[Histonet] Contamination..processor?

[Truscott, Tom]

If not already mentioned, wiping your heated forcep off with a kimwipe or paper towel before and after embedding each tissue helps prevent this problem at embedding.

-----Original Message-----
From: histonet-bounces <@t> lists.utsouthwestern.edu [mailto:histonet-bounces <@t> lists.utsouthwestern.edu] On Behalf Of Kim.Donadio <@t> bhcpns.org
Sent: Wednesday, March 24, 2010 10:01 AM
To: tigger13b <@t> aol.com
Cc: histonet <@t> lists.utsouthwestern.edu; histonet-bounces <@t> lists.utsouthwestern.edu
Subject: Re: [Histonet] Contamination..processor?

You are definite that the cells are in the block? If so I would change all 
the paraffins out as well, even the paraffin on your embedding center. 




Kim Donadio 
Pathology Supervisor
Baptist Hospital
1000 W Moreno St.
Pensacola FL 32501
Phone (850) 469-7718
Fax (850) 434-4996



tigger13b <@t> aol.com 
Sent by: histonet-bounces <@t> lists.utsouthwestern.edu
03/24/2010 11:40 AM

To
histonet <@t> lists.utsouthwestern.edu
cc

Subject
[Histonet] Contamination..processor?








Hello everyone.

     Today we have a problem with contamination.  The pathologist notes 
cells from tonsil specimens here and there on our GI biopsy slides.  The 
cells are in the block.  I'm trying to ascertain the source of the 
contamination. 
     The grossing pathologist grossed the tonsils AFTER all GI specimens 
yesterday (not source of contaminant).  We (the techs) embedded all GI 
specimens first, trimmed, cut, floated and stained ALL GI specimens BEFORE 
the tonsils (not source of contaminant).  The only other source of the 
contamination I can think of is from the tissue processor.  We have a 
Tissue Tek VIP closed processor.  Has anyone ever experienced any problems 
like this?  We had a similar issue a few weeks ago.  I thought the 
contaminant cells may be from a bladder tumor, which had multiple sections 
submitted.  In this instance the cells showed up days work of the bladder 
tumor, and in the following days work also (though the pathologists could 
not say for sure the cells were from the bladder case).  We changed our 
formalin solutions in the processor and the problem did not present the 
next day.  We also started putting all bladder tumor specimens in the 
microcassettes, to prevent tissue from escaping.  Has anyone had any 
problem like this, or does anyone have any ideas on how to prevent this in 
the future?  We had not seen this problem until these past two incidences, 
and this tonsil problem is particularly strange to me because we process 
tonsils and GI specimens in the same workload on a regular basis and have 
never had this issue before.  Any help is appreciated! 

Thanks!
Brandi


_______________________________________________
Histonet mailing list
Histonet <@t> lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet



-----------------------------------------
All electronic data transmissions originating from or sent to
Baptist Health Care Corporation (BHC) are subject to monitoring.
This message along with any attached data, are the confidential and
proprietary communications of BHC and are intended to be received
only by the individual or individuals to whom the message has been
addressed. If the reader of this message is not the intended
recipient, please take notice that any use, copying, printing,
forwarding or distribution of this message, in any form, is
strictly prohibited and may violate State or Federal Law. If you
have received this transmission in error, please delete or destroy
all copies of this message.  For questions, contact the BHC Privacy
Officer at (850) 434-4472.  Rev.10/07.
_______________________________________________
Histonet mailing list
Histonet <@t> lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet