[Histonet] new IHC billing and Sunquest CoPathPlus

2014-04-29 Thread Houston, Ronald
Besides manually entering IHC charges, has anyone worked out a way to 
automatically bill for 88342 and 88343 on cases in Sunquest CoPathPlus?

Thanks

Ronnie Houston, MS HT(ASCP)QIHC
Anatomic Pathology Manager
ChildLab, a Division of Nationwide Children's Hospital
www.childlab.com

700 Children's Drive
Columbus, OH 43205
(P) 614-722-5450
(F) 614-722-2899
ronald.hous...@nationwidechildrens.orgmailto:ronald.hous...@nationwidechildrens.org
www.NationwideChildrens.orghttp://www.nationwidechildrens.org/

One person with passion is better than forty people merely interested.
~ E.M. Forster

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RE: [Histonet] Negative controls

2014-04-29 Thread Sebree Linda A
We still run negative controls.

Linda A. Sebree 
University of Wisconsin Hospital  Clinics 
IHC/ISH Laboratory 
600 Highland Ave. 
Madison, WI 53792 
(608)265-6596 
FAX: (608)262-7174 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Beth Brinegar
Sent: Monday, April 28, 2014 4:56 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Negative controls

Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies 
Appropriate negative controls are used.

I apologize, I know this question has been asked before.  I'm trying to satisfy 
these requirements in one procedure.

Thank you all for your assistance!!

Beth Brinegar HTL(ASCP)
Anatomic Pathology Supervisor
Mercy Medical Center
Cedar Rapids, IA 52403
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Re: [Histonet] cryosectioning, bubbles between slide and section

2014-04-29 Thread Emily Brown
Hello,

This may be a little late, but we use a mix of half 30% sucrose and half
OCT to section.  It works really well with 14 to 25 micron sections and no
cooling or heating of the slide.  Our tissue is very small
though--embryonic spinal cord or brain from chick or mouse.  I just change
the way I pick it up to get rid of bubbles.  Have you tried rolling the
slide upwards when you pick it up (if that makes sense) as opposed to
rolling it from left to right (or the opposite)? Also as our cryostat gets
older, it tends to get more static and we cannot get rid of it.  This
causes the tissue to adhere to the slide faster, which definitely causes
bubbles.  That may the case, but I hope not!!

Emily

By bitching and bitching and bitching, they could exhaust the drama of
their own horror stories. Grow bored. Only then could they accept a new
story for their lives. Move forward.

-Chuck Palahniuk, Haunted


On Fri, Apr 25, 2014 at 2:58 AM, Christina Kreutzer 
christina.kreutze...@gmail.com wrote:

 Hello members,
 I would need some help regarding cryosectioning of spinal cord. I am
 currently establishing cryosectioning on the cryostat (Leica CM1950) for
 this tissue and am having some problems. I am cutting 4% PFA fixed and
 succrose infiltrated spinal cords, embedded in Tissue Tek at 10µm and a
 temperature of approximately -16°C . I get more or less smoth slices but
 once I let them adhere to the slide -directly from the knife, after
 straightening it carefully with a brush - I get massive air bubbles between
 the slide and the slice.

 I have experience cutting on cryostats and with different tissues and never
 have had this problem before.

 I tried to change the temperature of the chamber and/or chunk and tried to
 warm the slide before adhering the slice and I tried to cool the slide. But
 it didn't help. Do you think changing from 30% succrose to a mixture of
 Tissue Tek/Succrose or even Tissue Tek/PBS would help?
 Does anybody have an advice?

