RE: [Histonet] RE: Adopting a bar code system

2012-06-26 Thread Janice Mahoney

Marcia,I'm so glad you are going with Vantage, you will not be disappointed.  
Good luck and call me if you need any help.Jan MahoneyOmaha

Date: Tue, 26 Jun 2012 10:58:48 -0400
From: fu...@mercyhealth.com
To: tjohn...@gnf.org; histonet@lists.utsouthwestern.edu; 
loralee_mcma...@urmc.rochester.edu
Subject: [Histonet] RE: Adopting a bar code system
CC: 

We are installing Vantage system from Ventana and very excited - great things 
to follow.
Marcia
 
 
Marcia Funk 
Histology Laboratory
Mercy Medical Center North Iowa
Mason City, IA, 50401
641-428-7907
 McMahon, Loralee A loralee_mcma...@urmc.rochester.edu 06/21/2012 1:55 
 PM 
Sorry Teri must have missed the reply all button. 
And also Lablion claims to interface with any current lab equipment that you 
have.  So if you already have slide printers (either etchers or labelers) it 
can work.  Like I said.  I haven't seen it in action, but I sure would like to. 
 
Loralee McMahon, HTL (ASCP)
Immunohistochemistry Supervisor
Strong Memorial Hospital
Department of Surgical Pathology
(585) 275-7210

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Teri Johnson 
[tjohn...@gnf.org]
Sent: Thursday, June 21, 2012 2:26 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Adopting a bar code system
 
Here's a response I have received off list:
 
 
Teri,
 
We just looked at a barcode histology tracking system called LabLion.  I have 
never heard of them until yesterday.  It was developed by a histotech and some 
engineers.  It looks too good to be true.  We have looked at a lot of different 
systems and this ones seems to have everything that we need.   We have looked 
at the TBS system, Dako, Ventana, etc.
I think if you google them you can find it and the contact information.  If not 
let me know and I'll get it for you.  It is definitley worth your time to look 
at this system.  We are in serious negotiations with them.  But this is just my 
opinion from the demo.   I haven't had a chance to actually put my hands on it.
 

From: histonet-boun...@lists.utsouthwestern.edu 
[histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Teri Johnson 
[tjohn...@gnf.org]
Sent: Thursday, June 21, 2012 1:45 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Adopting a bar code system
 
Hi Histonetters,
 
I am interested in hearing from folks who went from a manual histology system 
to a barcoding system. I would like to look into to adopting bar coding and 
want to know the pitfalls, issues, and your successes in doing so.
 
Thanks!
 
Teri Johnson, HT(ASCP)QIHC
GNF Histology Lab Manager
Genomics Institute of the Novartis Research Foundation
858-332-4752
 
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RE: [Histonet] Barcoding specimen tracking, lessons you learned

2012-04-26 Thread Janice Mahoney

Great Question.  No system can eliminate errors, but using a good system with  
standard process will and has proven eliminated errors.  I used the Vantage 
System in my lab and the only errors we had in several years (about 1 to 2 per 
year) occurred when staff were not following standard work and single piece 
flow.  These are very important LEAN concepts that work. I can't imagine 
implementing a bar coding system without using LEAN workflow in a lab.  Doing 
so would be a great waste of money.JanOmaha

 From: pathloc...@gmail.com
 Date: Mon, 23 Apr 2012 12:23:37 -0700
 To: timothy.mor...@ucsfmedctr.org; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Barcoding specimen tracking, lessons you learned
 CC: 
 
 See Rich Pucci at UCSF Pathology. He would be a great resource.
 
 Sent from my Windows Phone
 From: Morken, Timothy
 Sent: 4/23/2012 10:31 AM
 To: Histonet
 Subject: [Histonet] Barcoding specimen tracking, lessons you learned
 To anyone who has implemented a barcoding/specimen tracking system in
 your lab. What lessons did you learn that would make it easier if you
 did it over? We're starting the process and I would like to get some
 input on things to look out for!
 
 Thanks for any info and comments!
 
 Tim Morken
 Department of Pathology
 UC San Francisco Medical Center
 505 Parnassus Ave, Box 1656
 Room S570
 San Francisco, CA 94132
 
 (415) 353-1266 (ph)
 (415) 514-3403 (fax)
 tim.mor...@ucsfmedctr.org
 
 
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RE: [Histonet] Farewell

2012-03-30 Thread Janice Mahoney

Enjoy retirement Sara, I'm loving it and have been for almost a year now.  
Still love and am very interested in Histology.  I think it stays in the blood 
forever.  I'm doing a little consulting but mostly enjoying my grandson and 
being home.  Never a boring minute, I'm as busy as I ever was,
Congratulations!Jan MahoneyOmaha

 Date: Fri, 30 Mar 2012 07:16:14 -0600
 From: sbree...@nmda.nmsu.edu
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Farewell
 
 Hard as it is to believe - and I probably won't until I've been away for
 a week or more - this is my LAST day to work.  Retirement? Who knew it
 would come around so fast? I remember having only fifteen years left to
 work and that was just yesterday!  Histology has been 'bery, 'bery good
 to me and although I fell into it by accident, it has been a
 fascinating, involving, liberating experience.  I'll be lurking on
 Histonet but under the alias of nmhisto and I'll probably do some p.r.n.
 work but I'm going home and throwing away my alarm clock and resetting
 the coffee maker for 6:00 a.m. instead of 3:45 a.m.  Thank you all for
 your advice, guidance, humor, relative insanity and wisdom.  Enjoy what
 you do and try to recruit at least one person into this field before
 it's your time to pick out the color of the tennis balls on your walker.
 
  
 
 Hail and Farewell and best of everything to every one of you.
 
  
 
 Sally Breeden, HT(ASCP)
 
 New Mexico Department of Agriculture
 
 Veterinary Diagnostic Services
 
 1101 Camino de Salud NE
 
 Albuquerque, NM  87102
 
 505-383-9278 (Histology Lab)
 
  
 
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RE: [Histonet] Farewell

2012-03-30 Thread Janice Mahoney

I meant Sally, sorry.

 From: mamaw...@hotmail.com
 To: sbree...@nmda.nmsu.edu; histonet@lists.utsouthwestern.edu
 Date: Fri, 30 Mar 2012 07:53:28 -1000
 Subject: RE: [Histonet] Farewell
 CC: 
 
 
 Enjoy retirement Sara, I'm loving it and have been for almost a year now.  
 Still love and am very interested in Histology.  I think it stays in the 
 blood forever.  I'm doing a little consulting but mostly enjoying my grandson 
 and being home.  Never a boring minute, I'm as busy as I ever was,
 Congratulations!Jan MahoneyOmaha
 
  Date: Fri, 30 Mar 2012 07:16:14 -0600
  From: sbree...@nmda.nmsu.edu
  To: histonet@lists.utsouthwestern.edu
  Subject: [Histonet] Farewell
  
  Hard as it is to believe - and I probably won't until I've been away for
  a week or more - this is my LAST day to work.  Retirement? Who knew it
  would come around so fast? I remember having only fifteen years left to
  work and that was just yesterday!  Histology has been 'bery, 'bery good
  to me and although I fell into it by accident, it has been a
  fascinating, involving, liberating experience.  I'll be lurking on
  Histonet but under the alias of nmhisto and I'll probably do some p.r.n.
  work but I'm going home and throwing away my alarm clock and resetting
  the coffee maker for 6:00 a.m. instead of 3:45 a.m.  Thank you all for
  your advice, guidance, humor, relative insanity and wisdom.  Enjoy what
  you do and try to recruit at least one person into this field before
  it's your time to pick out the color of the tennis balls on your walker.
  
   
  
  Hail and Farewell and best of everything to every one of you.
  
   
  
  Sally Breeden, HT(ASCP)
  
  New Mexico Department of Agriculture
  
  Veterinary Diagnostic Services
  
  1101 Camino de Salud NE
  
  Albuquerque, NM  87102
  
  505-383-9278 (Histology Lab)
  
   
  
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RE: [Histonet] Ventana xt

2012-02-17 Thread Janice Mahoney

I think the Ventana XT is the best instrument for adding slides as you go which 
makes it perfect for a LEAN lab.  This will reduce your TAT.The instrument is 
so easy to use it is virtually impossible to mess up with it's bar coding and 
visual control.  Very user friendly.
Jan Mahoney,Omaha, NE
 From: christiego...@msn.com
 To: dphill...@vetmed.lsu.edu; histonet@lists.utsouthwestern.edu
 Date: Thu, 16 Feb 2012 19:46:35 +
 Subject: RE: [Histonet] Ventana xt
 CC: 
 
 
 Pros:
 Lends itself well to labs that do basic IHC staining
 Antibodies are pre-diluted so no guess work on dilutions
 Good for batching runs
 Consistent quality of slides
 24 hour technical support
 Can run molecular probes
 protocols are easy to adjust
  
 Cons:
 Closed system
 Must use Ventana antibodies or purchase special dispensers if using non 
 Ventana products
 Pre-dilute antibodies are pricey
 Stand alone instrument so must have space for it
  
 I'm sure there is more but you just really need to see what your needs are. 
 We have the XT and Ultra as well as open systems. We love the Ventana's but 
 we also will always have open platforms because we do a lot of research. The 
 work flow is another thing you need to look at. How many slides do you turn 
 out in one day? What is your turn around time? The XT is a great instrument 
 but it depends on your lab. Hope this helps.
 Christie Gowan
 UAB Hospital
  
  
 
  From: dphill...@vetmed.lsu.edu
  To: histonet@lists.utsouthwestern.edu
  Date: Thu, 16 Feb 2012 12:29:37 -0600
  Subject: [Histonet] Ventana xt
  
  Looking for any pros and cons on the Ventana XT.
  
  
  
  Thanks
  
  Del
  
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RE: [Histonet] Ventana xt

2012-02-17 Thread Janice Mahoney

Thanks for correcting me.Jan

 Subject: RE: [Histonet] Ventana xt
 Date: Fri, 17 Feb 2012 08:23:33 -0600
 From: lseb...@uwhealth.org
 To: mamaw...@hotmail.com; christiego...@msn.com; dphill...@vetmed.lsu.edu; 
 histonet@lists.utsouthwestern.edu
 
 Side note: only the Ventana Ultra allows adding slides as you go, not
 the XT. 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Janice
 Mahoney
 Sent: Friday, February 17, 2012 7:52 AM
 To: Christie Gowan; dphill...@vetmed.lsu.edu; histonet
 Subject: RE: [Histonet] Ventana xt
 
 
 I think the Ventana XT is the best instrument for adding slides as you
 go which makes it perfect for a LEAN lab.  This will reduce your TAT.The
 instrument is so easy to use it is virtually impossible to mess up with
 it's bar coding and visual control.  Very user friendly.
 Jan Mahoney,Omaha, NE
  From: christiego...@msn.com
  To: dphill...@vetmed.lsu.edu; histonet@lists.utsouthwestern.edu
  Date: Thu, 16 Feb 2012 19:46:35 +
  Subject: RE: [Histonet] Ventana xt
  CC: 
  
  
  Pros:
  Lends itself well to labs that do basic IHC staining Antibodies are 
  pre-diluted so no guess work on dilutions Good for batching runs 
  Consistent quality of slides
  24 hour technical support
  Can run molecular probes
  protocols are easy to adjust
   
  Cons:
  Closed system
  Must use Ventana antibodies or purchase special dispensers if using 
  non Ventana products Pre-dilute antibodies are pricey Stand alone 
  instrument so must have space for it
   
  I'm sure there is more but you just really need to see what your needs
 are. We have the XT and Ultra as well as open systems. We love the
 Ventana's but we also will always have open platforms because we do a
 lot of research. The work flow is another thing you need to look at. How
 many slides do you turn out in one day? What is your turn around time?
 The XT is a great instrument but it depends on your lab. Hope this
 helps.
  Christie Gowan
  UAB Hospital
   
   
  
   From: dphill...@vetmed.lsu.edu
   To: histonet@lists.utsouthwestern.edu
   Date: Thu, 16 Feb 2012 12:29:37 -0600
   Subject: [Histonet] Ventana xt
   
   Looking for any pros and cons on the Ventana XT.
   
   
   
   Thanks
   
   Del
   
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RE: [Histonet] Vantage Printers

2012-01-23 Thread Janice Mahoney

ThermoShandon printmate.Jan,Omaha

 Date: Fri, 20 Jan 2012 10:45:54 -0600
 From: bauer.ka...@mayo.edu
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Vantage Printers
 
 Hi Histoland,
  
 For those of you that are using the Vantage from Ventana, what cassette
 printers have you found work the best?
  
 Thanks much!!
  
 Karen
  
 Karen L. Bauer HTL/HT (ASCP)
 Histology Supervisor - Pathology Department
 MOHS Lab Supervisor - Dermatology Department
 Mayo Clinic Health System in Eau Claire
 Phone:  715-838-3205
 E-mail:   bauer.ka...@mayo.edu mailto:bauer.ka...@mayo.edu 
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 www.mayoclinichealthsystem.org
  
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RE: [Histonet] Has anyone else noticed

2011-12-19 Thread Janice Mahoney

I have noticed it many many times.
Happy Holidays
Jan Mahoney, Omaha
 

 From: del...@musc.edu
 To: histonet@lists.utsouthwestern.edu
 Date: Mon, 19 Dec 2011 10:23:40 -0500
 Subject: [Histonet] Has anyone else noticed
 
 
 Wondering if anyone else has noticed that rinsing a wine glass with water 
 will turn a nice cabernet sauvignon residue blue (reminiscient of hematoxylin 
 staining solution) ??
 
 
 Yes, with so little positive in the news these days, I am definitely 
 anesthetizing myself this holiday season. 
 
 Vinnie Della Speranza, MS, HTL(ASCP)
 Manager for Anatomic Pathology Services
 Medical University of South Carolina
 165 Ashley Avenue MSC 908
 Charleston, SC 29425
 tel. 843-792-6353
 fax. 843-792-8974
 
 
 
 
 
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RE: [Histonet] bar codes for slides and cassettes

2011-11-16 Thread Janice Mahoney

Leticia,
We used Ventana Vantage in my lab and loved everything about it.  It is so much 
more than just a labeling system.  Check it out.  It is pricy but worth every 
penny in what you will gain in productivity and error reduction.
Jan Mahoney
Omaha, NE
 

 From: leticia.figliu...@roche.com
 To: histonet@lists.utsouthwestern.edu
 Date: Wed, 16 Nov 2011 15:31:02 -0500
 Subject: [Histonet] bar codes for slides and cassettes
 
 Hello everybody,
 
 Is anybody out there using bar code system for slides/cassettes?
 My supervisor asked me to find out pros and cons and more information about 
 this. I have no idea where to start...
 
 Thank you in advance!
 
 Leticia Figliuolo
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RE: [Histonet] Slide and Cassette printing

2011-11-15 Thread Janice Mahoney

Hi Dana,
We used the slide labels for the Vantage system without any problems for 
several years.  We labeled at the cutting station and NEVER had a label wash 
off or smear in about three years.  I highly recommend it.  You will also see a 
huge gain in productivity elimination double labeling.
Hope all is well with you.  Call me anytime, it would be great to hear form you.
Jan Mahoney
Omaha, NE
 

 Date: Tue, 15 Nov 2011 09:17:06 -0500
 From: dana.spen...@pcmh.com
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Slide and Cassette printing
 
 What hardware are you using for printing slides and cassettes? There are many 
 good systems out there and each have their flaws, but specifically I have 
 heard negative rumblings about the PrintMate and SlideMate Systems from 
 ThermoFisher. Are you using labels at the microtome? I would welcome any 
 feedback or recommendations esp from larger institutions with large volumes.
 
 Thanks,
 Dana Spencer, CT(ASCP)
 Anatomic Pathology Manager
 Pitt County Memorial Hospital
 Greenville, NC 27834
 
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RE: [Histonet] Specimen Tracking for courier

2011-11-04 Thread Janice Mahoney

Yes, Call your Ventana rep.  Vantage is able to track courier pick-ups and 
record what slides are sent, etc.
Jan Mahoney
Omaha
 

 From: cp...@x-celllab.com
 To: jennifer.b...@northwestpathology.com; histonet@lists.utsouthwestern.edu
 Date: Thu, 3 Nov 2011 11:13:02 -0400
 Subject: RE: [Histonet] Specimen Tracking for courier
 CC: 
 
 I would be interested in everyone responses.
 
 Cindy
 
 Cindy Pyse, CLT, HT (ASCP)
 Laboratory Manger
 X-Cell Laboratories
 e-mail cp...@x-celllab.com
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bull,
 Jennifer L.
 Sent: Thursday, November 03, 2011 10:43 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Specimen Tracking for courier
 
 
 
 I'm curious what methods other labs are using to track specimens that
 couriers pick up from clinic locations to ensure safe delivery to the lab.
 We currently utilize a logbook at the clinic site that the courier signs
 when they take the specimen but I have heard there are barcoded systems
 available out there as well. What works? What doesn't? Appreciate your
 feedback!
 
 Jenny
 
 
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RE: [Histonet] Staffing to work ratios

2011-11-04 Thread Janice Mahoney

I have always used the 5000 blocks per HT for the year. (not including IHC 
staff)
 
Jan Mahoney
Omaha,NE

 Date: Thu, 3 Nov 2011 13:03:44 -0400
 From: stacy_mclaugh...@cooley-dickinson.org
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Staffing to work ratios
 
 Hi,
 
 I know this subject has been discussed before, but I'm having trouble
 finding the info I need from the archives. 
 
 Would anyone know where I can find the work to staffing ratios for a
 Histology laboratory?
 
 Our volume was ~9750 surgical cases (2010). The majority of them are
 biopsies (GI, GYN, skin, etc) but we do some larger complex cases.
 
 We had 2569 billable IHC tests, 254 billable group I special stains, 722
 billable group II special stains.
 
 #blocks:
 
 23,380
 
 
 
 # HE slides : 49,524
 
 
 
 Thank you for your help!
 
 
 
 Stacy McLaughlin, HT(ASCP)
 
 Histology Supervisor
 
 Cooley Dickinson Hospital
 
 30 Locust Street
 
 Northampton, MA 01060
 
 (413)582-2019
 
 stacy_mclaugh...@cooley-dickinson.org
 
 
 
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RE: [Histonet] Staffing to work ratios

2011-11-04 Thread Janice Mahoney

Sorry, i meant to say 5000 cases, not blocks.
Jan
 
 
 From: mamaw...@hotmail.com
 To: stacy_mclaugh...@cooley-dickinson.org; histonet@lists.utsouthwestern.edu
 Date: Fri, 4 Nov 2011 06:05:22 -1000
 Subject: RE: [Histonet] Staffing to work ratios
 CC: 
 
 
 I have always used the 5000 blocks per HT for the year. (not including IHC 
 staff)
 
 Jan Mahoney
 Omaha,NE
 
  Date: Thu, 3 Nov 2011 13:03:44 -0400
  From: stacy_mclaugh...@cooley-dickinson.org
  To: histonet@lists.utsouthwestern.edu
  Subject: [Histonet] Staffing to work ratios
  
  Hi,
  
  I know this subject has been discussed before, but I'm having trouble
  finding the info I need from the archives. 
  
