RE: [Histonet] Slide and Block Storage

2010-04-30 Thread Nails, Felton
If you are supplying the professional component, then it is a good idea to 
maintain the blocks and slides.
If you are inspected and they do an audit trail you must be able to produce the 
slides and/or blocks. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Daniel Adams
Sent: Thursday, April 29, 2010 11:41 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Slide and Block Storage

My laboratory provides professional services to some clients and technical 
services to others.  The question has recently come up, who should store blocks 
and slides when the pathologist and histology laboratory are different 
companies?

- Dan

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RE: [Histonet] Slide and Block Storage

2010-04-30 Thread Nails, Felton
 I am able to reply to questions n the histonet but I am unable to post 
anything on the histonet. Is there a different address I should be using 
instead of histo...@list.utsouthwestern.edu?

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Nails, Felton
Sent: Friday, April 30, 2010 7:12 AM
To: 'Daniel Adams'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Slide and Block Storage

If you are supplying the professional component, then it is a good idea to 
maintain the blocks and slides.
If you are inspected and they do an audit trail you must be able to produce the 
slides and/or blocks. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Daniel Adams
Sent: Thursday, April 29, 2010 11:41 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Slide and Block Storage

My laboratory provides professional services to some clients and technical 
services to others.  The question has recently come up, who should store blocks 
and slides when the pathologist and histology laboratory are different 
companies?

- Dan

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RE: [Histonet] MAILING BIOPSIES

2010-04-30 Thread Canyon Bowie
Hi All,

There has been quite a large response to the shipping regulations of mailing
specimens, as I would expect to the guidelines changing consistently.  I
will be at the CLMA show in Vegas on May 4th and 5th.  Please feel free to
stop by at booth #626 and I will be available to answer more questions
regarding the regulations and make suggestions for you.  I will also have
samples of different specimen mailing kits.  You can bring me (or mail me)
your current kits and we will evaluate them for free, letting you know if
they meet regulations and if other improvements can be made.

Thanks,

Canyon Bowie 
Path-Tec  
3151 Williams Rd
Bldg C
Columbus, GA
w. 706.507.1575 


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sara
Baldwin/mhhcc.org
Sent: Thursday, April 29, 2010 8:19 AM
To: histonet
Subject: [Histonet] MAILING BIOPSIES


   HISTONETTERS

   I  was  wondering  if  there  are  any  REGS out =here about mailing
   formalin  filled  biopsies thru UPS or FED EX other than =he special
   package  and  the  spill  pad.  Anyone  have any knowledge about the
subject?

   Thanks
   Pathology Supervisor
   Kathy Ba=dwin, SCT (ASCP)
   Memorial Hospital and Health=bsp;Care Center
   [1]sbald...@mhhcc.org
   Ph 812-482-0210, 482-0216, nbs=;Fax 812-482-0232,
   Pager 812-481-0897

   =R Confidential information, Authorized use only.

References

   1. 3Dmailto:sbald...@mhhcc.org;
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RE: [Histonet] Slide and Block Storage

2010-04-30 Thread Elizabeth Kronenberger
If our lab does slide preps for other clients (Technical component only), we
hold the blocks at our facility.  The slides are read and reported by the
client, they hold the slides.

Liz

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Daniel Adams
Sent: Friday, April 30, 2010 12:41 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Slide and Block Storage

My laboratory provides professional services to some clients and  
technical services to others.  The question has recently come up, who  
should store blocks and slides when the pathologist and histology  
laboratory are different companies?

- Dan

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RE: [Histonet] Slide and Block Storage

2010-04-30 Thread Nails, Felton
So what if the reporting company need to order special stains, it adds too much 
time having to request the blocks or additional unstained slides. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Elizabeth 
Kronenberger
Sent: Friday, April 30, 2010 9:40 AM
To: 'Daniel Adams'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Slide and Block Storage

If our lab does slide preps for other clients (Technical component only), we 
hold the blocks at our facility.  The slides are read and reported by the 
client, they hold the slides.

Liz

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Daniel Adams
Sent: Friday, April 30, 2010 12:41 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Slide and Block Storage

My laboratory provides professional services to some clients and technical 
services to others.  The question has recently come up, who should store blocks 
and slides when the pathologist and histology laboratory are different 
companies?

- Dan

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RE: [Histonet] Slide and Block Storage

2010-04-30 Thread Elizabeth Kronenberger
Clients fax orders for deepers and special stains which we perform and send
them out with their next package for them to read and report.

-Original Message-
From: Nails, Felton [mailto:flna...@texaschildrens.org] 
Sent: Friday, April 30, 2010 10:48 AM
To: 'Elizabeth Kronenberger'; 'Daniel Adams';
histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Slide and Block Storage

So what if the reporting company need to order special stains, it adds too
much time having to request the blocks or additional unstained slides. 

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Elizabeth
Kronenberger
Sent: Friday, April 30, 2010 9:40 AM
To: 'Daniel Adams'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Slide and Block Storage

If our lab does slide preps for other clients (Technical component only), we
hold the blocks at our facility.  The slides are read and reported by the
client, they hold the slides.

Liz

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Daniel Adams
Sent: Friday, April 30, 2010 12:41 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Slide and Block Storage

My laboratory provides professional services to some clients and technical
services to others.  The question has recently come up, who should store
blocks and slides when the pathologist and histology laboratory are
different companies?

- Dan

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[Histonet] CD68

2010-04-30 Thread Cynthia Pyse
Happy Friday Everyone

What clone is everyone using for the CD68 antibody for FFPE human tissue?
Thanks for the info in advance. Everyone have a great weekend.

