Re: [Histonet] Personel

2016-11-28 Thread Jesus Ellin via Histonet
Like I stated there is a lot out there and I agree with you all interpretation 
of this can vary,, but again our world is changing and I hope our powers at be 
are being the advocate for these issues,, cause we then are forces to make the 
interpretations, which I get it we are again asking the Pathologist to do,, but 
this section in under General Quality Control,, not at all added to the 
report,, the report itself has this designated as well in that section as well 
as the section for predictive markers,, So again you can see the confusion and 
ambiguity of this situation.  We need those advocates to make this clear for us 
for sure

-Original Message-
From: Willis, Donna G. [mailto:donna.wil...@bswhealth.org] 
Sent: Monday, November 28, 2016 8:25 AM
To: Jesus Ellin; Morken, Timothy; Jennifer Valentine-Williams
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Personel

My interpretation of this is that for AP the "test" is the reporting of the 
results.  What is done in the Histology lab to prepare the slides is the 
pre-analytical portion of the test.  

For the revised ANP. 21395 the pathologist is mentioning in the report the 
results of the controls therefore it is in concurrent with the report.  We 
still check our results before taking the slides to the pathologist.

Donna Willis, HT/HTL(ASCP)
Anatomic Pathology Manager

Baylor University Medical Center
3500 Gaston Ave|Dallas, Texas  75246
214-820-2465 office|214-725-6184 mobile
BaylorScottandWhite.com

-Original Message-----
From: Jesus Ellin via Histonet [mailto:histonet@lists.utsouthwestern.edu] 
Sent: Monday, November 28, 2016 8:04 AM
To: Morken, Timothy; Jennifer Valentine-Williams
Cc: Histonet
Subject: [EXTERNAL] Re: [Histonet] Personel

I hope that everyone had a great weekend and a good thanksgiving,, 

Just to shed some light on the subject on the matter to have things in 
perspective,  when I called CAP and here is what the Rep shared with me,  it 
wasn't the interpretation  or the result but rather the QA/QC of the result.  
See below:  now here is the rub on this, as a person doing Special Stains, IHC, 
Digital Path and ISH,,  we as TECH's QA/QC before we hand into the Pathologist, 
our controls are supposed to be reviewed by the tech to make sure the reaction 
took  place, we don't say it looks brown, or red, or hey the colorful,, WE 
confirm the reaction, cause if not we redo.  This is what ALSO the CAP states 
that we do because it does say Pathologist or Designee , and it's the QA/QC 
step.  By no means are we resulting or giving Diagnosis/interpretation.  This 
is where I am having trouble with this statement, about 
testing/interpretation,, it has nothing to do with that at all.  CLIA also 
doesnt define QA/QC , just resulting/interpretation.

They are the same Steps that are being followed on digital path, were imaging 
of the slides require a person of High Complexity testing to be doing the 
scanning.  Again this is another QA/QC step, so I get all the stuff about CLIA 
and reporting, but CAP is specific and we are doing the QA/QC of this testing.

I also had a conversation about whether Licensure was acceptable or not,,  
without meeting the requirements, and I was told NO,, they need to meet the 
minimum requirements as stated in CLIA for high complexity testing,, again 
something to look at.

I then called ASCP to ask them about where they stood with this and was told we 
only do the licensure not the regs.

I called CMS to get a better understanding stating the issue, as for them the 
person interpreting and reporting is the Pathologist, but if CAP requires that 
the QA/QC be done with those regs,, then that is more than is required, but 
that is their regulation and to be adhered too.

Funny thing then when you go the CLIA website you get the high complexity 
testing, you can see where the testing methodologies are and can see when the 
test system came about. 

I know this is going to be a debatable situation and I have to agree with Tim,, 
please standardize and let us know,, but it is clear what they are saying about 
results, testing , interpretation and now QA/QC..  

Thoughts anyone,, but I see that this is going to change histology as a whole, 
since now this is being added too the mix.  I am not saying it is right or 
wrong,, but it does put forth effort that we need to classify what we do and 
also try to align the test system accordingly, because QA/QC is almost 
everything,, you can put this on instrumentation, protocols, procedures, etc.  

Also what do we do with those that have been doing this for years,, that have 
the knowledge and also the background,, again I don't wish to open up PANDORA's 
box,, I also know we are all going to look at this differently,, but the facts 
are we are changing and if we do not own the processes we currently do, someone 
else will that's for sure.

Jesus Ellin



**REVISED** 08/17/2016
ANP.21395 Special Stains/Studies Phase II For spec

Re: [Histonet] Personel

2016-11-28 Thread Jesus Ellin via Histonet
I hope that everyone had a great weekend and a good thanksgiving,, 

Just to shed some light on the subject on the matter to have things in 
perspective,  when I called CAP and here is what the Rep shared with me,  it 
wasn't the interpretation  or the result but rather the QA/QC of the result.  
See below:  now here is the rub on this, as a person doing Special Stains, IHC, 
Digital Path and ISH,,  we as TECH's QA/QC before we hand into the Pathologist, 
our controls are supposed to be reviewed by the tech to make sure the reaction 
took  place, we don't say it looks brown, or red, or hey the colorful,, WE 
confirm the reaction, cause if not we redo.  This is what ALSO the CAP states 
that we do because it does say Pathologist or Designee , and it's the QA/QC 
step.  By no means are we resulting or giving Diagnosis/interpretation.  This 
is where I am having trouble with this statement, about 
testing/interpretation,, it has nothing to do with that at all.  CLIA also 
doesnt define QA/QC , just resulting/interpretation.

They are the same Steps that are being followed on digital path, were imaging 
of the slides require a person of High Complexity testing to be doing the 
scanning.  Again this is another QA/QC step, so I get all the stuff about CLIA 
and reporting, but CAP is specific and we are doing the QA/QC of this testing.

I also had a conversation about whether Licensure was acceptable or not,,  
without meeting the requirements, and I was told NO,, they need to meet the 
minimum requirements as stated in CLIA for high complexity testing,, again 
something to look at.

I then called ASCP to ask them about where they stood with this and was told we 
only do the licensure not the regs.

I called CMS to get a better understanding stating the issue, as for them the 
person interpreting and reporting is the Pathologist, but if CAP requires that 
the QA/QC be done with those regs,, then that is more than is required, but 
that is their regulation and to be adhered too.

Funny thing then when you go the CLIA website you get the high complexity 
testing, you can see where the testing methodologies are and can see when the 
test system came about. 

I know this is going to be a debatable situation and I have to agree with Tim,, 
please standardize and let us know,, but it is clear what they are saying about 
results, testing , interpretation and now QA/QC..  

Thoughts anyone,, but I see that this is going to change histology as a whole, 
since now this is being added too the mix.  I am not saying it is right or 
wrong,, but it does put forth effort that we need to classify what we do and 
also try to align the test system accordingly, because QA/QC is almost 
everything,, you can put this on instrumentation, protocols, procedures, etc.  

Also what do we do with those that have been doing this for years,, that have 
the knowledge and also the background,, again I don't wish to open up PANDORA's 
box,, I also know we are all going to look at this differently,, but the facts 
are we are changing and if we do not own the processes we currently do, someone 
else will that's for sure.

Jesus Ellin



**REVISED** 08/17/2016
ANP.21395 Special Stains/Studies Phase II
For special stains, including histochemical stains, and studies using 
immunologic and
ISH methodology, positive and negative controls are verified and recorded as 
acceptable
prior to or concurrent with the reporting of patient results and records 
maintained.

NOTE: Controls must be verified and recorded as acceptable by a pathologist or 
designee
(provided the designee meets high complexity testing qualifications).

Positive tissue controls must contain the component specific to the special 
stain that is being
applied to the specimen.
Immunohistochemical tests using polymer-based detection systems (biotin-free) 
are sufficiently
free of background reactivity to obviate the need for a negative reagent 
control and such controls
may be omitted at the discretion of the laboratory director following 
appropriate validation.
If interpretation of the special stain or study is performed by a different 
laboratory, there must
be a procedure for the laboratory performing the stain or study to verify the 
acceptability of
the controls before transfer, if the controls are not sent with the patient 
slides (regardless of
the outside laboratory's accrediting organization). Records of this 
verification must be readily

ANP.23041 Testing Personnel Qualifications Phase II
Personnel who are responsible for evaluating or accepting the imaging system 
data are
qualified as high-complexity testing personnel.
NOTE: The qualifications to perform high complexity testing can be accessed 
using the following
link: CAP Personnel Requirements by Testing Complexity.
available to the laboratory performing the interpretation.

-Original Message-
From: Morken, Timothy [mailto:timothy.mor...@ucsf.edu] 
Sent: Wednesday, November 23, 2016 5:12 PM
To: Jennifer Valentine

Re: [Histonet] Personel

2016-11-22 Thread Jesus Ellin via Histonet
I am going to attach the information where you can find what is high complexity 
testing as defined by CLIA,, also CAP defines the QA/QC of this process to be 
the high complexity ,, also the antibody workup,,   here is the website where 
you can get this information from.   Again if you look at the CAP regs its 
states there the QA/QC as high complexity,,  We can cut pull controls, place on 
machine and run,, but we can not Qa/QC reaction,, weird huh.

On another note the inspector stated that the grandfather clause is good for 
those testing methologies and test that were pre 1997,,  so if still doing same 
testing after 1997 then good to go,, if test have changed for instance 
predictive markers, testing kits that are defined by the link I sent you ,, 
then they are not eligible unless they meet those requirments.

Your thoughts 

Jesus Ellin 


http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCLIA/Search.cfm

-Original Message-
From: Morken, Timothy [mailto:timothy.mor...@ucsf.edu] 
Sent: Tuesday, November 22, 2016 11:17 AM
To: Jesus Ellin
Cc: Histonet
Subject: RE: Personel

Jesus, that is very interesting information. 

Does anyone know of any CAP accreditation documents that state explicitly  that 
IHC slide staining is high complexity? I have not seen any. If anyone has those 
documents I'd like to see them. The only reference from CAP about that 
classification I have seen was in a Q session transcript from a CAP webinar 
on competency testing. The webinar had no information about IHC and complexity. 
However, a presenter answering a question about whether IHC staining at the 
bench is a high complexity "test," did state that IHC staining is high 
complexity so the techs doing the staining must have competency testing. Very 
strange!

That's not to say I don't think IHC is high complexity - I do, and so is every 
other test in histology. But under CLIA the testing personnel is the 
pathologist, not the bench tech. CAP can deem IHC bench testing as high 
complexity if it wishes (CLIA is a baseline and deemed accrediting agencies, 
and institutions, can have stricter requirements). But it seems the only way 
anyone can find out if CAP classifies IHC as high complexity is to call them 
and ask.

Your comment about new technology is interesting. In a modern scenario, which 
tech is the person who is "staining" the slide? And which of these is the "high 
complexity" part of the process?
1) person collating slides to stain
2) Person who programs the stainer
3) Person who dilutes the antibodies (still done!)
4) person who loads reagents on the stainer
5) person who loads the slides on the stainer
6) person who starts the stainer
7) person who unloads the slides from the stainer
8) person who labels and distributes the slides.
9) Person who checks QC slides (BTW, not a "test,").

In our lab these tasks are traded off by many different people throughout the 
day 

How about the person doing the validation of the stain? They are not doing a 
"test" but they are making the test possible to do.

Just some questions to ponder over the holidays!



Tim Morken
Pathology Site Manager, Parnassus
Supervisor, Electron Microscopy/Neuromuscular Special Studies Department of 
Pathology UC San Francisco Medical Center



-Original Message-
From: Jesus Ellin via Histonet [mailto:histonet@lists.utsouthwestern.edu] 
Sent: Tuesday, November 22, 2016 9:36 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Personel

So I know I am going to open Pandoras box,, but have people been paying 
attention to the Personal requirements from CAP.

I called the CAP and asked them about the criteria concerning Moderate or High 
complexity testing, after discussing with them the situations,   IF you have a 
tech that is Licensed and Also has a QIHC, but does not minimum requirement 
Defined by CLIA in education ,, they CAN NOT do any QA/OC of IHC and antibody 
work up,, as IHC is defined as High complexity testing.

I also asked about the test systems.  The grandfather clause is only good for 
test systems that occurred for those time periods.  For instance if CLIA 
defined the test system after those dates of 1997,, then they are not included 
and the person cannot perform test and technology created after those dates, 
since the testing was not in place during the grandfather clause time.  In a 
nut shell meaning if the IHC staining and antibody was developed after those 
dates,, you are not covered by the grandfather clause to do the testing ,, can 
some help clear this up,,

So any help on this matter will do

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[Histonet] Personel

2016-11-22 Thread Jesus Ellin via Histonet
So I know I am going to open Pandoras box,, but have people been paying 
attention to the Personal requirements from CAP.

I called the CAP and asked them about the criteria concerning Moderate or High 
complexity testing, after discussing with them the situations,   IF you have a 
tech that is Licensed and Also has a QIHC, but does not minimum requirement 
Defined by CLIA in education ,, they CAN NOT do any QA/OC of IHC and antibody 
work up,, as IHC is defined as High complexity testing.

I also asked about the test systems.  The grandfather clause is only good for 
test systems that occurred for those time periods.  For instance if CLIA 
defined the test system after those dates of 1997,, then they are not included 
and the person cannot perform test and technology created after those dates, 
since the testing was not in place during the grandfather clause time.  In a 
nut shell meaning if the IHC staining and antibody was developed after those 
dates,, you are not covered by the grandfather clause to do the testing ,, can 
some help clear this up,,

So any help on this matter will do

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Re: [Histonet] slide id

2014-10-05 Thread Jesus Ellin
We use the Sunquest PowerPath system,, it is completely Integrated and track 
almost all event within the facilities,, we are starting to look and track 
electronic assets, which are not new ideas but most systems out there are not 
designed with this in mind.  We can print off the assets number for old 
cassettes and slides so we can track in from older cases since the asset ID is 
created from one single database,,  with multiple databases there are issue  
with electronic assets,, this is an important  fact you must discuss with your 
APLIS and also any third party vendor,, this becomes even more complicated when 
you start talking about digital slides and electronic transactions . Good luck 
and keep going strong 


Jesus Ellin
Yuma Regional Medical Center 

Sent from my iPad

 On Oct 3, 2014, at 3:37 PM, Morken, Timothy timothy.mor...@ucsfmedctr.org 
 wrote:
 
 Brian, we use Copath ABT, not Vantage, but the principle is the same. We use 
 the old non-barcoded system for older block/slide sendouts. There is no way 
 to barcode old blocks, unless you want to enter it as a consult, and that 
 entails giving it a new number, which would just confuse things.
 
 It will take a few years but eventually we'll be sending out mostly barcoded 
 items. This is just one of the things you have to work with when changing 
 over to something new. 
 
 Tim Morken
 Supervisor, Histology, Electron Microscopy and Neuromuscular Special Studies
 UC San Francisco Medical Center
 San Francisco, CA
 
 CONFIDENTIALITY NOTICE: This email message, including any attachments, is for 
 the sole use of the intended recipient(s) and may contain confidential, 
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 the intended recipient, you may not use, copy, or distribute this email 
 message or its attachments. If you believe you have received this email 
 message in error, please contact the sender by reply email and destroy all 
 copies of the original message.
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cooper, Brian
 Sent: Friday, October 03, 2014 1:26 PM
 To: WILLIAM DESALVO; Rathborne, Toni
 Cc: Histonet@lists.utsouthwestern.edu; Tapper, Sheila J.
 Subject: RE: [Histonet] slide id
 
 How does Vantage work with blocks and slides that were in your institution 
 prior to the implementation of Vantage?  Suppose you needed to send materials 
 to another institution for further testing?  Do you generate new barcoded 
 labels and affix them to the materials prior to sending them out (for 
 tracking purposes)? 
 
 Thanks, 
 
 Brian
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of WILLIAM 
 DESALVO
 Sent: Friday, October 03, 2014 1:21 PM
 To: Rathborne, Toni
 Cc: Histonet@lists.utsouthwestern.edu; Tapper, Sheila J.
 Subject: Re: [Histonet] slide id
 
 Vantage works great. We use it to track all blocks and slides as they move in 
 and out of the core lab and in and out of archive. You must bar code and make 
 a decision on cassette printers. Techs scan their own bar code to log on the 
 system.
 
 Sent from my iPhone
 
 On Oct 3, 2014, at 1:17 PM, Rathborne, Toni toni.rathbo...@rwjuh.edu wrote:
 
 How do you like Vantage? Have you experienced any problems with it, and is 
 it easy to use?
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
 WILLIAM DESALVO
 Sent: Friday, October 03, 2014 4:02 PM
 To: Tapper, Sheila J.
 Cc: Histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] slide id
 
 We use Vantage Quality and Tracking system and the tech is captured 
 for embedding, microtomy and staining
 
 Sent from my iPhone
 
 On Oct 3, 2014, at 12:55 PM, Tapper, Sheila J. 
 sheila.tap...@essentiahealth.org wrote:
 
 We have our techs fast process the slides that they cut - so the tech is 
 documented in the processing history... same for embedding. 
 
 Sheila
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mike 
 Pence
 Sent: Friday, October 03, 2014 2:51 PM
 To: 'anita'; Histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] slide id
 
 We do.
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of anita
 Sent: Friday, October 03, 2014 2:50 PM
 To: Histonet@lists.utsouthwestern.edu
 Subject: [Histonet] slide id
 
 just wondering if techs are putting their id on the slides that they cut, 
 that way if a mistake is made with labeling the tech that cut it is 
 identified.
 
 thanks for your input,
 
 anita dudley
 
 providence hosp
 
 mobile alabama 
 
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[Histonet] RE: Pathology Report Templates

2014-04-25 Thread Jesus Ellin

This is for the MU (meaningful use)
-Original Message-
From: Mike Pence [mailto:mpe...@grhs.net] 
Sent: Friday, April 25, 2014 6:00 AM
To: Jesus Ellin; 'Victor A. Tobias'; histonet@lists.utsouthwestern.edu
Subject: RE: Pathology Report Templates

I went through all my CAP check list questions and I do not see this anywhere.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jesus Ellin
Sent: Thursday, April 24, 2014 12:54 PM
To: 'Victor A. Tobias'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Pathology Report Templates

This is a fact, to meet compliance the signing facility needs to be ID along 
with the CLIA#, ,haven't heard about the medical director issue, but who knows

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Victor A. Tobias
Sent: Thursday, April 24, 2014 10:51 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Pathology Report Templates

One of our facilities had a CAP inspection last week and I was asked to add the 
CLIA# and Medical Director to the template, immediately. Is this something new, 
as we had our CAP inspection last Aug. and there was no mention about CLIA# or 
having the Director's name on the templates?

I haven't been able to get any follow-up from the lab supervisor.

Victor Tobias HT(ASCP)
Clinical Applications Analyst
Harborview Medical Center
Dept of Pathology Room NJB244
Seattle, WA 98104
vtob...@u.washington.edumailto:vtob...@u.washington.edu
206-744-2735
206-744-8240 Fax
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[Histonet] RE: Pathology Report Templates

2014-04-24 Thread Jesus Ellin
This is a fact, to meet compliance the signing facility needs to be ID along 
with the CLIA#, ,haven't heard about the medical director issue, but who knows

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Victor A. Tobias
Sent: Thursday, April 24, 2014 10:51 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Pathology Report Templates

One of our facilities had a CAP inspection last week and I was asked to add the 
CLIA# and Medical Director to the template, immediately. Is this something new, 
as we had our CAP inspection last Aug. and there was no mention about CLIA# or 
having the Director's name on the templates?

I haven't been able to get any follow-up from the lab supervisor.

Victor Tobias HT(ASCP)
Clinical Applications Analyst
Harborview Medical Center
Dept of Pathology Room NJB244
Seattle, WA 98104
vtob...@u.washington.edumailto:vtob...@u.washington.edu
206-744-2735
206-744-8240 Fax
=
Privileged, confidential or patient identifiable information may be contained 
in this message. This information is meant only for the use of the intended 
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[Histonet] Molecular tests

2013-11-20 Thread Jesus Ellin
I would like two pose a questions out there on histonet.  How is everyone 
handling the ordering of the molecular testing within their facility, through 
an electronic EMR?  How are you keeping track of proper test utilization of 
this testing?

Thanks to all for your help

Jesus Ellin
Yuma Regional Medical Center

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[Histonet] RE: Anyone using Section Transfer System by Microm?

2013-11-14 Thread Jesus Ellin
I would also like to know

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Thursday, November 14, 2013 9:55 AM
To: Histonet
Subject: [Histonet] Anyone using Section Transfer System by Microm?

Is anyone using the Thermo/Microm Secton Transfer System on their microtome?


http://cellab.se/pdfbroschyr/Microm/STS.pdf

I'd like to get some input for using it to cut serial sections of microarrays.

Thanks!

Tim Morken
Supervisor, Electron Microscopy and Neuromuscular Special Studies UC San 
Francisco Medical Center Box 1656
505 Parnassus Ave
San Francisco, CA 94143
USA

415.353.1266  (office)
tim.mor...@ucsfmedctr.orgmailto:tim.mor...@ucsfmedctr.org


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RE: [Histonet] Specimen Tracking Systems

2013-11-01 Thread Jesus Ellin
I would like to chime in on this Bill and Tim both gave great examples of what 
it takes to move in this direction.  But I would also like to understand why 
there are so many challenges in getting the data back into the APLIS with 
updates and orders.   I would tell people the biggest concern that I have the 
data being produced by a system should be accessible across all gradients of 
the workflow and not just the unique tracking system.  Not only is this 
tracking system positioned to help out histology with what is being explained 
below, but it is the foundation work in taking steps to get to the next level 
when talking Digital Pathology, molecular, Personalized medicine,  Pathologist 
cockpit, and algorithm analysis.

