Efficacy and Safety of Clazosentan After Aneurysmal Subarachnoid Hemorrhage: An Updated Meta-Analysis

被引:12
|
作者
Muniz Pontes, Julia Pereira [1 ]
Costa Santos, Monica D'Alma [2 ]
Gibram, Franceliny Couto [3 ]
Vieira Rodrigues, Natasha Maranhao [4 ]
Cavalcante-Neto, Joaquim Francisco [5 ]
Maia Barros, Alexandre Drayton [6 ]
Solla, Davi J. Fontoura [7 ]
机构
[1] Univ Estado Rio De Janeiro, Pedro Ernesto Univ Hosp, Dept Surg Specialties, Neurosurg Teaching & Assistance Unit, 25 Dois Dezembro, BR-22220040 Rio De Janeiro, RJ, Brazil
[2] Univ Oeste Paulista, Hosp Reg Presidente Prudente, Sao Paulo, Brazil
[3] Univ Vale Sapucai, Dept Neurosurg, Pouso Alegre, MG, Brazil
[4] Univ Fed Amazonas, Hosp Univ Getulio Vargas, Manaus, AM, Brazil
[5] Univ Fed Ceara, Dept Neurosurg, Sobral, Ceara, Brazil
[6] Hosp Cardio Pulm, Dept Intervent Neuroradiol, Salvador, BA, Brazil
[7] Univ Sao Paulo, Hosp Clin Fac Med, Dept Neurol, Div Neurosurg, Sao Paulo, Brazil
关键词
Aneurysm; Clazosentan; Meta-analysis; Subarachnoid hemorrhage; Vasospasm; DOUBLE-BLIND; RECEPTOR ANTAGONIST; CEREBRAL VASOSPASM; ENDOTHELIN; ISCHEMIA;
D O I
10.1227/neu.0000000000002601
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND OBJECTIVES: Clazosentan has been studied to treat cerebral vasospasm after aneurysmal subarachnoid hemorrhage (aSAH).This meta-analysis of randomized controlled trials updates the current knowledge regarding the efficacy and safety of clazosentan compared with placebo after aSAH.METHODS: Databases were systematically searched for randomized controlled trials directly comparing the use of clazosentan and placebo for the treatment of cerebral vasospasm after aSAH. Additional eligibility criteria were the report of any of the outcomes of interest (vasospasm, morbidity, functional outcome, or mortality). The primary outcome was vasospasm-related delayed cerebral ischemia (DCI). The analyses were stratified by clazosentan dosage (low or high dose) and aneurysm treatment modality (clipping or coiling). The Cochrane RoB-2 tool was used for studies quality assessment.RESULTS: Six studies comprising 7 clinical trials were included, involving 2778 patients. Clazosentan decreased the risk of vasospasm-related DCI (risk ratio [RR] 0.56, 95% CI 0.38-0.81) and delayed ischemic neurological deficit (RR 0.63, 95% 0.50-0.80). Angiographic vasospasm (RR 0.54, 95% CI 0.47-0.61) was also decreased. Functional outcomes (favorable Glasgow Outcome Scale, RR 0.99, 95% CI 0.79-1.24) and death (RR 1.03, 95% CI 0.71-1.49) did not change. Meanwhile, adverse events were increased by clazosentan (RR 1.54, 95% CI 1.35-1.76).CONCLUSION: Clazosentan decreased vasospasm-related DCI and angiographic vasospasm but did not improve functional outcomes or mortality. Adverse events were increased by clazosentan.
引用
收藏
页码:1208 / 1219
页数:12
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