Re: [Histonet] RE: sections not sticking to charged slides

2015-02-25 Thread histot...@imagesbyhopper.com
We follow the same process as Jeff.

Michelle



On Feb 24, 2015, at 4:59 PM, Jeffrey Robinson 
jrobin...@pathology-associates.com wrote:

HI Renee-  I had a major problem in the past with tissue staining for IHC 
lifting off the slides no matter what I tried.  It turned out that when we 
precut our controls and put them in the oven and then used them later for the 
patient tissue that the charge on the slide was altered.  We currently still 
precut controls on control slides (we use Leica APEX) and then let them just 
air dry with no heat.  We then use those slides when needed and add the patient 
tissue to the bottom and then put the slides in the oven (we use 70C for one 
hour) prior to IHC staining.  The tissue lifting decreased dramatically- even 
on breast tissue.  Be sure to pick up your controls from the wrong (label) end 
when picking up your controls and do not let the bottom half of the slide get 
into the waterbath so as to avoid double-dipping which can also cause tissue 
adherence problems.

Jeff Robinson, Senior Histotechnologist, Sierra Pathology Lab, Clovis, CA.

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Renee H. Workman
Sent: Tuesday, February 24, 2015 1:33 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] sections not sticking to charged slides


Help, sections not sticking to charged slides.  We use Mercedes Medical charged 
slides.  Lately have been using sta-on but still have occasional problems 
especially during antigen retrieval.  I need any suggestions.

Renee H. Workman
Histology Supervisor
Virginia Urology
9105 Stony Point Drive
Richmond, VA  23235
W: 804-527-1316 | F: 804-270-0917
rhwork...@uro.com | www.uro.com





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Re: [Histonet] Requirements that tissue cassette storage cabinets be off floor

2015-02-09 Thread histot...@imagesbyhopper.com
I agree with Sheila.  At our place, it was fire code that everything be off the 
ground by 6... not just blocks, but anything being stored.

Michelle

Sent from my iPhone

On Feb 9, 2015, at 1:30 PM, Tapper, Sheila J. 
sheila.tap...@essentiahealth.org wrote:

In my experience, this is usually a local fire code requirement.

Sheila

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Debra Siena
Sent: Monday, February 09, 2015 11:35 AM
To: 'histonet@lists.utsouthwestern.edu'
Subject: [Histonet] Requirements that tissue cassette storage cabinets be off 
floor

Hi Histonetters-

Can anyone tell me if it is a JCAHO, CAP or CLIA requirement that tissue 
cassette storage cabinets be at least 6 inches off the floor? Also, If 
possible, could you tell me how I could find this informaiton?  Any information 
is appreciated, thanks for your help in advance.



 Debbie Siena, HT(ASCP)QIHC
StatLab Medical Products
Technical Support Manager
407 Interchange Street | McKinney, TX 75071
t: 800.442.3573 ext. 229 | f: 972.767.3992 dsi...@statlab.com 
mailto:bbro...@statlab.com%7C | www.statlab.comhttp://www.statlab.com/


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Re: [Histonet] Frozen Sections

2015-02-07 Thread histot...@imagesbyhopper.com
We provide assistance, primarily on the outpatient frozens, but help with 
in-patient ones as well.

What makes you ask?

Michelle

Sent from my iPhone

On Feb 6, 2015, at 10:37 PM, lsmal...@juno.com lsmal...@juno.com wrote:

Hi, I need to ask Histoland a questionHow many HT departments provide 
assistance to the pathologist in the performance of frozen sections (cutting 
and staining of slides) to be evaluated by the pathologist?   Thank you very 
much in advance!  
Lorraine


Fast, Secure, NetZero 4G Mobile Broadband. Try it.
http://www.netzero.net/?refcd=NZINTISP0512T4GOUT2

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Re: [Histonet] Re: Embedding

2015-01-21 Thread histot...@imagesbyhopper.com
We also use the para-trimmer. In my view, it is worth its weight in gold!  I 
can melt 5 blocks at a time, works like a charm.  I am one who does not mind 
the wax on the sides, as I am most confident that there is enough paraffin to 
support the cassette.

Michelle

Sent from my iPhone

On Jan 21, 2015, at 11:41 AM, Morken, Timothy timothy.mor...@ucsf.edu wrote:

I agree. We got one of these a couple years ago and the techs love it.  It is a 
heated block on which you rub the cassette. The paraffin melts away. It is 
especially good for preserving barcodes (but don't press the printed surface on 
the heat block too long - you can soften the print and cause some damage, but 
nothing like can happen with scraping).

Tim Morken
Supervisor, Histology, Electron Microscopy and Neuromuscular Special Studies
UC San Francisco Medical Center
San Francisco, CA

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-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Goins, Tresa
Sent: Wednesday, January 21, 2015 8:29 AM
To: gayle.cal...@bresnan.net; histonet@lists.utsouthwestern.edu
Subject: RE: [Histonet] Re: Embedding

I agree with Gayle.  We finally purchased a trimmer from Ted Pella - lowest 
price by far - and are saving our finger joints.  The amount of wax remaining 
on the cassette also appears to depend on the brand of mold used.

Tresa

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Gayle Callis
Sent: Wednesday, January 21, 2015 9:11 AM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Re: Embedding

After years of never winning the battle of paraffin on cassette edges after 
embedding,  we purchased a paraffin block trimmer.  It saves time and the 
stress on finger joints compared to scraping cassettes daily.  No matter how 
careful we were during embedding to keep excess paraffin off cassette edges,
we were never successful.   Several vendors have these and you may be able
to find a refurbished one.   



Gayle M. Callis

HTL/HT/MT(ASCP)

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[Histonet] Tesr

2015-01-09 Thread histot...@imagesbyhopper.com
Please disregard 

Sent from my iPhone

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Re: [Histonet] Automatic H E slide stainer recommendations

2015-01-09 Thread histot...@imagesbyhopper.com
I second the Leica XL.  That stainer is a reliable workhorse.

Sent from my iPhone

On Jan 7, 2015, at 8:08 PM, ian bernard ian.bern...@comcast.net wrote:

The Leica Autostainer XL has proven effective for our lab.

IRB

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu 
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Conway, Carla
Sent: Tuesday, January 06, 2015 2:24 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Automatic H  E slide stainer recommendations

Hello colleagues,

I would appreciate any recommendations for an automatic slide stainer. It will 
primarily be used for H  E staining, not IHC.

Thanks in advance,

Carla







Carla Conway
Histology Technician
Western Fisheries Research Center, USGS
6505 N.E. 65th Street
Seattle, WA 98115-5016 USA
Phone: 206-526-2042
Fax: 206-526-6654
E-mail: cmcon...@usgs.gov
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[Histonet] New 88344 CPT code question

2015-01-08 Thread histot...@imagesbyhopper.com
Hello Histonetters :)

With regards to billing for multiplex IHC stains, I have a scenario and 
question.
Scenario: 1 container, 2 blocks, 2 different cocktail IHC stains. Stain1 is 
done on both blocks A1 and A2.  Stain2 is done on block A1.
How would we bill for this?  Would it be 88344X2 - because there are two 
distinct cocktails. OR would it be 88344X1 - because you can only charge one 
per container?

Thanks in advance,
Michelle

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Re: [Histonet] Facility Name on Slides

2012-10-15 Thread histot...@imagesbyhopper.com
Mary, thank you for your reply.  Can you point me to a specific regulation from 
which I can quote?

Thanks!
Michelle


On Oct 15, 2012, at 9:36 AM, MARY T HODGES  hodges...@msn.com wrote:

 The nuber and name of patient as well as the hospital is required
 Sent from my Verizon Wireless BlackBerry
 
 -Original Message-
 From: Jesus Ellin jel...@yumaregional.org
 Date: Mon, 8 Oct 2012 23:40:37 
 To: histot...@imagesbyhopper.com
 Cc: histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Facility Name on Slides
 
 
 To my knowledge there is no regulation rather than having 2 identifiers,, 
 
 Sent from my iPad
 
 On Oct 8, 2012, at 1:46 PM, histot...@imagesbyhopper.com 
 histot...@imagesbyhopper.com wrote:
 
 Does anyone have any regs that you can point me to for both Joint Commission 
 and CAP which details definitively whether or not a facility name is 
 *required* to be included on slides? 
 
 I know it's a good idea, the larger question here is whether or not there is 
 a specific regulation for it?
 
 Thanks for all your help!
 Michelle
 
 
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Re: [Histonet] Reprocess Procedure

2012-10-15 Thread histot...@imagesbyhopper.com
Once the block has been faced, we melt the excess paraffin from around the 
tissue, being careful not to seal the exposed tissue in paraffin. We remove the 
tissue from it's embedded cassette, put it in a newly numbered cassette and 
place it in the processor for reprocessing. 

Works well in our lab!


On Oct 15, 2012, at 3:41 PM, kira...@sbcglobal.net wrote:

 Thank you for your input. I would like to know how others are handling 
 reprocess.
 Kiran
 Sent from my Verizon Wireless BlackBerry
 
 -Original Message-
 From: Grantham, Andrea L - (algranth) algra...@email.arizona.edu
 Sender: histonet-boun...@lists.utsouthwestern.edu
 Date: Mon, 15 Oct 2012 15:28:21 
 Cc: histonet@lists.utsouthwestern.eduhistonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Reprocess Procedure
 
 A few years ago this subject was discussed on histonet and somebody - I think 
 it was Joe the Toe - said that they just melted the paraffin away from the 
 tissue if it had been embedded and threw it back in to process with the next 
 batch of tissues. The theory being that the part of the tissue that was 
 processed ok was protected by the paraffin and the part that needed 
 additional processing was exposed. I don't have to reprocess often but when I 
 was gone a student had a problem with the processor and put in an emergency 
 call to me. I told her to do this and the tissues came out fine the next day.
 
 
 
 
 Andrea Grantham, HT (ASCP)
 Senior Research Specialist
 University of Arizona
 Cellular and Molecular Medicine
 Histology Service Laboratory
 P.O.Box 245044
 Tucson, AZ 85724
 
 algra...@email.arizona.edumailto:algra...@email.arizona.edu
 Tel: 520.626.4415 Fax: 520.626.2097
 
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[Histonet] Facility Name on Slides

2012-10-08 Thread histot...@imagesbyhopper.com
Does anyone have any regs that you can point me to for both Joint Commission 
and CAP which details definitively whether or not a facility name is *required* 
to be included on slides? 

I know it's a good idea, the larger question here is whether or not there is a 
specific regulation for it?

Thanks for all your help!
Michelle


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Re: [Histonet] RE: back up cryostat

2012-09-21 Thread histot...@imagesbyhopper.com
We have two back ups!  :)

We also have back up tissue processors and microtomes as well.

Sent from my iPhone

On Sep 21, 2012, at 8:15 AM, Manfre, Philip philip_man...@merck.com wrote:

 If you use anything often enough, it is wise to have a back-up, if possible. 
 Microtomes, and especially cryostats, tend to malfunction without warning and 
 can leave you stranded. We have a back-up that isn't ours, but we have 
 access to it.  That's another option.  Make friends with someone else who has 
 one and strike an arrangement with them.
 
 Philip Manfre, BA, HT(ASCP)
 Associate Principal Scientist
 Merck Research Laboratories
 WP45-251
 PO Box 4
 West Point, PA 19486
 
 215-652-9750
 215-993-0383 (fax)
 philip_man...@merck.com
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
 barbara.cr...@lpnt.net
 Sent: Friday, September 21, 2012 8:07 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] back up cryostat
 
 I would like to know what the consensus is on having a backup cryostat.
 Does anyone have a back up cryostat?
 
 I am nervous about not having a backup cryostat
 
 Antoinette Crill
 TEAM LEADER ANATOMIC PATHOLOGY
 X5451
 
 
 
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[Histonet] Milestone Histos 5

2012-09-20 Thread histot...@imagesbyhopper.com
Does anyone know of a company who buys used Histology equipment and would give 
quotes for used Milestone Histos 5 microwave tissue processors.

Thanks!
Michelle
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Re: [Histonet] (no subject)

2012-09-20 Thread histot...@imagesbyhopper.com
Here are some links for HT/HTL licensure in FL.
 
 
http://ww2.doh.state.fl.us/mqaservices/PractitionerServices.asp
 
 
http://www.doh.state.fl.us/mqa/ClinLab/clp_applications.html
There is a lot of information on that page, not just the application, so you 
might want to spend a few extra minutes looking around.
 
Further down on the page, you can find the link related to the application.  
I've made it easier for you, by including the direct link  here:
http://www.doh.state.fl.us/mqa/ClinLab/ap_licensure.pdf
 
The following URL is one resource for online CEUs.  You can take the classes 
online, print your certificates and mail them in with your application, all on 
the same day!
http://www.4ceuinc.com/home.asp?Profession=1
 
You will need to create a user id (using your email address is an easy way to 
remember your user name!) and password in order to see the next link. 
http://www.4ceuinc.com/courseDetails.asp?CourseId=344
 
This link takes you to the page for NEW FL licensee people.  I would suggest 
you take the online courses, so you can print your certificate at the end


On Sep 20, 2012, at 12:19 PM, Dorothy Glass techman...@yahoo.com wrote:

 What are the steps to applying and receiving a health care license to work in 
 florida for an HT or an HTL? I heard there is also a requirement or different 
 fees to be paid for a position as supervisor.
 Curious in Georgia.
 