With the looming cuts coming down the pike, we have to make sure the vendors 
understand we cannot have barriers when it comes to interface and 
interoperability with our system.  At the same token we cannot be charges an 
arm, leg and torso for interfacing what is rightfully ours and that is the 
patients data we produce.

Bill and Tim excellent job in giving a crash course in Tracking system 101,, I 
do believe we should see more of this explained at professional societies 
meeting and also what the new environments we are going to be working in 
because of this technology.  

Just my two cents

Jesus Ellin


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Thursday, October 31, 2013 3:45 PM
To: 'WILLIAM DESALVO'; Matthew D. Roark; histonet
Subject: RE: [Histonet] Specimen Tracking Systems

I agree with Bill on this. We have Cerner Copath Plus and looked at Cerebro, 
Vantage and Omnitrax. Only Cerebro and Vantage were capable of working with 
Copath. But the problem is that Copath requires you purchase their tracking 
system to use as an HL-7 interface to any third party system. AND there is not 
two-way communication between the systems. You MUST enter orders (cases, 
blocks, stains) in copath and it ports orders to the other system. The only 
feedback is status updates to copath - you cannot add items in the other system 
and expect them to show up in copath. That requirement effectively doubled the 
price of the system. So we are using only the Copath ABT system, which we are 
starting to implement now. They will finally have touch screen capability in 
the spring so we were satisfied with that. Touch screens were a primary spec we 
demanded. 

The key to tracking is how the tracking system works with your current LIS. Can 
it communicate in a true bi-directional fashion? Is it just an add on and all 
the tracking info is in the tracking component, not the LIS? There are 
tradeoffs and you need to figure out which you want to live with.

We spent two years investigating all these systems, doing site visits, and 
going through a 6-month total LEAN evaluation. The one thing every institution 
told us was: LEAN your system BEFORE adding barcoding.  Barcoding will NOT fix 
any inefficiencies you have. And you are pretty much stuck with what ever 
system you barcode - warts and all. So do all the hard work up front. 

We thought we were prepared but are daily finding all kinds of little details 
that have to be worked out. Detail out every single little thing about all your 
workflows before starting anything. Streamline everything.

Cassette printing is the heart of barcoding. The barcoded (actually usually 2D 
matrix codes) on the cassette drive grossing, tracking through processing, 
embedding and cutting. If that does not work reliably your system will not 
work. 

We went with Leica cassette printers. They are huge, but fast (5 sec per cass). 
We were going to use thermo, but they had their printhead problem and we 
dropped the order. They are 20+ seconds per cassttes, tho have a very compact 
footprint. You will find there are tradeoffs to everything.

Slide labeling is the other half of the equation. They must be reliable and 
survive all histology procedures. 

We will use thermal transfer label printers rather than direct slide (too 
expensive- we will have a printer at each microtome- and cumbersome to change 
out slide types). Slide labeling is a HUGE deal - you have to be sure it works 
for everything and can be used in your immuno stainers and coverslipping 
machines. We are using either Brady StainerBondz labels or LabTags Xylituff 
labels. These were the only ones that had the size we wanted (23 x 19 mm) and 
survived all processes. General data StainerShield are also good, but only come 
in 22 x 22 size. Plus are the most expensive.

You will find it much easier if you use labels and ribbons from one 
manufacturer, designed to use with specific printers. That simplifies a lot of 
the effort. We have tried to mix and match but it is very difficult because all 
manufacturers do not make matching labels and ribbons for all printers. 



Tim Morken

RE: [Histonet] Specimen Tracking Systems

2013-11-01 Thread Jesus Ellin
We scan in at the point of accessioning and do one piece flow. As Tim stated, 
even though the APLIS and technology can do certain things, it is only as good 
and streamlined as the process and people behind it.  

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Friday, November 01, 2013 9:50 AM
To: 'Michael Mihalik'; 'histonet'
Subject: RE: [Histonet] Specimen Tracking Systems

Michael, yes that is the sort of workflow item that has to be considered. We 
plan to use the scanned image at the gross bench to double check. 

Tim Morken
Supervisor, Electron Microscopy and Neuromuscular Special Studies UC San 
Francisco Medical Center San Francisco, CA


-Original Message-
From: Michael Mihalik [mailto:m...@pathview.com]
Sent: Friday, November 01, 2013 9:47 AM
To: Morken, Timothy; 'Bauer, Karen L.'; 'Jesus Ellin'; 'WILLIAM DESALVO'; 
'Matthew D. Roark'; 'histonet'
Subject: RE: [Histonet] Specimen Tracking Systems

Just a quick thought

If you scan your requisition into the LIS after accessioning, it might not be a 
bad idea to have your grossing personnel review the requisition at grossing to 
confirm that the patient name/specimen on the paperwork matches
what's in the LIS.   Yes, with barcodes this shouldn't happen, but it's a
nice double check.

Michael Mihalik
PathView Systems | cell: 214.733.7688 | 800.798.3540 | fax: 952.241.7369


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Friday, November 01, 2013 9:23 AM
To: 'Bauer, Karen L.'; 'Jesus Ellin'; 'WILLIAM DESALVO'; 'Matthew D. Roark'; 
'histonet'
Subject: RE: [Histonet] Specimen Tracking Systems

Karen, we are going to move to a system as you describe. At accessioning all 
paperwork will be scanned and none will follow the specimen. The critical trick 
is getting residents and pathologists to look at screens rather than hard 
copies. We spend way too much time printing and collating hard copies of 
reports ever day.

Tim Morken
Pathology
UC San Francisco Medical Center
San Francisco, CA


-Original Message-
From: Bauer, Karen L. [mailto:bauer.ka...@mayo.edu]
Sent: Friday, November 01, 2013 9:03 AM
To: Morken, Timothy; 'Jesus Ellin'; 'WILLIAM DESALVO'; 'Matthew D. Roark'; 
'histonet'
Subject: RE: [Histonet] Specimen Tracking Systems
Importance: Low

Jesus, Tim, and Bill...  Wonderful communication about specimen tracking, 
bi-directional capabilities, and creating a histology lab that will be 
effective in the years to come!!  I loved reading your information!

We also have the Vantage system and it's helped us decrease our slide labeling 
error rate to 0%!  It's wonderful and I'm so glad we finally had it implemented 
last April.  Our workflow seems much more efficient, since we no longer have to 
perform all of those manual reconciliation steps.

Yes, the bi-directionality of the systems (we have Sunquest CoPath) is a 
downfall of the software, but the pros of Vantage outweighed that flaw.  I'm 
hoping that in the years to come, that will be fixed.


A new question for the Histo group... 

We are trying to get away from printed grossing working drafts that are 
submitted with the slides and delivered to the pathologists.  We would like the 
docs to scan the slide at their microscope and have the patient information 
show up on their computer.  The pathologists still want the paper requisition 
from the specimen, so I suggested to have the requisition scanned and attached 
in the digital format.  This way, when the doc scans the slide, the CoPath 
working draft, the patient clinical hx, and the scanned req slip can be viewed.

Is anyone doing this in their lab right now?  If so, I would really like to 
hear more about how you and your LIS made that happen.  

Thanks so much and Happy Friday!:)

Karen

Karen L. Bauer HTL/HT (ASCP) | Histology Supervisor | Pathology | MOHS Lab 
Supervisor | Dermatology | Phone: 715-838-3205 | bauer.ka...@mayo.edu | Mayo 
Clinic Health System | 1221 Whipple Street | Eau Claire, WI 54702 | 
mayoclinichealthsystem.org

 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Friday, November 01, 2013 10:06 AM
To: 'Jesus Ellin'; 'WILLIAM DESALVO'; Matthew D. Roark; histonet
Subject: RE: [Histonet] Specimen Tracking Systems

Jesus, the topic of bi-directional interfaces is fraught with both technical 
and political issues. Technically it is certainly possible (As a software 
developer colleague of mine always told us - 'don't ask if I can do it, just 
tell me what you want. It's just software'). The issue is who pays for it, and 
who wants it. As I see it, the large LIS companies got caught flat-footed by 
the desire of histology labs to move to barcoding. Indeed, when

[Histonet] RE: Pathology charges

2013-10-09 Thread Jesus Ellin
I did not know this was going on,,  where is this being stated at

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Maray Weirauch
Sent: Wednesday, October 09, 2013 9:13 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Pathology charges

We've been told that before our pathologists can order/run any of these stains 
(CPT 88313, 88342 or 88360) on our pathology specimens, we must obtain a 
pre-authorization from the insurance carrier or the payment will be denied.
Has anyone else run into this?  How are you efficiently handling that?

Maray Weirauch
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RE: [Histonet] Unregistered HT

2013-09-11 Thread Jesus Ellin
Tim Well said

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Wednesday, September 11, 2013 8:54 AM
To: Histonet
Subject: RE: [Histonet] Unregistered HT

This discussion comes up every year and, of course is never resolved to our 
satisfaction because histotechs  really have only a little say in it. 

Personally I think labs are better off with certified techs. Uncertified techs 
should start as lab assistants and earn their certification before getting a 
histotech title.  The histotech title should be for someone who at least starts 
as a general histotech who can do the gamut of histology work - embedding, 
cutting, HE, specials and IHC/ISH. From that base they can branch out or 
specialize. It would be a dream to require formal schooling, as with med techs, 
but there are so few schools that it is just impractical. A certification is a 
baseline that shows a person who is OJT has learned the minimum required to 
understand histotechnology.

However, because we don't report out any results on our own authority there is 
no impetus for a pathologist or institution to make the position more than it 
is: a technical position that does do require fancy work, but in the end only 
provides the materials for someone else to use for interpretation, decisions 
and reporting. We don't even pick the sample, the test or even determine how to 
do the test - that is all determined by the Technical Director of the lab, 
usually a board certified pathologist. Our primary job is to provide good 
quality materials so they can do their job well. That does involved a lot of 
knowledge, organization and skill, but it is not at the level of making actual 
patient care decisions. 

Pathologists Assistants get a  bit more respect because they are required to 
make judgment decisions on how to sample a particular case. Even then, that 
sampling is strictly detailed in procedures developed by pathologists. 

The most we could ask for is licensing that requires certain qualifications to 
be a histotech. However, that has some drawbacks as well, namely the 
restriction of the profession to licensed people, and so is a barrier to entry. 
Would it lead to pay raises? Does anyone have studies showing pay before and 
after licesure requirements?  It is questionable whether it enhances the 
quality of the lab since most histotechs are OJT anyway, and simple licensure 
may not increase actual quality of work by an individual. (does anyone know of 
any studies that look at quality in states with and without licensing?).

The CLIA requirements at least set a baseline for education, if not actual 
certification. Asking pathologists to support universal certification and/or 
licensure is problematic - many independent labs won't support that because, as 
in licensure, it decreases the pool and increases costs (ie, pay). Since the 
pathologist is the person deemed responsible for quality and lab results, 
setting the bar higher is only in the interests of the technologists, not the 
pathologist. Now, some enlightened pathologists understand that better-educated 
and better-trained techs are good for the overall.

So in the end the histotech community, along with a few enlightened 
pathologists have to lobby for anything they want. But what is that? Increased 
pay? More say in lab operations?

My experience is that you can rise as high as you want if you take 
opportunities that come up. But that may mean either spending many years in one 
place slowly moving up, or moving around to take other opportunities. It will 
depend on the individual. In either case using your time in the lab to learn 
whatever there is to learn, even in other departments, or on various 
committees, pays off in the long run. And that includes management. The last 
thing you should do is limit yourself to a job description someone gives you. 
Take that as the base line, not the limit.  


Tim Morken
Supervisor, Electron Microscopy/Neuromuscular Special Studies Department of 
Pathology UC San Francisco Medical Center




-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Horn, Hazel V
Sent: Wednesday, September 11, 2013 6:30 AM
To: 'Weems, Joyce K.'; 'Jennifer MacDonald'; Marcum, Pamela A
Cc: histonet@lists.utsouthwestern.edu; histonet-boun...@lists.utsouthwestern.edu
Subject: RE: [Histonet] Unregistered HT

Histology does not get the respect or the recognition because histologists do 
not report results.  All of the complex testing we do is overlooked because the 
pathologists report the results.   CLIA standards are based on result 
reporting.   The CAP has looked the other way for years because pathologists 
would hire unregistered techs.  If pathologists would demand only registered 
techs half our battle would be won. 

Hazel Horn
Supervisor of 

Re: [Histonet] PowerPath Issues

2013-06-28 Thread Jesus Ellin
Donna this is Jesus Ellin and I am the Sunquest POwerPath Chair,, I am cc 
Debbie Balli on this,, how can we help?

Sent from my iPad

On Jun 28, 2013, at 1:58 PM, Willis, Donna G. donna.wil...@baylorhealth.edu 
wrote:

 Anyone out there in Histoland having issues with PowerPath (Sunquest) 
 customer service?
 
 Thanks,
 
 Donna Willis, HT/HTL (ASCP)
 Anatomic Pathology Manager
 Baylor University Medical Center-Dallas
 ph. 214-820-2465 office
 ph. 214-725-6184 mobile
 donna.wil...@baylorhealth.edu
 
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[Histonet] RE: Epic and PowerPath

2013-06-25 Thread Jesus Ellin
We use EPIC and PowerPath,, how can I help you... 

Jesus Ellin
Yuma Regional Medical Center 
928-336-1743
jel...@yumaregional.org



From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] on behalf of Tasha Fraser 
[tfra...@olympicmedical.org]
Sent: Tuesday, June 25, 2013 10:42 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Epic and PowerPath

Does anyone out there use Epic and PowerPath together?



Tasha R. Fraser, HT (ASCP)

Olympic Medical Center

939 Caroline Street

Port Angeles, WA 98362


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RE: [Histonet] Monitoring Histology Quality

2013-05-07 Thread Jesus Ellin
We use Sunquest PowerPath to electronically show this information as well as 
keep records for data minning and Quality improvement

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Roger Heyna
Sent: Tuesday, May 07, 2013 10:44 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Monitoring Histology Quality

Is anyone using an electronic system to communicate histology quality info from 
the pathologists to Histology management? Also, do you use this same system to 
demonstrate to the CAP that histology quality is being checked daily, and if 
so, how do you indicate that slide quality was checked when there are no 
quality issues on a given day?
 
We operate in Sunquest CoPath.
 
Thank you,
 
Roger Heyna
Histology Supervisor
Maywood, IL

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[Histonet] RE: Ventana Melanoma Cocktail

2013-04-03 Thread Jesus Ellin
You can only bill for 1

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
stephen.cla...@hcahealthcare.com
Sent: Wednesday, April 03, 2013 10:45 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] Ventana Melanoma Cocktail

I've got a question regarding Ventana's Melanoma Cocktail.  We've never done 
double or triple staining at our institution so my knowledge of the CPT codes 
for this is vague.  If we were to use this product, which has HMB-45, 
Tyrosinase, and Mart-1 in one dispenser, do I bill it as an 88342 three times?  
Or is there a separate CPT code that we would use?  Thanks for your input.

Steve Clark
Pathology Dept. Supervisor
Grand Strand Regional Medical Center
843-692-1486 Lab
843-692-1459 Desk
stephen.cla...@hcahealthcare.com

 [cid:image001.gif@01C9DADA.65BB9E10]



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Re: [Histonet] Validation of Her2

2013-03-19 Thread Jesus Ellin
What did you do to evaluate your system and algorithms.   Also the cases of ER 
and PR. Negative vs Postive concordance. 

Sent from my iPad

On Mar 19, 2013, at 4:57 PM, Vickroy, Jim vickroy@mhsil.com wrote:

 
 We are working on validating HER 2 testing in our laboratory.  I see that the 
 guidelines state that we should use 25 - 100 cases to complete our validation.
 In the past we sent our Her2 IHC testing to Clarient and they performed the 
 technical testing and then our pathologists would do the scoring.  So for 
 validation we used 25 of the cases we sent to Clarient and then did them in 
 house to compare.   Our comparison was nearly 100%.  Here is my question:
 
 Clarient uses the DAKO method while we are using Ventana's antibody Pathway 
 (4B5).   The validation guidelines state parallel by identical method in 
 another lab with the same validated assay is also acceptable.  Can I assume 
 that this means comparison with another lab for IHC HER2 testing and does not 
 have to be using the same clone (DAKO vs Ventana)?
 
 Jim
 
 James Vickroy BS, HT(ASCP)
 
 Surgical  and Autopsy Pathology Technical Supervisor
 Memorial Medical Center
 217-788-4046
 
 
 
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Re: [Histonet] High complexity test

2013-02-06 Thread Jesus Ellin
I would say this is high complexoty testing and the tech performing this has to 
have knowledge of the process and troubleshooting in case there is issues with 
the results.  I do not agree with the interpretation some people give,, but 
this is based on individual institutions 

Sent from my iPad

On Feb 6, 2013, at 2:05 PM, Rene J Buesa rjbu...@yahoo.com wrote:

 This issue has been discussed at length recently (please go to HistoNet 
 files).
 The complexity does not deals with the actual test but with the ability 
 of the technician to go above and beyond the robotic tasks but also able to 
 think and apply knowledge when something goes wrong.
 Sometimes dismissal of complexity is rooted on the desire in management to 
 pay less for tasks that require a higher licensure grade.
 René J. 
 
 From: Sara Baldwin/mhhcc.org sbald...@mhhcc.org
 To: histonet@lists.utsouthwestern.edu 
 Sent: Wednesday, February 6, 2013 2:54 PM
 Subject: [Histonet] High complexity test
 
 Hi histonetters
 Is ventana Ultra IHC only doing antibodies no FISH or CISH is this considered 
 High complexity testing?  We are doing ER/PR and some others.
 
 Thanks
 Histology/Cytology Supervisor
 S. Kathy Baldwin, SCT (ASCP)
 Memorial Hospital and Health Care Center
 sbald...@mhhcc.org
 Ph 812-996-0210, 0216, Fax 812-996-0232, 
 Pager 812-481-0897, Cell 812-887-3357
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RE: [Histonet] problem with 88305 reimbursement

2013-01-29 Thread Jesus Ellin
How is this if the biopsy procedure is being done at the physician's facility?  
I have heard though this is just the start of including the biopsy within the 
DRG if it comes back with positive for cancer,, but once again this is a hear 
say.  This is also to include any testing for IHC, ISH, or molecular testing.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cynthia Pyse
Sent: Tuesday, January 29, 2013 11:51 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] problem with 88305 reimbursement

Hi Histonetters

We are currently having a problem with our Medicare reimbursement on the tech 
component of the 88305. If the patient has been seen at a hospital, either 
in-patient or out- patient, we are told by Medicare that we have to contract 
with that hospital to bill for the 88305. The biopsy was not done at the 
hospital but in a doctor's office. According to Medicare if there the same date 
of service it can only be billed through the hospital. Medicare is calling it 
consolidated billing. I can't see how the hospital can bill for something that 
was done in the doctor's office then sent to an independent lab. Is anyone else 
having this problem? How are you handling it with Medicare? Any help would be 
appreciated. Thanks in advance

Cindy

 

 

Cindy Pyse, CLT, HT (ASCP)

Laboratory Manager

X-Cell Laboratories

20 Northpointe Parkway Suite 100

Amherst, NY 14228

716-250-9235 etx. 232

e-mail cp...@x-celllab.com

 

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[Histonet] RE: CAP guideline for fixation time

2013-01-07 Thread Jesus Ellin
We have it documented within the APLIS, when the order is placed within our 
EMR,, for requisitions we have them document them on the requisition at the 
time it is taking place with a sticker,, but since the most of our orders are 
electronic it is part of the workflow, this is done for all specimens as we see 
the importance of other biomarkers for future

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems, Joyce K.
Sent: Monday, January 07, 2013 11:00 AM
To: 'Victor A. Tobias'; 'histonet'
Subject: [Histonet] RE: CAP guideline for fixation time

Our OR and Breast Health staff have done pretty well getting on board with 
this. We rarely have one that hasn't been documented.



We have a place on the requisition (located just under the date field so they 
will see it) where time out of body (for the cold ischemic time), and time into 
formalin is documented. Then we document the rest on the requisition and the 
pathologist takes it from there.







Joyce Weems

Pathology Manager

678-843-7376 Phone

678-843-7831 Fax

joyce.we...@emoryhealthcare.org







www.saintjosephsatlanta.org

5665 Peachtree Dunwoody Road

Atlanta, GA 30342



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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Victor A. Tobias
Sent: Friday, January 04, 2013 6:21 PM
To: 'histonet'
Subject: [Histonet] CAP guideline for fixation time



Per CAP guideline, in our reports of predictive markers(ER/PR/Her2), 
Pathologists need to check that the total fixation time of specimens is within 
the CAP guideline. Is this information readily available to the pathologists at 
the time of writing the report? How are others documenting this?



Have a great weekend.



