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首页> 外文期刊>BMC Pregnancy and Childbirth >Maternal adverse effects of different antenatal magnesium sulphate regimens for improving maternal and infant outcomes: a systematic review
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Maternal adverse effects of different antenatal magnesium sulphate regimens for improving maternal and infant outcomes: a systematic review

机译:不同产前硫酸镁治疗方案对改善母婴结局的母体不良反应:系统评价

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Background Antenatal magnesium sulphate, widely used in obstetrics to improve maternal and infant outcomes, may be associated with adverse effects for the mother sufficient for treatment cessation. This systematic review aimed to quantify maternal adverse effects attributed to treatment, assess how adverse effects vary according to different regimens, and explore women’s experiences with this treatment. Methods Bibliographic databases were searched from their inceptions to July 2012 for studies of any design that reported on maternal adverse effects associated with antenatal magnesium sulphate given to improve maternal or infant outcomes. Primary outcomes were life-threatening adverse effects of treatment (death, cardiac arrest, respiratory arrest). For randomised controlled trials, data were meta-analysed, and risk ratios (RR) pooled using fixed-effects or random-effects models. For non-randomised studies, data were tabulated by design, and presented as RR, odds ratios or percentages, and summarised narratively. Results A total of 143 publications were included (21 randomised trials, 15 non-randomised comparative studies, 32 case series and 75 reports of individual cases), of mixed methodological quality. Compared with placebo or no treatment, magnesium sulphate was not associated with an increased risk of maternal death, cardiac arrest or respiratory arrest. Magnesium sulphate significantly increased the risk of 'any adverse effects’ overall (RR 4.62, 95% CI 2.42-8.83; 4 trials, 13,322 women), and treatment cessation due to adverse effects (RR 2.77; 95% CI 2.32-3.30; 5 trials, 13,666 women). Few subgroup differences were observed (between indications for use and treatment regimens). In one trial, a lower dose regimen (2?g/3?hours) compared with a higher dose regimen (5?g/4?hours) significantly reduced treatment cessation (RR 0.05; 95% CI 0.01-0.39, 126 women). Adverse effect estimates from studies of other designs largely supported data from randomised trials. Case reports supported an association between iatrogenic overdose of magnesium sulphate and life-threatening consequences. Conclusions Appropriate administration of antenatal magnesium sulphate was not shown to be associated with serious maternal adverse effects, though an increase in 'minor’ adverse effects and treatment cessation was shown. Larger trials are needed to determine optimal regimens, achieving maximal effectiveness with minimal adverse effects, for each antenatal indication for use. Vigilance in the use of magnesium sulphate is essential for women’s safety.
机译:背景技术产前硫酸镁被广泛用于产科以改善母婴结局,可能与母亲的不良反应有关,足以终止治疗。这项系统的评估旨在量化归因于治疗的孕产妇不良反应,评估不良反应如何根据不同的治疗方案而变化,并探讨女性接受这种治疗的经验。方法从书目数据库开始到2012年7月,检索任何设计的研究报告,这些设计报告了与改善产前或产妇预产期硫酸镁相关的孕产妇不良反应。主要结局是威胁生命的治疗不良反应(死亡,心脏骤停,呼吸停止)。对于随机对照试验,对数据进行荟萃分析,并使用固定效应或随机效应模型汇总风险比(RR)。对于非随机研究,数据按设计制成表格,并以RR,优势比或百分比表示,并以叙述方式进行汇总。结果共纳入143种方法学质量参差不齐的出版物(21项随机试验,15项非随机比较研究,32例病例系列和75例个别病例报告)。与安慰剂或不进行治疗相比,硫酸镁与孕产妇死亡,心脏骤停或呼吸停止的风险增加无关。硫酸镁显着增加总体上“出现任何不良反应”的风险(RR 4.62,95%CI 2.42-8.83; 4个试验,13,322名女性),以及因不良反应而终止治疗(RR 2.77; 95%CI 2.32-3.30; 5试验中,有13,666名女性)。几乎没有观察到亚组差异(在使用适应症和治疗方案之间)。在一项试验中,与高剂量方案(5μg/ 4?小时)相比,低剂量方案(2?g / 3?小时)显着降低了戒烟(RR 0.05; 95%CI 0.01-0.39,126名女性) 。其他设计研究的不良反应估计在很大程度上支持了随机试验的数据。病例报告支持医源性硫酸镁过量与威胁生命的后果之间的联系。结论尽管适当增加了“次要”不良反应和中止了治疗,但未证明适当给予产前硫酸镁与严重的产妇不良反应有关。对于每种使用的产前适应症,都需要进行较大的试验来确定最佳方案,以达到最大的效果,同时将不良反应降至最低。对硫酸镁的使用保持警惕对女性安全至关重要。

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