Re: [Histonet] Microtome Cleaning Company and What to do with Old Metal Blades

2016-10-26 Thread Drew Meyer via Histonet
Michael Dietrich and his team at Southeast Pathology Instrument Service is
outstanding!

www.southeastpathology.com

Thanks,
Drew Meyer, HT
Anatomic Pathology Independent Contractor

On Wed, Oct 26, 2016 at 10:56 AM, Michelle Aono via Histonet <
histonet@lists.utsouthwestern.edu> wrote:

> Can anyone suggest a good company that works on old microtomes?  Ours is
> not broken, it's just in need of some TLC.  Also, what is a reasonable
> price for such work (we have a RJ 2040)?
>
> Also, we have a lot of the old metal blades that you have to sharpen.  Any
> suggestions on how to sell, donate, recycle such items?  Do people even use
> these anymore?  I would hate to have them thrown out.
>
> Thanks!
> Michelle (Shelly) Aono
> ~~~
> Research Associate II
> 107B/124 Greene Hall
> Auburn University, Dept of APP
> Auburn, AL 36849
> (334) 844-5594
>
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Re: [Histonet] 2014 IHC CPT coding

2013-12-10 Thread Drew Meyer
This is from the CAP site... and here's the link:

http://www.cap.org/apps/cap.portal?_nfpb=truecntvwrPtlt_actionOverride=/portlets/contentViewer/show_windowLabel=cntvwrPtltcntvwrPtlt%7BactionForm.contentReference%7D=statline/index.html_state=maximized_pageLabel=cntvwr

*Immunohistochemistry: 88342 (PC  TC)*
CMS rejected the CAP’s proposal and instead will require the use of two new
G codes for this service, including G0461 to report one unit of service per
specimen and G0462 to report each additional stain. The following chart
documents the percentage reduction and payment rate change for the new G
codes compared to the current reimbursement for CPT code 88342:
 *CPT Code**Modifier* *88342 2013 Total Payment**2014 Total Payment* *Total
% Change from 2013 88342* G0461 $115.34 $88.04-24% G0461TC$73.15 $57.39-22%G0461
26$42.19 $30.65-27% G0462 $115.34 $68.08-41% G0462TC$73.15 $55.61-24% G0462
26$42.19 $12.48-70%

The changes occurred under the Affordable Care Act (ACA), which provided
CMS expanded authority to launch its “misvalued code” initiative. CMS
targeted the top expenditure codes from each specialty as potentially
overvalued. This action triggered the review of the three additional high
volume code families.

Moving forward, the CAP will work with the AMA and other groups to pressure
CMS to change their G code definitions so that payment is made ‘per slide’
rather than ‘per specimen.’


On Tue, Dec 10, 2013 at 5:22 PM, Kim Donadio one_angel_sec...@yahoo.comwrote:

 I got information they got rid of 88342 all together and added G codes.
 One for the 1st slide stained and another for each additional stain. Can
 anyone verify and give a link?

 Sent from my iPhone

 On Dec 10, 2013, at 4:33 PM, Cartun, Richard 
 richard.car...@hhchealth.org wrote:

  My understanding is that 88342 is used for the first IHC antibody, then
 88343 is used for each subsequent antibody (per specimen part).  Is that
 correct?  Thank you.
 
 
 
  Richard
 
 
 
  Richard W. Cartun, MS, PhD
 
  Director, Histology  Immunopathology
 
  Director, Biospecimen Collection Programs
 
  Assistant Director, Anatomic Pathology
 
  Hartford Hospital
 
  80 Seymour Street
 
  Hartford, CT  06102
 
  (860) 545-1596 Office
 
  (860) 545-2204 Fax
 
  richard.car...@hhchealth.orgmailto:richard.car...@hhchealth.org
 
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[Histonet] CD200

2012-07-20 Thread Drew Meyer
Is anyone out there running CD-200 with good results?  If so, I would really 
appreciate it if you would email me privately so I can ask you a few questions.