Victor



Victor Tobias HT(ASCP)

Clinical Applications Analyst

Harborview Medical Center

Dept of Pathology Room NJB244

Seattle, WA 98104

vtob...@u.washington.edumailto:vtob...@u.washington.edumailto:vtob...@u.washington.edu%3cmailto:vtob...@u.washington.edu

206-744-2735

206-744-8240 Fax

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[Histonet] RE: Meaningful Use-Pathology

2012-11-07 Thread Jesus Ellin
Meaningful use is one aspect,, but most of the time you can not do this in EPIC 
in a fashion that will be able to be searchable and structured.  There are 
other ways of doing this, but most of the time this is a work around

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
jessica.va...@hcahealthcare.com
Sent: Wednesday, November 07, 2012 10:21 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Meaningful Use-Pathology

How is everyone addressing meeting meaningful use in regards to pathology, when 
a positive/negative or numeric value is looked at?
Objective:
Incorporate clinical lab test results into EHR as structured data.
Measure:
More than 40 percent of all clinical lab test results ordered by the eligible 
professional during the EHR reporting period whose results are either in a 
positive/negative or numerical format are incorporated in certified EHR 
technology as structured data.



Jessica Vacca
Epic Anatomic Pathology
Application Lead
HCA Clinical Services Group
2545 Park Plaza
Nashville, TN 32703
t: 615-579-0121
o: 615-344-5370
e: jessica.va...@hcahealthcare.com

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Re: [Histonet] Devasting news on 88305TC component--Where the $18 came from

2012-11-06 Thread Jesus Ellin
Well in this article it does have differences, especially when talking about 
usage of technology,, but non the less it does expose our state of being within 
Anatomic Pathology,, ,, what are peoples thought on this

Sent from my iPad

On Nov 6, 2012, at 12:21 PM, Lester Raff MD lr...@uropartners.com wrote:

 Sent: Tuesday, November 06, 2012 12:35 PM
 To: 'histonet-boun...@lists.utsouthwestern.edu'
 Subject: RE: [Histonet] Devasting news on 88305TC component--Where the
 $18 came from
 
 The $18.00 figure came from an article published in Archives of
 Pathology and Lab Medicine: 
 
 Pathology Economic Model Tool
 A Novel Approach to Workflow and Budget Cost Analysis in an Anatomic
 Pathology Laboratory
 David Muirhead, BSc; Patricia Aoun, MD, MPH; Michael Powell, MS, FASHP;
 Flemming Juncker, MBA; Jens Mollerup, MSc, PhD
 
 
 (Arch Pathol Lab Med. 2010;134:1164-1169)
 
 Thanks to Joe Plandowski of IOL for providing me with the reference.
 
 Lester J. Raff, MD
 Medical Director
 UroPartners Laboratory
 2225 Enterprise Dr. Suite 2511
 Westchester, Il 60154
 Tel 708.486.0076
 Fax 708.492.0203
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Webster,
 Thomas S.
 Sent: Monday, November 05, 2012 3:01 PM
 To: 'histonet@lists.utsouthwestern.edu'
 Subject: [Histonet] Devasting news on 88305TC component
 
 I wish there was a way to put a positive spin on this but  I can't think
 of any. We can only hope it kills off client billing somehow.
 
 Whomever the stakeholder was that told CMS a typical 88305 costs 18
 bucks, I'd love to know how he/she came up with that number. It's
 insultingly low.
 
 http://www.acla.com/sites/default/files/ACLA%20comments%202012%20PFS%20p
 roposed%20rule%208-30-11_3.pdf
 
 I believe whoever it was had the goal to stop the proliferation of POLs.
 Wouldn't surprise me if they worked for a large national lab that had
 lost a lot of business to POLs.
 
 
 
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RE: [Histonet] Devasting news on 88305TC component

2012-11-02 Thread Jesus Ellin
AMEN

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cristi Rigazio
Sent: Friday, November 02, 2012 9:32 AM
To: Brendal Finlay
Cc: histonet@lists.utsouthwestern.edu; Webster, Thomas S.
Subject: Re: [Histonet] Devasting news on 88305TC component

Political yet?!  Seriously!  52%, while the PC is increased 2%... But in case 
anyone wondered both candidates for President are looking for the middle class! 
 Unbelievable!

Sent from my iPhone

On Nov 2, 2012, at 8:28 AM, Brendal Finlay 
brendal.fin...@medicalcenterclinic.com wrote:

 http://www.cap.org/apps/cap.portal?_nfpb=truecntvwrPtlt_actionOverride=%2Fportlets%2FcontentViewer%2Fshow_windowLabel=cntvwrPtltcntvwrPtlt%7BactionForm.contentReference%7D=statline%2Fspecial_report_final_2013_physician_fee_schedule.html_state=maximized_pageLabel=cntvwr
 
 
 Brendal Finlay, HT (ASCP)
 Medical Center Clinic
 brendal.fin...@medicalcenterclinic.com
 850.474.8758
 http://medicalcenterclinic.com
 -Original message-
 From: Davide Costanzo pathloc...@gmail.com
 Date: Fri, 02 Nov 2012 10:09:18 -0500
 To: Webster, Thomas S. twebs...@crh.org
 Subject: Re: [Histonet] Devasting news on 88305TCcomponent
 
 That is devastating! Do you have a link to this information?
 
 Sent from my iPhone
 
 On Nov 2, 2012, at 4:53 AM, Webster, Thomas S. wrote:
 
 Devastating I meant
 
 
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RE: [Histonet] Histology Supervisor Opening

2012-10-25 Thread Jesus Ellin
What does this lab entail

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
Jessica-Prometheus
Sent: Thursday, October 25, 2012 7:39 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Histology Supervisor Opening

Hey Histonet!

 

Prometheus Healthcare is on the search for a Histology Supervisor for a
hospital in Connecticut! The ideal candidate will be HTL (ASCP), have at
least 3 years of leadership experience and about ten years of histology
experience. If you are interested, or know anyone who might be, please
contact me at the information below. Thank you!

 

Jessica Sanchez

Account Manager 

Prometheus Healthcare 

Office 301-693-9057

Fax 301-368-2478

 mailto:jess...@prometheushealthcare.com jess...@prometheushealthcare.com

 http://www.prometheushealthcare.com/ www.prometheushealthcare.com

 http://twitter.com/PrometheusBlog http://twitter.com/PrometheusBlog

 http://www.youtube.com/watch?v=ZxkF54CRhLc Click Here to Meet Me!

 

 

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[Histonet] FW: HT/HTL PROGRAM DIRECTORS SURVEY

2012-10-10 Thread Jesus Ellin
Please read this and I would like to know what peoples thoughts are about this 
issue.  Also take into consideration where we are head and also testing.  This 
is extremely interesting.


From: Robert Newberry
Sent: Wednesday, October 10, 2012 3:39 PM
To: Jesus Ellin
Subject: FW: HT/HTL PROGRAM DIRECTORS SURVEY
Importance: High


FYI

From: Julie Stiak [mailto:julie.st...@phoenixcollege.edu]
Sent: Tuesday, October 09, 2012 11:12 AM
To: algra...@email.arizona.edu; ghurf...@carondelet.org; jfille...@shc.org; 
joyce.h...@bannerhealth.com; lhi...@cgrmc.org; michelle.man...@mihs.gov; Amy 
Wendel Spiczka; Andy Burnette; Aprill Watanabe; Arthur Sitelman; 
barbara.blasutta; Bill Miller; Bob Wenham; Brian Stillwell; Dana Lake; Donna 
Vollmer; Ethel Macrea; Gary; Gwin Filleman; Holly Hanson-Kollar; Ida Male; 
Irene Campbell; Janani Siva; Jodi Evers-Dewald; Joe Ferreira; Joseph Berryhill; 
Karen Lahti; Kathy Hill-Epperson; Meredith Hale; Nicol Wargocz; Scott Cockayne; 
Stacie Schimke; Susan Pitts; Sutter, Katarina; mary.ac...@bannerhealth.com; 
patricia.tom...@bannerhealth.com; rr...@phoenixchildrens.com; Amy Spinti; 
Robert Newberry; Brigitte.Miedzybrocki; Cary Nava; Chelle Johnson; Cheryl 
Mossing; Chris Garza; Chris Westhoff; dan.otis; Diana McGregor; Eadie Baie; 
Elaine Fought; Fabrizio Saraceni; Georgia Koehler; Hans Baijense; Holland, 
Libby; James Taylor; Jeff Wolz; Jimmie Evans; joyce.santis; Judy Davis; Julie 
Pilkington; Kathryn Wangsness; Kathy Knight; Laura Bell; leslie.lyford; Liz 
Beauford; Lori Watkins; Marie Holub; Mark Wooden; Maya Sinha; McMillan, Susan - 
SJHMC; Merrikay Vidal; Mimi Wettach; Nancy Behling; Pamela Green; Pattie Glick; 
Peter Michaelson; Phil Hynes; Rachel Baker; rick.ro...@bannerhealth.com; Robert 
Graham; Rosemarie Prater; Ruth Spates; Salene Slader; Sally Caglioti; Shannon 
Sadat-Abhary; Sherry Gamble; Sponsler, Pam; Suzanne Sullivan; Tajuan Hamilton; 
Terri Bowen; Tim Hersom; Tony Millett; Valerie Kolody; Victor Waddell; Ward, 
Marilyn
Subject: Fwd: HT/HTL PROGRAM DIRECTORS SURVEY

This survey is very TIMELY regarding ASCP's potential interest in resurrecting 
the Clinical Lab Assistant national certification and to expand the role to 
basic embedding and processing in Histology!

The timing is interesting for Phoenix College as we had record number of 
applicants for the current Histologic Technology and future Medical Laboratory 
Science cohorts,  BUT just decided late last week to CANCEL the FALL Laboratory 
Assisting program as we only had 6 students.

I am trying to garner administrative approval to facilitate an industry 
sponsored partnership to provide the fall cohort to a few local Lab employees 
to be able to complete the program via distance learning this fall.

The topic of a Clinical Lab Assistant will be added to the fall HT Advisory 
Council meeting and the spring Medical Laboratory Science Advisory Council 
meeting.

Please feel free to share your thoughts with me before the meeting about the 
potential expansion of a nationally certified Clinical Lab Assistant.

Many thanks!

Julie

-- Forwarded message --
From: Peggy Wenk pw...@beaumont.edumailto:pw...@beaumont.edu
Date: Tue, Oct 9, 2012 at 8:36 AM
Subject: HT/HTL PROGRAM DIRECTORS SURVEY
To: \car...@nsh.orgmailto:car...@nsh.org\.GWIA.MSD 
car...@nsh.orgmailto:car...@nsh.org, Aulthouse, Amy 
a-aultho...@onu.edumailto:a-aultho...@onu.edu, Bailey, Mark 
mabai...@mdanderson.orgmailto:mabai...@mdanderson.org, Barone, Carol 
cbar...@nemours.orgmailto:cbar...@nemours.org, Beamon, Nancy 
nancy.bea...@darton.edumailto:nancy.bea...@darton.edu, Becker, Carol 
carol.e.bec...@osfhealthcare.orgmailto:carol.e.bec...@osfhealthcare.org, 
Bischof, Carol 
carol.bisc...@minnesota.edumailto:carol.bisc...@minnesota.edu, Campagna, 
Gerard gcam...@conemaugh.orgmailto:gcam...@conemaugh.org, Christopher 
Mignogna 
(christopher.migno...@drexel.edumailto:christopher.migno...@drexel.edu) 
christopher.migno...@drexel.edumailto:christopher.migno...@drexel.edu, 
Colony, Pamela colo...@cobleskill.edumailto:colo...@cobleskill.edu, 
Counts, Lisa lisa...@yahoo.commailto:lisa...@yahoo.com, Cox, Beth 
bethc...@gmail.commailto:bethc...@gmail.com, Davidson, Kelli 
jreyno...@mail.accd.edumailto:jreyno...@mail.accd.edu, Della Speranza, 
Vincent del...@musc.edumailto:del...@musc.edu, Delost, Maria 
medel...@ysu.edumailto:medel...@ysu.edu, DiNardo, Helen 
helen.dina...@shermanhospital.orgmailto:helen.dina...@shermanhospital.org, 
Donna Broderick (dbroder...@harcum.edumailto:dbroder...@harcum.edu) 
dbroder...@harcum.edumailto:dbroder...@harcum.edu, Durkin, Zoe Ann 
zdur...@goodwin.edumailto:zdur...@goodwin.edu, Feaster, Kimberly 
kfeas...@hsc.wvu.edumailto:kfeas...@hsc.wvu.edu, 
lfoster-br...@christianacare.orgmailto:lfoster-br...@christianacare.org 
lfoster-br...@christianacare.orgmailto:lfoster-br...@christianacare.org, 
Galina Negrouk 
(gnegr

Re: [Histonet] Facility Name on Slides

2012-10-08 Thread Jesus Ellin
To my knowledge there is no regulation rather than having 2 identifiers,, 

Sent from my iPad

On Oct 8, 2012, at 1:46 PM, histot...@imagesbyhopper.com 
histot...@imagesbyhopper.com wrote:

 Does anyone have any regs that you can point me to for both Joint Commission 
 and CAP which details definitively whether or not a facility name is 
 *required* to be included on slides? 
 
 I know it's a good idea, the larger question here is whether or not there is 
 a specific regulation for it?
 
 Thanks for all your help!
 Michelle
 
 
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Re: [Histonet] Changing dynamics in histotechnology

2012-09-17 Thread Jesus Ellin
With mixed emotions I read this article, not because of its context or 
information, but rather the outlook for our future.  

I would like to pole on the histonet today, who is enter in:

1.  Digital Pathology
2.  Molecular Testing (ISH, PCR, Next Gene Sequencing)
3.  Automation Semi to complete
4.  Barcoding 

A good question to ask is, are we, as Histology professionals, positioned to 
make this change.  Case in point, how many people are signed up and preparing 
for this transition at the NSH convention this year?  

Sent from my iPad

On Sep 17, 2012, at 8:29 AM, Judy O'Rourke jorou...@allied360.com wrote:

 Hello...
 
 In Clinical Lab Products’ just-released September issue, the article
 “Changing Dynamics in Histotechnology” addresses the challenges and trends
 you face daily. William DeSalvo, B.S., HTL(ASCP), chair, NSH Quality Control
 Committee, is quoted.
 
 Please share comments on CLP’s Facebook page, where I’ve just posted the
 article: 
 http://www.facebook.com/pages/Clinical-Lab-Products/56624886500#!/pages/Clin
 ical-Lab-Products/56624886500
 
 Thank you!
 
 Judy 
 
 JUDY O’ROURKE |  Editor
 Clinical Lab Products
 6100 Center Drive, Suite 1020, Los Angeles, CA 90045
 office 619.659.1065 | fax 619.659.1065
 jorou...@allied360.com | www.clpmag.com
 
 Follow us on Facebook, and follow me on Twitter at @editorCLPmag
 
 
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Re: [Histonet] Changing dynamics in histotechnology

2012-09-17 Thread Jesus Ellin
I do agree with both Rene and Elizabeths assessment, but what are we doing as a 
profession to secure our foot hold in the future of pathology?  Are we teaching 
our students and staff members the new techniques and trouble shooting skills 
needed for this advancement in skills, or are we just still doing the basics?  
Don't get me wrong the basics are needed, but there are new basics that have 
presented themselves to us within out profession.  Such examples would be image 
theory, computational analysis, bio analytics, bio informatics, and Computer 
systems interoperability, etc... where are these items being taught to the 
techs of the future?   I know that there will always be a need for the basic 
techs, but even as the article stated, we are the ones that know tissue and its 
function,, we are the ones that understand the pre-analytics to make it 
successful.  

But then again every where i go i hear of not being able to keep up with the 
demand of our basic routine of getting the H and E out,, or not enough time to 
think about this.  Then the solutions becomes out of sight out of mind,, or we 
can get to that later.   The problem is that currently our governing agencies, 
CAP, ASCP, NSH, CMS, CLSI, etc are creating the frame work for the lab of the 
future that will handle this testing, and guess what Histotechs are NOT apart 
of this equation.

YOur thoughts


Sent from my iPad

On Sep 17, 2012, at 12:42 PM, Elizabeth Chlipala l...@premierlab.com wrote:

 I do agree that as histotechs we need to very much involved in Digital 
 Pathology and new technologies as much as possible, if we do not we will be 
 left behind.  Here is a quote that I reference with respects to new 
 technologies.  But I am an early adopter of digital pathology.
 
 Once a new technology hits you, if you are not part of the steamroller
 you are part of the road - Lee A. Iacocca
 
 1.  Digital Pathology - We have been scanning slides since 2007, very active 
 in this technology, board member of the Digital Pathology Association.
 2.  Molecular Testing (ISH, PCR, Next Gene Sequencing) - we will be actively 
 running ISH in the next couple months, have looked at the other technologies 
 but have not made the move yet to bring those into the lab yet, but its on 
 our radar.
 3.  Automation Semi to complete - automated HE, and immunostainers.
 4.  Barcoding - would love to barcode, its difficult in the research setting, 
 software is available in the clinical setting but not for research, we have 
 been looking for over a year on a system that would work in research and in 
 our setting.
 
 Liz
 
 Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
 Manager
 Premier Laboratory, LLC
 PO Box 18592
 Boulder, CO 80308-1592
 (303) 682-3949 office
 (303) 682-9060 fax
 (303) 881-0763 cell
 www.premierlab.com
 
 Ship to address:
 
 1567 Skyway Drive, Unit E
 Longmont, CO 80504
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jesus Ellin
 Sent: Monday, September 17, 2012 1:22 PM
 To: Judy O'Rourke
 Cc: histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Changing dynamics in histotechnology
 
 With mixed emotions I read this article, not because of its context or 
 information, but rather the outlook for our future.
 
 I would like to pole on the histonet today, who is enter in:
 
 1.  Digital Pathology - We have been scanning slides since 2007, very active 
 in this technology.
 2.  Molecular Testing (ISH, PCR, Next Gene Sequencing) - we will be actively 
 running ISH in the next couple months, have looked at the other technologies 
 but have not made the move yet to bring those into the lab yet, but its on 
 our radar.
 3.  Automation Semi to complete - automated HE, and immunostainers.
 4.  Barcoding - would love to barcode, its difficult in the research setting, 
 software is available in the clinical setting but not for research, we have 
 been looking for over a year on a system that would work in research.
 
 A good question to ask is, are we, as Histology professionals, positioned to 
 make this change.  Case in point, how many people are signed up and preparing 
 for this transition at the NSH convention this year?
 
 Sent from my iPad
 
 On Sep 17, 2012, at 8:29 AM, Judy O'Rourke jorou...@allied360.com wrote:
 
 Hello...
 
 In Clinical Lab Products' just-released September issue, the article
 Changing Dynamics in Histotechnology addresses the challenges and trends
 you face daily. William DeSalvo, B.S., HTL(ASCP), chair, NSH Quality Control
 Committee, is quoted.
 
 Please share comments on CLP's Facebook page, where I've just posted the
 article:
 http://www.facebook.com/pages/Clinical-Lab-Products/56624886500#!/pages/Clin
 ical-Lab-Products/56624886500
 
 Thank you!
 
 Judy
 
 JUDY O'ROURKE |  Editor
 Clinical Lab Products
 6100 Center Drive, Suite 1020, Los Angeles, CA 90045
 office 619.659.1065 | fax 619.659.1065
 jorou...@allied360.com

Re: [Histonet] Changing dynamics in histotechnology

2012-09-17 Thread Jesus Ellin
 they can and promoting getting more involved 
 with the entire system. 
 
 
 
 Tim Morken
 
 
 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jesus Ellin
 Sent: Monday, September 17, 2012 12:22 PM
 To: Judy O'Rourke
 Cc: histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Changing dynamics in histotechnology
 
 With mixed emotions I read this article, not because of its context or 
 information, but rather the outlook for our future.  
 
 I would like to pole on the histonet today, who is enter in:
 
 1.  Digital Pathology
 2.  Molecular Testing (ISH, PCR, Next Gene Sequencing) 3.  Automation Semi to 
 complete 4.  Barcoding 
 
 A good question to ask is, are we, as Histology professionals, positioned to 
 make this change.  Case in point, how many people are signed up and preparing 
 for this transition at the NSH convention this year?  
 
 Sent from my iPad
 
 On Sep 17, 2012, at 8:29 AM, Judy O'Rourke jorou...@allied360.com wrote:
 
 Hello...
 
 In Clinical Lab Products' just-released September issue, the article 
 Changing Dynamics in Histotechnology addresses the challenges and 
 trends you face daily. William DeSalvo, B.S., HTL(ASCP), chair, NSH 
 Quality Control Committee, is quoted.
 
 Please share comments on CLP's Facebook page, where I've just posted 
 the
 article: 
 http://www.facebook.com/pages/Clinical-Lab-Products/56624886500#!/page
 s/Clin
 ical-Lab-Products/56624886500
 
 Thank you!
 
 Judy
 
 JUDY O'ROURKE |  Editor
 Clinical Lab Products
 6100 Center Drive, Suite 1020, Los Angeles, CA 90045 office 
 619.659.1065 | fax 619.659.1065 jorou...@allied360.com | 
 www.clpmag.com
 
 Follow us on Facebook, and follow me on Twitter at @editorCLPmag
 
 
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 Thank You.
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Re: [Histonet] Changing dynamics in histotechnology

2012-09-17 Thread Jesus Ellin
Sorry hit the sent button,,

but as for this we are going to be required to be even more accurate with the 
uses of our tools for diagnosis.

