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13 价肺炎球菌结合疫苗对美国老年社区获得性肺炎住院治疗的有效性:一项基于检验的研究设计。

Effectiveness of 13-Valent Pneumococcal Conjugate Vaccine Against Hospitalization for Community-Acquired Pneumonia in Older US Adults: A Test-Negative Design.

机构信息

Pfizer Vaccines, Collegeville, Pennsylvania.

Department of Medicine, Division of Infectious Diseases, School of Medicine, University of Louisville, Kentucky.

出版信息

Clin Infect Dis. 2018 Oct 30;67(10):1498-1506. doi: 10.1093/cid/ciy312.

Abstract

BACKGROUND

Following universal recommendation for use of 13-valent pneumococcal conjugate vaccine (PCV13) in US adults aged ≥65 years in September 2014, we conducted the first real-world evaluation of PCV13 vaccine effectiveness (VE) against hospitalized vaccine-type community-acquired pneumonia (CAP) in this population.

METHODS

Using a test-negative design, we identified cases and controls from a population-based surveillance study of adults in Louisville, Kentucky, who were hospitalized with CAP. We analyzed a subset of CAP patients enrolled 1 April 2015 through 30 April 2016 who were aged ≥65 years and consented to have their pneumococcal vaccination history confirmed by health insurance records. Cases were defined as hospitalized CAP patients with PCV13 serotypes identified via culture or serotype-specific urinary antigen detection assay. Remaining CAP patients served as test-negative controls.

RESULTS

Of 2034 CAP hospitalizations, we identified PCV13 serotypes in 68 (3.3%) participants (ie, cases), of whom 6 of 68 (8.8%) had a positive blood culture. Cases were less likely to be immunocompromised (29.4% vs 46.4%, P = .02) and overweight or obese (41.2% vs 58.6%, P = .01) compared to controls, but were otherwise similar. Cases were less likely to have received PCV13 than controls (3/68 [4.4%] vs 285/1966 [14.5%]; unadjusted VE, 72.8% [95% confidence interval, 12.8%-91.5%]). No confounding was observed during adjustment for patient characteristics, including immunocompromised status, body mass index, and history of influenza and pneumococcal polysaccharide vaccination (adjusted VE range, 71.1%-73.3%).

CONCLUSIONS

Our study is the first to demonstrate real-world effectiveness of PCV13 against vaccine-type CAP in adults aged ≥65 years following introduction into a national immunization program.

摘要

背景

2014 年 9 月,美国针对 65 岁以上老年人推荐使用 13 价肺炎球菌结合疫苗(PCV13),此后我们进行了首次针对该人群中 PCV13 疫苗对住院治疗的疫苗型社区获得性肺炎(CAP)的实际效果(VE)的评估。

方法

我们使用了一种基于病例对照的研究设计,从肯塔基州路易斯维尔市的一项基于人群的成年人 CAP 住院监测研究中确定了病例和对照。我们分析了 2015 年 4 月 1 日至 2016 年 4 月 30 日期间入组的、年龄≥65 岁且同意通过医疗保险记录确认其肺炎球菌疫苗接种史的 CAP 患者的一个子集。病例定义为通过培养或血清型特异性尿抗原检测确定 PCV13 血清型的住院 CAP 患者。其余 CAP 患者作为阴性对照。

结果

在 2034 例 CAP 住院患者中,我们在 68 名(3.3%)患者(即病例)中鉴定出 PCV13 血清型,其中 6 名(8.8%)的血培养阳性。与对照组相比,病例组免疫功能低下(29.4%对 46.4%,P =.02)和超重或肥胖(41.2%对 58.6%,P =.01)的可能性较低,但其他方面无差异。病例组接受 PCV13 接种的可能性低于对照组(3/68 [4.4%] 对 1966/285 [14.5%];未调整 VE,72.8%[95%置信区间,12.8%-91.5%])。在调整患者特征(包括免疫功能低下状态、体重指数和流感及肺炎球菌多糖疫苗接种史)后,未观察到混杂(调整后的 VE 范围为 71.1%-73.3%)。

结论

本研究是首个在将 PCV13 纳入国家免疫计划后,针对 65 岁以上成年人疫苗型 CAP 的实际效果进行的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0116/6206101/29783ca5d77b/ciy31201.jpg

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