Cox Christopher E, Ashana Deepshikha C, Dempsey Katelyn, Olsen Maren K, Parish Alice, Casarett David, Johnson Kimberly S, Haines Krista L, Naglee Colleen, Katz Jason N, Al-Hegelan Mashael, Riley Isaretta L, Docherty Sharron L
Department of Medicine, Division of Pulmonary and Critical Care Medicine, Duke University, Durham, North Carolina.
Program to Support People and Enhance Recovery (ProSPER), Duke University, Durham, North Carolina.
JAMA Intern Med. 2025 Feb 1;185(2):173-183. doi: 10.1001/jamainternmed.2024.6838.
Few person-centered, scalable models of collaborative intensive care unit (ICU) clinician-palliative care specialist care exist.
To evaluate the effect of a collaborative palliative care intervention compared to usual care among family members of patients in the ICU.
DESIGN, SETTING, AND PARTICIPANTS: This parallel-group randomized clinical trial with patient-level randomization was conducted between April 2021 and September 2023. The study was set at 6 medical and surgical ICUs in 1 academic hospital and 1 community hospital. The study participants included critically ill older adult patients with 1 of 11 poor outcome phenotypes, their family members with elevated palliative care needs, and their attending ICU physicians.
An automated electronic health record-integrated, mobile application-based communication platform that displayed family-reported needs over 7 days, coached ICU attending physicians on addressing needs, and prompted palliative care consultation if needs were not reduced within 3 study days.
The primary outcome was change in the family-reported Needs at the End-of-Life Screening Tool (NEST) score between study days 1 and 3. The 13-item NEST score is a number between 0 and 130, with higher scores indicating a greater need. Secondary outcomes included quality of communication and goal of care concordance, as well as 3-month psychological distress.
Of 151 family members, the mean (SD) age was 57.4 (12.9) years, and 110 (72.9%) were female. Of 151 patients, the mean (SD) age was 69.8 (9.7) years, and 86 (57.0%) were male. Thirty-five ICU physicians were male (68.6%). Seventy-six patients were randomized to the intervention group and 75 to the control group. Treatment group differences in estimated mean NEST scores were similar at 3 days between the intervention and control groups (-3.1 vs -2.0, respectively; estimated mean difference in differences, -1.3 points [95% CI, -6.0 to 3.5]) and 7 days (-2.3 vs -2.2, respectively; estimated mean difference in differences, 0 points [95% CI, -6.2 to 6.2]). Median (IQR) need scores were lower among individuals who remained in the ICU at day 3 for intervention participants vs controls (24.5 [16.5-34.5] vs 27.5 [13.0-40.0], respectively); median (IQR) need scores were also lower among those who remained in the ICU at day 7 for intervention vs controls (22.0 [11.0-35.0] vs 28.0 [14.0-35.0], respectively). Goal concordance, quality of communication, and psychological distress symptoms did not differ. Twenty-nine intervention participants (38.2%) had palliative care consultations, compared to only 3 (4.0%) among controls, (P < .001); 66 intervention participants (87.0%) had a family meeting, compared to 48 (64.0%) among controls (P = .001).
In this randomized clinical trial, a collaborative, person-centered, ICU-based palliative care intervention had no effect on palliative care needs or psychological distress compared to usual care despite a higher frequency of palliative care consultations and family meetings among intervention participants.
ClinicalTrials.gov Identifier: NCT04414787.
很少有以患者为中心、可扩展的协作式重症监护病房(ICU)临床医生-姑息治疗专家护理模式。
评估与常规护理相比,协作式姑息治疗干预对ICU患者家属的影响。
设计、地点和参与者:这项采用患者层面随机分组的平行组随机临床试验于2021年4月至2023年9月进行。研究在1家学术医院和1家社区医院的6个内科和外科ICU开展。研究参与者包括患有11种不良预后表型之一的危重症老年患者、姑息治疗需求较高的家属以及他们的ICU主治医生。
一个基于移动应用程序的自动化电子健康记录集成通信平台,该平台显示家属报告的7天需求,指导ICU主治医生满足需求,并在3个研究日内需求未减少时促使进行姑息治疗会诊。
主要结局是研究第1天和第3天之间家属报告的临终筛查工具(NEST)评分的变化。13项NEST评分范围为0至130分,分数越高表明需求越大。次要结局包括沟通质量和护理目标一致性,以及3个月时的心理困扰。
151名家属中,平均(标准差)年龄为57.4(12.9)岁,110名(72.9%)为女性。151名患者中,平均(标准差)年龄为69.8(9.7)岁,86名(57.0%)为男性。35名ICU医生为男性(68.6%)。76名患者被随机分配到干预组,75名被分配到对照组。干预组和对照组在第3天的估计平均NEST评分差异相似(分别为-3.1和-2.0;差异的估计平均差异为-1.3分[95%置信区间,-6.0至3.5]),在第7天也相似(分别为-2.3和-2.2;差异的估计平均差异为0分[95%置信区间,-6.2至6.2])。第3天仍在ICU的干预组参与者与对照组相比,需求评分中位数(四分位间距)较低(分别为24.5[16.5 - 34.5]和27.5[13.0 - 40.0]);第7天仍在ICU的干预组与对照组相比,需求评分中位数(四分位间距)也较低(分别为22.0[11.0 - 35.0]和28.0[14.0 - 35.0])。护理目标一致性、沟通质量和心理困扰症状没有差异。29名干预组参与者(38.2%)进行了姑息治疗会诊,而对照组只有3名(4.0%)(P <.001);66名干预组参与者(87.0%)召开了家属会议,对照组为48名(64.0%)(P = 0.001)。
在这项随机临床试验中,与常规护理相比,基于ICU的协作式、以患者为中心的姑息治疗干预对姑息治疗需求或心理困扰没有影响,尽管干预组参与者进行姑息治疗会诊和家属会议的频率更高。
ClinicalTrials.gov标识符:NCT04414787。