[Histonet] Ink issues

2009-09-02 Thread Amspacher, September
Good Morning all- I am having issues getting ink to stick to the tissue 
surface, the black and blue that we are using are fine we have tried several 
different companies and even use a ink stay acetic acid spray on the tissue. 
My new pathologist has talked about dipping the tissue after it is inked into 
Bouins solution, and that they didn't have any issues with inks where he came 
from.  I have heard of this technique before, But I was just able to get rid of 
all of the bounins solutions in the lab and I am hesitant to bring it back, 
looking for Ideas and thought from all, also if you use the Bouins solution to 
fix your inks- I would love to learn your thoughts about the process. 
Thanks-a-million

September Amspacher HT(ASCP)
Technical Specialist- Histology Department
Laboratory Chemical Hygiene Officer
Bassett Healthcare
Cooperstown, New York



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[Histonet] RE: Ink issues

2009-09-02 Thread Walzer Susan
My Docs use acetone.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amspacher, 
September
Sent: Wednesday, September 02, 2009 7:03 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Ink issues

Good Morning all- I am having issues getting ink to stick to the tissue 
surface, the black and blue that we are using are fine we have tried several 
different companies and even use a ink stay acetic acid spray on the tissue. 
My new pathologist has talked about dipping the tissue after it is inked into 
Bouins solution, and that they didn't have any issues with inks where he came 
from.  I have heard of this technique before, But I was just able to get rid of 
all of the bounins solutions in the lab and I am hesitant to bring it back, 
looking for Ideas and thought from all, also if you use the Bouins solution to 
fix your inks- I would love to learn your thoughts about the process. 
Thanks-a-million

September Amspacher HT(ASCP)
Technical Specialist- Histology Department
Laboratory Chemical Hygiene Officer
Bassett Healthcare
Cooperstown, New York



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[Histonet] RE: Ink issues

2009-09-02 Thread Smith Wanda
Good Morning,
We dip the inked tissue in a container of Acetone.  We use the 7-dye kit from 
Bradley Products, Inc. 
Wanda 


WANDA G. SMITH, HTL(ASCP)HT
Pathology Supervisor
TRIDENT MEDICAL CENTER
9330 Medical Plaza Drive
Charleston, SC  29406
843-847-4586
843-847-4296 fax

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amspacher, 
September
Sent: Wednesday, September 02, 2009 7:03 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Ink issues

Good Morning all- I am having issues getting ink to stick to the tissue 
surface, the black and blue that we are using are fine we have tried several 
different companies and even use a ink stay acetic acid spray on the tissue. 
My new pathologist has talked about dipping the tissue after it is inked into 
Bouins solution, and that they didn't have any issues with inks where he came 
from.  I have heard of this technique before, But I was just able to get rid of 
all of the bounins solutions in the lab and I am hesitant to bring it back, 
looking for Ideas and thought from all, also if you use the Bouins solution to 
fix your inks- I would love to learn your thoughts about the process. 
Thanks-a-million

September Amspacher HT(ASCP)
Technical Specialist- Histology Department Laboratory Chemical Hygiene Officer 
Bassett Healthcare Cooperstown, New York



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RE: [Histonet] Ink issues

2009-09-02 Thread Weems, Joyce
We use acetic acid - 3-5% solution (vinegar). j

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Amspacher, September
Sent: Wednesday, September 02, 2009 07:03
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Ink issues

Good Morning all- I am having issues getting ink to stick to the
tissue surface, the black and blue that we are using are fine we have
tried several different companies and even use a ink stay acetic acid
spray on the tissue. My new pathologist has talked about dipping the
tissue after it is inked into Bouins solution, and that they didn't have
any issues with inks where he came from.  I have heard of this technique
before, But I was just able to get rid of all of the bounins solutions
in the lab and I am hesitant to bring it back, looking for Ideas and
thought from all, also if you use the Bouins solution to fix your
inks- I would love to learn your thoughts about the process.
Thanks-a-million

September Amspacher HT(ASCP)
Technical Specialist- Histology Department Laboratory Chemical Hygiene
Officer Bassett Healthcare Cooperstown, New York



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RE: [Histonet] HE preparation

2009-09-02 Thread Weems, Joyce

 the good ole days for sure - purple ceilings, purple walls, purple
people And cigarette ashes in the trash and food on the counter...

