[Histonet] CA 15-3 and CA 27.29

2017-01-27 Thread Roy, Lisa via Histonet
I was wondering if anyone out there knows of a lab that is performing CA 15-3 
and/or CA 27.29 by IHC on FFPE tissue?  Thanks in advance.

Lisa Roy, HT(ASCP)cm
Histology Supervisor
Worcester, MA

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[Histonet] Pancytokeratin (AE1/AE3) Protocol

2016-01-11 Thread Roy, Lisa via Histonet
All of a sudden our AE1 is no longer good for the pathologists.  Anyone willing 
to share their protocol for Ventana Benchmark XT or Ultra?  I have "tweaked" 
this protocol so many times.  It amazes me how often stains are great during 
optimization and validation, then months later, everyone hates it!!!  UGH.

Thanks

Lisa Roy, HT(ASCP)cm
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Re: [Histonet] OJT Histotechs/Training

2015-05-14 Thread Roy, Lisa
I currently have 3 open tech positions and don't have any qualified applicants 
applying for the job.  I have recently taken a lab aide that showed interest 
and aptitude and began OJT.  With less than 30 schools in the country actually 
teaching histology, this is one day going to be the way.  Already having a 
bachelors in biology, my aide qualifies to sit for the ASCP exam once he has 
completed one full year of tech work and has a pathologist willing to review 
his work and sign off on the ASCP paperwork.  Without going through a 
traditional program, one must have an associates or bachelor's degree with a  
certain amount of Chemistry and Science credits.  As far as the training, I 
started with embedding and moved on from there to cutting and then special 
staining.  All along way, working on troubleshooting and documenting 
EVERYTHING.  Some places will hire someone with only a high school diploma as 
long as they have previous HT experience.  I think the specifics of what each 
institutio
 n would deem a qualified trainee will vary from place to place.  Smaller 
hospitals or labs may be okay training someone with aptitude that doesn't 
necessarily fit the ASCP exam qualifications, but large corporations might 
really insist that the trainee be certifiable at some point.

Frankly, I think taking someone that shows an interest and has the knowledge to 
be a great tech is better than hiring someone that you may not know what you 
are getting.  Doing OJT ensures that you are teaching the candidate exactly how 
you want things done and not having to accept the bad habits of someone that 
has been doing it a long time and set in their own ways.

Good luck
Lisa

-Original Message-
From: Dessoye, Michael [mailto:mjdess...@commonwealthhealth.net] 
Sent: Thursday, May 14, 2015 7:44 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] OJT Histotechs/Training

Hello Histonet,

I'm curious how people are dealing with on-the-job-trained histotechs.  Many 
people are seeing a shortage in techs, and in my opinion OJT will become more 
common than it already is.  Does anyone have an 'official' training program?  
Requirements to pass the exam?  Qualifications to be able to be trained 
on-the-job?  I'd like to consider having some kind of plan in place when I 
don't have an HT/HTL applicant but have folks who, if they get the experience, 
are otherwise qualified to sit for the exam.  If anyone has a similar situation 
or experience to share I would appreciate it!

Thanks,
Mike

Michael J. Dessoye, M.S. | Histology/Toxicology/RIA Supervisor | Wilkes-Barre 
General Hospital | An Affiliate of Commonwealth Health | 
mjdess...@commonwealthhealth.netmailto:mjdess...@commonwealthhealth.net | 575 
N. River Street | Wilkes Barre, PA 18764 | Tel: 570-552-1432 | Fax: 570-552-1486



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Re: [Histonet] HE Stainer Question

2015-05-12 Thread Roy, Lisa
Paula
Here are my two cents

I currently use a Leica Autostainer XL with attached glass coverslipper.  It is 
consistent in its staining and easy to use.  The downfall is if you are a large 
volume lab or just have large volume days, each staining rack holds 30 slides 
and only one rack can be stained in each batch. The stainer also only has one 
on board oven, so the throughput of this machine is fairly low.  It is only 
staining 30 slides at a time, with one holding station for the next set.  It 
will run multiple batches concurrently, but gets to a point where it is all 
backed up.  We sometimes have 2 racks staining, one in the oven, one in the 
loading dock, and some sitting on top of the stainer until it can go on. 

