Studies in the 1960s demonstrated the problems of variability in susceptibi
lity testing methods, especially those affecting the performance of disc di
ffusion procedures. These studies made apparent the need for standardizatio
n and resulted in more clearly defined performance limits for growth medium
, incubation conditions, inoculum concentration, disc content for diffusion
methods, the setting of interpretative MIC breakpoints and the establishme
nt of quality control parameters. More recently, there has been a growing i
nterest in the use of instrumentation for reading disc diffusion tests and
the endpoints of agar or broth dilution MIC determinations. Instrumentation
ranges in complexity from the simple optical reading of zones of inhibitio
n or growth endpoints, requiring operator interpretation, to more sophistic
ated devices for reading, recording and 'expert system' analysis of results
with interfacing of instruments to laboratory information management syste
ms. Some of the more developed systems are fully automated and can also ide
ntify the organisms tested. The pressure to reduce labour costs and provide
results earlier favours the use of more automated systems whilst the requi
rement for resistance surveillance provides impetus for the use of systems
that provide quantitative results and electronic data handling.