As for the LIS,, we are still creating the same LIS to do the same process we 
currently have and not help us transform into this new world of technology and 
application

Digital Pathology,, all I can say is that why are we trying to make this thing 
do what a microscope does,, I have yet to understand that thinking.  It is not 
a microscope, because it offers more than it.  But no one has taken a look at 
what is the histologys usage of this technology  

Sent from my iPad

On Sep 17, 2012, at 2:12 PM, Jesus Ellin jel...@yumaregional.org wrote:

 Tim,
 
 I think basic histology is going to be manual,, but i see the explosion of 
 technology sweeping our field.
 
 As Bill states it all about standardization,, but try getting the same H and 
 E across the board,, thats not going to happen
 
 IHC will always we a bread and butter, but now since the government has 
 limited the amoun t of IHC per patient, we are going to see a lot changes 
 here.  With only 4 IHC per patient 
 
 Sent from my iPad
 
 On Sep 17, 2012, at 2:00 PM, Morken, Timothy 
 timothy.mor...@ucsfmedctr.org wrote:
 
 Histology is going to have a huge manual component for a long time. Even 
 though embedding has been automated to a certain extent it has not been 
 accepted by many...yet. Automated sectioning is a long way off - and who 
 would have the money to buy sectioning robots that could do as well as a 
 human? Would it even be cost effective (and that IS the question!)? 
 
 Much of this could be made much easier by proper application of 
 grossing/processing/embedding procedures. But we can't even get pathologists 
 to agree how long any particular tissue should be fixed - no matter what the 
 literature says. Good luck standardizing grossing and tissue processing 
 across a single large department, let alone the entire industry (though I 
 know Bill has done wonders with this in his company). Simply due to that 
 lack of standardization manual work will be with us for a LONG time since 
 every block requires individual care and decision making by the person 
 sectioning it. 
 
 IHC is bread and butter to the lab now. ISH is coming along but still too 
 rare to make much money off of it, if any at all. I don't think we do much 
 more of it percentage wise than 20 years ago. 
 
 The best IHC techs take interest in the cases, learn what the antibodies are 
 for and pay attention to the staining they get (if they have time before the 
 TAT deadline!).  They do research on diseases and can converse with 
 pathologist about the results.
 
 Molecular methods (ie, DNA/RNA, besides ISH) is quite different than 
 histology. Completely different training required, though I have no doubt 
 histotechs could do it, why would they hire a histotech when there are 
 umpteen biochemists applying for every biology job advertised (including 
 histology!!)?
 
 Digital pathology is still promising, just as it was 10 years ago, and 
 will be promising 5 or 10 years from now unless a technology comes along 
 to scan slides FAST - ie 10 seconds, not 5 minutes. Maybe someone will adapt 
 the Lytro Light Field Camera to slide scanning. Seems a perfect match 
 (google it!).
 
 Barcoding is on the way in. We are going to have a system by June 2013. But 
 it is in the growing stage and there are lots of tradeoffs. The hardware has 
 just become available in the last 5 years to make it reliable. Now the 
 vendors have to get going. Some have with great systems  - Ventana, possibly 
 Leica, Omnitrax. The LIS vendors have fallen flat on their faces on this - 
 totally missed the boat and ceded the specimen tracking space to histology 
 and IHC vendors. Shows what happens when your company is too big and you 
 don't pay attention to the possibilities. As recently as 3 years ago I had 
 an LIS vendor technical person ask me what on earth I would use bar coding 
 for in histology. I hope that guy has been fired by now for ignorance!
 
 Of course one huge disadvantage to having histology and IHC vendors 
 providing barcoding/tracking systems is some want to limit your choices to 
 their instruments. That is a big bugaboo right now. But I understand 
 Clinical Chemistry is dealing with the same issue - instrument vendors 
 forcing certain parameters on the lab.
 
 Training of histotechs is and always will be a problem. 95+% of histotechs 
 are trained OJT. I think there is only one program on the west coast. So, 
 for the most part forget formally trained techs (and those that are formally 
 trained should make the most of it!). It is all dependent on individual 
 initiative and the training skill of the lab managers they work for. NSH is 
 doing a pretty good job - and I only say that because while the various 
 meetings are great, only a small percentage attend. The vast majority of 
 histotechs don't ever get outside training

Re: [Histonet] Changing dynamics in histotechnology

2012-09-17 Thread Jesus Ellin
Go to CMS MUE's where only 4 IHC will be reimbursed for medicare patients,, 
granted you can add a modifier to justify usage, but you are not getting 
anymore money,, but this is been in place since last year and took into affect 
this year.  

Sent from my iPad

On Sep 17, 2012, at 2:17 PM, Mike Pence mpe...@grhs.net wrote:

 Just to shed more light on one thing: can you direct me to where it
 states that you can only bill for 4 IHC per patient. I am not
 questioning what you are saying, just want more info on this subject.
 
 Thanks, Mike
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jesus
 Ellin
 Sent: Monday, September 17, 2012 4:12 PM
 To: Morken, Timothy
 Cc: histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Changing dynamics in histotechnology
 
 
 Tim,
 
 I think basic histology is going to be manual,, but i see the explosion
 of technology sweeping our field.
 
 As Bill states it all about standardization,, but try getting the same H
 and E across the board,, thats not going to happen
 
 IHC will always we a bread and butter, but now since the government has
 limited the amoun t of IHC per patient, we are going to see a lot
 changes here.  With only 4 IHC per patient 
 
 Sent from my iPad
 
 On Sep 17, 2012, at 2:00 PM, Morken, Timothy
 timothy.mor...@ucsfmedctr.org wrote:
 
 Histology is going to have a huge manual component for a long time. 
 Even though embedding has been automated to a certain extent it has
 not been accepted by many...yet. Automated sectioning is a long way off
 - and who would have the money to buy sectioning robots that could do as
 well as a human? Would it even be cost effective (and that IS the
 question!)?
 
 Much of this could be made much easier by proper application of 
 grossing/processing/embedding procedures. But we can't even get
 pathologists to agree how long any particular tissue should be fixed -
 no matter what the literature says. Good luck standardizing grossing and
 tissue processing across a single large department, let alone the entire
 industry (though I know Bill has done wonders with this in his company).
 Simply due to that lack of standardization manual work will be with us
 for a LONG time since every block requires individual care and decision
 making by the person sectioning it.
 
 IHC is bread and butter to the lab now. ISH is coming along but still 
 too rare to make much money off of it, if any at all. I don't think we
 do much more of it percentage wise than 20 years ago.
 
 The best IHC techs take interest in the cases, learn what the 
 antibodies are for and pay attention to the staining they get (if they
 
 have time before the TAT deadline!).  They do research on diseases and
 
 can converse with pathologist about the results.
 
 Molecular methods (ie, DNA/RNA, besides ISH) is quite different than 
 histology. Completely different training required, though I have no 
 doubt histotechs could do it, why would they hire a histotech when 
 there are umpteen biochemists applying for every biology job 
 advertised (including histology!!)?
 
 Digital pathology is still promising, just as it was 10 years ago, 
 and will be promising 5 or 10 years from now unless a technology 
 comes along to scan slides FAST - ie 10 seconds, not 5 minutes. Maybe 
 someone will adapt the Lytro Light Field Camera to slide scanning. 
 Seems a perfect match (google it!).
 
 Barcoding is on the way in. We are going to have a system by June 
 2013. But it is in the growing stage and there are lots of tradeoffs. 
 The hardware has just become available in the last 5 years to make it 
 reliable. Now the vendors have to get going. Some have with great 
 systems  - Ventana, possibly Leica, Omnitrax. The LIS vendors have 
 fallen flat on their faces on this - totally missed the boat and ceded
 
 the specimen tracking space to histology and IHC vendors. Shows what 
 happens when your company is too big and you don't pay attention to 
 the possibilities. As recently as 3 years ago I had an LIS vendor 
 technical person ask me what on earth I would use bar coding for in 
 histology. I hope that guy has been fired by now for ignorance!
 
 Of course one huge disadvantage to having histology and IHC vendors 
 providing barcoding/tracking systems is some want to limit your 
 choices to their instruments. That is a big bugaboo right now. But I 
 understand Clinical Chemistry is dealing with the same issue - 
 instrument vendors forcing certain parameters on the lab.
 
 Training of histotechs is and always will be a problem. 95+% of 
 histotechs are trained OJT. I think there is only one program on the 
 west coast. So, for the most part forget formally trained techs (and 
 those that are formally trained should make the most of it!). It is 
 all dependent on individual initiative and the training skill of the 
 lab managers they work for. NSH is doing a pretty good job

[Histonet] RE: Slide printing systems

2012-08-15 Thread Jesus Ellin
Have you looked at the type of slides you are using?  We have both instruments 
as we do have challenges with printing in the beginning , we now do not have 
issues

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mitchell, 
Janice A
Sent: Wednesday, August 15, 2012 7:25 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Slide printing systems

Good Morning,

We currently are using Thermo-Fisher print-mate and slide-mate.  I am not very 
happy with the printing of the slides.  Some days I feel like spend most of my 
time re-writing and labeling printed slides. Then when the units  are  sent out 
for repair and it arrives back it is not a whole lot better.  Before we get our 
new LIS system and our Docs will be scanning the bar code(that sometimes do not 
print) I need to find a better system.  I will not be able to deal with how 
often my name will be called out when the scanning of the slides fail.

I would like any input on other systems pros and cons that are currently being 
used in histology labs.   I know no system will be perfect but something has to 
be better.

Thanks, Janice

Janice A. Mitchell, BS, HT(ASCP)
Histology Lead Tech
Children's Hospital of Philadelphia
Anatomic Pathology and Laboratory Medicine
324 S. 34th Street
Philadelphia, Pa 19104-4399
215-590-1738(lab)
267-426-7754(office)


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RE: [Histonet] compatibility of Thermo slide printers with Leica cassette printer

2012-05-30 Thread Jesus Ellin
We use both the Printmate and slidemate from Thermo.

We also have used the Leica IPS for slides.

The biggest thing to remember is when using these items is if you are passing 
them through your APLIS or the printers own proprietary software.  Either was 
you are going to have to look at this with a critical eye.  I would suggest 
using 2D barcodes for both items.  1D tend to increase as the data increases.  
But this hold true for all barcodes you place on either a slide or cassette.  
The main thing is the symobology you need in order to produce the barcode.  
There are several symoblogies out there to use.  We currently use the 
Datamatrix one.  This is all driven by either the APLIS or the database you are 
using.  

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morphisto GmbH
Sent: Tuesday, May 29, 2012 11:14 PM
To: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] compatibility of Thermo slide printers with Leica 
cassette printer

Hello Sandy,

we use a Leica Cassette and Slide Printer which are both connected to a 
database in which we organize all our specimens and print cassettes and slides, 
so it is not necessary to read the barcodes from cassettes to print them on the 
slides. However, there is of course not much space for barcode on the 
cassettes, but in most cases we can read the barcode with our smart phones.
I do not know if the barcodes of Leica and Thermo are compatible. I think you 
have to use the same type of barcode in both machines, so that the other one 
can read it.

Best regards
Michael





Am 29.05.2012 um 22:12 schrieb Harrison, Sandra C.:

 1)  Does anyone have a Leica Cassette Printer on which they are
 printing 2-Dimensional barcodes?
 
 
 
 2)  Is anyone using a Thermo slide printer, with bar code reader, to
 read cassettes printed off of a Leica Cassette Printer with 2-D bar
 codes?
 
 
 
 Thanks for your input.
 
 
 
 
 
 Sandy C. Harrison, HTL (ASCP)
 
 Histology Supervisor
 
 Minneapolis VA
 
 612-467-2449
 
 
 
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[Histonet] RE: CAP

2012-05-30 Thread Jesus Ellin
Have fun and good luck

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bernice 
Frederick
Sent: Wednesday, May 30, 2012 7:16 AM
To: Fellow HistoNetters
Subject: [Histonet] CAP

They're here!

Bernice Frederick HTL (ASCP)
Senior Research Tech
Pathology Core Facility
ECOGPCO-RL
Robert. H. Lurie Cancer Center
Northwestern University
710 N Fairbanks Court
Olson 8-421
Chicago,IL 60611
312-503-3723
b-freder...@northwestern.edumailto:b-freder...@northwestern.edu

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RE: [Histonet] RE: CAP vs. CLIA

2012-05-21 Thread Jesus Ellin
Bill I have to agree with you on this, but then again we have always been 
looked as a step children within the lab.  What I see is word play here,  Cyto 
tech and Med Tech (CLS) are to be credited with release of a result.  But 
because there Tech ID number is on the result they are accountable for this.  
As we move forward in the computer age within Anatomic Pathology we are going 
to be seeing the same shift, but we need our professional societies, to start 
to transform our profession.  I am talking about algorithm analysis, special 
stains, IHC, bio banking, etc.  There are many decisions that make us more than 
just a point and push tech, for lack there of a better term.

I do agree education is a barrier, but once again how did the CLS (Med Tech), 
Cyto tech evelove?  I do recall when they were taught on the job or through 
military training, so to say they are better because of a degree is far from 
the truth.  Many MANY tech these days are assets to our profession and as we 
move forward in the future they we need to look for ways to have properly 
credentialed and EXPERIANCED staff.  I my self am witness to the lack of basic 
lab knowledge a new grads have, but we are also responsible because our 
clinical rotation programs are scares and we do not have time to train.

The future is full of opportunity for all histology tech, educated and 
experience, we just need to move forward and have the healthy discussion and 
make the changes needed in order to establish our profession.


From: WILLIAM DESALVO [mailto:wdesalvo@hotmail.com]
Sent: Sunday, May 20, 2012 8:38 PM
To: Jesus Ellin; Timothy Morken; histonet
Subject: RE: [Histonet] RE: CAP vs. CLIA

I seemed to have missed something or it might have been all the fresh sea air I 
got in Tampa at the FSH, but I do not understand the outrage expressed towards 
CLIA and CAP because we are not listed as testing personnel. I applaud 
everyone's passion for Histotechnology and the outrage that we are not allowed 
to fully participate in the test system model, but I think we should be 
directing more of our outrage to the individuals working in Histotechnology 
that are not and will not take responsibility to increase the professionalism 
of our profession and our own acceptance of the current state of 
Histotechnology.

A TEST SYSTEM is the process that includes pre-analytic, analytic, and 
post-analytic steps used to produce a test result or set of results. As good as 
we are and as complex parts of the Histotechnology process may be, 
Histotechnicians, Histotechnologists and Pathology Assistants do not meet the 
standard stated and do not participate in the post-analytic phase, produce and 
release patient results. We simply are not able to be credentialed as is the 
Medical Technologists and Cytotechnologist. I am not saying any one laboratory 
professional group is better than the other, just that to be considered testing 
personnel, we must be properly credentialed.

Collectively, we as a discipline, science and group should be working to 
upgrade our education requirements and training so that we can become fully 
invested partners with the Pathologist. We, not CAP or CLIA, must greatly 
increase our professionalism before we can truly be considered competent to 
work in the post-analytical phase. I cannot today accept that every working 
Histotechnician, Histotechnologist and Pathologist Assistant is able to produce 
the result and release. I am quite sure that every Medical Technologist and 
Cytotechnologist is capable and competent to produce and release a patient 
result. As things stand today, Histotechnology and all of us the working in 
this discipline are a support function to the one person in our discipline, the 
Pathologist, that is educated, trained, credentialed and competent to produce 
and release a patient result. I also believe there are many opportunities 
within our process available now, such as histochemical staining for organisms, 
that could allow us to participate in the post-analytic step. There will be 
many more as personalized medicine continues to transform Histotechnology.

That said, how can we honestly promote our participation in the post-analytic 
phase, when there are far too many individuals (good, decent and hard working) 
that work every day, in every type and complexity of lab, that do not have a 
formal secondary education, have participated in defined clinical trials or 
have completed a certification exam (required and necessary credentials). Just 
think how many practitioners of Histotechnology are out there working today 
that are not properly credentialed. Now think if you know of any Medical 
Technologist or Cytotechnologist are working that do not have the required 
credentials.

We have many obstacles to increasing the professionalism of Histotechnology; 
wide and varied backgrounds, lack of standards, lack of automation, lack of 
certification, but I do not think

[Histonet] RE: CAP vs. CLIA

2012-05-17 Thread Jesus Ellin
I am going to have to go there,, sorry all I know I am going to stir-up a 
hornets nest, but here it goes, don't we think that this is done in lue of the 
fact that CAP are representing the Pathologist interest and not the interest of 
the Technicians.  Times have changed and the CAP is asking for more and more 
from Anatomic Pathology questions every year, not only to include technical, 
but also instrumentation (simple and complex), as well as information systems, 
predictive markers, Digital Pathology ( a huge one), etc.  I think the CAP need 
to re-evaluate this and re consider what high complexity testing is, because 
CLIA defines it not the CAP.  Remember CAP enforces CLIA regulation as well as 
their own.  I would challenge this.  I feel the staff under me do more than 
turn a wheel, or place tissue in a mold.  With Passion comes a need to start to 
create change, we need this done.

Jesus Ellin  HT/PA ASCP, BSBE,MSBE
Yuma Regional Medical Center
Anatomic Pathology Supervisor

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Horn, Hazel V
Sent: Thursday, May 17, 2012 7:05 AM
To: 'Willis, Donna G.'; 'Courtney Pierce'
Cc: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: CAP vs. CLIA

It was a CAP e alert dated April 2, 2012

Hazel Horn
Supervisor of Histology/Autopsy/Transcription
Anatomic Pathology
Arkansas Children's Hospital
1 Children's Way | Slot 820| Little Rock, AR 72202
501.364.4240 direct | 501.364.1302 office | 501.364.1241 fax
hor...@archildrens.org
archildrens.org




100 YEARS YOUNG!
JOIN THE PARTY AT
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-Original Message-
From: Willis, Donna G. [mailto:donna.wil...@baylorhealth.edu] 
Sent: Thursday, May 17, 2012 8:42 AM
To: Horn, Hazel V; 'Courtney Pierce'
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: CAP vs. CLIA

I have to say I disagree with this interpretation.  The commentary in the 
7/11/2011 checklists indicates that regulations apply to A laboratory must 
evaluate and document the competency of all testing personnel for each test 
system. A TEST SYSTEM is the process that includes pre-analytic, analytic, and 
post-analytic steps used to produce a test result or set of results.  To me 
this includes both histology and pathology office staff.

This is the opinion on myself and our compliance person.  Hazel can you tell us 
where to find the CAP quote.

Thanks,

Donna Willis, HT/HTL (ASCP)
Histology Lab Manager
Baylor University Medical Center-Dallas
ph. 214-820-2465 office
ph. 214-725-6184 mobile
donna.wil...@baylorhealth.edu


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Horn, Hazel V
Sent: Thursday, May 17, 2012 7:26 AM
To: 'Courtney Pierce'
Cc: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: CAP vs. CLIA

CAP does not consider us testing personnel. How they come by this is a mystery 
to me.   In a recent memo from CAP it describes this:

 Why does CAP require the completion of the Laboratory Personnel Evaluation 
Roster form and when was this process implemented? 

As part of CAP's deemed status with CMS as an accrediting organization, CMS 
required CAP to implement a more stringent process to document that accredited 
laboratories have appropriately qualified personnel and adequate documentation 
of personnel qualifications. The Laboratory Personnel Evaluation Roster form 
requires laboratories to confirm that personnel files contain the information 
necessary for laboratories to be in compliance with the CLIA personnel 
qualification regulations and CAP Checklist requirements prior to the 
inspection. It is also used by the inspection team to assist in the auditing of 
the records during the inspection to confirm compliance with the Checklist 
requirements. The process of completing the personnel form took effect in 
August 2009.

And goes on to say:
Do I need to list histologists on the Laboratory Personnel Evaluation Roster?  

Typical histologist duties (e.g., fixation, embedding, microtomy, staining and 
cover slipping) are not considered testing. Therefore, it is not necessary to 
list these personnel on the roster. However, if the histologist is performing 
any part of the macroscopic tissue examination which is considered high 
complexity testing, it is necessary to list those personnel on the roster. Such 
personnel must provide documentation at minimum of an associate's 
degree/transcripts or high school diploma or equivalent for individuals 
performing grossing at the same laboratory prior to September 1, 1997.

Hazel Horn
Supervisor of Histology/Autopsy/Transcription Anatomic Pathology Arkansas 
Children's Hospital
1 Children's Way | Slot 820| Little Rock, AR 72202
501.364.4240 direct | 501.364.1302 office | 501.364.1241 fax 
hor...@archildrens.org archildrens.org




100 YEARS YOUNG!
JOIN THE PARTY AT
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-Original Message

[Histonet] RE: CAP vs. CLIA

2012-05-17 Thread Jesus Ellin
I completely agree with you on this.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken, Timothy
Sent: Thursday, May 17, 2012 10:46 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: CAP vs. CLIA

Jesus wrote:

 I think the CAP need to re-evaluate this and re consider what high complexity 
testing is, because CLIA defines it not the CAP.  Remember CAP enforces CLIA 
regulation as well as their own.  

Certainly the regulations limit the high complexity designation to 
interpretation of procedure results, but that does not mean a facility does not 
need very highly trained and competent technologists to do the protocols that 
lead to good interpretation. It simply highlights the difference between 
running slides through protocols vs looking at the result and determining a 
diagnosis. I'm sure most here will see the difference. 

Remember that CAP is a simply a deemed agency of CLIA - that is, CMS (Centers 
for Medicare and Medicaid, which administers the CLIA regulations) delegates to 
CAP (and Joint Commission) the authority to accredit laboratories. CAP cannot 
make up new regulations, only enforce existing CLIA regulations. However, the 
CLIA regulations are by necessity very general so they can apply to any kind of 
laboratory operations, current or future. CAP has the leeway to look at what 
labs are doing and determine if the CLIA regulations apply to those tasks. 
However, CAP must submit their proposals to CMS/CLIA and CMS/CLIA must pass off 
on them before they are implemented. 

