Early Magnesium Treatment After Aneurysmal Subarachnoid Hemorrhage Individual Patient Data Meta-Analysis

被引:22
作者
Mees, Sanne M. Dorhout [1 ]
Algra, Ale [1 ,2 ]
Wong, George K. C. [3 ]
Poon, Wai S. [3 ]
Bradford, Celia M. [4 ]
Saver, Jeffrey L. [5 ]
Starkman, Sidney [6 ,7 ]
Rinkel, Gabriel J. E. [1 ]
van den Bergh, Walter M. [8 ]
机构
[1] Univ Med Ctr Utrecht, Rudolf Magnus Inst Neurosci, Dept Neurol & Neurosurg, Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Crit Care, Div Neurosurg, Hong Kong, Hong Kong, Peoples R China
[4] Royal N Shore Hosp, Dept Crit Care, Sydney, NSW, Australia
[5] Univ Calif Los Angeles, David Geffen Sch Med, Comprehens Stroke Ctr, Dept Neurol, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Comprehens Stroke Ctr, Dept Emergency Med, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, David Geffen Sch Med, Comprehens Stroke Ctr, Dept Neurol, Los Angeles, CA 90095 USA
[8] Univ Groningen, Univ Med Ctr Groningen, Dept Crit Care, NL-9700 RB Groningen, Netherlands
基金
英国医学研究理事会;
关键词
SULFATE;
D O I
10.1161/STROKEAHA.115.010575
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Delayed cerebral ischemia (DCI) is an important cause of poor outcome after aneurysmal subarachnoid hemorrhage (SAH). Trials of magnesium treatment starting <4 days after symptom onset found no effect on poor outcome or DCI in SAH. Earlier installment of treatment might be more effective, but individual trials had not enough power for such a subanalysis. We performed an individual patient data meta-analysis to study whether magnesium is effective when given within different time frames within 24 hours after the SAH. Methods-Patients were divided into categories according to the delay between symptom onset and start of the study medication: <6, 6 to 12, 12 to 24, and >24 hours. We calculated adjusted risk ratios with corresponding 95% confidence intervals for magnesium versus placebo treatment for poor outcome and DCI. Results-We included 5 trials totaling 1981 patients; 83 patients started treatment <6 hours. For poor outcome, the adjusted risk ratios of magnesium treatment for start <6 hours were 1.44 (95% confidence interval, 0.83-2.51); for 6 to 12 hours 1.03 (0.65-1.63), for 12 to 24 hours 0.84 (0.65-1.09), and for >24 hours 1.06 (0.87-1.31), and for DCI, <6 hours 1.76 (0.68-4.58), for 6 to 12 hours 2.09 (0.99-4.39), for 12 to 24 hours 0.80 (0.56-1.16), and for >24 hours 1.08 (0.88-1.32). Conclusions-This meta-analysis suggests no beneficial effect of magnesium treatment on poor outcome or DCI when started early after SAH onset. Although the number of patients was small and a beneficial effect cannot be definitively excluded, we found no justification for a new trial with early magnesium treatment after SAH. © 2015 American Heart Association, Inc.
引用
收藏
页码:3190 / 3193
页数:4
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