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13 价肺炎球菌结合疫苗在中国儿童社区获得性肺炎中的有效性:一项观察性队列研究。

Effectiveness of 13-valent pneumococcal conjugate vaccine against community acquired pneumonia among children in China, an observational cohort study.

机构信息

Department of Epidemiology, School of Public Health, Fudan University, Key Laboratory of Public Health Safety, Ministry of Education, Shanghai, China.

Suzhou Center for Disease Prevention and Control, Suzhou, China.

出版信息

Vaccine. 2021 Jul 30;39(33):4620-4627. doi: 10.1016/j.vaccine.2021.06.075. Epub 2021 Jul 9.

Abstract

BACKGROUND

In China, 13-valent pneumococcal conjugate vaccine (PCV13) has been available since 2017, but only via the private market with low uptake rate. We assessed the direct effectiveness of PCV13 against community acquired pneumonia (CAP) associated with PCV13 serotype carriage (VT-CAP).

METHODS

We conducted an observational cohort study of children born during 12-Dec-2016 to 30-Nov-2018 identified in the Suzhou Centers for Disease Control vaccine registry database, and who had at least one inpatient or outpatient record at the Suzhou University Affiliated Children's hospital (SCH) health-information-system (HIS) database. The vaccine registry cohort was followed through the HIS database through 30-Jun-2019 to identify hospitalized VT-CAP. Pneumococci were isolated from deep upper respiratory aspirates and serotyped with Quellung reactions.

RESULTS

We included 139,127 children of whom 9024 (6.5%) received 1 + PCV13 doses (95.8% received 2 + doses). Within the total cohort, we identified 548 children hospitalized at SCH for VT-CAP, of whom 10 had received 2 + PCV13 doses. Adjusted for demographics, receipt of other childhood vaccines, and underlying medical conditions, the first visit vaccine effectiveness among children who had received 2 + PCV13 doses was 60.9% (95% CI: 25.8% to 79.4%) for VT-CAP and 17.9% (95% CI: 5.5% to 28.6%) for clinical CAP. Incidence rate reductions per 100,000 child-years of observation for all visits were 208 (95% CI: 118 to 298) for VT-CAP and 720 (95% CI: 304 to 1135) for clinical CAP.

CONCLUSIONS

PCV13 was protective against hospitalized VT-CAP and clinical CAP with large associated incidence rate reductions among children living in Suzhou, China.

摘要

背景

在中国,13 价肺炎球菌结合疫苗(PCV13)自 2017 年起已获准上市,但仅通过私人市场提供,接种率较低。我们评估了 PCV13 对与 PCV13 血清型携带相关的社区获得性肺炎(CAP)(VT-CAP)的直接有效性。

方法

我们对 2016 年 12 月 12 日至 2018 年 11 月 30 日期间出生的儿童进行了一项观察性队列研究,这些儿童在苏州疾病预防控制中心疫苗登记数据库中被识别,并在苏州大学附属儿童医院(SCH)健康信息系统(HIS)数据库中至少有一次住院或门诊记录。通过 HIS 数据库对疫苗登记队列进行随访,直至 2019 年 6 月 30 日,以确定住院 VT-CAP。从深部上呼吸道抽吸物中分离肺炎球菌,并通过 Quellung 反应进行血清分型。

结果

我们纳入了 139127 名儿童,其中 9024 名(6.5%)接受了 1 剂+PCV13 剂量(95.8%接受了 2 剂+剂量)。在总队列中,我们在 SCH 识别了 548 名因 VT-CAP 住院的儿童,其中 10 名接受了 2 剂+PCV13 剂量。在调整了人口统计学因素、其他儿童疫苗接种情况和潜在医疗状况后,接受 2 剂+PCV13 剂量的儿童的首次就诊疫苗有效性为 VT-CAP 为 60.9%(95%CI:25.8%至 79.4%),临床 CAP 为 17.9%(95%CI:5.5%至 28.6%)。每 100000 名儿童观察年的发病率降低率为所有就诊的 VT-CAP 为 208(95%CI:118 至 298),临床 CAP 为 720(95%CI:304 至 1135)。

结论

在中国苏州,PCV13 可预防住院 VT-CAP 和临床 CAP,并与儿童发病率的大幅降低相关。

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