Table 3.
Summary of findings for medications to prevent superimposed preeclampsia
| Patient or population: Pregnant women at any gestational age at high risk of developing hypertensive disorders in pregnancy Settings: Hospital setting Intervention: Antiplatelet agents, anticoagulants, antioxidants, calcium, nitric oxide, and their combinations Comparator: Placebo or no treatment Outcome: Superimposed preeclampsia | ||||||||
|---|---|---|---|---|---|---|---|---|
| Total studies: 4 RCTs Total participants: 6,342 |
Direct estimates RR (95% CI) |
Certainty of evidence | Indirect estimates RR (95% CI) |
Certainty of evidence | Network estimates RR (95% CI) [95% PrI] |
Certainty of evidence | SUCRA | Commentsa |
| Antiplatelets (3 RCTs; 6,298 participants) | 0.72 (0.46 to 1.14) |
⊕⊕⊝⊝ Lowb,c |
Not estimable |
0.72 (0.46 to 1.14) [0.04 to 14.21] |
⊕⊕⊝⊝ Lowb,c |
69.0% | There was no evidence of inconsistency for global inconsistency test (P = 0.165) | |
| Antioxidants (1 RCT; 44 participants) | 0.67 (0.12 to 3.61) |
⊕⊝⊝⊝ Very lowd,e |
Not estimable |
0.67 (0.12 to 3.61) [< 0.001 to 37900] |
⊕⊝⊝⊝ Very lowd,e |
60.6% | ||
GRADE Working Group grades of evidence
High quality: Further research is very unlikely to change our confidence in the estimate of effect
Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
Very low quality: We are very uncertain about the estimate
The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI)
CI Confidence interval, PrI Prediction interval, RR Relative risk
aDias’s inconsistency tests of the node splitting not estimable
bWe downgraded (1) level for serious limitations in study design due to most of the studies being at unclear risk of bias
cWe downgraded (1) level for serious imprecision due to wide confidence interval
dWe downgraded (2) level for very serious limitations in study design due to most of the studies being at high risk of bias
eWe downgraded (2) level for very serious imprecision due to wide confidence interval and small number of events and sample size