Is it Friday yet?!!! 
J:)

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lynette
Pavelich
Sent: Wednesday, September 02, 2009 07:02
To: aaz...@hotmail.com; histonet@lists.utsouthwestern.edu;
kemlo.roger...@waht.swest.nhs.uk
Subject: RE: [Histonet] HE preparation

Ah, the good 'ol days!  Remember adding the oxidizinng agent (mecuric
oxide) too soon when it was still bubbling and having a volcano of
hematoxylin?!!!  LOLj Was remembering tho', that every day, before
using, we would top off
(add...oh, about 30ml) of fresh to the filtered used batch.  This really
kept the quality good.  Worked for 30 yrs until we started purchasing
it.  Gone are the morning coffee and donuts sitting next to our
microtomes too!! Sigh  Ya, yaI know!!!  
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[Histonet] Robotic Prostatectomy

2009-09-02 Thread Phyllis Thaxton
For the first time here, we have Urologists using the robotic method for 
removing prostates. The PA always receives them fresh, inks them, then puts the 
whole prostate in alcoholic fixative (currently Zfix from Anatech). The next 
day they are grossed in and processed.  The prostates we have received lately 
are raw in the middle and unable to be grossed in, whereas before they were 
fine.

Has anyone had similar experiences?
 Phyllis Thaxton HT(ASCP)QIHC
DCH Regional Medical Center
Tuscaloosa, AL 



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[Histonet] (no subject)

2009-09-02 Thread James, Jennifer
Does anyone have experience with the Cell Technology Apo-single stranded DNA 
antibody?  Please let me know if you do.
Thanks!

Jennifer James BS, HT(ASCP)HTL, QIHC, CRS
Research Assistant
Experimental Pathology Laboratory
Winthrop P.Rockefeller Cancer Institute, Room 429
Universtiy of Arkansas for Medical Sciences
4301 West Markham Street, #725
Little Rock, AR  72205
501-686-8265
jamesjennif...@uams.edumailto:jamesjennif...@uams.edu


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[Histonet] Cost to produce an HE slide

2009-09-02 Thread Amy Johnson
Hello Histonet.Has anyone ever figured out how much it costs to
produce an HE slide?  Are there any articles out there that would help
to figure this out?

I realize it may be different for each institution but a ball park
figure would be greatly appreciated.

Thanks 

Amylin Johnson

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Re: [Histonet] Robotic Prostatectomy

2009-09-02 Thread Rene J Buesa
And your problem will not be solved unless the prostates, after being inked, 
are cut in half before placing them in the fixative. I do not see any problem 
in cutting in half a properly inked prostate to assure proper fixation and 
subsequent processing.
René J. 

--- On Wed, 9/2/09, Phyllis Thaxton dch...@yahoo.com wrote:


From: Phyllis Thaxton dch...@yahoo.com
Subject: [Histonet] Robotic Prostatectomy
To: histonet@lists.utsouthwestern.edu
Date: Wednesday, September 2, 2009, 11:26 AM


For the first time here, we have Urologists using the robotic method for 
removing prostates. The PA always receives them fresh, inks them, then puts the 
whole prostate in alcoholic fixative (currently Zfix from Anatech). The next 
day they are grossed in and processed.  The prostates we have received lately 
are raw in the middle and unable to be grossed in, whereas before they were 
fine.