CAP checklists are far more complex than they were 20 years ago. But the histo 
lab is far more complex as well, and regulators (as well as the public) are 
looking much more closely at histology because of some major mistakes that have 
happened largely due to lack of rigor in testing validation and implementation. 
A lot of that has to do with small labs doing complex testing (interpretation) 
with methods they were/are not fully competent to do primarily due to lack of 
experience and expertise. 

While the accreditation process is getting more onerous, it is also forcing 
labs to be much more professional in their operations - always a good thing, I 
think.

Tim Morken

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Willis, Donna G.
Sent: Thursday, May 17, 2012 7:26 AM
To: 'Jesus Ellin'; 'Horn, Hazel V'; 'Courtney Pierce'
Cc: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: CAP vs. CLIA

Very well said Jesus.  I agree.

Donna Willis, HT/HTL (ASCP)
Histology Lab Manager
Baylor University Medical Center-Dallas
ph. 214-820-2465 office
ph. 214-725-6184 mobile
donna.wil...@baylorhealth.edu


-Original Message-
From: Jesus Ellin [mailto:jel...@yumaregional.org]
Sent: Thursday, May 17, 2012 9:24 AM
To: 'Horn, Hazel V'; Willis, Donna G.; 'Courtney Pierce'
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: CAP vs. CLIA

I am going to have to go there,, sorry all I know I am going to stir-up a 
hornets nest, but here it goes, don't we think that this is done in lue of the 
fact that CAP are representing the Pathologist interest and not the interest of 
the Technicians.  Times have changed and the CAP is asking for more and more 
from Anatomic Pathology questions every year, not only to include technical, 
but also instrumentation (simple and complex), as well as information systems, 
predictive markers, Digital Pathology ( a huge one), etc.  I think the CAP need 
to re-evaluate this and re consider what high complexity testing is, because 
CLIA defines it not the CAP.  Remember CAP enforces CLIA regulation as well as 
their own.  I would challenge this.  I feel the staff under me do more than 
turn a wheel, or place tissue in a mold.  With Passion comes a need to start to 
create change, we need this done.

Jesus Ellin  HT/PA ASCP, BSBE,MSBE
Yuma Regional Medical Center
Anatomic Pathology Supervisor

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Horn, Hazel V
Sent: Thursday, May 17, 2012 7:05 AM
To: 'Willis, Donna G.'; 'Courtney Pierce'
Cc: histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: CAP vs. CLIA

It was a CAP e alert dated April 2, 2012

Hazel Horn
Supervisor of Histology/Autopsy/Transcription Anatomic Pathology Arkansas 
Children's Hospital
1 Children's Way | Slot 820| Little Rock, AR 72202
501.364.4240 direct | 501.364.1302 office | 501.364.1241 fax 
hor...@archildrens.org archildrens.org




100 YEARS YOUNG!
JOIN THE PARTY AT
ach100.org



-Original Message-
From: Willis, Donna G. [mailto:donna.wil...@baylorhealth.edu]
Sent: Thursday, May 17, 2012 8:42 AM
To: Horn, Hazel V; 'Courtney Pierce'
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: CAP vs. CLIA

I have to say I disagree

Re: [Histonet] Aetna requiring CAP accreditation for non-hospital labs

2012-04-06 Thread Jesus Ellin
There are several frame of minds here, but most closely this aligns with the 
affordable care act and quality outcomes for patients.  I to agree with the 
statement that other agencies can provide good quality outcomes, but Anatomic 
pathology is changing so rapidly.  From all aspects, but if you look at who 
bills for most of the CMS testing it falls under hospital based laboratories, 
yet the government decides reimbursement based on what the large labs make..  
In the end we are seeing consolidation,, but I hope someone comes to the 
forefront to speak for us all. 
Sent from my iPad
On Apr 6, 2012, at 1:41 PM, Carol Torrence ctorre...@kmcpa.com wrote:

 I too have been through many CAP inspections in the past. Passing is not my
 concern - how about expense, prep time, time away to inspect a peer.We
 are a small private lab also so this a bit of a pain.  There is no way that
 CAP will be able to accommodate the workload that will ensue if this becomes
 a trend. Which I think it will and there will be more insurance companies
 aligning themselves with the larger labs as preferred.  My fear is that
 local healthcare will be so undercut that it will become more difficult if
 not impossible for even hospital labs to compete. I will never be convinced
 that big is better. 
 
 I believe Aetna will hear from CAP on this issue due to the increased
 workload to them...deadlines may have to be extended.  We are hearing from a
 CAP member that they will not be able to be accredited in such a short time,
 according to CAP.
 
 -Original Message-
 From: Kim Donadio [mailto:one_angel_sec...@yahoo.com] 
 Sent: Thursday, April 05, 2012 6:31 PM
 To: Katelin Lester
 Cc: Carol Torrence; histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Aetna requiring CAP accreditation for non-hospital
 labs
 
 My lab can pass any inspection I have no fear Bring it on
 utube.com/index?desktop_uri=%2Fgl=US#/watch?v=gAQCbczCt8s
 
 Sent from my iPhone
 
 On Apr 5, 2012, at 7:00 PM, Katelin Lester katelin09...@gmail.com wrote:
 
 We also received this notice. We contacted our local CLIA office who 
 had heard of it this week as well. We are a small lab, so we are not 
 sure yet how this change will impact us. I'd also be curious to know 
 what smaller, private labs are planning on doing.
 --
 Katelin Lester, HTL
 Gastroenterology Specialists of Oregon, P.C.
 Pathology Laboratory
 (971) 224-2408
 
 On Thu, Apr 5, 2012 at 12:16 PM, Carol Torrence ctorre...@kmcpa.com
 wrote:
 
 We have received notification from AETNA that they now require 
 non-hospital labs to be accredited by CLIA and CAP.  The letter makes 
 it obvious that by making such a request that they are not aware that 
 CLIA assigned deemed status to CAP and CLIA is actually the 
 gatekeeper.  Secondly we are told to be registered by May 1st and 
 accredited by August 1st (which CAP says is
 impossible) or we will have to send our lab to either Quest or 
 Ameripath which includes Dermpath Diagnostics division.  It fails to 
 mention that there are other CAP accredited non hospital labs in our 
 state.  The Aetna contact number is either 'mailbox full or even 
 after leaving a message, no return call.  Me thinks me smells a rat.
 
 
 
 If you are a non-hospital lab, have you heard of this?  Does your 
 dematopathologist or pathologist know this is coming?  I am 
 interested in your comments.
 
 
 
 Carol M. Torrence, HT(ASCP)CM
 
 
 
 
 
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Re: [Histonet] Aetna requiring CAP accreditation for non-hospital labs

2012-04-05 Thread Jesus Ellin
I think this is just the beginning,, hold on to your pants

Sent from my iPad

On Apr 5, 2012, at 2:16 PM, Kim Donadio one_angel_sec...@yahoo.com wrote:

 
 http://www.mohscollege.org/president/AETNAletter.pdf
 
 Sent from my iPhone
 
 On Apr 5, 2012, at 5:09 PM, Kim Donadio one_angel_sec...@yahoo.com wrote:
 
 Hmm I found a letter regarding this.
 
 mohscollege.org/president/AETNAletter
 
 I must say the time restraint  seems short but I am not surprised they are 
 wanting it. With today's reimbursement rates and the economy we are in ins 
 companies want to insure they get the highest quality of service for their  
 dollars. 
 I'm a little surprised they specifically want CAP though but nit that much. 
 CLIA has deemed CAP authority to guide in the area of quality accreditation. 
  
 No need to panic though. Remember. Times are changing and prosperity favors 
 the ones who act upon knowledge :) 
 Kim D
 Sent from my iPhone. 
 
 On Apr 5, 2012, at 3:16 PM, Carol Torrence ctorre...@kmcpa.com wrote:
 
 We have received notification from AETNA that they now require non-hospital
 labs to be accredited by CLIA and CAP.  The letter makes it obvious that by
 making such a request that they are not aware that CLIA assigned deemed
 status to CAP and CLIA is actually the gatekeeper.  Secondly we are told to
 be registered by May 1st and accredited by August 1st (which CAP says is
 impossible) or we will have to send our lab to either Quest or Ameripath
 which includes Dermpath Diagnostics division.  It fails to mention that
 there are other CAP accredited non hospital labs in our state.  The Aetna
 contact number is either 'mailbox full or even after leaving a message, no
 return call.  Me thinks me smells a rat.
 
 
 
 If you are a non-hospital lab, have you heard of this?  Does your
 dematopathologist or pathologist know this is coming?  I am interested in
 your comments.
 
 
 
 Carol M. Torrence, HT(ASCP)CM 
 
 
 
 
 
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Re: [Histonet] RE: NCCI policy update

2011-12-30 Thread Jesus Ellin
Don't you think we havea hand in this reporting out this CPT code so much,, I 
would expect this to be bundled here soon in a DRG for pathology services,, 
that's where it is headed.


Sent from my iPad

On Dec 30, 2011, at 2:22 PM, histot...@imagesbyhopper.com 
histot...@imagesbyhopper.com wrote:

 Wow.  What made them change their minds?  There are many times when we stain
 different blocks of a single specimen and only one lights up.
 
 I, too, would be interested in an official document stating the change.
 
 Thanks!
 Michelle
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amber
 McKenzie
 Sent: Friday, December 30, 2011 3:07 PM
 To: Martha Ward-Pathology; Webb, Dorothy L;
 'histonet@lists.utsouthwestern.edu'
 Subject: [Histonet] RE: NCCI policy update
 
 Where can I get the article to show my billing dept/pathologists?
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Martha
 Ward-Pathology
 Sent: Friday, December 30, 2011 1:13 PM
 To: Webb, Dorothy L; 'histonet@lists.utsouthwestern.edu'
 Subject: [Histonet] RE: NCCI policy update
 
 Oh yes, we are very aware and quite upset at the change!
 
 
 Martha Ward, MT (ASCP) QIHC
 Manager, Molecular Diagnostics Lab
 Dept. of Pathology
 Wake Forest University Baptist Medical Center Winston-Salem, NC 27157
 336-716-2104
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Webb,
 Dorothy L
 Sent: Friday, December 30, 2011 1:33 PM
 To: 'histonet@lists.utsouthwestern.edu'
 Subject: [Histonet] NCCI policy update
 
 Is everyone aware that beginning 1/1/12, we can no longer bill for each
 block regarding IHC billing, only one unit of billing for each part type no
 matter how many blocks are stained?  Also IHC cocktail stains, such as
 PIN4 must now be billed as one unit even though multiple antibodies are
 reported out.
 
 Kind of a surprising reversal of the policy set in motion 10/1/2009.
 SPECIMEN becomes the unit of service rather than block(s) for IHC codes
 88342, 88360, and 88361.
 
 Happy New Year to everyone out there.  May 2012 find you happiness and
 health!
 
 Dorothy Webb, HT
 Regions Histology TS
 651-254-2962
 
 
 
  
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[Histonet] RE: Tissue Cassette Printer Recommendations

2011-07-07 Thread Jesus Ellin
I would look at Thermo, Leica and General Data printers .

Jesus Ellin
Yuma Regional Medical Center

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rodriguez, 
Arnold
Sent: Thursday, July 07, 2011 9:38 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Tissue Cassette Printer Recommendations

Hello All,
 
We are interested in purchasing a new cassette printer and I would
sincerely appreciate any recommendations for this instrument. We are
particularly looking for reliability, print speed, LIS connectivity and
barcode technology.
 
Thank you very much.
 
Arnold Rodriguez, HT (ASCP)
Supervisor, Anatomic Pathology
Eisenhower Medical Center 
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[Histonet] RE: Tissue Cassette Printer Recommendations

2011-07-07 Thread Jesus Ellin
I do not have Vantage, so I cannot comment on that. But you have to take into 
account the environment and the scanning quality of the print.  I would also 
look at space, location, downtime, workflow, even clarity of barcode meaning 
Datamatirx, ect.  There are also issues with specific cassette colors and 
cassette surface texture playing a part in the scanning.

-Original Message-
From: Carol Bryant [mailto:cb...@lexclin.com] 
Sent: Thursday, July 07, 2011 9:55 AM
To: 'Elizabeth Chlipala'; Jesus Ellin; 'Rodriguez, Arnold'; 
histonet@lists.utsouthwestern.edu
Subject: RE: Tissue Cassette Printer Recommendations

I am intersted in this info also.  I would like to know what printers everyone 
are using with the Vantage system or a bar coding system. 
Thank you,
Carol 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Elizabeth 
Chlipala
Sent: Thursday, July 07, 2011 12:53 PM
To: 'Jesus Ellin'; 'Rodriguez, Arnold'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Tissue Cassette Printer Recommendations

I second Jesus's comments especially if you are moving towards bar coding.  You 
will need a cassette printer that can print a high quality 2D bar code.

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Manager
Premier Laboratory, LLC
PO Box 18592
Boulder, CO 80308-1592
(303) 682-3949 office
(303) 682-9060 fax
(303) 881-0763 cell
www.premierlab.com

Ship to address:

1567 Skyway Drive, Unit E
Longmont, CO 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jesus Ellin
Sent: Thursday, July 07, 2011 10:49 AM
To: 'Rodriguez, Arnold'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Tissue Cassette Printer Recommendations

I would look at Thermo, Leica and General Data printers .

Jesus Ellin
Yuma Regional Medical Center

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rodriguez, 
Arnold
Sent: Thursday, July 07, 2011 9:38 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Tissue Cassette Printer Recommendations

Hello All,

We are interested in purchasing a new cassette printer and I would
sincerely appreciate any recommendations for this instrument. We are
particularly looking for reliability, print speed, LIS connectivity and
barcode technology.

Thank you very much.

Arnold Rodriguez, HT (ASCP)
Supervisor, Anatomic Pathology
Eisenhower Medical Center
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RE: [Histonet] VENTANA ULTRA ER,PR,HER2

2011-06-28 Thread Jesus Ellin
We will be going through this transition, here at Yuma Regional Medical
Center.. Call me if you have questions


Jesus Ellin
928-336-1743

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
barbara.cr...@lpnt.net
Sent: Tuesday, June 28, 2011 7:54 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] VENTANA ULTRA  ER,PR,HER2

We are investigating getting the Ventana Ultra.
I discovered that the ER, PR,  HER2 are not yet FDA approved.

If you are using the Ventana Ultra how are you doing the ER, PR,  HER2?
Do you use the Benchmark XT?

Is anyone using the INFORM HER2 Dual ISH DNA Probe Cocktail Assay?




ANTOINETTE CRILL,
E-mail:  barbara.cr...@lpnt.netmailto:barbara.cr...@lpnt.net

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RE: [Histonet] QC documentation

2011-04-07 Thread Jesus Ellin
We currently use our LIS to support this issue,, the tech are able to go
into the case and make comments about controls, staining, technical work
etc. There are places for comment section, etc.  I also use the LIS to
document Fixation time for specimens.  Multiple specimens are an issue,
but we are able to document that as well.  I then use the LIS to drill
down the data and get me what I want.  I still am using paper work,
since the Pathologist needs to sign off.  But the reports are attached
and reviewed by the Pathologist.  This also allows us to trend issues we
are having within the Department. I like it a lot.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Victor
Tobias
Sent: Thursday, April 07, 2011 11:15 AM
To: Webb, Dorothy L
Cc: 'histonet@lists.utsouthwestern.edu'
Subject: Re: [Histonet] QC documentation

Dorothy,

I'm only going to address what we are doing for IHC.  We have a custom 
worksheet that is printed from the LIS for each patient. We were totally

manual until 3 weeks ago when we went live with the Bond. We are still 
using our custom worksheet for the techs and pathologists.  Boxes for 
them to check off and write comments.  We just modified our IHC 
resulting tool and added fields for the pathologist to electronically 
record the QC.  The manual QC paperwork gets returned to the lab and can

be used for CAP and we can generate an electronic report also.  
Hopefully we'll get more paperless with time.

Victor

Victor Tobias HT(ASCP)
Clinical Applications Analyst
University of Washington Medical Center
Dept of Pathology Room BB220
1959 NE Pacific
Seattle, WA 98195
vic...@pathology.washington.edu
206-744-2735
206-744-8240 Fax
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On 4/7/2011 9:59 AM, Webb, Dorothy L wrote:
 How does everyone handle their QC documentation on special stains and
IHC?  We currently print out the run information from our stainer(s) and
have the tech initial for her QC and the pathologist sign after they
review the slides.  I am hoping that someone has a way of doing this
electronically.  I hope to learn of a better way to save some trees!!!
Thank you ahead of time!

 Dorothy Webb, HT
 Regions Histology Technical Specialist




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RE: [Histonet] CAP checklist, question ANP.23041.

2011-03-16 Thread Jesus Ellin
Mark this is a new question and let me answer this for you from a
inspection point of view.  Currently there are 15 to 18 new questions
that deal with predicative markers and the digital images, most of these
are QA/QC related.  But the issue with images is that your people are
inspecting them.  When you are looking at an image it is more than just
click and go.  There are technical issues of Tiling, focus with z
stacking, AOI ( if the full image was captured), magnification, etc.
This is just technical to images, but then there are the aspects that
are to the histology world as in staining components, microtomy,
fixation, etc.  To say that they don't make a decision is a huge
understatement.  As far as I know CAP put this in because people were
just scanning images and sending them off.  There are also issues were
the scanner scans for possible algorithm studies.  You have to make sure
this is inline.  So as for the High complexity testing to what CLIA
defines, that is a back and forth issue.  Currently within our facility
you have to be licensed HT/HTL to do scanning.  This comes in line with
the CAP looking at creating a QM program and having the
technician/Technologist maintain competencies and assessments for this
technology.  There is also a competency and assessment due for the
pathologist as well for this technology.  I can go on and on, but you
can contact me off line for this.

Jesus Ellin
Yuma Regional Medical Center
928-336-1743

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mark
Turner
Sent: Wednesday, March 16, 2011 4:36 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] CAP checklist, question ANP.23041.

Regarding CAP checklist, question ANP.23041.  The operation of the
imaging system is performed by high-complexity testing personnel.

 

We have a question regarding the qualifications of the operators.  The
operators of the Aperio system are simply scanning entire slides to make
a record for us prior to returning slides to the client.  Our operators
make no evaluation of the image other than whether the scan is adequate
for recording purposes, and this is verified by our medical staff prior
to release of the materials.  In your opinion, does this constitute
high-complexity testing and require CLIA compliant qualifications for
the operators?

Mark Turner, Ph.D, HT(ASCP) QIHC

IHC / Histology Manager

CSI Laboratories

 

770-817-0817 x 394  

678-205-4669  FAX

mtur...@csilaboratories.com mailto:nmon...@csilaboratories.com 

csilaboratories.com
https://csi-srv-007/exchweb/bin/redir.asp?URL=http://www.csi-labs.com/


11525 Park Woods Circle

Alpharetta, GA 30005

 

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RE: [Histonet] Her2 Gastric cases

2011-03-11 Thread Jesus Ellin
Mark can you send me the information as well,  Thanks

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mark
Tarango
Sent: Friday, March 11, 2011 10:03 AM
To: Coppin, Margaret
Cc: Histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Her2 Gastric cases

We do use the Ventana antibody for gastric cases.  There is some
difference
in reading the slide for the pathologist.  I'll send you an article on
it in
a seperate e-mail (so I can attach it).

Mark

On Fri, Mar 11, 2011 at 8:54 AM, Coppin, Margaret
copp...@aruplab.comwrote:

 Hello,



 I am hoping someone can shed some light on whether or not Her2 4B5
 (Ventana's antibody) is okay to run on gastric biopsies. We are
getting
 some client requests for this and I wonder if I should re-direct them
 toward the Dako Hercep Test instead.



 Thank you.



 Margaret G. Coppin, HT(ASCP)

 Technical Supervisor--Immunohistochemistry



 ARUP Laboratories

 500 Chipeta Way

 Salt Lake City, UT 84108

 (801)583-2787 X3869

 copp...@aruplab.com








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RE: [Histonet] Histology Workflow Solutions

2011-02-28 Thread Jesus Ellin
Vendor's, whether we like it or not are going to monitor areas where we
are expressing ideas and concerns.  This cuts down on the need to do
studies and customer data mining.  I to think that vendors need to stay
neutral, but the email clearly has a disclaimer,, so I think enough said
on this one.

-Original Message-
From: Rathborne, Toni [mailto:trathbo...@somerset-healthcare.com] 
Sent: Monday, February 28, 2011 11:03 AM
To: Mahoney,Janice A; Jesus Ellin; Michael Mihalik; CHRISTIE GOWAN;
dana.spen...@pcmh.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions


I can say that I appreciated Michael's comments, but also think that he
should have left his contact information and the company he represents
off of the email. If anyone would have been interested in replying to
him privately, they still could have done so. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]On Behalf Of
Mahoney,Janice A
Sent: Monday, February 28, 2011 12:56 PM
To: 'Jesus Ellin'; Michael Mihalik; CHRISTIE GOWAN;
dana.spen...@pcmh.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions


Histonet Users.
Please help me understand something.  I may be opening a big can of
worms here but I'm confused.
Why is it that Michael Mihalik is allowed to expound on the subject of
workflow solutions when he is a competitor in that market?  I'm not
saying that some of his comments are not helpful but I thought this was
a users forum?  People usually freak out when a vendor tries to put
comment on a competitors products,
what is the difference here? I personally do not want to hear what he
has to say here because he obviously has another agenda regardless of
how it is disguised.
I openly admit that I am a Ventana Vantage user and will stand by that
system because I know it so well and know it's capabilities. The BIG
difference is, I am a user, not a Vendor.
Jan
Omaha



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jesus
Ellin
Sent: Monday, February 28, 2011 11:40 AM
To: Michael Mihalik; CHRISTIE GOWAN; dana.spen...@pcmh.com;
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions

Well put Michael!!

