Re: [Histonet] problem with brain sections falling off subbed slides

2011-11-03 Thread Kim Donadio
Good morning. I see you mention only part of your protocol so I am not sure if 
you are going directly to the stain? This procedure seems close to what you are 
working with, it has a few tips. Hope this helps. 
 
Procedure:
1. Mount frozen or vibratomesections on 
gelatin coated or positive charged plus slides. Air 
dry sections or bake slides on slide warmer overnight.  
2. Place slides directly into 1:1   
alcohol/chloroform overnight and then rehydrate through 100% and 95 
% alcohol to distilled water. DON’T put frozen sections directly to 
water otherwise they will come off the slides.This is called 
de-fat step that will reduce background fat
staining.
3. Stain in 0.1% cresyl violet solution for 5-10
minutes. Notes:Staining in warmed cresyl violet solution (warm up in 
37-50 ºC oven) can improve penetration and 
enhancing even staining. It is  particularly 
beneficial for thicker (30 um) sections.
4. Rinse quickly in distilled water.
5. Differentiate in 95% ethyl alcohol   for 
2-30 minutes and check microscopically for best result. 
6. Dehydrate in 100% alcohol 2x5 min.
7. Clear in  xylene 2x5 min.
8. Mount with permanent mountingmedium.
 
http://www.ihcworld.com/_protocols/special_stains/nissl-frozen-section.htm
 
Kim Donadio



From: John Kiernan jkier...@uwo.ca
To: Douglas M Burns dmbur...@gmail.com; histonet@lists.utsouthwestern.edu
Sent: Wednesday, November 2, 2011 11:19 PM
Subject: Re: [Histonet] problem with brain sections falling off subbed slides

Gelatin alone is not an adhesive because it dissolves in water. Chrome 
alum-gelatin is an excellent adhesive for sections and costs almost nothing to 
make. Subbed slides are one coated with chrome gelatin, dried and stored. The 
following web link shows a 1999 publication giving the rationale and methods 
for a variety of section adhesives.
     http://publish.uwo.ca/~jkiernan/adhesivs.htm

John Kiernan 
Anatomy,UWO 
London, Canada
= = = 
On 02/11/11, Douglas M Burns dmbur...@gmail.com wrote:

 
 Hello,
 
       I am new to working with brain, and I am having a bad problem with
 both thin and thick rat brain sections sliding off of subbed slides.
 
       We tried commercial treated slides first, but then  moved on to
 subbing them. The subbing was done with gelatin according to a printed
 protocol, and I can see the film on the dried slide. When kept horizontal
 they seem okay, but as soon as they are put into a slide holder for washing
 or anything, they begin to slide off or even move around. After a short
 while, many/most of mysteriously vanished (into the wash solution).
 
       Our slices are sliced by cryostat from a rat brain that has been
 fixed with 4% paraformaldehyde and 30% sucrose. The slice comes right off
 the cryostat, and then I m ove it onto a warm slide. (Perhaps they are not
 warm enough?? I have seen others blow on them to warm them.) Slides
 destined for Cresyl violet staining were dried for 3 days at room
 temperature before being moved.
 
        It is the Cresyl violet protocol that causes the most trouble, but I
 am seeing some problems with any type of large volume wash. At this point,
 I don't have enough experience with this specific tissue and our protocols
 to be able to tell for sure what is happening. Thus, I am entirely open to
 advice - any advice that might help with the problem.
 
                      Thank  you    -    Doug Burns, Kansas City
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[Histonet] problem with brain sections falling off subbed slides

2011-11-03 Thread King,Michael A
Apart from Dr. Kiernan's recommendation, you can try putting your 
mounted slides in fixative for a few minutes, we've found this to work 
with gelatin-only coated slides, or chrome-alum gelatin subbed slides 
with thick brain sections.  If you're trying to rescue material already 
on slides, dip briefly in warm 1% gelatin, air dry, fix for a few 
minutes in 10% NBF, and proceed to counterstaining.


---
Message: 14
Date: Wed, 2 Nov 2011 17:06:48 -0500
From: Douglas M Burns dmbur...@gmail.com
Subject: [Histonet] problem with brain sections falling off subbed
slides
Hello,
  I am new to working with brain, and I am having a bad problem 
with

both thin and thick rat brain sections sliding off of subbed slides...


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[Histonet] Specimen Tracking for courier

2011-11-03 Thread Bull, Jennifer L.


I'm curious what methods other labs are using to track specimens that couriers 
pick up from clinic locations to ensure safe delivery to the lab. We currently 
utilize a logbook at the clinic site that the courier signs when they take the 
specimen but I have heard there are barcoded systems available out there as 
well. What works? What doesn't?  Appreciate your feedback!

Jenny


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RE: [Histonet] Specimen Tracking for courier

2011-11-03 Thread Cynthia Pyse
I would be interested in everyone responses.

Cindy

Cindy Pyse, CLT, HT (ASCP)
Laboratory Manger
X-Cell Laboratories
e-mail cp...@x-celllab.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bull,
Jennifer L.
Sent: Thursday, November 03, 2011 10:43 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Specimen Tracking for courier



I'm curious what methods other labs are using to track specimens that
couriers pick up from clinic locations to ensure safe delivery to the lab.
We currently utilize a logbook at the clinic site that the courier signs
when they take the specimen but I have heard there are barcoded systems
available out there as well. What works? What doesn't?  Appreciate your
feedback!

Jenny


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all 
 copies of the original message.
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RE: [Histonet] Specimen Tracking for courier

2011-11-03 Thread Houston, Ronald
Our lab as a whole uses the Gajema Specimen Transport And Tracking System for 
all courier deliveries


Ronnie Houston, MS HT(ASCP)QIHC
Anatomic Pathology Manager
Nationwide Children's Hospital
Columbus OH 43205
(614) 722 5450

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cynthia Pyse
Sent: Thursday, November 03, 2011 11:13 AM
To: 'Bull, Jennifer L.'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Specimen Tracking for courier

I would be interested in everyone responses.

