Effectiveness of 13-valent pneumococcal conjugate vaccine against medically-attended lower respiratory tract infection and pneumonia among older adults

J. Lewnard, K. Bruxvoort, Heidi Fischer, V. Hong, L. Grant, L. Jodar, A. Cane, B. Gessner, S. Tartof
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引用次数: 21

Abstract

Importance: In 2014, the US Advisory Committee on Immunization Practices (ACIP) extended existing pneumococcal vaccination recommendations for adults aged [≥]65 years to include 13-valent pneumococcal conjugate vaccine (PCV13), primarily to prevent non-bacteremic pneumonia. Objective: To determine PCV13 effectiveness against all-cause inpatient plus outpatient medically-attended lower-respiratory tract infection (LRTI) and pneumonia among US older adults. Design: Prospective, open cohort study following participants from 2016 to 2019. We conducted analyses in a self-matched framework, comparing outcomes during participants' follow-up periods before and after receipt of PCV13. Setting: Kaiser Permanente Southern California (KPSC) integrated healthcare delivery system. Participants: Adults aged [≥]65 years who received PCV13 between 2016-2019. Exposures: Receipt of PCV13 at ages [≥]65 years, concordant with ACIP guidelines. Main outcomes and measures: We estimated the adjusted hazards ratio (aHR) for first LRTI and pneumonia episodes during each respiratory season, comparing PCV13-exposed and PCV13-unexposed time at risk for each participant using a self-matched inference framework. We computed aHR estimates using Cox proportional hazards models. We defined vaccine effectiveness (VE) as (1-aHR)*100%. We also estimated PCV13-attributable absolute reductions in incidence of LRTI and pneumonia. Results: Observations were available both before and after PCV13 receipt for 42,700 participants. Among these individuals, 1,419 experienced LRTI and 969 experienced pneumonia over approximately 26,000 combined years of follow-up before PCV13 receipt; 3,849 experienced LRTI and 2,727 experienced pneumonia over approximately 74,000 combined years of follow-up after PCV13 receipt. In adjusted analyses, VE was 9.5% (95% confidence interval: 2.2% to 16.3%) against all-cause medically-attended LRTI and 8.8% (-0.2% to 17.0%) against all-cause medically-attended pneumonia. In contrast, we did not identify evidence of protection against LRTI and pneumonia following receipt of 23-valent pneumococcal polysaccharide vaccine. We estimated that PCV13 prevented 0.7 (0.2 to 1.4) and 0.5 (0.0 to 1.0) cases of LRTI and pneumonia, respectively, per 100 vaccinated persons annually. Over a five-year time horizon, one case of LRTI and pneumonia, respectively, was prevented for every 27 (14 to 116) and 42 (-97 to 268) individuals receiving PCV13. Conclusions and relevance: PCV13 vaccination among older adults reduced the burden of medically-attended respiratory illness in this population.
13价肺炎球菌结合疫苗对老年人下呼吸道感染和肺炎的有效性
重要性:2014年,美国免疫实践咨询委员会(ACIP)扩大了现有的65岁以上成人肺炎球菌疫苗接种建议,包括13价肺炎球菌结合疫苗(PCV13),主要用于预防非菌源性肺炎。目的:确定PCV13对美国老年人全因住院和门诊医疗护理下呼吸道感染(LRTI)和肺炎的有效性。设计:前瞻性、开放式队列研究,2016 - 2019年随访。我们在一个自我匹配的框架中进行了分析,比较了参与者在接受PCV13之前和之后的随访期间的结果。环境:南加州凯撒医疗机构(KPSC)综合医疗保健服务系统。参与者:2016-2019年期间接受PCV13治疗的65岁[≥]成年人。暴露:年龄[≥]65岁接受PCV13,符合ACIP指南。主要结局和测量:我们估计了每个呼吸季节首次LRTI和肺炎发作的调整危险比(aHR),使用自匹配推断框架比较每个参与者暴露于pcv13和未暴露于pcv13的风险时间。我们使用Cox比例风险模型计算aHR估计。我们将疫苗有效性(VE)定义为(1-aHR)*100%。我们还估计了pcv13可导致下呼吸道感染和肺炎发生率的绝对降低。结果:42,700名参与者在接受PCV13之前和之后都有观察结果。在这些个体中,1419人经历了LRTI, 969人经历了肺炎,在接受PCV13之前的随访时间总计约26,000年;在接受PCV13后约74,000年的随访中,3,849例发生LRTI, 2,727例发生肺炎。在校正分析中,全因医务人员参与的LRTI组VE为9.5%(95%可信区间:2.2%至16.3%),全因医务人员参与的肺炎组VE为8.8%(-0.2%至17.0%)。相反,我们没有发现接种23价肺炎球菌多糖疫苗后对LRTI和肺炎有保护作用的证据。我们估计,每年每100名接种疫苗的人中,PCV13分别预防了0.7(0.2至1.4)和0.5(0.0至1.0)例下呼吸道感染和肺炎。在五年的时间范围内,每27例(14至116例)和42例(-97至268例)接受PCV13的个体分别预防1例下呼吸道感染和肺炎。结论和相关性:老年人接种PCV13疫苗减轻了这一人群接受医疗护理的呼吸道疾病负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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