Department of Medicine, Division of Nephrology, University of Tennessee Health Science Center, Memphis, TN, USA.
Department of Medicine, Nephrology Section, Memphis VA Medical Center, Memphis, TN, USA.
Nephrol Dial Transplant. 2019 Jul 1;34(7):1084-1089. doi: 10.1093/ndt/gfz088.
Patients with end-stage renal disease (ESRD) experience extremely high morbidity and mortality and there are virtually no therapeutic interventions besides dialysis treatment that are proven in properly designed randomized controlled trials (RCTs) to improve patients' outcomes. Historically, the number of RCTs performed in the ESRD population has been very low compared with other medical subspecialties, and several of the few large RCTs have yielded inconclusive or negative results, dampening enthusiasm for future investment in similar trials. Recent initiatives promoting a focus on patient-centered outcomes and more active patient and caregiver involvement in the planning and conduct of clinical trials may result in more clinically relevant RCTs and broader participation from patients representing the diversity of the ESRD population. The adoption of novel clinical trial design elements characteristic of pragmatic clinical trials and platform trials could help improve both the internal and external validity of RCTs in ESRD, ultimately resulting in the adoption of therapeutic interventions that can be rapidly translated to clinical practice.
终末期肾病(ESRD)患者的发病率和死亡率极高,除了透析治疗之外,实际上几乎没有任何经过适当设计的随机对照试验(RCT)证明可以改善患者的预后。从历史上看,与其他医学亚专科相比,在 ESRD 人群中进行的 RCT 数量非常少,而且少数几项大型 RCT 的结果也没有定论或为阴性,这降低了对未来类似试验投资的积极性。最近的一些举措强调以患者为中心的结果,并促使患者和护理人员更积极地参与临床试验的规划和实施,这可能会产生更有临床意义的 RCT,并使更多来自 ESRD 人群多样性的患者参与进来。采用实用临床试验和平台试验的新型临床试验设计要素可以帮助提高 ESRD 中 RCT 的内部和外部有效性,最终使能够迅速转化为临床实践的治疗干预措施得到采用。