No clinical data is present in the provided text, which consists only of the journal's editorial board and contact information.
Does enoxaparin with or without aspirin improve live-birth rate in women with recurrent miscarriage compared to aspirin alone?
Enoxaparin, with or without aspirin, does not significantly improve live birth rates compared to aspirin alone in women with recurrent miscarriage.
Recurrent miscarriage affects 1-2% of women. In more than half of all recurrent miscarriage the cause still remains uncertain. Thrombophilia has been identified in about 50% of women with recurrent miscarriage and thromboprophylaxis has been suggested as an option of treatment. A randomised double-blind (for aspirin) multicentre trial was performed among 207 women with three or more consecutive first trimester (<13 weeks) miscarriages, two or more second trimester (13-24 weeks) miscarriages or one third trimester fetal loss combined with one first trimester miscarriage. Women were analysed for thrombophilia. After complete work-up, women were randomly allocated before seven weeks' gestation to either enoxaparin 40 mg and placebo (n=68), enoxaparin 40 mg and aspirin 100 mg (n=63) or aspirin 100 mg (n=76). The primary outcome was live-birth rate. Secondary outcomes were pregnancy complications, neonatal outcome and adverse effects. The trial was ended prematurely because of slow recruitment. A live birth rate of 71% relative risk (RR) 1.17, 95% confidence interval (CI) 0.92-1.48 was found for enoxaparin and placebo and 65% RR 1.08, 95% CI 0.83-1.39 for enoxaparin and aspirin when compared to aspirin alone (61%, reference group). In the whole study group the live birth rate was 65% (95% CI 58.66-71.74) for women with three or more miscarriages (n=204). No difference in pregnancy complications, neonatal outcome or adverse effects was observed. No significant difference in live birth rate was found with enoxaparin treatment versus aspirin or a combination of both versus aspirin in women with recurrent miscarriage.
Visser et al. (Wed,) reported a other. No clinical data is present in the provided text, which consists only of the journal's editorial board and contact information.