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Aspirin in pregnancy: a review of indications, timing, dosing and efficacy
1Division of Maternal-Fetal Medicine and Obstetrics, Department of Obstetrics and Gynecology, Stanford University Hospital, Stanford, California, USA.
Insights
Low-dose daily aspirin (LDA) use effectively reduces preeclampsia risk, especially at higher doses initiated early in pregnancy. LDA also shows promise in preventing preterm birth and intrauterine growth restriction.
Area of Science:
- Obstetrics and Gynecology
- Perinatal Medicine
- Pharmacology
Background:
- Preeclampsia and adverse perinatal outcomes pose significant risks to maternal and infant health.
- Low-dose daily aspirin (LDA) is increasingly studied for its prophylactic role in pregnancy.
- Evidence review is needed to clarify optimal dosing and timing for LDA therapy.
Approach:
- Systematic review of recent meta-analyses and randomized controlled trials.
- Evaluation of varying aspirin dosages and initiation times for preeclampsia prevention.
- Assessment of LDA's impact on other perinatal sequelae like preterm birth and fetal growth.
Key Points:
- Consistent evidence shows LDA reduces preeclampsia risk in high-risk individuals.
- Higher aspirin doses (above 81 mg) may offer greater reduction in preterm preeclampsia.
- LDA use is associated with reduced risk of preterm birth, small for gestational age (SGA), and intrauterine growth restriction (IUGR).
Conclusions:
- Initiating LDA before 16 weeks of gestation, potentially at doses higher than 81 mg, may decrease preeclampsia rates.
- LDA shows promise for improving outcomes like preterm delivery and IUGR, but further research is needed.
- Updated guidelines reflect evolving understanding of risk identification and LDA's role in prevention.
Purpose Of Review:
The aim of this study was to evaluate the recent literature examining the utility of low-dose daily aspirin (LDA) in the prevention of preeclampsia and other potential adverse perinatal sequelae. The evidence supporting various aspirin doses and timing of initiation of treatment for this purpose will be examined. The potential benefits of LDA therapy in pregnancy will be discussed weighing against any potential associated harm.
Recent Findings:
Findings from several recent meta-analyses of randomized controlled trials are consistent with prior studies in showing a reduction in risk for preeclampsia with LDA use in individuals at an increased risk for this complication. Some studies suggest aspirin at a dose greater than the current recommended 81 mg is associated with the highest reduction in preterm PE.Several studies have demonstrated a reduction in risk for preterm birth, small for gestational age (SGA) infant or intrauterine growth restriction (IUGR), and a reduction in the risk of perinatal mortality associated with aspirin use. The findings of reduced preterm birth (PTB) and IUGR were also demonstrated among low-risk patients.Identifying patients at risk was re-evaluated, with resulting changes to existing United States Preventive Services Task Force (USPSTF) guidelines.
Summary:
This review of recent evidence suggests a decreased rate of preeclampsia at aspirin doses higher than the standardly used 81 mg when treatment is initiated prior to 16 weeks of gestation. Although LDA use seems promising for other outcomes such as preterm delivery and IUGR, further studies to strengthen recommendations are warranted.
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