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[Histonet] Open Position - Laboratory Supervisor - Pathology

2012-08-28 Thread histot...@imagesbyhopper.com
Please see the following link for more information and online application.

https://uhs.ats.hrsmart.com/cgi-bin/portal/highlightjob.cgi?jobid=75412

Manatee Memorial Hospital, a 319-bed acute care facility is located on the 
banks of the Manatee River in Bradenton, Florida. The hospital has been a major 
provider of quality healthcare in the Tampa Bay Region since 1953. Manatee 
Memorial Hospital has a medical staff of over 500 physicians and the only 
residency program in the county. The spectacular four-story patient tower 
welcomes visitors as they cross over the bridge from Palmetto to Bradenton. The 
hospital offers a comprehensive range of medical services, including 24-hour 
emergency services, cardiac, cardiovascular, surgery, outpatient services, 
women’s and children’s services and orthopedic services, in addition to 
specialty programs in chest pain, a primary stroke center and the only 
pediatric center and Level ll Neonatal Intensive Care Unit in the county. 
Manatee Memorial Hospital currently has a Supervisor- Laboratory Pathology 
position available.

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Re: [Histonet] RE: disposal of formalin

2012-08-18 Thread histot...@imagesbyhopper.com
We use Aldex, neutralize the formalin and dispose of the neutralized gel in the 
biohazard trash. The manufacturer says it can go in regular trash, but we 
choose to put it in biohazard trash.

Michelle

On Aug 17, 2012, at 4:18 PM, Vanessa Perez vpe...@pathreflab.com wrote:

 We use formalex green.  
 http://americanbiosafety.com/PDF/ABS_FXG_Instructions.pdf
 
 is a link to the instructions for it
 
 we also keep a disposal log every time we dump the neutralized formalin down 
 the drain..
 
 Vanessa Perez Garcia
 Histology Supervisor
 Pathology Reference Lab
 210-892-3746
 210-892-3732
 vpe...@pathreflab.com
 
 
 -Original Message-
 From: Johnson, Pamela [mailto:pamela.john...@stjude.org] 
 Sent: Friday, August 17, 2012 3:09 PM
 To: Vanessa Perez; Lake,Debbie; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] RE: disposal of formalin
 
 May I ask what your neutralization protocol is?
 
 Pam Johnson, BS, HT (ASCP)
 Lab Manager
 Veterinary Pathology Core Lab
 St. Jude Children's Research Hospital
 262 Danny Thomas Place
 Memphis, TN  38105-3678
 Office - 901-595-3355
 
 -Original Message-
 From: Vanessa Perez [mailto:vpe...@pathreflab.com]
 Sent: Friday, August 17, 2012 10:25 AM
 To: Lake,Debbie; histonet@lists.utsouthwestern.edu
 Subject: [Histonet] RE: disposal of formalin
 
 We neutralize it and then dump down the drain with tons of running water.
 
 Vanessa Perez Garcia
 Histology Supervisor
 Pathology Reference Lab
 210-892-3746
 210-892-3732
 vpe...@pathreflab.com
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Lake,Debbie
 Sent: Friday, August 17, 2012 10:29 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] disposal of formalin
 
 Would anyone be willing to share how formalin is disposed of at your 
 facility?  Neutralization, disposal off site, etc.  Thank you.
 
 
 
 Debra Lake  MT(ASCP)
 
 Manager Micro, Blood Bank, Pathology
 
 Marion General Hospital
 
 Marion, IN  46952
 
 (765) 660-6521
 
 Fax: (765-651-7330)
 
 
 
 
 
 
 
 
 
 
 
 If you are not the intended recipient(s), you are notified that any 
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Re: [Histonet] Leica CV5030 coverslipper issues

2012-05-22 Thread histot...@imagesbyhopper.com
We do have the Ventana labeled slides, but coverslip them by hand. The issues 
we have are with standard, non-labeled slides

In fairness to both Leica and the repair company we use, it has been a couple 
of months since we have had a real problem. Not sure if that is saying a lot, 
just wanted to be fair.

Michelle

On May 22, 2012, at 5:40 AM, Angela Bitting akbitt...@geisinger.edu wrote:

 If you are using slides with labels (esp. Ventana's), don't think the upgrade 
 will fix it. We tear our hair out most days of the week with our 2 CV5030s. I 
 wish Ventana would just make a coverslipper to use with their labels or 
 change their labels to something thinner. Symphony takes too long to use as a 
 coverslipper.
 
  histot...@imagesbyhopper.com histot...@imagesbyhopper.com 5/21/2012 
  3:30 PM 
 We have the CV5030 and have had *many* issues. I have a graveyard of the 
 composite racks with broken ears on them. The machine has broken racks and 
 slides, thrown coverslips, dropped slides and we kept being told that we just 
 needed adjustments. Later we were told that a new electronics board upgrade 
 would fix the issue. My understanding is that the upgraded board is 
 approximately $4000! 
 
 I love Leica products, but this particular unit has not lived up to their 
 reputation. These issues began almost immediately after purchase and continue 
 5 years later. We keep getting it repaired, but I have told the repair 
 company, it was my position that Leica should have stepped up and replaced 
 the board free of charge given all the issues we have endured!
 
 Michelle
 
 On May 21, 2012, at 3:00 PM, Horn, Hazel V hor...@archildrens.org wrote:
 
  We have a CV5030 coverslipper and we have had a few issues but Leica has 
  been quick to resolve them.  
  
  Hazel Horn
  Supervisor of Histology/Autopsy/Transcription
  Anatomic Pathology
  Arkansas Children's Hospital
  1 Children's Way | Slot 820| Little Rock, AR 72202
  501.364.4240 direct | 501.364.1302 office | 501.364.1241 fax
  hor...@archildrens.org
  archildrens.org
  
  
  
  
  100 YEARS YOUNG!
  JOIN THE PARTY AT
  ach100.org
  
  
  -Original Message-
  From: histonet-boun...@lists.utsouthwestern.edu 
  [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems, 
  Joyce K.
  Sent: Monday, May 21, 2012 1:15 PM
  To: 'Linda'; histonet@lists.utsouthwestern.edu
  Cc: kristy.han...@leica-microsystems.com; 
  jack.ke...@leica-microsystems.com; paul.raimo...@leica-microsystems.com
  Subject: RE: [Histonet] Leica CV5030 coverslipper issues
  
  We've had some issues that were mostly due to operator errors and lack of 
  housekeeping, but they have been very good about correcting the problems.
  
  Joyce Weems
  Pathology Manager
  678-843-7376 Phone
  678-843-7831 Fax
  joyce.we...@emoryhealthcare.org
  
  
  
  www.saintjosephsatlanta.org
  5665 Peachtree Dunwoody Road
  Atlanta, GA 30342
  
  This e-mail, including any attachments is the property of Saint Joseph's 
  Hospital and is intended for the sole use of the intended recipient(s).  It 
  may contain information that is privileged and confidential.  Any 
  unauthorized review, use, disclosure, or distribution is prohibited. If you 
  are not the intended recipient, please delete this message, and reply to 
  the sender regarding the error in a separate email.
  
  
  -Original Message-
  From: histonet-boun...@lists.utsouthwestern.edu 
  [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Linda
  Sent: Monday, May 21, 2012 1:58 PM
  To: histonet@lists.utsouthwestern.edu
  Cc: kristy.han...@leica-microsystems.com; 
  jack.ke...@leica-microsystems.com; paul.raimo...@leica-microsystems.com
  Subject: [Histonet] Leica CV5030 coverslipper issues
  
  Hello Everyone,
  
  
  I purchase a brand new Leica CV5030 coverslipper, which I received at the 
  beginning of February.  I have had non- stop issues with this coverslipper 
  from it throwing slides, coverslips and now the sensor not working properly.
  
  I have emailed Leica several times now requesting a new coverslipper.  If I 
  have this many issues at three months what is it going to do in a year?
  
  The tech service support person has been great with fixing all of the 
  issues.
  
  This is my reply I received from the President, North America, Jack Kenny-
  
  We do not believe that it is appropriate at this point to replace this 
  system.   We will continute to monitor the situation but not upgrade at 
  this time.
  
  
  I am not looking for an upgrade I would just like a new coverslipper that 
  works.
  
  Has anyone else had problems with Leica not replacing defective equipment?  
  Please let me know.  How did you resolve the issue?
  
  Thank you in advance,
  
  
  Linda Dee, BGS, HT(ASCP)
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Re: [Histonet] Cytology Staining

2012-05-22 Thread histot...@imagesbyhopper.com
Is Cyto prep considered a high complexity task?


On May 17, 2012, at 12:59 PM, Yang, Mari my...@emc.org wrote:

 Sheila,
 
 Maybe the inspector was referring to the prep? Many cytology labs use 
 automated staining. If you find out any information, I'd love to know.
 
 Thanks,
 Mari
 
 Mari Yang, MHA, CT(ASCP)CMHTLCM 
 Cytology Supervisor
 Tel: 760.773.2009
 
 P Save a tree, please don't print this e-mail unless you really need to.
 
 Confidentiality Note: The preceding e-mail message (including any 
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 applicable legal privileges, or constitute non-public information. It is 
 intended to be conveyed only to the designated recipient(s). If you are not 
 an intended recipient of this message, please notify the sender by replying 
 to this message and then delete it from your system. Use, dissemination, 
 distribution or reproduction of this message by unintended recipients is not 
 authorized and may be unlawful. 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Sheila Haas
 Sent: Thursday, May 17, 2012 4:22 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Cytology Staining
 
 Hello all. During an inspection yesterday, the inspector made a brief, vague
 reference to cytology staining now being deemed high complexity. Does
 anyone have information and/or a reference for this? 
 I'd appreciate any information anyone could provide.
 Thanks a bunch.
  
 Sheila Haas
 Laboratory Manager
 MicroPath Laboratories, Inc.
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Re: [Histonet] Leica CV5030 coverslipper issues

2012-05-21 Thread histot...@imagesbyhopper.com
We have the CV5030 and have had *many* issues. I have a graveyard of the 
composite racks with broken ears on them. The machine has broken racks and 
slides, thrown coverslips, dropped slides and we kept being told that we just 
needed adjustments. Later we were told that a new electronics board upgrade 
would fix the issue. My understanding is that the upgraded board is 
approximately $4000! 

I love Leica products, but this particular unit has not lived up to their 
reputation. These issues began almost immediately after purchase and continue 5 
years later. We keep getting it repaired, but I have told the repair company, 
it was my position that Leica should have stepped up and replaced the board 
free of charge given all the issues we have endured!

Michelle

On May 21, 2012, at 3:00 PM, Horn, Hazel V hor...@archildrens.org wrote:

 We have a CV5030 coverslipper and we have had a few issues but Leica has been 
 quick to resolve them.  
 
 Hazel Horn
 Supervisor of Histology/Autopsy/Transcription
 Anatomic Pathology
 Arkansas Children's Hospital
 1 Children's Way | Slot 820| Little Rock, AR 72202
 501.364.4240 direct | 501.364.1302 office | 501.364.1241 fax
 hor...@archildrens.org
 archildrens.org
 
 
 
 
 100 YEARS YOUNG!
 JOIN THE PARTY AT
 ach100.org
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems, Joyce 
 K.
 Sent: Monday, May 21, 2012 1:15 PM
 To: 'Linda'; histonet@lists.utsouthwestern.edu
 Cc: kristy.han...@leica-microsystems.com; jack.ke...@leica-microsystems.com; 
 paul.raimo...@leica-microsystems.com
 Subject: RE: [Histonet] Leica CV5030 coverslipper issues
 
 We've had some issues that were mostly due to operator errors and lack of 
 housekeeping, but they have been very good about correcting the problems.
 
 Joyce Weems
 Pathology Manager
 678-843-7376 Phone
 678-843-7831 Fax
 joyce.we...@emoryhealthcare.org
 
 
 
 www.saintjosephsatlanta.org
 5665 Peachtree Dunwoody Road
 Atlanta, GA 30342
 
 This e-mail, including any attachments is the property of Saint Joseph's 
 Hospital and is intended for the sole use of the intended recipient(s).  It 
 may contain information that is privileged and confidential.  Any 
 unauthorized review, use, disclosure, or distribution is prohibited. If you 
 are not the intended recipient, please delete this message, and reply to the 
 sender regarding the error in a separate email.
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Linda
 Sent: Monday, May 21, 2012 1:58 PM
 To: histonet@lists.utsouthwestern.edu
 Cc: kristy.han...@leica-microsystems.com; jack.ke...@leica-microsystems.com; 
 paul.raimo...@leica-microsystems.com
 Subject: [Histonet] Leica CV5030 coverslipper issues
 
 Hello Everyone,
 
 
 I purchase a brand new Leica CV5030 coverslipper, which I received at the 
 beginning of February.  I have had non- stop issues with this coverslipper 
 from it throwing slides, coverslips and now the sensor not working properly.
 
 I have emailed Leica several times now requesting a new coverslipper.  If I 
 have this many issues at three months what is it going to do in a year?
 
 The tech service support person has been great with fixing all of the issues.
 
 This is my reply I received from the President, North America, Jack Kenny-
 
 We do not believe that it is appropriate at this point to replace this 
 system.   We will continute to monitor the situation but not upgrade at this 
 time.
 
 
 I am not looking for an upgrade I would just like a new coverslipper that 
 works.
 
 Has anyone else had problems with Leica not replacing defective equipment?  
 Please let me know.  How did you resolve the issue?
 
 Thank you in advance,
 
 
 Linda Dee, BGS, HT(ASCP)
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 If you have received this message in error, please contact the sender by 
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Re: [Histonet] cassette marker

2011-12-03 Thread histot...@imagesbyhopper.com
I like the StatLab markers.



On Dec 3, 2011, at 1:38 PM, Rathborne, Toni 
trathbo...@somerset-healthcare.com wrote:

Can anyone recommend a marker for using on cassettes? We currently use pencil, 
which sometimes smudges. We've tried a few markers already, but some fade, 
while others hold up well for processing, but won't when placed in decalcifier.
Vendors are welcome to respond.
Thanks,
Toni




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promptly delete this message and notify the sender of the delivery error
by e-mail or you may call Somerset Medical Center's computer Help Desk
at 908-685-2200, ext. 4050.