Thanks,
Drew

Sent from my iPhone
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Re: [Histonet] DAKO Autostainer Issues

2012-03-12 Thread Drew Meyer
There's a circuit board on the arm near the barcode scanner that controls the 
movement and orientation of the arm. If that circuitboard malfunctions, then 
you can see some of the erratic behavior that you are describing. That's one 
possibility I can think of that might cause that kind of problem. However, the 
technician who looked at it should be able to troubleshoot and replace that 
board if it is a problem.

Drew

Sent from my iPhone

On Mar 12, 2012, at 2:31 PM, friedrich_h...@bd.com wrote:

 
   We  have been having issues with our Autostainer since bringing it out
   of  storage.  All  parts  are  in  excellent  shape,  according to the
   technician  that  performed the PM.  It worked fine for a month of so,
   but  then  began  malfunctioning after only a couple of staining runs.
   At some point in the staining process, the machine appears to lose its
   XY  homing  and jams itself against the front right corner, dispensing
   buffer  onto the floor of the chamber and occasionally making grinding
   noises.   We've  had  a  technician  take  a  look  at it, 'clean' the
   software,  and  we thought we had it resolved, but the problem appears
   to be back.
   Has  anyone  experienced  this  issue?  If  so,  was  it  hardware- or
   software- based?
   Thanks in advance!
 
   -
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[Histonet] Surgipath Millenium VSP3001/Leica Vogel 35396 Slide Writer

2012-02-23 Thread Drew Meyer
So apparently this model of slide writer is no longer manufactured, at
least from what I can tell.  My Leica rep says they don't make it anymore,
but I really need to get my hands on one.  Normally, I'm not a big fan of
this printer for larger volume labs, but the way we make slides here at our
immuno lab is perfectly conducive for the specific design of slide writer.
I'm wondering if anyone out there in Histoland knows where I can get one
new or used.  Also, do you know if Leica still sells the ribbons that go
with them?  Finally, the ideal circumstance would be where we could demo
one here; you know how it is getting the funding approved!  However, one of
our Pathologists has straight up said he'd buy it himself and worry about
getting reimbursed for it later.  Anyways, please let me know if you can
help or point me in the right direction!

Thanks,
Drew Meyer, HT
CSI Laboratories
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Re: [Histonet] H. Pylori - IHC

2011-11-16 Thread Drew Meyer
We use the Rabbit Polyclonal H. pylori from Cell Marque on the Ventana
Ultra's... We're a natinowide reference laboratory and our clients are all
very happy with the specificty of the staining.  Let me know if there's any
more information you need.

Drew
On Wed, Nov 16, 2011 at 17:15, beth@hcahealthcare.com wrote:

 Does anyone have recommendations for a good vendor for H.Pylori  for IHC?
  We have tried many, but our pathologists complain that they are not
 specific for H.Pylori and that all gram negative bacteria are staining.
  Currently we are not running this but our pathologists are interested in
 it.

 Thanks!

 Beth A. Fye, CT (ASCP)
 Pathology Technical  Manager
 HCA Richmond Hospital Laboratories
 office:  (804)228-6564
 fax: (804)323-8638
 mailto:beth@hcahealthcare.com




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Re: [Histonet] Varicella Zoster

2011-10-28 Thread Drew Meyer
abcam has a few Varicella Zoster strains to choose from... I haven't used them 
before, so I can't speak of how well they work or provide much insight to 
dilutions and protocols for the Ventana, but the other antibodies I've used 
from them work well.  

Drew

Sent from my iPhone

On Oct 28, 2011, at 12:11 PM, Donna Liaros dlia...@bioreference.com wrote:

 Anyone have any recommendations for a vendor that supplies a concentrated 
 antibody for Varicella Zoster Virus (herpes zoster)? I would be optimizing it 
 on the Ventana Ultra.
 The information transmitted in this email and any of its attachments is 
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 privileged, confidential, or subject to copyright belonging to BioReference 
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Re: [Histonet] Creative Waste Solutions

2011-08-17 Thread Drew Meyer
I may be wrong about this, but I don't think Rex has anyone else distributing 
his stuff yet.  However, some of the stuff they sell is merely products that 
they relabel to distribute themselves.  So, it depends on what specific 
products you're talking about. 

Drew

Sent from my iPad

On Aug 17, 2011, at 9:42 AM, Anita Buchiane abuchi...@bmhvt.org wrote:

 Does anyone know of a distributor of Creative Waste Solutions products?
 
