The impact of 13-valent pneumococcal conjugate vaccination on virus-associated community-acquired pneumonia in elderly Exploratory analysis of the CAPiTA trial

被引:16
|
作者
Huijts, S. M. [1 ,2 ]
Coenjaerts, F. E. J. [3 ]
Bolkenbaas, M. [2 ]
van Werkhoven, C. H. [2 ]
Grobbee, D. E. [2 ,4 ]
Bonten, M. J. M. [2 ,3 ]
机构
[1] UMC Utrecht, Dept Resp Med, Utrecht, Netherlands
[2] UMC Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] UMC Utrecht, Dept Med Microbiol, Utrecht, Netherlands
[4] Julius Clin, Zeist, Netherlands
关键词
13-valent pneumococcal conjugate vaccine; Community-acquired pneumonia; Influenza virus; Viral community-acquired pneumonia; Viral pneumonia; STREPTOCOCCUS-PNEUMONIAE; RESPIRATORY VIRUSES; INFLUENZA-VIRUS; DISEASE; ADULTS;
D O I
10.1016/j.cmi.2017.10.006
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: 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. Methods: 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. Results: 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. Conclusion: 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. (c) 2017 The Authors. Published by Elsevier Ltd on behalf of European Society of Clinical Microbiology and Infectious Diseases.
引用
收藏
页码:764 / 770
页数:7
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