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Re: [Histonet] Difference between Neutral Buffered Formalin 10% and NB formaldehyde 3.7 to 4%

2011-10-08 Thread histot...@imagesbyhopper.com
Wow. Just Wow!  :o(

Sent from my iPhone

On Oct 5, 2011, at 7:03 PM, Jenny Vega histotech...@gmail.com wrote:

 Ok I want to know the diferrence between Neutral Buffered Formalin 10% and
 NB formaldehyde 3.7 to 4% . I was taugh at college that they were the same
 thing and in the book from Frieda Carson it says that but my supervisor
 swears they are different chemicals. In the laboratory she has used 10%
 neutral buffered formalin all the time, but when we ran out of it  we were
 sent NB formaldehyde 3.7 to 4 %she sent it back and we were sent NB
 formaldehyde 3.7 to 4% once again. She says that 10% NBF is more
 concentrated and pure than 3.7 to 4 % formaldehyde and that the tissues are
 going to  putrefied if they are put in that solution.
 
 Am I wrong or is she wrong? thanks
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Re: [Histonet] Automatic HE stainer with coverslipper (glass)

2011-09-02 Thread histot...@imagesbyhopper.com
We use the Leica autostainer, bridge  coverslipper. We use the premimum 
coverslips from Fisher and seldom have any issues with them sticking together 
(and we're in FL!)

Does anyone have issues with the coverslipper breaking off the ears on the 
grey/black racks?  I have a cupboard graveyard for my broken racks.  :o(

Michelle

Sent from my iPhone

On Sep 2, 2011, at 5:48 AM, Bartlett, Jeanine (CDC/OID/NCEZID) j...@cdc.gov 
wrote:

 We use high quality slides from Mercedes Medical with no problems at all. We 
 also use traditional slidesno rounded corners and have no problems.
 
 Jeanine Bartlett
 Infectious Diseases Pathology Branch
 (404) 639-3590 
 jeanine.bartl...@cdc.hhs.gov
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Fleming, 
 Jackie M
 Sent: Thursday, September 01, 2011 4:41 PM
 To: Bea DeBrosse-Serra; 'Ernestine Middleton'; 
 histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Automatic HE stainer with coverslipper (glass)
 
 Must use the Leica coverslips - OR it's a lot of downtime!
 Stainer is slower than we had hoped, but we have a really high volume.
 Great service!
 
 Jackie Fleming HT ASCP
 Allina Medical Laboratries
 Histology Technical Consultant
 phone: 612-863-4773
 pager: 612-654-2135
 
 
 From: histonet-boun...@lists.utsouthwestern.edu 
 [histonet-boun...@lists.utsouthwestern.edu] on behalf of Bea DeBrosse-Serra 
 [bdebrosse-se...@isisph.com]
 Sent: Thursday, September 01, 2011 3:38 PM
 To: 'Ernestine Middleton'; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Automatic HE stainer with coverslipper (glass)
 
 Leica...all the way!
 
 Beatrice DeBrosse-Serra HT(ASCP)QIHC
 Isis Pharmaceuticals
 Antisense Drug Discovery
 1896 Rutherford Road
 Carlsbad, CA 92008
 760-603-2371
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Ernestine 
 Middleton
 Sent: Wednesday, August 31, 2011 6:24 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Automatic HE stainer with coverslipper (glass)
 
 Hi;
 Looking and need comments on those of you that are using combination HE 
 stainer with glass coverslipper.
 Thank you.
 
 Ernestine Middleton, Manager,  HT, HTL ,BS ,MPA
 Montefiore Medical Center
 Bronx, New York
 718-920-4157
 emidd...@montefiore.org
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Re: [Histonet] training techs

2011-08-29 Thread histot...@imagesbyhopper.com
Way to go Patsy!! :o)

Sent from my iPhone

On Aug 29, 2011, at 5:36 PM, Patsy Ruegg pru...@ihctech.net wrote:

 Hey Everyone,
 
 
 
 The third tech I trained in the last 3 years just passed her HTL exam last
 Friday, that all makes me feel pretty good.  I just signed an affiliate
 agreement to be a clinical training site for the Histology program at UND
 today, they are sending me another student who will be with me for 2
 semesters.  
 
 
 
 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  mailto:pru...@ihctech.net pru...@ihctech.net
 web site  http://www.ihctech.net www.ihctech.net
 
 
 
 
 This email is confidential and intended solely for the use of the Person(s)
 ('the intended recipient') to whom it was addressed. Any views or opinions
 presented are solely those of the author. It may contain information that is
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 any dissemination, distribution, copying, or other use of this message, or
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Re: [Histonet] peggy wenk comments on HT/HTL practical

2011-08-29 Thread histot...@imagesbyhopper.com
Interestingly, I have never been required to section tissue in a job interview. 
I have worked at four hospitals, three private labs and one research facility 
(hubby moved us around a bit!)

I just recently hired two techs, directly out of school with no real world 
experience. I did ask them to cut some slides for me!  ;o)

Michelle

Sent from my iPhone

On Aug 29, 2011, at 9:05 AM, joelle weaver joellewea...@hotmail.com wrote:

 
 
 I was required to know and understand all this as well. I often have had to 
 perform various aspects on an interview, and had no problems with this.
 Joelle
 
 Joelle Weaver MAOM, BA, (HTL) ASCP
 
 
 From: b-freder...@northwestern.edu
 To: lpw...@sbcglobal.net; mad...@verizon.net; 
 histonet@lists.utsouthwestern.edu
 Date: Mon, 29 Aug 2011 12:35:50 +
 Subject: RE: [Histonet] peggy wenk comments on HT/HTL practical
 CC: 
 
 I remember having to know, regarding Peggy's comment on why a reagent was on 
 a piece of tissue, for my HTL what was going in every step of the retic 
 (oxidation,reduction,toning etc) and believe me it was on the exam. We were 
 taught to know the why from the techs that trained us and had taken the exam. 
 If you chose to ignore what they said, it was on your head.
 
 As to the microtomy during an interview, I'm all for it as I have done it in 
 the past (as an interviewer and interviewee)  and most recently, as we had a 
 tech come in from Romania and how were we to know what she knew? Their 
 program is a CLS degree and she chose histo from that. Great tech by the way- 
 histo is not much different the world over, from what I can see.
 
 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 Lee  Peggy 
 Wenk
 Sent: Sunday, August 28, 2011 6:41 PM
 To: mad...@verizon.net; histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] peggy wenk comments on HT/HTL practical
 
 Now add in a few other things, that I didn't directly mention in the original 
 2006 HistoNet reply.
 
 How many people are now using:
 - automated HE stainers
 - automated special stainers, including IHC stainer
 - automated coverslippers
 - automated microtomes
 - disposable blades
 
 Can you see why nearly everyone passed the practical? If they could cut a 
 half-way decent section (with better microtomes and blades, easier to do), 
 just put the slide on a machine and let the machine stain it. To fail, they 
 basically had to NOT follow a LOT of directions, such as submitting colon for 
 small intestine, submitting autolyzed gall bladder, doing the wrong stain 
 (like doing a Prussian blue for iron, instead of the requested colloidal 
 iron), grossing the tissue too small, microtoming too thick, putting the 
 institution's name on the label, etc. Automation makes it easier to produce 
 better sections and better stains, particularly if someone is a mediocre tech 
 to begin with.
 
 As to whether the person understands the theory when using automated stainers 
 - well, the fact that many of the people submitting the practical could pass 
 the practical but would fail the written - that has been going on since 
 ancient times, when staining was done by hand. They could follow the 
 directions, but didn't know the reasons. Pour on solution A for 5 minutes, 
 pour it off, pour on solution B for 10 minutes, rinse it off, and it's done. 
 No idea what is in solution A or B, or what chemicals are binding to what 
 components in the tissue, etc. Whether someone is doing the stain by hand or 
 by machine, it's up to the person to have the curiosity to find out what is 
 going on. Some people don't have it, and don't feel the urge to learn.
 
 That's one of the reasons I like going to state and national meetings, and 
 reading HistoNet. These people WANT to learn! Hurrah for them! And there are 
 a lot of people in the histology community willing to help people who WANT to 
 learn - answering HistoNet, giving talks at state and national meetings, 
 being a mentor, etc. Hurrah for them too!
 
 Peggy A. Wenk, HTL(ASCP)SLS
 Beaumont Health Systems
 Royal Oak, MI 48073
 
 The above are my opinions and not those of my institution.
 
 -Original Message-
 From: mad...@verizon.net
 Sent: Sunday, August 28, 2011 2:23 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] peggy wenk comments on HT/HTL practical
 
 
The  dropping of the practical was explained so well by Peggy Wenk. I
   never  got  into  the  debate(glad  I  did  not  after  reading Peggys
   comments),  I  would  have argued to keep it.  That said, indeed it is
   outdated.  The  fact  that  we  were  the last to do it I guess speaks
   volumes.  I did struggle getting 

Re: [Histonet] harrasment for humble histotechs

2011-08-27 Thread histot...@imagesbyhopper.com
:o). I'm not even sure I could find my results after all these years and 9 
moves!

I *do* remember how picture perfect those slides had to be though. Tiny air 
bubble=graded down. Folds=forget it. Knife marks=bad.

I did both the HT and the HTL practicals and now new students don't even have 
to submit them.  I didn't cheat, but over the years I saw students attempting 
to cheat. If I saw them, I would remind them that they were to work 
independently, but who knows what they did when I wasn't looking?

Integrity is what you do when no one is looking.



Sent from my iPhone

On Aug 27, 2011, at 3:25 PM, mad...@verizon.net wrote:

 
   Gentle  harrassment.  I  encourage  you to look at you scores for your
   practical  and  written  exam.  Between gigs I am getting my important
   documents  together  and  found my old scores for the HTL, no thte HT,
   however,  both parts of the exam were taken by yours truly.  Never got
   into  the  talk of practical vs no practical.  I do think it si a good
   idea to keep it. Honest techs will be proud to do a practical. Looking
   at  scores  made  me feel good that the next great job is right around
   the corner.
 
   Nick(Rocky) Madary, HT/HTL(ASCP)QIHC
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Re: [Histonet] Returning to Histology-Another Idea Won't Work

2011-08-27 Thread histot...@imagesbyhopper.com
Sorry, I misread, the experience must be within the last 10 years.

Michelle

Sent from my iPhone

On Aug 27, 2011, at 1:45 PM, Lee  Peggy Wenk lpw...@sbcglobal.net wrote:

 It looks like the time limits prohibit me from trying this, since I did it 
 so long ago
 
 What is IT? What is prohibiting you from taking the HTL exam? What does 
 having taken and passed the HT exam have to do with taking the HTL exam?
 
 Sorry, I'm really lost as to what you need, and how to help you.
 
 Peggy A. Wenk, HTL(ASCP)SLS
 Beaumont Hospital
 Royal Oak, MI 48073
 
 The above response reflects my opinion, and not the hospital's view.
 
 -Original Message- From: Paula
 Sent: Thursday, August 25, 2011 3:31 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Returning to Histology-Another Idea Won't Work
 
 I thought it might be good to study and try for the HTL (already have school 
 for HT and am certified) but it looks like the time limits prohibit me from 
 trying this, since I did it so long ago. Anyone else have any ideas? I'd 
 gladly buy the books and study. Cannot get into a lab here in NC without 
 current experience. The closest school is in western NC, about 5 hours away. 
 I didn't see anything near me in Raleigh. I was going to purchase the 
 textbooks but now I see this won't work either:
 
 Histotechnologist, HTL(ASCP)
 
 Application Fee: $210
 
 To be eligible for this examination category, an applicant must
 satisfy the requirements of at least one of the following routes:
 
 Route 1: Baccalaureate degree from a regionally
 accredited college/university with a combination of 30 semester hours
 (45 quarter hours) of biology and chemistry AND successful completion of
 a NAACLS accredited Histotechnician or Histotechnology program within
 the last 5 years; OR
 
 Route 2: Baccalaureate degree from a regionally
 accredited college/university with a combination of 30 semester hours
 (45 quarter hours) of biology and chemistry AND one year full time
 acceptable experience in a histopathology (clinical, veterinary,
 industry or research) laboratory in the U.S., Canada or an accredited
 laboratory* within the last ten years.
 
 *laboratory accredited by a CMS approved accreditation organization (i.e., 
 AABB, CAP, COLA, DNV, The Joint Commission, etc.)
 
 Clinical Laboratory Experience
 
 To fulfill the experience requirement for the Histotechnologist
 examination, you must have experience, within the last ten years, in the
 following areas:
 
 Fixation
   Microtomy
   Processing
   Staining Any ideas? I have posted this before, but I keep on trying!
 
 Paula
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Re: [Histonet] Returning to Histology-Another Idea Won't Work

2011-08-27 Thread histot...@imagesbyhopper.com
10 years experience to qualify for taking the exam?  Is that an ASCP 
requirement?  It sounds like they might be exchanging experience for the 
bachelor's degree?  Have you checked out the online courses?  I believe there 
are some that offer the bachelor's degree.

Michelle

Sent from my iPhone

On Aug 27, 2011, at 1:45 PM, Lee  Peggy Wenk lpw...@sbcglobal.net wrote:

 It looks like the time limits prohibit me from trying this, since I did it 
 so long ago
 
 What is IT? What is prohibiting you from taking the HTL exam? What does 
 having taken and passed the HT exam have to do with taking the HTL exam?
 
 Sorry, I'm really lost as to what you need, and how to help you.
 
 Peggy A. Wenk, HTL(ASCP)SLS
 Beaumont Hospital
 Royal Oak, MI 48073
 
 The above response reflects my opinion, and not the hospital's view.
 
