Kenyon S, Boulvain M, Neilson J
ORACLE Clinical Co-ordinating Centre, Leicester Royal Infirmary, Department of Obstetrics, Clinical Sciences Building, PO Box 65, Leicester, UK, LE2 7ZR.
Cochrane Database Syst Rev. 2003(2):CD001058. doi: 10.1002/14651858.CD001058.
Premature birth carries substantial neonatal morbidity and mortality. One cause, associated with preterm rupture of membranes (pROM), is often subclinical infection. Maternal antibiotic therapy might lessen infectious morbidity and delay labour, but could suppress labour without treating underlying infection.
To evaluate the immediate and long-term effects of administering antibiotics to women with pROM before 37 weeks, on maternal infectious morbidity, fetal and neonatal morbidity and mortality, and longer term childhood development.
We searched the Cochrane Pregnancy and Childbirth Group trials register (January 2003) and the Cochrane Controlled Trials Register (The Cochrane Library, Issue 4, 2002).
Randomised controlled trials comparing antibiotic administration with placebo that reported clinically relevant outcomes, were included. In addition, trials, in which no placebo was used, were included for the outcome of perinatal death alone.
Data were extracted from each report without blinding of either the results or the treatments that women received. Unpublished data were sought from a number of authors.
Nineteen trials involving over 6000 women and their babies were included. The use of antibiotics following pROM is associated with a statistically significant reduction in chorioamnionitis (relative risk (RR) 0.57, 95% confidence interval (CI) 0.37 to 0.86). There was a reduction in the numbers of babies born within 48 hours (RR 0.71, 95% CI 0.58 to 0.87) and seven days of randomisation (RR 0.80, 95% CI 0.71 to 0.90). The following markers of neonatal morbidity were reduced: neonatal infection (RR 0.68, 95% CI 0.53 to 0.87), use of surfactant (RR 0.83, 95% CI 0.72 to 0.96), oxygen therapy (RR 0.88, 95% CI 0.81 to 0.96), and abnormal cerebral ultrasound scan prior to discharge from hospital (RR 0.82, 95% CI 0.68 to 0.98). Co-amoxiclav was associated with an increased risk of neonatal necrotising enterocolitis (RR 4.60, 95% CI 1.98 to 10.72).
REVIEWER'S CONCLUSIONS: Antibiotic administration following pROM is associated with a delay in delivery and a reduction in major markers of neonatal morbidity. These data support the routine use of antibiotics in pPROM. The choice as to which antibiotic would be preferred is less clear as, by necessity, fewer data are available. Co-amoxiclav should be avoided in women at risk of preterm delivery because of the increased risk of neonatal necrotising enterocolitis. From the available evidence, erythromycin would seem a better choice.
早产会导致大量新生儿发病和死亡。胎膜早破(pROM)相关的一个原因通常是亚临床感染。产妇使用抗生素治疗可能会降低感染发病率并延迟分娩,但也可能在未治疗潜在感染的情况下抑制分娩。
评估在孕37周前对胎膜早破的女性使用抗生素对产妇感染发病率、胎儿及新生儿发病率和死亡率以及儿童长期发育的近期和长期影响。
我们检索了Cochrane妊娠与分娩组试验注册库(2003年1月)和Cochrane对照试验注册库(《Cochrane图书馆》,2002年第4期)。
纳入比较抗生素给药与安慰剂并报告临床相关结果的随机对照试验。此外,仅纳入未使用安慰剂的试验中关于围产期死亡的结果。
从每份报告中提取数据,不对结果或女性接受的治疗进行盲法处理。向多位作者索取未发表的数据。
纳入了19项涉及6000多名女性及其婴儿的试验。胎膜早破后使用抗生素与绒毛膜羊膜炎的统计学显著降低相关(相对危险度(RR)0.57,95%置信区间(CI)0.37至0.86)。随机分组后48小时内出生的婴儿数量减少(RR 0.71,95%CI 0.58至0.87)以及7天内出生的婴儿数量减少(RR 0.80,95%CI 0.71至0.90)。以下新生儿发病指标降低:新生儿感染(RR 0.68,95%CI 0.53至0.87)、表面活性剂的使用(RR 0.83,95%CI 0.72至0.96)、氧疗(RR 0.88,95%CI 0.81至0.96)以及出院前脑超声扫描异常(RR 0.82,95%CI 0.68至0.98)。阿莫西林克拉维酸与新生儿坏死性小肠结肠炎风险增加相关(RR 4.60,95%CI 1.98至10.72)。
胎膜早破后使用抗生素与分娩延迟以及新生儿主要发病指标降低相关。这些数据支持在胎膜早破时常规使用抗生素。由于可用数据较少,关于首选哪种抗生素的选择不太明确。对于有早产风险的女性应避免使用阿莫西林克拉维酸,因为其会增加新生儿坏死性小肠结肠炎的风险。根据现有证据,红霉素似乎是更好的选择。