Costantine Maged M, Weiner Steven J
From the Department of Obstetrics and Gynecology at the University of Texas Medical Branch, Galveston, Texas; and the George Washington University Biostatistics Center, Washington, DC.
Obstet Gynecol. 2009 Aug;114(2 Pt 1):354-364. doi: 10.1097/AOG.0b013e3181ae98c2.
To review the evidence regarding neuroprotective effects of antenatal exposure to magnesium sulfate.
We conducted database searches of MEDLINE, the Cochrane Library and Controlled Trials Register, as well as the ClinicalTrials.gov and International Clinical Trials Register websites. Bibliographies of all relevant articles were reviewed.
Randomized controlled trials comparing magnesium sulfate with placebo/other treatment in patients at risk of preterm delivery were evaluated for inclusion and methodological quality. The primary outcome was death or cerebral palsy by 18-24 months corrected age. Secondary outcomes were death, cerebral palsy, moderate-severe cerebral palsy, and death or moderate-severe cerebral palsy. Separate analyses were performed according to the gestational age (GA) at randomization (less than 32 to 34 weeks and less than 30 weeks) and for studies in which magnesium sulfate was used exclusively for fetal neuroprotection.
TABULATION, INTEGRATION, AND RESULTS: Five randomized controlled trials were included (5,235 fetuses/infants). When analyzed by GA at randomization, in utero exposure to magnesium sulfate at less than 32-34 weeks did not reduce the rate of death or cerebral palsy (relative risk [RR] 0.92, 95% confidence interval [CI] 0.83-1.03). However, cerebral palsy (RR 0.70, 95% CI 0.55-0.89), moderate-severe cerebral palsy (RR 0.60, 95% CI 0.43-0.84), and death or moderate-severe cerebral palsy were significantly reduced, without an evident increase in the risk of death (RR 1.01, 95% CI 0.89-1.14). Similar results were obtained when the GA at randomization was less than 30 weeks. When only neuroprotection trials (four trials, 4,324 fetuses/infants) are analyzed, in utero exposure to magnesium sulfate additionally reduced the primary outcome of death or cerebral palsy. The number needed to treat to prevent one case of cerebral palsy among those who survive until age 18-24 months is 46 (95% CI 26-187) in infants exposed to magnesium sulfate in utero before 30 weeks, and 56 (95% CI 34-164) in infants exposed to magnesium sulfate in utero before 32 to 34 weeks.
Fetal exposure to magnesium sulfate in women at risk of preterm delivery significantly reduces the risk of cerebral palsy without increasing the risk of death.
综述产前暴露于硫酸镁的神经保护作用的相关证据。
我们对MEDLINE、Cochrane图书馆和对照试验注册库以及ClinicalTrials.gov和国际临床试验注册网站进行了数据库检索。对所有相关文章的参考文献进行了审查。
评估比较硫酸镁与安慰剂/其他治疗方法对有早产风险患者的随机对照试验,以确定其纳入情况和方法学质量。主要结局为校正年龄18 - 24个月时的死亡或脑瘫。次要结局为死亡、脑瘫、中重度脑瘫以及死亡或中重度脑瘫。根据随机分组时的孕周(GA)(小于32至34周和小于30周)以及仅将硫酸镁用于胎儿神经保护的研究进行单独分析。
列表、整合与结果:纳入了五项随机对照试验(5235例胎儿/婴儿)。按随机分组时的GA分析,孕32 - 34周前宫内暴露于硫酸镁并未降低死亡或脑瘫发生率(相对危险度[RR] 0.92,95%置信区间[CI] 0.83 - 1.03)。然而,脑瘫(RR 0.70,95% CI 0.55 - 0.89)、中重度脑瘫(RR 0.60,95% CI 0.43 - 0.84)以及死亡或中重度脑瘫显著降低,且死亡风险无明显增加(RR 1.01,95% CI 0.89 - 1.14)。随机分组时GA小于30周时也得到了类似结果。仅分析神经保护试验(四项试验,4324例胎儿/婴儿)时,宫内暴露于硫酸镁还降低了死亡或脑瘫这一主要结局。对于在孕30周前宫内暴露于硫酸镁的婴儿,预防一例存活至18 - 24个月时脑瘫所需治疗人数为46(95% CI 26 - 187);对于在孕32至34周前宫内暴露于硫酸镁的婴儿,所需治疗人数为56(95% CI 34 - 164)。
有早产风险的女性胎儿暴露于硫酸镁可显著降低脑瘫风险且不增加死亡风险。