Effectiveness of pneumococcal Haemophilus influenzae protein D conjugate vaccine against pneumonia in children: A cluster-randomised trial

被引:12
作者
Kilpi, T. M. [1 ]
Jokinen, J. [1 ]
Puumalainen, T. [1 ]
Nieminen, H. [2 ]
Ruokokoski, E. [1 ]
Rinta-Kokko, H. [1 ]
Traskine, M. [3 ]
Lommel, P. [3 ]
Moreira, M. [3 ]
Ruiz-Guinazu, J. [3 ]
Borys, D. [3 ]
Schuerman, L. [3 ]
Palmu, A. A. [2 ]
机构
[1] Natl Inst Hlth & Welf, Dept Hlth Protect, POB 30, FI-00271 Helsinki, Finland
[2] Natl inst Hlth & Welf, Dept Hlth Protect, FinnMedi 1,Biokatu 6, FI-33520 Tampere, Finland
[3] GSK, Vaccine Res & Dev, Parc Noire Epine 20,Ave Fleming, B-1300 Wavre, Belgium
关键词
Vaccine effectiveness; Pneumococcus; Clinical trial; Pneumonia; Infant; PLACEBO-CONTROLLED-TRIAL; DOUBLE-BLIND; STREPTOCOCCUS-PNEUMONIAE; STANDARDIZED INTERPRETATION; SEROTYPE REPLACEMENT; CHEST RADIOGRAPHS; DISEASE; EFFICACY; YOUNGER; PREVENTION;
D O I
10.1016/j.vaccine.2018.08.020
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Pneumococcal conjugate vaccines have potential to prevent significant proportion of childhood pneumonia. Finnish Invasive Pneumococcal disease vaccine trial was designed to assess the vaccine effectiveness (VE) of the 10-valent pneumococcal Haemophilus influenzae protein D conjugate vaccine (PHiD-CV10) against several outcomes. We now report results for pneumonia. Methods: In this nationwide, cluster-randomised, double-blind trial, children younger than 19 months received PHiD-CV10 in 52 clusters or hepatitis vaccines as control in 26 clusters. Infants younger than 7 months at the first vaccination received either 3+1 or 2+1 vaccination schedule, children aged 711 months received 2+1, and those 12-18 months of age two-dose schedule. All hospitalizations and outpatient visits to hospital associated with ICD-10 codes compatible with pneumonia were identified through the National Care Register and 1-3 frontal chest X-ray images per event were collected. External readers who were unaware of the patients' vaccination status retrospectively interpreted the images. The evaluated outcomes were hospital-diagnosed, hospital-treated pneumonia as primary diagnosis, and radiologically confirmed pneumonia during the blinded, intention-to-treat follow-up period from the first vaccination to the end of 2011. Total VE was calculated as 1 minus rate ratio of all pneumonia episodes. Results: 47 366 children were enrolled from February 2009, to October 2010. VE against all episodes of hospital-diagnosed pneumonia was 27% (95% confidence interval [CI]: 14%, 38%), 32% (95% CI: 3%, 52%), and 23% (95% CI: -5%, 44%) in subjects enrolled at age <7, 7-11, and 12-18 months, respectively. Corresponding rate reductions were 3.4, 4.7, and 2.5 per 1000 person-years. VE estimates against pneumonia with alveolar consolidation or pleural effusion (WHO criteria) in the three cohorts were 45% (95% CI: 26%, 60%), 56% (95% CI: 14%, 77%), and 48% (95% CI: 2%, 73%), respectively. Conclusion: PHiD-CV10 vaccination remarkably reduced disease burden due to pneumonia in infants and young children. (C) 2018 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:5891 / 5901
页数:11
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