From the GSK, Rockville, Maryland.
National Autonomous University of Santo Domingo, Santo Domingo, Dominican Republic.
Pediatr Infect Dis J. 2019 Aug;38(8):866-872. doi: 10.1097/INF.0000000000002387.
In an exploratory analysis of an inactivated quadrivalent influenza vaccine (IIV4) trial in children 6-35 months without risk factors for influenza, we evaluated clinical presentation of influenza illness and vaccine impact on health outcomes.
This phase III trial was conducted in 13 geographically diverse countries across 5 influenza seasons (2011-2014). Children were randomized 1:1 to IIV4 or control. Active surveillance was performed for influenza-like episodes (ILE); influenza was confirmed by reverse transcription polymerase chain reaction (RT-PCR). The total vaccinated cohort was evaluated (N = 12,018).
5702 children experienced ≥1 ILE; 356 (IIV4 group) and 693 (control group) children had RT-PCR-confirmed influenza. Prevalence of ILE was similar in RT-PCR-positive and RT-PCR-negative cases regardless of vaccination. Breakthrough influenza illness was attenuated in children vaccinated with IIV4; moderate-to-severe illness was 41% less likely to be reported in the IIV4 group than the control group [crude odds ratio: 0.59 (95% confidence intervals: 0.44-0.77)]. Furthermore, fever >39°C was 46% less frequent following vaccination with IIV4 than with control [crude odds ratio: 0.54 (95% confidence intervals: 0.39-0.75)] in children with breakthrough illness. Health outcome analysis showed that, each year, IIV4 would prevent 54 influenza cases per 1000 children and 19 children would need to be vaccinated to prevent 1 new influenza case.
In addition to preventing influenza in 50% of participants, IIV4 attenuated illness severity and disease burden in children who had a breakthrough influenza episode despite vaccination.
在一项针对无流感高危因素的 6-35 个月儿童的四价灭活流感疫苗(IIV4)试验的探索性分析中,我们评估了流感疾病的临床表现和疫苗对健康结局的影响。
这项 III 期试验在 13 个地理位置不同的国家进行,横跨 5 个流感季节(2011-2014 年)。儿童以 1:1 的比例随机分配至 IIV4 组或对照组。进行了流感样病例(ILE)的主动监测;通过逆转录聚合酶链反应(RT-PCR)确认流感。对总接种组(N=12018)进行了评估。
5702 名儿童经历了≥1 次 ILE;356 名(IIV4 组)和 693 名(对照组)儿童的 RT-PCR 检测结果为流感阳性。无论接种情况如何,RT-PCR 阳性和 RT-PCR 阴性病例的 ILE 发生率相似。接种 IIV4 可减轻儿童突破性流感疾病的严重程度;与对照组相比,IIV4 组中度至重度疾病的报告发生率降低了 41%[粗比值比:0.59(95%置信区间:0.44-0.77)]。此外,与对照组相比,接种 IIV4 后发热>39°C 的频率降低了 46%[粗比值比:0.54(95%置信区间:0.39-0.75)],这在突破性疾病患儿中更为明显。健康结局分析表明,每年 IIV4 将预防 1000 名儿童中 54 例流感病例,需要接种 19 名儿童才能预防 1 例新的流感病例。
除了在 50%的参与者中预防流感外,IIV4 还减轻了突破性流感事件中儿童的疾病严重程度和疾病负担。