Li Tianjing, Wieland L Susan, Oh Esther, Neufeld Karin J, Wang Nae-Yuh, Dickersin Kay, Sieber Frederick E
1 Center for Clinical Trials and Evidence Synthesis, Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
2 Center for Integrative Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Clin Trials. 2017 Jun;14(3):299-307. doi: 10.1177/1740774516687253. Epub 2017 Jan 9.
Background Delirium is an acute change in mental status characterized by sudden onset, fluctuating course, inattention, disorganized thinking, and abnormal level of consciousness. The objective of the randomized controlled trial "A STrategy to Reduce the Incidence of Postoperative Delirium in Elderly Patients" (STRIDE) is to assess the effectiveness of light versus heavy sedation on delirium and other outcomes in elderly patients undergoing hip fracture repair surgery. Our goal is to describe the design considerations and lessons learned in planning and implementing the STRIDE trial. Methods Discussed are challenges encountered including (1) how to ensure that we quickly identify, assess the eligibility of, and randomize traumatic hip fracture patients; (2) how to implement interventions that involve continuous monitoring and adjustment during the surgery; and (3) how to measure and ascertain the primary outcome, delirium. Results To address the first challenge, we monitored the operating room schedule more actively than anticipated. We constructed and organized eligibility assessment data collection forms by purpose and by source of information needed to complete them. We decided that randomization needs to take place in the operating room. To address the second challenge, we designed and implemented a treatment protocol and covered the bispectral index monitor to prevent the Anesthesiologist/Anesthetist from being influenced by the bispectral index reading while administering the intervention. Finally, clinical assessment of delirium consisted of standardized interviews of the patient using validated instruments, interviews of those caring for the patient, and review of the medical record. A consensus panel made the final determination of a delirium diagnosis. We note that STRIDE is a single-center trial. The decisions we took may have different implications for multi-center trials. Conclusions Lessons learned are likely to provide useful information to others designing trials in emergency and surgical setting and for those who are interested in unbiased assessment of delirium.
谵妄是一种精神状态的急性改变,其特征为起病突然、病程波动、注意力不集中、思维紊乱以及意识水平异常。随机对照试验“降低老年患者术后谵妄发生率的策略”(STRIDE)的目的是评估轻度镇静与深度镇静对接受髋部骨折修复手术的老年患者谵妄及其他结局的有效性。我们的目标是描述在规划和实施STRIDE试验过程中的设计考量和经验教训。方法:讨论了所遇到的挑战,包括(1)如何确保我们快速识别、评估创伤性髋部骨折患者的 eligibility 并将其随机分组;(2)如何实施在手术期间需要持续监测和调整的干预措施;(3)如何测量和确定主要结局谵妄。结果:为应对第一个挑战,我们比预期更积极地监测手术室日程安排。我们根据目的以及完成所需信息的来源构建并组织了 eligibility 评估数据收集表。我们决定随机分组需要在手术室进行。为应对第二个挑战,我们设计并实施了一项治疗方案,并覆盖脑电双频指数监测仪,以防止麻醉医生在实施干预时受到脑电双频指数读数的影响。最后,谵妄的临床评估包括使用经过验证的工具对患者进行标准化访谈、对照顾患者的人员进行访谈以及查阅病历。一个共识小组对谵妄诊断做出最终判定。我们注意到STRIDE是一项单中心试验。我们所做的决定可能对多中心试验有不同的影响。结论:经验教训可能会为其他在急诊和手术环境中设计试验的人以及那些对谵妄的无偏倚评估感兴趣的人提供有用信息。 (注:原文中“eligibility”未翻译,可能是特定术语,需根据上下文确定准确含义)