  Would anyone know where I can find the work to staffing ratios for a
  Histology laboratory?
  
  Our volume was ~9750 surgical cases (2010). The majority of them are
  biopsies (GI, GYN, skin, etc) but we do some larger complex cases.
  
  We had 2569 billable IHC tests, 254 billable group I special stains, 722
  billable group II special stains.
  
  #blocks:
  
  23,380
  
  
  
  # HE slides : 49,524
  
  
  
  Thank you for your help!
  
  
  
  Stacy McLaughlin, HT(ASCP)
  
  Histology Supervisor
  
  Cooley Dickinson Hospital
  
  30 Locust Street
  
  Northampton, MA 01060
  
  (413)582-2019
  
  stacy_mclaugh...@cooley-dickinson.org
  
  
  
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RE: [Histonet] Training and Competency Assessment for HE Slide Review

2011-11-04 Thread Janice Mahoney

A great way to do this is by using the results of the Histo QIP from CAP and 
the NSH.  If you participate you get wonderful study and competency materials 
to use for routine HE's special stains and IHC.
Jan Mhaoney
Omaha
 

 From: joellewea...@hotmail.com
 To: diana.har...@viha.ca; histonet@lists.utsouthwestern.edu
 Date: Thu, 3 Nov 2011 17:42:53 +
 Subject: Re: [Histonet] Training and Competency Assessment for HE Slide 
 Review
 CC: 
 
 Any certified histologist has gone through this, but the NSH has good 
 resources for this.
 Sent from my Verizon Wireless BlackBerry
 
 -Original Message-
 From: Harris Diana diana.har...@viha.ca
 Date: Thu, 3 Nov 2011 17:34:03 
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Training and Competency Assessment for HE Slide Review
 
 Any suggestions for creating a Training and Competency (TC) Assessment for 
 HE slide review?  We currently QC all HE slides macroscopically and 15% 
 microscopically.  I would like to have all Histotechs trained and competent 
 to QC HE slides.  Has anyone gone thru this process?
 
 Thanks
 Diana Harris
 QC  Method Development Technologist
 Royal Jubilee Hospital
 Victoria, BC  Canada
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RE: [Histonet] Staffing to work ratios

2011-11-04 Thread Janice Mahoney

I believe the NSH published standards a few years back that suggested the 
average for embedding is one minute per block and 2.5 minutes for sectioning.  
My personal opinion is that one minute is too fast for sectioning, unless you 
have already faced in and are just taking a section off the top of the block. 
It can be done, no doubt, but for how long and at what expence?  I would think 
that after about an hour the quality would suffer as well as the tech from 
repetative motion.  I hope you are taking your ergonomic breaks.
Jan Mahoney
Omaha, NE
 

 From: b-freder...@northwestern.edu
 To: mpe...@grhs.net; mamaw...@hotmail.com; 
 stacy_mclaugh...@cooley-dickinson.org; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Staffing to work ratios
 Date: Fri, 4 Nov 2011 16:36:28 +
 
 I wish! Try at least 100blk /day. And that is on an easy day. Can I work with 
 you all? We were taught to cut a block a minute, levels or not. At slowest, 
 one ice tray of 14 blocks in 20 minutes ,with quality. And yes ,I can still 
 do it after all these years. When I started I had 3 months (probation) to get 
 the quality and quantity of techs that had been around for at least 10 years 
 and I was straight out of histo school. Well taught, I might add. 
 Bernice
 
 Bernice Frederick HTL (ASCP)
 Senior Research Tech
 Pathology Core Facility
 ECOGPCO-RL
 Robert. H. Lurie Cancer Center
 Northwestern University
 710 N Fairbanks Court
 Olson 8-421
 Chicago,IL 60611
 312-503-3723
 b-freder...@northwestern.edu
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Mike Pence
 Sent: Friday, November 04, 2011 11:16 AM
 To: Janice Mahoney; stacy_mclaugh...@cooley-dickinson.org; histo net
 Subject: RE: [Histonet] Staffing to work ratios
 
 That is only 20 blocks per working day (Mon-Fri)!
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Janice Mahoney
 Sent: Friday, November 04, 2011 11:05 AM
 To: stacy_mclaugh...@cooley-dickinson.org; histo net
 Subject: RE: [Histonet] Staffing to work ratios
 
 
 
 I have always used the 5000 blocks per HT for the year. (not including IHC 
 staff)
 
 Jan Mahoney
 Omaha,NE
 
  Date: Thu, 3 Nov 2011 13:03:44 -0400
  From: stacy_mclaugh...@cooley-dickinson.org
  To: histonet@lists.utsouthwestern.edu
  Subject: [Histonet] Staffing to work ratios
  
  Hi,
  
  I know this subject has been discussed before, but I'm having trouble 
  finding the info I need from the archives.
  
  Would anyone know where I can find the work to staffing ratios for a 
  Histology laboratory?
  
  Our volume was ~9750 surgical cases (2010). The majority of them are 
  biopsies (GI, GYN, skin, etc) but we do some larger complex cases.
  
