Integrating Patient and Expert Perspectives to Conceptualize High-Quality Palliative Cancer Care for Symptoms in the US Veterans Health Administration: A Qualitative Study

被引:0
|
作者
O'Hanlon, Claire E. [1 ,2 ,10 ]
Giannitrapani, Karleen F. [3 ,4 ]
Gamboa, Raziel C. [3 ,4 ]
Walling, Anne M. [2 ,5 ]
Lindvall, Charlotta [6 ,7 ]
Garrido, Melissa [8 ,9 ]
Asch, Steven M. [3 ,4 ]
Lorenz, Karl A. [3 ,4 ]
机构
[1] RAND Corp, Santa Monica, CA USA
[2] Ctr Study Healthcare Innovat Implementat & Policy, Los Angeles, CA USA
[3] Ctr Innovat Implementat Ci2i, Palo Alto, CA USA
[4] Stanford Univ, Sch Med, Stanford, CA USA
[5] Univ Calif Los Angeles, Los Angeles, CA USA
[6] Dana Farber Canc Inst, Boston, MA USA
[7] Brigham & Womens Hosp, Boston, MA USA
[8] Partnered Evidence Based Policy Resource Ctr PEPRe, Boston, MA USA
[9] Boston Univ, Sch Publ Hlth, Boston, MA USA
[10] Dept Vet Affairs, 11301 Wilshire Blvd 151, Los Angeles, CA 90073 USA
关键词
palliative care; cancer; advanced cancer; quality measurement; quality improvement; qualitative research; END-OF-LIFE; CENTERED CARE; INDICATORS; FAMILY;
D O I
10.1177/00469580231160374
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
Quality measurement is typically the domain of clinical experts and health system leaders; patient/caregiver perspectives are rarely solicited. We aimed to describe and integrate clinician and patient/caregiver conceptualizations of high-quality palliative symptom care for patients receiving care for advanced cancer within the US Veterans Health Administration in the context of existing quality measures. We conducted a secondary qualitative analysis of transcripts from prioritization discussions of process quality measures relevant to cancer palliative care. These discussions occurred during 2 modified RAND-UCLA appropriateness panels: a panel of 10 palliative care clinical expert stakeholders (7 physicians, 2 nurses, 1 social worker) and a panel of 9 patients/caregivers with cancer experience. Discussions were recorded, transcribed, and independently double-coded using an a priori logical framework. Content analysis was used to identify subthemes within codes and axial coding was used to identify crosscutting themes. Patients/caregivers and clinical experts contributed important perspectives to 3 crosscutting themes. First, proactive elicitation of symptoms is critical. Patients/caregivers especially emphasized importance of comprehensive and proactive screening and assessment, especially for pain and mental health. Second, screening and assessment alone is not enough; information elicited from patients must inform care. Measuring screening/assessment and management care processes separately has important limitations. Lastly, high-quality symptom management can be broadly defined if it is patient-centered; high-quality care takes an individualized approach and might include non-medical or non-pharmacological symptom management. Integrating the perspectives of clinical experts and patients/caregivers is critical for health systems to consider as they design and implement quality measures for palliative cancer care.
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页数:10
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