Good Morning and Happy Friday Histoland!
Just curious if anyone out there is using the Athena Healthcare Computer system
for your AP lab. If so, do have any special Macros you have created, or do you
use a separate LIS system? I would greatly appreciate any feedback you can
provide.
Akemi
Have an opening for a part-time/ full-time histotechnologist in private
pathology laboratory. Primarily 85% dermpath specimens, 15% AP specimens.
Hours : 3am-11:30am. location: Nashville, Tn
Contact email for more information if interested.
madeathri...@pastnashville.com
Good Morning and Happy Friday Histoland!
Just curious if anyone out there is using the Athena Healthcare Computer system
for your AP lab. If so, do you have any special Macros you have created, or do
you use a separate LIS system? From my research, it appears to be a billing a
patient
Good Grips make a jar opener that will handle up to a 480.
Robert Jacox
Manager, Global Tactical Marketing
Anatomic Pathology
Thermo Fisher Scientific
Tel: 269-544-5651 l Mobile: 269-598-0747
robert.ja...@thermofisher.com l www.thermoscientific.com
-Original Message-
From: Stacy
Hi Histo-land,
I have a really quick question: about how long does it take to decal a bone
marrow biopsy?
Thanks a bunch!
Adrienne
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Hello,
We have a pathologist with a repetitive motion injury from opening the screw
top specimen containers.
Does anyone know of devices that would help with this?
Happy Friday!
Stacy
Stacy McLaughlin, HT(ASCP)
Histology Supervisor
Cooley Dickinson Hospital
30 Locust Street
Northampton,MA 01060
Hi Adrienne,
It all depends on what you use for decal. We use 5% Nitric acid for 1 hour or
so. Sometimes it needs a bit more time.
Have a good weekend!
Jessica
-Original Message-
From: Adrienne Anderson [mailto:rennie1...@yahoo.com]
Sent: Friday, June 05, 2015 1:25 PM
To:
Per CLIA we only need to keep paraffin blocks two years. What is the proper way
to dispose of them?
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Robin Simpkins
On Jun 5, 2015, at 10:19 AM, histonet-requ...@lists.utsouthwestern.edu
histonet-requ...@lists.utsouthwestern.edu wrote:
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Dear Peter,
Some of the information you mention as anecdotal is wrong. Formaldehyde and
paraformaldehyde are well documented in original peer-reviewed papers and in
all textbooks in the fields of histotechnology and histochemistry.
Your anecdote about high concentrations of formaldehyde
Formaldehyde 37% (commonly called 100% formalin) compared to 4% ( commonly
known as 10% neutral buffered formalin)-in theory the 37% should fix quicker
and better BUT anecdotally it is said that high concentrations of
formaldehyde quickly form a shell in the tissue and will stop good
penetration
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