 Regards
 Christina
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RE: [Histonet] Negative controls

2014-04-29 Thread Debra Siena
I just wanted to clarify there are two types of negative controls, one is a 
negative reagent control and one is a tissue that is known negative.  A lot of 
time, we tend to focus on the negative reagent control and forget about the 
negative tissue control.  I know that a lot of smart folks out there on 
histonet will be able to give you some direction as far as how to write a 
policy to cover both but just wanted to clarify that the two types of negative 
controls are different and the negative reagent control may be abandoned if you 
are running a polymer detection kit but the known negative tissue controls are 
still required.  Thanks

  Debbie Siena, HT(ASCP)QIHC
StatLab Medical Products
Technical Support Manager
407 Interchange Street | McKinney, TX 75071
t: 800.442.3573 ext. 229 | f: 972.436.1369
dsi...@statlab.com | www.statlab.com


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Beth Brinegar
Sent: Monday, April 28, 2014 4:56 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Negative controls

Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies 
Appropriate negative controls are used.

I apologize, I know this question has been asked before.  I'm trying to satisfy 
these requirements in one procedure.

Thank you all for your assistance!!

Beth Brinegar HTL(ASCP)
Anatomic Pathology Supervisor
Mercy Medical Center
Cedar Rapids, IA 52403
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RE: [Histonet] Negative controls

2014-04-29 Thread Weems, Joyce K.
This is what I put in my procedure shortly after Richard sent his email. There 
wasn't a problem at inspection.

Following his announcement at NSH/ISH Forum in Windsor, CT, Dr. Richard 
Carten sent an email to Histonet on July 17, 2102, regarding CAP guidelines for 
negative controls. The checklist will be changed to reflect that
negative controls will no longer be required for polymer based procedures. The 
new wording contains the following statement:
“Immunohistochemical tests using polymer-based 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”. Dr. Stargel has approved the discontinuation of 
negative controls as of July 20, 2012.

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

This e-mail, including any attachments is the property of Saint Joseph’s 
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review, use, disclosure, or distribution is prohibited. If you are not the 
intended recipient, please delete this message, and reply to the sender 
regarding the error in a separate email.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Beth Brinegar
Sent: Monday, April 28, 2014 5:56 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Negative controls

Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies 
Appropriate negative controls are used.

I apologize, I know this question has been asked before.  I'm trying to satisfy 
these requirements in one procedure.

Thank you all for your assistance!!

Beth Brinegar HTL(ASCP)
Anatomic Pathology Supervisor
Mercy Medical Center
Cedar Rapids, IA 52403
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[Histonet] cryosectioning - still bubbles between slide and section, spinal cord

2014-04-29 Thread Christina Kreutzer
Dear members,
first I wanna thank all the people who responded to my first email (Andrea,
Mesru and Emily).Your tips were very helpful. Unfortunately I am still
fighting agains bubbles/ wrinkles/bubble-shaped wrinkles between my slices
and the slide.

During the last couple of days I tried:

i) to adjust the temperature of the chamber and the sample, seems like
-16°C brings the best slices

ii) to cool the slide by putting it into the chamber and warming it with my
thumb just the second I held it towards the slice to adher

iii) to warm the slides by putting them on a 37°C warm heating-plate after
attachement

iv) to moisten the slides with a little bit of bidest before letting the
slices attach and put these slides on a 37°C heating plate
afterwards...that was kind of desperate try to straighten the slices slowely

v)  3 different intermedia before embedding the sample in pure Tissue Tek,
a) 30% Succrose, b) half 30% succrose and half Tissue Tek, c) half Tissue
Tek half PBS

but...nothing really helped. I still have wrinkles aka bubbles. Tomorrow I
am going the cut perfusion fixed rat spinal cord, hoping that this makes a
difference.

Anyway, I think I have some options left 1) trying to cut on a different
mikrotome and 2) Leica promised to send me some slide/embedding
solution/blade samples that worked for other groups.

Can anybody think of something I havent tried yet? Besides of raising slide
thickness and cutting for freefloating procedure?

I would be so thankful for any ideas/suggestions/tips!

Regards
Christina
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[Histonet] Your experience with barcoding and materials tracking in grossing and histology

2014-04-29 Thread Morken, Timothy
Hi all, I am giving a talk at NSH about implementing barcoding and materials 
tracking in histology. I have that experience with Cerner Copath ABT, but not 
other systems. I'd like to hear from others, especially with other systems, 
about their experiences in implementing barcoding in their lab with their own 
LIS, third party vendors (ie, Vantanage, Cerebro, Lab Lion, Dako, others). Pros 
and cons, lessons learned, etc that would help others starting down that path. 
The point of the talk is the generalities of implementation, not a marketing 
talk on any particular system, though I would like to know why you chose a 
given system, whether you were able to use your own LIS for barcoding or had to 
use a third party vendor.