Has anyone had similar experiences?
 Phyllis Thaxton HT(ASCP)QIHC
DCH Regional Medical Center
Tuscaloosa, AL 



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[Histonet] Re: Ink issues

2009-09-02 Thread Robert Richmond
About what to put on tissue to make the marking ink stick to it:

I don't use anything. The trick is to blot the surfaces thoroughly dry
with a paper towel before you try to put the ink on. Of course,
there's nothing you can use that will make ink adhere well to
cauterized surfaces (some breast biopsy specimens, LEEP cones, and
such. The pathologist can however identify cauterized margins under
the microscope.)

Because of the picric acid (and because it stains your clothes)
Bouin's fixative is unacceptable. So is acetone, which is a serious
explosion hazard. If you must use something, use 3% acetic acid (white
vinegar diluted half-strength).

I've been grossing since 1965, worked on maybe sixty different
pathology services.

Bob Richmond
Samurai Pathologist
Knoxville TN

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[Histonet] Re: Gloves

2009-09-02 Thread Robert Richmond
Janet Bonner notes:

We use Aloe Touch Nitrile gloves, powder-free from Medline (MDS195084 for 
small size)  www.medline.com.(1-800 - medline) These gloves are not 
stiff, they fit the hand 'like a glove' .  They say on the box not intended 
to be used as a chemical barrier, but they do a great job when exposed to 
Histology chemicals.

Not familiar with this product, but with nitrile rubber gloves brand
name is important, as the quality of nitrile rubber gloves worsens.
When they first came out and were made in the USA, I could make a pair
last for two weeks of grossing. As manufacture moved to the
latex-producing countries, nitrile rubber (if that's what they
actually are) gloves became no better than latex. At present I use two
pairs of gloves when I gross.

There's a little-known product called chemotherapy gloves - thick
blue latex. I filched a box of these and use them - they last for
several days. Obviously re-using gloves offsets the high initial cost
of purchase, but that's not good MBA thinking.

OSHA says not to handle formaldehyde (and I suppose xylene) with latex
gloves, but has not specified an alternative.

It's disgraceful how little the powers that be care about the hands of
pathologists and histotechnologists. You can bet that if it were
nurses who had this problem, it'd get solved in a hurry.

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] Re: Ink issues

2009-09-02 Thread Galbraith, Joe
I concur with the Samurai Pathologist.  Long ago, we used Bouin's but
have stopped that procedure and prefer to just blot dry but do also use
3% acetic acid, especially if blotting could potentially damage a
delicate tissue.  Good luck.

Joe Galbraith
University of Iowa
joseph-galbra...@uiowa.edu


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Robert
Richmond
Sent: Wednesday, September 02, 2009 12:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Ink issues

About what to put on tissue to make the marking ink stick to it:

I don't use anything. The trick is to blot the surfaces thoroughly dry
with a paper towel before you try to put the ink on. Of course,
there's nothing you can use that will make ink adhere well to
cauterized surfaces (some breast biopsy specimens, LEEP cones, and
such. The pathologist can however identify cauterized margins under
the microscope.)

Because of the picric acid (and because it stains your clothes)
Bouin's fixative is unacceptable. So is acetone, which is a serious
explosion hazard. If you must use something, use 3% acetic acid (white
vinegar diluted half-strength).

I've been grossing since 1965, worked on maybe sixty different
pathology services.

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] Re: Gloves

2009-09-02 Thread Bonner, Janet
It says on the box that these aloe touch nitrile gloves are Latex-free, 
powder-free nitrile examination gloves, single use, non-sterile. Tested for use 
with chemotherapy drugs 
   We've had a terrible time with getting good gloves, and then when we get 
some good ones, they are replaced the following year with a cheaper brand until 
our PAs start screaming.  You're right - Surgery wouldn't even have to whistle!!
 
Janet 



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Robert Richmond
Sent: Wed 9/2/2009 1:34 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Gloves



Janet Bonner notes:

We use Aloe Touch Nitrile gloves, powder-free from Medline (MDS195084 for 
small size)  www.medline.com.(1-800 - medline) These gloves are not 
stiff, they fit the hand 'like a glove' .  They say on the box not intended 
to be used as a chemical barrier, but they do a great job when exposed to 
Histology chemicals.