 -Original Message- From: Paula
 Sent: Thursday, August 25, 2011 3:31 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Returning to Histology-Another Idea Won't Work
 
 I thought it might be good to study and try for the HTL (already have school 
 for HT and am certified) but it looks like the time limits prohibit me from 
 trying this, since I did it so long ago. Anyone else have any ideas? I'd 
 gladly buy the books and study. Cannot get into a lab here in NC without 
 current experience. The closest school is in western NC, about 5 hours away. 
 I didn't see anything near me in Raleigh. I was going to purchase the 
 textbooks but now I see this won't work either:
 
 Histotechnologist, HTL(ASCP)
 
 Application Fee: $210
 
 To be eligible for this examination category, an applicant must
 satisfy the requirements of at least one of the following routes:
 
 Route 1: Baccalaureate degree from a regionally
 accredited college/university with a combination of 30 semester hours
 (45 quarter hours) of biology and chemistry AND successful completion of
 a NAACLS accredited Histotechnician or Histotechnology program within
 the last 5 years; OR
 
 Route 2: Baccalaureate degree from a regionally
 accredited college/university with a combination of 30 semester hours
 (45 quarter hours) of biology and chemistry AND one year full time
 acceptable experience in a histopathology (clinical, veterinary,
 industry or research) laboratory in the U.S., Canada or an accredited
 laboratory* within the last ten years.
 
 *laboratory accredited by a CMS approved accreditation organization (i.e., 
 AABB, CAP, COLA, DNV, The Joint Commission, etc.)
 
 Clinical Laboratory Experience
 
 To fulfill the experience requirement for the Histotechnologist
 examination, you must have experience, within the last ten years, in the
 following areas:
 
 Fixation
   Microtomy
   Processing
   Staining Any ideas? I have posted this before, but I keep on trying!
 
 Paula
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Re: [Histonet] Cleanser for blades/instruments

2011-08-26 Thread histot...@imagesbyhopper.com
Liquinox and bleach soulution works for us.

Michelle

Sent from my iPhone

On Aug 26, 2011, at 6:24 PM, Jeter, Brent brent.je...@gwu-hospital.com 
wrote:

 Histonetters,
 
 Can anyone recommend a good cleanser for soaking scissors/blades/instruments?
 
 Thanks in advance -
 
 Brent Jeter
 Anatomic Pathology Supervisor
 The George Washington University Hospital
 202-715-5076 (phone)
 202-715-4691 (fax)
 brent.je...@gwu-hospital.comhttps://mail.uhsinc.com/owa/redir.aspx?C=2e2500d5f8774abea919776f9edf4c8dURL=mailto%3abrent.jeter%40gwu-hospital.com
 
 
 
 UHS Confidentiality Notice:  This e-mail message, including any attachments, 
 is for the sole use of the intended recipient (s) and may contain 
 confidential and privileged information.  Any unauthorized review, use, 
 disclosure or distribution of this information is prohibited.  If this was 
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Re: [Histonet] Cassette Marking Pen

2011-08-22 Thread histot...@imagesbyhopper.com
Statlab pens for both cassettes (when we hand write them) and for slides.

Michelle

Sent from my iPhone

On Aug 22, 2011, at 11:26 AM, Sherwood, Margaret  msherw...@partners.org 
wrote:

 We use the marking pencils, exlusively, for our cassettes and StatLab marker
 pens for our slides. 
 
 
 Peggy Sherwood
 Lab Associate, Photopathology
 Wellman Center for Photomedicine (EDR 214)
 Massachusetts General Hospital
 50 Blossom Street
 Boston, MA 02114-2696
 617-724-4839 (voice mail)
 617-726-6983 (lab)
 617-726-1206 (fax)
 msherw...@partners.org
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of dkb...@chs.net
 Sent: Monday, August 22, 2011 11:16 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Cassette Marking Pen
 
 I know I have seen this thread before, but what marking pens are you using 
 to write on your cassettes?  We are using the KP Marker Plus from Mercedes 
 and haven't had a problem until this shipment.
 
 Debbie M. Boyd, HT(ASCP) l Chief Histologist l Southside Regional Medical 
 Center I 
 200 Medical Park Boulevard l Petersburg, Va.  23805 l T: 804-765-5050 l F: 
 804-765-5582 l dkb...@chs.net
 
 
 
 
 
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Re: [Histonet] Shipping prepared histology slides

2011-08-10 Thread histot...@imagesbyhopper.com
Good gosh, don't tell that to the reference labs who routinely send out 
finished slides!!


Sent from my iPhone

On Aug 10, 2011, at 5:30 PM, b427...@aol.com wrote:

 
 Can someone provide a quick reference to ANYTHING I can use to prove to my 
 EHS that fixed, processed, coverslipped slides are not HAZMAT?
 They insist shipping finished slides cannot be performed by histotechs.  Wha?
 Thanks.
 
 
 
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Re: [Histonet] Re: Knife for trimming paraffin from blocks

2011-08-08 Thread histot...@imagesbyhopper.com
I agree, the Para-Trimmer is the next best thing since sliced bread!  I'll 
never go back to the knife again.

We use lid from one of the Ventana special stains boxes to catch the wax.  I 
have also fashioned a drip tray out of the cardboard boxes that the coverslips 
come in.

We're all McGuyver's at heart, aren't we?  :o)

Sent from my iPhone

On Aug 8, 2011, at 11:14 AM, John Shelley jshel...@sanfordburnham.org wrote:

 Hi All,
 
 I likewise use the Para-trimmer and instead of a specimen cup I just use the 
 top lid of a 1/2 gross microscope slide box. Once filled I just throw away in 
 the trash.
 
 Kind Regards!
  
 John J Shelley
 Senior Research Associate, Histology Core 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Cormier, 
 Kathleen
 Sent: Monday, August 08, 2011 11:04 AM
 To: gayle callis; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Re: Knife for trimming paraffin from blocks
 
 We use the paratrimmer too. What we do for a paraffin catcher is to use
 a specimen cup (I call them urine cups, but whatever) to catch the
 paraffin. When it get fullish, we place in the slide oven to melt the
 paraffin, when melted pour off, and reuse the cup... :)
 
 Kathy Cormier
 Histology Manager
 Charles River Laboratories
 251 Ballardvale Street 
 Wilmington, MA 01887
 Ph: 781-222-6803
 Fax: 978-988-8793
 kathleen.corm...@crl.com
 Accelerating Drug Development. Exactly.
 Notice - This email and any files transmitted with it are confidential
 and may contain privileged and/or proprietary information. You must not
 disclose this message to another party without Charles River's express
 written consent. If you are not the intended recipient you must not
 copy, distribute or use this email or the information contained in it
 for any purpose other than to notify us. If you have received this
 message in error, please notify Charles River immediately, and delete it
 from your system.
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of gayle
 callis
 Sent: Monday, August 08, 2011 10:56 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Re: Knife for trimming paraffin from blocks
 
 You Wrote: 
 
 
 
 I am looking for a stainless steel knife that we use to scrape off the 
 
 paraffin from the embedded blocks.  I could not find the 6 inches size 
 
 knife in any catalog. 
 
 
 
 Thanks in advance
 
 
 
 Mala
 
 
 
 Nirmala Srishan
 
 Histology Supervisor
 
 Holy Name Medical Center.
 
 
 
 
 *
 
 Dear Mala, 
 
 
 
 In the past, we used an old style permanent edge scalpel blade but after
 a
 disaster with one person seirously cutting himself while trimming
 paraffin
 from a block, we purchased a Paratrimmer with a heated, slanted metal
 surface.  This trimmer has made everyone happy by eliminating the
 potential
 for serious injury and does an even better job of getting rid of excess
 paraffin. 
 
 
 
 There are two models sold, one from Thermo Scientific and the other one
 was
 recently spotted on a vendor website. (Sorry, I didn't jot the name
 down).
 The trimmers  are worth the investment to keep you and your employees
 safe
 from nasty cuts, no matter what the knife/blade, etc could be used.  
 
 
 
 The only drawback to the Para Trimmer is the messy paraffin drippings
 have
 to be collected in some separate container that the manufacturer doesn't
 supply.  This is more than a bit annoying.  It seems to me the
 manufacturer
 of these devices would design the trimmer with a paraffin catch tray.  A
 small aluminum baking pan (from grocery store) could be used and
 disposed of
 (not a Green consideration).
 
 
 
 Be safe rather than sorry.  
 
 
 
 Gayle M. Callis 
 
 HTL/HT/MT(ASCP) 
 
 
 
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Re: [Histonet] (no subject)

2011-07-26 Thread histot...@imagesbyhopper.com
Ruthie,
In order to unsubscribe from the list, you must click on the link at the bottom 
of the email, scroll to the bottom of the webpage and enter your email 
requesting to be unsubscribed. You have the power to unsubscribe yourself!

Good Luck!

Michelle

Sent from my iPhone

On Jul 26, 2011, at 12:50 AM, Ruthie Wilson wilsonj...@yahoo.com wrote:

 Please unsubscribe me
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[Histonet] HE protocol question

2011-07-25 Thread histot...@imagesbyhopper.com
Hi Histonetters!

I'm looking for thoughts on preferences/pros/cons between using a progressive 
and a regressive HE on routine daily work.

Which hematoxylins do you prefer (commercially prepared), which eosin?

Anyone have a tried and true protocol for each method?

Thanks!

Michelle

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[Histonet] Recycled alcohol

2011-07-22 Thread histot...@imagesbyhopper.com
Hi Histonetters!

For those who use recycled alcohol, I have a few questions.

Do you use it in your automatic HE stainers?
Are you having any troubles with proper, consistent HE staining?

We are using recycled alcohol, and wish to continue to do so IF we can.  We are 
having issues with our staining - hematoxylin isn't as purple as it should be, 
eosin is way too pink/red. We use recycled alcohol when deparaffinizing and 
running down to water. For the record, we are also using recycled xylene.  
After staining, we use 2 recycled 100s and two fresh 100s. I have increased the 
hem time, decreased the eosin time, adjusted the acid alcohol and bluing... I'm 
tearing my hair out trying to troubleshoot this!  Can anyone help me?

Thanks!
Michelle
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Re: [Histonet] NBF waste disposal

2011-07-22 Thread histot...@imagesbyhopper.com
Sharon,

We use a product called Aldex to neutralize our formalin.  It binds with the 
aldehyde groups and neutralizes them. According to the mfr, you can dispose of 
it in regular trash, but I am more cautious and throw it away in red bag trash.

Michelle

Sent from my iPhone

On Jul 22, 2011, at 1:01 PM, Campbell, Sharon scampb...@celligent.net wrote:

 Happy Friday everyone,
 I am currently researching ways to dispose of NBF waste. I would like to know 
 if you are neutralizing the waste and then putting it down the drain or if 
 you are shipping it off to be handled by another company. I am looking for 
 the best and most cost effective way to handle this waste. We are not in a 
 position to reclaim the formalin as space is not available for the still.
 Thank you for your help on this.
 
 Sharon Campbell
 
 Sharon Campbell HT, HTL (ASCP)
 Histology Supervisor
 
 Celligent Diagnostics, LLC
 106 Venture Blvd.
 Spartanburg, SC  29306
 (864) 583-3850
 
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Re: [Histonet] RE: Assisting with Autopsies

2011-07-20 Thread histot...@imagesbyhopper.com
We do, on average, about 15 autopsies per year.  We have a diener who does them 
for us. The pathologists are present and are often are hands on during the 
autopsy.  Sometimes a lab aide will be there in the mode of a scribe. Our 
histotechs do not participate in autopsies.

Michelle



On Jul 20, 2011, at 6:06 AM, Podawiltz, Thomas tpodawi...@lrgh.org wrote:

 We have always helped with autopsies, just comes with the territory. 
 
 
 
 Tom Podawiltz HT (ASCP)
 Histology Section Head/Laboratory Safety Officer. 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
 susan.wal...@hcahealthcare.com
 Sent: Wednesday, July 20, 2011 3:32 AM
 To: as...@georgetownhospitalsystem.org; histonet@lists.utsouthwestern.edu
 Subject: [Histonet] RE: Assisting with Autopsies 
 
 We are a small hospital and though we no longer do in house autopsies we 
 still had an autopsy assistant.(most prefer to be called this) We always had 
 a pool of people available to do this job. Training as a histotech does not 
 include this job and I have always refused to do it. I know there are techs 
 who do not mind and some who supplement their income doing it but histotechs 
 should not be forced to do them, certainly not free of charge. If enough 
 histotechs in an area stand together and refuse the pathologists will find 
 assistants.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amy Self
 Sent: Tuesday, July 19, 2011 3:12 PM
 To: 'histonet@lists.utsouthwestern.edu'
 Subject: [Histonet] Assisting with Autopsies 
 
 Hello All,
 
 We are small hospital that does approximately 5-10 autopsies a year.  This 
 being said our administration department does not want to hire a diener to 
 assist with these autopsies. So I have decided to turn to all of you out 
 there in histoland for a little poll.
 
 Does your facility use histotechs or a diener to assist with the autopsy?
 
 
 Thanks in advance for all of your help, Amy
 
 
 Amy Self
 Georgetown Hospital System
 843-527-7179
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Re: AW: [Histonet] Quick Drying Mounting Media

2011-07-14 Thread histot...@imagesbyhopper.com
Have you tried drying them under a blow dryer?  That's how we used to dry our 
slides before we sent them out. It was a commercially available slide dryer.

Michelle

Sent from my iPhone

On Jul 14, 2011, at 3:57 AM, Gudrun Lang gu.l...@gmx.at wrote:

 I think it's more depending on the organic solvent used before
 coverslipping.
 We use butyl acetate in the last trogh in the stainer and in the
 coverslipper. This reagent dries/ evaporates very fast. So after 15 min
 there is hardly a smell of it and we deliver our slides immediately.
 We use Pertex as coverslipping medium.
 
