Development and Pilot Test of a Culturally Relevant Toolkit to Enhance Advance Care Planning With Chinese American Patients

被引:9
作者
Dhingra, Lara [1 ,2 ]
Lam, Kin [3 ]
Cheung, William [3 ]
Hynes, Gavin [4 ]
Fleming-Damon, Colleen [1 ]
Hicks, Stephanie [1 ]
Huang, Philip [5 ]
Chen, Jack [6 ]
Chang, Victor [7 ,8 ]
Portenoy, Russell [1 ,2 ,9 ]
机构
[1] MJHS Inst Innovat Palliat Care, 39 Broadway,3rd Floor, New York, NY 10006 USA
[2] Albert Einstein Coll Med, Dept Family & Social Med, Bronx, NY 10467 USA
[3] Community Private Practice, New York, NY USA
[4] Natl Univ Ireland, Galway, Ireland
[5] Univ Kansas, Dept Psychol, Lawrence, KS 66045 USA
[6] Cohen Childrens Med Ctr, Gen Pediat, New Hyde Pk, NY USA
[7] Vet Affairs New Jersey Hlth Care Syst, Sect Hematol Oncol, East Orange, NJ USA
[8] Rutgers NJMS, Dept Med, Newark, NJ USA
[9] Albert Einstein Coll Med, Dept Neurol, Bronx, NY USA
关键词
Chinese American; advance care planning; provider toolkit; elderly; end-of-life care disparities; BARRIERS; COMMUNICATION; FACILITATORS; PERCEPTIONS; PREFERENCES; KNOWLEDGE; ADULTS; US;
D O I
10.1016/j.jpainsymman.2021.02.031
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
Background. First-generation Chinese American patients have low engagement in advance care planning (ACP). Among the causes may be clinician uncertainty about traditional cultural values. Aim. Based on a survey identifying barriers to ACP among older ethnic Chinese American patients, we created a toolkit to support clinicians in culturally relevant ACP practices and conducted a pilot test to evaluate usability, acceptability, and preliminary outcomes. Design/Setting/Participants. The toolkit includes culturally relevant information and an ACP guideline with a prompt list of questions. Six clinicians (three physicians, two nurse practitioners, and one physician assistant) in two New York City-based practices piloted the toolkit through discussions with 66 patients. Results. Patients' age averaged 70.2 years (SD=12.4); 56.1% were women. Almost two-thirds had not finished high school and 53.0% spoke only Cantonese. More than three-quarters (78.8%) did not understand the purpose of ACP before the discussion. During the discussion, 58 patients (87.9%) completed a new proxy naming a health care agent, 21 (31.8%) requested a nonhospital DNR order, and two (3%) completed a living will. Topics discussed included treatment preferences (discussed with 80.3% of patients); health care values (77.3%); treatment decisions (72.7%); goals of care (68.2%), and hospice (1.5%). Five of the six clinicians expressed satisfaction ("very" or "somewhat") with the toolkit, four were "very" comfortable using it, and three stated that it helped them "a lot" with effective discussions. Conclusions. An ACP toolkit may facilitate culturally relevant ACP discussions by increasing clinician competency and patient engagement. Further studies of this approach are needed. J Pain Symptom Manage 2021;62:e186-e191. (c) 2021 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:E186 / E191
页数:6
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