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危及生命的疾病临床试验中的决策:治疗预期,而非误解。

Decision making in a clinical trial for a life-threatening illness: Therapeutic expectation, not misconception.

机构信息

Department of Clinical Research, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, UK; Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Social Aspects of Health Programme, MRC/UVRI & LSHTM Uganda Research Institute, Entebbe, Uganda; Department of Global Health and Development, Faculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, UK.

出版信息

Soc Sci Med. 2022 Jul;305:115082. doi: 10.1016/j.socscimed.2022.115082. Epub 2022 May 25.

Abstract

Potential participants for clinical trials which aim to define treatments for life-threatening conditions are often extremely unwell. When exploring why individuals participate in clinical trials one common observation is a misplaced expectation of personal benefit - a therapeutic misconception. The care offered in some clinical trials is of a higher standard than is routinely available and this has led to criticism around the freedom of choice to enrol - structural coercion. We embedded an ethnographic study within a randomised controlled trial for HIV-associated cryptococcal meningitis in Gaborone, Botswana and Kampala, Uganda. We aimed to gain an understanding of decision-making around the trial and how this was impacted by the study design and broader social context. We conducted in-depth interviews with trial participants, surrogate decision makers and researchers, combined these with direct observations and analysed data using thematic analysis. Between January 2020 and June 2021 we interviewed 89 individuals. We found previous exposure to and awareness of clinical research was limited, as was understanding of the trial objectives and design. Through observations and engagement with healthcare facilities decision-makers were able to identify the trial as providing the best possible chance of survival. Hesitation and reluctance were mostly due to fear of lumbar punctures which was sometimes based on rumours but often based on tragic personal experience. Despite fear, and sometimes conviction that they would die, individuals agreed to consent, often against the wishes of family members. Reassurance and confidence came from trust in routine care staff and the research team but also from fellow participants and their surrogates. We argue that participants made informed decisions based on a therapeutic expectation from the trial and that rather than being the result of structural coercion this was an informed and voluntary choice.

摘要

参与旨在确定危及生命疾病治疗方法的临床试验的潜在参与者通常病情极为严重。在探讨为什么个人参与临床试验时,一个常见的观察结果是对个人获益的错误期望——治疗误解。一些临床试验提供的护理标准高于常规护理标准,这导致了对入组自由选择的批评——结构性强制。我们在博茨瓦纳的哈博罗内和乌干达的坎帕拉的随机对照试验中嵌入了一项民族志研究。我们旨在了解试验决策过程,并了解研究设计和更广泛的社会背景对此的影响。我们对试验参与者、替代决策人和研究人员进行了深入访谈,将这些访谈与直接观察相结合,并使用主题分析对数据进行分析。在 2020 年 1 月至 2021 年 6 月期间,我们采访了 89 人。我们发现,他们之前对临床研究的接触和认识有限,对试验目标和设计的理解也有限。通过观察和与医疗机构决策者的接触,决策者能够确定该试验提供了生存的最佳机会。犹豫和不情愿主要是由于对腰椎穿刺的恐惧,这种恐惧有时是基于谣言,但往往是基于悲惨的个人经历。尽管个人担心,有时甚至确信自己会死亡,但他们还是同意同意,这通常违背了家庭成员的意愿。他们从对常规护理人员和研究团队的信任中获得了安慰和信心,但也从其他参与者及其代理人那里获得了安慰和信心。我们认为,参与者根据试验的治疗期望做出了知情决策,而不是结构性强制的结果,这是一种知情和自愿的选择。

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