Until 1943, blood-grouping tests were performed mainly on glass slides
or tiles but, following the description of the antiglobulin test, tub
e techniques became widespread. With increasing workloads and pressure
to be ever more cost-efficient, other 'reaction vessels' such as micr
oplates have been developed for blood-group serological testing. The i
ndirect antiglobulin test has been shown to be the most effective and
reliable method for detecting clinically significant antibodies. As a
result, this test has been developed, for example by the introduction
of enhancement media such as low-ionic-strength saline and polyethylen
e glycol. However, the problems and inconvenience associated with the
labelling and washing of large numbers of tubes were not overcome unti
l the introduction of the solid-phase antiglobulin test and the newer
microtubes containing gel or glass microbeads. These techniques are no
w replacing the conventional tube tests, but they too have their own l
imitations. There is still no single technique that will detect all cl
inically significant red-cell antibodies. Therefore, the safe transfus
ion of red cells that would survive optimally in the recipient depends
not on a single test but on a series of tests and procedures, such as
correct patient identification, blood-grouping, antibody-screening an
d compatibility-testing.