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成人肺炎球菌疫苗接种的疗效:随机对照试验的荟萃分析

Efficacy of pneumococcal vaccination in adults. A meta-analysis of randomized controlled trials.

作者信息

Fine M J, Smith M A, Carson C A, Meffe F, Sankey S S, Weissfeld L A, Detsky A S, Kapoor W N

机构信息

Department of Medicine, University of Pittsburgh, Pa.

出版信息

Arch Intern Med. 1994;154(23):2666-77. doi: 10.1001/archinte.1994.00420230051007.

Abstract

BACKGROUND

Because of the prevalence of pneumococcal pneumonia, the substantial morbidity and mortality associated with many pneumococcal infections, and an increase in the incidence of antibiotic resistance among pneumococcal isolates, considerable efforts for disease prevention have been made using a polyvalent polysaccharide pneumococcal vaccine. Despite numerous clinical trials of the vaccine, its efficacy in the prevention of pneumococcal infections and other clinically relevant medical outcomes in adults remains uncertain.

METHODS

To assess quantitatively the efficacy of pneumococcal vaccination, a MEDLINE literature search, manual reviews of article bibliographies, and communications with pneumococcal vaccine investigators were used to identify randomized controlled trials of the pneumococcal vaccine. Independent review of 594 articles revealed nine randomized trials with 12 vaccine and control study groups that evaluated clinically relevant outcomes in adults. To estimate a summary effect size for all outcomes, Mantel-Haenszel odds ratios (ORs) and Dersimonian and Laird rate differences (RDs) and their associated 95% confidence intervals (CIs) were computed.

RESULTS

Summary ORs demonstrated a statistically significant protective effect of the vaccine for four pneumococcal infection-related outcomes: definitive pneumococcal pneumonia (OR = 0.34; 95% CI = 0.24 to 0.48), definitive pneumococcal pneumonia for vaccine-containing pneumococcal antigen types only (vaccine types only) (OR = 0.17; 95% CI = 0.09 to 0.33), presumptive pneumococcal pneumonia (OR = 0.47; 95% CI = 0.35 to 0.63), and presumptive pneumococcal pneumonia (vaccine types only) (OR = 0.39; 95% CI = 0.26 to 0.59). The summary RDs, which account for heterogeneity among studies, confirmed a statistically significant protective effect for two of these same outcomes: definitive pneumococcal pneumonia (RD = 4/1000; 95% CI = 0/1000 to 7/1000) and definitive pneumococcal pneumonia (vaccine types only) (RD = 8/1000; 95% CI = 1/1000 to 16/1000). Summary ORs and RDs failed to demonstrate a protective effect for pneumonia (all causes), bronchitis, and mortality (all causes) or mortality due to pneumonia or pneumococcal infection. Subgroup analyses showed that for all four pneumococcal infection-related outcomes, vaccine efficacy differed for high- and low-risk subjects, demonstrating efficacy for low-risk subjects and lack of efficacy for high-risk subjects.

CONCLUSIONS

Pneumococcal vaccination appears efficacious in reducing bacteremic pneumococcal pneumonia in low-risk adults. However, evidence from randomized controlled trials fails to demonstrate vaccine efficacy for pneumococcal infection-related or other medical outcomes in the heterogeneous group of subjects currently labeled as high risk.

摘要

背景

由于肺炎球菌肺炎的普遍存在、许多肺炎球菌感染所导致的高发病率和死亡率,以及肺炎球菌分离株中抗生素耐药性的增加,人们已做出大量努力使用多价多糖肺炎球菌疫苗来预防疾病。尽管对该疫苗进行了大量临床试验,但其在预防成人肺炎球菌感染及其他临床相关医疗结局方面的疗效仍不确定。

方法

为了定量评估肺炎球菌疫苗的疗效,我们通过医学文献数据库(MEDLINE)进行文献检索、人工查阅文章参考文献,并与肺炎球菌疫苗研究人员进行沟通,以确定肺炎球菌疫苗的随机对照试验。对594篇文章进行独立评审后,发现有9项随机试验,包含12个疫苗组和对照组,评估了成人的临床相关结局。为了估计所有结局的汇总效应量,计算了曼特尔-亨泽尔优势比(OR)、德西蒙尼安和莱尔德率差(RD)及其相关的95%置信区间(CI)。

结果

汇总OR显示,疫苗对四种与肺炎球菌感染相关的结局具有统计学显著的保护作用:确诊的肺炎球菌肺炎(OR = 0.34;95%CI = 0.24至0.48)、仅针对含疫苗肺炎球菌抗原类型的确诊肺炎球菌肺炎(仅疫苗类型)(OR = 0.17;95%CI = 0.09至0.33)、疑似肺炎球菌肺炎(OR = 0.47;95%CI = 0.35至0.63)以及疑似肺炎球菌肺炎(仅疫苗类型)(OR = 0.39;95%CI = 0.26至0.59)。考虑到研究间异质性的汇总RD,证实了对其中两个相同结局具有统计学显著的保护作用:确诊的肺炎球菌肺炎(RD = 4/1000;95%CI = 0/1000至7/1000)和确诊的肺炎球菌肺炎(仅疫苗类型)(RD = 8/1000;95%CI = 1/1000至16/1000)。汇总OR和RD未能显示出对(所有病因的)肺炎、支气管炎以及(所有病因的)死亡率或肺炎或肺炎球菌感染所致死亡率的保护作用。亚组分析表明,对于所有四种与肺炎球菌感染相关的结局,高风险和低风险受试者的疫苗疗效不同,显示出对低风险受试者有效,而对高风险受试者无效。

结论

肺炎球菌疫苗似乎对降低低风险成人的菌血症性肺炎球菌肺炎有效。然而,随机对照试验的证据未能证明该疫苗对目前被标记为高风险的异质性受试者群体中的肺炎球菌感染相关或其他医疗结局有效。

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