 
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Re: [Histonet] Ventana Benchmark Ultra-Red Problems

2011-08-01 Thread Drew Meyer
Have you tried using a different lot of the Ultra View Red... Ours has been 
working fine, so maybe you got a bad lot?

Drew

Sent from my iPhone

On Aug 1, 2011, at 12:18 PM, Susan Foreman sfore...@labpath.com wrote:

 We have been having an issue lately with a precipitate (possibly bacterial
 contaminant) using the Ultra View Red Detection Kit that is not showing up
 on stains using the Ultra View DAB Detection Kit.  The red speckles appear
 on the tissue and also on the glass away from the tissue.  We have alerted
 tech support, done several decontaminations and changed our water from
 purified to distilled.  Has anyone experienced similar problems with the
 new formulation of the Ultra Red Detection kit or any other similar
 situations?   Any thoughts on the subject would be greatly appreciated.
 Benchmark Ultra stainer
 
 
 
 I appreciate your input,
 
 Susan
 
 KDL Pathology
 
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Re: [Histonet] Ventana Benchmark Ultra-Red Problems

2011-08-01 Thread Drew Meyer
Is it appearing on every slide run with that detection regardless of the 
antibody?  What are you using to remove the liquid coverslip?  If it's 
dish-soap, did you just recently change brands or use one with a different 
formula?

Drew

Sent from my iPhone

On Aug 1, 2011, at 12:24 PM, Susan Foreman sfore...@labpath.com wrote:

 We have tried both lots of the Ultra View Red
 
 -Original Message-
 From: Drew Meyer [mailto:41dm...@gmail.com] 
 Sent: Monday, August 01, 2011 12:27 PM
 To: Susan Foreman
 Cc: histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Ventana Benchmark Ultra-Red Problems
 
 Have you tried using a different lot of the Ultra View Red... Ours has been
 working fine, so maybe you got a bad lot?
 
 Drew
 
 Sent from my iPhone
 
 On Aug 1, 2011, at 12:18 PM, Susan Foreman sfore...@labpath.com wrote:
 
 We have been having an issue lately with a precipitate (possibly bacterial
 contaminant) using the Ultra View Red Detection Kit that is not showing up
 on stains using the Ultra View DAB Detection Kit.  The red speckles appear
 on the tissue and also on the glass away from the tissue.  We have alerted
 tech support, done several decontaminations and changed our water from
 purified to distilled.  Has anyone experienced similar problems with
 the
 new formulation of the Ultra Red Detection kit or any other similar
 situations?   Any thoughts on the subject would be greatly appreciated.
 Benchmark Ultra stainer
 
 
 
 I appreciate your input,
 
 Susan
 
 KDL Pathology
 
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Re: [Histonet] special stain controls

2011-04-29 Thread Drew Meyer
I can provide you with all the H. pylori you could ever want if you have some 
good fungus blocks.  Let me know if you'd like to trade!

Drew

Sent from my iPhone

On Apr 29, 2011, at 6:20 PM, histot...@imagesbyhopper.com wrote:

 Hi,
 
 
 
 I am in need of control blocks for special stains, H. Pylori, pneumocystis
 and AFB.  I am attempting to grow our own AFB, but am having difficulty
 getting the other control blocks.  Commercial vendors charge a LOT of money
 for these controls!  I was hoping to find a way to swap controls, if I
 could.   Does anyone have any suggestions for me?  I don't mind buying them,
 but tend to cringe when the costs are around $10/slide!!
 
 
 
 Thanks!
 
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[Histonet] Sunquest CoPath Rep

2011-01-26 Thread Drew Meyer
Could any Sunquest CoPath sales rep please contact me privately off the
list?

Thanks,
Drew Meyer
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Re: [Histonet] Billing question

2011-01-06 Thread Drew Meyer
Hey Joyce,

My understanding has always been that if the pathologist specifically
mentions the stain in the report, then it's OK to charge all the fees.
However, if the pathologist chooses to leave any mention of the stain/immuno
in the report, then you can't bill for it.  So if the pathologist mentions a
specific stain was done, but that the findings were negative, you can still
charge.  In the case of an exhausted tumor, I think the ultimate discretion
comes to whether or not the pathologist chooses to mention it in the
report.  That's just from my experience, but I would love to hear how others
are handling instances such as these, too!