  We had 2569 billable IHC tests, 254 billable group I special stains,
  722 billable group II special stains.
  
  #blocks:
  
  23,380
  
  
  
  # HE slides : 49,524
  
  
  
  Thank you for your help!
  
  
  
  Stacy McLaughlin, HT(ASCP)
  
  Histology Supervisor
  
  Cooley Dickinson Hospital
  
  30 Locust Street
  
  Northampton, MA 01060
  
  (413)582-2019
  
  stacy_mclaugh...@cooley-dickinson.org
  
  
  
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RE: [Histonet] CPT CODE

2011-10-27 Thread Janice Mahoney

Shane,
It depends on the prep you use.  If it is a smear it should be 88104, if a thin 
prep 88312.
Jan
Omaha
 

 Date: Thu, 27 Oct 2011 11:29:25 -0700
 From: nelsonr...@verizon.net
 To: Histonet@lists.utsouthwestern.edu
 CC: 
 Subject: [Histonet] CPT CODE
 
 Does anyone know the CPT code for Anal pap smear
 
 
 THANK YOU,
  
 PATTI RUBEN-NELSON  H.T.(ASCP) 
 nelsonr...@verizon.net
  
  
 CONFIDENTIALITY NOTICE:
 This message and any included attachments are from Patti Nelson, PNP 
 Laboratory Consultants 
  and are intended only for the addressee.  The information contained in this 
 message is confidential and may contain privileged, confidential, proprietary 
 and/or exemption from disclosure under applicable
 law.  Unauthorized forwarding, printing, copying, distribution, or use of
 such information is strictly prohibited and may be unlawful.  If you are not
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RE: [Histonet] CPT CODE

2011-10-27 Thread Janice Mahoney

Sorry, non-gyn thin prep, 88112.
Jan
 

 Date: Thu, 27 Oct 2011 11:29:25 -0700
 From: nelsonr...@verizon.net
 To: Histonet@lists.utsouthwestern.edu
 CC: 
 Subject: [Histonet] CPT CODE
 
 Does anyone know the CPT code for Anal pap smear
 
 
 THANK YOU,
  
 PATTI RUBEN-NELSON  H.T.(ASCP) 
 nelsonr...@verizon.net
  
  
 CONFIDENTIALITY NOTICE:
 This message and any included attachments are from Patti Nelson, PNP 
 Laboratory Consultants 
  and are intended only for the addressee.  The information contained in this 
 message is confidential and may contain privileged, confidential, proprietary 
 and/or exemption from disclosure under applicable
 law.  Unauthorized forwarding, printing, copying, distribution, or use of
 such information is strictly prohibited and may be unlawful.  If you are not
 the addressee, please promptly delete this message and notify the sender of
 the delivery error by e-mail or you may call  909-841-9761.
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RE: [Histonet] cochineal mentioned in comic strip

2011-10-24 Thread Janice Mahoney

I concur Peggy, great book and great article.
Jan Mahoney HT(ASCP)
Omaha, NE
 

 From: lpw...@sbcglobal.net
 To: Histonet@lists.utsouthwestern.edu
 Date: Sun, 23 Oct 2011 19:04:34 -0400
 CC: 
 Subject: [Histonet] cochineal mentioned in comic strip
 
 Just for fun: Check to see if your Sunday comic section carries Jump Start. 
 Check out today’s 10/23/11 strip.
 
 Jump Start, a comic strip about a couple (policeman and nurse) and their 
 kids, has the oldest girl wanting to be a cochineal insect for Halloween – 
 which is where histology gets carmine dye for the mucicarmine stain.
 http://www.gocomics.com/jumpstart/2011/10/23
 
 If you want to read a fascinating book about the the role of carmine in the 
 exploration of the America’s, enslaving the people of Central and South 
 America, pirates stealing ships loaded with the dye, spying, politics, 
 government and religion, and the “unions” of the dyeing industry back then – 
 find or buy a copy of “A Perfect Red: Empire, Espionage, and the Quest for 
 the Color of Desire” by Amy Butler Greenfield, 2006.
 
 If you want a more abbreviated version, Anatech’s newsletter ”The Innovator” 
 had an article about carmine in their Winter 2007 issue – all about the 
 history, and about why the quality of Mucicarmine has gone downhill in the 
 past few years. (And also towards the end of the newsletter - what Anatech 
 has done to try to improve the quality of the carmine. The article includes 
 promoting their version of mucicarmine, so just a head’s up – this is their 
 newsletter to promote their products. But they do a great job at educating in 
 general, too. So I enjoy reading and learning from their newsletters. Great 
 photos of what stains SHOULD look like.)
 http://www.anatechltdusa.com/Innovators/Innovator12_06.pdf
 
 No – I don’t get any money talking about the comic strip, the book or 
 Anatech. I just think it’s neat to read about the history of dyes. And really 
 great to to read about cochineal in a Sunday comic strip!
 
