镁作为尼莫地平辅助治疗蛛网膜下腔出血:荟萃分析。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Journal of Yeungnam medical science Pub Date : 2025-01-01 Epub Date: 2025-02-02 DOI:10.12701/jyms.2025.42.26
Riva Satya Radiansyah, Yuri Pamungkas, Ilham Ikhtiar
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引用次数: 0

摘要

背景:蛛网膜下腔出血(SAH)是一种具有高发病率和死亡率的破坏性神经系统疾病。尽管尼莫地平被广泛用于SAH的治疗,但镁作为辅助治疗的潜在益处尚不清楚。本荟萃分析旨在评价镁联合尼莫地平治疗SAH的疗效和安全性。方法:利用PubMed、ScienceDirect、谷歌Scholar和Cochrane Library进行全面的文献检索。随机对照试验和前瞻性队列研究比较镁加尼莫地平与尼莫地平单独治疗SAH患者。主要结局包括脑血管痉挛(CV)、延迟性脑缺血(DCI)、功能结局、死亡率和不良事件。结果:纳入了12项研究,涉及2338例患者。镁与尼莫地平联合用药可显著降低CV发生率(优势比[OR], 0.53;95%置信区间[CI], 0.29-0.95;p=0.03)和DCI (OR, 0.52;95% ci, 0.31-0.87;P =0.01)。然而,在功能结局方面没有发现显著差异(修正Rankin量表:OR, 0.97;p = 0.75;格拉斯哥结局量表:OR, 0.81;p=0.24),死亡率(OR, 0.97;p=0.83)或继发性脑梗死(or, 0.38;p = 0.12)。联合用药组不良事件发生率较高;然而,这种差异没有统计学意义(OR, 3.14;p = 0.33)。结论:在尼莫地平治疗中加入镁可能有助于降低SAH患者的CV和DCI发生率,但不能显著改善功能结局或死亡率。需要进一步的大规模研究来优化给药方案并证实这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Magnesium as an adjunct to nimodipine in subarachnoid hemorrhage: a meta-analysis.

Background: Subarachnoid hemorrhage (SAH) is a devastating neurological condition with high morbidity and mortality rates. Although nimodipine is widely used in the management of SAH, the potential benefits of magnesium as adjunct therapy remain unclear. This meta-analysis aimed to evaluate the efficacy and safety of combining magnesium with nimodipine for the management of SAH.

Methods: A comprehensive literature search was conducted using PubMed, ScienceDirect, Google Scholar, and the Cochrane Library. Randomized controlled trials and prospective cohort studies comparing magnesium plus nimodipine versus nimodipine alone in patients with SAH were included. Key outcomes included cerebral vasospasm (CV), delayed cerebral ischemia (DCI), functional outcomes, mortality, and adverse events.

Results: Twelve studies involving 2,338 patients were included. The combination of magnesium and nimodipine significantly reduced the incidence of CV (odds ratio [OR], 0.53; 95% confidence interval [CI], 0.29-0.95; p=0.03) and DCI (OR, 0.52; 95% CI, 0.31-0.87; p=0.01) compared to nimodipine alone. However, no significant differences were found in functional outcomes (modified Rankin Scale: OR, 0.97; p=0.75; Glasgow Outcome Scale: OR, 0.81; p=0.24), mortality (OR, 0.97; p=0.83), or secondary cerebral infarction (OR, 0.38; p=0.12). The incidence of adverse events was higher in the combination group; however, this difference was not statistically significant (OR, 3.14; p=0.33).

Conclusion: Adding magnesium to nimodipine therapy in patients with SAH may help reduce CV and DCI incidence but does not significantly improve functional outcomes or mortality. Further large-scale studies are needed to optimize the dosing regimens and confirm these findings.

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