Department of Medicine, University of Pennsylvania, Philadelphia, 19104-6021, USA.
Clin Trials. 2012 Jun;9(3):348-57. doi: 10.1177/1740774512438981. Epub 2012 Mar 2.
There is substantial need to rigorously evaluate existing and new therapies for pulmonary arterial hypertension (PAH) and other severe and relatively rare conditions affecting younger patients. However, the ability to conduct meaningful randomized clinical trials (RCTs) in such contexts often is limited by difficulties obtaining adequate patient enrollment.
To understand the motivations of patients with PAH for participating in RCTs so as to facilitate enrollment in future trials among patients with similar diseases.
We conducted semistructured interviews of a diverse sample of patients with World Health Organization (WHO) Group I PAH. We purposefully recruited a diverse sample of participants until theoretical saturation was reached. We randomly assigned patients to review hypothetical RCTs that did or did not allow continuation of background PAH therapies and elicited their reasons for or against enrolling. Interviews were transcribed and analyzed using constant comparison techniques to code and sort data into discrete themes.
The 26 PAH patients enrolled before theoretical saturation was reached identified 24 factors that would influence their RCT enrollment decisions. These factors grouped naturally into four themes: (1) personal medical benefits, (2) personal medical risks/harms, (3) nonmedical benefits, and (4) nonmedical burdens. Personal benefits were cited as commonly as altruistic motives. One third of the patients (9/26) suggested that they would defer enrollment decisions to their treating clinicians. Seventy-nine percent of patients (11/14) assigned to consider trials without background therapies expressed concerns about clinical deterioration (vs. 17% (2/12) among patients assigned to consider trials allowing background therapies).
The sample was recruited from a single academic center. Furthermore, the use of hypothetical trials may not elicit identical decision-making processes as may be used among patients contemplating actual trial participation.
For PAH patients considering RCT enrollment, the potentials for personal benefit and risk are at least as important as altruistic motives. Minimizing the time demands of participating, financial remuneration, and allowing participants to continue current therapies are factors, which might enhance enrollment to trials in similar disease areas.
对于肺动脉高压(PAH)和其他影响年轻患者的严重且相对罕见的疾病,迫切需要严格评估现有和新疗法。然而,在这种情况下进行有意义的随机临床试验(RCT)的能力通常受到难以获得足够的患者入组的限制。
了解 PAH 患者参与 RCT 的动机,以便促进在具有类似疾病的患者中进行未来试验的入组。
我们对一组不同的 I 组 PAH 患者进行了半结构化访谈。我们有目的地招募了不同的参与者,直到达到理论饱和。我们随机分配患者查看是否允许继续进行 PAH 背景治疗的假设 RCT,并引出他们赞成或反对入组的理由。对访谈进行转录,并使用恒定比较技术进行分析,对数据进行编码和分类为离散主题。
在达到理论饱和之前,26 名 PAH 患者入组,确定了 24 个影响他们 RCT 入组决策的因素。这些因素自然分为四个主题:(1)个人医疗收益,(2)个人医疗风险/危害,(3)非医疗收益,和(4)非医疗负担。个人收益与利他动机一样常见。三分之一的患者(9/26)表示他们将把入组决策推迟给他们的治疗医生。在考虑没有背景治疗的试验的患者中,有 79%(11/14)表示对临床恶化表示担忧(而在考虑允许背景治疗的试验的患者中,这一比例为 17%(2/12))。
该样本是从一个学术中心招募的。此外,使用假设试验可能不会引出与考虑实际试验参与的患者可能使用的相同决策过程。
对于考虑 RCT 入组的 PAH 患者,个人收益和风险的潜力至少与利他动机同样重要。尽量减少参与时间要求、经济报酬,并允许参与者继续当前治疗,这些因素可能会增强在类似疾病领域进行试验的入组。