[Histonet] margins without frozen

2010-12-29 Thread Tench, Bill
If the margin is grossly close, then re-excision without a frozen is
entirely appropriate.
 
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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[Histonet] cassette labelers, etc

2010-12-17 Thread Tench, Bill
The response by M. Mihalik nails the problem.  Anything that is batched
(cassette labeling, slide labeling, case labeling) is known to be high
risk for mistakes even though it may seem to be more efficient.
On-demand-labeling is the key to significantly reducing identification
errors.
 
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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[Histonet] Procedure manual review

2010-11-15 Thread Tench, Bill
All procedures must be reviewed annually (and that means WITHIN 12
months, not just once a calender year)
This may be done by the appropriate supervisor or pathologist, not
necessarily the Director (Director must review all new or changed
procedures)
The review should confirm that the procedure in operation matches what
really happens.
The laboratory must have in place a mechanism that demonstrates that the
users of those procedures are familiar with them (and without digging up
the CAP standards, i rely on my memory that this must also be documented
in some format on an annual basis).  I believe we accomplish this with
an annual signed statement from the employees confirming they are
familiar with the procedures they use. 
 
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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[Histonet] rapid h and e

2010-11-13 Thread Tench, Bill
We have never noticed any significant cell loss if dehemoglobinzing is
done on bloody smears either before or after regular staining (as noted,
this is used ONLY when the smear is very bloody.  If it is very bloody
there can be very significant obscuration.  This is especially true of
liver FNA's).  As for regular staining, we have not found that the
addition of OG offers anything special (the rare case of keratinized
cells still stands out with the regular h and e stain).
 
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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[Histonet] rapid h and e

2010-11-12 Thread Tench, Bill
We use the same materials and timing we use for a frozen section, which
as a cytopathologist works just fine for me.  Approx 1 min Hematox,
several dips wash, dips in blueing UNTIL BLUE (people tend to shorten
this critical step), no more than 5 dips in eos, 100 ETOH X 2, xylene
dipped until runs smooth, coverslip.  Takes about 1 min 45 sec.  If
there was a lot of blood, one can start with quick fix and dips in acid
alcohol, or the histo people can destain and restain the case at a later
date.
 
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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[Histonet] Saponin

2010-10-25 Thread Tench, Bill
Lots of blood can be a problem in cyto specimens, especially smears.  If
you are making smears from fresh specimens in particular you may elute
the obscuring hemoglobin by dipping the smear directly in acid alcohol
(i think 5% hcl-95% etoh).  We do this frequently for CT guided FNA's
(particularly of the liver and thyroid, which tend to be bloody).  We
also do this post facto on those smears even when they have already
been stained with H and E.  The red cell stroma disappears into the
background).  Just lift the coverslip and back up to 95%, use acid
alcohol ( i think it is sold on the commercial market as
differentiating agent), and then start staining process all over.
With fresh specimens you can see the hemoglobin elute from the surface
while you dip the slide.  We typically go back into regular 95% Etoh
just to get rid of the acid background (effects the blueing down the
line).
 
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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[Histonet] eosin

2010-10-22 Thread Tench, Bill
I think the use in a processor becomes a local culture.  I think
everyone in my community does it (someone spread the word), so now we
all do.  I believe that we are all putting it in the last alcohol.  It
really makes facing a block on minute pieces a whole lot easier.  We
found marking the tissue directly tedious, and it didn't persist as well
in the processing.
  Because there is often so little visible material in our FNA cell
blocks, we mark the histogel pellet with Davidson ink, and when the tech
has just faced off the ink, he/she knows its time to start collecting
sections.
 
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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[Histonet] formalin containers

2010-10-22 Thread Tench, Bill
We haven't heard anything about this (and we were inspected at the end
of July). If you have any additional information, please post it.
It is a little hard to image a locking Lid on a disposable plastic
container of reasonable cost that is large enough to hold a a total
colon resection or large mastectomy.
 
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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[Histonet] FX

2010-10-19 Thread Tench, Bill
it's too cold.  set your cryostat at 20.  put your tumb on the block
 
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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[Histonet] fx

2010-10-19 Thread Tench, Bill
that's suppose to be  put your thumb on the block. 
 
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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[Histonet] clinical trial blocks

2010-10-18 Thread Tench, Bill
The fundamental philosophy that we have is that we do not want to stand
in the way of the patient receiving any kind of treatment.  That being
said, we also have the policy that whether or not we own the material
(patients are actually suppose to sign an admission consent that says
they give up any ownership rights), we are clearly the legal custodians
of the material, and as such are responsible for insuring that no
irreparable distruction occurs.  So, we prefer to not send out blocks
unless the clilnical trial says there are no alternatives.  We contact
them and ask if we can send recuts from which they can obtain the
information they desire.  We also review what we have.  If we have only
one section, we cut a recut for the file before sending out any blocks.
If we have only one block, with not much in it, we again discuss the
issue with the trial coordinator.  We do insist on return of the block,
and assuming that there is an outside review of the material, we insist
on a copy of the report.  We also have the patient sign a release
informing them that they need to understand that this process may
exhaust any tissue that would be useful for some other new treatment
which may come up down the line. Since we have to pull this material for
review and usually make recuts, we bill the clinical trial.  Years back,
they never had any budget allowances for this, and it was always a
hassle.  More recently, we get a lot less BS.  They know they have to
pay, and they do.  Unfortunately, nothing is free any more.
 
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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[Histonet] change in CPT coding rule

2010-10-14 Thread Tench, Bill
The change in place now allows for billing multiple blocks from the same
specimen for the same special stain (it isn't just immunos)  BUT you
must justify this (should be done by a statement in the report micro).
You are not permitted just because you wanted to stain multiple blocks
to increase your chance of identifying the target, rather you must
indicate that EACH additional block presents additional information.
This could be assumed to always be the case for sentinel nodes (you are
specifically looking for tumor in each block), but would not be true if
you have a multiple blocks of a lung tumor that you were testing for
some specifc marker.
 
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] RE: New Cap Guidelines for Her2 and ER/PR

2010-10-13 Thread Tench, Bill
 Have you validated this processing?  Leaving the tissue in 70% alcohol for 48 
hours is not standard, and thus requires all of the hassles associated with 
validation.


