VanBuren John M, Yeatts Sharon D, Holubkov Richard, Moler Frank W, Topjian Alexis, Page Kent, Clevenger Robert G, Meurer William J
Department of Pediatrics, University of Utah, Salt Lake City, UT.
Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC.
Pediatr Crit Care Med. 2025 Feb 1;26(2):e227-e236. doi: 10.1097/PCC.0000000000003667. Epub 2024 Dec 19.
To determine the optimal cooling duration for children after out-of-hospital cardiac arrest (OHCA) using an adaptive Bayesian trial design.
The Pediatric Influence of Cooling duration on Efficacy in Cardiac Arrest Patients (P-ICECAP) trial is a randomized, response-adaptive duration/dose-finding clinical trial with blinded outcome assessment. Participants are randomized to one of several cooling durations (0, 12, 18, 24, 36, 48, 60, 72, 84, or 96 hr). The first 150 participants are randomized 1:1:1 to 24-, 48-, and 72-hour durations. Response-adaptive randomization is used thereafter to allocate participants based on emerging duration-response data.
PICUs.
Up to 900 pediatric patients 2 days to younger than 18 years old who have survived OHCA and been admitted to an ICU.
Duration of targeted temperature management using a surface temperature control device.
The primary outcome is the Vineland Adaptive Behavior Scales-Third Edition mortality composite score, assessed at 12 months. Secondary outcomes include changes in the Pediatric Cerebral Performance Category and Pediatric Resuscitation after Cardiac Arrest scores, as well as survival at 12 months. Bayesian modeling is employed to evaluate the duration-response curve and determine the optimal cooling duration. The trial is designed to adaptively update randomization probabilities every 10 weeks, maximizing the allocation of participants to potentially optimal cooling durations. Over 90% power is achieved for the hypothesized scenarios.
The P-ICECAP trial aims to identify the shortest cooling duration that provides the maximum treatment effect for pediatric OHCA patients. The adaptive design allows for flexibility and efficiency in handling various clinical scenarios, potentially transforming pediatric cardiac arrest care by optimizing hypothermia treatment protocols.
采用适应性贝叶斯试验设计确定院外心脏骤停(OHCA)后儿童的最佳降温持续时间。
降温持续时间对心脏骤停患者疗效的儿科影响(P-ICECAP)试验是一项随机、反应适应性持续时间/剂量探索性临床试验,结果评估采用盲法。参与者被随机分配到几个降温持续时间(0、12、18、24、36、48、60、72、84或96小时)中的一种。前150名参与者按1:1:1随机分配到24小时、48小时和72小时的持续时间组。此后采用反应适应性随机化,根据新出现的持续时间-反应数据分配参与者。
儿科重症监护病房。
最多900名年龄在2天至18岁以下、OHCA后存活并入住重症监护病房的儿科患者。
使用表面温度控制装置进行目标温度管理的持续时间。
主要结局是在12个月时评估的《文兰适应性行为量表第三版》死亡率综合评分。次要结局包括儿科脑功能分类和心脏骤停后儿科复苏评分的变化,以及12个月时的生存率。采用贝叶斯模型评估持续时间-反应曲线并确定最佳降温持续时间。该试验设计为每10周自适应更新随机化概率,最大限度地将参与者分配到潜在的最佳降温持续时间组。对于假设的情况,检验效能超过90%。
P-ICECAP试验旨在确定为儿科OHCA患者提供最大治疗效果的最短降温持续时间。适应性设计允许在处理各种临床情况时具有灵活性和效率,可能通过优化低温治疗方案改变儿科心脏骤停的护理。