Who is at risk of 13-valent conjugated pneumococcal vaccine failure?

被引:7
|
作者
Yildirim, Melike [1 ]
Keskinocak, Pinar [1 ,2 ]
Pelton, Stephen [3 ,4 ]
Pickering, Larry [5 ]
Yildirim, Inci [5 ,6 ]
机构
[1] H Milton Stewart Sch Ind & Syst Engn, Atlanta, GA USA
[2] Georgia Inst Technol, Coll Engn, Atlanta, GA 30332 USA
[3] Boston Med Ctr, Dept Pediat, Boston, MA USA
[4] Boston Univ, Dept Epidemiol, Sch Publ Hlth, Boston, MA USA
[5] Emory Univ, Dept Pediat, Atlanta, GA 30322 USA
[6] Rollins Sch Publ Hlth, Dept Epidemiol, Atlanta, GA USA
关键词
Vaccine failure; 13-valent conjugated pneumococcal vaccine; Children; STREPTOCOCCUS-PNEUMONIAE; HAEMOPHILUS-INFLUENZAE; MASSACHUSETTS CHILDREN; DISEASE; COLONIZATION; INFECTIONS; ERA;
D O I
10.1016/j.vaccine.2019.12.060
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: Despite high vaccine coverage rates in children and efficacy of pneumococcal conjugate vaccines, invasive pneumococcal disease (IPD) episodes due to serotypes included in the vaccine following completion of the recommended course of immunisation (i.e. vaccine failure) have been reported. Methods: We used data gathered from a population-based enhanced passive surveillance for IPD in children under 18 years of age in Massachusetts and an ensemble model composed of three machine-learning algorithms to predict probability of 13-valent pneumococcal conjugated vaccine (PCV13) failure and to evaluate potential associated features including age, underlying comorbidity, clinical presentation, and vaccine schedule. Vaccine failure was defined as diagnosis of IPD due to vaccine serotype (VST), in a child who received age recommended doses recommended by Advisory Committee of Immunization Practices. Results: During the 7-year study period, between April 01, 2010 and March 31, 2017, we identified 296 IPD cases. There were 107 (36%) IPD cases caused by VST, mostly serotype 19A (49, 17%), 7F (21, 7%), and 3 (18, 6%). Thirty-seven (34%) were in children who were completely vaccinated representing 13% of all IPD cases. Vaccine failure was more likely among children older than 60 months (predicted probability 0.40, observed prevalence 0.37, model prediction accuracy 79%), children presenting with pneumonia (predicted probability 0.27, observed prevalence 0.31, model accuracy 77%), and children with underlying comorbidity (predicted probability 0.24, observed prevalence 0.23, model accuracy 96%). Vaccine failure probability for those >60 months of age and had an underlying risk factor was 45% (observed prevalence 0.33, model accuracy 82%). The likelihood of vaccine failure was lowest among children who had completed 3 primary doses plus one booster dose PCV13 (predicted probability 0.14, observed prevalence 0.14, model prediction accuracy 100%). Conclusion: PCV13 vaccine failure is more frequent among older children with underlying comorbidity, and among those who present with pneumococcal pneumonia. Our study provides a preliminary framework to predict the patterns of vaccine failures and may contribute to decision-making processes to optimize PCV immunization schedules. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1671 / 1677
页数:7
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