Patient and Caregiver Prioritization of Palliative and End-of-Life Cancer Care Quality Measures

被引:3
|
作者
O'Hanlon, Claire E. [1 ]
Giannitrapani, Karleen F. [2 ,3 ]
Lindvall, Charlotta [4 ,5 ]
Gamboa, Raziel C. [2 ]
Canning, Mark [1 ]
Asch, Steven M. [2 ,3 ]
Garrido, Melissa M. [6 ,7 ]
Walling, Anne M. [1 ,8 ,9 ]
Lorenz, Karl A. [2 ,3 ]
Bernstein, Erica
Branstetter, John
Bunch, Dean
Carroll, Frederick
Guzman, Eric
Krutz, Mary
Maizel, Jonathan
Moe, John
机构
[1] VA Greater Los Angeles Hlth Care Syst, Ctr Study Healthcare Innovat Implementat & Policy, Los Angeles, CA 90073 USA
[2] VA Palo Alto Hlth Care Syst, Ctr Innovat Implementat Ci2i, Palo Alto, CA USA
[3] Stanford Univ, Sch Med, Div Primary Care & Populat Hlth, Stanford, CA 94305 USA
[4] Dana Farber Canc Inst, Dept Psychosocial Oncol & Palliat Care POPC, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA
[6] VA Boston Healthcare Syst Res & Dev, Partnered Evidence Based Policy Resource Ctr PEPR, Boston, MA USA
[7] Boston Univ, Sch Publ Hlth, Dept Hlth Law Policy & Management, Boston, MA USA
[8] Univ Calif Los Angeles, Div Gen Internal Med, Los Angeles, CA USA
[9] Univ Calif Los Angeles, Hlth Serv Res, Los Angeles, CA USA
关键词
FAMILY;
D O I
10.1007/s11606-021-07041-8
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: Development and prioritization of quality measures typically relies on experts in clinical medicine, but patients and their caregivers may have different perspectives on quality measurement priorities. OBJECTIVE: To inform priorities for health system implementation of palliative cancer and end-of-life care quality measures by eliciting perspectives of patients and caregivers. DESIGN: Using modified RAND-UCLA Appropriateness Panel methods and materials tailored for knowledgeable lay participants, we convened a panel to rate cancer palliative care process quality measure concepts before and after a 1-day, in-person meeting. PARTICIPANTS: Nine patients and caregivers with experience living with or caring for patients with cancer. MAIN MEASURES: Panelists rated each concept on importance for providing patient- and family-centered care on a nine-point scale and each panelist nominated five highest priority measure concepts ("top 5"). KEY RESULTS: Cancer patient and caregiver panelists rated all measure concepts presented as highly important to patient- and family- centered care (median rating >= 7) in pre-panel (mean rating range, 6.9-8.8) and post-panel ratings (mean rating range, 7.2-8.9). Forced choice nominations of the "top 5" helped distinguish similarly rated measure concepts. Measure concepts nominated into the "top 5" by three or more panelists included two measure concepts of communication (goals of care discussions and discussion of prognosis), one measure concept on providing comprehensive assessments of patients, and three on symptoms including pain management plans, improvement in pain, and depression management plans. Patients and caregivers nominated one additional measure concept (pain screening) back into consideration, bringing the total number of measure concepts under consideration to 21. CONCLUSIONS: Input from cancer patients and caregivers helped identify quality measurement priorities for health system implementation. Forced choice nominations were useful to discriminate concepts with the highest perceived importance. Our approach serves as a model for incorporating patient and caregiver priorities in quality measure development and implementation.
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页码:1429 / 1435
页数:7
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