Drew

On Thu, Jan 6, 2011 at 12:22, Weems, Joyce jwe...@sjha.org wrote:

 When you have performed a special stain or immuno that does not help the
 pathologist (tumor exhausted, etc) do you still charge for the technical
 component and the pathologist credits the professional fee? Just curious..

 Happy New Year, Everyone!

 Thanks! j


 Joyce Weems
 Pathology Manager
 Saint Joseph's Hospital
 5665 Peachtree Dunwoody Rd NE
 Atlanta, GA 30342
 678-843-7376 - Phone
 678-843-7831 - Fax


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[Histonet] VIP 1000 Help

2010-12-22 Thread Drew Meyer
We've got the old workhorse, the VIP 1000, that we still use.  During a
move, the guide, which shows all the commands you can do with that magnet,
got lost.  Is there anyone out there that has this and could send or fax me
a copy?  It would be much appreciated!

Thanks,
Drew Meyer

-- 








































































~Love is like a booger. You keep picking at it until you get it, then wonder
what to do with it.
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Re: [Histonet] Oil Red O control

2010-11-10 Thread Drew Meyer
There was a discussion on this recently, so you may want to search the
archives for it.  In my opinion, the easiest and best control to use is
Mayo.  Just smear it on a slide as you need it and there you go.  Cheap and
easy.

Drew

On Wed, Nov 10, 2010 at 09:45, Inman, Anna anna.in...@stmarygj.org wrote:

 Hello -

 How does everyone handle having a positive control for Oil Red O - We
 very infrequently have this stain and have had difficulty keeping
 control on hand.





 Thank you

 Anna

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Re: [Histonet] hi-profile blades

2010-10-19 Thread Drew Meyer
I agree with Bernice... I've used both the low and high profile Sakura
AccuEdge nothing comes close to their quality and consistency.

Drew

On Tue, Oct 19, 2010 at 11:44, Bernice Frederick 
b-freder...@northwestern.edu wrote:

 I've been using Accu-edge blades from Sakura and have found nothing to
 equal
 them. We use low profile here, but high are the same quality.


 Bernice Frederick HTL (ASCP)
 Northwestern University
 Pathology Core Facility
 ECOGPCO-RL
 710 N Fairbanks Court
 Olson 8-421
 Chicago,IL 60611
 312-503-3723


 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Margiotta,
 Michele
 Sent: Tuesday, October 19, 2010 7:14 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] hi-profile blades

 Hi All,

 One of my techs loves using hi-profile blades but recently she has been
 having problems with the quality and consistency of the blades.  One will
 cut great and the next one will give her problems cutting.  I'd appreciate
 any suggestions for blade type/company that histotechs are happy with so we
 can try them out.

 Thanks,
 Michele Margiotta
 BMHMC
 Histology Supervisor
 631-654-7192




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Re: [Histonet] Question about Oil Red O controls

2010-10-06 Thread Drew Meyer
Just use Mayo (not fat free, of course!) and smear it on the slide like you
would a blood smear.  It stains beautifully.

Drew

On Wed, Oct 6, 2010 at 09:15, Komal Gada kjg...@gmail.com wrote:

 Hello Histonetters,

 I am trying to find a procedure for using butter and egg yolks as controls
 for the Oil Red O stain (to show the fat).

 Does anyone have something they would be able to share with me?

 Thanks,
 Komal
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Re: [Histonet] Precipitate in Processor

2010-08-09 Thread Drew Meyer
My guess is that either your 70% wasn't made up properly and was a higher
concentration or it's been so long since you've changed the solution that
the water is fully saturated with the formalin salts.  If it becomes a
regular problem, you might consider reducing your first alcohol's
concentration to 60% or even 50%.  Good luck!

Drew

On Mon, Aug 9, 2010 at 12:00, Adrienne Aperghis Kavanagh 
aaperg...@uspath.com wrote:

 Hello Everyone,

 Has anyone ever seen a (salt?) precipitate in their alcohols following
 formalin?  While changing the processor this morning, I noticed a
 precipitate in the 80% alcohol and 95% alcohol (NOT in the 70% alcohol).  It
 is white and grainy.  The alcohols were otherwise unaffected.

