What is the absolute risk reduction of preeclampsia with low-dose Aspirin (acetylsalicylic acid) in a healthy 30-year-old woman in her first pregnancy?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 9, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Absolute Risk Reduction of Preeclampsia with Low-Dose Aspirin in Healthy First Pregnancy

The absolute risk reduction of preeclampsia with low-dose aspirin in a healthy 30-year-old woman in her first pregnancy is approximately 1.7%, based on a reduction from about 6.3% to 4.6% risk. 1

Risk Assessment and Benefit

  • Low-dose aspirin reduces the risk of preeclampsia by 24% in women at increased risk (relative risk reduction), with an absolute risk reduction ranging from 2% to 5% 2
  • The number needed to treat (NNT) to prevent one case of preeclampsia is 42 in women at increased risk 2
  • For a healthy nulliparous woman (first pregnancy), the NICHD Network of Maternal-Fetal Medicine Units trial showed a reduction from 6.3% to 4.6% incidence of preeclampsia with 60mg daily aspirin 1
  • The benefit appears most significant in women with initial systolic blood pressure between 120-134 mmHg, where the reduction was from 11.9% to 5.6% 1

Dosage and Timing Considerations

  • The most commonly studied dosages are 60 mg/day and 100 mg/day, with 81 mg/day being a reasonable dosage in the United States 2
  • Low-dose aspirin should be initiated between 12 and 16 weeks of gestation for optimal effect 2, 3
  • There is no evidence of additional benefit when starting aspirin earlier than 16 weeks compared to later initiation 2
  • Some evidence suggests aspirin should be continued until delivery, though practices vary with about 52% of physicians continuing it until delivery 3
  • Recent research indicates that aspirin can be safely discontinued at 24-28 weeks in women with normal biomarkers (sFlt-1:PlGF ratio ≤38) without increasing preeclampsia risk 4

Safety Profile

  • Low-dose aspirin does not increase the risk of:
    • Placental abruption (pooled analysis) 2
    • Postpartum hemorrhage 2
    • Fetal intracranial bleeding 2
    • Perinatal mortality 2
  • However, one study noted an increased risk of abruptio placentae in the aspirin group (11 women vs. 2 in placebo) 1
  • No significant differences were found in cesarean delivery rates between aspirin and placebo groups 2

Considerations for Healthy Nulliparous Women

  • While the USPSTF recommendations focus on women at high risk for preeclampsia, the NICHD trial specifically studied healthy nulliparous women 1
  • For women with moderate risk factors (including first pregnancy), the evidence for aspirin benefit is less certain but may still be beneficial 2
  • Early administration of aspirin (≤16 weeks) appears to be more effective at reducing severe preeclampsia (78% reduction) than mild preeclampsia (no significant reduction) 5

Additional Benefits

  • Low-dose aspirin also provides:
    • 14% reduction in risk of preterm birth 2
    • 20% reduction in risk of intrauterine growth restriction (IUGR) 2
    • Increased mean birthweight by approximately 130g 2

Clinical Application

  • For a healthy 30-year-old woman in her first pregnancy without other risk factors, the absolute risk reduction is modest but may be clinically significant
  • The decision to use aspirin should consider the woman's baseline blood pressure, as those with systolic BP 120-134 mmHg appear to benefit most 1
  • The low risk of adverse effects and potential benefits beyond preeclampsia prevention (reduced preterm birth and IUGR) may justify consideration even in women without high-risk factors 2

Common Pitfalls and Caveats

  • Failing to start aspirin early enough (before 16 weeks) may reduce effectiveness 5
  • Discontinuing aspirin too early (before 36 weeks) without biomarker assessment may reduce protective effects 3
  • Not considering moderate risk factors in combination when assessing preeclampsia risk 3
  • Overlooking the potential benefit in women with higher-normal blood pressure readings 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.