Key result
Endothelin-receptor antagonists did not improve overall mortality (RR 1.03) or unfavorable outcomes (RR 1.07) compared to placebo in patients with aneurysmal subarachnoid hemorrhage.
Why the study?
Do endothelin-receptor antagonists improve clinical outcomes in patients with aneurysmal subarachnoid hemorrhage?
Meta-Analysis (n=2,595)
Double-blind
Yes
Yes
Do endothelin-receptor antagonists improve clinical outcomes in patients with aneurysmal subarachnoid hemorrhage?
Answers are grounded in this paper and cite their sources.
Endothelin-receptor antagonists do not improve clinical outcomes in aneurysmal subarachnoid hemorrhage and are associated with increased adverse events including lung complications, hypotension, and anemia.
INTRODUCTION: The previous meta-analysis on the use of endothelin-receptor antagonists (ETRAs) to treat aneurysmal subarachnoid hemorrhage (SAH) has become outdated due to recently published phase 3 clinical trials. An up-to-date meta-analysis is needed to provide the best available evidence for the efficacy of ETRAs for aneurysmal SAH. METHODS: We performed a systematic review and meta-analysis of published randomized controlled trials that investigate efficacy of ETRAs in patients with aneurysmal SAH. Mortality, unfavorable outcome, delayed ischemic neurological deficit (DIND), delayed cerebral infarction (DCI), angiographic vasospasm and adverse events were analyzed. Meta-analysis was performed in terms of the risk ratio (RR) and 95% confidence interval (CI). RESULTS: Five eligible studies were reviewed and analyzed, involving 2,595 patients. The pooled RRs of mortality and unfavorable outcome after SAH were 1.03 (95% CI = 0.77 to 1.36) and 1.07 (95% CI = 0.93 to 1.22), respectively. The pooled RRs were 0.87 (95% CI = 0.74 to 1.03) for DCI, 0.77 (95% CI = 0.66 to 0.90) for DIND, and 0.66 (95% CI = 0.57 to 0.77) for angiographic vasospasm. There were significant increases in lung complications (RR = 1.80, 95% CI = 1.55 to 2.09), hypotension (RR = 2.42, 95% CI = 1.78 to 3.29) and anemia (RR = 1.47, 95% CI = 1.19 to 1.83) in patients administered ETRAs. CONCLUSION: There is no evidence that ETRAs could benefit clinical outcome in patients with SAH. Owing to the increased adverse events, further clinical trials of ETRAs in SAH patients should be more carefully formulated and designed. The present results also suggest that DCI may be a better outcome measure than vasospasm and DIND in SAH clinical trials and observational studies.
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Ma et al. (2012) conducted a meta-analysis in Aneurysmal subarachnoid hemorrhage (n=2,595). Endothelin-receptor antagonists vs. Placebo was evaluated on Mortality (RR 1.03, 95% CI 0.77 to 1.36). Endothelin-receptor antagonists did not improve overall mortality (RR 1.03) or unfavorable outcomes (RR 1.07) compared to placebo in patients with aneurysmal subarachnoid hemorrhage.
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