 We are using a 10% NBF containing:
 Formaldehyde
 Water
 Sodium Phosphate, monobasic
 Sodium Phosphate, dibasic
 Methanol

 And our alcohols are all reagent grade.

 Any help would be very much appreciated!  Thank you in advance!


 Adrienne Aperghis Kavanagh
 US PATH
 30 W. Century Road
 Suite 255
 Paramus NJ 07652


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Re: [Histonet] Embedding multiple GI pieces on end in a paraffin block

2010-07-16 Thread Drew Meyer
We regularly embed 6-12 pieces on end in one block without any special
method.  You just have to be quick... and don't leave the block on the cold
plate very long... just touch the cold plate briefly while embedding the
individual piece, then lift the block off the plate until you grab the next
piece... repeat quickly and you'll run out of room in the mold before you'll
have to worry about it hardening too much.

Drew

On Fri, Jul 16, 2010 at 11:23, kgrob...@rci.rutgers.edu wrote:

 Is there a way to do this without one or more pieces falling over?  I saw
 in the archive the method for frozen sections-embed them on their sides in
 OCT, then cut on the end, but I don't think I'd be able to do that in
 paraffin.  Would one of the tissue microarray methods work?  (I've never
 done that before, so I have no idea.)

 Thanks in advance for all your help,
 Kathleen


 Principal Lab Technician
 Neurotoxicology Labs
 Molecular Pathology Facility Core
 Dept of Pharmacology  Toxicology
 Rutgers, the State University of NJ
 41 B Gordon Road
 Piscataway, NJ 08854
 (732) 445-6914

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Re: [Histonet] VIP 2000

2010-07-09 Thread Drew Meyer
You can always call Sakura... they'll at least tell you what the codes
means...

Drew

On Fri, Jul 9, 2010 at 10:15, sgoe...@xbiotech.com wrote:


   Hello all,

   I  recently  purchased a refurbished VIP.  ; This would have been the
   3rd  time  I  have  run it, but wait...diagnose flas hes and I get an
   error  code 73.  Of course the manual doesn't say what this is or how
   to  fix it, and I can't seem to find anything online either.   I know
   this  is  an  older  machine  and lots of you have used it, was ju st
   wondering if anyone knew what the heck diagnose code 73 is?

   Th anks

   Sarah Goebel, B.A., HT (ASCP) /div
   Histotechnician
   XBiotech USA Inc.
   8201 E ast Riverside Dr. Bldg 4 Suite 100
iA ustin, Texas  78744
   (512)386-51 07
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Re: [Histonet] used histology equipment

2010-07-06 Thread Drew Meyer
Absolutely... Southeast Pathology Instrument Service out of Charleston, SC.
The owner's name is Michael Dietrich.  I've done business with him before
and they are great people, very honest and they stand behind their
instruments.  I would highly recommend them to anyone.  Contact Michael
directly and tell him Drew Meyer from Atlanta referred you.

http://southeastpathology.com/

Drew

On Tue, Jul 6, 2010 at 18:29, dcoj...@tampabay.rr.com wrote:

 Does anyone know of a reputable dealer for used equipment?

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[Histonet] H. pylori RTU antibody

2010-06-30 Thread Drew Meyer
I was just wondering if a lot of people use the RTU antibodies available out
there for H. pylori.  Currently, we're testing the RTU from Dako and we're
having issues with a lot of background staining.  After tweaking the
protocol a lot, I've managed to get a lot of it removed, but there are still
some issues.  I was wondering if most people are making their own dilutions
to get a better stain or if the RTUs are commonplace.  I appreciate the
feedback!

Thanks,
Drew
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[Histonet] Re: H. pylori RTU antibody

2010-06-30 Thread Drew Meyer
I'm getting tons of responses from people about other antibodies that work
well, which I appreciate very much... However, I'm curious to hear from
someone that's actually using the Dako RTU and having success...

