Chang Dong, Parrish Jennifer, Kamangar Nader, Liebler Janice, Lee May, Neville Thanh
Los Angeles BioMedical Research Institute, Harbor-University of California Los Angeles Medical Center, Torrance, CA, United States.
Olive View Medical Center, Sylmar, CA, United States.
JMIR Res Protoc. 2019 Nov 25;8(11):e16301. doi: 10.2196/16301.
Invasive intensive care unit (ICU) treatments for patients with advanced medical illnesses and poor prognoses may prolong suffering with minimal benefit. Unfortunately, the quality of care planning and communication between clinicians and critically ill patients and their families in these situations are highly variable, frequently leading to overutilization of invasive ICU treatments. Time-limited trials (TLTs) are agreements between the clinicians and the patients and decision makers to use certain medical therapies over defined periods of time and to evaluate whether patients improve or worsen according to predetermined clinical parameters. For patients with advanced medical illnesses receiving aggressive ICU treatments, TLTs can promote effective dialogue, develop consensus in decision making, and set rational boundaries to treatments based on patients' goals of care.
The aim of this study will be to examine whether a multicomponent quality-improvement strategy that uses protocoled TLTs as the default ICU care-planning approach for critically ill patients with advanced medical illnesses will decrease duration and intensity of nonbeneficial ICU care without changing hospital mortality.
This study will be conducted in medical ICUs of three public teaching hospitals in Los Angeles County. In Aim 1, we will conduct focus groups and semistructured interviews with key stakeholders to identify facilitators and barriers to implementing TLTs among ICU patients with advanced medical illnesses. In Aim 2, we will train clinicians to use protocol-enhanced TLTs as the default communication and care-planning approach in patients with advanced medical illnesses who receive invasive ICU treatments. Eligible patients will be those who the treating ICU physicians consider to be at high risk for nonbeneficial treatments according to guidelines from the Society of Critical Care Medicine. ICU physicians will be trained to use the TLT protocol through a curriculum of didactic lectures, case discussions, and simulations utilizing actors as family members in role-playing scenarios. Family meetings will be scheduled by trained care managers. The improvement strategy will be implemented sequentially in the three participating hospitals, and outcomes will be evaluated using a before-and-after study design. Key process outcomes will include frequency, timing, and content of family meetings. The primary clinical outcome will be ICU length of stay. Secondary outcomes will include hospital length of stay, days receiving life-sustaining treatments (eg, mechanical ventilation, vasopressors, and renal replacement therapy), number of attempts at cardiopulmonary resuscitation, frequency of invasive ICU procedures, and disposition from hospitalization.
The study began in August 2017. The implementation of interventions and data collection were completed at two of the three hospitals. As of September 2019, the study was at the postintervention stage at the third hospital. We have completed focus groups with physicians at each medical center (N=29) and interviews of family members and surrogate decision makers (N=18). The study is expected to be completed in the first quarter of 2020, and results are expected to be available in mid-2020.
The successful completion of the aims in this proposal may identify a systematic approach to improve communication and shared decision making and to reduce nonbeneficial invasive treatments for ICU patients with advanced medical illnesses.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/16301.
对于患有晚期疾病且预后不良的患者,侵入性重症监护病房(ICU)治疗可能只会延长痛苦且获益甚微。不幸的是,在这些情况下,临床医生与重症患者及其家属之间的护理计划和沟通质量差异很大,经常导致侵入性ICU治疗的过度使用。限时试验(TLT)是临床医生与患者及决策者之间达成的协议,即在规定的时间段内使用某些医疗疗法,并根据预先确定的临床参数评估患者的病情是改善还是恶化。对于接受积极ICU治疗的晚期疾病患者,限时试验可以促进有效的对话,在决策中达成共识,并根据患者的护理目标为治疗设定合理的界限。
本研究的目的是检验一种多成分质量改进策略,该策略将程序化限时试验作为患有晚期疾病的重症患者默认的ICU护理计划方法,是否会在不改变医院死亡率的情况下减少无益的ICU护理的持续时间和强度。
本研究将在洛杉矶县的三家公立教学医院的医学ICU中进行。在目标1中,我们将与关键利益相关者进行焦点小组讨论和半结构化访谈,以确定在患有晚期疾病的ICU患者中实施限时试验的促进因素和障碍。在目标2中,我们将培训临床医生将协议强化的限时试验作为接受侵入性ICU治疗的晚期疾病患者默认的沟通和护理计划方法。符合条件的患者将是那些根据危重症医学会的指南,治疗ICU医生认为接受无益治疗风险高的患者。ICU医生将通过理论讲座、病例讨论和模拟课程接受培训,在模拟场景中由演员扮演家庭成员。由经过培训的护理经理安排家属会议。改进策略将在三家参与医院依次实施,并使用前后研究设计评估结果。关键过程结果将包括家属会议的频率、时间和内容。主要临床结果将是ICU住院时间。次要结果将包括住院时间、接受维持生命治疗(如机械通气、血管加压药和肾脏替代治疗)的天数、心肺复苏尝试次数、侵入性ICU操作频率以及出院情况。
该研究于2017年8月开始。三家医院中的两家已完成干预措施的实施和数据收集。截至2019年9月,第三家医院处于干预后阶段。我们已完成每个医疗中心与医生的焦点小组讨论(N = 29)以及对家属和替代决策者的访谈(N = 18)。该研究预计于2020年第一季度完成,结果预计于2020年年中公布。
本提案目标的成功完成可能会确定一种系统方法,以改善沟通和共同决策,并减少对患有晚期疾病的ICU患者的无益侵入性治疗。
国际注册报告标识符(IRRID):DERR1-10.2196/16301。