Not familiar with this product, but with nitrile rubber gloves brand
name is important, as the quality of nitrile rubber gloves worsens.
When they first came out and were made in the USA, I could make a pair
last for two weeks of grossing. As manufacture moved to the
latex-producing countries, nitrile rubber (if that's what they
actually are) gloves became no better than latex. At present I use two
pairs of gloves when I gross.

There's a little-known product called chemotherapy gloves - thick
blue latex. I filched a box of these and use them - they last for
several days. Obviously re-using gloves offsets the high initial cost
of purchase, but that's not good MBA thinking.

OSHA says not to handle formaldehyde (and I suppose xylene) with latex
gloves, but has not specified an alternative.

It's disgraceful how little the powers that be care about the hands of
pathologists and histotechnologists. You can bet that if it were
nurses who had this problem, it'd get solved in a hurry.

Bob Richmond
Samurai Pathologist
Knoxville TN

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the 
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RE: [Histonet] Re: Ink issues

2009-09-02 Thread Morken, Tim
Maybe it is the acetic acid in Bouin's that is the active ingredient for dye 
adherence!

Tim Morken
Supervisor, Histology / IPOX
UCSF Medical Center
San Francisco, CA  
 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Galbraith, Joe
Sent: Wednesday, September 02, 2009 10:49 AM
To: Robert Richmond; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Ink issues

I concur with the Samurai Pathologist.  Long ago, we used Bouin's but
have stopped that procedure and prefer to just blot dry but do also use
3% acetic acid, especially if blotting could potentially damage a
delicate tissue.  Good luck.

Joe Galbraith
University of Iowa
joseph-galbra...@uiowa.edu


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Robert
Richmond
Sent: Wednesday, September 02, 2009 12:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Ink issues

About what to put on tissue to make the marking ink stick to it:

I don't use anything. The trick is to blot the surfaces thoroughly dry
with a paper towel before you try to put the ink on. Of course,
there's nothing you can use that will make ink adhere well to
cauterized surfaces (some breast biopsy specimens, LEEP cones, and
such. The pathologist can however identify cauterized margins under
the microscope.)

Because of the picric acid (and because it stains your clothes)
Bouin's fixative is unacceptable. So is acetone, which is a serious
explosion hazard. If you must use something, use 3% acetic acid (white
vinegar diluted half-strength).

I've been grossing since 1965, worked on maybe sixty different
pathology services.

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] Ink issues (UNCLASSIFIED)

2009-09-02 Thread Gladney, Diane C Ms CIV USA MEDCOM MACH
Classification:  UNCLASSIFIED 
Caveats: NONE

We use Distilled White Vinegar. I buy it at the grocery store by the
gallon. It is the acetic acid in bouin's solution that fixes the ink to
the tissue, not the picric acid. I have been using white vinegar for
more years than I care to remember. Hope this helps.

Diane Gladney
Supervisor, Histology Dept.
Moncrief Army Community Hospital
Ft. Jackson, SC

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
Amspacher, September
Sent: Wednesday, September 02, 2009 7:03 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Ink issues

Good Morning all- I am having issues getting ink to stick to the
tissue surface, the black and blue that we are using are fine we have
tried several different companies and even use a ink stay acetic acid
spray on the tissue. My new pathologist has talked about dipping the
tissue after it is inked into Bouins solution, and that they didn't have
any issues with inks where he came from.  I have heard of this technique
before, But I was just able to get rid of all of the bounins solutions
in the lab and I am hesitant to bring it back, looking for Ideas and
thought from all, also if you use the Bouins solution to fix your
inks- I would love to learn your thoughts about the process.
Thanks-a-million

September Amspacher HT(ASCP)
Technical Specialist- Histology Department
Laboratory Chemical Hygiene Officer
Bassett Healthcare
Cooperstown, New York