Cindy

Cindy Pyse, CLT, HT (ASCP)
Laboratory Manger
X-Cell Laboratories
e-mail cp...@x-celllab.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bull, Jennifer 
L.
Sent: Thursday, November 03, 2011 10:43 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Specimen Tracking for courier



I'm curious what methods other labs are using to track specimens that couriers 
pick up from clinic locations to ensure safe delivery to the lab.
We currently utilize a logbook at the clinic site that the courier signs when 
they take the specimen but I have heard there are barcoded systems available 
out there as well. What works? What doesn't?  Appreciate your feedback!

Jenny


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RE: [Histonet] Specimen Tracking for courier

2011-11-03 Thread Dustin Paul Campbell
Jenny,

I know Triangle Urology Associates in NC is using TBS' SHUR/Mark-TVT
tracking and verification system and love it! If you would like
additional info I will be happy to get it for you?

Dustin Campbell   


-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cynthia
Pyse
Sent: Thursday, November 03, 2011 11:13 AM
To: 'Bull, Jennifer L.'; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Specimen Tracking for courier

I would be interested in everyone responses.

Cindy

Cindy Pyse, CLT, HT (ASCP)
Laboratory Manger
X-Cell Laboratories
e-mail cp...@x-celllab.com



-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bull,
Jennifer L.
Sent: Thursday, November 03, 2011 10:43 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Specimen Tracking for courier



I'm curious what methods other labs are using to track specimens that
couriers pick up from clinic locations to ensure safe delivery to the
lab.
We currently utilize a logbook at the clinic site that the courier signs
when they take the specimen but I have heard there are barcoded systems
available out there as well. What works? What doesn't?  Appreciate your
feedback!

Jenny


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[Histonet] Staffing to work ratios

2011-11-03 Thread Stacy McLaughlin
Hi,

I know this subject has been discussed before, but I'm having trouble
finding the info I need from the archives.  

Would anyone know where I can find the work to staffing ratios for a
Histology laboratory?

Our volume was ~9750 surgical cases (2010).  The majority of them are
biopsies (GI, GYN, skin, etc) but we do some larger complex cases.

We had 2569 billable IHC tests, 254 billable group I special stains, 722
billable group II special stains.

#blocks:

23,380

 

# HE slides : 49,524

 

Thank you for your help!

 

Stacy McLaughlin, HT(ASCP)

Histology Supervisor

Cooley Dickinson Hospital

30 Locust Street

Northampton, MA 01060

(413)582-2019

stacy_mclaugh...@cooley-dickinson.org

 

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[Histonet] Names of Hospitals with Histology in Alabama

2011-11-03 Thread Donna Hunter




Fishing for some Names in Alabama that have Histology Labs?



Thanks

Donna Hunter HTII








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[Histonet] Training and Competency Assessment for HE Slide Review

2011-11-03 Thread Harris, Diana
Any suggestions for creating a Training and Competency (TC) Assessment for HE 
slide review?  We currently QC all HE slides macroscopically and 15% 
microscopically.  I would like to have all Histotechs trained and competent to 
QC HE slides.  Has anyone gone thru this process?

Thanks
Diana Harris
QC  Method Development Technologist
Royal Jubilee Hospital
Victoria, BC  Canada
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Re: [Histonet] Training and Competency Assessment for HE Slide Review

2011-11-03 Thread joelle weaver
Any certified histologist has gone through this, but the NSH has good resources 
for this.
Sent from my Verizon Wireless BlackBerry

-Original Message-
From: Harris  Diana diana.har...@viha.ca
Date: Thu, 3 Nov 2011 17:34:03 
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Training and Competency Assessment for HE Slide Review

Any suggestions for creating a Training and Competency (TC) Assessment for HE 
slide review?  We currently QC all HE slides macroscopically and 15% 
microscopically.  I would like to have all Histotechs trained and competent to 
QC HE slides.  Has anyone gone thru this process?

Thanks
Diana Harris
QC  Method Development Technologist
Royal Jubilee Hospital
Victoria, BC  Canada
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[Histonet] Brain sections...

2011-11-03 Thread Cheryl
This works if you are doing traditional specials--never worked out if it 
affected IHC.  We used it for autopsy brained -called it double cook--and you 
can't scratch the tissue off with a knife after they're handled like this. 
 
Dry your slides in low heat the way you always would.  Then cool completely.  
Heat them again til the wax melts and the slide is up to the higher temp (about 
10 minutes).  Cool and handle as usual. 
 
Something about the expanding and contracting of going in and out of the heat 
twice 'snuggles' the tissue onto the slide.  

Cheryl Kerry, HT(ASCP) 
Full Staff Inc. 
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RE: [Histonet] Brain sections...

2011-11-03 Thread Weems, Joyce
And I've always found that letting them air dry overnight before drying in the 
oven works well too.  j 


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 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cheryl
Sent: Thursday, November 03, 2011 15:08
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Brain sections...

This works if you are doing traditional specials--never worked out if it 
affected IHC.  We used it for autopsy brained -called it double cook--and you 
can't scratch the tissue off with a knife after they're handled like this. 
 
Dry your slides in low heat the way you always would.  Then cool completely.  
Heat them again til the wax melts and the slide is up to the higher temp (about 
10 minutes).  Cool and handle as usual. 
 
Something about the expanding and contracting of going in and out of the heat 
twice 'snuggles' the tissue onto the slide.  

Cheryl Kerry, HT(ASCP)
Full Staff Inc.
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