Re: [Histonet] "cooked" biopsy

2021-07-07 Thread Tony Henwood (SCHN) via Histonet
Hi Paula,

We can check the purity of the xylene quite easily:

Xylene Purity Test Procedure 

Note: The recommended and most accurate method of determining the purity of the 
recycled xylene is by doing a Gas Chromatography analysis.  The following 
method can be used to obtain an acceptable confidence level in the purity of 
the recycled xylene (CBG Biotech).

Testing Procedure

1.  To a clean, dry 100 ml mixing cylinder graduate, add sufficient 
recovered xylene so that the bottom of the meniscus is aligned with the top 
edge of the 85 ml mark on the graduate. 

2.  Add water to the graduate until the bottom of the meniscus aligns with 
the top edge of the 100 ml mark on the graduate. At this point, 15 ml of water 
will have been added to 85 ml of recovered xylene.

3.  Stopper the graduate and invert the mixture.  Allow the mixture to 
settle, making sure that all of the water settles to the bottom of the 
graduate.  No water should remain clinging to the sides of the graduate above 
the xylene/water separation point. This separation point should be near the 15 
ml level of the graduate. (Note: xylene floats on top of the water).

4.  Carefully inspect and record the point of separation between the water 
and xylene using the bottom of the meniscus as the separation point.

5.  Subtract 15 ml from the quantity of water indicated in step 5.  The 
remainder plus an additional 0.1 correction factor equals the percentage of 
recovered xylene impurities.

EXAMPLE:

Xylene/Water separation point is indicated to be 15.5 ml.
(15.5 - 15) + 0.1 = 0.6% impurities.  
Therefore, the recovered xylene is 99.4% pure.


Regards
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA)
Principal Scientist, the Children’s Hospital at Westmead
Adjunct Fellow, School of Medicine, University of Western Sydney
Tel: 612 9845 3306
Fax: 612 9845 3318
Pathology Department
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA


From: Paula via Histonet 
Sent: Thursday, 8 July 2021 04:53
To: 'Erick Rodriguez'
Cc: histonet@lists.utsouthwestern.edu
Subject: Re: [Histonet] "cooked" biopsy

Thank you, everyone...
I looked at my reagents and saw the color pink in the xylene, which tells me 
that there is water or too much water in it so I changed it.
We recycle xylene, so I need to get the recycler looked at now.
Thanks again,
Paula


-Original Message-
From: Erick Rodriguez [mailto:rodriguez.er...@icloud.com]
Sent: Wednesday, July 07, 2021 11:24 AM
To: Paula
Subject: Re: [Histonet] "cooked" biopsy

Did you change the processor reagents before running your tissues? Cooked 
tissue usually means the tissue wasn’t dehydrated properly and the leftover 
water boiled and fried your tissue. I would double check the alcohols.

> On Jul 7, 2021, at 11:00 AM, Paula via Histonet 
>  wrote:
>
> Hello, good day,
>
>
>
> Our pathologist is complaining about the tissues today that they are
> "cooked, burnt, crushed, shrunken" those are the adjectives she is using.
>
>
>
> Can you tell me the cause?  Usually, the work comes out beautiful but today
> they are not. Nothing has changed on our processing times.
>
>
>
> What should I investigate?
>
>
>
> Thank you in advance,
>
> Paula
>
> Bio-Path Medica Group
>
>
>
> ___
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet


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[Histonet] Histotechnician/Grosser Needed Long Island NY

2021-07-07 Thread Olivia Sloane via Histonet
Good Afternoon-

New permanent histology opening!

*Histotechnician/Grosser Needed Long Island, NY*

   - Permanent full time position
   - Shift is Tuesday to Saturday 6:00am - 2:30pm but seems to have
   flexibility
   - Candidates must have New York State Clinical Laboratory
   Technologist/Technician or Histological Technician License
   - Ideally would like to see candidates with 1+ year of experience
   - In this role you will embed, cut, stain and coverslip specimens. Set
   up specimens and their paperwork for grossing. Maintain the tissue
   processor, embedding centers, microtomes, stainers and coverslipper, etc.
   - Full benefits included and much more!!!
   - Position is located on Western Long Island- only about 35 miles from
   Manhattan.