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 Phyllis Thaxton
Sent: Wednesday, October 13, 2010 7:32 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 antigenicity for 
either Her2 or ER/PR?  Any information or suggestions will be greatly 
appreciated.  Thanks :)


Ronda Souders
Hagerstown Medical Laboratory
301-665-4980
fax 301-665-4941
ronda.soud...@wchsys.orgmailto:ronda.soud...@wchsys.org


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[Histonet] relaxation of her2 standards

2010-10-13 Thread Tench, Bill
Don't hold your breath.  I have had multiple conversations with at least
one of the primary individuals who set the standards and i have not
detected ANY willingness to modify the standards and that includes a
hard and fast insistence on good validation for ANYTHING that differs
from standard processing.  If you are not in compliance you are asking
for a world of hurt (which may extend to the patient).  Of course, your
other comments about the tissue management are right on.
 
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] Quality Assurance for Histology

2010-10-11 Thread Tench, Bill
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] Quality Assurance for Histology

2010-10-11 Thread Tench, Bill
 Sorry, you are right about that. But, one wonders, if the problem has been 
solved before they get the slides, what's the usefulness of the activity (that 
would be a CAP debate)


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: Laurie Colbert [mailto:laurie.colb...@huntingtonhospital.com] 
Sent: Monday, October 11, 2010 9:07 AM
To: Tench, Bill; Podawiltz, Thomas; Rene J Buesa; 
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Quality Assurance for Histology

Actually, it is a CAP requirement: 
ANP.11713 There is documented evidence of daily review of the technical 
quality of histologic preparations by the pathologist.

-Original Message-
From: Tench, Bill [mailto:bill.te...@pph.org]
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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[Histonet] CAP programs

2010-10-04 Thread Tench, Bill
There are now online CAP PIP programs.  I have done one on prostate.
Also there are online programs for the cytology part.  Review the
catalogue.
 
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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[Histonet] change in immuno machines

2010-10-01 Thread Tench, Bill
If you changed machines, you need to validate the staining on that
machine just as if you never had the first machine.
 
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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[Histonet] giving back tissue

2010-09-09 Thread Tench, Bill
In all of this discussion, it is important to understand that there are
significant variations in state laws that relate to this issue, so if
this problem arises, have your hospital/lab attorney check into state
laws very carefully.  In California, the laboratory may not own the
tissue (again, depending on releases never read but signed by the
patient on admission) but it clearly is the responsible custodian.
This applies to sending out slides and blocks for research and for
clinical testing.
 
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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[Histonet] decal arteries

2010-09-09 Thread Tench, Bill
We routinely decal these.  Most often for part of a day, but if really
dense, overnight.
 
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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[Histonet] billing consults

2010-09-08 Thread Tench, Bill
we ask the consultant to bill the patient's insurance.  If they don't do
that, they bill the hospital and the hospital passes the charges on to
the patient.  we do not make any distinction based on where the request
for the consultation came from (us, the patient, the treating
clinician).  The patient is the beneficiary of the service.  On the very
rare case when it clearly is an issue of intellectual curiosity (i can
think of only 3 examples), the practice will pay the charge.
 
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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[Histonet] returning tissue

2010-09-08 Thread Tench, Bill
We do not return any tissue to patient unless there is a religious
request that must be initiated by the patient (ie, staff are not
permitted to offer this option--we consider that coaching).  Then it is
a big hassle with the issues of hazard exposure, disposal, etc.
 
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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[Histonet] caris and genoptix experience

2010-09-03 Thread Tench, Bill
We have had almost identical experiences with both organizations.
Caris has been informed that it is not welcome; genoptix is on the same
list
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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[Histonet] tonsils

2010-08-31 Thread Tench, Bill
I have seen malignancy in tonsils that did not show a 5 cm difference in
the gross size.  I would be very concerned about missing a significant
lesion using that criterion.

 

Dr Bill Tench

Assoc Dir. Lab Services

Chief Cytology

Palomar Medical Center

555 E. Valley Parkway

Escondido, Ca 92025

Voice: 760-739-3037

Fax:  760-739-2604

 


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[Histonet] (no subject)

2010-08-31 Thread Tench, Bill
You need to review all of the notes that go with the standard:

 

NOTE: Microwave devices should be placed in an appropriate ventilation
hood to contain airborne

chemical contaminants and potentially infectious agents. Before
operation of the microwave device,

flammable and corrosive reagents should be removed from the hood, to
prevent fire or chemical

damage to the electronic components of the device. Microwave devices
used outside a fume hood

should have an integral fume extractor that is certified by the
manufacturer for use in a clinical

laboratory.

The effectiveness of ventilation should be monitored at least annually.

This checklist requirement does not apply if only non-hazardous reagents
(and non-infectious

specimens) are used in the device (e.g. water, certain biological
stains, paraffin sections). The

laboratory should consult the MSDS sheets received with reagents and
stains to assist in determining

proper handling requirements and safe use.

This checklist item does not apply to microwave devices that are
designed by the manufacturer to

operate without venting.

 

How much of this applies to you?  What are you microwaving? If it is
nonhazardous, as indicated above, then this is an N/A.

Or, is this a device designed to operate without venting?

If situation #1 above applies, then yes, you must comply.

 

Reading the detail in the notes is critical to understanding the
standards.  They are a lot more detailed and specific than what I have
seen in the past in other regulatory resources.

 

Dr Bill Tench

Assoc Dir. Lab Services

Chief Cytology

Palomar Medical Center

555 E. Valley Parkway

Escondido, Ca 92025

Voice: 760-739-3037

Fax:  760-739-2604

 


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[Histonet] cutting standards

2010-08-27 Thread Tench, Bill
I asked this question earlier in the spring.  someone sent me some
national standards from surveys, so if you go to the archives you should
find this information. i will see if i can find the information.
 
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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[Histonet] gross specimen retention

2010-08-27 Thread Tench, Bill
We generally do not return specimens to patients, so this is not so much
of an issue for us.  We do retain processed specimens longer than 2
weeks (more like 2 months).  Fresh placentas (requiring refrigerated
storage) are an exception.
 
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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[Histonet] preparation of frozen sections

2010-08-24 Thread Tench, Bill
So as a pathologist, i have to ask you why you would want to air dry a
section?  From a diagnostic perspective, we consider air dried samples
unacceptable in my lab.  All of our standard histologic interpretation
is based on fixed sections.  So, why not drop the slide in a jar or ETOH
and keep it there until you are ready to stain?
 
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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[Histonet] grossing manual

2010-08-12 Thread Tench, Bill
Yes, you do need a standard procedure manual for the management of all
of your specimens.  Life has gotten more complicated with the reporting
standards now in place for reporting cancer which includes the gross
examination.  A good start for the non-neoplastic cases would be the
appendix of a good surgical pathology text like Rosai (i haven't seen
the latest editions, but i think it is still there).  Other standard
references also have this information.  And then, go to the CAP website
and download the standard protocols and convert them to how your
pathologists want them.  All of this may be online, but you also need a
copy in the gross room.  It's a pretty sizable job if you don't have any
of it done already.
 
