O'Halloran Amanda, Sannino James, Dominick Cheryl, Bailey Christine, Boyle Lori, Shepard Lindsay N, Nadkarni Vinay, Wolfe Heather, Morgan Ryan W, Nishisaki Akira, Lane-Fall Meghan, Sutton Robert
Division of Critical Care, Department of Anesthesiology and Critical Care Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA.
Department of Anesthesiology and Critical Care Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Pediatr Crit Care Med. 2025 Aug 15. doi: 10.1097/PCC.0000000000003811.
Excessive ventilation adversely affects cardiopulmonary resuscitation (CPR) hemodynamics and outcomes. Pediatric providers rarely achieve guideline-recommended CPR ventilation rates. We aimed to use human factors engineering to design a metronome to improve compliance with recommended CPR ventilation rates. We hypothesized that in usability testing, our novel metronome would achieve: 1) a System Usability Scale (SUS) score greater than 68 and 2) greater than 70% of CPR epochs with ventilation rates within target range, which would be sufficient to support a pilot trial in our PICU.
Prospective single-center mixed-methods study.
Seventy-five-bed academic PICU.
Multidisciplinary clinicians.
None.
We elicited clinician feedback on the proposed ventilation rate metronome with a survey. Participatory design sessions determined optimal metronome components. During high-fidelity simulation usability testing, we collected qualitative and quantitative measures reflecting participant feedback and performance. Average ventilation rates were calculated during 30-second epochs of CPR, with average rates ± 2 breaths/min (bpm) from the target considered to be within goal range. Among 107 survey respondents, perceptions of appropriateness, acceptability, and feasibility of the ventilation rate metronome were favorable. The final prototype used a bell sound for high saliency in noisy environments and a scrolling timed vertical bar, with pre-set options for three guideline-recommended CPR ventilation rates (infants: 30 bpm, children 1-17 yr old: 20 bpm, adults: 10 bpm). In usability testing (three groups, 34 clinicians), median SUS was 92.5 of 100 (interquartile range, 89.4-93.1), with 0 attributable errors. Overall, 34 of 36 (94% [95% CI, 81-99%]) epochs of simulated CPR with metronome use had ventilation rates ± 2 bpm from the target rate.
Utilizing human factors engineering and implementation science, we successfully designed a novel ventilation rate metronome. When deployed during high-fidelity cardiac arrest simulations, metronome use had high usability scores and resulted in excellent compliance with recommended ventilation rates.
过度通气会对心肺复苏(CPR)的血流动力学及预后产生不利影响。儿科急救人员很少能达到指南推荐的CPR通气频率。我们旨在运用人因工程学设计一种节拍器,以提高对推荐CPR通气频率的依从性。我们假设在可用性测试中,我们的新型节拍器将实现:1)系统可用性量表(SUS)得分大于68分;2)超过70%的CPR周期通气频率在目标范围内,这足以支持在我们的儿科重症监护病房(PICU)进行一项试点试验。
前瞻性单中心混合方法研究。
拥有75张床位的学术性PICU。
多学科临床医生。
无。
我们通过一项调查征求临床医生对拟议的通气频率节拍器的反馈意见。参与式设计会议确定了节拍器的最佳组件。在高保真模拟可用性测试期间,我们收集了反映参与者反馈和表现的定性和定量指标。在CPR的30秒周期内计算平均通气频率,目标频率±2次呼吸/分钟(bpm)的平均频率被视为在目标范围内。在107名调查受访者中,对通气频率节拍器的适宜性、可接受性和可行性的看法较为积极。最终原型在嘈杂环境中使用铃声以提高显著性,并采用滚动计时垂直条,预设了三种指南推荐的CPR通气频率选项(婴儿:30 bpm,1 - 17岁儿童:20 bpm,成人:10 bpm)。在可用性测试中(三组,共34名临床医生),SUS中位数为100分中的92.5分(四分位间距,89.4 - 93.1),无归因错误。总体而言,在使用节拍器进行模拟CPR的36个周期中,有34个(94% [95% CI,81 - 99%])周期的通气频率与目标频率相差±2 bpm。
利用人因工程学和实施科学,我们成功设计了一种新型通气频率节拍器。在高保真心脏骤停模拟过程中使用时,节拍器具有较高的可用性得分,并能使通气频率极佳地符合推荐频率。