 Peggy A. Wenk, HTL(ASCP)SLS
 Beaumont Hospital
 Royal Oak, MI 48073
 
 (The opinions expressed are my own.)
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RE: [Histonet] (no subject)

2011-10-06 Thread Janice Mahoney

Very good question Cindi.Jan

 Date: Thu, 6 Oct 2011 09:26:18 -0400
 From: robin...@mercyhealth.com
 To: mamaw...@hotmail.com; histonet@lists.utsouthwestern.edu; 
 christiego...@msn.com
 Subject: RE: [Histonet] (no subject)
 
 It is a good thing this vendor does not work in a histo lab because with that 
 comment/attitude he/she would not last long. I have heard the water bath 
 theory but upon investigation this has never been the source because every 
 histotech I work with cleans it each and every time. We have traced floaters 
 back to grossing stations, processors...especially placenta getting 'snagged' 
 on a piece of bone...embedding forceps (we now use ones with no grooves), 
 forcep warmers, stains and coverslippers. We have significantly reduced the 
 number we see since we make the effort to track each one found as an ongoing 
 QA project, but we still see the occasional floater.  We did find that we 
 have to put tissue types which fragment easily into mesh cassettes or bags 
 but this can cause issues with fluid exchange and carryover during 
 processing. It is a balancing act. I have always wondering about the newer 
 processors with orientation cassettes which are embed and then cut without 
 opening. Do they see less floaters with this type of 'closed' system? 
 
 
 
 Cindi Robinson HT(ASCP)
 Mercy Medical Center
 Dunes Medical Laboratories
 350 W Anchor Dr
 Dakota Dunes SD 57049
 phone-712-279-2768
 robin...@mercyhealth.com
 
 
  CHRISTIE GOWAN christiego...@msn.com 10/6/2011 7:44 AM 
 
 I agree with you Jan. In my 30 + years as a histotech (yes, I am old too) I 
 have seen floaters come from a variety of places but I am hard pressed to 
 remember any floater coming from the water bath. Today we are blessed with 
 DNA fingerprinting to determine if the floater is or is not from the patient 
 but that still does not address the real issue of where did it come from and 
 how do we stop it. The vendors stating that it is not an issue have never 
 been re-biopsied because of a floater in with their tissue. Good discussion 
 and long overdue. I look forward to the day when it is no longer an automatic 
 response from all involved that it is Histology's fault. Hope you are 
 enjoying your new adventures in retirement. See you next year in Canada!
  
 
  From: mamaw...@hotmail.com 
  To: histonet@lists.utsouthwestern.edu 
  Date: Wed, 5 Oct 2011 14:11:25 -1000
  Subject: [Histonet] (no subject)
  
  
  Hello everyone,After being home from the NSH for a few weeks I have been 
  pondering an issue that I think bears discussion on the histonet.There have 
  been several papers published regarding floaters and the amount 
  determined to come from traditional staining buckets. There was also a 
  poster presented at the NSH this year on the subject.When I approached 
  several vendors of HE stainers about this issue. The answers were 
  surprisingly pretty much the same. It is not an issue! Now I understand how 
  one company can make this claim as their stainer uses fresh stain on each 
  slide. The explanations from the other companies were insulting and just 
  plain did not make sense to me. I was told by a Histo tech vendor that All 
  Histo techs know that floaters come from the water bath. Well, she was 
  talking to a histo tech and I know for a fact that floaters come from a 
  variety of places. I have seen them from the doctor's office or procedure 
  room to the stainer and every step in between. Sometimes if the floater 
  is in the block it is very difficult to determine where it originated. We 
  can however eliminate the water bath and stainer as the origin in these 
  cases. One company told me that the design of the solution bottle 
  eliminated floaters because floaters float and their stainer draws 
  solutions from the bottom of the bottle. I have probably changed thousands 
  of staining dishes during my 40+ year career (yes, I am old) and I have 
  seen lots of little pieces of tissue at the bottom of the staining dishes. 
  So, no, not all floaters float. I would love to hear feedback from others 
  on this. I guess I would appreciate feedback about the floater issue as 
  well as how a few vendors can make such claims and expect Histology techs 
  to buy it. I really felt that a few comments were insulting to our 
  profession and to the knowledge and expertise we possess. JanOmaha 
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RE: [Histonet] Tissue left in processor

2011-10-06 Thread Janice Mahoney

I agree with Rene, as long as the temp is only a few degrees above the melting 
point of the paraffin.Jan,Omaha

 Date: Thu, 6 Oct 2011 07:13:54 -0700
 From: rjbu...@yahoo.com
 To: histonet@lists.utsouthwestern.edu; rchar...@pa.gov
 Subject: Re: [Histonet] Tissue left in processor
 CC: 
 
 I do not think that a well fixed, well processed tissue left in molten 
 paraffin for 2 hours after the processor finished will have any adverse 
 outcome.
 René J.
 