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Classification:  UNCLASSIFIED 
Caveats: NONE


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[Histonet] Uranyl Nitrate

2009-09-02 Thread kristen arvidson
I am looking for an alternate disposal method for my Uranyl Nitrate.  I was 
quoted at about $3000 from our haz. waste disposal company.  I would like to 
find a cheaper method.  I cannot ship it outside the US.  Would anyone be able 
to take it and add it to their waste?  I have about 500ml of a 1% aq. 
solution to get rid of.  Please let me know if this might be a possibility, I 
will pay for service.  Thank you!!



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[Histonet] (no subject)

2009-09-02 Thread sheila adey


Does anyone have a good recipe for making up a dissect aid in house?

 


Sheila Adey HT MLT 



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RE: [Histonet] Re: Gloves

2009-09-02 Thread Merced M Leiker
I was just doing some research on the original question posted of gloves 
suitable for handling xylene.  Nitrile is a synthetic rubber made of 
acrylnitrile and butadiene, devoid of allergy-causing proteins like in 
latex and natural rubber.


The U.S. Dept. of Energy suggests using nitrile when handling xylenes, 
Ansell suggests either their laminate film gloves, PVA, or nitrile on their 
very detailed chart offering technical permeabilty data (for instance, it 
takes 75 min for xylene to break through their nitrile gloves). Now 
according to OSHA, nitrile does not provide adequate protection, but gives 
other glove types that are in agreement with what is suggested by some of 
the other sites I saw. Some of the sites don't seem to say how THICK these 
gloves are that they are rating, which I think would be a factor for 
permeability rate. Most of Ansell's gloves were quite THICK (like for 
industrial use).


Another factor for permeability would be how long xylene will be in contact 
with your glove, if you change gloves frequently or soon after getting 
xylene on them it seems you'd be ok. I find nitrile (the flexible thin 
healthcare ones) to be pretty cost-effective. At least, I've dipped my 
nitrile-gloved fingers in a xylene bath and when I changed my gloves a few 
minutes later my skin and the inside of the glove was still dry.


References:
http://www.aps.anl.gov/Safety_and_Training/User_Safety/gloveselection.html

http://www.ansellpro.com/download/Ansell_7thEditionChemicalResistanceGuide.pdf

http://www.osha.gov/SLTC/healthguidelines/xylene/recognition.html


Regards,
Merced

--On Wednesday, September 02, 2009 1:53 PM -0400 Bonner, Janet 
janet.bon...@flhosp.org wrote:



It says on the box that these aloe touch nitrile gloves are Latex-free,
powder-free nitrile examination gloves, single use, non-sterile. Tested
for use with chemotherapy drugs We've had a terrible time with
getting good gloves, and then when we get some good ones, they are
replaced the following year with a cheaper brand until our PAs start
screaming.  You're right - Surgery wouldn't even have to whistle!!
Janet



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Robert
Richmond Sent: Wed 9/2/2009 1:34 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Gloves



Janet Bonner notes:


We use Aloe Touch Nitrile gloves, powder-free from Medline (MDS195084
for small size)  www.medline.com.(1-800 - medline) These gloves
are not stiff, they fit the hand 'like a glove' .  They say on the box
not intended to be used as a chemical barrier, but they do a great job
when exposed to Histology chemicals.


Not familiar with this product, but with nitrile rubber gloves brand
name is important, as the quality of nitrile rubber gloves worsens.
When they first came out and were made in the USA, I could make a pair
last for two weeks of grossing. As manufacture moved to the
latex-producing countries, nitrile rubber (if that's what they
actually are) gloves became no better than latex. At present I use two
pairs of gloves when I gross.

There's a little-known product called chemotherapy gloves - thick
blue latex. I filched a box of these and use them - they last for
several days. Obviously re-using gloves offsets the high initial cost
of purchase, but that's not good MBA thinking.

