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用于预防老年人流感的疫苗。

Vaccines for preventing influenza in the elderly.

作者信息

Jefferson Tom, Di Pietrantonj Carlo, Al-Ansary Lubna A, Ferroni Eliana, Thorning Sarah, Thomas Roger E

机构信息

Vaccines Field, The Cochrane Collaboration, Via Adige 28a, Anguillara Sabazia, Roma, Italy, 00061.

出版信息

Cochrane Database Syst Rev. 2010 Feb 17(2):CD004876. doi: 10.1002/14651858.CD004876.pub3.

Abstract

BACKGROUND

Vaccines have been the main global weapon to minimise the impact of influenza in the elderly for the last four decades and are recommended worldwide for individuals aged 65 years or older. The primary goal of influenza vaccination in the elderly is to reduce the risk of complications among persons who are most vulnerable.

OBJECTIVES

To assess the effectiveness of vaccines in preventing influenza, influenza-like illness (ILI), hospital admissions, complications and mortality in the elderly. To identify and appraise comparative studies evaluating the effects of influenza vaccines in the elderly. To document types and frequency of adverse effects associated with influenza vaccines in the elderly.

SEARCH STRATEGY

We searched the Cochrane Central Register of Controlled Trials (CENTRAL), which contains the Cochrane Acute Respiratory Infections (ARI) Group's Specialised Register (The Cochrane Library 2009, issue 4); MEDLINE (January 1966 to October Week 1 2009); EMBASE (1974 to October 2009) and Web of Science (1974 to October 2009).

SELECTION CRITERIA

Randomised controlled trials (RCTs), quasi-RCTs, cohort and case-control studies assessing efficacy against influenza (laboratory-confirmed cases) or effectiveness against influenza-like illness (ILI) or safety. Any influenza vaccine given independently, in any dose, preparation or time schedule, compared with placebo or with no intervention was considered.

DATA COLLECTION AND ANALYSIS

We grouped reports first according to the setting of the study (community or long-term care facilities) and then by level of viral circulation and vaccine matching. We further stratified by co-administration of pneumococcal polysaccharide vaccine (PPV) and by different types of influenza vaccines. We analysed the following outcomes: influenza, influenza-like illness, hospital admissions, complications and deaths.

MAIN RESULTS

We included 75 studies. Overall we identified 100 data sets. We identified one RCT assessing efficacy and effectiveness. Although this seemed to show an effect against influenza symptoms it was underpowered to detect any effect on complications (1348 participants). The remainder of our evidence base included non-RCTs. Due to the general low quality of non-RCTs and the likely presence of biases, which make interpretation of these data difficult and any firm conclusions potentially misleading, we were unable to reach clear conclusions about the effects of the vaccines in the elderly.

AUTHORS' CONCLUSIONS: The available evidence is of poor quality and provides no guidance regarding the safety, efficacy or effectiveness of influenza vaccines for people aged 65 years or older. To resolve the uncertainty, an adequately powered publicly-funded randomised, placebo-controlled trial run over several seasons should be undertaken.

摘要

背景

在过去四十年里,疫苗一直是全球将流感对老年人影响降至最低的主要手段,并且在全球范围内被推荐用于65岁及以上的人群。老年人接种流感疫苗的主要目标是降低最易感染人群出现并发症的风险。

目的

评估疫苗在预防老年人流感、流感样疾病(ILI)、住院、并发症及死亡方面的有效性。识别并评价评估流感疫苗对老年人影响的比较研究。记录老年人中与流感疫苗相关的不良反应类型及发生频率。

检索策略

我们检索了Cochrane对照试验中心注册库(CENTRAL),其中包含Cochrane急性呼吸道感染(ARI)小组的专业注册库(《Cochrane图书馆》2009年第4期);MEDLINE(1966年1月至2009年10月第1周);EMBASE(1974年至2009年10月)以及科学引文索引(1974年至2009年10月)。

选择标准

评估针对流感(实验室确诊病例)的疗效或针对流感样疾病(ILI)的有效性或安全性的随机对照试验(RCT)、半随机对照试验、队列研究和病例对照研究。任何独立给予的流感疫苗,无论剂量、制剂或时间安排如何,与安慰剂或无干预措施相比均在考虑范围内。

数据收集与分析

我们首先根据研究背景(社区或长期护理机构)对报告进行分组,然后按病毒传播水平和疫苗匹配情况进行分组。我们还根据肺炎球菌多糖疫苗(PPV)的联合使用情况以及不同类型的流感疫苗进行了进一步分层。我们分析了以下结局:流感、流感样疾病、住院、并发症和死亡。

主要结果

我们纳入了75项研究。总体而言,我们识别出100个数据集。我们识别出一项评估疗效和有效性的RCT。尽管这似乎显示出对流感症状有效果,但检测对并发症的任何影响的能力不足(1348名参与者)。我们其余的证据基础包括非RCT。由于非RCT的总体质量较低且可能存在偏差,这使得这些数据难以解释且任何确凿结论都可能产生误导,因此我们无法就疫苗对老年人的影响得出明确结论。

作者结论

现有证据质量较差,无法为65岁及以上人群流感疫苗的安全性、疗效或有效性提供指导。为解决不确定性,应开展一项由公共资金资助、有足够效力、在多个季节进行的随机、安慰剂对照试验。

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