Palliative Care Initiated in the Emergency Department: A Cluster Randomized Clinical Trial.

Q1 Medicine
Corita R Grudzen, Nina Siman, Allison M Cuthel, Oluwaseun Adeyemi, Rebecca Liddicoat Yamarik, Keith S Goldfeld, Benjamin S Abella, Fernanda Bellolio, Sorayah Bourenane, Abraham A Brody, Lauren Cameron-Comasco, Joshua Chodosh, Julie J Cooper, Ashley L Deutsch, Marie Carmelle Elie, Ahmed Elsayem, Rosemarie Fernandez, Jessica Fleischer-Black, Mauren Gang, Nicholas Genes, Rebecca Goett, Heather Heaton, Jacob Hill, Leora Horwitz, Eric Isaacs, Karen Jubanyik, Sangeeta Lamba, Katharine Lawrence, Michelle Lin, Caitlin Loprinzi-Brauer, Troy Madsen, Joseph Miller, Ada Modrek, Ronny Otero, Kei Ouchi, Christopher Richardson, Lynne D Richardson, Matthew Ryan, Elizabeth Schoenfeld, Matthew Shaw, Ashley Shreves, Lauren T Southerland, Audrey Tan, Julie Uspal, Arvind Venkat, Laura Walker, Ian Wittman, Erin Zimny
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引用次数: 0

Abstract

Importance: The emergency department (ED) offers an opportunity to initiate palliative care for older adults with serious, life-limiting illness.

Objective: To assess the effect of a multicomponent intervention to initiate palliative care in the ED on hospital admission, subsequent health care use, and survival in older adults with serious, life-limiting illness.

Design, setting, and participants: Cluster randomized, stepped-wedge, clinical trial including patients aged 66 years or older who visited 1 of 29 EDs across the US between May 1, 2018, and December 31, 2022, had 12 months of prior Medicare enrollment, and a Gagne comorbidity score greater than 6, representing a risk of short-term mortality greater than 30%. Nursing home patients were excluded.

Intervention: A multicomponent intervention (the Primary Palliative Care for Emergency Medicine intervention) included (1) evidence-based multidisciplinary education; (2) simulation-based workshops on serious illness communication; (3) clinical decision support; and (4) audit and feedback for ED clinical staff.

Main outcome and measures: The primary outcome was hospital admission. The secondary outcomes included subsequent health care use and survival at 6 months.

Results: There were 98 922 initial ED visits during the study period (median age, 77 years [IQR, 71-84 years]; 50% were female; 13% were Black and 78% were White; and the median Gagne comorbidity score was 8 [IQR, 7-10]). The rate of hospital admission was 64.4% during the preintervention period vs 61.3% during the postintervention period (absolute difference, -3.1% [95% CI, -3.7% to -2.5%]; adjusted odds ratio [OR], 1.03 [95% CI, 0.93 to 1.14]). There was no difference in the secondary outcomes before vs after the intervention. The rate of admission to an intensive care unit was 7.8% during the preintervention period vs 6.7% during the postintervention period (adjusted OR, 0.98 [95% CI, 0.83 to 1.15]). The rate of at least 1 revisit to the ED was 34.2% during the preintervention period vs 32.2% during the postintervention period (adjusted OR, 1.00 [95% CI, 0.91 to 1.09]). The rate of hospice use was 17.7% during the preintervention period vs 17.2% during the postintervention period (adjusted OR, 1.04 [95% CI, 0.93 to 1.16]). The rate of home health use was 42.0% during the preintervention period vs 38.1% during the postintervention period (adjusted OR, 1.01 [95% CI, 0.92 to 1.10]). The rate of at least 1 hospital readmission was 41.0% during the preintervention period vs 36.6% during the postintervention period (adjusted OR, 1.01 [95% CI, 0.92 to 1.10]). The rate of death was 28.1% during the preintervention period vs 28.7% during the postintervention period (adjusted OR, 1.07 [95% CI, 0.98 to 1.18]).

Conclusions and relevance: This multicomponent intervention to initiate palliative care in the ED did not have an effect on hospital admission, subsequent health care use, or short-term mortality in older adults with serious, life-limiting illness.

Trial registration: ClinicalTrials.gov Identifier: NCT03424109.

在急诊科开展姑息治疗:一项随机临床试验。
重要性:急诊科(ED)提供了一个机会,启动姑息治疗的老年人严重,限制生命的疾病。目的:评估在急诊科启动姑息治疗的多组分干预对患有严重、限制生命的疾病的老年人住院、随后的医疗保健使用和生存率的影响。设计、环境和参与者:集群随机、楔形分步临床试验,包括在2018年5月1日至2022年12月31日期间访问美国29个急诊科中1个急诊科的66岁或以上患者,既往有12个月的医疗保险登记,Gagne合并症评分大于6,短期死亡风险大于30%。养老院的病人被排除在外。干预:多组分干预(初级姑息治疗急诊医学干预)包括(1)循证多学科教育;(2)基于模拟的大病传播研讨会;(3)临床决策支持;(4)对急诊科临床工作人员进行审核和反馈。主要转归指标:主要转归指标为住院率。次要结局包括随后的医疗保健使用情况和6个月的生存率。结果:研究期间有98次 922次ED首次就诊(中位年龄77岁[IQR, 71-84岁];50%为女性;13%是黑人,78%是白人;加涅合并症评分中位数为8分[IQR, 7-10])。干预前的住院率为64.4%,干预后为61.3%(绝对差值为-3.1% [95% CI, -3.7%至-2.5%];校正优势比[OR], 1.03 [95% CI, 0.93 ~ 1.14])。干预前和干预后的次要结局没有差异。干预前重症监护病房的入院率为7.8%,干预后为6.7%(校正OR为0.98 [95% CI, 0.83至1.15])。干预前至少1次复查ED的比率为34.2%,干预后为32.2%(校正OR为1.00 [95% CI, 0.91至1.09])。干预前的安宁疗护使用率为17.7%,干预后为17.2%(校正OR为1.04 [95% CI, 0.93至1.16])。干预前家庭健康使用率为42.0%,干预后为38.1%(调整比值比为1.01 [95% CI, 0.92至1.10])。干预前至少1次再入院率为41.0%,干预后为36.6%(校正OR为1.01 [95% CI, 0.92 ~ 1.10])。干预前死亡率为28.1%,干预后死亡率为28.7%(校正OR为1.07 [95% CI, 0.98 ~ 1.18])。结论和相关性:这种在急诊科启动姑息治疗的多组分干预对患有严重、限制生命的疾病的老年人的住院率、随后的医疗保健使用或短期死亡率没有影响。试验注册:ClinicalTrials.gov标识符:NCT03424109。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
45.40
自引率
0.00%
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0
期刊介绍: JAMA, published continuously since 1883, is an international peer-reviewed general medical journal. JAMA is a member of the JAMA Network, a consortium of peer-reviewed, general medical and specialty publications.
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