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Michael
Mihalik
Sent: Monday, February 28, 2011 10:35 AM
To: 'CHRISTIE GOWAN'; dana.spen...@pcmh.com;
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions

As many as you know this is a topic that is near and dear to my heart so
I'd
like to expound on this subject if you'll permit me.  For those of you
who
already have solutions, or perhaps have more favored topics, please feel
to
move on to the next subject.

First off, while I have some knowledge of both products, I am a user of
neither.  In fact I am a competitor of both, to some degree.  Both
products
offer advantages and disadvantages.  You really need to think about how
they
fit in your lab.  When I say 'in your lab', I mean not only the
histology
area, but everyone, including the accessioning clerks, secretaries,
pathologists, and even cytotechnologists.

To me, one of the items that is more relevant to your situation is
whether
you want an integrated solution (IMPAC) or a standalone/interfaced
solution.
For instance,

1.  How will information get into Vantage?  Will it have to be manually
accessioned/entered or will there be an interface?  In the IMPAC
solution
this is a non issue.  Also, keep in mind that there may be an interface
cost
from BOTH vendors should you decide an interface is in order.

2.  How will information get OUT of Vantage or put another way, does the
pathologist or secretary need to see information gathered/stored by
Vantage?
This may be resolved by another interface, but it may also be resolved
by
putting Vantage on more and more PCs.

3.  Who is going to configure, manage and maintain Vantage?  This is
going
to be a whole other computer system in your lab.  Will your IT
department
support it, maintain it, administer it, etc.  Who will understand and
set up
the files, etc.?  You have the same issue with IMPAC, but I bet someone
is
already handling all these issues.

4.  Can you use barcodes generated from Ventana on IMPAC?  I don't know
the
answer to this question.  It's not that each system can't read the
barcode.
It's a matter of whether IMPAC calls their slide, slide X and Vantage
calls
it 'y'.  For instance, maybe IMPAC calls it case#.spnid.blockid.slideid
and
maybe Vantage calls it slideidNN.  That means whenever the pathologist
scans
the slide at his IMPAC workstation, IMPAC won't recognize it.  Perhaps
this
is not an issue, but I thought I would bring it up.

5.  Management Reports:  I know IMPAC supports Crystal

RE: [Histonet] Histology Workflow Solutions

2011-02-28 Thread Jesus Ellin
I am coming from the stand point of an informed decision, there are a
lot of other products out there other than a Vantage,, but it is the one
with the most visibility currently.  I do agree that Vendors do need to
be neutral when giving perspective.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Mahoney,Janice A
Sent: Monday, February 28, 2011 11:10 AM
To: 'Rathborne, Toni'; Jesus Ellin; Michael Mihalik; CHRISTIEGOWAN;
dana.spen...@pcmh.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions

So you suggest that vendors pretend to be users by not stating who they
are?  I don't get it?
I do not mean to be argumentative, I REALLY do not see how we are
allowing this.
Jan

-Original Message-
From: Rathborne, Toni [mailto:trathbo...@somerset-healthcare.com]
Sent: Monday, February 28, 2011 12:03 PM
To: Mahoney,Janice A; Jesus Ellin; Michael Mihalik; CHRISTIE GOWAN;
dana.spen...@pcmh.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions


I can say that I appreciated Michael's comments, but also think that he
should have left his contact information and the company he represents
off of the email. If anyone would have been interested in replying to
him privately, they still could have done so.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu]On Behalf Of
Mahoney,Janice A
Sent: Monday, February 28, 2011 12:56 PM
To: 'Jesus Ellin'; Michael Mihalik; CHRISTIE GOWAN;
dana.spen...@pcmh.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions


Histonet Users.
Please help me understand something.  I may be opening a big can of
worms here but I'm confused.
Why is it that Michael Mihalik is allowed to expound on the subject of
workflow solutions when he is a competitor in that market?  I'm not
saying that some of his comments are not helpful but I thought this was
a users forum?  People usually freak out when a vendor tries to put
comment on a competitors products,
what is the difference here? I personally do not want to hear what he
has to say here because he obviously has another agenda regardless of
how it is disguised.
I openly admit that I am a Ventana Vantage user and will stand by that
system because I know it so well and know it's capabilities. The BIG
difference is, I am a user, not a Vendor.
Jan
Omaha



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jesus
Ellin
Sent: Monday, February 28, 2011 11:40 AM
To: Michael Mihalik; CHRISTIE GOWAN; dana.spen...@pcmh.com;
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions

Well put Michael!!

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Michael
Mihalik
Sent: Monday, February 28, 2011 10:35 AM
To: 'CHRISTIE GOWAN'; dana.spen...@pcmh.com;
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Histology Workflow Solutions

As many as you know this is a topic that is near and dear to my heart so
I'd
like to expound on this subject if you'll permit me.  For those of you
who
already have solutions, or perhaps have more favored topics, please feel
to
move on to the next subject.

First off, while I have some knowledge of both products, I am a user of
neither.  In fact I am a competitor of both, to some degree.  Both
products
offer advantages and disadvantages.  You really need to think about how
they
fit in your lab.  When I say 'in your lab', I mean not only the
histology
area, but everyone, including the accessioning clerks, secretaries,
pathologists, and even cytotechnologists.

To me, one of the items that is more relevant to your situation is
whether
you want an integrated solution (IMPAC) or a standalone/interfaced
solution.
For instance,

1.  How will information get into Vantage?  Will it have to be manually
accessioned/entered or will there be an interface?  In the IMPAC
solution
this is a non issue.  Also, keep in mind that there may be an interface
cost
from BOTH vendors should you decide an interface is in order.

2.  How will information get OUT of Vantage or put another way, does the
pathologist or secretary need to see information gathered/stored by
Vantage?
This may be resolved by another interface, but it may also be resolved
by
putting Vantage on more and more PCs.

3.  Who is going to configure, manage and maintain Vantage?  This is
going
to be a whole other computer system in your lab.  Will your IT
department
support it, maintain it, administer it, etc.  Who will understand and
set up
the files, etc.?  You have the same issue with IMPAC, but I bet someone
is
already handling all these issues.

4.  Can you use barcodes generated from Ventana on IMPAC?  I

RE: [Histonet] CAP

2011-02-23 Thread Jesus Ellin
Akemi, were you inspected with the new CAP checklist or the old one?
The situation in our lab is that we were given the checklist and then
they changed us to the new format.  Your thoughts

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Akemi
Allison
Sent: Wednesday, February 23, 2011 7:03 AM
To: histonet
Subject: [Histonet] CAP

Lot's of Labs in LA are in their CAP window!  We had our CAP inspection 
yesterday and having our summation this morning at 9:00.  I think our
department 
did pretty good.  Keeping my fingers crossed.  
 Akemi Allison BS, HT(ASCP)HTL


  
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[Histonet] Information Please

2011-02-16 Thread Jesus Ellin
Wanting to get information on anyone that has already implemented Epic
and offered the Epic ambulatory piece to there clients.  Are you also
offering this technology with interface to competitive laboratories
like, Quest, Lab Corp, etc?


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[Histonet] Re: CMS Postpones Deadline for Physician Signatures

2010-12-22 Thread Jesus Ellin
Yes we received the update.  But there is still questions about difference from 
electronic ordering CPOE vs review and verify correct entry before proccessing 
by a clinician.  Even though it states that this does not address electronic 
orders. We feel that this can be a problem for the future.  

Sent via DROID one Verizon Wireless


-Original message-


From: WILLIAM DESALVO wdesalvo@hotmail.com
To: trathbo...@somerset-healthcare.com, Jesus Ellin 
jel...@yumaregional.org, jwe...@sjha.org, histonet 
histonet@lists.utsouthwestern.edu
Sent: Wed, Dec 22, 2010 15:44:34 GMT+00:00
Subject: CMS Postpones Deadline for Physician Signatures


I have just received notice that the CMS requirement for Physician 
Signature Deadline of Jan 1, 2011 has been postponed.
 
http://www.cms.gov/ClinicalLabFeeSched/
 
CMS has decided that in the first quarter of 2011 they will be 
developing educational and outreach materials to help educate all of us that 
are affected by the policy change. Looks like we have a little more time to 
figure this new process out.  

William DeSalvo, B.S., HTL(ASCP)




 
 From: wdesalvo@hotmail.com
 To: trathbo...@somerset-healthcare.com; jel...@yumaregional.org; 
jwe...@sjha.org; histonet@lists.utsouthwestern.edu
 Date: Fri, 17 Dec 2010 12:38:12 -0700
 Subject: RE: [Histonet] Physician Signatures
 CC: 
 
 
 They sign into the case prior to surgery, they have Physician 
Assistant (PA) assigned to the case, a nurse is assigned to the case and they 
then enter additional information into the system after they complete surgery. 
It meets requirements. In Pathology, many of your Frozen Section specimens 
arrive in the lab on verbal orders or nursing applying a signature and we have 
processed for years. I believe the key point that you have to wrap your head 
around is that the electronic orders by the surgeon are complete before there 
is any delivery of results, the signed and preliminary or final report by the 
pathologist and that meets regulatory requirements. I have more concern on the 
clinical side. Orders can be entered, tests performed and results delivered 
more easily than in Pathology. 
 
 William DeSalvo, B.S., HTL(ASCP)
 
 
 
 
 
  Subject: RE: [Histonet] Physician Signatures
  Date: Fri, 17 Dec 2010 14:06:04 -0500
  From: trathbo...@somerset-healthcare.com
  To: wdesalvo@hotmail.com; jel...@yumaregional.org; 
jwe...@sjha.org; histonet@lists.utsouthwestern.edu
  
  So how do the surgeons electronically order a test? Do they order 
it before the procedure? What if they discover something and need to add an 
additional specimen? Our orders are electronically entered in the OR during the 
procedure. The surgeon is scrubbed and performing the procedure while the 
circulating nurse places the order.
  
  -Original Message-
  From: histonet-boun...@lists.utsouthwestern.edu
  [mailto:histonet-boun...@lists.utsouthwestern.edu]on Behalf Of 
WILLIAM
  DESALVO
  Sent: Friday, December 17, 2010 1:56 PM
  To: Jesus Ellin; jwe...@sjha.org; histonet
  Subject: RE: [Histonet] Physician Signatures
  
  
  
  I previously did not go into to deep detail about security and 
compliance, but in our system all computer portals are password protected, 
orders are signed with electronic signature of the ordering person and when a 
hard copy paper form is printed, the ordering physician's electronic signature 
is applied. It is the same type of process and signature that is used by the 
pathologist to electronically sign off all pathology reports. I absolutely 
agree that you must control access to ordering and maintain integrity in the 
system. As you work through your process to develop a more electronic system, 
you will have the opportunity to build in and require proper controls. With 
those controls implemented, you can then become confident that the electronic 
process can and will meet your regulatory requirements. 
  
  William DeSalvo, B.S., HTL(ASCP)
  
  
  
  
  
   Subject: RE: [Histonet] Physician Signatures
   Date: Fri, 17 Dec 2010 10:46:15 -0700
   From: jel...@yumaregional.org
   To: jwe...@sjha.org; wdesalvo@hotmail.com; 
histonet@lists.utsouthwestern.edu
   
   This is true about electronic ordering but there is a provision 
on what
   is acceptable for electronic order, just ordering in a system and
   spitting out requisitions does not comply, There needs to be 
password
   verification and review of this information

RE: [Histonet] CAP Question regarding procedure manual

2010-12-22 Thread Jesus Ellin
Currently Victor we use to have the techs sign off on all the policies
and procedures.  As Bill stated this is a big pain.  We are now all
electonic and have gone live with I-Passport our document control
software,, this has saved tons of time and effort.  Electronic is the
way to go especially for updates and new information.  Users are notifed
by email and it allows the supervisor to keep track of edits and much
more. 


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of WILLIAM
DESALVO
Sent: Wednesday, December 22, 2010 4:46 PM
To: vic...@pathology.washington.edu; histonet
Subject: RE: [Histonet] CAP Question regarding procedure manual


You will need a signature for the manual and for each procedure that is
implemented or amended during your cycle year. If your manual is very
stable, a yearly signature page for the entire manual may suffice, but
the inspector will note the date everyone signed the manual review page
and then go through the manual to see if there are any implementation
dates or procedure change dates after the manual review date. Each
occurrence found one can be a deficiency.

In my lab, it is not uncommon for new procedures to be written and
implemented or existing procedures implemented during a cycle year and
all these events require a signature by System Medical Director, Site
Medical Director, Site Lab Director, System Technical Specialist
(responsible for physically writing) and all employees affected. You
must prove to CAP that all personnel know where the procedure manual is
located, that they have reviewed the manual as a whole and that they
have reviewed all additions implemented. We have employees sign each
technical alert, procedure update/change and new procedures, along with
a once a year review of all manuals.

This type of signature trail is part of and right in line with quality
management and document control. This process alone can be a daunting
task and requires a lot or forethought. To better manage this process,
we are moving to an electronic on-line, web based procedure manual with
document control functions that tracks usage by employee and captures
electronic signatures for each step of the creation, review and
implementation process. Thankfully, this process is the responsibility
of our Technical Specialist for Anatomic Pathology and our System
Quality Department.


William DeSalvo, B.S., HTL(ASCP)





 Date: Wed, 22 Dec 2010 15:16:37 -0800
 From: vic...@pathology.washington.edu
 To: Histonet@lists.utsouthwestern.edu
 CC: 
 Subject: [Histonet] CAP Question regarding procedure manual
 
 Is there a requirement to have a signature of every staff member on a 
 procedure if they perform that procedure in a manual? Wouldn't one 
 signature on a cover page suffice that you have read and understand 
 what is in the manual?
 
 Victor
 
 --
 Victor Tobias
 Clinical Applications Analyst
 University of Washington Medical Center Dept of Pathology Room BB220
 1959 NE Pacific
 Seattle, WA 98195
 vic...@pathology.washington.edu
 206-598-2792
 206-598-7659 Fax
 =
 Privileged, confidential or patient identifiable information may be 
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RE: [Histonet] Physician Signatures

2010-12-17 Thread Jesus Ellin
This is true about electronic ordering but there is a provision on what
is acceptable for electronic order, just ordering in a system and
spitting out requisitions does not comply, There needs to be password
verification and review of this information by the clinician before it
is ordered and sent to the laboratory performing the service when the
requisition is created.  They go on to say that orders and requisitions
are different aspects and should not be confused. IF the orders are just
received through an electronic interface then there is a difference.
But if the specimen is received using any paper form then this needs to
be signed by the clinician either electronically or manually.

We are looking at this really closely, with using paper requisitions,
even orders from the OR for frozens, molecular studies, interoperative
work, all needs to be signed by the surgeon.  Can you imagine the impact
that this is going to cause. 

Our current solutions is to have maybe standing orders in place and move
and look at process within the  Main OR's, outpatient OR and clients.
Once again a huge problem,, but Bill is right this will lead to more and
more paperless enviroments.


Jesus Ellin
Yuma Regional Medical Center   

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RE: [Histonet] Tissue Processor Advice

2010-10-22 Thread Jesus Ellin
How are you meeting the hours of fixation requirement for Breast?  With
2 and 4 and 8 hours,, But recently there are articles calling for Her 2
to be done on GI cases.  Just want to know you insight on this?

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Feher,
Stephen
Sent: Friday, October 22, 2010 2:12 PM
To: caymanfl...@gmail.com; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Tissue Processor Advice

We are using the Peloris with a 2 hr, 4 hr and 8 hr protocol.  We run 2
hour protocols throughout the day with an average of 4-5 runs per day
depending on specimen volume.  We really like this processor.  We have
had them for 10 months now, are using factory protocols and have not had
any specimens that have been either under or over processed.  The techs
and the pathologists are very pleased with it. 


Steve

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
caymanfl...@gmail.com
Sent: Friday, October 22, 2010 4:17 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Tissue Processor Advice

We are in need of some advice regarding rapid tissue processors.  Models
we are considering:

Sakura Xpress
Leica Peloris
Thermo STP 420

It seems none of these models are perfect in every respect.  I'm
interested in anyone's opinions of these processors and your experience
with them.

All input is appreciated!
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RE: [Histonet] RE: New Cap Guidelines for Her2 and ER/PR

2010-10-13 Thread Jesus Ellin
OK I usually do not like to chime in on this, but here I go.  How can a
true validation of a specific target be obtained if the wiggle room is 6
to 48 hr, or 8 to 72 hr.  Where is the precision and accuracy on the
results for this testing if you are going to be varying process for the
weekend vs weekday?  This is the flaw in the guidelines in my
perspective, when this much time is allowed it is like anything else.
We are going to go the path of least resistance to change, instead of
what is right.  I know that as techs we always want the best, but are
pushed to produce next day.  Techs for years have been saying more
fixation is needed on tissue.  Well enough of that.

What we do is we hold at 12 hours of fixation for all specimens no
matter what?  We document ischemic cold time through our LIS, to include
time placed in formalin, and time of first cut.  We feel that all
specimens need the same fixation times.  This is imperative to
standardize the process, but once again we also have our processors set
up in such a way that they come off at different times and our
production of H an E is in sync with this.  It might sound like a lot,
but we get most of our work done around 96 to 97 % of cases within 24
hours or less using conventional processing techniques.  

With the future relying more and more on, patient centered care, through
personalized medicine, we need to really look on how we can do the
optimal requirements, not do the minimal requirements to reach our
goals.


Jesus Ellin  

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Kuhnla,
Melissa
Sent: Wednesday, October 13, 2010 7:45 AM
To: Phyllis Thaxton; Mahoney,Janice A; Mike Pence; Joyce Cline;
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] RE: New Cap Guidelines for Her2 and ER/PR

For the weekend, we have our processor set for 36 hours in formalin and
then a hold in 70%. This allows for complete fixation and cuts down on
prolonged time in 70%

 



From: Phyllis Thaxton [mailto:dch...@yahoo.com] 
Sent: Wednesday, October 13, 2010 10:32 AM
To: Kuhnla, Melissa; Mahoney,Janice A; Mike Pence; Joyce Cline;
histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] RE: New Cap Guidelines for Her2 and ER/PR

 


 We run a weekend (Friday til Monday AM)  breast run where the tissues
are in 10% NBF for 8 hours, then in 70% alcohol for 48 hours in order to
complete processing on Monday morning. So far no problems.

 

Phyllis Thaxton HT(ASCP)QIHC
DCH Regional Medical Center
Tuscaloosa, AL 

 

 



From: Kuhnla, Melissa melissa.kuh...@chsli.org
To: Mahoney,Janice A janice.maho...@alegent.org; Mike Pence
mpe...@grhs.net; Joyce Cline joyce.cl...@wchsys.org;
histonet@lists.utsouthwestern.edu
Sent: Tue, October 12, 2010 12:02:32 PM
Subject: RE: [Histonet] RE: New Cap Guidelines for Her2 and ER/PR

I disagree.  Prolonged formalin fixation (over 48 hrs), diminishes
signals

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Mahoney,Janice A
Sent: Tuesday, October 12, 2010 12:05 PM
To: 'Mike Pence'; Joyce Cline; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] RE: New Cap Guidelines for Her2 and ER/PR

Formalin fixation time does not impact the results of FISH as it does
IHC.
Jan M
Omaha

-Original Message-
From: Mike Pence [mailto:mpe...@grhs.net]
Sent: Tuesday, October 12, 2010 11:00 AM
To: Mahoney,Janice A; Joyce Cline; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] RE: New Cap Guidelines for Her2 and ER/PR

I don't think it matters if you do Her2 by FISH or IHC the time is still
48hr. I hope I am wrong, but I don't think I am.

Mike

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Mahoney,Janice A
Sent: Tuesday, October 12, 2010 10:25 AM
To: 'Joyce Cline'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: New Cap Guidelines for Her2 and ER/PR


We have decided to reflex to FISH those breasts that do not fall within
the recommended formalin fixation time.  We do work on Saturdays so it
is only the rare 3 day weekends that this comes into play. Jan M Omaha

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joyce
Cline
Sent: Tuesday, October 12, 2010 10:10 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] New Cap Guidelines for Her2 and ER/PR

Does anyone have any experience with storing formalin fixed breast
tissue in 70% before processing?  I am trying to comply with the new
guidelines set forth by CAP and ASCO with regard to Her2 and ER/PR and
since my lab does not operate on the weekend we have been well above the
48 hour recommended formalin fixation time.  Does 70% affect

RE: [Histonet] Quality Assurance for Histology

2010-10-11 Thread Jesus Ellin
We have a place in out LIS that the Pathologist can choose and document 
everything, then we run a report that tabulates and give us the values and 
solutions.  One thing I am seeing here is that we also need to address the 
solution.  A lot of people that I have inspected do great with marking the 
issues, but solutions and tracking they do not do well.

