RE: [Histonet] fume hood

2010-06-17 Thread Feher, Stephen
Hi Brandy,

I have recently had the opportunity to build a Path lab from scratch.
In the design we decided to completely separate the grossing area from
the microtomy and IHC area of the lab.  We built a room within a room,
made it negative pressure, installed 2 Thermo elevating grossing
stations that are vented to the outside.  Since we are using the
hospital ventilation system in addition to the blowers built in to the
back draft, downdraft capabilities of the grossing stations, we were
able to set these to pull at 500 cfm each.  We also put 2 Peloris
processors, with their own charcoal filters, within this room.  The
result is that we are well under the limits for all fumes and, in the
event we get fresh tissue, we can segregate the area from the rest of
the lab.  Many labs that have to do autopsy on babies or near full term
fetus' use their grossing stations to do so.  Since we are in a separate
area, we can block these procedures from view.

We also put in a Labconco Fume hood (vented to the outside) in the IHC
area of the lab and a Thermo Bio Hood in the cytoprep area.  This has
all worked out very well for us and it affords us the opportunities to
have these items in place for future growth.  A renovation done
correctly, with an eye towards strategic planning for the future, will
go a long way towards saving the hospital money in the long run. 


Steve Feher
Pathology Supervisor
Catholic Medical Center
Manchester, NH

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Brandi
Higgins
Sent: Tuesday, June 15, 2010 9:51 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] fume hood

Hello,

Our hospital is doing some renovation and we need to look into new fume
hoods for our new location.  Currently we have one fume hood over our
grossing area, and one fume hood in our coverslipping area (two
different rooms).  The hospital wants to put our grossing room and
histo/cyto rooms together.  I am still going to need two separate hoods.
Does anyone have any experience/knowledge/input about fume hoods?  I'm
trying to look into the ductless ones, although I imagine changing the
filters will end up being more expensive over time (I have no idea what
would be involved in running a duct/vent).  Also I have seen a benchtop
downdraft type that sucks the air down, and does not have a top.  It is
advertised as being good for xylene.
Does anyone use this in their coverslipping area?  Any input would be
greatly appreciated.  I'm pretty clueless on the whole issue.  I want to
make sure that what I get will be safe for me and my coworker as we will
be spending most of our day in this room.  Any input is appreciated!
Thank You!

Brandi Higgins, BS, HT(ASCP)
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[Histonet] Thermo Slide Mate Print Mate

2010-06-17 Thread Mike Pence
Is anyone using the Thermo Slide Mate  Print Mate with CoPath as your
AP LIS?  I am trying to decide if I am going to look at this as a stand
alone process or integrate it with my AP LIS.  I would like to hear from
those that use it both ways and if it is okay to contact you off line.
 
Thanks,
 
Mike
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RE: [Histonet] Thermo Slide Mate Print Mate

2010-06-17 Thread Laurie Colbert
Mike,

We have the Print Mate and 5 Slide Mates.  We are not connected to our
LIS - we use it as a stand alone process.  Everything is set up very
basic and the system works very well for us.  Feel free to contact me
offline.

Laurie Colbert
Huntington Hospital
Pasadena, CA
(626) 397-8620

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mike
Pence
Sent: Thursday, June 17, 2010 6:33 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Thermo Slide Mate  Print Mate

Is anyone using the Thermo Slide Mate  Print Mate with CoPath as your
AP LIS?  I am trying to decide if I am going to look at this as a stand
alone process or integrate it with my AP LIS.  I would like to hear from
those that use it both ways and if it is okay to contact you off line.
 
Thanks,
 
Mike
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[Histonet] how to prevent foldings on femoral head cartilage tissue

2010-06-17 Thread Reuel Cornelia
Hello histonetters especailly hard tissue group
I have a  pig femoral head bone tissue embedded in paraffin and I have a hard 
time getting rid of the folding problem. I tried to remedy by lowering my 
temperature to 38 C and putting them in 5% alcohol before placing them in water 
bath I still have a lots of folding formation on some areas of the cartilage. 
Is there any other technique to remedy this problem. I appreciate your help. 
Thank you.

reuel



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RE: [Histonet] how to prevent foldings on femoral head cartilage tissue

2010-06-17 Thread Liz Chlipala
Sometimes placing them on a hot plate at about 60C will help get out the
folds, the paraffin needs to melt and the sections need to turn clear
then take it off the hot plate.  If you leave it too long on the
hotplate the articular cartilage may fold over on itself.

