Department of Epidemiology and Biostatistics, College of Public Health, University of Georgia, Athens, GA 30602, USA.
Fam Pract. 2013 Apr;30(2):125-33. doi: 10.1093/fampra/cms059. Epub 2012 Sep 20.
Oseltamivir is widely used for the treatment of influenza. Previous systematic reviews suggest that they reduce complications, but had significant methodologic limitations.
To assess the effect of oseltamivir on duration of symptoms, complications and hospitalizations in adults.
We searched Medline without time or language restrictions, and trial registries maintained by the manufacturer. We included published and unpublished randomized double-blinded, placebo-controlled trials of oseltamivir in adults with suspected influenza that reported duration of symptoms, complications or hospitalizations. We abstracted data regarding study quality, the duration of symptoms and rates of complications and hospitalization.
Three published and eight unpublished studies met our inclusion criteria. For the intention-to-treat (ITT) population, the mean reduction in the duration of symptoms was 20.7 hours [95% confidence interval (CI) 13.3 to 28.0 hours]. Two large unpublished studies in the elderly and in adults with chronic disease did not find a significant reduction in the symptom duration. There was no difference in the likelihood of hospitalization in the ITT population (33/2633 patients for oseltamivir versus 20/1694 for placebo). The rate of complications in the intention-to-treat infected (ITTI) population was reduced when acute bronchitis was included (-2.8%, 95% CI -0.6 to -4.9), but not when it was excluded. The risk of pneumonia was reduced in the ITTI population (-0.9%, 95% CI -0.1 to -1.7) but not in the ITT population.
There is no evidence that oseltamivir reduces the likelihood of hospitalization, pneumonia or the combined outcome of pneumonia, otitis media and sinusitis in the ITT population.
奥司他韦被广泛用于流感的治疗。此前的系统评价表明,奥司他韦可以减少并发症,但存在显著的方法学局限性。
评估奥司他韦对成人流感症状持续时间、并发症和住院治疗的影响。
我们对 Medline 数据库进行了无时间和语言限制的检索,并检索了制造商维护的试验注册数据库。我们纳入了已发表和未发表的奥司他韦治疗成人疑似流感的随机双盲、安慰剂对照试验,这些试验报告了症状持续时间、并发症和住院治疗的结果。我们提取了有关研究质量、症状持续时间以及并发症和住院治疗发生率的数据。
有 3 项已发表研究和 8 项未发表研究符合我们的纳入标准。对于意向治疗(ITT)人群,症状持续时间的平均缩短时间为 20.7 小时[95%置信区间(CI)为 13.3 至 28.0 小时]。两项针对老年人和慢性病成人的大型未发表研究并未发现症状持续时间的显著缩短。在 ITT 人群中,住院治疗的可能性没有差异(奥司他韦组 2633 例患者中有 33 例,安慰剂组 1694 例中有 20 例)。在 ITTI 感染人群中,当包括急性支气管炎时,并发症发生率降低(-2.8%,95%CI-0.6 至-4.9%),但当排除急性支气管炎时则没有降低。在 ITTI 人群中,肺炎的风险降低(-0.9%,95%CI-0.1 至-1.7%),但在 ITT 人群中没有降低。
在 ITT 人群中,奥司他韦并未减少住院治疗、肺炎或肺炎、中耳炎和鼻窦炎的联合结局的发生风险。