 Gudrun
 Histolab, Akh Linz, Austria
 
 
 -UrsprĂĽngliche Nachricht-
 Von: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] Im Auftrag von Katelin
 Lester
 Gesendet: Mittwoch, 13. Juli 2011 19:42
 An: Histonet
 Betreff: [Histonet] Quick Drying Mounting Media
 
 Hi histonet,
 We have a brand new Leica CV5030 Coverslipper and I am looking for the
 quickest drying media available. We are currently using Micromount by
 Surgipath/Leica and it is not drying fast enough.
 Any suggestions are appreciated as we have to package our slides for
 shipping and the media is either sticking to the bubble wrap or creating
 circles on the slides from the pressure of the bubble wrap.
 
 
 --
 Katelin Lester, HTL
 Gastroenterology Specialists of Oregon, P.C.
 Pathology Laboratory
 (971) 224-2408
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[Histonet] Waste disposal

2011-07-11 Thread histot...@imagesbyhopper.com
For those who use the Ventana IHC and special stainers, how do you dispose of 
the liquid waste that is generated?

Thanks!
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Re: [Histonet] Re: Embedding Media

2011-07-11 Thread histot...@imagesbyhopper.com
Amita,

The paraffin that we use is also a Leica product. It was formerly sold under 
the Surgipath label, but since to companies have merged together, it now sells 
under the Leica name. It is a beaded pellet paraffin and has a version 
suitable for infiltration and a version suitable for embedding.  The box of the 
embedding paraffin suggests it can be utilized for *both* purposes, however we 
do not choose to use it that way.  So yes, we use two different types of 
paraffin.

Hope that helps!
Michelle

On Jul 11, 2011, at 2:07 AM, amitapan...@torrentpharma.com wrote:

 I continuation of same discussion , i would like to have clarification for 
 our lab..we use beaded paraffin Leica Paraplast  both for processing 
 and embedding . Do you advice us to use different paraffin for both steps?
 
 
 Paula, Please share if you get any feed back on Richard Allan product.
 
 Amita
 
 
 From:   Tim Higgins thigg...@cddmedical.com
 To: histonet@lists.utsouthwestern.edu
 Date:   07/08/2011 11:34 PM
 Subject:[Histonet] Re: Embedding Media
 Sent by:histonet-boun...@lists.utsouthwestern.edu
 
 
 
 Hi Paula,
 
 Obviously there are no compression free paraffin's on the market.  Look
 for a paraffin with a higher polymer content, this makes the paraffin 
 firmer
 and less likely to compress.  Other factor for into section compression 
 but
 paraffin is a good place to start.
 
 The higher polymer paraffin's are not as suited for processing, it is more
 for the embedding portion of the process.
 
 Use a paraffin with lower polymers content in the processor and higher for
 embedding and you will like the results.
 
 
 Tim
 
 
 Date: Fri, 8 Jul 2011 09:44:51 -0700
 From: Paula Lucas plu...@biopath.org
 Subject: [Histonet] Embedding Media
 To: histonet@lists.utsouthwestern.edu
 Message-ID: 9251EDA88CA748D6861A0C3BB0E32FCB@biopath.local
 Content-Type: text/plain; charset=us-ascii
 
 Hello,
 
 
 
 We are considering a switch to a different brand of paraffin and this is
 because I feel we are having too many compressions in some of our tissue
 sections.  Currently, we use Tissue Path Paraplast, regular.
 
 
 
 I would like to get feedback from you as to what you prefer.  Looking on
 line, Richard Allan has a product called Signature Series Paraffin that
 comes in a type L that offers compression-free sections and I was also
 hoping to get any feedback on that product.
 
 
 
 I would greatly appreciate any suggestions and thoughts.
 
 Thanks in advance,
 
 Paula
 
 
 
 
 
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Re: [Histonet] Test

2011-07-11 Thread histot...@imagesbyhopper.com
CONGRATS!!!  :-D

Sent from my iPhone

On Jul 11, 2011, at 12:08 PM, sdys...@mirnarx.com wrote:

 So I got married and my name changed (meaning so did my email) tried
 sending out a broad email, but it didn't work.  Just making sure I'm
 updated now =)
 
 Happy Monday all!!
 
 
 
 Sarah Goebel-Dysart, BA, HT(ASCP)
 
 Histotechnologist
 
 Mirna Therapeutics
 
 2150 Woodward Street
 
 Suite 100
 
 Austin, Texas  78744
 
 (512)901-0900 ext. 6912
 
 
 
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Re: [Histonet] Embedding Media

2011-07-08 Thread histot...@imagesbyhopper.com
We use the infiltration  embedding paraffin from Surgipath/Leica and are very 
happy with it.

Michelle

Sent from my iPhone

On Jul 8, 2011, at 12:44 PM, Paula Lucas plu...@biopath.org wrote:

 Hello,
 
 
 
 We are considering a switch to a different brand of paraffin and this is
 because I feel we are having too many compressions in some of our tissue
 sections.  Currently, we use Tissue Path Paraplast, regular.
 
 
 
 I would like to get feedback from you as to what you prefer.  Looking on
 line, Richard Allan has a product called Signature Series Paraffin that
 comes in a type L that offers compression-free sections and I was also
 hoping to get any feedback on that product.
 
 
 
 I would greatly appreciate any suggestions and thoughts.
 
 Thanks in advance,
 
 Paula
 
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Re: [Histonet] Isopropyl alcohol

2011-07-06 Thread histot...@imagesbyhopper.com
Rene,
I was just as surprised!  When we purchased the mw, we were led to believe that 
we could use the recycled alcohol, but I was told later that we should not for 
quality reasons - that recycled is never 100% pure and that water contamination 
will adversely affect the processing.

So, can I use it on my HE stainer without negatively affecting the stain 
quality?

As always, thanks for you thoughts,
Michelle


On Jul 5, 2011, at 11:58 AM, Rene J Buesa rjbu...@yahoo.com wrote:

 First of all, if you recycle correctly your 2-propanol there is no objective 
 reason why you cannot use it in your MW processor, unless your provider wants 
 you to buy your 2-propanol from them.
 René J.
 
 --- On Tue, 7/5/11, histot...@imagesbyhopper.com 
 histot...@imagesbyhopper.com wrote:
 
 From: histot...@imagesbyhopper.com histot...@imagesbyhopper.com
 Subject: [Histonet] Isopropyl alcohol
 To: Histonet@Lists. Utsouthwestern. Edu histonet@lists.utsouthwestern.edu
 Date: Tuesday, July 5, 2011, 10:42 AM
 
 We recycle our isopropyl alcohol. We have been told by our microwave 
 manufacturer that we cannot use the recycled alcohol on the microwave 
 processor.
 
 As a result, I am trying to find additional uses for the recycled isopropyl.  
 Is there any reason why I can't use the iso in place of ethanol when running 
 the slides down to water on the HE stainer? 
 
 Any others uses?
 
 Any input is greatly appreciated!  :o)
 
 Michelle
 
 
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[Histonet] Isopropyl alcohol

2011-07-05 Thread histot...@imagesbyhopper.com
We recycle our isopropyl alcohol. We have been told by our microwave 
manufacturer that we cannot use the recycled alcohol on the microwave processor.

As a result, I am trying to find additional uses for the recycled isopropyl.  
Is there any reason why I can't use the iso in place of ethanol when running 
the slides down to water on the HE stainer? 

Any others uses?

Any input is greatly appreciated!  :o)

Michelle


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Re: [Histonet] Could you please recommend? (Bascaramurty, Saro)

2011-06-29 Thread histot...@imagesbyhopper.com
I second the Leica!  :o)

Michelle

Sent from my iPhone

On Jun 29, 2011, at 1:14 PM, White, Lisa M. lisa.whi...@va.gov wrote:

 We use the Leica CM1850 UV.  It is easy to use for sectioning as well as
 UV decontamination.  Pricing fell in line with other vendors.  I have
 used Shandon, Leitz, Leica and a unit so old I think it came with Noah
 on the boat don't even remember the maker.  Leica is the favorite.  It
 sections well and was the first one that the anti-roll plate would work
 correctly.  It decontaminates well.  No regrets, love it and would
 recommend. 
 
 
 
 Lisa White, HT(ASCP)
 
 Supervisory HT
 
 James H. Quillen VAMC
 
 PO Box 4000
 
 Corner of Veterans Way and Lamont
 
 PLMS 113
 
 Mountain Home, TN 37684
 
 423-979-3567
 
 423-979-3401 fax
 
 
 
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Re: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-28 Thread histot...@imagesbyhopper.com
OMG, 100 blocks/hour?  Seriously?  I am fast , but even I can't touch that!  
That's simply insane!!  :o(



Sent from my iPhone

On Jun 28, 2011, at 6:20 PM, Grantham, Andrea L - (algranth) 
algra...@email.arizona.edu wrote:

 I'd do it - along with Rene's paper which was published and the Canadian 
 paper that was referenced yesterday.
 
 Ask these people - if they would want their child's tissue bx treated in this 
 manner?
 
 They have no clue as to what we do - you might suggest that you put together 
 an inservice for the lab managers on histopathology. Not hard to do using a 
 little power point, you can take your own pictures of the steps that the 
 tissue samples go through. Emphasize that cutting something like a fallopian 
 tube is different than cutting cervix or bone. They might be happy that you 
 are interested enough in providing insight into histopathology. I have 
 something like this that I use often when speaking to service groups and high 
 school students in my community.
 
 If they don't want to consider all that you have to do - look for another job!
 
 I had a problem with the OR people one time so I did a presentation for them 
 on the importance of fixation and I took them through all the steps from 
 patient to slide to pathologist. They were floored because they never thought 
 it was such an involved process, and my tissues were treated much better by 
 the OR staff.
 
 Andi
 
 
 
 On Jun 28, 2011, at 1:49 PM, Stella Mireles wrote:
 
 Joanne is not alone.
 
 The lab I work at has informed us that due to their own research, a single
 histotech should be able to do 100 blocks an hour.
 I'm not sure if they expect embedding, trimming, writing slides, sectioning
 and manual staining in this goal.
 
 I am a seasoned histotech, and have tried to speak to my lab manager and lab
 supervisor, (both are med. techs and have very little insight into what is
 involved in producing a high quality slide), but their goal remains the
 same.
 
 I have an idea:  I feel like printing some of your responses to Joanne
 question and showing them that their goal is unattainable as well.
 
 Any other suggestions.
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Re: [Histonet] How many tissues an histo tech is suppose to cut per

2011-06-25 Thread histot...@imagesbyhopper.com
Not to add fuel and all that... but I can, and regularly do, cut  single slide 
blocks in less than minute per block.  I am not a new tech though, been around 
the microtome a few times!

I think the proper approach would be to have the tech *average* the number of 
slides the cut over a period of time.  Then watch the trend, are you showing 
improvement over time?  I think forward progress is what should be watched for, 
while maintaining quality. Quality is prarmount.

Sent from my iPhone

On Jun 25, 2011, at 6:27 PM, Rittman, Barry R barry.r.ritt...@uth.tmc.edu 
wrote:

 Joanne
 I assume that you are not having us on as this seems a ridiculous goal to set.
 I would ask to look at previous personnel records to determine where the 
 employer managed to find a robot that did this previously and ask  your 
 supervisor to show how he/she cuts one block per minute.
 It is obvious that the time taken to carry out cutting depends to a large 
 extent on the challenge of the tissue blocks.
 It is also obvious that with such an attitude there will be less attention to 
 quality and a greater likelihood of errors occurring.I would point out to 
 management the potential lawsuits that might occur if a mistake is made and I 
 suspect that they have not thought this through at all or are just trying to 
 see how far they can go.
 An alternate solution would be for you to ask for a set sum per block and see 
 their response.
 53 is no age at all kid so hang in there and if you get an unfavorable 
 response from management point out the big job market out there and the 
 severe lack of skilled histotechs.
 My response to them would be more graphic.
 Barry
 
 
 
 
 From: histonet-boun...@lists.utsouthwestern.edu 
 [histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Joanne 
 [joanne0...@comcast.net]
 Sent: Saturday, June 25, 2011 4:50 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] How many tissues an histo tech is suppose to cut per
 
 i've only been working 2 months.  although older, i am new as a histotech 
 (graduated in may 2010, found a job in april 2011).  seems management is 
 setting a goal of a block per minute as far as cutting goes for me.  i have 
 until october to attain this goal. this minute for cutting is to include 
 facing, writing out slides, cutting, and putting tray into symphony stainer 
 (not to mention getting up to answer the phone, fielding questions regarding 
 send-out cases, and other slight cutting interruptions).   this seems an 
 extreme, possibly unattainable goal.  i'm up for a challenge  at age 53, but 
 any advice would be SWONDERFUL :)
 
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Re: [Histonet] Retirement

2011-06-19 Thread histot...@imagesbyhopper.com
And remember mouth pipeting? oops, that's the cotton...

Eating and smoking in the lab was the norm.

Our alcohol had the tax stamp on it!  :o)

Michelle


On Jun 19, 2011, at 4:19 PM, Paula Sicurello pat...@gmail.com wrote:

 Sheesh!  We used to have people smoke while working with propylene oxide.
 
 Eating in your control pigs was part of the benefit of being a
 graduate student to save on grocery money.
 
 Film?  My TEM used glass plates.
 
 Lab mates used to routinely drink diet coke and 100% ethanol on Fridays.
 
 Wearing closed toed shoes was for wimps, you were just fast if you
 dropped a steel wedge blade.
 
 We even wrote using the entire word and proper grammar, none of this
 acronym stuff for us.
 
 Retirement?  What's that?
 
 Paula :-)
 
 On Sun, Jun 19, 2011 at 12:31 PM, Amos Brooks amosbro...@gmail.com wrote:
 Agarose Gels!
... Listen you whipersnapper Agarose is the easy way out. When I learned
 it we used to have to make up our own polyacrylamide gels. That was after
 having to walk to work up hill both ways in 30 feet of snow!
 