Thanks in advance for any and all information.


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

415.514-6042  (office)
tim.mor...@ucsfmedctr.orgmailto:tim.mor...@ucsfmedctr.org


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[Histonet] Re: Negative Controls

2014-04-29 Thread Terri Braud
On Message 7 - Negative Controls
While it is true that if you run polymers, you no longer have to run a
negative reagent control, HOWEVER, you still must have a negative tissue
control, which to quote CAP: must  show no staining of tissues known to
lack the antigen
Any of the following can serve as a negative tissue control:
1. Multi tissue blocks.  These can provide simultaneous positive and
negative tissue controls and are considered best practice...
The type of negative tissue control used (i.e. separate sections,
internal controls, or multitissue blocks) must be specified in the
laboratory manual.
Thus sayeth CAP, the almighty.  Please see ANP.22570
Our lab has defined our negative controls as a piece of Uterus as the
negative tissue in a multitissue block as a negative tissue control for
most of our antibodies, though for a few that might be too reactive in
uterus, we use a piece of skin.
I hope this helps.

Terri L. Braud, HT(ASCP)
Anatomic Pathology Supervisor
Holy Redeemer Hospital Laboratory
1648 Huntingdon Pike
Meadowbrook, PA 19046
Ph: 215-938-3676
Fax: 215-938-3874

Message: 7
From: Beth Brinegar bbrinegar...@gmail.com
Subject: [Histonet] Negative controls
Hello fellow histonetters,

What is are other labs doing to satisfy the ANP.22570 QC - Antibodies
Appropriate negative controls are used.


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[Histonet] Seventh Wave Pathology or Other Contract Pathology Labs!

2014-04-29 Thread Jennifer Oskins
Histonetters-

   I am trying to help a co-worker find contact information for
Seventh Wave Pathology. Does anyone have information for this Lab? Are
there any other Histology/Pathology Labs that are recommended for
processing, staining and evaluating tissue samples? Thank you so much in
advance!

Jennifer
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RE: [Histonet] Seventh Wave Pathology or Other Contract Pathology Labs!

2014-04-29 Thread Garcia, Lori, M.Sc.
Here is contact person:

Kim Sagartz
President  Chief Operating Officer
Senior Director, Client Services
Seventh Wave Laboratories LLC
743 Spirit 40 Park Drive, Suite 209
Chesterfield MO 63005
Telephone: 636-519-4885
Facsimile: 636-519-4886
www.7thwavelabs.com

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jennifer Oskins
Sent: Tuesday, April 29, 2014 11:02 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Seventh Wave Pathology or Other Contract Pathology Labs!

Histonetters-

   I am trying to help a co-worker find contact information for 
Seventh Wave Pathology. Does anyone have information for this Lab? Are there 
any other Histology/Pathology Labs that are recommended for processing, 
staining and evaluating tissue samples? Thank you so much in advance!

Jennifer
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RE: [Histonet] Seventh Wave Pathology or Other Contract Pathology Labs!

2014-04-29 Thread Douglas Porter
Jennifer,

You can send your samples to us.  We'd be happy to evaluate them for you.  My 
contact information is below.

I guess I should ask what kind of samples you have first though...!

Douglas A. Porter, HT (ASCP) 
Grossing Technician 
IT Coordinator
Cancer Registrar 

CAP-Lab, PLC 
2508 South Cedar Street 
Lansing, MI 48910-3138 

517-372-5520 (phone) 
517-372-5540 (fax) 

doug.por...@caplab.org 

www.caplab.org  
 
 
The information contained in this message may be privileged and/or confidential 
and protected from disclosure. If the reader of this message is not the 
intended recipient, you are hereby notified that any dissemination, 
distribution, copying, forwarding or capture of this communication is strictly 
prohibited. If you have received this communication in error, please notify me 
immediately by return e-mail and delete this and all copies. Thank-you.


