A small randomised trial of low-dose aspirin in women at high risk of pre-eclampsia

Eur J Obstet Gynecol Reprod Biol. 2004 Feb 10;112(2):142-4. doi: 10.1016/s0301-2115(03)00269-0.

Abstract

Objective: To determine if aspirin (ASA) therapy reduces the incidence of pre-eclampsia in women at high risk of this condition.

Study design: Randomised clinical trial. We recruited pregnant women with gestational age at randomisation <14 weeks, who satisfied the following criteria: chronic hypertension, history of severe pre-eclampsia or eclampsia or intrauterine growth retardation (IUGR) or intrauterine foetal death. Nineteen women in the no-treatment group and 16 in the ASA group were successfully followed up.

Results: The mean birthweight was higher in the ASA group than in the no-treatment group (2790 g (S.D. 340 g) versus 2616 g (S.D. 779 g)), but the difference was not statistically significant. We found no statistically significant differences between the groups in the proportion of infants with birthweight below 2500 g (13.3% versus 29.4%) and the number of cases with pregnancy-induced hypertension (PIH)/pre-eclampsia (31.3% versus 36.8%).

Conclusion: These limited data give some support to the potential favourable effect of early treatment with ASA in pregnant women at risk of PIH and IUGR.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Aspirin / administration & dosage*
  • Chi-Square Distribution
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Female
  • Follow-Up Studies
  • Gestational Age
  • Humans
  • Incidence
  • Italy
  • Maternal Age
  • Pre-Eclampsia / epidemiology
  • Pre-Eclampsia / prevention & control*
  • Pregnancy
  • Pregnancy, High-Risk
  • Probability
  • Reference Values
  • Risk Assessment
  • Treatment Outcome

Substances

  • Aspirin