Jesus Ellin

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tench, Bill
Sent: Monday, October 11, 2010 9:02 AM
To: Podawiltz, Thomas; Rene J Buesa; histonet@lists.utsouthwestern.edu; Laurie 
Colbert
Subject: RE: [Histonet] Quality Assurance for Histology

Why would you want to have the pathologists fill out a QA sheet for a function 
you have already performed (and should document).  This would seem to be a 
meaningless exercise (ie, waste of time) for the pathologist. 


Bill Tench
Associate Dir. Laboratory Services
Chief, Cytology Services
Palomar Medical Center
555 E. Valley Parkway
Escondido, California  92025
bill.te...@pph.org
Voice: 760- 739-3037
Fax: 760-739-2604

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Podawiltz, 
Thomas
Sent: Monday, October 11, 2010 8:28 AM
To: 'Rene J Buesa'; histonet@lists.utsouthwestern.edu; Laurie Colbert
Subject: RE: [Histonet] Quality Assurance for Histology

I actually randomly review the slides before they are sent to the Pathologist 
any slide with incomplete sections, chatter or other major defects get re-cut 
at that time. Since doing this complaints from the Pathologist disappeared 
about the quality of the slides they were getting. They get the QA form with 
the last book of slides for the day. They fill it out then give it back to me. 
Works well for us. I do know this will not work for others, but it works for 
us. 

Tom 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
Sent: Monday, October 11, 2010 11:21 AM
To: histonet@lists.utsouthwestern.edu; Laurie Colbert
Subject: Re: [Histonet] Quality Assurance for Histology

After many different forms and many efforts to make the pathologists to provide 
feed back about the quality of the sections and procedures, this is what I 
finished doing:
to ask the pathologists to simply separate the slides they considered of poor 
quality and those unacceptable for diagnoses.
It was then my job to define the problem and to addressed it with the histotech 
who made the slide, to determine the re-training or any other administrative 
action deemed necessary.
After I did that I started to receive slides while before seldom any 
pathologist was willing to use any time to evaluate the slides. In all reality 
they are quite busy to take time to fill forms that, in any event, I also had 
to review, re-evaluate and discuss with the histotech.
This procedure worked very well for me and the quality of the work was improved 
considerably, as well as the rejections diminished.
Try this approach.
René J.

--- On Mon, 10/11/10, Laurie Colbert laurie.colb...@huntingtonhospital.com 
wrote:


From: Laurie Colbert laurie.colb...@huntingtonhospital.com
Subject: [Histonet] Quality Assurance for Histology
To: histonet@lists.utsouthwestern.edu
Date: Monday, October 11, 2010, 11:08 AM


I am revising our daily QA sheet that we hand out to the pathologists with the 
HE's in the morning. I would like to gather some ideas from other sites.  Does 
anyone have a form/chart that they would be willing to share with me?



Laurie Colbert

Huntington Hospital

Pasadena CA

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RE: [Histonet] RE: LIS systems

2010-08-31 Thread Jesus Ellin
We have used PowerPath here and it works great for us.  It also depends
on what you want to accomplish with the LIS.  This is very important to
look at this aspect and define what your goals are, costs, and future
functionality.  The smaller system will be able to customize well, while
the larger systems are pretty much set in there ways.  If I had to pick
top 3 it would be PowerPath, Pathview, and Pathlogic.  The larger
systems have issues and unless if you are part of an enterprise system
that requires you to be one vendor, I would keep my mind open.  But ask
these systems about workflow and how they are going to meet the role of
the new future of QA and QC within the AP Laboratory.  They are so
pathologist centric and they forget about the other aspects of the AP
lab to include cytology, molecular, grossing, etc.



Jesus Ellin HT/PA ASCP BSBE
Anatomic Pathology Supervisor
Department of Pathology 
Information Systems
Yuma Regional Medical Center
Yuma,AZ
jel...@yumaregional.org
928-336-1743
928-336-7319

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Victor
Tobias
Sent: Tuesday, August 31, 2010 7:30 AM
To: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] RE: LIS systems

  We have used PowerPath since 1999 and have made so many custom changes

that we probably can't ever leave. If I were looking today I would 
consider http://www.pathview.com/.

Victor

Victor Tobias
Clinical Applications Analyst
University of Washington Medical Center
Dept of Pathology Room BB220
1959 NE Pacific
Seattle, WA 98195
vic...@pathology.washington.edu
206-598-2792
206-598-7659 Fax
=
Privileged, confidential or patient identifiable information may be
contained in this message. This information is meant only for the use
of the intended recipients. If you are not the intended recipient, or
if the message has been addressed to you in error, do not read,
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transmission. Instead, please notify the sender by reply e-mail, and
then destroy all copies of the message and any attachments.


On 8/31/2010 7:23 AM, Blazek, Linda wrote:
 I've never used Meditech so I don't know what the down side is to that
system.  I have used PowerPath and it was a great system but if you want
a system that has most of what PowerPath has but not the enormous cost
you may want to look at Pathlogix.  http://www.pathlogix.com/
 I use it now and like it.  It does have some glitch things but they
are not major and there is a simple workaround for them.


 Linda Blazek HT (ASCP)
 Manager/Supervisor
 GI Pathology of Dayton
 Digestive Specialists, Inc
 7415 Brandt Pike
 Huber Heights, OH 45424
 Phone: (937) 396-2623
 Email: lbla...@digestivespecialists.com



 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Mitchell, Janice A
 Sent: Tuesday, August 31, 2010 9:43 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] LIS systems

 Good Morning,
 We are looking for new LIS system.  Right now there are two options, a
system  for all of Clinical Labs  AP or  a new system for just AP.
Right now we use Meditech. Any advice on which systems work best for AP.
I know each system will have some flaw since nothing is perfect but,
anything has got to be better than Meditech.

 Thanks, Janice

 Janice A. Mitchell, BS, HT(ASCP)
 Assistant Histology Supervisor
 Children's Hospital of Philadelphia
 Anatomic Pathology and Laboratory Medicine
 324 S. 34th Street
 Philadelphia, Pa 19104-4399
 215-590-1738(lab)
 267-426-7754(office)

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RE: [Histonet] decontamination of cryostat

2010-07-21 Thread Jesus Ellin
Bill and company

This is a very difficult, there are times were decontamination is needed
immediately depending on the outcome of the frozen or there is scheduled
maintenance that needs to occur with the decontamination as well.  The
UV light is not sufficient enough to call this decontamination.  CAP has
stated that it needs a specific reagent used in this decontamination
procedure.  My Chair was upset by this statement from the College and
called them to ask for clarification.  The main purpose is documented
and scheduled times of decontamination is what we received back from the
College.  Of course there are circumstances when a case presents itself,
action needs to be taken and documented.  I would say is look at
creating a scheduled decontamination that is appropriate for you
facility.  We have elected for a monthly Decontamination of cryostats,
this is based on usage and history.  This is documented and the
appropriate solution is used during decontamination.  This is done
during the normally work day since we have two cryostats.  This usually
takes 3 days to do right, but some facilities might not be able to do
this.


Jesus Ellin
Yuma Regional Medical Center

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tench,
Bill
Sent: Wednesday, July 21, 2010 8:36 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] decontamination of cryostat

I would suggest that if you are a CAP certified lab that you read the
appropriate section in the current LAP standards list.  The note
associated with the standard is pretty specifiic.  I believe that if you
use the cryostat daily, you need to decontaminate once a week, but i
don't have the standard available.
 
Bill Tench
Associate Dir. Laboratory Services
Chief, Cytology Services
Palomar Medical Center
555 E. Valley Parkway
Escondido, California  92025
bill.te...@pph.org
Voice: 760- 739-3037
Fax: 760-739-2604
 

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RE: [Histonet] decontamination of cryostat

2010-07-21 Thread Jesus Ellin
We use the Lysol Brand IC and Envirocide.  We switch off every other
month to prevent resistance to the cleaner that is being used within the
instrument.  


Jesus Ellin
Yuma Regional Medical Center
928-336-1743

-Original Message-
From: anni...@gmail.com [mailto:anni...@gmail.com] 
Sent: Wednesday, July 21, 2010 9:24 AM
To: Jesus Ellin; histonet-boun...@lists.utsouthwestern.edu; Tench, Bill;
Histonet
Subject: Re: [Histonet] decontamination of cryostat

If I may ask, what do you contaminate with when doing a full meltdown
defrost clean up after a suspect TB or hep B pos case?
Formalin?
Some proprietary decontaminant?
AnnieinArabia
Empower your Business with BlackBerry(r) and Mobile Solutions from
Etisalat

-Original Message-
From: Jesus Ellin jel...@yumaregional.org
Sender: histonet-boun...@lists.utsouthwestern.edu
Date: Wed, 21 Jul 2010 09:01:19 
To: Tench, Billbill.te...@pph.org; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] decontamination of cryostat

Bill and company

This is a very difficult, there are times were decontamination is needed
immediately depending on the outcome of the frozen or there is scheduled
maintenance that needs to occur with the decontamination as well.  The
UV light is not sufficient enough to call this decontamination.  CAP has
stated that it needs a specific reagent used in this decontamination
procedure.  My Chair was upset by this statement from the College and
called them to ask for clarification.  The main purpose is documented
and scheduled times of decontamination is what we received back from the
College.  Of course there are circumstances when a case presents itself,
action needs to be taken and documented.  I would say is look at
creating a scheduled decontamination that is appropriate for you
facility.  We have elected for a monthly Decontamination of cryostats,
this is based on usage and history.  This is documented and the
appropriate solution is used during decontamination.  This is done
during the normally work day since we have two cryostats.  This usually
takes 3 days to do right, but some facilities might not be able to do
this.


Jesus Ellin
Yuma Regional Medical Center

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Tench,
Bill
Sent: Wednesday, July 21, 2010 8:36 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] decontamination of cryostat

I would suggest that if you are a CAP certified lab that you read the
appropriate section in the current LAP standards list.  The note
associated with the standard is pretty specifiic.  I believe that if you
use the cryostat daily, you need to decontaminate once a week, but i
don't have the standard available.
 
Bill Tench
Associate Dir. Laboratory Services
Chief, Cytology Services
Palomar Medical Center
555 E. Valley Parkway
Escondido, California  92025
bill.te...@pph.org
Voice: 760- 739-3037
Fax: 760-739-2604
 

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RE: [Histonet] New CAP question ANP.22760

2010-06-26 Thread Jesus Ellin
I have been reading the post to this question and it seems to me that there are 
different standards depending on the lab that is operating the methodology.  I 
do agree that the core lab for years have had the instruction and training in 
the performance of validation.  One thing that comes to mind as well is why has 
histology not had this training?  Why are we not getting this from our 
certification agency, our professional societies and biggest reason where is 
our standardization.  It seems to me that with all these regualtions in plac 
for so long, why were we missed.  Is it because when inspected through CAP we 
are being inspected by a pathologist rather than a histo tech?  These are some 
of the questions at hand.  I to see new standards within the CAP checklist as 
well as other regulatory organizations that will affect the future of the 
Anatomic Pathology community.  But I think we need is to provide a underlying 
architecture for our peers, so that we can begin the transition to the future.  
This is only the beginning, there is still Digital Image Analysis and 
Telepathology.  It funny we are looking to become a hybrid of radiology and the 
core lab, but with the best of both worlds.  Tim great structure for the 
validation study.  


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu on behalf of Morken, Tim
Sent: Wed 6/23/2010 9:48 AM
To: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] New CAP question ANP.22760
 
Joe,

You wrote : The folks in the 'clinical' lab have been performing more 
comprehensive and complex validation procedures for a very long time ...

Those were my thoughts exactly. While the person replying may or may not have 
specific histology experience she will have clinical lab experience (however, 
my guess is that she is exposed to histology regularly at CAP). Clinical labs 
have a bit of an easier time, actually, because they validate primarily to 
known concentration controls - analytical controls manufactured at a range of 
known concentrations for instance. The institution then adds in their normal 
controls for validation.

As far as the current question about validating a new lot of reagent the best 
practice is to run parallel tests on the same machine. If that is not easily 
possible on a particular manufacturer's instrument then the question should be 
asked of them: Why not? If this is a requirement the manufacturer should 
provide an easy path to meeting the requirement. However, if that is not the 
case then the institution simply writes a procedure to get around the 
inadequacies of the instrument (Maybe the vendor can help with that). Then 
follow the procedure. That should satisfy inspectors.

An ...appropriate panel of tissues... is whatever the institution deems 
appropriate for the given antibody or reagent. This is a perfect place for 
tissue arrays. You can make your own or buy them.

IHC must meet CLIA validation guidelines but since IHC is generally qualitative 
the requirements must be understood and methods adapted to a qualitative 
scenario. Several IHC and Histotechnology books discuss the subject at length 
(Taylor, Dabbs, Bancroft for instance).

Below is a brief overview of how to do that. (for more in-depth info this was 
covered in an NSH teleconference I gave last year - PowerPoint, audio and 
references available from NSH-, and will be covered in a similar workshop at 
NSH in Seattle this year).


1)
CAP General Validation
CAP GEN.42020-42163 Test Method Validation Follows CLIA CFR Sec 493.1253 Does 
not apply well to IHC (IHC is usually qualitative)

But the general principle applies:
The laboratory must have data on each test's accuracy, precision, analytic 
sensitivity, interferences and reportable range.

Unmodified FDA-cleared or approved tests:  the lab may use manufacturer 
information or published reports but lab must verify outside data.

Non-FDA cleared: Lab MUST verify or establish analytic accuracy, precision, 
sensitivity, specificity and reportable range.

2) Validation includes:
Accuracy:
Compare results with New antibody to a previously validated antibody
on the same tissues

Precision:
Test samples with varying antigen expression
Intra-run, Inter-run tests, 10 slides each (reproducibility)

Sensitivity:
True Positive vs False Negative (higher % FN = less sensitive)

Interferences [Specificity]:
True Negative vs False Positive (Higher % FP = less specific)
Delineate what could interfere to give a false positive or false
negative result.

Reportable Range
Establish a scoring system
Provide the definition of a positive result

3)Sensitivity

Analytic Sensitivity:
Lowest amount of substance detectable by the test
Can only be done with controls of known concentration

Diagnostic Sensitivity:
Ability of the test to determine true diagnostic positive verses false  
negative (higher % FN = less 

RE: [Histonet] Antibody Validation

2010-06-15 Thread Jesus Ellin
There are other issue that you have to take into consideration with both
instruments, With digital image analysis you also have to look at the
questions that CAP just instituted for this.  This includes the machine
being run by someone that can do high complexity testing.  This means
that you have to have a tech do this machine, not a TA or Lab aid.
There are also issue with consistent calibration of the Image analysis
machines, continued education of the techs, and validating not only
anitbodies but continued validation of the image algorythms.. Do not
listen to vendors, rely on your instinct and validate.  


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


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RE: [Histonet] Antibody Validation - long response

2010-06-15 Thread Jesus Ellin
Well said Elizabeth 


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Liz Chlipala
Sent: Tuesday, June 15, 2010 9:01 AM
To: Rene J Buesa; histo...@pathology.swmed.edu; teri.hall...@midmichigan.org
Subject: RE: [Histonet] Antibody Validation - long response

Bottom line it's not the vendors responsibility to validate their equipment or 
antibodies in your lab. Some vendors may help you do this, but ultimately the 
lab needs to validate the equipment and IHC in their lab.  The vendors normally 
calibrate the equipment prior to shipment and once they set the instrument up 
in your lab, they should be able to provide you with the documentation that 
states that they calibrated the instrument.  Your instruments need to be 
calibrated prior to being validated. 

As far as your scanner goes some vendors can provide validation, but it's at a 
cost and that cost is not cheap depending upon what you actually want 
validated.  If you are using the scanner and associated algorithms for analysis 
then you need to validate that separately.  There are several steps required to 
validate a scanner - 1.  you validate the scanner 2.  if you are using a 
database to store your images then that also may need to be validated and 3.  
if you are using algorithms that provide you with data then those algorithms 
need to be validated.   

For example prior to running a validation protocol on a tissue processor its 
needs to be calibrated for temperature.  All of your major equipment needs to 
be on a calibration schedule.  We calibrate all of our instruments once a year 
and validation is completed only once unless we change the instrument location 
or how we use the instrument. Pipettors are calibrated every 6 months.  All 
instruments are validated it may just be a one pager for the basic lab 
equipment but instruments like the tissue processor, slide staining, IHC 
stainer and scanner require written protocols some of these are 80 pages in 
length and go into great detail.  

The same goes for your antibodies.  Antibodies are validated initially with 25 
tissue samples (10 strongly positive tissues, 10 moderate to weakly positive 
tissues and 5 tissues that have no reactivity) This type of validation is 
required for routine antibodies, prognostic markers such as Her-2, ER and PR 
require additional tissue samples.  New lots require 3 tissue samples one 
strongly positive on moderate to weakly positive and one negative.  If you 
change the antibody source or detection system or retrieval it needs to be 
validated again - This information comes from the paper Standarization of 
Immunohistochemistry from CAP its available on line - I have a copy if you need 
it.  There are also new guidelines for ER/PR and a new article on validation of 
ER/PR in the June issue of Archives of pathology from CAP.

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC Manager Premier Laboratory, LLC PO Box 
18592 Boulder, Colorado 80308 office (303) 682-3949 fax (303) 682-9060 
www.premierlab.com
 
 
Ship to Address:
1567 Skyway Drive, Unit E
Longmont, Colorado 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
Sent: Tuesday, June 15, 2010 8:50 AM
To: histo...@pathology.swmed.edu; teri.hall...@midmichigan.org
Subject: Re: [Histonet] Antibody Validation

Teri:
You are right about the validations you propose although I am not surprised 
that your vendor does not think it is necessary. They are in the business of 
selling and you are in the business of assuring the high quality of your work 
to obtaining the most accurate work for patients' sake.
There is where the difference resides. Ignore your vendor and keep validating 
your protocols.
René J.

--- On Tue, 6/15/10, teri.hall...@midmichigan.org 
teri.hall...@midmichigan.org wrote:


From: teri.hall...@midmichigan.org teri.hall...@midmichigan.org
Subject: [Histonet] Antibody Validation
To: histo...@pathology.swmed.edu
Date: Tuesday, June 15, 2010, 7:55 AM


I am being questioned by our vendor as to why we need to validate our automated 
immunostainer and image analysis instrument. They would like documentation 
pertaining to the requirement of validation and the number of specimens 
utilized for validation.  I am requesting that each antibody be validated on 
the instrument against a previously validated instrument. Additionally, I am 
requesting that each new lot of antibody be validated upon receipt against 
previously ran specimens. This would also apply to the image analysis 
antibodies. (Her2 has been validated by
FISH.) The vendor has apparently polled users in the area and 

RE: [Histonet] Barcoding and Tracking Information

2010-05-03 Thread Jesus Ellin
There are several systems that are out there.  But I am glad to see that
you are wanting to interface with the LIS.  That is a key step.  But I
would look at all of them and come up with a pretty good RFP process for
selection.  Make sure also they are live with at least 3 to 4 sites with
the interface. 


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Blake
Taylor
Sent: Monday, May 03, 2010 6:43 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Barcoding and Tracking Information

Does anyone currently use an automated barcoding and tracking system
that interfaces with CoPath-Sunquest??  If so can you please tell me
which company you are using?  Thanks so much

Blake Taylor
Section Supervisor
Dept. of Pathology
Lexington Medical Center
803-936-8214
bcdu...@lexhealth.org


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RE: [Histonet] (no subject)

2010-04-26 Thread Jesus Ellin
I would look at this very carefully, especially in light of the new
regulation that were just released by the CAP on ER and PR.  But that is
up to each individual lab 


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Urim,
Lyudmila
Sent: Monday, April 26, 2010 8:10 AM
To: Histonet@lists.utsouthwestern.edu
Subject: [Histonet] (no subject)

Hi,

I am looking into purchasing a microwave tissue processor. 

I would be interested to hear from people who has had experience with
microwave tissue processing. And what brands would you recommend?

Thanks a lot,

Lucy

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RE: [Histonet] Leica Peloris

2010-04-15 Thread Jesus Ellin
Please answer this we are looking at buying one next year! 


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mike
Pence
Sent: Thursday, April 15, 2010 11:58 AM
To: Davis, Michael J; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Leica Peloris

We use the Peloris and have had no big problems with it. Certainly not
that affect our stain, however, we do not use it xylene-free. Her may
lay the problem.


I think the FDA question should be answered by someone from Leica.

Mike

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Davis,
Michael J
Sent: Thursday, April 15, 2010 1:33 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Leica Peloris


Moving into a new lab and have tested several processors.  Need some
info on the peloris.  Good and Bad.  We demoed the machine for about 2
months and had an issue with our biopsy tissue staining too light (HE).
We could not get this problem resolved - we were running our tissue thru
the xylene free process.  Also any truth to the rumor that I heard today
thay the FDA has placed a hold on this machine?

Michael J Davis, HT (ASCP)
Histology
Lancaster General Hospital
555 N Duke St
Lancaster, PA 17601



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RE: [Histonet] Communication when pathologist are not in sameareaas lab

2010-04-14 Thread Jesus Ellin
I agree with
Janice processes need to be defined and then look at the right technology
to implement.  This is were LIS plays a key role.  But I would warn you
that the LIS company needs to be forward thinking and open to
ingtergration with vendors. Just my thoughts.

Michael Mihalik m...@pathview.com wrote:

Thank you for heading in that direction.  The 'right' LIS makes a BIG
difference.