OSHA says not to handle formaldehyde (and I suppose xylene) with latex
gloves, but has not specified an alternative.

It's disgraceful how little the powers that be care about the hands of
pathologists and histotechnologists. You can bet that if it were
nurses who had this problem, it'd get solved in a hurry.

Bob Richmond
Samurai Pathologist
Knoxville TN

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Merced M Leiker
Research Technician II
Cardiovascular Medicine
348 Biomedical Research Building
State University of New York at Buffalo
3435 Main St, Buffalo, NY 14214  USA
lei...@buffalo.edu
716-829-6118 (Ph)
716-829-2665 (Fx)

No trees were harmed in the sending of this email.

RE: [Histonet] Cost to produce an HE slide

2009-09-02 Thread Burton, Lynn
I don't know what the COST to produce an HE is but we charge outside entities 
$8 each to stain them.
 
Lynn Burton
Lab Assoc. I
Animal Disease Lab
Galesburg, Il 61401



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Amy Johnson
Sent: Wed 9/2/2009 11:11 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Cost to produce an HE slide



Hello Histonet.Has anyone ever figured out how much it costs to
produce an HE slide?  Are there any articles out there that would help
to figure this out?

I realize it may be different for each institution but a ball park
figure would be greatly appreciated.

Thanks

Amylin Johnson

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RE: [Histonet] Re: Gloves

2009-09-02 Thread hymclab
We also use the Aloetouch gloves for all aspects of Histology and have had no 
issues with them.  They fit like a glove and are very durable but continue to 
have good flexability.
Luckily Medline is on contract with HPG (our buying group)!!!

Dawn D. Schneider, HT(ASCP)
Howard Young Medical Center
Woodruff, WI  54568
(715)356-8174
dawn.schnei...@ministryhealth.org



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bonner, Janet
Sent: Wednesday, September 02, 2009 12:54 PM
To: Robert Richmond; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Gloves

It says on the box that these aloe touch nitrile gloves are Latex-free, 
powder-free nitrile examination gloves, single use, non-sterile. Tested for use 
with chemotherapy drugs
   We've had a terrible time with getting good gloves, and then when we get 
some good ones, they are replaced the following year with a cheaper brand until 
our PAs start screaming.  You're right - Surgery wouldn't even have to whistle!!

Janet



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Robert Richmond
Sent: Wed 9/2/2009 1:34 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Gloves



Janet Bonner notes:

We use Aloe Touch Nitrile gloves, powder-free from Medline (MDS195084 for 
small size)  www.medline.com.(1-800 - medline) These gloves are not 
stiff, they fit the hand 'like a glove' .  They say on the box not intended 
to be used as a chemical barrier, but they do a great job when exposed to 
Histology chemicals.

Not familiar with this product, but with nitrile rubber gloves brand name is 
important, as the quality of nitrile rubber gloves worsens.
When they first came out and were made in the USA, I could make a pair last for 
two weeks of grossing. As manufacture moved to the latex-producing countries, 
nitrile rubber (if that's what they actually are) gloves became no better than 
latex. At present I use two pairs of gloves when I gross.

There's a little-known product called chemotherapy gloves - thick blue latex. 
I filched a box of these and use them - they last for several days. Obviously 
re-using gloves offsets the high initial cost of purchase, but that's not good 
MBA thinking.

OSHA says not to handle formaldehyde (and I suppose xylene) with latex gloves, 
but has not specified an alternative.

It's disgraceful how little the powers that be care about the hands of 
pathologists and histotechnologists. You can bet that if it were nurses who had 
this problem, it'd get solved in a hurry.

Bob Richmond
Samurai Pathologist
Knoxville TN

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RE: [Histonet] Endogenous biotin blocking

2009-09-02 Thread JMyers1
Sally:
 
The simple answer to the question of whether or not biotin blocking is 
required is ‘no’.  As you stated in your inquiry, blocking need only be 
performed when excessive nonspecific staining, attributable to endogenous 
biotin, 
is observed. 