Thanks,
Drew

On Wed, Jun 30, 2010 at 10:41, Drew Meyer 41dm...@gmail.com wrote:

 I was just wondering if a lot of people use the RTU antibodies available
 out there for H. pylori.  Currently, we're testing the RTU from Dako and
 we're having issues with a lot of background staining.  After tweaking the
 protocol a lot, I've managed to get a lot of it removed, but there are still
 some issues.  I was wondering if most people are making their own dilutions
 to get a better stain or if the RTUs are commonplace.  I appreciate the
 feedback!

 Thanks,
 Drew

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[Histonet] Trichrome Help

2010-05-03 Thread Drew Meyer
I'm trying to troubleshoot a problem we had today with a Trichrome stain and
I was wondering if anyone out there could help.  We do Gomori Blue Collagen
Trichrome Stain... 10 minutes in Weigert's Hematoxylin and then 15 min in
the Gomori Blue Collagen stain followed by a quick change through acetic
acid, alcohol and xylene.  When it's all done, there is this weird film
that is present over the entire surface of the slide... almost like the thin
gray film that you sometimes see when you leave slides too long in the
silver solution for a GMS.  Anyways, I'm not sure what's causing it and
putting the slide in xylene or alcohol for a long time doesn't get rid of
it.  It can easily be wiped off, but obviously we can't wipe the section
off.  If anyone could help me narrow down what step might be causing this,
I'd appreciate it!

Thanks,
Drew
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[Histonet] Amyloid Stain

2010-04-05 Thread Drew Meyer
Hey Guys,

I was hoping to get some help with the best way to approach a request for an
amyloid stain.  The only thing I've ever done in the past is the traditional
Congo Red... however we were wondering how the Amyloid A Immuno stain is.
Our pathologists were wondering if the Amyloid A is more/less reliable and
if there are any limitations associated with this antibody.  I just don't
know that much about it and was hoping you guys could enlighten me!  Thanks
for the help!

Drew
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Re: [Histonet] help

2010-03-23 Thread Drew Meyer
So sorry... the only thing I know to fix it is time... about a week or
two... :)

Drew

On Tue, Mar 23, 2010 at 11:59, Patsy Ruegg pru...@ihctech.net wrote:

 After you stop laughing seriously I need some help here, apparently I got
 my
 fingers in some silver nitrate yesterday and touched my face under my nose
 over my lip and now I have black spots that won't come off.  I have done
 this on my hands before but never on my face.  So far I have tried soaking
 a
 cloth in hydrogen peroxide hoping to bleach it with no luck, I even tried
 putting some gold chloride on it to see if I could tone it down, to no
 avail.  Any ideas?  Make up only goes so far and lasts so long.



 Regards,



 Patsy



 Patsy Ruegg, HT(ASCP)QIHC
 IHCtech, LLC
 Fitzsimmons BioScience Park
 12635 Montview Blvd. Suite 215
 Aurora, CO 80010
 P-720-859-4060
 F-720-859-4110
 wk email pru...@ihctech.net
 web site www.ihctech.net




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Re: [Histonet] glass coverslipper

2010-03-04 Thread Drew Meyer
We use the Tissue-Tek Glas with great results.  Knowing how Sakura loves to
just relabel Leica equipment, it might be the same as the CV5030, but I'm
not sure.  Either way, I've been very impressed with the Tissue-Tek machine.

Drew

On Thu, Mar 4, 2010 at 15:00, Derek Papalegis derek.papale...@tufts.eduwrote:

 Hi Everyone,
 I am looking for a glass coverslipper and was wondering what people
 recommend. I am in a small research lab so having a small footprint is very
 important. It doesn't have to be very fast but I need something dependable
 that will give consistent results.

 Thanks,
 Derek

 --
 Derek Papalegis HT (ASCP)
 Senior Histology Technologist
 Division of Laboratory Animal Medicine
 Tufts University 136 Harrison Avenue
 Boston, MA 02111




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Re: [Histonet] time tissue stays in paraffin

2009-12-10 Thread Drew Meyer

What is the make/model of your tissue processor?

