RE: [Histonet] RE: Microwave verification

2012-05-24 Thread joelle weaver

Try the CLSI guideline. It is being revised now, but the original is pretty 
detailed.




Joelle Weaver MAOM, HTL (ASCP) QIHC
  From: tajib...@echd.org
 To: lbustama...@cvm.tamu.edu; histonet@lists.utsouthwestern.edu; 
 histonet-boun...@lists.utsouthwestern.edu
 Date: Wed, 23 May 2012 14:33:33 -0500
 CC: 
 Subject: [Histonet] RE: Microwave verification
 
 Can you please give more details about this question?
 
  Tunde Ajibade BS, HTL(ASCP)QIHC
  Histology Supervisor
  Medical Center Hospital
  Odessa,TX
  Tel:  432-640-2348
  Fax:432-640-2303
  
 -Original Message-
 From: histonet-boun...@lists.utsouthwestern.edu 
 [mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Bustamante, 
 Lin
 Sent: Wednesday, May 23, 2012 1:42 PM
 To: histonet@lists.utsouthwestern.edu
 Subject: [Histonet] Microwave verification
 
 Does anyone knows a protocol for Microwave verification? (CAP requirement).
 Thank you.
 Lin Bustamante
 Central Texas Gastrointestinal Clinic
 Histology laboratory.
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[Histonet] RE: Microwave verification

2012-05-23 Thread Weems, Joyce K.
Someone else asked about this as well.. hope the attachment of our very simple 
instructions is ok to send. Sor far this has worked for us...j

Here is CAP checklist:

ANP.27170 Microwave Usage Phase I
Microwave devices are used in accordance with manufacturer's instructions.
NOTE: Microwave devices should be used in accordance with manufacturer's 
instructions, unless
CAP requirements are more stringent.
Evidence of Compliance:
✓ Written procedure for microwave usage

ANP.28290 Microwave Monitoring Phase I
Microwave devices are at least annually monitored for reproducibility.
NOTE: “Reproducibility” is defined as consistency in diagnostic quality 
obtained from microwave
equipment and procedures. For some devices, reproducibility may be evaluated by 
monitoring the
temperatures of identical samples after microwave processing. For those 
microwave devices
(particularly those incorporated into histology processing equipment) that use
temperature-independent methods to evaluate reproducibility, the laboratory 
should have a written
procedure for monitoring reproducibility that follows instrument manufacturer's 
instructions.
Information on such procedures is given in the reference to this checklist 
requirement (see below).
The microwave device should be tested for radiation leakage if there is visible 
damage to the device.
Evidence of Compliance:
✓ Written procedure for monitoring the diagnostic quality of specimens 
processed using microwaves

ANP.28860 Microwave Container Venting Phase I
All containers used in microwave devices are vented.
NOTE: Venting of containers is necessary so that processing occurs at 
atmospheric pressure, to
prevent explosion. For procedures using pressure above that of the atmosphere, 
specialized
containers must be used, with strict adherence to manufacturer instructions.
Evidence of Compliance:
✓ Written procedure for the use of appropriately vented containers

ANP.29430 Microwave Venting Phase I
Microwave devices are properly vented.
NOTE: Microwave devices should be placed in an appropriate ventilation hood to 
contain airborne
chemical contaminants and potentially infectious agents. Before operation of 
the microwave device,
36 of 43
Emory/Saint Josephs, Inc
Main Laboratory
Anatomic Pathology Checklist 01.04.2012
flammable and corrosive reagents should be removed from the hood, to prevent 
fire or chemical
damage to the electronic components of the device. Microwave devices used 
outside a fume hood
should have an integral fume extractor that is certified by the manufacturer 
for use in a clinical
laboratory.
The effectiveness of ventilation should be monitored at least annually.
This checklist requirement does not apply if only non-hazardous reagents (and 
non-infectious
specimens) are used in the device (e.g. water, certain biological stains, 
paraffin sections). The
laboratory should consult the MSDS sheets received with reagents and stains to 
assist in determining
proper handling requirements and safe use.
This checklist item does not apply to microwave devices that are designed by 
the manufacturer to
operate without venting.
Evidence of Compliance:
✓ Records of annual evaluation of ventilation effectiveness



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 Bustamante, Lin
Sent: Wednesday, May 23, 2012 2:42 PM
To: histonet@lists.utsouthwestern.edu
Subject: [Histonet] Microwave verification

Does anyone knows a protocol for Microwave verification? (CAP requirement).
Thank you.
Lin Bustamante
Central Texas Gastrointestinal Clinic
Histology laboratory.
___
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet



This e-mail message (including any attachments) is for the sole use of
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If you have received this message in error, please contact
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[Histonet] RE: Microwave verification

2012-05-23 Thread Weems, Joyce K.
Ok - attachment didn't work. Whoever wants the procedure, just let me know it 
is ok to send separately! j

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 Weems, Joyce K.
Sent: Wednesday, May 23, 2012 4:27 PM
To: 'Bustamante, Lin'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Microwave verification

Someone else asked about this as well.. hope the attachment of our very simple 
instructions is ok to send. Sor far this has worked for us...j

Here is CAP checklist:

ANP.27170 Microwave Usage Phase I
Microwave devices are used in accordance with manufacturer's instructions.
NOTE: Microwave devices should be used in accordance with manufacturer's 
instructions, unless CAP requirements are more stringent.
Evidence of Compliance:
✓ Written procedure for microwave usage