On the flip side, the Sakura Prisma is a workhorse.  It is very similar to the 
Leica in the sense that it is linear and very consistent in staining.  It has 
two on board ovens and each basket can hold 20 slides.  The difference is that 
the Sakura can stain 3 racks (60 slides) per batch, with two batches in the 
oven at the same time.  That gives you 120 slide throughput for each batch.  
This stainer also has an attached coverslipper (Sakura Film), but it is film 
coverslips.  I know, I know.no one likes the film coverslips.  One 
advantage to the film, is that the slides are dry almost immediately and can be 
filed away the same day.  No waiting for 3-4 days for the glass ones to fully 
cure.  I can say that the last lab I worked in had the film coverslips and 
after 10 years, the slides were still in pristine condition.  There are many 
pathologists that do not like to read film covered slides, but once ours got 
used to it, they had no problems.  Some say the film yellows or comes off 
 with the tissue still attached.  I can say that I never seen this in my past 
position.  It is very dependent on Xylene only during coverslipping.  You 
cannot use a xylene substitute in the coverslip portion and expect to get good 
results.

Hope it helpsgood luck.
Lisa

-Original Message-
From: Paula Sicurello [mailto:pat...@gmail.com] 
Sent: Monday, May 11, 2015 5:04 PM
To: HistoNet
Subject: [Histonet] HE Stainer Question

Me again...

UCSD is in the market for a new HE stainer for our new hospital opening next 
year.

We need a workhorse, not a prima dona, something with a coverslipper built in 
would be nice.

What do you use?

Suggestions gratefully accepted-even from you two Keith and Matt  ;)

Opinions about the good, the bad, and the ugly (as long as it works really
well) will be helpful.

Thanks oodles!

Paula  :-)
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Re: [Histonet] HE Stainer Question

2015-05-12 Thread Roy, Lisa
Depends on which model you have...hence XL.  Ours only has one oven so you're 
really only getting 3-4 racks stained at a time.

-Original Message-
From: Simmons, Christopher [mailto:sim...@upmc.edu] 
Sent: Tuesday, May 12, 2015 8:33 AM
To: Roy, Lisa; Paula Sicurello; HistoNet
Subject: RE: [Histonet] HE Stainer Question

To be fair, a batch of slides for Leica is actually 270- slides, It can run 9 
racks at a time, but, the 9th rack from start to coverslip is 3 hours+ You can 
always skip the on-board oven and place your slides in a slide dryer (most labs 
have them) and then every 3 minutes you can load a rack (1st xylene step 3 
minutes) Then it goes much faster.
As for tape..ugh..it is only guaranteed to last 7 years, after that they pull 
off the slide and take the tissue with it.
CAP is starting to frown on this as you need to keep the initial HE slides for 
up to 10+ years.

Chris Simmons B.S., A.S., HTL(ASCP)
Supervisor, UPP Dermatopathology
412.864.3880 office
412.612.0881 cell


-Original Message-
From: Roy, Lisa [mailto:ro...@labcorp.com]
Sent: Tuesday, May 12, 2015 8:19 AM
To: Paula Sicurello; HistoNet
Subject: Re: [Histonet] HE Stainer Question

Paula
Here are my two cents

I currently use a Leica Autostainer XL with attached glass coverslipper.  It is 
consistent in its staining and easy to use.  The downfall is if you are a large 
volume lab or just have large volume days, each staining rack holds 30 slides 
and only one rack can be stained in each batch. The stainer also only has one 
on board oven, so the throughput of this machine is fairly low.  It is only 
staining 30 slides at a time, with one holding station for the next set.  It 
will run multiple batches concurrently, but gets to a point where it is all 
backed up.  We sometimes have 2 racks staining, one in the oven, one in the 
loading dock, and some sitting on top of the stainer until it can go on. 

On the flip side, the Sakura Prisma is a workhorse.  It is very similar to the 
Leica in the sense that it is linear and very consistent in staining.  It has 
two on board ovens and each basket can hold 20 slides.  The difference is that 
the Sakura can stain 3 racks (60 slides) per batch, with two batches in the 
oven at the same time.  That gives you 120 slide throughput for each batch.  
This stainer also has an attached coverslipper (Sakura Film), but it is film 
coverslips.  I know, I know.no one likes the film coverslips.  One 
advantage to the film, is that the slides are dry almost immediately and can be 
filed away the same day.  No waiting for 3-4 days for the glass ones to fully 
cure.  I can say that the last lab I worked in had the film coverslips and 
after 10 years, the slides were still in pristine condition.  There are many 
pathologists that do not like to read film covered slides, but once ours got 
used to it, they had no problems.  Some say the film yellows or comes off 
 with the tissue still attached.  I can say that I never seen this in my past 
position.  It is very dependent on Xylene only during coverslipping.  You 
cannot use a xylene substitute in the coverslip portion and expect to get good 
results.

