You must match your blocks and slides. This will eliminate a lot of your
mistakes/ NOT ALL!
Mike
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lynette
Pavelich
Sent: Thursday, November 19, 2009 9:52 PM
Lynette,
You might want to also investigate different fonts if that is an option.
Keeping the same size but using a different font can make a world of
difference.
Victor
Victor Tobias
Clinical Applications Analyst
University of Washington Medical Center
Dept of Pathology Room BB220
1959 NE
Thanks for the suggestions. One clarification: matching blocks and slides
CATCHES mistakes; it does not reduce or eliminate them.
Tim
-Original Message-
From: Mike Pence [mailto:mpe...@grhs.net]
Sent: Friday, November 20, 2009 6:38 AM
To: Lynette Pavelich;
Hello,
I am trying to find the guidelines for CAP that describes how long IHC
positive control slides are to be kept on file ... does anyone know?
Thanks in advance!
Tiana
This email and/or any documents in this transmission is intended for the
addressee(s) only and may contain legally
What is the current practice for meeting this regulation? Is a general
statement (disclaimer) placed on all pathology reports that have
immunocytochemistry and/or
FISH and ISH or is the disclaimer placed only on the reports where the class 1
ASR antibody or nucleic acid have been used?
Thanks
I am looking for a conference/course to attend in 2010. I am experienced in IF
and IHC and would like to learn more about any new techniques and products that
might be available. Does anyone have a recommendation for a course or a
conference in the US? I am not a certified HT but I pretend to
We used to add that the methods were experimental.
René J.
--- On Fri, 11/20/09, Foshey, Annette afos...@chw.org wrote:
From: Foshey, Annette afos...@chw.org
Subject: [Histonet] CAP QUESTION ANP.12425 ASR disclaimer on pathology reports
To: (histonet@lists.utsouthwestern.edu)
We write a macro-protocol at the time of grossing with all blocknumbers
and additional identifer.
This paper is matched the first time with all blocks after embedding and
before cutting. Missing blocks or wrong labelled blocks are found.
The second time the paper is matched with all slides after
We add ours to only the Class I ASR cases.
Joyce Weems
Pathology Manager
Saint Joseph's Hospital
5665 Peachtree Dunwoody Rd NE
Atlanta, GA 30342
678-843-7376 - Phone
678-843-7831 - Fax
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
They should be kept to comply with your policies and the state requirements.
Remember that CAP has regulations but cannot override state nor institutional
policies.
René J.
--- On Fri, 11/20/09, Tiana Fountain tfount...@exchange.hsc.mb.ca wrote:
From: Tiana Fountain
Take a look at the National Society for Histotechnology (www.nsh.org). There
are several State and Regional Society meetings coming up in the spring of 2010
and then of course there is the National Symposium/Convention in the Fall of
2010 in Seattle, WA.
Jack Ratliff
NSH -Hard Tissue
Linda, Yes, I should have said matching blocks and slides after staining
catches mistakes but does not eliminate them.
We are looking at: isolating block to be cut, labeling slide just before or
after sectioning, matching block to slide after sectioning at the cutting
station.
Unfortunately
I am processing adult rat brain sections for routine histological stains, but
am having a terrible time getting them to stick to the slide. After
transcardial perfusion the rat brains are dissected out and processed for
frozen sectioning. I post-fix overnight in PFA, cryoprotect in
Check out this Applied Immunohistochemistry and Molecular Pathology (AIMP)
meeting coming at end of January 2009 in Florida.
the fourth annual international retreat on applied IHC and molecular
pathology.
Please visit
http://www.pathlearning.com/Pathology_Learning_Centers/Welcome.html for
We use the statement for all reports that any IHC/ISH, regardless if
they are ASRs or not.
Martha Ward
Wake Forest University Baptist Medical Center
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Foshey,
I am processing adult rat brain sections for routine histological stains, but
am having a terrible time getting them to stick to the slide. After
transcardial perfusion the rat brains are dissected out and processed for
frozen sectioning. I post-fix overnight in PFA, cryoprotect in
The disclaimer is only for ASR antibodies. They don't have to be labeled
experimental because a CLIA certified lab has full capability and authority
to validate any antibody they want to use for any purpose. You do have to
document your validation procedure and results.
You can also use RUO
Just can't bill for RUO, correct?
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Morken,
Tim
Sent: Friday, November 20, 2009 13:24
To: Foshey, Annette; (histonet@lists.utsouthwestern.edu)
Subject: RE:
Dear Histonetters,
I am collecting any hand-outs, pamphlets, archives, books, CD's, anything you
may have extra or may be willing to share that can help me prepare for the New
York State Histologic Technician Examination. The examination may be similar
to the HT and HTL exam; so anything
Dear Histonetters,
I have a problem with my ISH and maybe one of you can help me.
I used probes I *know* they are working. I put the mice embryos (E 10.5)
in BM Purple for staining. Unfortunately they turned black in a short time.
They were not stained in the inside. It looks like that the
Good Friday Afternoon,
Does anyone know if there is a modifier for 88307 for Lumpectomies when
20-30 blocks are submitted.
We are currently charging 88307 but the pathologist thinks there should be
a modifier.
Thanks.
Debbie M. Boyd, HT(ASCP) I Chief Histologist I Southside Regional Medical
According the one of our pathologist the above mentioned update
clarified that CMS allows the billing of special stains performed on
different blocks of the same Pathology specimen. Previously, it was
understood that a special stain could only be billed once per specimen.
Now it appears that a
Joyce,
That's very interesting, as I remember going to great lengths a few
years ago to be sure we had a billing limiter in place in CoPath to
prevent the multiple charging of CPT codes on the same specimen.
However, I looked up the document released on 10/1/09 and here's what
I found in regards
Hi friends,
My PI is asking for Notch 4 IHC on FFPE tissue. Can any of you suggest me a
good Ab (preferably mot mouse but anti-human Notch4) and protocol please!
Thanks in advance,
Naira
Naira V. Margaryan, D.V.M., Ph.D.
Research Scientist
Children's Memorial Research Center
2300
I am interested in the same antibody.
Thanks,
Beatrice DeBrosse-Serra
Pathology Scientist
Pfizer Global Research Development
CB4, 2150
10646 Science Center Drive
San Diego, CA 92121
Phone# 858-622-5986
Fax# 858-678-8290
-Original Message-
From:
Debbie,
as far as I know, there is no modifier, all you can charge is a 88307.
That's the same case when you have a skin excision at a 88305. Even if it's
a melanoma excision and it takes 20 blocks, you can only charge an 88305.
The system is FAR from perfect.
JTT
- Original Message
I have a question similar to this one.
If I take 2 IVD antibodies say cytokeratin AE1/AE3 and 34BF12 and make these
into one cytokeratin cocktail, is this considered an ASR because I combined
them into another antibody?
Joe
- Original Message -
From: Morken, Tim
Alcohol will cause the stain to fade, even the small amt. that is carried over
to the xylene over the course of the day. Make sure your xylene is fresh and
coverslip immediately after staining
Rena Fail
- Original Message
From: Gudrun Lang gu.l...@gmx.at
To:
Rena,
we use butylacetat for clearing and before coverslipping with Pertex
(xylolbased, resinous). Butylacetat tolerates ethanol-carryover more than
xylene, but evapourates very fast after couverslipping.
But is it possible, that butylacetat or Pertex itself cause the fading?
Do you think
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