Michael Mihalik
PathView Systems | cell: 214.733.7688 | 800.798.3540 | fax: 952.241.7369





-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Mahoney,Janice A
Sent: Wednesday, April 14, 2010 2:47 PM
To: 'malbena...@gmail.com'; Scott, Allison D
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Communication when pathologist are not in same
area
as lab

With the right LIS and standard work you may never have to or get to,
depending on your perspective, speak with a Pathologist again.
Jan
Omaha

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Malika
Benatti
Sent: Wednesday, April 14, 2010 2:38 PM
To: Scott, Allison D
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Communication when pathologist are not in same
area
as lab

Well our 5 pathologists, advance practitioner and SPR are just across the
way from us, until last July all request were made personally by
pathologist
to staff and if there were any query with regard to the request made it
was
sorted then and then and it was pretty straight forward.

But the good all days of face to face communication changed when we
started
to get requests via email, although a good idea, in principle, requests
via
email are not without pitfalls and therefore face to face communication
between lab staff and pathologist is still necessary.



 say email request can be problematic as very often request.

On Wed, Apr 14, 2010 at 4:09 PM, Scott, Allison D 
allison_sc...@hchd.tmc.edu wrote:

 Hello to all in histoland.  What are you doing to minimize the
 communication breakdown, when the pathologist are not housed in the lab.
 We will be moving to a new lab and the pathologist will not be in the
 new bldg with us.  They will be in the old building next door. Are you
 relying upon email and phone interactions.   My directors concern is how
 will this effect the flow of information, especially when they are used
 to face to face interactions.

 Allison Scott HT(ASCP)
 LBJ Hospital
 5656 Kelley
 Houston, Texas 77026
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RE: [Histonet] (no subject)

2010-04-07 Thread Jesus Ellin
I have to agree Vantage is an excellent system, just make sure that
other basis are covered, interfacing, future instrumentation costs and
also bi directional interfacing with LIS.  These are costly

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Mahoney,Janice A
Sent: Wednesday, April 07, 2010 10:21 AM
To: 'Santiago, Albert'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] (no subject)

In my opinion Ventana's Vantage is miles ahead of anyone else.  We've
had the system for over a year and love it.  My techs would not want to
work without it.  It is much more than a tracking system, you will be
amazed at the information Vantage can give you.  Very user friendly and
takes very little space.
Jan Mahoney
Omaha, NE

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Santiago, Albert
Sent: Wednesday, April 07, 2010 11:57 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] (no subject)

Hello fellow histonetters, we're in the process of researching bar
coding/specimen tracking system for our lab and I was wondering if
anyone had any recommendation of any particular system and/or vendor
that I should look into. Thank you

Albert Santiago, HT(ASCP)
Laboratory Manager
Dermatopathology
215-662-6759/6539-office
215-662-6150-fax



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RE: [Histonet] Thermo Slide and Cassette printers

2010-03-18 Thread Jesus Ellin
We have the Printmate coming on board and have used the slide mate.  The 
Printmate is excellent, the slide mate is good but if you have it connected to 
LIS there is lag time.  Also take into consideration that the barcodes have to 
be read and that traditional scrapping does hinder this.  You will need to look 
at getting a hot plate for the blocks so that the read is clear, clean and 
concise.  Also the color will play in issue.  AS mike said there are different 
vendors out there, but for me for space and accuracy, since every histology 
labs has space, I would go with looking at thermo or General Data.  If you have 
any questions feel free to give me a call.


Jesus Ellin  HT/PA  ASCP
Yuma Regional Medical Center
928-336-1743

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Michael Mihalik
Sent: Thursday, March 18, 2010 8:48 AM
To: 'Sharon.Davis-Devine'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Thermo Slide and Cassette printers

Hi Sharon,

We're an LIS vendor working with a client that just purchased 6 of these.
They're 30 days away from go live, but we've played with them for a bit.  

If you or anyone else is curious about what our experiences have been, feel
free to email me.

We also trialed cassette labelers from several other companies before our
client selected these labelers.


Michael Mihalik
PathView Systems | cell: 214.733.7688 | 800.798.3540 | fax: 952.241.7369
 
 
 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Sharon.Davis-Devine
Sent: Thursday, March 18, 2010 10:30 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Thermo Slide and Cassette printers

Does anyone out there in Histo land have any experience with the new
Thermo Scientific PrintMate and SlideMate system?  Or do any of you have
another system similar to this that you have experience with?  We are
looking into some of these systems to help reduce errors and make our
laboratory more lean. I would appreciate any and all opinions and
advice.  

 

Thank you.

 

Sharon Davis-Devine, CT (ASCP)

Cytology-Histology  Supervisor

Carle Foundation Hospital

Laboratory and Pathology Services

611 West Park Street

Urbana, Illinois 61801

217-383-3572

sharon.davis-dev...@carle.com

 

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RE: [Histonet] Block patient IDs

2010-03-12 Thread Jesus Ellin
In the latest CAP inspection list that we were handed, block and slides are 
said to have two perminant identifiers.  There are alot of new items in this 
checklist that raise questions.  This raises the question if there are alot of 
labs out of compliance?  There are also new questions that pertain to fna 
samples at the bedside, etc.  Also those doing digital imaging there are about 
15 new questions from calibration to personal able to do the testing.  There 
are new revisions on how we should be validating antibodies.  What we are 
seeing is a paradigm shift in quality management.  This is the biggest thing 
that I see, but what we are not seeing the resources that need to be deployed 
for this type of shift.  Any takers on this.  I acctually gave a presentation 
on this for the Arizona Society of Histology last November in Tucson.

Jesus Ellin HT/PA  ASCP
Yuma Regional Medical Center
928-336-1144


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu on behalf of hymclab
Sent: Fri 3/12/2010 10:08 AM
To: 'Nails, Felton'; 'Anne van Binsbergen'; 
histonet-requ...@lists.utsouthwestern.edu; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Block patient IDs
 
It refers to the original container the specimen came to you in.  The block is 
considered a secondary container, therefore, two identifiers are not required.

Dawn

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[https://connect.yumaregional.org/CitrixFEI/composemessage.asp?to=histonet-boun...@lists.utsouthwestern.edu]
 On Behalf Of Nails, Felton
Sent: Friday, March 12, 2010 9:55 AM
To: 'Anne van Binsbergen'; histonet-requ...@lists.utsouthwestern.edu; 
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Block patient IDs

It is my understand that the two patient identifier applies to the completed 
slide not the block.
You can verify this by looking at the CAP Checklist for anatomical pathology

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[https://connect.yumaregional.org/CitrixFEI/composemessage.asp?to=histonet-boun...@lists.utsouthwestern.edu]
 On Behalf Of Anne van Binsbergen
Sent: Friday, March 12, 2010 9:42 AM
To: histonet-requ...@lists.utsouthwestern.edu; histonet@lists.utsouthwestern.edu
Subject: [Histonet] Block patient IDs

A question for all you CAP fundis: how many patient Identifiers are needed on 
each paraffin block

We currently just write the unique, LIS generated number on the block face, but 
have recently been advised that CAP and JCIA require not one, but TWO patient 
IDS on the block

Comments please

--
Anne van Binsbergen (Hope)
Abu Dhabi
UAE
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RE: [Histonet] New cryostat decontamination CAP statndard

2010-02-23 Thread Jesus Ellin
To me the key word in here is interval.  If a regularly scheduled interval is 
set, this could be daily , weekly, monthly or quarterly.  Obviously there are 
going to be the times when a contaminant is there and the machine has to be 
brought down, but also I do not see the mention of the UV light.  We have a 
Leica that has an internal UV button.  This is pressed everyday as well as 
normal daily maintenance.  Once a month our cryostat is brought down for 
decontamination.  This is part of the normal maintenance.  I agree that is the 
CAP wants this to happen, it needs to be clearly defined within the question 
and not up to interpretation.

Jesus Ellin  HT/PA  ASCP

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mike Pence
Sent: Tuesday, February 23, 2010 8:18 AM
To: Pamela Marcum; Jeffrey Silverman
Cc: histonet@lists.utsouthwestern.edu; Jeffrey Silverman
Subject: RE: [Histonet] New cryostat decontamination CAP statndard

The way I read this is if I don't use my cryostat 7 days a week, 365 days a 
year, then I don't use it daily and therefore I will set my own routine 
decontamination schedule.
Mike
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Pamela Marcum
Sent: Tuesday, February 23, 2010 9:06 AM
To: Jeffrey Silverman
Cc: histonet@lists.utsouthwestern.edu; Jeffrey Silverman
Subject: Re: [Histonet] New cryostat decontamination CAP statndard




Thank you Jeffery.  I am not sure how we get to CAP on this however; it makes 
no sense for a really busy lab unless they want to give us enough cryostats to 
make up for the problem this will cause.  Is this something NSH might decide to 
help with?  



It may be time to bombard them (CAP) with questions and report the issues it 
will cause with patient care.  None of us want to use a contaminated cryostat 
but we also know how to decontaminate without being in danger and stopping 
surgery for frozens . 



Pam Marcum 

UAMS - Anatomic Pathology 



- Original Message - 
From: Jeffrey Silverman   JSilverman @ NSHS . edu  
To: histonet @lists. utsouthwestern . edu 
Cc: Jeffrey Silverman   JSilverman @ NSHS . edu  
Sent: Tuesday, February 23, 2010 8:23:39 AM GMT -06:00 US/Canada Central 
Subject: [ Histonet ] New cryostat decontamination CAP statndard 

Here is the new standard for cryostat decontamination. No references are given 
documenting or supporting the need for this onerous and cumbersome weekly 
requirement. I suggest we lobby the CAP and demand  both documentation 
supporting the need for weekly defrosting or, better, a more user friendly and 
sensible standard. 

Jeff Silverman 


**REVISED** 06/15/2009 
ANP .12087 Phase II N/A YES NO 
Is there a documented procedure for the routine decontamination of the cryostat 
at defined intervals, 
and are decontamination records evident? 
NOTE: The cryostat must be defrosted and decontaminated with a tuberculocidal 
disinfectant at an 
interval appropriate for the institution; this must be weekly for instruments 
used daily. Trimmings and 
sections of tissue that accumulate inside the cryostat must be removed during 
decontamination. Although 
not a requirement, steel mesh gloves should be worn when changing knife blades. 





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RE: [Histonet] Ventana ULTRA Immuno Stainer

2009-09-11 Thread Jesus Ellin
Excellent stainer, but you need to look at your process to help facilitate the 
technology. if you have nay questions you can reach me.

Jesus Ellin
Yuma Regional Medical Center 
928-336-1144


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu on behalf of Gomez, Milton
Sent: Thu 9/10/2009 7:35 PM
To: Histonet
Subject: [Histonet] Ventana ULTRA Immuno Stainer
 
Dear Histonetters,
 
Is anyone out there using the Ventana ULTRA Immuno Stainer?  What is your 
experience with them?  What are the advantages, disadvantages, pros and cons?
 
Thank you very much in advance?
 
Milton A. Gomez, HTL (ASCP)
Technical Supervisor
Immunohistochemistry Department
ARUP Laboratories, Inc.
500 Chipeta Way
Salt Lake City, UT 84108-1221
Desk Phone:  801-583-2787, ext.3869
Lab. Phone:   801-584-5257/5242
Fax:  801-584-5217
E-mail:  milton.go...@aruplab.com 
https://connect.yumaregional.org/CitrixFEI/composemessage.asp?to=milton.go...@aruplab.com
 
Web:  www.aruplab.com http://www.aruplab.com/ 

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RE: [Histonet] ABT systems

2009-08-25 Thread Jesus Ellin
There are several ones that are out there, Ventana-vantage, Dako-TPID,
Cerner's solution, There is also Omintrax, but the majority of the
solutions are primarly barcode with some tracking feature.. I would ask
you if you have an LIS to communicate see if they would interface to a
third party vendor,, this usually costs extra.


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Donna
Millard
Sent: Tuesday, August 25, 2009 1:20 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] ABT systems

Hello,

We are investigating purchasing an Automated Bar Code and Tracking
System. So far we're looking at Ventana's Vantage system, and Cerner
CoPath's system. Is anyone aware of other systems out there? We're not
looking for just the bar-coding, we also want the tracking features.

 

Thanks

 

Donna Millard, B.S.

Histology Supervisor

Physicians Reference Laboratory, LLC

7800 W. 110th Street

Overland Park, KS  66210

Direct: 913-339-0485

Fax: 913-319-4156

 


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RE: [Histonet] Information Systems: Specimen Tracking MiddleWare

2009-03-27 Thread Jesus Ellin
I do agree that computers are tools that are indeed an asset to anatomic
path laboratories.  Michael I applaud you for your efforts in getting
the staff and engaging them.  This is the basis of my entire theory, in
order to create efficiencies within histology that there are 3 distinct
area of the process  Histology, Transcription, and Pathologist.  Unlike
the clinical laboratory we are not a straight test result type of
methodology, rather a fair straight forward process that has
inter-connected components.  Those components have for so long relied o
the fact of internal checks and balances, but with the explosion that
has happened within AP in the last 10-15 years we are seeing those
checks and balances begin to have cracks and stress points.   

I would applaud anyone that takes advance courses in anything, but I
would caution an IT person looking at Anatomic Pathology that does not
have the clinical background that is necessary to see the cracks and
stress points.  I use PowerPath as my LIS and as the University of
Washington our facility has made strides in stream lining and innovation
with our LIS,, but I am open to help anyone that is looking to get
information on this subject. 


 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: jel...@yumaregional.org 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of joelle
weaver
Sent: Friday, March 27, 2009 2:48 AM
To: m...@pathview.com; Histonet
Subject: RE: [Histonet] Information Systems: Specimen Tracking 
MiddleWare


Yes, I do agree, that is why I call it a tool for people to use. I
think that it is a stereotype to think that histologists are not
experienced or knowledgable about computers. There are some histologists
who have had a fairly good introduction to computer systems, how
computers work, what they can and cannot do, software, applications,
interfaces, databases, and have worked with 5 or more LIS systems,
barcodes etc. Though admittedly, in my experience this is a rarity. Most
of what I have learned about computers, I have gotten from formal
classes, but I also have used this knowledge in other arenas, and wish I
could use it more in my job. I am just not fortunate enough to have been
given the opportunity to have much influence on the processes, or the
computer systems. I think that many who have been promoted into
management simply also accept this stereotype that histologists know
only technical information, and so we are not consulted, though we do
the work everyday.I wish that you could come to our lab and educate
those who have been given this authority! I would love to have a
computer geek come to our lab and inform us of what is available to
help us to our jobs better.

 

Joelle Weaver HTL (ASCP)
 
 From: m...@pathview.com
 To: joellewea...@hotmail.com; jel...@yumaregional.org; 
 histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Information Systems: Specimen Tracking  
 MiddleWare
 Date: Thu, 26 Mar 2009 18:14:21 -0500
 
 People are always at the forefront. Someone has to build that new 
 tool, or come up with some new process or whatever. That's why before 
 we do any installation of our software, we spend what probably amounts

 to 100 to 200 hours interviewing and watching each clerk, PA, 
 histotech, secretary, cytotech, and pathologist and THEN we propose 
 how we would install and tailor our software. By the way, at the end 
 of that analysis, people are usually pretty tired of hearing me ask 
 'why do you do that', but guess what
 -- you are way, way more likely to get 'buy in' from the staff. That 
 tech you spoke to at 3 a.m. remembers that some computer geek took the

 time and effort and asked them how they would do things better.
 
 
 ...but let me address a real world issue. I am not versed in the 
 technologies of many aspects of the AP/Cytology department (you'll 
 never hear me speak on subjects of which stainer is better for 
 instance), but I do know a few things about work flow and 
 computerization. I like to illustrate via example, so let's try this
one:
 
 In the real world, a histotechnologist may have only worked in let's 
 say 3 or 4different labs in their life, and perhaps only 1 or 2 
 different computer systems. With that background, how are they 
 supposed to know what's possible or not possible to do with computer 
 technology. Personally, I think it's the job of the LIS vendor to work

 TOGETHER with the histotechnologist and other department personnel to 
 come up with better solutions. In this example, each side has 
 knowledge and experience that needs to be conveyed to the other. When 
 that communication occurs, magic happens. Barcodes are not the magic. 
 It's how you use those barcodes in your work flow.
 
 
 It's always about the people.
 
 
 

[Histonet] Error question

2008-11-24 Thread Jesus Ellin
Was wanting to know how people handle accession errors within the
pathology information system,, to elaborate on this, is when a person
receives in the specimen with a requisition and they have to do data
entry into the system.  What is allowable?, what is the percent error
rate?, how are people dealing with errors?  How are you dealing with
personnel??  This is becoming an issue and I wanted to survey people out
there how they are handling this issue,? Any help would greatly be
appreciated.

 

 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

* Office:  (928) 336-1743

*Fax:  (928) 336-7319

*Email: [EMAIL PROTECTED] 

 




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[Histonet] Antibody protocol

2008-11-18 Thread Jesus Ellin
Needing some help with the staining protocol for  HSA (Hepatocyte
Specific Antigen) clone OCH1E5, made by Cell marquee to be ran on the
Ventana LT/Benchmark platform.. Would anyone be willing to share
protocol information with us, as well as staining methodology.  Thank
you for the help.  

 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: [EMAIL PROTECTED] 



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RE: [Histonet] HT grossing specimens

2008-10-17 Thread Jesus Ellin
$1.00 dollar per hour

 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: [EMAIL PROTECTED] 

-Original Message-
From: Tom McNemar [mailto:[EMAIL PROTECTED] 
Sent: Friday, October 17, 2008 10:13 AM
To: Jesus Ellin; Weems, Joyce; Snyder, Wendy;
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] HT grossing specimens

Is that $1 per specimen or $1 per hour?


Tom McNemar, HT(ASCP)
Histology Co-ordinator
Licking Memorial Health Systems
(740) 348-4163
(740) 348-4166
[EMAIL PROTECTED]
www.LMHealth.org


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] Behalf Of Jesus
Ellin
Sent: Friday, October 17, 2008 11:38 AM
To: Jesus Ellin; Weems, Joyce; Snyder, Wendy;
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] HT grossing specimens


But did not finish answering the question, there is a augmentation of
pay depending on years of experience and specimen type,, most of these
specimens are GI or Prostate so we give a $1.00 augmentation,, but most
of the time the PA do the gross and the Pathologist still like doing the
large specimens or complex ones.

 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: [EMAIL PROTECTED] 


-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Jesus
Ellin
Sent: Friday, October 17, 2008 8:35 AM
To: Weems, Joyce; Snyder, Wendy; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] HT grossing specimens

Just for everyone's FYI if you are Processing specimen's under CAP
regulation, but you are collecting from Medicare, The Medicare
regulation is completely different and if audited by Medicare can be
subject to huge fines for not meeting the requirement..  Help me out on
this one Charles E.

 

Jesus A Ellin  HT/PA  ASCP

Department of Pathology/Histology

Yuma Regional Medical Center

2400 South Ave A

Yuma, AZ  85364 - 7170

( Office:  (928) 336-1743

(Fax:  (928) 336-7319

*Email: [EMAIL PROTECTED] 

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Weems,
Joyce
Sent: Friday, October 17, 2008 8:30 AM
To: Snyder, Wendy; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] HT grossing specimens

Just part of the gross room position here.. But it is called
Processing according to the latest CAP check list...

Joyce 

-Original Message-
From: [EMAIL PROTECTED]
[mailto:[EMAIL PROTECTED] On Behalf Of Snyder,
Wendy
Sent: Friday, October 17, 2008 11:25 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] HT grossing specimens

I am looking for HT and or MLT/MT's grossing small specimens.  If so,
are you getting a difference in your salary/hourly wage for this added
responsibility.
 
Thanks,
 
Wendy Snyder, HT(ASCP), MT(AMT), MLT(ASCP) Lead Histology Technician
United Hospital Center
(304) 624-2652
[EMAIL PROTECTED]
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RE: [Histonet] Waste on Benchmark XT

2008-10-07 Thread Jesus Ellin
I am surprised that ,, and also Ventana has not informed you of a way to 
neutralize the waste.. I know that they have the protocols you might want to 
get intouch with them about this.. and also follow your facilites regulatory 
guidlines,,

Jesus Ellin  HT/PA  ASCP


-Original Message-
From: [EMAIL PROTECTED] on behalf of Laurie Colbert
Sent: Tue 10/7/2008 7:19 AM
To: Senn, Amy R; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Waste on Benchmark XT
 
We have the same hazardous waste company that picks up our formalin,
alcohol, xylene waste pick up all of the waste from the Benchmarks.

Laurie Colbert

-Original Message-
From: [EMAIL PROTECTED]
[https://connect.yumaregional.org/CitrixFEI/[EMAIL PROTECTED] On Behalf Of Senn,
Amy R
Sent: Tuesday, October 07, 2008 5:34 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Waste on Benchmark XT

 

 



From: Senn, Amy R 
Sent: Tuesday, October 07, 2008 8:33 AM
To: Senn, Amy R
Subject: 

 

Hello Histoland,

 

We have a Benchmark XT.  The sales rep told us it was ok to dump the
waste down the drain.  THEN we were told that the waste is hazardous and
actually causes mutant changes in lab animals.  (wow, I could turn into
Rogue or Storm! My luck, I'd be Beast or Toad . . . . .)

 

Anyway, can I get some feedback from you guys about how you dispose of
the waste from the Benchmark XT?  We had someone here to test it, but
we're still waiting for results.

 

Thanks!

 

Amy, Camp Hill PA

 



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