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] correct CPT code

2010-08-09 Thread Tench, Bill
You need to be more specific about what it is you are doing.  If you are
looking at imprints or smears intraoperatively then the correct code
is 88333.  I would say that neither a PA or HT is qualified for this
job, but a cytotech is.  If anyone other than a pathologist does it,
however, you cannot charge for it. 


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 Houston,
Ronald
Sent: Monday, August 09, 2010 12:09 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] correct CPT code

How do others code analysis of renal bxs and cilia bxs for specimen
adequacy; and can this be performed by a PA and/or HT who is CLIA
qualified to gross?

I know of 88172, but this is for adequacy of FNA specimens; can you use
88329, pathology consultation during surgery?

Thanks
Ronnie

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...@nationwidec
hildrens.org
www.NationwideChildrens.orghttp://www.NationwideChildrens.org




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RE: [Histonet] correct CPT code

2010-08-09 Thread Tench, Bill
 OK, so that's a different story (and we look at renal cores for
glomeruli as well).  I believe the correct code for that is
88329--intraoperative consultation.  It is not a frozen section so that
code, 88331, does not apply.  Again, I believe that to be paid, this
activity must be performed by a 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: Houston, Ronald [mailto:ronald.hous...@nationwidechildrens.org] 
Sent: Monday, August 09, 2010 12:57 PM
To: Tench, Bill
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] correct CPT code

Bill, 

I'm specifically referring to visualization of a renal biopsy under a
dissecting scope to see if the specimen is adequate for analysis (i.e.
are there glomeruli present?) and examining a ciliary biopsy, again
under dissecting microscope, to check for the presence of motile cilia

Ronnie Houston
Anatomic Pathology Manager
Nationwide Children's Hospital
Columbus OH 43205
(614) 722 5450
-Original Message-
From: Tench, Bill [mailto:bill.te...@pph.org]
Sent: Monday, August 09, 2010 3:17 PM
To: Houston, Ronald
Cc: histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] correct CPT code

You need to be more specific about what it is you are doing.  If you are
looking at imprints or smears intraoperatively then the correct code
is 88333.  I would say that neither a PA or HT is qualified for this
job, but a cytotech is.  If anyone other than a pathologist does it,
however, you cannot charge for it. 


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 Houston,
Ronald
Sent: Monday, August 09, 2010 12:09 PM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] correct CPT code

How do others code analysis of renal bxs and cilia bxs for specimen
adequacy; and can this be performed by a PA and/or HT who is CLIA
qualified to gross?

I know of 88172, but this is for adequacy of FNA specimens; can you use
88329, pathology consultation during surgery?

Thanks
Ronnie

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...@nationwidec
hildrens.org
www.NationwideChildrens.orghttp://www.NationwideChildrens.org




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[Histonet] dissection aide

2010-07-28 Thread Tench, Bill
I don't see much advantage of this over plain old Carnoy's fixative,
other than missing the wiff of choroform.  Ethanol should not be a
problem with IHC, but as you said, revalidation is required.  The magic
number of nodes is 12.
 
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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[Histonet] REFRIG FORMALIN

2010-07-28 Thread Tench, Bill
You must have a heck of a lot of space in the frig.  I am envious. I
don't think refrigerating your specimens would create any problems.
Everyone i know stores them in some inconvenient corner of a morgue at
room temperature.
 
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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[Histonet] special stain storage

2010-07-26 Thread Tench, Bill
The critical issue that your CLIA, or perhaps CAP, inspector is going to
be asking is:  is it necessary to storage stain reagent X in a
refrigerator with a temperature range of Y.  That answer lies in your
procedure.  If it says refrigerate (perhaps with a range) reagent X,
then you must document that you have done so by tracking the frig
temperature. If it really is not necessary to refrigerate the reagent
(perhaps it is done so just to keep it from evaporating) indicate that
in the procedure.
 
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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[Histonet] powder stain expiration

2010-07-26 Thread Tench, Bill
If the manufacturer has not included an expiration date for these, i
think there probably isn't one.  I would call the CAP LAP folks and ask
them about that.  When this kind of issue arises during an inspection,
it is always better to call while the inspectors are still there.  You
can get an answer right then and there and it will save everyone a lot
of time and hassle.
 
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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[Histonet] hpv testing on head and neck ca's

2010-07-22 Thread Tench, Bill
We do p16 on squamous ca of the head and neck region routinely
 
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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[Histonet] decontamination of cryostat

2010-07-21 Thread Tench, Bill
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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[Histonet] workload limits

2010-07-18 Thread Tench, Bill


I am a little concerned about some possible misunderstandings regarding slide 
limits, so below is a CAP article written on the topic that still applies.  
Understand that the elevated limits for image related instruments (which now 
include the ThinPrep Imager and the SurePath GS systems) have specific limits 
set for specific ways those instruments are used--and they are not the same for 
both instruments).  Note well, liquid based paps do NOT count as 1/2 slides 
under any circumstances.  You can only get to 200 slides per day if you are 
using the ThinPrep Imager and ONLY looking at fields of view. If you have to do 
a full manual review of the slide, you must reduce you limit accordingly.

   
CAP Today

August 2004
Special Section

Q  A

Q.  We use a combination of manual and location-guided screening in my 
laboratory. How do I calculate cytotechnologist workload limits in this setting?

A.  Maximum workload limits should be calculated based on the following factors:

Manual versus computer-assisted screening. CLIA regulations specify a 100-slide 
maximum limit for manual screening in 24 hours over a minimum eight-hour work 
day. This translates to a maximum screening rate of 12.5 slides per hour for 
manual screening. The Centers for Medicare and Medicaid Services recently set 
the maximum workload limit for location-guided screening at 200 slides per day. 
This limit is equivalent to 25 slides per hour for location-guided screening. 
All Pap tests count as whole slides. Slides from nongynecologic cases count as 
whole slides except for concentration and liquid-based techniques that confine 
the material to less than one-half of the slide surface, which may be counted 
as one-half slides. Quality control and five-year retrospective rescreens are 
also included in the workload accounting.
Number of hours spent screening. The maximum workload limit should be prorated 
based on the total number of hours spent screening, using the 12.5 slides per 
hour maximum rate for manual screening and 25 slides per hour for 
computer-assisted screening. This time does not include computer data entry, 
reporting, and other duties.
Cytotechnologist ability, experience, QC data, etc. It must be emphasized that 
the maximum workload limits are the maximum allowable by CLIA/CMS and are not 
to be used as a productivity goal. Each cytotechnologist's workload limit 
should be carefully determined and individualized based on expertise, time 
spent screening, and screening method(s) used. Here are a few scenarios to 
illustrate maximum workload limit calculations in different settings:
Cytotechnologist A works in a high-volume laboratory and screens Paps using 
location-guided screening. She is a highly skilled cytotechnologist with 10 
years of experience and has no other duties (no data entry or reporting, no 
answering phone). Her maximum workload limit is 200 slides per day over eight 
hours (25 slides/hour). This case scenario is a rare exception. Most 
cytotechnologists have other duties or have a lower personal workload limit set 
by the laboratory supervisor and medical director.
Cytotechnologist B's laboratory just brought a computerized imaging system in 
house and is gradually making a transition to computer-assisted screening. She 
now screens about two hours per day using the computer-assisted device and 
three hours per day screening Paps manually. She spends the rest of her day 
doing clerical and cytopreparatory work. Her maximum workload allowed by CLIA 
is: (2 hrs x 25 slides/hr) + (3 hrs x 12.5 slides/hr)=87.5 slides
Cytotechnologist C screens Paps every morning using location-guided screening 
and screens nongyns in the afternoon. Today he spent four hours screening Paps. 
Although the maximum limit by CLIA would be 25 x 4=100, his individual maximum 
screening limit is set a bit lower (20 slides per hour), so his maximum limit 
is 80 for four hours of screening. This afternoon is busy with several FNAs, 
each of about 20 slides. With four hours left of screening time at 12.5 slides 
per hour, he is allowed by CLIA to screen a maximum of 50 slides this 
afternoon. However, his individual workload limit is less, and he will be 
permitted to screen a maximum of 35 of the FNA slides, and other 
cytotechnologists will screen the rest.
Although computer-assisted screening methods afford greater productivity, care 
should be taken to set reasonable maximum workload limits based on the ability 
of the individual cytotechnologist, to avoid compromising screening accuracy.

Theresa M. Voytek, MD
Department of Pathology




Bill Tench
Palomar Medical Center
555 E Valley Parkway
Escondido, Ca 92025
Voice: 760-739-3037
Fax: 760-739-2604



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[Histonet] Re Grossing assistants

2010-06-25 Thread Tench, Bill
I would suggest that you review the archives on this topic.  There has
been much discussion recently.  The short answer is that ANYONE
performing ANY grossing in the AP laboratory must meet the requirements
for high complexity testing.
 
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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[Histonet] afb contamination

2010-05-21 Thread Tench, Bill
We had a problem with contamination on our AFB stains, and we discovered
that it was the control slide flaking off in the copland jar which was
being used for staining the control and target slide at the same time
(makes sense as a real control').  We identified these contaminants
because they were frequently large clusters (by large I would say 4-8
organisms) which we almost never see in real cases, and fortunately,
they were also not in the same plane of focus (but that can be subtle).
they did create problems.  Our solution was to stain the control
separately from the case.  No more problems. 

 

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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[Histonet] charging for cytospins

2010-05-19 Thread Tench, Bill
Can you charge for two different stains for the urine cytospin?

 

The answer to this question is a depends.  If you are just doing any
of the optional stains that may be used on a cytology preparation
(namely Pap, HE, romanovsky) you are NOT permitted to charge for each
of these (they are not considered special stains).  If you did an iron
stain, or melanin stain, or mucin stain, you could charge separately for
these special stains.

 

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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[Histonet] Grossing assistants-pathologist assistants

2010-05-18 Thread Tench, Bill
Yes, the Pathology Assistant national organization is a great resource
as is the CAP.  As I said before, please remember that the CAP
inspection standards represent compliance with FEDERAL CMS standards.  I
would encourage contact with the CAP LAP  in regard to these FEDERAL
standards.  Individual states may also have requirements specific for
that state, which certainly may complicate things, so contact with your
state pathology society will help with that. 

 

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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[Histonet] urine cytology

2010-05-18 Thread Tench, Bill
I don't think I know of any labs that do air dried Diff quik type stains
on urine cytologies any more.  You need to use some sort of
concentration technique, and the most frequently used for labs without
liquid-base processing apparatus is the cytospin.  Several companies
make cytospin devices.  High quality preparation with good fixation is
critical, as is specimen quality.  If you don't have training in
cytology (at least cytology preparation) I would stay away from this.

 

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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[Histonet] Grossing assistants

2010-05-17 Thread Tench, Bill
The rules are established by CMS through CLIA regulations.  They are
applied based on the complexity of the activity.  Grossing is
considered high complexity and thus is subject to rather stringent
rules (which become more complicated because there are grandfather
clauses).  For years, the CAP took a more liberal view of how various
parts of the grossing activity could be defined.  CMS reviews the CAP
standards.  So, the result is a tightening of those standards (ie,
don't blame the CAP for this one). The CAP has provided rather clear cut
guidelines, and if you find them confusing, then you may contact the LAP
program there and someone will assist you. You may ask the CAP to lobby
for you (which I suspect they have done) or you can appeal to CMS (which
will largely not listen to anything reasonable, and if it does, will
tell you it will take multiple years to make any changes).

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
histonet-requ...@lists.utsouthwestern.edu
Sent: Sunday, May 16, 2010 10:24 AM
To: histonet@lists.utsouthwestern.edu
Subject: [BULK] Histonet Digest, Vol 78, Issue 22


--



--

Message: 2
Date: Sat, 15 May 2010 17:46:58 -0400
From: Robert Richmond rsrichm...@gmail.com
Subject: [Histonet] Re: Grossing Technician Qualifications
To: histonet@lists.utsouthwestern.edu
Message-ID:
aanlktinp8attp0bpdbthkldm-8nx5sjphnrl3agrl...@mail.gmail.com
Content-Type: text/plain; charset=ISO-8859-1

Tanisha Neely HT(ASCP) asks: Are the guidelines for a tech who is
strictly limited to grossing
anatomic pathology specimens different than for those of a full time
histotech? Could a bachelor degree'd person with the right course work
qualify for this position? If so, does anyone have documentation of
this? I'd like to present this as a staffing option to my management
if possible.

Well, I'm giving a talk on the subject to the Tennessee Society for
Histotechnology meeting in Chattanooga, and I'm pretty confused about
the question of who's allowed to gross - the rules seem to be
changing, and different certifying organizations have different
requirements. If somebody can spell out in detail who it is that's
requiring what, I'd appreciate it.

