I agree.  That's the easiest solution.

My colleague at a sister institution does not allow breast excisions on Friday.

We need more people to do studies on fixation beyond 72 hours. My hunch is that 
another 24 hours won't affect ER , Pgr, and Her2 results.

Garrey

Sent from my iPhone

> On Jul 29, 2015, at 5:01 PM, Joanne Clark via Histonet 
> <histonet@lists.utsouthwestern.edu> wrote:
> 
> 
> I would do a delayed start on your tissue processor Friday night to include 
> the extra two hours you need of fixation time and just have the run come off 
> two hours later on Saturday morning.  Just adjust the hours of your per diem 
> Saturday tech to come in later.
> 
> Joanne Clark, HT
> Director of Histology
> Pathology Consultants of New Mexico
> 
> 
> Message: 4
> Date: Wed, 29 Jul 2015 08:01:31 -0700
> From: "Heckford, Karen - SMMC-SF" <karen.heckf...@dignityhealth.org>
> To: "histonet@lists.utsouthwestern.edu"
>    <histonet@lists.utsouthwestern.edu>
> Subject: [Histonet] Breast fixation
> Message-ID:
>    <d329219d3b967447a9e3ed3242117e3206fedc7...@phx-msg-007-n1.chw.edu>
> Content-Type: text/plain; charset="us-ascii"
> 
> Good Morning,
> I have a question about breast fixation.   I am in a little bit of a pickle 
> with the 6-72 hour rule for the fixation on breast tissue.   Friday I am 
> getting 2 breast cases in the afternoon and both will not have the required 
> minimum 6 hour formalin fixation for my per diem to cut early Saturday 
> morning.   He will not be able to make it in again until Monday night.  The 
> tissue will be about 3-4 hours (this includes time on the processor)  over 
> the 72 hour maximum.    Does anyone have any suggestions on what can be done? 
>  We are a one person show here.
> 
> Thanks,
> 
> Karen Heckford HT ASCP CE
> Lead Histology Technician
> St. Mary's Medical Center
> 450 Stanyan St.
> San Francisco, Ca. 94117
> 415-668-1000 ext. 6167
> karen.heckf...@dignityhealth.org
>                                                                               
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> ------------------------------
> 
> Message: 5
> Date: Wed, 29 Jul 2015 12:10:19 -0300
> From: Emily Dewar <emilydewar32...@gmail.com>
> To: histonet@lists.utsouthwestern.edu
> Subject: [Histonet] NetWell inserts and IHC with TUNEL stain
> Message-ID:
>    <CAJ7MPPp=h9pgEkH-SxJG=KkDiDxi4=6_ttrap7rcb5nsjnm...@mail.gmail.com>
> Content-Type: text/plain; charset=UTF-8
> 
> Hello,
> 
> I will be performing a number of immunos within the next couple of months,
> and have been wondering what the best way to do so might be with no tissue
> damage during the process. Does anyone know whether using NetWell inserts
> for immunos to transfer tissue affects morphology? The tissue will be
> placed into the insert, and submersed in solution within a well plate to be
> incubated on a shaker. The problem is that contact with the NetWell insert
> could damage the tissue, not only with the rocking, but with transfer from
> one solution to another.
> 
> I am under the impression that with TUNEL staining, is often difficult to
> differentiate whether the damage in cells caused by handling/extraction, or
> from the treatment itself. While not impossible, I will not have the time
> to develop or perform such a procedure.
> 
> If anyone has any knowledge or insight, it would be greatly appreciated.
> 
> Thank you for your time,
> 
> Emily Dewar
> Laboratory Technician
> 
> 
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