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Companion May 2012 - BSAVA

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donor can be difficult. Practically type A donor<br />

blood would be an appropriate choice for AB cats<br />

as it contains low levels of anti-B antibodies to<br />

react with the recipient’s AB erythrocytes. As is<br />

clearly apparent from this discussion,<br />

administering compatible type-specific blood is<br />

mandatory in feline transfusion. See Table 1.<br />

DOnOR<br />

BLOOD<br />

GROUp<br />

RecipienT BLOOD GROUp<br />

A B AB<br />

A OK <strong>May</strong>be fatal Possible<br />

reaction<br />

B Reaction OK Reaction<br />

AB Reaction <strong>May</strong>be fatal OK<br />

Table 1: Reactions produced between donor and recipient<br />

blood types<br />

Mik antigen<br />

Recently a blood group antigen, and clinically<br />

relevant alloantibody, distinct from the AB blood<br />

group system has been discovered. Researchers<br />

have named this Mik. The absence of Mik can be<br />

associated with naturally occurring anti-Mik<br />

alloantibodies. In light of this knowledge, and given<br />

that more blood group antigens are likely to become<br />

known in the future, it is clear that the AB blood group<br />

system is simplistic. Therefore, ideally all cats should<br />

be cross-matched prior to transfusion, particularly if<br />

multiple transfusions are likely.<br />

Cross-matching<br />

Cross-matching is the gold standard laboratory test<br />

used to determine the serological compatibility<br />

between the donor and recipient red blood cells<br />

and is recommended in all cases. Practically<br />

however, cross-matching can not always be<br />

performed and its use is typically restricted to<br />

animals likely to receive more than one transfusion<br />

or before a second transfusion.<br />

From a pragmatic point of view, use of typed rather<br />

than cross-matched blood is likely to be suitable in<br />

most general practice situations. A brief guide to<br />

cross-matching, from a previous How to article<br />

(companion April 2011) is reproduced in Box 1.<br />

BOX 1: ABBreviAted slide crOss‑mAtch<br />

pROceDURe<br />

1. Collect blood into an EDTA tube from recipient and<br />

donor.<br />

2. Centrifuge tubes to settle the RBCs, remove the<br />

supernatant and transfer to a clean, labelled glass or<br />

plastic tube.<br />

3. For each donor prepare 3 slides labelled as major,<br />

minor and recipient control.<br />

4. Place 1 drop of RBCs and 2 drops of plasma on to each<br />

slide according to the following:<br />

■■ Major cross-match = donor RBCs + recipient plasma<br />

■■ Minor cross-match = recipient RBCs + donor plasma<br />

■■ Recipient control = recipient RBCs + recipient<br />

plasma<br />

5. Gently rock the slides to mix the plasma and red<br />

cells and examine for haemagglutination after<br />

1–5 minutes (presence of agglutination indicates<br />

incompatibility); recipient control agglutination will<br />

invalidate results.<br />

Despite using type-specific blood and performing<br />

a cross-match, it is still possible for transfusion<br />

reactions to occur, even when donor and recipient<br />

appear compatible, and close monitoring is vital<br />

during any transfusion. Similarly, warning clients of<br />

the possibility of transfusion reactions inspite of<br />

compatibility testing, is mandatory before any<br />

feline transfusion.<br />

Feline blood typing<br />

The principle of all veterinary blood typing methods is<br />

a visible haemagglutination reaction between patient<br />

RBC surface antigens and known reagent monoclonal<br />

or polyclonal antisera. There are several different<br />

typing kits available.<br />

Feline donors and recipients must always be<br />

blood-typed due to the naturally occurring antibodies<br />

and this can be achieved using simple in-house test<br />

kits (for example Alvedia Quick Test A+B) which will<br />

type for A, B and AB blood types (Figure 2). It is<br />

worth noting that profound autoagglutination, as might<br />

be seen with IMHA, will prevent blood typing by<br />

in-house methods. Furthermore when an AB result is<br />

received it should be checked by an external<br />

laboratory for confirmation.<br />

companion | 17

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