If you would like to talk further about these openings I am working on
please send an updated resume to oli...@ka-recruiting.com with the best
time and phone number for me to reach you! Or feel free to reach out to my
direct line which is  617-746-2743 .

You can also schedule an appointment with my calendar:
https://calendly.com/olivia-ka/15min

*Other Permanent Histology Openings Nationwide*

FL - Tampa Area- Histology Manager

GA – 1.5 Hours South of Atlanta - Histotech (3 am - 11 am)

NC – Winston-Salem Area - Histotech

NY- Bronx Area- Histotech

NY - Buffalo Area- CLT Histology Lab Pathology

NY - Westchester - Histotech

NY - Westchester - IHC Lab Tech (Histotech)

NY - Westchester - IHC Lead Tech (Histotech)

NY – Syracuse Area - Histotech

NY – Long Island - Histotechnician or Histotechnologist

NY - Rochester Area- Histotechnologist (Day shift)

OR - Northwest- Grossing Histotech

OR - Northwest - Histotech

PA - Southeast - Histotechnologist

PA - Southeast - Histotech

TN - Nashville Area- Histotech

VA - Southeast - Senior Histotech

VA - Southeast - Histotech

VA – Roanoke Area - Histotech

WI – Greater Green Bay Area - Histotech

WI – Greater Green Bay Area - Lab Histotech Trainer

Talk to you soon,

Olivia Sloane
Healthcare Recruiter, K.A. Recruiting, Inc.
* 617-746-2743   *
oli...@ka-recruiting.com   www.ka-recruiting.com
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[Histonet] Iron stain on Bone Marrow crush specimens

2021-07-07 Thread Johnson, Carole via Histonet
Hello,

Would anyone be willing to share their protocol for performing iron stains on 
bone marrow crush specimens?  We are trying to convert from doing the stain 
manually to automated on a Ventana Special Stainer using the iron stain kit 
from Roche.  We are using the following protocol:


1.   Fix slide in methanol x 2 minutes

2.   Allow slide to air dry

3.   Rinse slide in distilled water

4.   Place slide on special stainer (Ventana only allows adjusting 
counterstain time, currently set at 4 minutes)

My plan is to pull additional crush smears and trying different counterstain 
times, but if anyone has other suggestions, it would be greatly appreciated.

Best Regards,
Carole

Carole L Johnson, HT, QIHC (ASCP)

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Re: [Histonet] "cooked" biopsy

2021-07-07 Thread Paula via Histonet
Thank you, everyone...
I looked at my reagents and saw the color pink in the xylene, which tells me 
that there is water or too much water in it so I changed it. 
We recycle xylene, so I need to get the recycler looked at now.
Thanks again,
Paula


-Original Message-
From: Erick Rodriguez [mailto:rodriguez.er...@icloud.com] 
Sent: Wednesday, July 07, 2021 11:24 AM
To: Paula
Subject: Re: [Histonet] "cooked" biopsy

Did you change the processor reagents before running your tissues? Cooked 
tissue usually means the tissue wasn’t dehydrated properly and the leftover 
water boiled and fried your tissue. I would double check the alcohols. 

> On Jul 7, 2021, at 11:00 AM, Paula via Histonet 
>  wrote:
> 
> Hello, good day,
> 
> 
> 
> Our pathologist is complaining about the tissues today that they are
> "cooked, burnt, crushed, shrunken" those are the adjectives she is using.  
> 
> 
> 
> Can you tell me the cause?  Usually, the work comes out beautiful but today
> they are not. Nothing has changed on our processing times.
> 
> 
> 
> What should I investigate?
> 
> 
> 
> Thank you in advance,
> 
> Paula
> 
> Bio-Path Medica Group
> 
> 
> 
> ___
> Histonet mailing list
> Histonet@lists.utsouthwestern.edu
> http://lists.utsouthwestern.edu/mailman/listinfo/histonet


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[Histonet] "cooked" biopsy

2021-07-07 Thread Paula via Histonet
Hello, good day,

 

Our pathologist is complaining about the tissues today that they are
"cooked, burnt, crushed, shrunken" those are the adjectives she is using.  

 

Can you tell me the cause?  Usually, the work comes out beautiful but today
they are not. Nothing has changed on our processing times.

 

What should I investigate?

 

Thank you in advance,

Paula

Bio-Path Medica Group

 

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