Low molecular weight heparins (LMWHs) are as efficient as unfractionated he
parin (UFH) for prevention and treatment of thromboembolism. There is no ev
idence that monitoring the dose improves the clinical efficacy. In contrast
, any overdosage increases the risk of hemorrhage. Because renal function p
lays a significant role in the elimination of LMWH, curative treatment shou
ld be monitored with an anti-factor Xa assay in patients presenting renal i
nsufficiency, in the elderly, and in patients presenting an increased hemor
rhagic risk. It is advisable to sample the patient at peak activity (3 to 5
hours after the subcutaneous [sc] administration) and to target the mean a
nti-factor Xa activity that was found efficient and safe in the clinical tr
ial. This target is different for each LMWH and each dose regimen.