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[老年人流感疫苗接种:关于死亡率的试验在伦理上是否可接受?]

[Influenza vaccination in the elderly: is a trial on mortality ethically acceptable?].

作者信息

Verhees Ruud A F, Dondorp Wybo, Thijs Carel, Dinant G J, Knottnerus André

机构信息

Universiteit Maastricht, Care and Public Health Research Institute (CAPHRI), vakgroep Huisartsgeneeskunde.

Contact: R.A.F. Verhees (

出版信息

Ned Tijdschr Geneeskd. 2018 Sep 6;162:D3177.

Abstract

The effectiveness of influenza vaccination in the elderly has long been a topic of debate, fueled by the absence of direct evidence on its effect on mortality. It is argued that new placebo-controlled trials should be undertaken to resolve this uncertainty. However, such trials may be ethically questionable. We provide an overview of the ethical challenges of an influenza vaccine efficacy trial designed to evaluate mortality in the elderly. An important condition in the justification of a trial is the existence of genuine uncertainty regarding the answer to a research question. Therefore an extensive analysis of the existing levels of knowledge is needed to support the conclusion that an effect of vaccination on mortality is uncertain. Even if a so-called 'clinical equipoise' status applies, denying a control group vaccination would be problematic because vaccination is considered 'competent care' and withholding vaccination could substantially increase patients' risk for influenza and its complications. Given the high burden of disease and proven benefits of vaccination, the importance of a trial is unlikely to outweigh the risk patients are exposed to. While a placebo-controlled trial in vaccine refusers may be considered, such a trial is unlikely to meet methodological standards regarding trial size and generalizability. We conclude that a new trial is unlikely to provide a direct answer, let alone change current policy. At the same time, given the lack of consensus on this topic, we invite researchers considering vaccine efficacy trials on mortality to address the ethical challenges as discussed.

摘要

流感疫苗对老年人的有效性长期以来一直是一个争论的话题,由于缺乏关于其对死亡率影响的直接证据,这一争论愈发激烈。有人认为应该进行新的安慰剂对照试验来解决这一不确定性。然而,此类试验在伦理上可能存在问题。我们概述了一项旨在评估老年人死亡率的流感疫苗疗效试验所面临的伦理挑战。试验合理性的一个重要条件是对于研究问题的答案存在真正的不确定性。因此,需要对现有知识水平进行广泛分析,以支持疫苗接种对死亡率的影响尚不确定这一结论。即使存在所谓的“临床 equipoise”状态,拒绝给对照组接种疫苗也会有问题,因为接种疫苗被视为“合理医疗”,而不给患者接种疫苗可能会大幅增加他们感染流感及其并发症的风险。鉴于疾病负担沉重且疫苗接种已证实具有益处,试验的重要性不太可能超过患者所面临的风险。虽然可以考虑在拒绝接种疫苗者中进行安慰剂对照试验,但这样的试验不太可能达到关于试验规模和普遍性的方法学标准。我们得出结论,新的试验不太可能提供直接答案,更不用说改变当前政策了。与此同时,鉴于在这个问题上缺乏共识,我们邀请考虑进行死亡率疫苗疗效试验的研究人员解决本文所讨论的伦理挑战。

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