In patients with an acute cerebral infarction, anticoagulation may spa
re tissue in the ischaemic penumbra from irreversible necrosis by prev
enting thrombus extension from a vascular bed with good collateral cir
culation to one with poor collateral circulation. In addition to the p
ossibility of limiting infarct volume, anticoagulation may be given ac
utely to prevent early recurrent cerebral infarction or to prevent or
treat thrombus outside the nervous system (i.e. deep venous thrombosis
or pulmonary embolus). In one controlled trial of a low molecular wei
ght heparin, administration of nadroparin calcium within 48 hours of o
nset of cerebral infarction decreased the combined incidence of depend
ency and all-cause mortality at 6 months. Another controlled trial in
patients with cerebral venous thrombosis demonstrated the benefit of c
ontinuous intravenous adjusted-dose unfractionated (UF) heparin compar
ed with placebo. Although results of anticoagulation appear promising
in patients with acute cerebral infarction and cerebral venous thrombo
sis, the benefits of these agents remain unconfirmed. The results of l
arge multicentre trials using a heparinoid (ORG 10172) and subcutaneou
s UF heparin in patients with acute cerebral infarction are expected w
ithin the year.