ANP.28290 Microwave Monitoring Phase I
Microwave devices are at least annually monitored for reproducibility.
NOTE: “Reproducibility” is defined as consistency in diagnostic quality 
obtained from microwave equipment and procedures. For some devices, 
reproducibility may be evaluated by monitoring the temperatures of identical 
samples after microwave processing. For those microwave devices (particularly 
those incorporated into histology processing equipment) that use 
temperature-independent methods to evaluate reproducibility, the laboratory 
should have a written procedure for monitoring reproducibility that follows 
instrument manufacturer's instructions.
Information on such procedures is given in the reference to this checklist 
requirement (see below).
The microwave device should be tested for radiation leakage if there is visible 
damage to the device.
Evidence of Compliance:
✓ Written procedure for monitoring the diagnostic quality of specimens 
processed using microwaves

ANP.28860 Microwave Container Venting Phase I All containers used in microwave 
devices are vented.
NOTE: Venting of containers is necessary so that processing occurs at 
atmospheric pressure, to prevent explosion. For procedures using pressure above 
that of the atmosphere, specialized containers must be used, with strict 
adherence to manufacturer instructions.
Evidence of Compliance:
✓ Written procedure for the use of appropriately vented containers

ANP.29430 Microwave Venting Phase I
Microwave devices are properly vented.
NOTE: Microwave devices should be placed in an appropriate ventilation hood to 
contain airborne chemical contaminants and potentially infectious agents. 
Before operation of the microwave device,
36 of 43
Emory/Saint Josephs, Inc
Main Laboratory
Anatomic Pathology Checklist 01.04.2012
flammable and corrosive reagents should be removed from the hood, to prevent 
fire or chemical damage to the electronic components of the device. Microwave 
devices used outside a fume hood should have an integral fume extractor that is 
certified by the manufacturer for use in a clinical laboratory.
The effectiveness of ventilation should be monitored at least annually.
This checklist requirement does not apply if only non-hazardous reagents (and 
non-infectious
specimens) are used in the device (e.g. water, certain biological stains, 
paraffin sections). The laboratory should consult the MSDS sheets received with 
reagents and stains to assist in determining proper handling requirements and 
safe use.
This checklist item does not apply to microwave devices that are designed by 
the manufacturer to operate without venting.
Evidence of Compliance:
✓ Records of annual evaluation of ventilation effectiveness



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 Bustamante, Lin
Sent: Wednesday, May

[Histonet] RE: Microwave verification

2012-05-23 Thread Bustamante, Lin
Thank you so much.
You are all great.
Lin :-)


From: Weems, Joyce K. [joyce.we...@emoryhealthcare.org]
Sent: Wednesday, May 23, 2012 3:33 PM
To: Weems, Joyce K.; Bustamante, Lin; histonet@lists.utsouthwestern.edu
Subject: RE: Microwave verification

Ok - attachment didn't work. Whoever wants the procedure, just let me know it 
is ok to send separately! j

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 Weems, Joyce K.
Sent: Wednesday, May 23, 2012 4:27 PM
To: 'Bustamante, Lin'; histonet@lists.utsouthwestern.edu
Subject: [Histonet] RE: Microwave verification

Someone else asked about this as well.. hope the attachment of our very simple 
instructions is ok to send. Sor far this has worked for us...j

Here is CAP checklist:

ANP.27170 Microwave Usage Phase I
Microwave devices are used in accordance with manufacturer's instructions.
NOTE: Microwave devices should be used in accordance with manufacturer's 
instructions, unless CAP requirements are more stringent.
Evidence of Compliance:
✓ Written procedure for microwave usage

ANP.28290 Microwave Monitoring Phase I
Microwave devices are at least annually monitored for reproducibility.
NOTE: “Reproducibility” is defined as consistency in diagnostic quality 
obtained from microwave equipment and procedures. For some devices, 
reproducibility may be evaluated by monitoring the temperatures of identical 
samples after microwave processing. For those microwave devices (particularly 
those incorporated into histology processing equipment) that use 
temperature-independent methods to evaluate reproducibility, the laboratory 
should have a written procedure for monitoring reproducibility that follows 
instrument manufacturer's instructions.
Information on such procedures is given in the reference to this checklist 
requirement (see below).
The microwave device should be tested for radiation leakage if there is visible 
damage to the device.
Evidence of Compliance:
✓ Written procedure for monitoring the diagnostic quality of specimens 
processed using microwaves

ANP.28860 Microwave Container Venting Phase I All containers used in microwave 
devices are vented.
NOTE: Venting of containers is necessary so that processing occurs at 
atmospheric pressure, to prevent explosion. For procedures using pressure above 
that of the atmosphere, specialized containers must be used, with strict 
adherence to manufacturer instructions.
Evidence of Compliance:
✓ Written procedure for the use of appropriately vented containers

ANP.29430 Microwave Venting Phase I
Microwave devices are properly vented.
NOTE: Microwave devices should be placed in an appropriate ventilation hood to 
contain airborne chemical contaminants and potentially infectious agents. 
Before operation of the microwave device,
36 of 43
Emory/Saint Josephs, Inc
Main Laboratory
Anatomic Pathology Checklist 01.04.2012
flammable and corrosive reagents should be removed from the hood, to prevent 
fire or chemical damage to the electronic components of the device. Microwave 
devices used outside a fume hood should have an integral fume extractor that is 
certified by the manufacturer for use in a clinical laboratory.
The effectiveness of ventilation should be monitored at least annually.
This checklist requirement does not apply if only non-hazardous reagents (and 
non-infectious
specimens) are used in the device (e.g. water, certain biological stains, 
paraffin sections). The laboratory should consult the MSDS sheets received with 
reagents and stains to assist in determining proper handling requirements and 
safe use.
This checklist item does not apply to microwave devices that are designed by 
the manufacturer to operate without venting.
Evidence of Compliance:
✓ Records of annual evaluation of ventilation effectiveness



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