SPAM-LOW: RE: [Histonet] Responses to IHC CAP Validation question
Patsy Ruegg
pruegg <@t> ihctech.net
Thu May 6 12:32:42 CDT 2010
I believe the point of validating is supposed to be to use samples that are
processed in your own facility, so if you use controls you have not fixed
and processed yourself it would not be valid.
Regards,
Patsy
Patsy Ruegg, HT(ASCP)QIHC
IHCtech, LLC
Fitzsimmons BioScience Park
12635 Montview Blvd. Suite 215
Aurora, CO 80010
P-720-859-4060
F-720-859-4110
wk email pruegg <@t> ihctech.net
web site www.ihctech.net
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-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu
[mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of
tonia.richmond <@t> gracepathology.com
Sent: Thursday, May 06, 2010 9:28 AM
To: McMahon, Loralee A
Cc: histonet <@t> lists.utsouthwestern.edu; thisisann <@t> aol.com
Subject: SPAM-LOW: RE: [Histonet] Responses to IHC CAP Validation question
If you are a brand new lab, how do you validate IHC if you are no=
yet receiving patient specimens? Can the validation be done on cont
rol tissues only?
Sincerely,
Tonia Richmond, AS, HT (ASCP)
Chief Operations Officer = Laboratory
Grace Pathology
PH: (501) 765-7367
Email: =1]tonia.=ichmond <@t> gracepathology.com
-----histonet-bounces <@t> lists.utsouthwestern.edu wrote: -----
<=FONT>
To: "thisisann@= aol.com" <thisisann <@t> aol.com>,
"histonet <@t> lists.utsouthwestern.edu" <
;histonet <@t> lists.utsouthwestern.edu>
From: "McMahon, Loralee A" <Lo=alee_Mcmahon <@t> URMC.Rochester.edu>
Sent by: histonet-bounces <@t> lists.u=southwestern.edu
Date: 04/28/2010 02:01PM
Subject: RE: [Histonet] Re=ponses to IHC CAP Validation question
Any inspection that I have under=one we have used the 25 to 30
case rule. Except for the Er/Pr//Her-2= We use closer to 50
cases. We also use a TMA to make our live= easier. The TMA
contains known positives and known negatives.
I=n cases of t-cell or b-cell markers or cytokeratins. 25 to 30
cases i= easy. But when you are validated for more hard to find
markers (SV-=0) then fewer cases is acceptable. We always throw
in a slide that w= know will not stain for sv-40 like a tonsil -
then you can say it has spe=ificity.
Any inspector that I have come across is usually understanding=f
this. But I am sure that there are exceptions to this.........esp
ecially if they are not familiar with immunohistochemistry.
Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong M=morial Hospital
Department of Surgical Pathology
(585) 275-7210
______________________ 5F__=5F______________
From: histonet-bounces <@t> lis= ts.utsouthwestern.edu
[histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf= Of
thisisann <@t> aol.com [thisisann <@t> aol.com]
Sent: Wednesday, April 28, 201= 2:47 PM
To: histonet <@t> lists.utsouthwestern.edu
Subject: [Histonet] R=sponses to IHC CAP Validation question
The following is one respone= rec'd:
1. I asked CAP who told me that they do not currentl= have a
guideline on
validating but that they
recommend what is in t=e following book:
Quality Management In Anatomic Pathology, Promoting P=tient
Safety
Through Systems Improvement and Error
by Raouf E. Nakhl=h, MD & Patrick Fitzgibbons, MD editors
sold by CAP !
Chapter 8-=uality Management in IHC
That is what we follow.
I. Get a new antib=dy and optimize it with your positive control.
II. Once optimized you n=ed to run it on cases expected to be
positive
(how many?)
"a suffien= size ..."
III. Must also be run on cases expected to be negative. (how=any?
IV. In a situation where you cannot expect a lot of cases or such
a
case has
never been presented in your lab, then you must say just =hat.
(ex. some of the hormones we just use a pituitary)
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References
1. 3D"mailto:tonia.richmond <@t> gracepathology.com"
2. 3D"http://lists.utsouthwestern.edu/mailman/listinfo/histonet"
3. 3D"http://=
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