Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, Netherlands.
Department of Internal Medicine, St Antonius Hospital, Nieuwegein, Netherlands.
Lancet Respir Med. 2018 Apr;6(4):257-264. doi: 10.1016/S2213-2600(18)30055-9. Epub 2018 Feb 27.
Respiratory syncytial virus (RSV) infection is associated with subsequent wheeze and asthma. We previously reported on the causal relationship between prevention of RSV infection during infancy and reduced frequency of subsequent wheeze using a double-blind, randomised, placebo-controlled trial (MAKI). We continued follow-up and analysed the effect of RSV prevention during infancy on asthma and lung function at age 6 years.
We studied 429 infants born at 32-35 weeks of gestation between 2008-10 who had randomly received either palivizumab for RSV immunoprophylaxis or placebo during the RSV season of their first year of life. After the first year of follow-up, single, assessor-blind follow-up of children continued until they were aged 6 years. Primary outcomes were parent-reported current asthma and forced expiratory volume in 0·5 s (FEV). The trial is registered in the ISRCTN registry, number ISRCTN73641710.
395 (92%) of 429 participants completed this 6-year follow-up study. Parent-reported current asthma was reported in 28 (14·1%) of 199 children in the RSV prevention group and 47 (24·0%) of 196 children in the placebo group (absolute risk reduction [ARR] 9·9%, 95% CI 2·2 to 17·6). The difference in current asthma, which was a composite endpoint, was due to a difference in infrequent wheeze (one to three episodes in the past year; 12 [6·0%] of 199 vs 26 [13·4%] of 194, ARR 7·4%, 95% CI 1·5 to 13·2). FEV percentage predicted values were similar between the RSV prevention group (89·1% [SD 10·6]) and placebo group (90·1% [11·1]), with a mean difference of 1·0 (95% CI -1·3 to 3·3). The proportion of children with current physician-diagnosed asthma was similar between the RSV prevention group (19 [10·3%] of 185) and placebo group (18 [9·9%] of 182), with an ARR of -0·4 (95% CI -6·5 to 5·8).
In otherwise healthy preterm infants, this single-blind, randomised, placebo-controlled trial showed that RSV prevention did not have a major effect on current asthma or lung function at age 6 years. Future research will inform on the effect of RSV prevention on asthma at school age in the general population.
AbbVie.
呼吸道合胞病毒(RSV)感染与随后的喘息和哮喘有关。我们之前曾报道过,在婴儿期使用双盲、随机、安慰剂对照试验(MAKI)预防 RSV 感染与随后喘息频率降低之间存在因果关系。我们继续进行随访,并分析了婴儿期 RSV 预防对 6 岁时哮喘和肺功能的影响。
我们研究了 2008 年至 2010 年间在 32-35 周龄出生的 429 名婴儿,他们在婴儿期的 RSV 季节随机接受了 RSV 免疫预防的帕利珠单抗或安慰剂。在第一年随访结束后,对儿童进行单次、评估者盲法随访,直到他们 6 岁。主要结局是父母报告的当前哮喘和用力呼气量占预计值的百分比(FEV)。该试验在 ISRCTN 注册处注册,编号为 ISRCTN73641710。
429 名参与者中有 395 名(92%)完成了这项 6 年随访研究。在 RSV 预防组的 199 名儿童中有 28 名(14.1%)报告了当前哮喘,在安慰剂组的 196 名儿童中有 47 名(24.0%)报告了当前哮喘(绝对风险降低[ARR]9.9%,95%CI 2.2 至 17.6)。当前哮喘的差异,这是一个复合终点,是由于偶发性喘息的差异(过去一年有一到三次发作;199 名儿童中的 12 名[6.0%]与 194 名儿童中的 26 名[13.4%],ARR 7.4%,95%CI 1.5 至 13.2)。RSV 预防组(89.1%[SD 10.6])和安慰剂组(90.1%[11.1])的 FEV 预计值百分比相似,平均差异为 1.0(95%CI-1.3 至 3.3)。在 RSV 预防组(185 名儿童中的 19 名[10.3%])和安慰剂组(182 名儿童中的 18 名[9.9%])中,当前有医生诊断为哮喘的儿童比例相似,ARR 为-0.4(95%CI-6.5 至 5.8)。
在其他健康的早产儿中,这项单盲、随机、安慰剂对照试验表明, RSV 预防对 6 岁时的当前哮喘或肺功能没有重大影响。未来的研究将阐明 RSV 预防对普通人群中哮喘的影响。
艾伯维。