For what its worth, I think that some folks believe biotin blocking is 
required because they've miscontrued information contained within the College 
of 
American Pathologists AP checklist, which states: “If the laboratory uses 
an avidin-biotin complex (ABC) detection system...is there a policy that 
addresses nonspecific false positive staining from endogenous biotin?  As 
written, this question only implies that an assessment of false positive 
staining 
be performed.  Therefore, provided that the lab conducts the recommended 
assessment, documents their results within appropriate policies/procedures, 
and then incorporates biotin blocking steps where they're needed, it does not 
have to perform blocking at all times. 

I'd welcome additonal input if my understanding is incorrect. 
Regards, 
Joe Myers, M.S., CT(ASCP) 


--

Message: 9
Date: Tue, 1 Sep 2009 08:31:56 -0400
From: Sally Price sprice2...@gmail.com
Subject: [Histonet] Endogenous biotin blocking
To: histonet@lists.utsouthwestern.edu

I recently had a discussion with one of my coworkers about the 
need/requirement for blocking of endoegnous biotin whenever an avidin-biotin 
detection 
system is used, and I was hoping that the IHC
experts on the histonet might be able to provide us with some feeback.  Its 
been my understanding that blocking is only necessary when one is certain 
that background staining is caused by endogenous biotin, but maybe I'm 
off-base here.  I look forward to eveyone's input.
Sally
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RE: [Histonet] Cost to produce an HE slide

2009-09-02 Thread Rittman, Barry R
The cost around $12 to produce a regularly stained section.
The cost to produce a stained section by an very experienced 
histotech...priceless.



From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Burton, Lynn 
[lynn.bur...@illinois.gov]
Sent: Wednesday, September 02, 2009 2:02 PM
To: Amy Johnson; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Cost to produce an HE slide

I don't know what the COST to produce an HE is but we charge outside entities 
$8 each to stain them.

Lynn Burton
Lab Assoc. I
Animal Disease Lab
Galesburg, Il 61401



From: histonet-boun...@lists.utsouthwestern.edu on behalf of Amy Johnson
Sent: Wed 9/2/2009 11:11 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Cost to produce an HE slide



Hello Histonet.Has anyone ever figured out how much it costs to
produce an HE slide?  Are there any articles out there that would help
to figure this out?

I realize it may be different for each institution but a ball park
figure would be greatly appreciated.

Thanks

Amylin Johnson

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[Histonet] pERK IHC

2009-09-02 Thread Nancy Lemke
Does anyone have any suggestions for antibody, protocol, etc.,  regarding 
staining FFPE sections with pERK?  Any information would be greatly appreciated.
Thanks in advance,
Nancy Lemke
Research Coordinator
Hermelin Brain Tumor Center
Henry Ford Hospital
Detroit


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RE: [Histonet] Cost to produce an HE slide

2009-09-02 Thread WILLIAM DESALVO

Over the years I have not found any published cost calculations that have 
addressed individual categories that fluctuate constantly in the department and 
it seems that there are as many models as there are institutions/companies. In 
the past I have found if I separate costs into a minimum of 4 categories, I can 
provide a reasonable calculation for the technical component successfully. Full 
calculation will require that you have a cost for all shared tasks in the 
department that contribute to the production of the slide (i.e. accessioning, 
grossing, embedding, cutting) and be able to allocate a portion of that 
technical cost to the final slide. I have also been asked to add to the 
calculation to account for items such as Training/Education for staff, 
taxes/shipping cost and professional fees. I suggest you communicate with 
Finance to see what detail is required and to capture all costs for your 
department. I hope this gets you started.

