UMR-S 707, UPMC-Paris 6, Paris, France.
PLoS One. 2010 Nov 17;5(11):e13998. doi: 10.1371/journal.pone.0013998.
Facemasks and respirators have been stockpiled during pandemic preparedness. However, data on their effectiveness for limiting transmission are scarce. We evaluated the effectiveness of facemask use by index cases for limiting influenza transmission by large droplets produced during coughing in households.
A cluster randomized intervention trial was conducted in France during the 2008-2009 influenza season. Households were recruited during a medical visit of a household member with a positive rapid influenza A test and symptoms lasting less than 48 hours. Households were randomized either to the mask or control group for 7 days. In the intervention arm, the index case had to wear a surgical mask from the medical visit and for a period of 5 days. The trial was initially intended to include 372 households but was prematurely interrupted after the inclusion of 105 households (306 contacts) following the advice of an independent steering committee. We used generalized estimating equations to test the association between the intervention and the proportion of household contacts who developed an influenza-like illness during the 7 days following the inclusion. Influenza-like illness was reported in 24/148 (16.2%) of the contacts in the intervention arm and in 25/158 (15.8%) of the contacts in the control arm and the difference between arms was 0.40% (95%CI: -10% to 11%, P = 1.00). We observed a good adherence to the intervention. In various sensitivity analyses, we did not identify any trend in the results suggesting effectiveness of facemasks.
This study should be interpreted with caution since the lack of statistical power prevents us to draw formal conclusion regarding effectiveness of facemasks in the context of a seasonal epidemic.
clinicaltrials.gov NCT00774774.
在大流行准备期间,已储备了口罩和呼吸器。然而,关于其限制传播效果的数据却很少。我们评估了面罩在限制大飞沫传播方面的效果索引病例在家庭中咳嗽时产生的流感。
在 2008-2009 年流感季节,法国进行了一项集群随机干预试验。在一名家庭成员出现阳性快速流感 A 检测和症状持续不到 48 小时的医疗就诊期间,招募了家庭。家庭被随机分为口罩或对照组,持续 7 天。在干预组中,索引病例必须从就诊时起佩戴外科口罩,并且必须佩戴 5 天。该试验最初打算纳入 372 户家庭,但在咨询了一个独立指导委员会后,在纳入 105 户家庭(306 名接触者)后提前中断。我们使用广义估计方程来检验干预与家庭接触者在纳入后 7 天内出现流感样疾病的比例之间的关联。在干预组中,有 24/148(16.2%)的接触者出现流感样疾病,在对照组中,有 25/158(15.8%)的接触者出现流感样疾病,两组之间的差异为 0.40%(95%CI:-10%至 11%,P=1.00)。我们观察到对干预措施的良好依从性。在各种敏感性分析中,我们没有发现任何趋势表明口罩有效。
由于缺乏统计学效力,我们无法得出关于口罩在季节性流行情况下有效性的正式结论,因此应谨慎解释这项研究。
clinicaltrials.gov NCT00774774。