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jennifer Oskins
Sent: Tuesday, April 29, 2014 2:02 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Seventh Wave Pathology or Other Contract Pathology Labs!

Histonetters-

   I am trying to help a co-worker find contact information for 
Seventh Wave Pathology. Does anyone have information for this Lab? Are there 
any other Histology/Pathology Labs that are recommended for processing, 
staining and evaluating tissue samples? Thank you so much in advance!

Jennifer
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RE: [Histonet] Seventh Wave Pathology or Other Contract Pathology Labs!

2014-04-29 Thread Douglas Porter
Jennifer,

If your samples happen to be of a non-human nature, let me suggest the 
following lab:

Amy S. Porter, HT(ASCP) QIHC
Michigan State University
Investigative HistoPathology Laboratory
William S. Spielman, Ph.D. - Director
Department of Physiology / Human Pathology
Biomedical Physical Sciences Building 
567 Wilson Road - Room 2133
East Lansing, MI  48824-3320
Phone:  517-884-5026
Fax:  517-432-1368
port...@msu.edu
www.humanpathology.msu.edu

Douglas A. Porter, HT (ASCP) 
Grossing Technician 
IT Coordinator
Cancer Registrar 

CAP-Lab, PLC 
2508 South Cedar Street 
Lansing, MI 48910-3138 

517-372-5520 (phone) 
517-372-5540 (fax) 

doug.por...@caplab.org 

www.caplab.org  
 
 
The information contained in this message may be privileged and/or confidential 
and protected from disclosure. If the reader of this message is not the 
intended recipient, you are hereby notified that any dissemination, 
distribution, copying, forwarding or capture of this communication is strictly 
prohibited. If you have received this communication in error, please notify me 
immediately by return e-mail and delete this and all copies. Thank-you.


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Jennifer Oskins
Sent: Tuesday, April 29, 2014 2:02 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Seventh Wave Pathology or Other Contract Pathology Labs!

Histonetters-

   I am trying to help a co-worker find contact information for 
Seventh Wave Pathology. Does anyone have information for this Lab? Are there 
any other Histology/Pathology Labs that are recommended for processing, 
staining and evaluating tissue samples? Thank you so much in advance!

Jennifer
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[Histonet] Job Opening in East Tennessee

2014-04-29 Thread rgrow
Blount Memorial Hospital in Maryville, TN will have a histology technician 
position opening in May. One of our histotechnician's is retiring after a 
long career for some well deserved time to do as she wants.
We are located in east Tennessee just minutes from the beautiful Smoky 
Mountains National Park and experience 4 wonderful seasons!
Applicants must meet the educational and training requirements necessary 
for certification by the American Society of Clinical Pathology as a 
Histology Technician, HTL, or have experience equal to certification. 
Salary commiserate with experience. Please respond via email with resume 
attached to: rg...@bmnet.com .
Thank you

Renee Grow, BA., HT (ASCP)
rg...@bmnet.com
Histology Supervisor
Blount Memorial Hospital
907 E. Lamar Alexander Pkwy.
Maryville, TN  37804-5016
(865) 977-4744
(865) 977-5766 Fax

This communication may contain protected health information (PHI) that is 
legally protected from inappropriate disclosure by the Privacy Standards 
of the Health Insurance Portability and Accountability Act (HIPAA) and 
relevant Tennessee Laws. If you are not the intended recipient, please 
note that any dissemination, distribution or copying of this communication 
is strictly prohibited. If you have received this message in error, you 
should notify the sender immediately by telephone or by return e-mail and 
delete this message from your computer. Direct questions to the Blount 
Memorial Hospital Privacy Officer at 865-977-4675.
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[Histonet] CAP question ANP.22978 - Her2 assay validation

2014-04-29 Thread Martha Ward-Pathology
Hello all,

I have been reading through the most recent revisions and want to see how 
others are handling this question.   The explanation states that it is for new 
and existing assays and that if your validation does not meet current standards 
that you must supplement and bring it into compliance.  Furthermore if you do 
not have any documentation from the initial validation the assay must be fully 
revalidated and documented.