Liz

Elizabeth A. Chlipala, BS, HTL(ASCP)QIHC
Manager
Premier Laboratory, LLC
PO Box 18592
Boulder, Colorado 80308
office (303) 682-3949 
fax (303) 682-9060
www.premierlab.com
 
 
Ship to Address:
1567 Skyway Drive, Unit E
Longmont, Colorado 80504

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Reuel
Cornelia
Sent: Thursday, June 17, 2010 11:10 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] how to prevent foldings on femoral head cartilage
tissue

Hello histonetters especailly hard tissue group
I have a  pig femoral head bone tissue embedded in paraffin and I have a
hard time getting rid of the folding problem. I tried to remedy by
lowering my temperature to 38 C and putting them in 5% alcohol before
placing them in water bath I still have a lots of folding formation on
some areas of the cartilage. Is there any other technique to remedy this
problem. I appreciate your help. Thank you.

reuel



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Re: [Histonet] Breast Specimen handling

2010-06-17 Thread BSullivan
Sara,
 Funny that this comes up now. I attended a meeting last week and this was
one of the topics. It was suggested that the tissue be stored in 70%
alcohol. I personally have not done this but I am going to start doing
this.

Beatrice Sullivan, HT(A.S.C.P.) HTL , AAS, CLSP(N.C.A.)
AP Supervisor
Shore Memorial Hospital
609-653-3590


   
 Sara 
 Baldwin/mhhcc.org 
   To 
 sbald...@mhhcc.o Histo Net   
 rg   histonet@lists.utsouthwestern.edu 
 Sent by:   cc 
 histonet-bounces@ 
 lists.utsouthwest Subject 
 ern.edu   [Histonet] Breast Specimen handling 
   
   
 06/17/2010 01:24  
 PM
   
   





   Hi histonetters

   Was  wondering  if  anyone  saw the new gui= delines for breast Cancer
   specimen  handling  ?  I am sure you have.nbs= p; What my Pathologist
   is  wondering is if you have a large specimen and do = not use all the
   tissue  for  processing  what  would  the agent  be  to  apply= to the
   specimen  to  stop penetration of the formlalin before the 72 hour ti
me arrives?  Would it be sodium chloride?  Can someone help?
   = /DIV
   Thanks
   Pathology Supervisor
   Kathy Baldwin, S= CT (ASCP)
   Memorial Hospital and Health Carenbs= p;Center
   [1]sbald...@m= hhcc.org
   Ph 812-482-0210, 482-0216,  Fax 81= 2-482-0232,
   Pager 812-481-0897
   Confidential information, Authorized use only.

References

   1. 3Dmailto:sbald...@mhhcc.org;
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RE: [Histonet] how to prevent foldings on femoral head cartilage tissue

2010-06-17 Thread Jack Ratliff

Reuel,

 

Do the opposite and turn up the temp on the waterbath and let the section float 
out a little before the wax starts to break up. You can even gently use the 
forcepts to tease out any folds and this will definitely help to release any 
wrinkles in the cartilage. Then, make sure the section is free of large 
droplets of water before transfer of the slide to the slide warmer. Next, let 
slide sit on slide warmer until the wax is melted and then bake the section for 
a few minutes at a higher temperature to firmly secure the section to the glass 
slide. Bob Skinner at UAMS showed me this technique at the beginning of the 
year and it works nicely, especially for even larger human femoral heads!

 

Jack


 
 Date: Thu, 17 Jun 2010 12:10:10 -0500
 From: reuel.corne...@tsrh.org
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] how to prevent foldings on femoral head cartilage tissue
 
 Hello histonetters especailly hard tissue group
 I have a pig femoral head bone tissue embedded in paraffin and I have a hard 
 time getting rid of the folding problem. I tried to remedy by lowering my 
 temperature to 38 C and putting them in 5% alcohol before placing them in 
 water bath I still have a lots of folding formation on some areas of the 
 cartilage. Is there any other technique to remedy this problem. I appreciate 
 your help. Thank you.
 
 reuel
 
 
 
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RE: [Histonet] intervertebral disc

2010-06-17 Thread Jack Ratliff

Jennifer,

 

What do you wish to accomplish histologically? Do you only wish to see the disc 
material? Do you care about the cranial and caudal vertebral bodies? Are you 
wanting to perform IHC? Please tell me a little more so that I can provide you 
with a more detailed options. I am assuming that this is an IVD project and 
maybe you only wish to see the treatment of the nucleus pulposus?

