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针对错误问题的精确答案:老年及高危成年人肺炎球菌疫苗的前瞻性临床试验与荟萃分析

Precise answers to the wrong question: prospective clinical trials and the meta-analyses of pneumococcal vaccine in elderly and high-risk adults.

作者信息

Fedson David S, Liss Charles

机构信息

Aventis Pasteur MSD, Lyon, France.

出版信息

Vaccine. 2004 Feb 25;22(8):927-46. doi: 10.1016/j.vaccine.2003.09.027.

Abstract

Ten prospective clinical trials conducted in elderly and high-risk adults have failed to show that pneumococcal vaccine prevents pneumococcal bacteraemia and all pneumonia. Several of these trials focused on unrepresentative populations and most had serious methodological problems. Few adequately considered sample size requirements in pre-trial planning. Retrospective sample size calculations based on the findings of the individual trials showed that none was large enough to rule out false negative results. Five published meta-analyses have attempted to determine the efficacy of pneumococcal vaccine by pooling the results of the individual clinical trials. The resulting study populations often were not representative of the populations of elderly and high-risk adults for whom vaccination is recommended. The meta-analysts often omitted clinical trials that should have been evaluated, included other trials that should have been omitted and miscounted the numbers of subjects and outcome events in the individual trials. Retrospective sample size calculations showed that none of the meta-analyses included an adequate number of person years of observation to rule out false negative results. The prospective clinical trials and meta-analyses of pneumococcal vaccine in elderly and high-risk adults have been inconclusive, but they should not be regarded as negative studies. The clinical effectiveness of vaccination in preventing pneumococcal bacteraemia in elderly and high-risk adults has been demonstrated in observational studies, and vaccination is cost-effective. This evidence is sufficient to justify wider use of pneumococcal vaccine.

摘要

在老年人和高危成年人中进行的十项前瞻性临床试验未能表明肺炎球菌疫苗可预防肺炎球菌菌血症和所有类型的肺炎。其中几项试验关注的是缺乏代表性的人群,并且大多数试验存在严重的方法学问题。很少有试验在试验前规划中充分考虑样本量要求。根据各个试验的结果进行的回顾性样本量计算表明,没有一个试验的样本量足以排除假阴性结果。五项已发表的荟萃分析试图通过汇总各个临床试验的结果来确定肺炎球菌疫苗的疗效。由此产生的研究人群往往不能代表建议接种疫苗的老年人和高危成年人。荟萃分析者常常遗漏了本应评估的临床试验,纳入了本应排除的其他试验,并且在各个试验中错误计算了受试者和结局事件的数量。回顾性样本量计算表明,没有一项荟萃分析纳入足够的人年观察数来排除假阴性结果。在老年人和高危成年人中进行的肺炎球菌疫苗前瞻性临床试验和荟萃分析尚无定论,但不应将它们视为阴性研究。在观察性研究中已证明接种疫苗在预防老年人和高危成年人肺炎球菌菌血症方面具有临床有效性,并且接种疫苗具有成本效益。这一证据足以证明更广泛地使用肺炎球菌疫苗是合理的。

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