Our lab has been performing the Herceptest from Dako (FDA approved) since 
before 2008 and participating in the HER2 proficiency testing since it was 
first offered.   We have our statistical results comparing our IHC patient 
results to FISH Her2 results since 2008 and we have always done well on our CAP 
proficiency testing (95%-100%).We do inter-pathologist result comparisons, 
using know CAP slides and have 95% to 100% agreements.   

What I do not have however is the original results of the slides that were 
stained to set up the original assay.   Under these circumstances will we need 
to completely revalidate the assay, using the mandated 20+/20- cases, or can we 
simply do a retroactive formal review and write up of our past performances on 
our proficiency testing challenges?

Thanks in advance for your help with this!

 
Martha Ward, MT (ASCP) QIHC
Manager
 
Molecular Diagnostics Lab
Medical Center Boulevard  \  Winston-Salem, NC 27157


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[Histonet] RE: CAP question ANP.22978 - Her2 assay validation

2014-04-29 Thread Vanessa Perez
From what I have read and understand you should be able to do a write up the 
retroactive review based on the PT results.  What we did here was bought a 
microarray slide that came with the HER2/ER/PR results, ran them on our 
machine, and compared our results to the ones that came with the slide.


Vanessa Perez Garcia
Pathology Reference Lab
210-892-3746
210-892-3732
vpe...@pathreflab.com

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Martha 
Ward-Pathology
Sent: Tuesday, April 29, 2014 2:47 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] CAP question ANP.22978 - Her2 assay validation

Hello all,

I have been reading through the most recent revisions and want to see how 
others are handling this question.   The explanation states that it is for new 
and existing assays and that if your validation does not meet current standards 
that you must supplement and bring it into compliance.  Furthermore if you do 
not have any documentation from the initial validation the assay must be fully 
revalidated and documented.

Our lab has been performing the Herceptest from Dako (FDA approved) since 
before 2008 and participating in the HER2 proficiency testing since it was 
first offered.   We have our statistical results comparing our IHC patient 
results to FISH Her2 results since 2008 and we have always done well on our CAP 
proficiency testing (95%-100%).We do inter-pathologist result comparisons, 
using know CAP slides and have 95% to 100% agreements.   

What I do not have however is the original results of the slides that were 
stained to set up the original assay.   Under these circumstances will we need 
to completely revalidate the assay, using the mandated 20+/20- cases, or can we 
simply do a retroactive formal review and write up of our past performances on 
our proficiency testing challenges?

Thanks in advance for your help with this!

 
Martha Ward, MT (ASCP) QIHC
Manager
 
Molecular Diagnostics Lab
Medical Center Boulevard  \  Winston-Salem, NC 27157


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Re: [Histonet] Your experience with barcoding and materials tracking in grossing and histology

2014-04-29 Thread Sue


So we have the Vantage system with CoPath ABT.  With CoPath you cannot use 
Vantage 

unless you get ABT.  I actually like Vantage alot.  There are some issues that 
make it a 

little difficult to use and I would love to talk to you directly since trying 
to put it all in an e-mail 

is crazy.  If you want you can call my cell 856-905-1549. 



Sue Paturzo 

TJUH 




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[Histonet] Question about high complexity testing for histotechnologists

2014-04-29 Thread Delia, Catherine
Does anyone know if there is a regulatory agency that requires high complexity 
testing certification for histotechnologists.

Catherine Susan Delia, BS. HT. ASCP
Chief Technologist, Anatomic Pathology
University Hospital
150 Bergen Street
E-151
Newark, New Jersey 07103
Phone: 973-972-5717
Cell: 908-391-1060
Fax: 973-972-5724
deli...@uhnj.orgmailto:deli...@uhnj.org

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