 

Jack


 
 From: jander...@halozyme.com
 To: histonet@lists.utsouthwestern.edu
 Date: Wed, 16 Jun 2010 13:30:51 -0700
 Subject: [Histonet] intervertebral disc
 
 Greetings.
 What is the best way to process intervertebral disc tissue from pig? Right 
 now I have 4 intact vertebrae with attached discs in formalin. Should I just 
 use a sharp knife?
 Thanks so much for your expertise.
 
 Jennifer M. Anderson, Scientist
 Halozyme Therapeutics, Inc.
 11388 Sorrento Valley Road
 San Diego, CA 92121
 858-704-8333 (office)
 jander...@halozyme.commailto:jander...@halozyme.com
 
 
 
 
 The information transmitted in this email is confidential and is intended 
 only for the person(s) or entity to which it is addressed. Delivery of this 
 message to any person other than the intended recipient(s) is not intended in 
 any way to waive confidentiality or any applicable privilege. Any review, 
 retransmission, dissemination or other use of, or taking of any action in 
 reliance upon, this information by individuals or entities other than the 
 intended recipient is prohibited by Halozyme and may be in violation of 
 applicable laws. If you received this in error, please contact the sender and 
 delete/destroy this email.
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[Histonet] release of tissues

2010-06-17 Thread Mary_Joy

   Hi all,


   How  would  you  handle  a  request  from  a surgeon, f= or release of
   gallstones  or  any  tissue,  to  a  patient? Assuming a 'Rele= ase of
   Tissue'  request form, indicating the biohazard staus of the tissue,is 
signed by the patient, is this commom practice?


   Thanks for your responses,

   Mary Sue
   CONFID=  ENTIALITY  NOTICE:  This  e-mail and attachments, if any, may
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   the  designated  ad=  dressee  only.  If  you  are  not the designated
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   distribution  of  this  e-ma=  il  and its attachments, if any, may be
   unlawful  and  may  subject  you=  to  legal consequences. If you have
   received  this  e-mail  and its attachmen= ts in error, please contact
   the  St.  Mary's  Hospital Helpdesk at (301) 4= 75-6166 and delete the
   e-mail  and  its  attachments from your computer. Than= k you for your
   attention.
   Please  consider  the  environment: = do you really need to print this
   email?
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[Histonet] Immuno

2010-06-17 Thread Carol Fields
Hi All,

Does anyone out there know a lab that is able to do a Human Herpes
Virus, Type 6 immuno?
Thanks for any help on this.  We haven't been able to find a reference
lab that does this.
Carole

Carole Fields, HT (ASCP)
Histology Supervisor
Northside Hospital
Atlanta, GA 30342
carol.fie...@northside.com



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of it, or any attachments. If you have received this message in error, please 
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There is no intent on the part of the sender to waive any privilege.

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Re: [Histonet] release of tissues

2010-06-17 Thread Karen Sly
Mary Sue,

Our hospital regular releases gallstones to patients and/or their doctors.  We 
make a record of it in our computer system as to where and to who the 
gallstones were sent/released to.

Karen Sly BS Biology
Pathology Department
Central Michigan Community Hospital
Mt Pleasant MI.


Please consider the environment before printing this e-mail 

 Please consider the environment before printing this e-mail

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RE: [Histonet] New CAP question ANP.22760

2010-06-17 Thread Ellen Yee
Sorry, I should have included it.  
   
ANP.22760  Are new lots of antibody and detection system reagents tested in 
parallel with old lots?  (NOTE: New lots of primary antibody and detection 
system reagents must be compared to the previous lot using an appropriate panel 
of control tissues.)  
   
Ellen Yee
  _  

  From: Laurie Colbert [mailto:laurie.colb...@huntingtonhospital.com]
To: Ellen Yee [mailto:e...@dpmginc.com]
Sent: Thu, 17 Jun 2010 08:47:38 -0700
Subject: RE: [Histonet] New CAP question ANP.22760

Can you give us the wording of that question/checklist item?
Laurie

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Ellen
Yee
Sent: Wednesday, June 16, 2010 10:10 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] New CAP question ANP.22760

How are IHC labs complying with this question? What is considered an
appropriate panel of control tissues? What do you stain to test your
detection systems? 

Ellen Yee 

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