Screening has become central to the effective prevention of several disease
s, but implementation suffers from difficulties with targeting and rates of
compliance. Such issues are also complicated by the need to consider legal
provisions regarding confidentiality of patients and other human rights is
sues.
Screening has been an inexact science in relation to eg faecal occult blood
testing for colorectal cancer, false positive and false negative tests for
HIV and there have been inadequate quality controls in breast cancer scree
ning programmes. The public need to be made aware of what the screening pro
grammes really offer, balanced against the expectations they may have. Ther
e needs to be a clearer understanding of the nature of the contractual and
other legal rights of patients/consumers as against providers. A positive s
creening test may carry adverse consequences as well as benefits. It could
alert an insurance company to a risk and lead to additional weighting or ev
en outright rejection for life insurance policies. Job prospects may also b
e affected for employees.
The method of informing patients in relation to screening and screening fai
lure has already been considered by the courts. Realistic information about
both screening and treatment efficiency needs to be offered to patients so
that they can have a real understanding of what can and cannot be achieved
by current science. The development of understanding of the human genome m
akes the need for clearer legislation in this are more urgent.