Division of Pulmonary, Allergy, Sleep and Critical Care, Department of Medicine, The Pulmonary Center.
Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Kansas School of Medicine, Kansas City, Kansas.
Ann Am Thorac Soc. 2021 Sep;18(9):1560-1566. doi: 10.1513/AnnalsATS.202009-1124SD.
The unprecedented public health burdens of coronavirus disease (COVID-19) have intensified the urgency of identifying effective, low-cost treatments that limit the need for advanced life support measures and improve clinical outcomes. However, personal protective equipment and staffing shortages, disease virulence, and infectivity have created significant barriers to traditional clinical trial practices. We present the novel design of a pragmatic, adaptive, multicenter, international, prospective randomized controlled clinical trial evaluating the safety and effectiveness of awake prone positioning in spontaneously breathing patients with COVID-19 (APPEX-19 [Awake Prone Position for Early Hypoxemia in COVID-19]). Key innovations of this trial include ) a novel smartphone-based communication process that facilitates rapid enrollment and intervention delivery while allowing social distancing and conservation of personal protective equipment, ) Bayesian response-adaptive randomization to allow preferential assignment to the most effective intervention and expedite trial completion compared with frequentist designs, ) remote electronic collection of patient-reported outcomes and electronic medical record data, and ) pragmatic prospective use of patient-reported data and data collected as part of routine clinical care. Clinical trial registered with www.clinicaltrials.gov (NCT04344587).
冠状病毒病(COVID-19)带来了前所未有的公共卫生负担,这使得寻找有效且低成本的治疗方法变得更加紧迫,这些方法可以限制对高级生命支持措施的需求并改善临床结果。然而,个人防护设备和人员短缺、疾病的毒力和传染性给传统的临床试验实践带来了重大障碍。我们提出了一项实用、适应性、多中心、国际性、前瞻性随机对照临床试验的新设计,该试验评估了 COVID-19 患者清醒俯卧位(APPEX-19 [COVID-19 中早期低氧血症的清醒俯卧位])的安全性和有效性。该试验的主要创新包括:)一种新的基于智能手机的沟通流程,该流程可在允许保持社交距离和节约个人防护设备的同时,促进快速入组和干预措施的实施;)贝叶斯响应适应性随机化,与传统设计相比,允许优先分配到最有效的干预措施并加快试验完成;)患者报告结局和电子病历数据的远程电子采集;)实用的前瞻性使用患者报告数据和常规临床护理中收集的数据。该临床试验已在 www.clinicaltrials.gov(NCT04344587)上注册。