 

Cindy Pyse, CLT, HT (ASCP)

Histology Supervisor

X-Cell Laboratories

e-mail cp...@x-celllab.com

 

 

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Re: [Histonet] CD68

2010-04-30 Thread Mark Tarango
Hi Cindy,

My lab uses KP-1.

Mark

On Fri, Apr 30, 2010 at 8:48 AM, Cynthia Pyse cp...@x-celllab.com wrote:

 Happy Friday Everyone

 What clone is everyone using for the CD68 antibody for FFPE human tissue?
 Thanks for the info in advance. Everyone have a great weekend.



 Cindy Pyse, CLT, HT (ASCP)

 Histology Supervisor

 X-Cell Laboratories

 e-mail cp...@x-celllab.com





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RE: [Histonet] CD68

2010-04-30 Thread Drew Sally A
We also use KP1 


Sally

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cynthia
Pyse
Sent: Friday, April 30, 2010 10:49 AM
To: 'Histonet'
Subject: [Histonet] CD68

Happy Friday Everyone

What clone is everyone using for the CD68 antibody for FFPE human
tissue?
Thanks for the info in advance. Everyone have a great weekend.

 

Cindy Pyse, CLT, HT (ASCP)

Histology Supervisor

X-Cell Laboratories

e-mail cp...@x-celllab.com

 

 

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[Histonet] Repeat validation when IHC protocol changed?

2010-04-30 Thread Kevin_Kurtz
Recently our IHC vendor sent a tech to help us out with some weak staining 
affecting multiple antibodies.  Several staining protocols were changed, 
including adjusting the incubation time and adding amplification.  The 
results were great in the slides that I was shown.

The tech said that revalidation was unnecessary, since the changes to the 
protocol were considered minor.  However, I personally disagree, since 
we don't know how the change in the staining protocol could potentially 
affect staining of other tissues (especially tissues that would be 
expected to be negative). Before subjecting our lab to the cost and effort 
of revalidation, I'd like to get your opinion.

For new antibodies, I usually validate using 10 cases expected to be 
positive and 10 cases expected to be negative for the antibody in 
question. For revalidation, I was thinking of running 5 positive cases and 
5 negative cases.

Thanks for your input - 

Kevin Kurtz, M.D.
St. Mary's Hospital
Madison, Wisconsin

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[Histonet] How to troubleshoot a cytology slide with dehydration problems

2010-04-30 Thread Valerie R.
I am an HTL but I have to stain pap smears. In the Papanicalou procedure for
fine needle aspirations I have to stain the slides in sodium chloride first
for 25 seconds in total (15 seconds in one container and 10 in another
container). This for me is the trickiest part when staining cytology because
if slides are not well dehydrated in saline then the cells are not going to
absorb the stains well, and the result will be a pinkish slide, when it is
suppose to look blue-greenish.

I had this problem today where I stained an entire rack of slides, and all
the slides turned blue (which means they stained correctly) except 4 slides
which turned out pinkish (which is a sign that they did not dehydrated
properly in sodium chloride (h20 saline).

Is there a solution to this issue. Can these slides be re-stained?

I know this newsgroup is for histology only but I would like to know if
histotech and cytotechs have encountered this issue in their labs and how
they ended up solving the problem.

Thanks in advance
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[Histonet] Re: How to troubleshoot a cytology slide with dehydration problems

2010-04-30 Thread Valerie R.
I forgot to include the complete protocol that my lab uses so you can help
me better:

1.After dehydrating in sodium chloride for 25 seconds you have to dip the
slides in alcohol 95.
2. 10 dips in water then 1.30 minutes in hematoxylin, it used to be 1 min,
then rinse in water.
3. 1 min in rinse solution
4.10 dips in water.
5. 1 min in bluing solution
6. 10 dips in water.
7. 10 dips in alcohol.
8. 10 dips in alcohol.
9. 1 min in orange solution
10. 15 dips in 95 alcohol.
11. 15 dips in 95 alcohol.
12.  3.15 mins in EA solution
13. The slides are then dipped in 3 containers of 95 alcohol (20 dips each)
14. Slides are dipped in 3 containers of 99 alcohol (15 dips in each)
15. Then they are dipped in Isoxylene which is a combination of xylene and
99 alcohol (15 dips)
16. And lastly Xylene 10 dips


When the slides do not absorb the h20 saline seems that the slides absorb
more EA than hematoxylin.  I don't know why.

On Fri, Apr 30, 2010 at 5:34 PM, Valerie R. vrodrigue...@gmail.com wrote:

 I am an HTL but I have to stain pap smears. In the Papanicalou procedure
 for fine needle aspirations I have to stain the slides in sodium chloride
 first for 25 seconds in total (15 seconds in one container and 10 in another
 container). This for me is the trickiest part when staining cytology because
 if slides are not well dehydrated in saline then the cells are not going to
 absorb the stains well, and the result will be a pinkish slide, when it is
 suppose to look blue-greenish.

 I had this problem today where I stained an entire rack of slides, and all
 the slides turned blue (which means they stained correctly) except 4 slides
 which turned out pinkish (which is a sign that they did not dehydrated
 properly in sodium chloride (h20 saline).

 Is there a solution to this issue. Can these slides be re-stained?

 I know this newsgroup is for histology only but I would like to know if
 histotech and cytotechs have encountered this issue in their labs and how
 they ended up solving the problem.

 Thanks in advance



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