Can Community Health Workers Increase Palliative Care Use for African American Patients? A Pilot Study

被引:16
|
作者
Sedhom, Ramy [1 ]
Nudotor, Richard [2 ]
Freund, Karen M. [3 ]
Smith, Thomas J. [4 ]
Cooper, Lisa A. [5 ,6 ]
Owczarzak, Jill T. [6 ]
Johnston, Fabian M. [2 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Dept Surg, Baltimore, MD 21205 USA
[3] Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA
[4] Johns Hopkins Univ, Sch Med, Palliat Care Program, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[5] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Hlth Behav & Soc, Baltimore, MD USA
基金
美国医疗保健研究与质量局;
关键词
END-OF-LIFE; ADVANCE DIRECTIVES; ETHNIC-DIFFERENCES; MEDICAL-CARE; CANCER; NAVIGATION; OUTCOMES; DISPARITIES; BARRIERS; PARTICIPATION;
D O I
10.1200/OP.20.00574
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE African American patients with cancer underutilize advance care planning (ACP) and palliative care (PC). This feasibility study investigated whether community health workers (CHWs) could improve ACP and PC utilization for African American patients with advanced cancer. METHODS African American patients diagnosed with an advanced solid organ cancer (stage IV or stage III disease with a palliative performance score, 60%) were enrolled. Patients completed baseline surveys that assessed symptom burden and distress at baseline and 3 months post-CHW intervention. The CHW intervention consisted of a comprehensive assessment of multiple PC domains and social determinants of health. CHWs provided tailored support and education on the basis of iterative assessment of patient needs. Intervention feasibility was determined by patient and caregiver retention rate above 50% at 3 months. RESULTS Over a 12-month period, 24 patients were screened, of which 21 were deemed eligible. Twelve patients participated in the study. Patient retention was high at 3 months (75%) and 6 months (66%). Following the CHW intervention, symptom assessment as measured by Edmonton Symptom Assessment System improved from 33.8 at baseline to 18.8 (P = .03). Psychological distress improved from 5.5 to 4.7 (P = .36), and depressive symptoms from 42.2 to 33.6 (P = .09), although this was not significant. ACP documentation improved from 25% at baseline to 75% at study completion. Sixty-seven percentage of patients were referred to PC, with 100% of three decedents using hospice. CONCLUSION Utilization of CHWs to address PC domains and social determinants of health is feasible. Although study enrollment was identified as a potential barrier, most recruited patients were retained on study. (C) 2021 by American Society of Clinical Oncology.
引用
收藏
页码:E158 / E167
页数:10
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