Department of Respiratory Medicine, UMC Utrecht, Utrecht, The Netherlands; Julius Centre for Health Sciences and Primary Care, UMC Utrecht, Utrecht, The Netherlands.
Department of Medical Microbiology, UMC Utrecht, Utrecht, The Netherlands.
Clin Microbiol Infect. 2018 Jul;24(7):764-770. doi: 10.1016/j.cmi.2017.10.006. Epub 2017 Oct 16.
Our objective was to evaluate whether vaccination with the 13-valent pneumococcal conjugate vaccine (PCV13) prevents the incidence of community-acquired pneumonia (CAP) caused by influenza (influenza-associated CAP, IA-CAP) or other respiratory viruses in the elderly.
This analysis was part of the Community-Acquired Pneumonia immunization Trial in Adults (CAPiTA); a double blind, randomized, placebo-controlled trial in 84 496 immunocompetent individuals aged ≥65 years. CAP was defined by clinical and radiological criteria, and oropharyngeal swabs were collected from all individuals referred to a sentinel centre with a clinical suspicion of pneumonia. Presence of influenza A and B, parainfluenza 1, 2, 3 and 4, human adeno-, boca-, corona-, metapneumo-, rhino- and respiratory syncytial viruses was determined by real-time PCR.
Of 3209 episodes of suspected pneumonia, viral aetiology was tested in 2917 and proportions with influenza virus, human metapneumovirus and respiratory syncytial virus were 4.6%, 2.5% and 3.1%, respectively. There were 1653 oropharyngeal swabs for PCR testing available from 1814 episodes that fulfilled criteria for CAP, yielding 23 first episodes of IA-CAP in the PCV13 and 35 in the in placebo group-vaccine efficacy for IA-CAP of 34.4% (95% CI -11.1% to 61.2%; p 0.117). Annual influenza vaccination was received by 672 (87.2%) in the PCV13 group and 719 (87.7%) in the placebo group of the confirmed CAP cases.
In a randomized study of 84 496 elderly individuals with a high uptake of influenza vaccination, PCV13 was not associated with a statistically significant reduction of influenza or virus-associated CAP. Overall incidence of non-influenza viral pneumonia was low.
本研究旨在评估 13 价肺炎球菌结合疫苗(PCV13)接种能否预防老年人社区获得性肺炎(CAP)由流感(流感相关 CAP,IA-CAP)或其他呼吸道病毒引起。
该分析为成人社区获得性肺炎免疫接种试验(CAPiTA)的一部分;这是一项在 84496 名免疫功能正常的年龄≥65 岁的个体中进行的双盲、随机、安慰剂对照试验。CAP 的定义为临床和影像学标准,所有疑似肺炎患者均采集咽拭子进行检测。采用实时 PCR 检测流感 A 和 B、副流感 1、2、3 和 4、人腺病毒、博卡病毒、冠状病毒、副黏液病毒、鼻病毒和呼吸道合胞病毒。
3209 例疑似肺炎病例中,2917 例进行了病毒病因学检测,流感病毒、人偏肺病毒和呼吸道合胞病毒的比例分别为 4.6%、2.5%和 3.1%。1814 例符合 CAP 标准的病例中有 1653 例可进行 PCR 检测,其中 PCV13 组有 23 例首次出现 IA-CAP,安慰剂组有 35 例,PCV13 组对 IA-CAP 的疫苗疗效为 34.4%(95%CI -11.1%至 61.2%;p=0.117)。PCV13 组确诊 CAP 病例中,672 例(87.2%)和安慰剂组中 719 例(87.7%)接种了年度流感疫苗。
在一项针对 84496 名老年人的随机研究中,流感疫苗接种率较高,PCV13 与流感或病毒相关 CAP 的发生率降低无关。非流感病毒性肺炎的总体发生率较低。