Drew

Sent from my iPhone

On Dec 10, 2009, at 10:56 AM, Dunlap, Charles dunl...@umkc.edu  
wrote:



We have a software glitch in our tissue processor, it  stops in the
first paraffin and will not progress to paraffins 2 and 3 then  
complete
the cycle.   If we catch it quickly, we can instruct it to continue  
but

the cycle happens around 5:00 am so we sometimes are not here, tissuet
may spend an extra 30 minutes or even an hour in the first paraffin.
Estimated cost of repairing is a whopping  6 thousand $$.Does this
have a major effect on quality of slidessometimes ours are less  
than

ideal but I am not sure if the problem is in the paraffin cycle or
elsewhere...sectioning, staining, etc.  Any ideas?   Charles Dunlap

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Re: [Histonet] paper on osteoclasts

2009-12-08 Thread Drew Meyer
Is this it?

http://www.jbmronline.org/doi/full/10.1359/jbmr.2000.15.8.1477?cookieSet=1

I've never read the paper, so I don't know exactly what you're looking
for... but I sometimes find Google Scholar to be a better search
engine for journal articles (which is what I used to find the above
article).

Drew

On Tue, Dec 8, 2009 at 01:36, louise renton louise.ren...@gmail.com wrote:
 Hi all,

 I am going crazy - and its not even friday yet! A little while ago (OK about
 3 years) i came across a paper where the researcher had shown the transition
 of macrophages to osteoclasts  using immuno staining - i cannot seem to find
 it on Pubmed, dont know the author date or journal.

 i hope soemone out there can help

 best egards

 --
 Louise Renton
 Bone Research Unit
 University of the Witwatersrand
 Johannesburg
 South Africa
 There are nights when the wolves are silent and only the moon howls.
 George Carlin
 No trees were killed in the sending of this message.
 However, many electrons were terribly inconvenienced.
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Re: [Histonet] CAP question

2009-12-03 Thread Drew Meyer
There has already been a lot of responses to this, but I thought I'd
add mine anyway.

For all our specimens in-house that are delivered from surgery, we
have three identifiers present: name, DOB and MR number.  We
eliminated the use of SSN (from our reports as well), since we all
know how dangerous it is to have your SSN just floating around.

Specimens received from outside facilities are a little different,
because the outside facility can't possibly label the specimen with
our MR number; it's assigned once the specimen arrives at our
location.  In those instances, just the name and DOB are used.

At the time of accession, we do add the in-house pathology case number
to all the specimens as well.  You might call this overkill, but it
helps greatly when we need to pull a specimen later on and it helps
cut down on grossing errors.

The big thing from CAP is the two identifiers.  When you're
specifically dealing with outpatient centers where you might not be
able to get the medical record number on the container at the time of
collection, it seems to me that the best choice is to use name and
DOB.  Just my 2 cents.

Drew

On Wed, Dec 2, 2009 at 11:49, Una McGiven lost.dragon...@yahoo.com wrote:
 Hi everyone,

 On the most recent CAP checklist there is a requirement for 2 patient 
 identifiers.  For those labs who are CAP and receive all or a large portion 
 of their cases from outside facilities (=not from your facility), what are 
 you using as the identifiers on your specimen containers?  Name and 
 birthdate?  SS#?  Med record?  Something else?

 Thank you in advance!



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Re: [Histonet] (no subject)

2009-11-25 Thread Drew Meyer
I'd be curious to see how you have your processor times set for each
station.  I'm sure you're using a different setting on the weekends to
account for the longer time.  Have you made sure that all the other
stations are getting the same time they normally get during the week?

Drew

On Wed, Nov 25, 2009 at 10:13, Taylor, Robin
robin.tay...@prexushealth.com wrote:
 We have been having processing problems for a while now and cannot resolve 
 it. It only happens on weekends. When we embed and cut on Monday morning, 
 alot of our larger pieces of tissue, especially  breast, are not fixed and 
 processed well. I would expect the opposite especially since they are in 
 formalin for an additional 48 hours. We do not work Saturdays (sorry guys) so 
 the tissue is grossed and submitted on Friday. Does anyone have any ideas as 
 to why this would be and what I can do to fix it. Thanks so much.
 Robin Taylor HT
 Butler County Medical Center
 Hamilton, OH


 
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Re: [Histonet] CMS/NCCI Update Dated October 1, 2009