Bob Richmond
Samurai Pathologist
Knoxville TN



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[Histonet] histogel technique

2010-05-13 Thread Tench, Bill
Next day, pellet cells and resuspend them in a small amount (100-200 
microliters) of Histogel or Agar.  When the gel cools cut the microcentrifuge 
tube open with a scalpel or razor blade.  Now you have a nice cell pellet 
shaped like the bottom of your centrifuge tube, and you can treat it just like 
any piece of tissue. Pop it in a tissue processing cassette and then to your 
ethanol dehydrating steps.

We use histogel routinely for clinical specimens.  We have found several things 
that improve the process:
1)after you pellet the cells and decant, use a cotton tip swab to pick up the 
last little droplet of fluid adjacent to the button.  It will hold together 
much better.
2)after you have added histogel, vortex and centrifuge to pellet. Put tube in 
ice bath, add a few drops of formalin, and wait a few minutes.  With minimal 
prodding the plug will essentially pour out of the tube.  No need to cut.

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-
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[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
histonet-requ...@lists.utsouthwestern.edu
Sent: Thursday, May 13, 2010 7:41 AM
To: histonet@lists.utsouthwestern.edu
Subject: [BULK] Histonet Digest, Vol 78, Issue 17

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Today's Topics:

   1. RE: FFPE cell pellet prep (JR R)
   2. xylene substitutes (Perry, Margaret)
   3. RE: AMT Cover (Jones, Laura)
   4. RE: AMT Cover (wanda.sm...@hcahealthcare.com)
   5. RE: AMT Cover (Jennifer Anderson)
   6. RE: RE: AMT Cover (Terri Brown)
   7. RE: AMT Cover (Bell, Lynne)
   8. RE: AMT Cover (Elliott, Rachel A.)
   9. 2010 Louisiana Society for Histotechnology State Meeting  -
  Reservation Extension! (Montina Van Meter)
  10. Re: Xylene substitutes (V. Neubert)
  11. Gastric biopsies (Cristi stephenson)
  12. RE: Forwarding Request for Control Mehtod (Tony Henwood)
  13. Re: Gastric biopsies (Brandi Higgins)
  14. Re: Gastric biopsies (susanfpl...@aim.com)
  15. How do I subscribe? (Michelle MacVeigh-Aloni)
  16. job opening for cytology/ FISH and histology supervisor   -
  Florida (dcoj...@tampabay.rr.com)
  17. RE: Gastric biopsies (Gill, Caula A.)
  18. RE: Are Histotechs considered exempt employees?
  (Heckford, Karen - SMMC-SF)
  19. RE: Gastric biopsies (Cynthia Pyse)
  20. Re: Gastric biopsies (Rene J Buesa)
  21. RE: Gastric biopsies (Weems, Joyce)
  22. RE: Gastric biopsies (Joyce Cline)
  23. Tilapia Fish Eye (Marquisha Paul)


--

Message: 1
Date: Wed, 12 May 2010 10:36:15 -0700
From: JR R rosenfeld...@hotmail.com
Subject: RE: [Histonet] FFPE cell pellet prep
To: histonet@lists.utsouthwestern.edu
Message-ID: bay135-w681d7f121be89ca27acdcdb...@phx.gbl
Content-Type: text/plain; charset=iso-8859-1


Here's how I do it.

I hate the lens paper method.

I transfer suspended cells from a T75 flask to a 50 ml Falcon tube and 
centrifuge at 400 X g for 5 minutes.  Aspirate most of the media so that cells 
plus media are about 1 ml.  Transfer cells plus media to a 1.7 ml 
microcentrifuge tube.  Pellet cells at 400 x G for 5 minutes.  Rinse with PBS 
if needed.  Suspend cells in NBF and fix over night.  

Next day, pellet cells and resuspend them in a small amount (100-200 
microliters) of Histogel or Agar.  When the gel cools cut the microcentrifuge 
tube open with a scalpel or razor blade.  Now you have a nice cell pellet 
shaped like the bottom of your centrifuge tube, and you can treat it just like 
any piece of tissue. Pop it in a tissue processing cassette and then to your 
ethanol dehydrating steps.

Jerry Ricks
Research Scientist
University of Washington
Department of Pathology





 Date: Wed, 12 May 2010 06:50:14 -0700
 From: kmerriam2...@yahoo.com
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] FFPE cell pellet prep
 
 Sorry - I forgot to put a subject line.
 
 
 Good morning,
 
 I am trying to make some nice FFPE cell pellet blocks, but I seem to lose a 
 lot of cells along the way (especially when trying to take the cells out of 
 the tube).  We are fixing the cells in NBF, spinning them down, adding 70% 
 and spinning down again.  At that point, I am trying to scoop out the cells 
 (with a weighing scoop) and wrap them in lens paper for processing.  I am 
 

[Histonet] routine specials

2010-05-13 Thread Tench, Bill
Grumpy old pathologist trying to pay attention to costs:

Livers:  if the biopsy was for anything other than metastatic ca, then retic, 
trichrome, and iron are pretty much standard. If for met ca, you are wasting 
money.

Gastrics for h pylori:  Just because the GI guys asked for it doesn't mean 
there is any chance it is there.  In my practice, the pathologist MUST request 
the stain, and only if there is histologic evidence to support the dx (or the 
GI really whines).  We did an internal study and found in 6 months ZERO (0) 
cases that were positive when there was no supporting histologic change. (we do 
immunos)  In 95% of the cases (or more) the bugs are easily identified on H and 
E (you just gotta look)

Bone Marrows:  doing an iron is pretty much standard. Smear is best, at least 
in my lab, because it seems to go away in blocks.

Esophagus bx:  lots of folks want alcian blue for Barrett's.  Again, more than 
95% of the time, the dx is obvious and the special is superfluous.

Gastric bx:  same issue with alcian blue.  It is purported to increase the 
sensitivity for intestinal metaplasia.  I find it hard to believe that a 
competent pathologist cannot interpret IM without a special stain in more than 
98% (or greater) of the cases.

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-
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Sent: Thursday, May 13, 2010 7:41 AM
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Subject: [BULK] Histonet Digest, Vol 78, Issue 17

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Today's Topics:

   1. RE: FFPE cell pellet prep (JR R)
   2. xylene substitutes (Perry, Margaret)
   3. RE: AMT Cover (Jones, Laura)
   4. RE: AMT Cover (wanda.sm...@hcahealthcare.com)
   5. RE: AMT Cover (Jennifer Anderson)
   6. RE: RE: AMT Cover (Terri Brown)
   7. RE: AMT Cover (Bell, Lynne)
   8. RE: AMT Cover (Elliott, Rachel A.)
   9. 2010 Louisiana Society for Histotechnology State Meeting  -
  Reservation Extension! (Montina Van Meter)
  10. Re: Xylene substitutes (V. Neubert)
  11. Gastric biopsies (Cristi stephenson)
  12. RE: Forwarding Request for Control Mehtod (Tony Henwood)
  13. Re: Gastric biopsies (Brandi Higgins)
  14. Re: Gastric biopsies (susanfpl...@aim.com)
  15. How do I subscribe? (Michelle MacVeigh-Aloni)
  16. job opening for cytology/ FISH and histology supervisor   -
  Florida (dcoj...@tampabay.rr.com)
  17. RE: Gastric biopsies (Gill, Caula A.)
  18. RE: Are Histotechs considered exempt employees?
  (Heckford, Karen - SMMC-SF)
  19. RE: Gastric biopsies (Cynthia Pyse)
  20. Re: Gastric biopsies (Rene J Buesa)
  21. RE: Gastric biopsies (Weems, Joyce)
  22. RE: Gastric biopsies (Joyce Cline)
  23. Tilapia Fish Eye (Marquisha Paul)


--

Message: 1
Date: Wed, 12 May 2010 10:36:15 -0700
From: JR R rosenfeld...@hotmail.com
Subject: RE: [Histonet] FFPE cell pellet prep
To: histonet@lists.utsouthwestern.edu
Message-ID: bay135-w681d7f121be89ca27acdcdb...@phx.gbl
Content-Type: text/plain; charset=iso-8859-1


Here's how I do it.

I hate the lens paper method.

I transfer suspended cells from a T75 flask to a 50 ml Falcon tube and 
centrifuge at 400 X g for 5 minutes.  Aspirate most of the media so that cells 
plus media are about 1 ml.  Transfer cells plus media to a 1.7 ml 
microcentrifuge tube.  Pellet cells at 400 x G for 5 minutes.  Rinse with PBS 
if needed.  Suspend cells in NBF and fix over night.  

Next day, pellet cells and resuspend them in a small amount (100-200 
microliters) of Histogel or Agar.  When the gel cools cut the microcentrifuge 
tube open with a scalpel or razor blade.  Now you have a nice cell pellet 
shaped like the bottom of your centrifuge tube, and you can treat it just like 
any piece of tissue. Pop it in a tissue processing cassette and then to your 
ethanol dehydrating steps.

Jerry Ricks
Research Scientist
University of Washington
Department of Pathology





 Date: Wed, 12 May 2010 06:50:14 -0700
 From: kmerriam2...@yahoo.com
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] FFPE cell pellet prep
 
 Sorry - I forgot to put a subject line.
 
 
 Good morning,
 
 I am trying to make some nice FFPE cell 

[Histonet] clo test

2010-05-05 Thread Tench, Bill
The Clo test is a clinical lab test.  You need to go to that part of the
CPT coding book (sorry I don't have it available).  88300 is an anatomic
code (gross only, ie, it requires examination of a piece of tissue or
foreign body) and is entirely inappropriate for this test.

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
histonet-requ...@lists.utsouthwestern.edu
Sent: Wednesday, May 05, 2010 1:36 PM
To: histonet@lists.utsouthwestern.edu
Subject: [BULK] Histonet Digest, Vol 78, Issue 6




Hi everyone,
 
I am looking to see what CPT code everyone is using for reading Clo
Tests in the pathology department. I have heard of using 87081 but I am
not sure if this is accurate as this is for culture and the CLO is
biochemical reaction not a culture.  Currently I have been using 88300
gross only.
Any help would be appreciated.
 
Thank you,
Amy Farnan

***

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[Histonet] Cap guidelines and Clia

2010-04-27 Thread Tench, Bill
It is important to understand that CLIA is the driving force for most of
the various regulations promulgated by CAP, and this is true of the
issue regarding the requirements for Gross room assistants.  The CAP
simply tries to interpret the morass of regulatory garbage into
understandable standards, which must be approved by CLIA.  There are
some CAP standards that have grown out of good laboratory practices
and not specific CLIA regulations, but this is not one of them.

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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[Histonet] Patient ID on cassettes

2010-04-27 Thread Tench, Bill
A statement was made in a previous posting indicating CAP requirements for 2 
unique identifiers throughout the entire analytic process: To conform to CAP 
and state regulations that require two unique patient identifiers on a specimen 
at all analytical steps.
The CAP standards GEN 40491, ANP 11460, and ANP12092 specifically indicate two 
unique identifiers on the PRIMARY specimen container, not on every container 
throughout the process, and there are notes explaining the requirements.  There 
may be variations in State laws, but these are the most up to date CAP 
standards.  There is no need to go through a lot of contortions adding 
additional information to cassettes. (however, at least the ones we use also 
have a side panel which can be written on)

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 
histonet-requ...@lists.utsouthwestern.edu
Sent: Sunday, April 25, 2010 10:01 AM
To: histonet@lists.utsouthwestern.edu
Subject: [BULK] Histonet Digest, Vol 77, Issue 31

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Today's Topics:

   1. Patient ID on cassettes (Jeffrey Silverman)
   2. Re: Gram stain (Maxim Peshkov)
   3. Best books for the HTL? (Paula Sicurello)


--

Message: 1
Date: Sat, 24 Apr 2010 10:28:55 -0700 (PDT)
From: Jeffrey Silverman pathmas...@yahoo.com
Subject: [Histonet] Patient ID on cassettes
To: joyce.cl...@wchsys.org
Cc: histonet@lists.utsouthwestern.edu
Message-ID: 690158.71961...@web08.mail.gq1.yahoo.com
Content-Type: text/plain; charset=iso-8859-1

To conform to CAP and state regulations that require two unique patient 
identifiers on a specimen at all analytical steps, and to cope with a 
persnickety cassette labeller that is down more than up, we have taken to 
writing the patient's first and last initials in the upper left corner of the 
writing surface of the cassette, above the S10- . Our pencil sharpeners are 
running non -stop  but it works. Only problem is when a block is sent out for 
IHC the returned slides are labelled with the initials as part of the reference 
slides accession numbers and my boss doesn't care for that. Originally we 
dropped the S in S10- and replaced with the initials to get a little more room, 
now  we added back the S and placed initials above S10-.

