A Systematic Approach to Assessing and Addressing Palliative Care Needs in an Outpatient Population

被引:3
作者
Bischoff, Kara E. [1 ,5 ]
Vanegas, Gabriela [1 ]
O'Riordan, David L. [1 ]
Sumser, Bridget [1 ]
Long, Judy [1 ,2 ]
Lin, Jessica [1 ]
Berkey, Ann R. [3 ]
Kobayashi, Edward [4 ]
Zapata, Carly [1 ]
Rabow, Michael W. [1 ]
Pantilat, Steven Z. [1 ]
机构
[1] Univ Calif San Francisco, Dept Med, Div Palliat Med, San Francisco, CA USA
[2] Univ Med Partners, Stanford Healthcare, Stanford, CA USA
[3] Berkey Grp, San Francisco, CA USA
[4] Univ Calif San Francisco, Dept Family & Community Med, San Francisco, CA USA
[5] Univ Calif San Francisco, Dept Med, Div Palliat Med, Box 0125,521 Parnassus Ave,Floor 5, San Francisco, CA 94143 USA
关键词
Palliative care; serious illness; population health; systematic assessment; palliative care needs; advance care planning; ETHNIC DISPARITIES; REFERRAL CRITERIA; SURPRISE QUESTION; CANCER CARE; IMPACT; TOOLS;
D O I
10.1016/j.jpainsymman.2023.06.024
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Context/Objectives. A critical frontier for palliative medicine is to develop systems to routinely and equitably address the palliative care (PC) needs of seriously ill populations. Methods. An automated screen identified Medicare primary care patients who had serious illness based on diagnosis codes and utilization patterns. A stepped-wedge design was used to evaluate a six-month intervention through which a healthcare navigator assessed these seriously ill patients and their care partners for PC needs in the domains of 1) physical symptoms, 2) emotional distress, 3) practical concerns, and 4) advance care planning (ACP) via telephone surveys. Identified needs were addressed with tailored PC interventions. Results. A total of 292/2175 (13.4%) patients screened positive for serious illness. A total of 145 completed an intervention phase; 83 completed a control phase. Severe physical symptoms were identified in 27.6%, emotional distress in 57.2%, practical concerns in 37.2%, and ACP needs in 56.6%. Twenty-five intervention patients (17.2%) were referred to specialty PC compared to six control patients (7.2%). Prevalence of ACP notes increased 45.5%-71.7% (p = 0.001) during the intervention and remained stable during the control phase. Quality of life remained stable during the intervention and declined 7.4/10-6.5/10 (P =0.04) during the control phase. Conclusion. Through an innovative program, patients with serious illness were identified from a primary care population, assessed for PC needs, and offered specific services to meet those needs. While some patients were appropriate for specialty PC, even more needs were addressed without specialty PC. The program resulted in increased ACP and preserved quality of life. J Pain Symptom Manage 2023;66:270-280. & COPY; 2023 The Authors. Published by Elsevier Inc. on behalf of American Academy of Hospice and Palliative Medicine. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
引用
收藏
页码:270 / 280.e8
页数:19
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