protocol. For
standard processing we had/have two stations with 60 min each at 40 °C. For fat
processing the time is doubled.
That works for our specimens well enough.
Gudrun
-Ursprüngliche Nachricht-
Von: Ann Specian via Histonet [mailto:histonet@lists.utsouthwestern.edu]
Gesendet: Freitag
.
Will Cavett, II
-Original Message-
From: Ann Specian via Histonet
Sent: Wednesday, April 24, 2024 2:00 PM
To: histonet@lists.utsouthwestern.edu
Subject: [EXTERNAL][Histonet] Epredia xylene substitute
We are thinking of changing from xylene to this substitute. Does anybody have
any
We are thinking of changing from xylene to this substitute. Does anybody have
any Processing protocols using Epredia Xylene substitute that they could share?
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Can anyone let me know if CAP, New York State or ISO have any required
credentials for someone to be able to embed human tissue?
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Is anyone familiar with this new technology?
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We just received a recycler and would like to know if anyone has performed a
validation on the recycler prior to putting into use (separate from the
processing validation). If you have, is it possible to share it with me?
Thank you, Ann
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Is anyone using a xylene substitute when staining their PAPs and imaging using
the Hologic Imagers? If you are, can you tell me which xylene substitute you
are using (as long as it is FDA approved). Have you had any issues? Thank
you, Ann
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Is anyone aware of any NYS/CAP/CLIA regulations regarding credentialing
required to perform embedding in NJ?Thank you, Ann
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Can someone tell me if there has been a change in the training and education
requirements in the New Jersey/New York area for Histotech’s. Were there any
regulatory changes?
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Does anybody have a reference as to the proper temperature to store paraffin
blocks. What is the highest temp permitable.
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Has anyone used Proscia for digital imaging? Comments?
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Can someone tell me the correct way to bill an IUD that has tissue. If there is
no tissue then we just bill cpt code 88300. If there is tissue should you bill
88305 or 88300 and 88305?
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Does anyone have a staining procedure for the fuelgen stain for urine cytology
that they can share
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Does anyone have a procedure for an acid hematoxylin stain for urine cytology?
I believe Bostwick used to/does perform it..
Ann
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Is anyone familiar with the Sakura Automated Embeddingcenter or their Express
processor? If so, can you let me know yourthoughts.
Thanks,
Ann
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Does anyone know where to find the requirements to start aschool for
Histotechnology in nj?
Ann
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Has anyone had to validate a microtome (manual/automatic). If so, how did you
do it?
Ann
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Does anyone have any information in regard to using digitalimages as the
primary diagnostic tool?
Thanks,
ann
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I am looking to purchase a cassette printer. Does anyone have any suggestions
as to which are the best and which should be avoided?
Thanks,
Ann
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We are moving out Peloris tissue processors to another room, so we have to
validate. I was wondering what other labs do as a validation for this type of
move? Do you run tissue on every progam utilizing each processor for at least
one of the protocols? Any help would be appreciated.
thanks,
Does anyone have a procedure where in you can lift the stained sections off of
a slide and place them on another slide?
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Does anyone post fix their IHC slides in formalin in an effort to try to reduce
tissue loss? If so, does anyone have a protocol for this that they have used
and have seen good results?
If you have any other suggestions which can help to reduce tissue loss during
IHC staining, I would love to
Can someone tell me the range you set your slide drying oven at and what you
base it on.
thanks,
Ann
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I have to write an sop for submission of slides for HQIP. Does anyone have one
they can share?
Thanks, Ann
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Can anyone tell me the average cost for preparing an IHC slide?
thanks, Ann
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I need a radiation sop specific to Histology. Does anyone have one they can
share? thanks, Ann
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Has anyone written a procedure for this new checklist item? If so, what
procedure are you using to verify equipment/instrument performance prior to
use? Ann
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I am getting complaints in regard to insufficient cell blocks. We currently
spin, pour off the supernatant, retrieve the sediment and process in lens paper.
Does anyone have a more current technique which renders better cellularity?
Also, do you know which renders a better cell block: a
ANP.12087 states that the cryostat needs to be defrosted and wiped clean with a
tuberculocidal.
Can someone tell me what they use that meets the CAP criteria listed above.
thankis,
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Can someone tell me the CAP approved chemical that can be used to clean the
cryostat?
thanks, Ann
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I am looking for a voice recognition system for the gross room. It needs to be
a system that will interface with our LIS.
Does anyone have any recommendations in regard to vendors?
Thank you,
Ann Specian
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I have a question in regard to eliminating the use of negative controls when
using a non-avidin-biotin detection system.
Do you not feel that negative controls may still need to be run in tissues
which are likely to be pigmented such as lymph node, skin and liver?
We were thinking to
We are having a problem with floaters in our blocks which occur during
embedding. We have multiple forceps which are placed in heated wells and each
cassette is embedded with a new forcep. We also wipe with a gauze, but we are
still getting floaters embedded in the cassette from time to
we clean them at the start of our shift, but not during embedding. do you
clean them during embedding too?
-Original Message-
From: Norton, Sally sally.nor...@seattlechildrens.org
To: 'Ann Specian' thisis...@aol.com; histonet
histonet@lists.utsouthwestern.edu
Sent: Fri, May 25, 2012
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