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奥司他韦在儿童中的疗效和安全性:随机对照试验的系统评价和个体患者数据分析荟萃分析。

Efficacy and Safety of Oseltamivir in Children: Systematic Review and Individual Patient Data Meta-analysis of Randomized Controlled Trials.

机构信息

University of Michigan School of Public Health, Ann Arbor.

Department of Pediatrics, University of Turku and Turku University Hospital, Finland.

出版信息

Clin Infect Dis. 2018 May 2;66(10):1492-1500. doi: 10.1093/cid/cix1040.

Abstract

BACKGROUND

Oseltamivir has been used to treat children with influenza for nearly 2 decades, with treatment currently approved for infants aged ≥2 weeks. However, efficacy and safety remain controversial. Newer randomized, placebo-controlled trials (RCTs), not included in previous meta-analyses, can add to the evidence base.

METHODS

We conducted a systematic review to identify RCTs of oseltamivir therapy in children. We obtained individual patient data and examined protocol-defined outcomes. We then conducted a 2-stage, random-effects meta-analysis to determine the efficacy of treatment in reducing the duration of illness, estimated using differences in restricted mean survival time (RMST) by treatment group. We also examined complications and safety.

RESULTS

We identified 5 trials that included 2561 patients in the intention-to-treat (ITT) and 1598 in the intention-to-treat infected (ITTI) populations. Overall, oseltamivir treatment significantly reduced the duration of illness in the ITTI population (RMST difference, -17.6 hours; 95% confidence interval [CI], -34.7 to -0.62 hours). In trials that enrolled patients without asthma, the difference was larger (-29.9 hours; 95% CI, -53.9 to -5.8 hours). Risk of otitis media was 34% lower in the ITTI population. Vomiting was the only adverse event with a significantly higher risk in the treatment group.

CONCLUSIONS

Despite substantial heterogeneity in pediatric trials, we found that treatment with oseltamivir significantly reduced the duration of illness in those with influenza and lowered the risk of developing otitis media. Alternative endpoints may be required to evaluate the efficacy of oseltamivir in pediatric patients with asthma.

摘要

背景

奥司他韦用于治疗儿童流感已近 20 年,目前批准用于≥2 周龄的婴儿。然而,其疗效和安全性仍存在争议。新的随机、安慰剂对照试验(RCT),未包含在之前的荟萃分析中,可以为证据基础提供补充。

方法

我们进行了一项系统评价,以确定奥司他韦治疗儿童流感的 RCT。我们获取了个体患者数据并检查了方案定义的结局。然后,我们进行了两阶段、随机效应荟萃分析,以确定治疗组在减少疾病持续时间方面的疗效,通过治疗组的受限平均生存时间(RMST)差异来估计。我们还检查了并发症和安全性。

结果

我们确定了 5 项试验,其中 ITT 人群包括 2561 例患者,ITTI 人群包括 1598 例患者。总体而言,奥司他韦治疗显著缩短了 ITTI 人群的疾病持续时间(RMST 差异,-17.6 小时;95%置信区间[CI],-34.7 至-0.62 小时)。在纳入无哮喘患者的试验中,差异更大(-29.9 小时;95%CI,-53.9 至-5.8 小时)。在 ITTI 人群中,中耳炎的风险降低了 34%。在治疗组中,呕吐是唯一具有更高风险的不良事件。

结论

尽管儿科试验存在很大的异质性,但我们发现奥司他韦治疗显著缩短了流感患儿的疾病持续时间,并降低了发生中耳炎的风险。可能需要替代终点来评估奥司他韦在患有哮喘的儿科患者中的疗效。

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