2009-11-20 Thread Drew Meyer
Joyce,

That's very interesting, as I remember going to great lengths a few
years ago to be sure we had a billing limiter in place in CoPath to
prevent the multiple charging of CPT codes on the same specimen.
However, I looked up the document released on 10/1/09 and here's what
I found in regards to the special and immuno CPT codes:

8. The unit of service for special stains (CPT codes 88312-88313) and
immunohistochemistry (CPT codes 88342, 88360, 88361) is each stain. If
it is medically reasonable and necessary to perform the same stain on
more than one specimen or more than one block of tissue from the same
specimen, additional units of service may be reported for the
additional specimen(s) or block(s). Physicians should not report more
than one unit of service for a stain performed on a single tissue
block. For example it is common practice to cut multiple levels from a
tissue block and stain each level with the same stain. The multiple
levels from the same block of tissue stained with the same stain
should not be reported as additional units of service. Only one unit
of service should be reported for the stain on multiple levels from
the single tissue block. Additionally, controls performed with special
stains should not be reported as separate units of service for the
stain.

From what all I can see, you're right; it seems that we can bill for
multiple special stains on the same specimen, just not the same block
(so tell Drs. Stargel and Sears it won't help them :)  ).  I'm going
to present this to our pathologists and billing auditors for review.
Thanks so much for sharing this with everyone!!!

Drew

On Fri, Nov 20, 2009 at 14:28, Weems, Joyce jwe...@sjha.org wrote:
 According the one of our pathologist the above mentioned update
 clarified that CMS allows the billing of special stains performed on
 different blocks of the same Pathology specimen.  Previously, it was
 understood that a special stain could only be billed once per specimen.
 Now it appears that a stain could be billed twice if performed on block
 1 and block 3 of the same specimen. Has anyone else reached this
 conclusion?



 Thanks,

 Joyce



 Joyce Weems
 Pathology Manager
 Saint Joseph's Hospital
 5665 Peachtree Dunwoody Rd NE
 Atlanta, GA 30342
 678-843-7376 - Phone
 678-843-7831 - Fax

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Re: [Histonet] B5 alternate

2009-11-16 Thread Drew Meyer

Essentially it's a zinc formalin.

Drew

Sent from my iPhone

On Nov 16, 2009, at 4:53 PM, John Kiernan jkier...@uwo.ca wrote:


What is this B plus fixative?  Is it a trade-secret brew?

John Kiernan
Anatomy, UWO
London, Canada
= = =
- Original Message -
From: Anne van Binsbergen anni...@gmail.com
Date: Friday, November 13, 2009 10:01
Subject: Re: [Histonet] B5 alternate
To: Drew Meyer 41dm...@gmail.com
Cc: Knutson, Deanne dknut...@primecare.org, histonet@lists.utsouthwestern.edu 
 histonet@lists.utsouthwestern.edu



B plus is the one - we use it as stated and it works like a charm
immunos are good too - we are proudly mercury free
Annie

2009/11/13 Drew Meyer 41dm...@gmail.com


In my lab, we're using B-Plus Fixative by BBC

Biochemical.  I know

many other labs that are also using it as their B5

alternative.  The

biggest pro, of course, is that it's mercury free and not hazardous.
Also, it's not as sensitive to over-fixation like B5 is.  The
guideline I use is 4 hours minimum fixation for Bone Marrows and
Lymphoid tissue.  After that, routine formalin processing

is all you

need to do.  You can, however, leave the specimen in B-

Plus for up to

48 hours without adversely effecting the tissue sample.

Hope this help.

Drew Meyer

On Fri, Nov 13, 2009 at 09:43, Knutson, Deanne

dknut...@primecare.org wrote:

Am looking for advice on what alternate fixative to use to

replace B5.

What

do the majority of you histonetters use?  Does it work

well with immunos?

The pros and cons?  Thank you for your recommendations.



Deanne Knutson

Anatomic Pathology Supervisor

St. Alexius Medical Center

900 E. Broadway

Bismarck, North Dakota  58506

(701)-530-6730

dknut...@primecare.org mailto:dknut...@primecare.org



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--
Anne van Binsbergen (Hope)
Abu Dhabi
UAE
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