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  • [ATTACH]707[/ATTACH] A suggestion: I would leave out this part. The weakest of the in-vitro incompatible units will be given to the patient. See attachment; I think calling them least incompatibl

  • Deny Morlino
    Deny Morlino

    In this situation we still classify this as incompatible since the identification is incomplete. The physician signs a release of the unit indicating that counseling of the risks involved have been e

  • Emergency Release Form.doc

comment_49997

[ATTACH]707[/ATTACH]

A suggestion: I would leave out this part.

The weakest of the in-vitro

incompatible units will be given to the patient.

See attachment; I think calling them least incompatible gives a false sense of security that the reaction will be less severe, which has not been proven. We just call them incompatible and let the physician decide to consider the risk of that.

Some have also called these units "serologically incompatible" which is another acceptable alternative. There is no correlation between in-vitro grading and actual in-vivo result in the patient.

comment_50000
Here's what I came up with as a draft. We manage using O negs RBCs for Emergencies. I basically combined both our Emergency Release and Least Incompatible forms into 1.

" The compatibility testing has been completed but there were serological testing problems encountered thathave not been fully identified or resolved. The medical status of the patient necessitates transfusion of theseblood products. I am aware of the risks of transfusion.

Crossmatch compatible units are available, but all testing is not complete. "

The two statements contradict, just a heads up.

  • Author
comment_50001

" The compatibility testing has been completed but there were serological testing problems encountered thathave not been fully identified or resolved. The medical status of the patient necessitates transfusion of theseblood products. I am aware of the risks of transfusion.

Crossmatch compatible units are available, but all testing is not complete. "

The two statements contradict, just a heads up.

What I was going for is that the crossmatch may be compatible, but antigen typing or complete rule-outs of other possible antibodies may not have been completed yet.

comment_50002
What I was going for is that the crossmatch may be compatible, but antigen typing or complete rule-outs of other possible antibodies may not have been completed yet.

In this situation we still classify this as incompatible since the identification is incomplete. The physician signs a release of the unit indicating that counseling of the risks involved have been explained and the responsibility and liability now lies with them.

  • 1 year later...
comment_59603

[ATTACH]707[/ATTACH]

A suggestion: I would leave out this part.

The weakest of the in-vitro

incompatible units will be given to the patient.

See attachment; I think calling them least incompatible gives a false sense of security that the reaction will be less severe, which has not been proven. We just call them incompatible and let the physician decide to consider the risk of that.

Some have also called these units "serologically incompatible" which is another acceptable alternative. There is no correlation between in-vitro grading and actual in-vivo result in the patient.

 

EXACTLY!  We shouldn't be talking 'least incompatible' anymore and we need to teach our MDs to stop talking that way, too. 

 

BTW:  Since it is under the BB MD license to choose blood for patients, we do not put this burden on the ordering MD who is likely not well versed in all these BB variables.  

 

We have written protocol regarding how to deal with warm/cold panagglutinins which I won't go into on this string. But, I will say if we have to give out RBCs that are truly incompatible, it is because we are not given the time to find antigen-negative RBCs or to complete our investigative testing.  If this happens, the MD is required to sign for 'Emergency Release'.

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