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流感疫苗对发病率影响的现场调查

Field investigation of influenza vaccine effectiveness on morbidity.

作者信息

Carrat F, Tachet A, Rouzioux C, Housset B, Valleron A J

机构信息

Unité de Recherches Epidémiologie et Sciences de l'Information, Institut Fédératif Saint-Antoine de Recherche sur la Santé, Paris, France.

出版信息

Vaccine. 1998 May-Jun;16(9-10):893-8. doi: 10.1016/s0264-410x(97)00307-1.

Abstract

Our objective was to evaluate influenza vaccine effectiveness during an influenza epidemic by means of a matched case-control study. The study was performed by 35 general practitioners who collected specimens for influenza virus testing from 610 patients who consulted for infectious syndrome: 168 (28%) were influenza-positive. Two designs were used for selecting controls to take into account the high incidence-rate of influenza-like illness and the various possible protective effects of the vaccine. A first disease-free control matched for age and sex was selected during the same week as the case. A second control matched for age and sex was selected at the end of the epidemic period, irrespective of disease history during the epidemic period. Upper and lower bounds of vaccine effectiveness can be derived from these case-control designs. After adjustment for chronic conditions and exposure to an index case, analysis of the matched-pairs whose case was influenza-positive showed, with the first group of controls, an influenza vaccine effectiveness of 68% (95% CI, 10% to 88%) and, in the second group, 53% (95% CI, -19% to 82%). Among the pairs whose case was negative for influenza, vaccine effectiveness was, respectively, 31% (95% CI, -17% to 59%) and 12% (95% CI, -47% to 47%). Vaccine effectiveness was highest for the H3N2 subtype whose vaccine strain was identical to that of the wild-type strain. The results suggest that influenza vaccine is effective in the field in preventing influenza morbidity.

摘要

我们的目标是通过一项匹配病例对照研究评估流感流行期间流感疫苗的有效性。该研究由35名全科医生进行,他们从610名因感染综合征前来就诊的患者中采集了流感病毒检测样本:168人(28%)流感检测呈阳性。为了考虑到流感样疾病的高发病率以及疫苗可能存在的各种保护作用,采用了两种设计来选择对照。第一种是在与病例相同的那一周选择年龄和性别匹配的无病对照。第二种对照是在流行期结束时选择,不考虑流行期内的疾病史,年龄和性别与之匹配。疫苗有效性的上限和下限可从这些病例对照设计中得出。在对慢性病和接触指示病例进行调整后,对病例为流感阳性的匹配对进行分析,结果显示,与第一组对照相比,流感疫苗有效性为68%(95%CI,10%至88%),与第二组对照相比为53%(95%CI,-19%至82%)。在病例流感检测呈阴性的配对中,疫苗有效性分别为31%(95%CI,-17%至59%)和12%(95%CI,-47%至47%)。对于疫苗株与野生型株相同的H3N2亚型,疫苗有效性最高。结果表明,流感疫苗在预防流感发病方面在实际应用中是有效的。

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