 --- On Thu, 10/6/11, Charles, Roger rchar...@pa.gov wrote:
 
 
 From: Charles, Roger rchar...@pa.gov
 Subject: [Histonet] Tissue left in processor
 To: Histonet (histonet@lists.utsouthwestern.edu) 
 histonet@lists.utsouthwestern.edu
 Date: Thursday, October 6, 2011, 10:05 AM
 
 
 Hi All,
 Is there any standard on how long tissue cassettes can remain in the 
 processor after processing before the tissue is subjected to unwanted 
 outcomes?  And if so  what type of artifacts can one expect from tissue that 
 was in the processor in molten paraffin for 2 hours after the processing was 
 completed?
 Thanks so much.
 Roger
 
 Roger Charles| Microbiologist II
 Pennsylvania Veterinary Laboratory
 2305 North Cameron Street | Harrisburg, PA 17110
 Phone: 717.787.8808 | Fax: 717.772.3895
 www.agriculture.state.pa.ushttp://www.agriculture.state.pa.us
 
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[Histonet] (no subject)

2011-10-05 Thread Janice Mahoney

Hello everyone,After being home from the NSH for a few weeks I have been 
pondering an issue that I think bears discussion on the histonet.There have 
been several papers published regarding floaters and the amount determined to 
come from traditional staining buckets.  There was also a poster presented at 
the NSH this year on the subject.When I approached several vendors of HE 
stainers about this issue.  The answers were surprisingly pretty much the same. 
  It is not an issue!  Now I understand how one company can make this claim as 
their stainer uses fresh stain on each slide.  The explanations from the other 
companies were insulting and just plain did not make sense to me.  I was told 
by a Histo tech vendor that All Histo techs know that floaters come from the 
water bath.  Well, she was talking to a histo tech and I know for a fact that 
floaters come from a variety of places.  I have seen them from the doctor's 
office or procedure room to the stainer and every step in between.  Sometimes 
if the floater is in the block it is very difficult to determine where it 
originated.  We can however eliminate the water bath and stainer as the origin 
in these cases.  One company told me that the design of the solution bottle 
eliminated floaters because floaters float and their stainer draws solutions 
from the bottom of the bottle.  I have probably changed thousands of staining 
dishes during my 40+ year career (yes, I am old) and I have seen lots of little 
pieces of tissue at the bottom of the staining dishes.  So, no, not all 
floaters float.  I would love to hear feedback from others on this.  I guess I 
would appreciate feedback about the floater issue as well as how a few vendors 
can make such claims and expect Histology techs to buy it.  I really felt that 
a few comments were insulting to our profession and to the knowledge and 
expertise we possess. JanOmaha
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RE: [Histonet] Slide/Block Retention

2011-10-03 Thread Janice Mahoney

CAP standard is 10 years for tissue blocks.  I would caution not keeping them 
for that period for several reasons.  One is that it may put you in a bad 
position regarding legal cases.  You could be asked why you don't follow the 
most strict standard and be expected to explain why.  The second is for 
subsequent patient care.  When Her-2 first come on the scene we were pulling 
blocks from cases older than 2 years old.  You never know what new 
prognostic/predictive markers will appear on the scene.  If you don't have the 
original tumor material you may be doing your patients a disservice.  If I had 
blocks at your institution I would want to keep them myself rather than have 
them destroyed.Jan M.Omaha

 Date: Mon, 3 Oct 2011 07:00:51 -0700
 From: rjbu...@yahoo.com
 To: histonet@lists.utsouthwestern.edu; mjdess...@wvhcs.org
 Subject: Re: [Histonet] Slide/Block Retention
 CC: 
 
 We keep our blocks 9 years.
 René J.
 
 --- On Mon, 10/3/11, Dessoye, Michael J mjdess...@wvhcs.org wrote:
 
 
 From: Dessoye, Michael J mjdess...@wvhcs.org
 Subject: [Histonet] Slide/Block Retention
 To: histonet@lists.utsouthwestern.edu
 Date: Monday, October 3, 2011, 9:50 AM
 
 
 Hello Histonet,
 
 What policy is everyone following for slide and block retention?  We are
 not CAP, however we currently keep slides and blocks for 10 years.  My
 director wants to decrease that period to 2 years, which is the Joint
 Commission standard.  I would like to keep 10 years because we
 frequently are asked to send slides for consult and review that are
 several years old.  It is also helpful when looking for hard-to-find
 control tissue.  However these reasons are apparently not sufficient.  
 
 I'm leaning towards keeping the 10 year policy, but I need additional
 justification.  Or does anyone think the 2 year period is sufficient?
 
 Thanks,
 Mike
 
 Michael J. Dessoye, M.S. | Histology Supervisor | Wyoming Valley Health
 Care System | mjdess...@wvhcs.org mailto:mjdess...@wvhcs.org  |
 575 N. River Street | Wilkes Barre, PA 18764 | Tel: 570-552-1485 | Fax:
 570-552-1526 
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