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comment_54765

LOL! And then all potential recipients are screened for the Rh's and K, and given the appropriate antigen negative units to avoid sensitation?  (as some here say they do for E antigen for patients that show only anti-c, but are antigen negative for E and c?)

 

Scott

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  • Malcolm Needs
    Malcolm Needs

    In the UK, the National External Quality Assurance Scheme (NEQAS) does not require that either anti-E be excluded in the case of an anti-c or anti-C be excluded in the case of an anti-e, but would exp

  • I also want to know to know if there is a anti-E hiding in there behind the anti-c. We usually have a RZR1 cell on one of our panels, or can beg a drop from our reference lab, conveniently located jus

  • Malcolm Needs
    Malcolm Needs

    I do know that there was a theory put about some years ago that anti-cE caused more severe HDFN than does a mixture of anti-c (monospecific) and anti-E (monospecific) and, as a result, we have been ti

comment_54766

Yes, but only really for females of "child-bearing potential" (horrible phrase - makes them sound like farm animals) and for those who are transfusion dependent.

comment_54768

Well, we are especially careful with those over here also.  Then there's endless-txn patients like those living with sickle-cell anemia.

 

Someday someone is going to figure out how to make decent artificial blood, and this will all be academic!

 

Scott

comment_54769

Prof Dave Anstee is well on the way to growing red cells from CD34+ cells.

They have foetal type antigens, such as ii, Ch-, Rg-, weak Lutheran antigens, etc.

He's got as far as about half a universal bottle's worth, but, of course, scaling it all up is the key.

comment_54779

Depends on where you work and what your resources are. It would be "nice" to give R1R1 to a patient with anti-E or anti-c who is negative for the other; or to give R2R2 to a patient with anti-e or anti-C who is negative for the other. But especially with the R2R2 units...you are taking valuable resources from patients with anti-e if your patient just has an anti-C (and some Donor Facilities won't give that up unless you have an anti-e). While it is true they may go on to make the other antibody; it is not a high enough frequency that we have done it most places I have worked.

Brenda Hutson

  • 2 weeks later...
comment_54975

Ya.

Still... if we wanted to be really careful, we would completely phenotype for every significant antigen for both the patient and donor units. And I think that is where we are headed when we screen for E with anti-c patients, or for e with anti-C patients.

(In general, I think we are already enough anal-retentive!)

Scott

Molecular people would agree with your first statement. rjt

comment_54989

All,

 

What do you report on a CAP survey, when anti-c is identified in a sample that you can't rule-in or rule-out anti-E?

Isn't there always the option to select "other" and fill in the answer, or choose that you would send it out for further testing? Different labs have different resources.

  • 2 weeks later...
comment_55208

In our reference lab, when a patient demonstrates an anti-c, we phenotype for E. If the patient is E- we recommend giving c and E negative units even if we have ruled out an anti-E. Percentages are very high for the development of an anti-E to ignore the E. We don't do the reverse for anti-e because of the lower antigenicity of C (unless of course it's a patient that will be transfused multiple times)

  • 10 months later...
comment_59428

So you can rule out anti-E with a heterozygous cell in the presence of anti-c, just like you would anti-C and anti-E in the presence of anti-D?  I haven't seen that on any lists, but I would love to be able to use it.

comment_59431

Unless you have an RzRz, Rzry or ryry cell sample handy, I think you are going to have to mollyredone.

 

Cells aren't heterozygous; genes are heterozygous!

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