Feasibility of Implementing a Palliative Care Intervention for People with Heart Failure: Learnings from a Pilot Randomized Clinical Trial

被引:14
|
作者
O'Riordan, David L. [1 ,2 ]
Rathfon, Megan A. [1 ,2 ]
Joseph, Denah M. [1 ]
Hawgood, Jane [1 ]
Rabow, Michael W. [1 ,2 ]
Dracup, Kathleen A. [3 ]
De Marco, Teresa [2 ]
Pantilat, Steven Z. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Med, Div Palliat Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Sch Med, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Sch Nursing, San Francisco, CA 94143 USA
关键词
feasibility; heart-related quality of life; pain; pilot study; randomized clinical trial; QUESTIONNAIRE; RELIABILITY; VALIDITY;
D O I
10.1089/jpm.2018.0633
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: People with heart failure (HF) have high morbidity and mortality and may benefit from palliative care (PC). Objective: To pilot a randomized, clinical trial of a PC intervention for people with HF. Design: Participants were randomized to usual care (UC) or intervention (UC plus specialty PC) between January 2012 and December 2013. The initial PC consultation was conducted in-hospital, with six additional contacts from the PC team over six months. Setting/Subjects: The study was undertaken in a large, urban, academic medical center with patients (n = 30) with New York Heart Association HF Class II-IV. Measurements: Patients completed a survey at baseline, three and six months, assessing pain, dyspnea, depression, and quality of life (QoL). Results: Although there were significant improvements in mean scores from baseline to six months for pain (4.3 vs. 2.4, p = 0.05), dyspnea (3.9 vs. 2.2, p = 0.03), and QoL (59.2 vs. 42.7, p = 0.001), there were no differences between study groups over time. On average, participants in the intervention group received 5 out of 6 contacts and were satisfied with the intervention. Conclusions: The intervention was well accepted by patients, safe, and feasible. Our findings suggest that PC interventions for people with HF should match the PC needs of the patient. Given the trajectory of HF, studies may need to recruit outpatients and follow patients for a longer period to fully evaluate the impact of PC interventions. Clinical trials Identifier: NCT01461681.
引用
收藏
页码:1583 / 1588
页数:6
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