Patient safety dictates that a prossector verify a match among  the labelled 
cassette and the labelled specimen containers and against the requisition and 
the number dictated into the gross computer/transcriber. Case by case, on every 
case. There is no substitute. As for placing the wrong cassettes on the wrong 
specimen containers, that seems to me to be pure carelessness and a 
disciplinary issue if it continues. 

When labelling, matching the initials that the microtomist writes on the slide 
with the patient's name printed on the slide labels provides a final  ID double 
check if the numbers on the slide get transcribed incorrectly. The initials 
thing takes minimal effort, but you need to be able to write small LOL.

Jeff Silverman. 


--

Message: 2
Date: Sat, 24 Apr 2010 23:08:48 +0400
From: Maxim Peshkov maxim...@mail.ru
Subject: Re: [Histonet] Gram stain
To: Perry, Margaret margaret.pe...@sdstate.edu
Cc: histonet@lists.utsouthwestern.edu
Message-ID: 573298402.20100424230...@mail.ru
Content-Type: text/plain; charset=windows-1251

Margaret:
We uses 1% aqueous neutral red as red counterstain
with very good results.
Do not forget rinse slides at 10-15 secs in DW
with 1-2 drop of glacial acetic acid before neutral
red and after this, because this dye have red color
at pH  6.
Sincerely,
Maxim Peshkov,
Russia,
Taganrog.

---Original message---
 Date: Fri, 23 Apr 2010 16:25:30 -0500
 From: Perry, Margaret margaret.pe...@sdstate.edu
 Subject: [Histonet] Gram stain
 To: histonet@lists.utsouthwestern.edu
 histonet@lists.utsouthwestern.edu
 Message-ID:

 fca5ef47f9bc694cbb4c58fea04219634ccfb69...@sdsu-mbx.jacks.local
 Content-Type: text/plain; charset=us-ascii

 Now that I'm done with my rant I have a real
 question.  We are trying to do a gram stain on fish
 and the safranine O is staining everything red.  What
 other stain 

[Histonet] histotech positions in San Diego area

2010-04-26 Thread Tench, Bill
Life is uncertain, but
We may have an opening in the future.  You may send resumes directly to
this email address and I will forward them on to the appropriate people.

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-
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histonet-requ...@lists.utsouthwestern.edu
Sent: Monday, April 26, 2010 10:02 AM
To: histonet@lists.utsouthwestern.edu
Subject: [BULK] Histonet Digest, Vol 77, Issue 32

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Today's Topics:

   1. Re: [IHCRG] ER clone 1D5 or SP1 ? (Richard Cartun)
   2. Region 1 conference (Amos Brooks)
   3. Re: [IHCRG] ER clone 1D5 or SP1 ? (ancillaryp...@mac.com)
   4. Mysterious artifact on GI biopsies HE stain (Urim, Lyudmila)
   5. paraformaldayhde (Perry, Margaret)
   6. RE: Mysterious artifact on GI biopsies HE stain (Weems, Joyce)
   7. anti 8 hydroxyguanosine (Fabrice gankam)
   8. RE: Mysterious artifact on GI biopsies HE stain (Mike Pence)
   9. Any Histology openings in San Diego area? (Jill Cox)
  10. (no subject) (Urim, Lyudmila)
  11. Re: Two antibodies from the same host with tyramide
  (Johnson, Teri)
  12. RE: (no subject) (Kaye Ryan)
  13. RE: (no subject) (Nails, Felton)
  14. RE: Best books for the HTL? (Morken, Tim)
  15. RE: (no subject) (Jesus Ellin)
  16. RE: [IHCRG] ER clone 1D5 or SP1 ? (Van Eyck, Deb)
  17. RE: [IHCRG] ER clone 1D5 or SP1 ? (Patsy Ruegg)


--

Message: 1
Date: Sun, 25 Apr 2010 15:04:28 -0400
From: Richard Cartun rcar...@harthosp.org
Subject: [Histonet] Re: [IHCRG] ER clone 1D5 or SP1 ?
To: 'ih...@googlegroups.com' ih...@googlegroups.com,
'histonet@lists.utsouthwestern.edu'
histonet@lists.utsouthwestern.edu,jtay...@meriter.com
Message-ID: 4bd459fb.7400.007...@harthosp.org
Content-Type: text/plain; charset=US-ASCII

I have looked at several clones over the years and I prefer clone 6F11.

Richard

Richard W. Cartun, Ph.D.
Director, Histology  Immunopathology
Director, Biospecimen Collection Programs
Assistant Director, Anatomic Pathology
Hartford Hospital
80 Seymour Street
Hartford, CT  06102
(860) 545-1596 Office
(860) 545-2204 Fax


 Taylor, Jean jtay...@meriter.com 4/23/2010 11:17 AM 

I'm wondering which clone of ER most labs are using?

Thanks,
Jean Taylor, HT(ASCP)QIHC
IHC Tech
Meriter Health Services
Madison, WI


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--

Message: 2
Date: Sun, 25 Apr 2010 19:14:49 -0400
From: Amos Brooks amosbro...@gmail.com
Subject: [Histonet] Region 1 conference
To: histonet@lists.utsouthwestern.edu
Message-ID:
y2z582736991004251614m979ddea5yea99650b77ced...@mail.gmail.com
Content-Type: text/plain; charset=ISO-8859-1

Hi,
I would like to ask if anyone has any photos of the Region 1
conference
to consider emailing them to me. I was going to post some on the Region
1
Conference web page and possibly put some in the Paraffin Press. If you
are
interested, please drop me a line.

Thanks,
Amos

amosbro...@gmail.com


--

Message: 3
Date: Sun, 25 Apr 2010 20:36:18 -0400
From: ancillaryp...@mac.com
Subject: [Histonet] Re: [IHCRG] ER clone 1D5 or SP1 ?
To: ihcrg Group (E-mail) ih...@googlegroups.com,histonet
netserver histonet@lists.utsouthwestern.edu
Message-ID: 0d48ea46-525d-45a6-bfcd-24662d59f...@mac.com
Content-Type: text/plain;   charset=us-ascii;   format=flowed;
delsp=yes

When we started our lab 3 years ago, we began with SP1 from day 1, so  
I don't have any experience with either 1D5 or 6F11 except in my  
previous labs. 1D5 is an excellent clone, and seems to be more  
specific than SP1 in the work-up of metastatic carcinoma of unknown  
primary site, based on the published literature. The advantage of 6F11  
is that, for those of us who use the Allred scoring system, it's the  
only clone that was clinically validated by Harvey et al. (JCO 1999)  
for this purpose. I agree with Rich.