 (No nearer retirement)
 Crotchety Amos
 
 
 
 Message: 7
 Date: Fri, 17 Jun 2011 13:24:12 -0400
 From: Emily Sours talulahg...@gmail.com
 Subject: Re: [Histonet] Retirement
 To: histonet@lists.utsouthwestern.edu
 Message-ID: banlktinejxtxyop-byfweuxn3yw-ff3...@mail.gmail.com
 Content-Type: text/plain; charset=UTF-8
 
 Retirement? I think by the time I get to that point, social security will
 have run out.
 Then again, technology will be so advanced, I can tell stories about the old
 days, where I logged on to the bbs by modem to post messages to my friends
 and typed in my own html coding.
 We didn't have google when I was young!! Our cameras used film! And you
 couldn't see how bad your pictures were until you developed that film!!
 There was no PCR to sequence your DNA, you ran an agarose gel and hoped for
 the best!! You could drink the 100% ethanol, there was no denaturing! (okay
 that was before my time) You could smoke in the lab while you sectioned
 without gloves!! (okay that was too)
 
 Emily
 
 A great book should leave you with many experiences, and slightly exhausted.
 You should live several lives while reading it.
 -William Styron
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Re: [Histonet] (no subject)

2011-06-15 Thread histot...@imagesbyhopper.com
Dorothy,

Is your question related to the fact that a protocol will have the currently 
active lot number and you want to use a different lot number?  Or is this a 
brand new antibody that has not been in use before and therefore has not ever 
been validated?

Michelle


On Jun 15, 2011, at 11:41 AM, Dorothy Glass techman...@yahoo.com wrote:

 Dear Histonets, 
 How is it possible to validate a antibody on the Ventana Ultra or XT, when 
 the 
 antibodys afre prediluted or made into a prep-kit?
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Re: [Histonet] Keeping Histo room floor clean?

2011-06-14 Thread histot...@imagesbyhopper.com
We don't keep it off the floor, but do use a wide-bladed putty knife attached 
to a mop handle to scrape the residual wax off the floor. It woks quite nicely 
and doesn't remove the actual floor wax like a razor blade scrapper would.

Michelle

Sent from my iPhone

On Jun 14, 2011, at 6:44 PM, JR R rosenfeld...@hotmail.com wrote:

 
 We keep getting a lot of paraffin on the floor of one histo room--especially 
 around the microtome and the embedding station.
 
 Short of laying down a tarp, what do folks do keep wax off of the floor?
 
 Thanks,
 
 Jerry Ricks
 Research Scientist
 University of Washington
 Department of Pathology
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Re: [Histonet] Submission of tonsils to pathology

2011-06-05 Thread histot...@imagesbyhopper.com
We do micros on every one of them.



On Jun 3, 2011, at 12:13 PM, Horn, Hazel V hor...@archildrens.org wrote:

 Generally all are gross only.  There are some exceptions depending on patient 
 history or if one is significantly larger than the other the pathologists 
 have the discretion to do a microscopic. 
 
 Hazel Horn
 Hazel Horn, HT/HTL (ASCP)
 Supervisor of Autopsy/Histology/Transcription
 Arkansas Children's Hospital
 1 Children's WaySlot 820
 Little Rock, AR   72202
 
 phone   501.364.4240
 fax501.364.3155
 
 visit us on the web at:www.archildrens.org
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rene J Buesa
 Sent: Friday, June 03, 2011 11:11 AM
 To: Histonet; Richard Cartun
 Subject: Re: [Histonet] Submission of tonsils to pathology
 
 Labelled gross only.
 René J.
 
 --- On Fri, 6/3/11, Richard Cartun rcar...@harthosp.org wrote:
 
 
 From: Richard Cartun rcar...@harthosp.org
 Subject: [Histonet] Submission of tonsils to pathology
 To: Histonet histonet@lists.utsouthwestern.edu
 Date: Friday, June 3, 2011, 11:55 AM
 
 
 What is your policy on the submission of tonsils to pathology for examination 
 (gross or microscopic)?  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
 
 
 
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Re: [Histonet] RE: printed requisitions

2011-06-02 Thread histot...@imagesbyhopper.com
We currently use paper reqs, but gasp coming soon, we will be going 
paperless.  I am not sure I am going to like this... ;o). Surgical staff will 
enter the req in the computer, we receive the order  the specimen and enter 
into our AP system.

There are going to be growing pains!!!


Sent from my iPhone

On Jun 2, 2011, at 8:18 AM, Horn, Hazel V hor...@archildrens.org wrote:

 We still use paper reqs.
 
 Hazel Horn
 Hazel Horn, HT/HTL (ASCP)
 Supervisor of Autopsy/Histology/Transcription
 Arkansas Children's Hospital
 1 Children's WaySlot 820
 Little Rock, AR   72202
 
 phone   501.364.4240
 fax501.364.3155
 
 visit us on the web at:www.archildrens.org
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Rathborne, 
 Toni
 Sent: Wednesday, June 01, 2011 3:13 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] printed requisitions
 
 
 Does everyone still receive printed requisitions with your surgical 
 specimens? How many of your OR's have a printer in each room? Our OR has a 
 shared printer for all of the procedure rooms, but would like to have a 
 printer for each OR suite. Our  IT department is saying there would be 
 problems and has suggested that we go paperless. I see many problems arising 
 from this. If anyone is doing this successfully, I'd be very interested in 
 hearing how you accomplished it.
 
 
 Toni
 
 Regards,
 Toni Rathborne
 Pathology Supervisor
 Somerset Medical Center
 110 Rehill Ave.
 Somerville, NJ 08876
 
 
 
 
 CONFIDENTIALITY NOTICE
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 and are intended only for the addressee.  The information contained in this
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Re: [Histonet] RE: Keyboard and mouse covers

2011-06-01 Thread histot...@imagesbyhopper.com
For the keyboard, what about using the silicon style?  A lab near me uses them 
exclusively.  They are easy to keep clean, as they basically watertight - just 
wipe down with a sani-wipe!  And, they are fairly inexpensive - I got one from 
Office Max (or was it Staples?) for $10.



Sent from my iPhone

On Jun 1, 2011, at 1:21 PM, Weems, Joyce jwe...@sjha.org wrote:

 Actually, we put the mouse in a baggie. But the whole thing is covered.  
 
 
 Joyce Weems 
 Pathology Manager 
 Saint Joseph's Hospital 
 5665 Peachtree Dunwoody Rd NE 
 Atlanta, GA 30342 
 678-843-7376 - Phone 
 678-843-7831 - Fax 
 
 
 -Original Message-
 From: Rathborne, Toni [mailto:trathbo...@somerset-healthcare.com] 
 Sent: Wednesday, June 01, 2011 13:19
 To: Weems, Joyce; Dessoye, Michael J; histonet@lists.utsouthwestern.edu
 Subject: RE: Keyboard and mouse covers
 
 Do you completely wrap your mouse? Or do you leave the ball exposed?
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems, Joyce
 Sent: Wednesday, June 01, 2011 1:16 PM
 To: Dessoye, Michael J; histonet@lists.utsouthwestern.edu
 Subject: [Histonet] RE: Keyboard and mouse covers
 
 We use plastic wrap... Easy to change out and keep clean! 
 
 
 Joyce Weems
 Pathology Manager
 Saint Joseph's Hospital
 5665 Peachtree Dunwoody Rd NE
 Atlanta, GA 30342
 678-843-7376 - Phone
 678-843-7831 - Fax 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Dessoye, 
 Michael J
 Sent: Wednesday, June 01, 2011 13:01
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Keyboard and mouse covers
 
 Hi,
 
 We're upgrading our grossing areas with new workstations that require the 
 techs to interact with a keyboard and mouse.  I'd like to get keyboard and 
 mouse covers to protect them from the usual hazards of grossing!  But I can't 
 seem to find any big vendors that sell them...does anyone use them and could 
 recommend a vendor for these covers?  Thanks!
 
 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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 Any views expressed in this message are those of the individual sender, 
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 and/or trade secret information entitled to protection and/or exemption from 
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 distribution, or use of such information is strictly prohibited and may be 
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 and notify the sender of the delivery error by e-mail or you may call 
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 Be sure to visit Somerset Medical Center's Web site - 
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 It may contain 

Re: [Histonet] hematoxylin washed off

2011-05-07 Thread histot...@imagesbyhopper.com
We had a similar thing happen last week, except in our case it was the eosin 
was very pale  the hematoxylin was more blue than purple.  Through our 
troubleshooting steps, we determined it could have only been the processor 
reagents.  We fully changed it and the problem went away. While I am delighted 
that the staining has returned to normal, I have no idea what really happened.

Here are some of my first thoughts:

Have you checked your reagents on the stainer? Same lot numbers, differerent 
lot number? Do you use progressive or regressive technique? If regressive, are 
your differentiating/bluing reagents new since the processor change? Did you 
use new/different reagents on the processor?  Did you wash the bottles/dishes 
with a cleaning solution that, maybe, didn't get fully rinsed out? Or do the 
dishes need stronger cleaning?

Michelle

Sent from my iPhone

On May 7, 2011, at 2:42 AM, V. Neubert histonet.nos...@vneubert.com wrote:

 Is it only the HTX which is pale? Did you change anything else? Like
 dewaxing?
 
 anuradha shrivastava:
 Hello Every body,
 We changed the solutions testerday in the processor, and today Dr. 
 complained about pale hematoxylin. Can u suggest what is wrong.
 thanks.
 anu.
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[Histonet] Florida Law Question

2011-03-29 Thread histot...@imagesbyhopper.com
Hi Histonetters!

Can anyone tell me (maybe even provide a req) as to whether or not a lab aide 
can run the Histos 5 microwave tissue processor?  It's semi-automatic, which 
involves the person (lab aide, tech etc) moving a carousel of cassettes from 
one beaker to another.

Any help is greatly appreciated!

Michelle
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Re: [Histonet] April 1st Fun

2011-03-29 Thread histot...@imagesbyhopper.com
We had a patient we named Oscar Meyer... it was a piece of hot dog that we put 
in formalin, the doc grossed it, we cut it (and it cut very well, I might add!) 
and they got to the point of looking under the scope before they realized the 
joke!  ;o)

Michelle

On Mar 29, 2011, at 2:13 PM, Breeden, Sara sbree...@nmda.nmsu.edu wrote:

 Dead cockroach on autopsy/necropsy table as legitimate specimen;
 goldfish processed as patient Barry Cuda; change family photos to
 total strangers; butterscotch pudding in (unused) specimen jar and
 subsequent tasting with applicator stick; activated charcoal on oculars
 (a la Colonel Potter in MASH); single hair attached to ocular with
 super-glue (tickling nose); cut fingertips off gloves; pumpkin/squash in
 animal shapes to slide; bug in block;
 foam-rubber-stuffed-box-with-toy-rat-to-burst-out-and-cause-startlement
 (toy rat to morph into histo lab mascot complete with appropriate
 holiday costume); process beef jerky as legitimate specimen; light
 coating of oil on 'scope oculars; - and the latest one I just received -
 a small slip of paper on the underside of the (computer's) mouse.  Oh -
 the joy!  What shall I do first?!  Happy Annoying!  This ought to cover
 the last several months I've not done the Friday Hour of Fuming...
 
 
 
 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] Bone marrow charges

2011-02-24 Thread histot...@imagesbyhopper.com
It is my understanding that you may now charge for every stain, even if it's 
two blocks from one bottle.  The CMS requirements changed in Oct of 2009, if 
memory serves correctly.  Perhaps some one else can site the reference or go 
back into the archives for it.  I'm not at my computer, or I would do it myself!

Sent from my iPhone

On Feb 23, 2011, at 10:06 AM, Rathborne, Toni 
trathbo...@somerset-healthcare.com wrote:

 Are your blocks (1 bx and 1 clot) separate specimens, or just one specimen 
 with 2 blocks?
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu]On Behalf Of Goodwin,
 Diana
 Sent: Monday, February 21, 2011 11:40 AM
 To: 'histonet@lists.utsouthwestern.edu'
 Subject: [Histonet] Bone marrow charges
 
 
 Greetings, Histonetters.
 
 How many times can I charge 88313 for a bone marrow case that has an Iron 
 stain on 2 separate blocks (one for the bx and one for the aspirate clot) and 
 also on 1 smear made from the aspirate clot, a PAS on the 2 blocks, a 
 Trichrome and a Retic on the bx. block, and a Wright/ Giemsa on 4 smears?
 
 Thank you!!!
 Diana Goodwin
 Supervisor, Histology Laboratory
 RWJUHHNJ
 
 
 Diana Goodwin
 Supervisor, Histology Laboratory
 xt. 6996
 
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Re: [Histonet] Bacterial contamination

2011-01-27 Thread histot...@imagesbyhopper.com
Another place to check is the holding water that the slides rest in just 
prior to staining.  We run our slides to water on the HE stainer and then 
transfer the rack to a holding water dish.  We bleach this dish nightly, as 
we have found it contaminated in the past.  We don't know what caused the 
contamination, but we have not it since the bleaching started!  ;o)

Good luck!

Michelle


On Jan 27, 2011, at 1:41 PM, bsulli...@shorememorial.org wrote:

 One place you need to look is the floatation bath where you cut your
 slides.
 
 Beatrice Sullivan, HT(A.S.C.P.) HTL , AAS, CLSP(N.C.A.)
 AP Supervisor
 Shore Memorial Hospital
 609-653-3590
 
 
 Speak only well of people and you need never whisper
 
 
 
 Breeden, Sara   
 sbree...@nmda.nm 
 su.eduTo 
 Sent by:  Histonet  
 histonet-bounces@ histonet@lists.utsouthwestern.edu 
 lists.utsouthwest  cc 
 ern.edu   Ragsdale, John
   jragsd...@nmda.nmsu.edu   
   Subject 
 01/27/2011 01:39  [Histonet] Bacterial contamination  
 PM
 
 
 
 
 
 
 
 
 
 My pathologist tells me I have floating bacteria in both special stains
 I did this morning (GMS and Gram); some slides have these floating
 critters and some don't.   Because the only common solutions are those
 for processing and deparaffinization and because these bacteria appear
 to be floating above the plane of the tissue - I can't figure out where
 to start looking.   My DI water is from a central source and is
 routinely quality-checked, and this is a new building (Sep. 2010)  I
 don't want to blame that. Knowing full well that I am probably
 overlooking the obvious, I'm asking for help figuring this out.  I need
 a Sputnik Moment.  Thanks!
 
