Department of Community Medicine, University of Hong Kong, China.
Clin Infect Dis. 2010 Mar 1;50(5):707-14. doi: 10.1086/650458.
Large clinical trials have demonstrated the therapeutic efficacy of oseltamivir against influenza. We assessed the indirect effectiveness of oseltamivir in reducing secondary household transmission in an incident cohort of influenza index patients and their household members.
We recruited index outpatients whose rapid test results were positive for influenza from February through September 2007 and January through September 2008. Household contacts were followed up for 7-10 days during 3-4 home visits to monitor symptoms. Nose and throat swabs were collected and tested for influenza by reverse-transcription polymerase chain reaction or viral culture.
We followed up 384 index patients and their household contacts. Index patients who took oseltamivir within 24 h of symptom onset halved the time to symptom alleviation (adjusted acceleration factor, 0.56; 95% confidence interval [CI], 0.42-0.76). Oseltamivir treatment was not associated with statistically significant reduction in the duration of viral shedding. Household contacts of index patients who had taken oseltamivir within 24 h of onset had a nonstatistically significant lower risk of developing laboratory-confirmed infection (adjusted odds ratio, 0.54; 95% CI, 0.11-2.57) and a marginally statistically significant lower risk of clinical illness (adjusted odds ratio, 0.52; 95% CI, 0.25-1.08) compared with contacts of index patients who did not take oseltamivir.
Oseltamivir treatment is effective in reducing the duration of symptoms, but evidence of household reduction in transmission of influenza virus was inconclusive.
大型临床试验已经证明奥司他韦治疗流感的疗效。我们评估了奥司他韦在减少流感指数患者及其家庭接触者继发性家庭传播方面的间接效果。
我们招募了 2007 年 2 月至 9 月和 2008 年 1 月至 9 月期间快速检测结果阳性的流感门诊指数患者及其家庭接触者。家庭接触者在 3-4 次家访中接受了 7-10 天的随访,以监测症状。采集鼻喉拭子,通过逆转录聚合酶链反应或病毒培养检测流感。
我们随访了 384 名指数患者及其家庭接触者。在症状出现后 24 小时内服用奥司他韦的指数患者症状缓解时间减半(调整后的加速因子为 0.56;95%置信区间为 0.42-0.76)。奥司他韦治疗与病毒脱落持续时间的显著降低无关。在发病后 24 小时内服用奥司他韦的指数患者的家庭接触者实验室确诊感染的风险较低(调整后的比值比为 0.54;95%置信区间为 0.11-2.57),临床疾病的风险略有统计学意义降低(调整后的比值比为 0.52;95%置信区间为 0.25-1.08)与未服用奥司他韦的指数患者的接触者相比。
奥司他韦治疗可有效缩短症状持续时间,但家庭传播流感病毒的证据尚不确定。