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首页> 外文期刊>Vaccine >Precise answers to the wrong question: prospective clinical trials and the meta-analyses of pneumococcal vaccine in elderly and high-risk adults
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Precise answers to the wrong question: prospective clinical trials and the meta-analyses of pneumococcal vaccine in elderly and high-risk adults

机译:正确答案的错误:老年人和高危成年人的前瞻性临床试验和肺炎球菌疫苗的荟萃分析

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摘要

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
机译: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肺炎。其中一些试验针对的是代表性人群,大多数试验存在严重的方法学问题。在审前计划中很少考虑到样本量要求。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功效。结果得出的研究人群通常不能代表建议接种疫苗的老年人和高危成人人群。荟萃分析人员通常会省略应进行评估的临床试验,包括应予省略的其他试验,并会误算个别试验中的受试者人数和结局事件。回顾性样本量计算表明,所有荟萃分析均未包含足够的人年观察数以排除假阴性结果。对老年人和高危成年人进行肺炎球菌疫苗的前瞻性临床试验和荟萃分析尚无定论,但不应视为阴性研究。在观察性研究中已经证明了预防老年人和高危成年人肺炎球菌菌血症的疫苗接种的临床有效性,并且疫苗接种具有成本效益。该证据足以证明广泛使用肺炎球菌疫苗是合理的

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