 

Cost Analysis for HE:
Staining Materials + Labor + Instrumentation + Company Cost Allocation
 
Materials - Reagents, Stains, Slides, Cover slips
Each item will need to be calculated to number of units (slides) per ordered 
unit (i.e. gallon, quart, pint, milliliters). Can take total monthly cost of 
all staining material and divide by total slides stained per month.
Example: Hematoxylin = 1500 slides stained per 620 ml (specific to slide 
staining instrument) or 2.42 slides / mL; Hematoxylin is ordered by the pint or 
473 mL; Cost per pint = $29.80 or $0.063/mL; Cost per slide = .063 mL / 2.42 
slides or $0.026 per slide. This is only for the Hematoxylin
 
Labor – Average salary and benefits for all employees that will perform task. 
Average labor cost will be divided by time spent to perform task.
Example: Average hourly labor cost = $24.00; time spent to perform staining 
task = 4 hours; number of slides stained in 4 hours = 480 slides; Cost per 
slide = 24 x 4 / 480 = $0.20 per slide
 
Instrumentation – Cost to purchase plus the cost of repairs and/or maintenance 
contract or lease/rental cost per year and then the allocation per your 
institution amortization schedule. Divide by total number of slides stained per 
year
Example: Cost of instrument = $60,000; Amortized over 7 years = 60,000 / 7 = 
$8572; Cost of service contract per year = $3,000; Total number of slides 
stained = 100,000; Cost per slide = 8572 + 3,000 / 100,000 = $0.12 per slide. 
All instruments used in the process will need to be added to the cost 
calculation (i.e. cover slip instrument).
 
Company Cost Allocation - This could be a variety of additional cost allocated 
to your department. Air conditioning, lease rental for building, lights, etc.  
Acquire monthly or year total from Finance.
Eample: Allocated casts assigned= $12,000; 100,00 slides per year; Cost per 
slide = 12000 / 10 = $0.012 per slide

William DeSalvo, B.S., HTL(ASCP)
 
 Date: Wed, 2 Sep 2009 11:11:50 -0500
 From: ajohn...@aipathology.com
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Cost to produce an HE slide
 
 Hello Histonet.Has anyone ever figured out how much it costs to
 produce an HE slide? Are there any articles out there that would help
 to figure this out?
 
 I realize it may be different for each institution but a ball park
 figure would be greatly appreciated.
 
 Thanks 
 
 Amylin Johnson
 
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Re: [Histonet] Re: anti-GFP antibody

2009-09-02 Thread Adam .
Hi all,

Just to update you, I ordered Abcam's ab13970 chicken anti-GFP and tested it
out in paraffin embedded sections with HIER for 10 minutes in Dako target
retrieval system. I came in with a Dylight 488 secondary from Jackson
Immunoresearch at 1 ug / mL. It worked beautifully at 1:500, 1:1000, and
1:2000. I should've titered it even further down.

Thanks for all your help,
Adam

On Thu, Aug 20, 2009 at 1:38 PM, Hobbs, Carl carl.ho...@kcl.ac.uk wrote:


 I am sure someone has a cunning combination!
  I use Abcam's ab13970 chicken anti  GFP in Pwax sections after HIER.
 For me, it is very good
 Image at Abcam or here : http://www.immunoportal.com/index.php
 Good luck!
 carl



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[Histonet] Tissue Embedder

2009-09-02 Thread Perry, Margaret
We are in the market for a new embedder.  What do you suggest?   I tried 
searching the archives but only came up with older comments.
Vendors please feel free to contact 
frank@sdstate.edumailto:frank@sdstate.edu.  We may have to go with a 
used instrument so would like comments on good vendors.

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[Histonet] Dragon dictating system

2009-09-02 Thread judy webb
Histonet,
Has anyone had any experience with the Dragon dictating system? Pro's or Con's?

Thanks for your opinions

Judy McKinney    
John Peter Smith Hospital
Fort Worth Texas
817-927-1024
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[Histonet] Ink issues

2009-09-02 Thread judy webb
We  blot the tissue dry, ink specimen and dip into 50% vinegar .  Black and 
green work best, but all colors work.

Judy McKinney
JPS Hospital
Fort Worth Texas
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