Thromboprophylaxis in pregnancy and the puerperium |
















































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PREGNANCY
THROMBOPROPHYLAXIS
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Agents for
Thromboprophylaxis
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Low molecular weight heparin
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Lancet.
1994 Mar 12;343(8898):619-29.
CLASP: a randomised trial of low-dose aspirin for the prevention and
treatment of pre-eclampsia among 9364 pregnant women. CLASP (Collaborative
Low-dose Aspirin Study in Pregnancy) Collaborative Group.
[No authors listed]
Pre-eclampsia is a common and serious complication of pregnancy that affects
both mother and child. Review of previous small trials of antiplatelet
therapy, particularly low-dose aspirin, suggested reductions of about
three-quarters in the incidence of pre-eclampsia and some avoidance of
intrauterine growth retardation (IUGR), but larger trials have not confirmed
these results. In our multicentre study 9364 women were randomly assigned 60
mg aspirin daily or matching placebo. 74% were entered for prophylaxis of
pre-eclampsia, 12% for prophylaxis of IUGR, 12% for treatment of pre-eclampsia,
and 3% for treatment of IUGR. Overall, the use of aspirin was associated
with a reduction of only 12% in the incidence of proteinuric pre-eclampsia,
which was not significant. Nor was there any significant effect on the
incidence of IUGR or of stillbirth and neonatal death. Aspirin did, however,
significantly reduce the likelihood of preterm delivery (19.7% aspirin vs
22.2% control; absolute reduction of 2.5 [SD 0.9] per 100 women treated; 2p
= 0.003). There was a significant trend (p = 0.004) towards progressively
greater reductions in proteinuric pre-eclampsia the more preterm the
delivery. Aspirin was not associated with a significant increase in
placental haemorrhages or in bleeding during preparation for epidural
anaesthesia, but there was a slight increase in use of blood transfusion
after delivery. Low-dose aspirin was generally safe for the fetus and
newborn infant, with no evidence of an increased likelihood of bleeding. Our
findings do not support routine prophylactic or therapeutic administration
of antiplatelet therapy in pregnancy to all women at increased risk of pre-eclampsia
or IUGR. Low-dose aspirin may be justified in women judged to be especially
liable to early-onset pre-eclampsia severe enough to need very preterm
delivery. In such women it seems appropriate to start low-dose aspirin
prophylactically early in the second trimester.
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