Homozygous sickle cell disease is one of the most common genetic abnor
malities in the world; it affects approximately 100,000 births annuall
y in Nigeria alone. With this scale of public health problem, the newe
r high technology approaches to prevention, such as antenatal diagnosi
s, or to treatment, such as bone marrow transplantation, are unlikely
to be affordable or to have a discernible population impact. Experienc
e in Jamaica suggests that many low technology affordable procedures c
an markedly reduce the morbidity and mortality of the disease. Further
more, certain aspects of current management in the United Kingdom, suc
h as frequent hospital admission and transfusion, not only consume sca
rce resources but may increase morbidity. Prophylactic penicillin to p
revent pneumoccocal complications, education of parents so as to reduc
e the mortality from acute splenic sequestration, awareness of the fea
tures and epidemic pattern of aplastic crises, and exchange transfusio
n for the acute chest syndrome represent cost-effective measures which
may markedly influence outcome. Reducing dependency on inpatient faci
lities might actually reduce morbidity and save resources that could b
e used to improve day care and outpatient management.