Hope it helpsgood luck.
Lisa

-Original Message-
From: Paula Sicurello [mailto:pat...@gmail.com]
Sent: Monday, May 11, 2015 5:04 PM
To: HistoNet
Subject: [Histonet] HE Stainer Question

Me again...

UCSD is in the market for a new HE stainer for our new hospital opening next 
year.

We need a workhorse, not a prima dona, something with a coverslipper built in 
would be nice.

What do you use?

Suggestions gratefully accepted-even from you two Keith and Matt  ;)

Opinions about the good, the bad, and the ugly (as long as it works really
well) will be helpful.

Thanks oodles!

Paula  :-)
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RE: [Histonet] (no subject)

2015-04-30 Thread Roy, Lisa
How long do you bake slides for before staining, at what temperature?  Does 
your stainer use agitation?

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Carolyn Nelson
Sent: Thursday, April 30, 2015 11:41 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] (no subject)

Hi, I was hoping someone can help me with tissue falling off the slides. I have 
tried regular slides with and without adhesive in the water bath. Charged 
slides with and without adhesive in the water bath. I have not changed the type 
of slides I’m using. All the chemicals are fresh in the processor and the stain 
line, as well as the paraffin in the processor. It is the worst on needle bx ( 
prostate and breast ). I am SO frustrated, any help would be greatly 
appreciated! 


Carolyn






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RE: [Histonet] Over- decalcified tissue

2015-04-29 Thread Roy, Lisa
Good article on IHC world about restoring nuclear detail to over decalcified 
tissueit is called Problem Number 23.  Good luck.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of WILLIAM DESALVO
Sent: Wednesday, April 29, 2015 12:21 PM
To: pablo.sanc...@usc.es
Cc: Histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] Over- decalcified tissue

I would suggest not allowing decalcification to be extended. Better to leave in 
fixative until you can control the time of endpoint of decalcification. What 
type of decal solution are you using? I am not a big fan of trying to adjust 
the chemistry of the stain to compensate for over decalcification. Is there 
opportunity to submit another sample?

Sent from my iPhone

 On Apr 29, 2015, at 9:08 AM, pablo.sanc...@usc.es wrote:
 
 As I usually process gross pieces of bone -that need abouth thirty hours 
 decalcifying- I suffer the same nuissance. Also would thank any hint.
 
 Pablo Sanchez
 
 
 
 Laurie Colbert lcolb...@pathmdlabs.com escribiu:
 
 I have tissue that was left in decal over the weekend and now has very poor 
 nuclear staining.  Is there a fix for this so that I can get better 
 nuclear staining (other than restaining for a long time in the hematoxylin)?
 
 Laurie Colbert, HT (ASCP)
 Histology Supervisor
 PATH MD
 8158 Beverly Blvd.
 Los Angeles, CA  90048
 (323) 648-3214 direct
 (424) 245-7284 main lab
 
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[Histonet] Nuclear Artifact

2015-04-21 Thread Roy, Lisa
Hi HistoNetters:
I have run into quite a problem.  My lab currently processes all tissue types 
from 3 different sites.  Recently, we have been getting complaints from one of 
the sites that the biopsies have a nuclear artifact.  It is described as 
washed out or poor to no nuclear detail.  Pictures have been uploaded 
(Nuclear Artifact).  The Medical Director at said site is convinced that a 
processor error is occurring.  Our site is not seeing this on any of our 
slides.  Biopsies from all three sites are processed and embed together.  We 
have done all trouble shooting that we can think of.  Leica service has come to 
inspect our Peloris processor and all areas checked out as functioning 
properly.  The problem is not consistent daily.  Seems to be worst toward the 
end of the week.
We have been running the same processing protocol, staining protocol and 
cutting protocols for years now.  This problem has just developed over the last 
2 months.  Any ideas, no matter how far-fetched, would be greatly appreciated 
at this point.

Lisa Roy, HT(ASCP)
Histology Supervisor
LabCorp at St. Vincent Hospital
123 Summer St
Worcester, MA
(508)363-9420

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