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在赞比亚卢萨卡,评估口服霍乱疫苗一剂效力的替代观察性设计。

Alternative observational designs to estimate the effectiveness of one dose of oral cholera vaccine in Lusaka, Zambia.

机构信息

Epicentre, Paris, France.

Ministry of Health, Lusaka, Zambia.

出版信息

Epidemiol Infect. 2020 Mar 13;148:e78. doi: 10.1017/S095026882000062X.

Abstract

We conducted a matched case-control (MCC), test-negative case-control (TNCC) and case-cohort study in 2016 in Lusaka, Zambia, following a mass vaccination campaign. Confirmed cholera cases served as cases in all three study designs. In the TNCC, control-subjects were cases with negative cholera culture and polymerase chain reaction results. Matched controls by age and sex were selected among neighbours of the confirmed cases in the MCC study. For the case-cohort study, we recruited a cohort of randomly selected individuals living in areas considered at-risk of cholera. We recruited 211 suspected cases (66 confirmed cholera cases and 145 non-cholera diarrhoea cases), 1055 matched controls and a cohort of 921. Adjusted vaccine effectiveness of one dose of oral cholera vaccine (OCV) was 88.9% (95% confidence interval (CI) 42.7-97.8) in the MCC study, 80.2% (95% CI: 16.9-95.3) in the TNCC design and 89.4% (95% CI: 64.6-96.9) in the case-cohort study. Three study designs confirmed the short-term effectiveness of single dose OCV. Major healthcare-seeking behaviour bias did not appear to affect our estimates. Most of the protection among vaccinated individuals could be attributed to the direct effect of the vaccine.

摘要

我们在 2016 年赞比亚卢萨卡开展了一项匹配病例对照(MCC)、检验阴性病例对照(TNCC)和病例队列研究,该研究是在一次大规模疫苗接种活动之后进行的。所有三种研究设计均将确诊霍乱病例作为病例。在 TNCC 中,对照病例是霍乱培养和聚合酶链反应结果均为阴性的病例。在 MCC 研究中,通过年龄和性别与确诊病例相匹配的对照病例是从确诊病例的邻居中选择的。对于病例队列研究,我们招募了一组居住在被认为存在霍乱风险地区的随机选择的个体作为队列。我们招募了 211 例疑似病例(66 例确诊霍乱病例和 145 例非霍乱腹泻病例)、1055 例匹配对照病例和一个 921 人的队列。MCC 研究中一剂口服霍乱疫苗(OCV)的调整疫苗有效性为 88.9%(95%置信区间(CI)为 42.7-97.8),TNCC 设计为 80.2%(95%CI:16.9-95.3),病例队列研究为 89.4%(95%CI:64.6-96.9)。三项研究设计均证实了一剂 OCV 的短期有效性。主要的医疗寻求行为偏倚似乎并未影响我们的估计。接种疫苗个体的大部分保护作用可归因于疫苗的直接作用。

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