 
 
 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] Leica autostainer XL

2011-01-26 Thread histot...@imagesbyhopper.com
I have a run set up to bake the slides  run them down to water ( for my 
specials), another just to start at hematoxylin down to xylene etc.  The 
stainer allows for nearly any custom program you can think of. :o)

If you have any questions about how to set the program up, please let me know  
I will be happy to help you with it.

Michelle



On Jan 26, 2011, at 11:52 AM, Langenberg, Stacey 
stacey.langenb...@ucdenver.edu wrote:

 You can set up a just depar run.
 
 Sent from myTouch 4G
 
 - Reply message -
 From: Nicole Tatum nic...@dlcjax.com
 To: histonet@lists.utsouthwestern.edu histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Leica autostainer XL
 Date: Wed, Jan 26, 2011 9:48 am
 
 
 
 Does anyone know if you can just deparaffinize slides in the stainer.
 
 Im just wondering if I also need a small stain line to dewax specials.
 
 Thank you,
 Nicole
 
 
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Re: [Histonet] Lost Blocks

2011-01-08 Thread histot...@imagesbyhopper.com
Our method isn't as technology savvy, but it works well for us.  All blocks 
submitted for processing are written down on our piece sheet. At the end of 
the grossing day, two staff members compare the blocks in the processing basket 
to those listed on the piece sheet. At embedding, the histotech checks off the 
blocks prior to embedding.


On Jan 7, 2011, at 3:25 PM, Patrick Laurie foreig...@gmail.com wrote:

 Here we take a picture of the blocks before they go on the processor.  We
 have a barcoding system that lets me know who embedded what and when.  With
 over 140,000 blocks/year we only have had one instance where a block was
 lost between grossing and embedding.  Because we have some off-site
 pathologists and grossing staff, our lab relies very heavily on tracking
 every specimen that comes in, every block that goes to histology and every
 stained slide that goes to our pathologists.
 
 Good luck, it can be frustrating when you lose a block.
 
 On Fri, Jan 7, 2011 at 9:45 AM, Paula Wilder hist...@hotmail.com wrote:
 
 
 HI all,
 
 Does anyone have a procedure outlining checks and balances to assure blocks
 have been placed on the processor, blocks that are missing, either before or
 after embedding, etc.  Any help would be greatly appreciated!
 Thank you,
 
 Paula Wilder
 St. Joseph Medical Center
 Towson, MD 21204
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 -- 
 Patrick Laurie HT(ASCP)QIHC
 CellNetix Pathology  Laboratories
 1124 Columbia Street, Suite 200
 Seattle, WA 98104
 plau...@cellnetix.com
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Re: [Histonet] Stupid, stupid static!!

2011-01-07 Thread histot...@imagesbyhopper.com
I have a tech who complains about static/compression in our cell blocks, but I 
don't seem to have the same problem as her.  The difference? I face my blocks 
and then soak it on my waterbath for about 15 -30 seconds and then it goes onto 
the ice tray.  The additional moisture that is soaked up in the block seems to 
correct the issue for me.  Sort of like breathing heavily on the block!

Michelle


On Jan 6, 2011, at 4:36 PM, Johnson, Nacaela nacaela.john...@usoncology.com 
wrote:

 I am also having issues with static, but only on my particle blocks.
 This happens in the summer as well.  The static is actually in the
 block.  The core biopsies cut wonderfully.  Does anyone else run into
 this problem?  I can see the effects of the static when I'm embedding,
 the particles float to the edges of the mold instead of in a clump. 
 
 
 Thanks,
 
 Nacaela Johnson
 Histology Technician
 KCCC Pathology
 12000 110th St., Ste. 400
 Overland Park, KS 66210
 Office:  913-234-0576
 Fax:  913-433-7639
 Email:  nacaela.john...@usoncology.com
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of
 sgoe...@mirnarx.com
 Sent: Wednesday, January 05, 2011 1:15 PM
 To: Histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Stupid, stupid static!!
 
 So where the microtome is here that I have to use we have to wear those
 blue hospital booties and disposable lab coats (the white paper type
 ones).  With me and several other people walking around in those booties
 the amount of static electricity is to say the least frusterating!!
 Does anyone know of anything I can do to get rid of the static?
 
 Thanks
 
 
 
 Sarah Goebel, BA, HT(ASCP)
 
 Histotechnologist
 
 Mirna Therapeutics
 
 2150 Woodward Street
 
 Suite 100
 
 Austin, Texas  78744
 
 (512)901-0900 ext. 6912
 
 
 
 
 
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 this message. If received in error, please immediately inform the sender and 
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Re: [Histonet] No Mail??

2010-12-17 Thread histot...@imagesbyhopper.com
Oh man!  The first time Histonet stopped working, I thought it was my email... 
but this time I knew better!  And I too didn't realize how much I looked 
forward to the messages/thoughts/questions shared on this board.

So histonet, what's been causing the problem?


Michelle

On Dec 17, 2010, at 11:29 AM, Harrison, Sandra C. sandra.harris...@va.gov 
wrote:

 Wow...didn't realize how addicted to Histonet I'd become till
 this week!
 
 Sandy Harrison
 Histology Supervisor
 VA Medical Center
 Minneapolis, MN 55417
 612-467-2449
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems,
 Joyce
 Sent: Friday, December 17, 2010 9:54 AM
 To: Behnaz Sohrab; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] No Mail??
 
 And I kept getting a returned msg yesterday that I was trying to post. I
 am experiencing withdrawal!!! :)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 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Behnaz
 Sohrab
 Sent: Friday, December 17, 2010 10:48
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] No Mail??
 
 Any Problem? I have not received any email from Histo-net last few days
 ??
 Behnaz
 
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 not the intended recipient, please delete this message, and 
 reply to the sender regarding the error in a separate email. 
 
 
 
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Re: [Histonet] Cardboard slide flat storage

2010-11-15 Thread histot...@imagesbyhopper.com
Hi Meghan,

We use grey colored boxes that will hold either 8 cardboard drawers of blocks 
or 4 cardboard drawers of slides.  I am at home right now,  don't have the 
specific ordering information, but will share it tomorrow when I get to work.  
I just didn't want to let the question languish w/o some sort of response!

Michelle

On Nov 15, 2010, at 9:30 AM, Meghan Tucker meghan.tuc...@yahoo.com wrote:

 Good morning,
  
 Are there any suggestions on a place to order a storage shelf for cardboard 
 slide flats, which may have 6-8 'cubbies' that can be used to organize the 
 flats?
  
 Thanks!
  
 Meghan
  
 meghan.tuc...@yahoo.com
 
 
 
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Re: [Histonet] Formalin

2010-11-11 Thread histot...@imagesbyhopper.com
Not in Florida either.  We use Aldex to neutralize the formalin  then dispose 
of it on the biohazard trash.  The mfr says once neutralized you can put it in 
regular trash, but we don't.

Michelle


On Nov 11, 2010, at 7:45 PM, jmacdon...@mtsac.edu wrote:

 Absolutely not here in southern California.
 
 
 Sent via BlackBerry by ATT
 
 -Original Message-
 From: godsgal...@aol.com godsgal...@aol.com
 Sender: histonet-boun...@lists.utsouthwestern.edu
 Date: Thu, 11 Nov 2010 17:44:52 
 To: Histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Formalin
 
 Ok, so how many of you are allowed to dump formalin down the drain?
 
 Sent from my Verizon Wireless Phone
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Re: [Histonet] Re: Frozen Section TAT

2010-11-02 Thread histot...@imagesbyhopper.com
We have a calendar book in the frozen section room. The pathologist places the 
patient label on the book on the appropriate date, writes both the start  stop 
times.  I don't count the multiple block ones, but I don't tell them that!  ;o) 
 If they stay in the habit, all the better for me!  Oh yeah, we have a large 
clock on the wall, easy to find, see and read!

Michelle

On Nov 2, 2010, at 5:46 PM, Robert Richmond rsrichm...@gmail.com wrote:

 Some comments on this dismal piece of busy work:
 
 It helps to have a time stamper so the person receiving the specimen
 can stamp the time on the requisition.
 
 A work sheet for each frozen section case makes it easier for the
 pathologist to record the time the report is telephoned, the frozen
 section diagnosis, and other useful information.
 
 A clock by the frozen section microscope is both a reminder and a
 hint, particularly for those of us who don't wear wrist watches in the
 lab.
 
 Turning a single block case around in 20 minutes isn't very difficult.
 The usual cause of delay is a difficult diagnosis where more than one
 pathologist looks at the slides.
 
 There is no TAT requirement for multiple block cases.
 
 Pathologist compliance is a major issue. Some pathologists entirely
 refuse to record TAT. Frozen sections are the highest stress area of
 most pathologists' practice, and it's easy to forget procedural
 details, particularly this one, which is of no benefit to the patient,
 nor to anyone else except the paper-pushers.
 
 Bob Richmond
 Samurai Pathologist
 Knoxville TN
 
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Re: [Histonet] Frozen Section TAT

2010-11-01 Thread histot...@imagesbyhopper.com
Allison, 

I have created an excel spreadsheet where you put time started, time completed 
 it will calculate the amount time spent doing the frozen. It highlights any 
time grater than 20 min.  Let me know if you are interested in something like 
that.

 Michelle



On Nov 1, 2010, at 2:54 PM, Scott, Allison D allison_sc...@hchd.tmc.edu 
wrote:

 Hello to all in histoland.  How is everyone calculating the FS TAT.
 Does any anyone have a file that automatically calculates that tat when
 you plug in the data, that they would be willing to share.  Any help
 would be appreciated.  
 
 Allison Scott
 Histology Supervisor
 LBJ Hospital.
 CONFIDENTIALITY NOTICE:
 If you have received this e-mail in error, please immediately notify the
 sender by return e-mail and delete this e-mail and any attachments from 
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 To the extent the information in this e-mail and any attachments contain 
 protected health information as defined by the Health Insurance Portability 
 and Accountability Act of 1996 (HIPAA), PL 104-191; 45 CFR Parts 160 and 
 164; or Chapter 181, Texas Health and Safety Code, it is confidential and/or 
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Re: [Histonet] eosin

2010-10-22 Thread histot...@imagesbyhopper.com
It sounds like I am in the minority in pitting the eosin in the *first* 100% 
alcohol!  

I agree with Bill, it really makes a HUGE difference in small, minute tissues.  
We did run into one issue though, we were using orange biopsy cassettes and the 
red-orange tissue was difficult to spot in the orange cassettes!  We have since 
switched to an aqua color and no more hiding specimens!  ;o)

Michelle



On Oct 22, 2010, at 10:51 AM, Tench, Bill bill.te...@pph.org wrote:

 I think the use in a processor becomes a local culture.  I think
 everyone in my community does it (someone spread the word), so now we
 all do.  I believe that we are all putting it in the last alcohol.  It
 really makes facing a block on minute pieces a whole lot easier.  We
 found marking the tissue directly tedious, and it didn't persist as well
 in the processing.
  Because there is often so little visible material in our FNA cell
 blocks, we mark the histogel pellet with Davidson ink, and when the tech
 has just faced off the ink, he/she knows its time to start collecting
 sections.
 
 Bill Tench
 Associate Dir. Laboratory Services
 Chief, Cytology Services
 Palomar Medical Center
 555 E. Valley Parkway
 Escondido, California  92025
 bill.te...@pph.org
 Voice: 760- 739-3037
 Fax: 760-739-2604
 
 
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 which it is addressed, and may contain information that is privileged, 
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 distribution, or copying of this e-mail or the information herein by anyone 
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Re: [Histonet] Eosin to dye small Biopsies

2010-10-21 Thread histot...@imagesbyhopper.com
We use about 40ml of eosin in the first 100% alcohol in both of our large 
specimen  small biopsy machines.

Michelle



On Oct 21, 2010, at 4:33 PM, Scott, Allison D allison_sc...@hchd.tmc.edu 
wrote:

 Hello to all in histoland.  Are any of you using eosin on the processor
 to dye your small bx's?  If so, are you putting it in the 100% alcohol
 to do so?  Any help in this matter will be greatly appreciated.
 
 
 Allison Scott HT(ASCP)
 Histology Supervisor
 LBJ Hospital
 Houston, Texas 77026
 CONFIDENTIALITY NOTICE:
 If you have received this e-mail in error, please immediately notify the
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 To the extent the information in this e-mail and any attachments contain 
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 and Accountability Act of 1996 (HIPAA), PL 104-191; 45 CFR Parts 160 and 
 164; or Chapter 181, Texas Health and Safety Code, it is confidential and/or 
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Re: [Histonet] Cassette Marking

2010-10-19 Thread histot...@imagesbyhopper.com
Statlab pens for us.  We have a cassette printer, but we hand write our slides. 
 I *love* the statlab pens!!

Sent from my iPod

On Oct 19, 2010, at 5:26 PM, Sherwood, Margaret  msherw...@partners.org 
wrote:

 Victor,
 
 We are a research lab and don't generate near the amount of specimens that a
 clinical lab would.  We were happy to get an automatic stainer and 
 coverslipper!
 
 Peggy 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Victor Tobias
 Sent: Tuesday, October 19, 2010 4:57 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Cassette Marking
 
 
  I'm somewhat surprised that many labs are still handwriting blocks and 
 slides. If you are using a LIS, can it integrate printing blocks and 
 slides? Is the cost too high to add the printing capability? The cost of 
 equipment is so cheap compared with one lawsuit.
 
