Table 2.
Effectiveness of aspirin on superimposed preeclampsia in regard to gestation age at initiation
| Author | Year | Population | Purpose | Design | Main findings | Risk of bias |
|---|---|---|---|---|---|---|
| Sinha, Singh et al [68] | 2023 | 113 pregnant women at high risk | To compare the efficacy of aspirin 150 mg versus 75 mg in the prevention of PE if initiated between 12 and 16 weeks of gestation | Parallel, open-label, randomized control trial | There were five times greater odds of preeclampsia in those who received aspirin 75 mg compared to those who received 150 mg (cOR = 5.341, CI = 1.829–15.594) | Moderate |
| Ashraf, Ali et al [3] | 2024 | 156 pregnant women with moderate to high risk of PE | To determine the efficacy of aspirin 75 mg vs. 150 mg in moderate and high-risk women if initiated between 11 and 14 weeks | Parallel arm randomized control open-label study | Aspirin 150 mg in moderate and high-risk pregnancies starting at 11–14 weeks was more effective and safer than 75 mg in reducing the incidence of Preeclampsia | Low |
| Richards, Giorgione et al [58] | 2023 | 2150 pregnant women with chronic hypertension | To determine the efficacy of aspirin 60 mg, 75 mg, 100 mg, 150 mg in the prevention of SIP among women with stage 1 hypertension if initiated before 20 weeks | Systematic review and meta-analysis of nine (three retrospective cohort studies and six randomized trials) studies | Low-dose aspirin prophylaxis did not reduce the odds of pre-eclampsia (OR 0.91, 95% CI 0.64–1.29) | Moderate |
| Chaemsaithong, Cuenca-Gomez et al [14] | 2020 | 1426 pregnant women at high risk of PE | To determine whether aspirin initiated before 11 weeks’ gestation reduces the rate of preeclampsia | Systematic Review and meta-analysis of 8 randomized controlled trials | Low-dose aspirin initiated at < 11 weeks’ gestation was associated with a no significant reduction in the risk of preeclampsia (relative risk, 0.52; 95% confidence interval, 0.23–1.17, P =.115), gestational hypertension (relative risk, 0.49; 95% confidence interval, 0.20–1.21; P =.121) | Moderate |
| Shen, Martinez‐Portilla et al [66] | 2021 | 1592 women at risk of PE | To examine the efficacy of aspirin 150 mg in reducing the risk of PE initiated between 11 and 13 weeks | Secondary analysis of data from the ASPRE trial | The use of 150 mg aspirin in women with chronic hypertension did not have a significant effect compared to those without chronic hypertension | Moderate |
| Banala, Moreno et al. [6] | 2020 | 457 women with chronic hypertension | To assess the impact of the ACOG guideline regarding low-dose aspirin initiated between 12 and 16 weeks of gestation for prevention of SIP In Women With Chronic Hypertension | Retrospective cohort study | No significant decrease in SIP was noted after the implementation of aspirin 81 mg initiated between 12 to 16 weeks of gestation | Moderate |
| Huai, Lin et al [33] | 2021 | 397 women with stage 1 hypertension | To evaluate the preventive effect of aspirin 100 mg in women with stage 1 hypertension initiated before 16 weeks of gestation | Secondary analysis of data from a randomized controlled trial | The incidence of PE was not significantly reduced in the aspirin group compared to the control group | Moderate |
| Xiao, Ling et al [77] | 2023 | 266 women at high risk | To assess the efficacy of aspirin 75 mg in preventing PE in high-risk pregnancies | Retrospective chart review | A lower incidence of preeclampsia was observed among women who started taking aspirin before 16 weeks than those who started after 16 weeks (4.69%) vs (17.65%, p = 0.0239). Chronic hypertension was associated with a higher incidence of PE despite taking aspirin (p = 0.0001) | Low |