For those who use SP1, it's a very good clone as a predictive marker  
in breast cancer. But again, in the setting of metastatic workup, it  
is NOT recommended, as it will pick up too many primary lung cancers  
and some colon 

[Histonet] CLIA requirements

2010-04-15 Thread Tench, Bill
You may define whatever QA monitors for grossing that you wish.  These
are not CLIA mandated, but contribute to improved performance.  When it
comes to the individuals doing the grossing, you need to understand that
this has been interpreted as a high complexity activity with strict CLIA
requirements (see recent postings and CAP standards).

 

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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[Histonet] CPT coding question

2010-04-09 Thread Tench, Bill
Michelle,  the example that you raised of having two tonsils, one with a
stitch, isn't quite the same as your problem.  The two tonsils would
otherwise not be identifiable as left or right.  That is not a problem
with a fetus and a placenta.  Each is separately identifiable and each
should be coded separately.  You will simplify any coding review if each
is a separate line on your report.

 

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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[Histonet] RE: [BULK] Histonet Digest, Vol 76, Issue 45

2010-03-31 Thread Tench, Bill
For placentas, you will find that you get consistently good sections if you 
gross the placenta fresh, take the samples you will want from the cord, disc 
and make a membrane role (which is easily done if they are not fixed).  Fix 
your samples overnight and trim for blocks the next day. For the membrane role, 
grab the free edge of the membrane with a large forceps, role the membrane up 
on the forceps toward the disc, stick two pins through the space between the 
forceps, and cut from disc, then slightly release grip on forceps and slide 
role into formalin cup.

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 
histonet-requ...@lists.utsouthwestern.edu
Sent: Wednesday, March 31, 2010 7:42 AM
To: histonet@lists.utsouthwestern.edu
Subject: [BULK] Histonet Digest, Vol 76, Issue 45

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Today's Topics:

   1. Coverslipping with SubX (Vanessa Avalos)
   2. Haunted cryostat/Thanks! (mtitf...@aol.com)
   3. GMS on decal tissue (Morken, Tim)
   4. questions (Webb, Dorothy L)
   5. Re: her2 validation (Pat Laurie)
   6. FREE MONEY! (Jackie M O'Connor)
   7. RE: questions (Garrison, Becky)
   8. Thermo's Excelsior Tissue Processor Program's
  (Akemi Allison-Tacha)
   9. re: cyto prep tech (Kim Tournear)
  10. her-2 neu validation (Debbie Nannenga)
  11. RE: questions (Tony Henwood)
  12. RE: RE: Leica Paraplast (connie grubaugh)
  13. (no subject) (Green JumpyOne)
  14. Fwd: [Histonet] (no subject) (Malika Benatti)
  15. RE: Thermo's Excelsior Tissue Processor Program's
  (Heckford, Karen - SMMC-SF)
  16. RE: RE: Leica Paraplast (Nails, Felton)
  17. Thermo Fisher Excelsior Tissue Processor Programs (Ann Bennett)
  18. Texas Society for Histotechnology April 23-25, 2010
  (kdwyer3...@aol.com)
  19. cassette labels erased by processor (Catherine Breen)
  20. RE:  her2 validation (Weems, Joyce)
  21. RE: cassette labels erased by processor (Sherwood, Margaret )
  22. FW: [Histonet] cassette labels erased by processor (Cheri Miller)
  23. Re: cassette labels erased by processor (Malika Benatti)


--

Message: 1
Date: Tue, 30 Mar 2010 11:15:38 -0700
From: Vanessa Avalos vava...@allergydermatology.com
Subject: [Histonet] Coverslipping with SubX
To: 'HISTONET LISTS' histonet@lists.utsouthwestern.edu
Message-ID: 01cad035$00d2f5b0$0278e1...@com
Content-Type: text/plain;   charset=us-ascii

Is anyone using SubX ? I am trying it out and am having some difficulty
coverslipping. I am using the Subx glue as directed since Acrymount didn't
seem to work as well. I still get a hazy film under the glass and am getting
big air bubbles as well. I can eventually get them out but its just takes a
while and you know how time is precious when you have a line of slides to
stain. The process is not as smooth as before. I really would like this to
work out for me and eliminate xylene.

Any suggestions??

 

Vanessa

Fax: 602-277-2134

 



--

Message: 2
Date: Tue, 30 Mar 2010 14:44:26 -0400
From: mtitf...@aol.com
Subject: [Histonet] Haunted cryostat/Thanks!
To: histo...@pathology.swmed.edu
Message-ID: 8cc9e5028adfb36-1500-2...@webmail-m010.sysops.aol.com
Content-Type: text/plain; charset=us-ascii



Thank you everyone who responded to my problem with a Leica CM 1850 cryostat 
turning itself off. About 11 people responded with tips. Thank you!! The 
Histonet is great!!
In answer to some enquirys:
1) The cryostat is set to defrost at 2 a.m.. The manual says it defrosts for an 
hour. Jackie O' Conner asks if it is set to go back on after the defrost. I 
have no idea. It defrosts well the rest of the time, and turns itself back on. 
Brian Cornett-Early recommends changing the start device on the compressor.
2) Someone else asked if power is getting to the cryostat -  Yes, when it turns 
itself off, the on/off switch is on off. All you have to do is flip the 
switch and it starts pumping and  cooling.
3) Mari Ann Mailhiot with Leica recommends changing a cicuit breaker on the 
side of the compressor. That is probably where we will start. Mari Ann works 
for Leica so it sounds like good advice.

Thank you everyone. Since it 

[Histonet] technologist productivity

2010-03-17 Thread Tench, Bill
I apologize in advance if I offend anyone with this inevitably touchy
question.

In the last two years we have lost one older histotechnologist, and
the routine reliable services of another of that group and are now
facing the issue of what can be expected from their replacements.  I
have little feel for this other than my experience with these and other
previous employees, so I am hoping that some of you would be willing to
share your thoughts/data with me either in response on this listserv, or
alternatively off line directly to my email address.  I am interested
in some numbers on how many blocks one could expect to have embedded
within an hour, with break down for simple larger or single pieces vs
multiple small bx's like GI bx's or prostate needle bx's.  I am looking
for similar information in regard to the number of sections one could
expect to be cut in an hour from routine blocks (and for this purpose,
small and large bxs should be included in the same analysis-there is so
much variation in regard to the number of sections that labs routinely
cut from smalls, so just a general mix of the number of slides would
be helpful.)  Thank you in advance for sharing-we are just trying to
maintain reasonable expectations from our new/replacement technologists.

 

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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