 It would also reduce the stress of loosing your job over a labeling 
 mistake. Just seems like a win win for everyone.
 
 Victor
 
 Victor Tobias
 Clinical Applications Analyst
 University of Washington Medical Center
 Dept of Pathology Room BB220
 1959 NE Pacific
 Seattle, WA 98195
 vic...@pathology.washington.edu
 206-598-2792
 206-598-7659 Fax
 =
 Privileged, confidential or patient identifiable information may be
 contained in this message. This information is meant only for the use
 of the intended recipients. If you are not the intended recipient, or
 if the message has been addressed to you in error, do not read,
 disclose, reproduce, distribute, disseminate or otherwise use this
 transmission. Instead, please notify the sender by reply e-mail, and
 then destroy all copies of the message and any attachments.
 
 
 On 10/19/2010 1:38 PM, Sean McBride wrote:
 Nita,
 
 We use HistoTec pens by Newcomer Supply
 
 ~Sean
 
 
 On Oct 19, 2010, at 2:22 PM, Nita Searcy wrote:
 
 ** High Priority **
 
 If you HAVE to manually mark cassettes - what are you using? Cassette pens ?
 Pencils ? What is the rest of the world doing?
 
 Anything else on the market?
 
 Thanks
 
 
 
 Nita Searcy, HT/HTL (ASCP)
 Scott and White Hospital
 Division Manager, Anatomic Pathology
 2401 S. 31st. Street
 254-724-2438
 Temple, Texas, 76502
 nsea...@swmail.sw.org
 
 
 254-724-2438
 
 Nita Searcy.vcf___
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 but does not contain patient information, please contact the sender and 
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Re: [Histonet] Re: Histonet Digest, Vol 83, Issue 20

2010-10-15 Thread histot...@imagesbyhopper.com
Can you please provide the specific CMS update number?  The website doesn't 
seem to be too user friendly ...   thanks!



On Oct 14, 2010, at 12:22 PM, Weems, Joyce jwe...@sjha.org wrote:

 
 CMS/NCCI Update Dated October 1, 2009 
 
 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. 
 
 
 -Original Message-
 From: Mike Pence [mailto:mpe...@grhs.net] 
 Sent: Thursday, October 14, 2010 11:31
 To: Weems, Joyce; histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Re: Histonet Digest, Vol 83, Issue 20
 
 Can you site your source, please.
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Weems, Joyce
 Sent: Thursday, October 14, 2010 10:25 AM
 To: histonet@lists.utsouthwestern.edu
 Subject: RE: [Histonet] Re: Histonet Digest, Vol 83, Issue 20
 
 
 
 
 The change is that you can bill per block now and not per specimen. This is 
 for immunos and special stains. It does make a huge difference! 
 
 Best, 
 
 Joyce Weems
 Pathology Manager
 Saint Joseph's Hospital
 5665 Peachtree Dunwoody Rd NE
 Atlanta, GA 30342
 678-843-7376 - Phone
 678-843-7831 - Fax 
 
 
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Chris Evanish
 Sent: Thursday, October 14, 2010 11:10
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Re: Histonet Digest, Vol 83, Issue 20
 
 Has anyone heard of a cpt coding change that allows us to bill 88342 per 
 slide run instead of per antibody? One of our Pathologist was at a conference 
 and was told that we could do that. It makes a big difference with running 
 cytokeratins on multiple blocks and levels of sentinel nodes.
 
  Thanks,
 Chris Evanish
 Montgomery Hospital
 Norristown PA
 
 Chris D. Evanish
 Histology Supervisor
 Montgomery Hospital
 610-270-2379 
 
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Re: [Histonet] (no subject)

2010-09-30 Thread histot...@imagesbyhopper.com
Sean, what state are you in?  If FL, there is a company called Southern Biomed 
who could probably help you out.

Michelle




On Sep 29, 2010, at 10:28 PM, Sean McBride smcbr...@andrew.cmu.edu wrote:

 Hello everyone,
 
 I have an old Leica RM 2065 microtome that is in need of repair (the
 clutch stopped working), but according to Leica, the machine is no longer
 supported by the company.  Does anyone have any suggestions for a company
 or technician who might be able to repair the machine?
 
 Thanks in advance,
 
 ~Sean
 
 
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Re: [Histonet] Ventana vs Leica

2010-08-26 Thread histot...@imagesbyhopper.com
Unless someone corrects me (or even agrees with me!) in FL only a technologist 
is allowed to load the IHC machine, so no additional lean for us.  :o(

I would be interested to hear more about the savings though, as we are 
preparing to be in the market for a new IHC machine.  We currently have the 
Benchmark XT.



On Aug 26, 2010, at 10:08 AM, Mahoney,Janice A janice.maho...@alegent.org 
wrote:

 We love our Ventana instruments too Jay.  I don't quite believe the 40% 
 difference in cost.  I'd like to see those numbers.  I know I save in tech 
 time and the instruments are very easy to use.  We have histo assistants and 
 secretaries trained to load and unload the instruments, saving out techs to 
 do the things only techs can do.  Talk about LEAN!
 A little more from a LEAN perspective, the Ultra is the only instrument out 
 there that is TRUE continuous flow. As soon as there is an open spot on the 
 instrument and the antibody is on board, I can add a slide.  I don't have to 
 wait till one of the 10 slide modules is finished.  Leica is still a batch 
 instrument, it is just smaller batches than the older IHC models. I'm not 
 putting Leica down, it is a fine instrument but I think it is important for 
 people to know the facts.
 Jan Mahoney
 Omaha
 
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of 
 bsulli...@shorememorial.org
 Sent: Tuesday, August 24, 2010 2:05 PM
 To: Jay Lundgren
 Cc: histonet; histonet-boun...@lists.utsouthwestern.edu
 Subject: Re: [Histonet] Ventana vs Leica
 
 Jay,
 I currently use the Ventana and am very pleased with the results I get.
 The only draw back is the cost to run the instrument. It can get quite
 pricey. They added space on the antibody wheel but took space away from the
 slide area. This has impacted our work flow greatly. We are however looking
 to purchase a second one. This one will have continual through put. That
 should help out with TAT. Hope this helps.
 
 Beatrice Sullivan, HT(A.S.C.P.) HTL , AAS, CLSP(N.C.A.)
 AP Supervisor
 Shore Memorial Hospital
 609-653-3590
 
 
 
 Jay Lundgren
 jaylundg...@gmai
 l.com To
 Sent by:  histonet
 histonet-bounces@ histonet@lists.utsouthwestern.edu
 lists.utsouthwest  cc
 ern.edu
   Subject
   [Histonet] Ventana vs Leica
 08/24/2010 02:30
 PM
 
 
 
 
 
 
 
 
 I was wondering if anyone out there had experience with both the
 Ventana Ultra and the Leica Bond immunostainers.  I realize that most
 people
 have a personal preference as to brands, but I'm not looking for a
 knee-jerk
 opinion (LEICA RULZ11 or VENTANA FTW!!), just someone who has had
 actual
 experience working on a daily basis with both instruments.  If this is you,
 could you please tell me which you preferred and why.
 I'm currently working for a facility in MT which has narrowed down its
 search to these two instruments.  No vendors please, they've already given
 their pitches.
 
 Thanks,
  Jay A.
 Lundgren M.S., HTL (ASCP)
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Re: [Histonet] HE stainers

2010-06-30 Thread histot...@imagesbyhopper.com
We have the new version of the Leica XL stainer (looks just like the  
old one!) with the bridge-transfer station  coverslipper  love it.   
We had the old stainer for 10 years before getting the new one... and  
even managed to sell the old one!


Michelle



On Jun 30, 2010, at 9:57 AM, Webb, Dorothy L dorothy.l.w...@healthpartners.com 
 wrote:


We are in the market for a new HE automated stainer and am hoping I  
get some feedback on this request!  I wold like to hear from the  
techs who work with either the Prisma from Sakura or the Leica auto  
or multi stainers, PLEASE!!  You can email me directly if you would  
like your comments private at  dorothy.l.w...@healthpartners.com


Thanks much ahead of time!!



 
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RE: [Histonet] toe nails falling off slides - Email found in subject

2010-04-28 Thread histot...@imagesbyhopper.com
We have very good success in facing the block and soaking it on the  
water bath for 30-60 seconds and then allowing it to cool down on a  
very wet ice tray.  Ours cut like butter too!  :o)



On Apr 28, 2010, at 8:58 AM, Cazares, Ruth rcaza...@schosp.org  
wrote:


Or you could soak them in 10% sodium hydroxide for 20-30 minutes  
prior to processing. My techs say they cut like butter!



Ruth Cazares, HT (ASCP)
Histology Supervisor
Department of Pathology
Swedish Covenant Hospital
5145 North California Ave
Chicago, IL 60625

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet- 
boun...@lists.utsouthwestern.edu] On Behalf Of Maria Katleba

Sent: Tuesday, April 27, 2010 5:22 PM
To: zodia...@comcast.net; histonet@lists.utsouthwestern.edu
Subject: [SPAM-HC] - RE: [Histonet] toe nails falling off slides -  
Email found in subject


HOW TO CUT NAILS (or other difficult tissue) SO THAT THEY STAY on  
slide!


(1) Cut the slides and place on Plus(+) slide
(2) shake off excess water
(3) place slide immediately in plastic Coplin jar with 1-3 drops of  
formalin at bottom.

(4) place in hot oven for 5 mins (50-60 degrees)
(5) remove from Coplin jar under a hood as formalin drops are now  
carcinogenic vapour
(6) place slides in rack in oven so that the formalin moisture  
dries...

(7) slide is ready for use

Maria Katleba HT(ASCP), MS
Pathology Dept. Mgr.
Queen of the Valley Medical Center
707-294-9229 cell
707-252-4411 x3689

-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu [mailto:histonet- 
boun...@lists.utsouthwestern.edu] On Behalf Of zodia...@comcast.net

Sent: Tuesday, April 27, 2010 12:17 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] toe nails falling off slides

To all,


I was wondering if anyone out there had any tips on how to keep  
toenail sections from falling off slides. We mount them on positive  
slides, air dry for about an hour but they still fall off. Any  
insight on the subject would be greatly appreciated.



Thanks,


Jenny
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Re: [Histonet] Bone Marrow Clots - falling off slides

2010-04-27 Thread histot...@imagesbyhopper.com
Thanks for all the input.  I will check the collection method.  B-plus  
is the fixative we normally use but I am not convinced that this clot  
ended up in it!  Other tissues are not being dramatically affected and  
not even all the bone marrows!  We do soak the blocks too.


This is very frustrating.  :o(

Michelle



On Apr 27, 2010, at 7:59 AM, Lynette Pavelich  
lpave...@hurleymc.com wrote:


In my experience, it can be all of the above that can cause it.  By  
the
tissue not getting enough penetration by any of the solutions will  
alter

the outcome.  That is why I asked about the thickness (remember...only
as thick as a nickel).  Blood is also so dense, so it would really  
apply
here.  Try that.  Do 1 change at a time.  I've been in your shoes,  
it is

very frustrating.  Then if the thickness is good, work on something
else.starting with fixation times.



histot...@imagesbyhopper.com 4/27/2010 7:32 AM 

Mary,
Thanks for the suggestion.  We do check the alcohols with a hydrometer
and
if not 100%, we will use that alcohol as the base for dilution
alcohols.  We
check quality of the xylene by putting 10ml of water in a graduated
cylinder
and then add 10ml of the recycled xylene to it and shake it vigorosly.
Good, clean xylene should have a perfect separation and no  mixing
with
the water.

Lynette,
I am leaning towards the processing too, but which part??  The clot
seems to
be more dry than moist, so it's not under dehydrated.  Fixation? It
spends 3
hours in formalin on the tissue processor and whatever time it can be
in
formalin prior to the processor.  Paraffin impregnation?  About the
only
thing I could think of here was if the wax wasn't changed fast enough
and/or
we got too much carry over from the xylene.  Could that cause this?

Thanks for the help!

Michelle



-Original Message-
From: Lynette Pavelich [mailto:lpave...@hurleymc.com]
Sent: Tuesday, April 27, 2010 6:56 AM
To: histot...@imagesbyhopper.com; histonet@lists.utsouthwestern.edu;
MARY
HODGES
Subject: RE: [Histonet] Bone Marrow Clots - falling off slides


When I start losing tissue on the slide, I have found that it is
usually a
processing issue.  Is the clot too thick?  Try cutting them in half
before
processing.

Hope this helped,
Lynette

Lynette Pavelich, HT(ASCP)
Histology Supervisor
MSH Competency Coordinator
Hurley Medical Center
One Hurley Plaza
Flint, MI  48503
email: lpave...@hurleymc.com
ph:  810-257-9948
Lab:  810-257-9138
fax:  810-762-7082



MARY T HODGES hodges...@msn.com 4/27/2010 12:18 AM 


recycled anything is not back to it original state always use a hydo
meter
and add new to back product of a better quality you will find this  
also

with
alcohols


From: histot...@imagesbyhopper.com
To: histonet@lists.utsouthwestern.edu
Date: Mon, 26 Apr 2010 23:26:43 -0400
Subject: [Histonet] Bone Marrow Clots - falling off slides

Hi Histonetters!

We have started to have an issue with our bone marrow clots falling

off the

slides. We are using plus slides, making sure they drain well (just

like

our other slides), but when we stain them routinely, we are getting

a
fair

amount of tissue coming off the slides.

It has been suggested that it's related to our using recycled

xylene.
Does

anyone have any experience with recycled xylene and this type of

tissue

fall-off?

Another suggestion was that the tissues sat in xylene too long. I

don't see

how that could happen, under routine conditions, but is that a

possibility

for causing this?

All thoughts will be appreciated!

Michelle


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