Munday Judy, Sturgess David, Oishi Sabrina, Bendeich Jess, Kearney Allison, Douglas Clint
Centre for Healthcare Transformation & School of Nursing, Queensland University of Technology (QUT) and Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia.
The University of Queensland (UQ) and Surgical Treatment and Rehabilitation Service (STARS), Brisbane, Queensland, Australia.
Patient Saf Surg. 2022 Sep 24;16(1):32. doi: 10.1186/s13037-022-00341-w.
Continuous body temperature monitoring during perioperative care is enabled by using a non-invasive "zero-heat-flux" (ZHF) device. However, rigorous evaluation of whether continuous monitoring capability improves process of care and patient outcomes is lacking. This study assessed the feasibility of a large-scale trial on the impact of continuous ZHF monitoring on perioperative temperature management practices and hypothermia prevention.
A feasibility study was conducted at a tertiary hospital. Participants included patients undergoing elective surgery under neuraxial or general anesthesia, and perioperative nurses and anesthetists caring for patient participants. Eighty-two patients pre and post introduction of the ZHF device were enrolled. Feasibility outcomes included recruitment and retention, protocol adherence, missing data or device failure, and staff evaluation of intervention feasibility and acceptability. Process of care outcomes included temperature monitoring practices, warming interventions and perioperative hypothermia.
There were no adverse events related to the device and feasibility of recruitment was high (60%). Treatment adherence varied across the perioperative pathway (43 to 93%) and missing data due to electronic transfer issues were identified. Provision of ZHF monitoring had most impact on monitoring practices in the Post Anesthetic Care Unit; the impact on intraoperative monitoring practices was minimal.
Enhancements to the design of the ZHF device, particularly for improved data retention and transfer, would be beneficial prior to a large-scale evaluation of whether continuous temperature monitoring will improve patient outcomes. Implementation research designs are needed for future work to improve the complex area of temperature monitoring during surgery. TRIAL REGISTRATION: Prospective registration prior to patient enrolment was obtained from the Australian and New Zealand Clinical Trials Registry (ANZCTR) on 16 April 2021 (Registration number: ACTRN12621000438853).
使用非侵入性“零热流”(ZHF)设备可在围手术期护理期间进行连续体温监测。然而,目前缺乏对连续监测能力是否能改善护理过程和患者预后的严格评估。本研究评估了一项关于ZHF连续监测对围手术期体温管理实践和预防体温过低影响的大规模试验的可行性。
在一家三级医院进行了一项可行性研究。参与者包括接受神经轴索或全身麻醉的择期手术患者,以及护理患者参与者的围手术期护士和麻醉师。纳入了82名在引入ZHF设备前后的患者。可行性结果包括招募和保留情况、方案依从性、数据缺失或设备故障,以及工作人员对干预可行性和可接受性的评估。护理过程结果包括体温监测实践、保暖干预和围手术期体温过低情况。
未发生与该设备相关的不良事件,招募可行性较高(60%)。围手术期各阶段的治疗依从性各不相同(43%至93%),并发现了因电子传输问题导致的数据缺失。提供ZHF监测对麻醉后护理单元的监测实践影响最大;对术中监测实践的影响最小。
在对连续体温监测是否能改善患者预后进行大规模评估之前,改进ZHF设备的设计,特别是提高数据保留和传输能力,将是有益的。未来的工作需要实施研究设计,以改善手术期间体温监测这一复杂领域。试验注册:于2021年4月16日从澳大利亚和新西兰临床试验注册中心(ANZCTR)获得患者入组前的前瞻性注册(注册号:ACTRN12621000438853)。