Palliative Care Interventions for Patients with Heart Failure: A Systematic Review and Meta-Analysis

被引:144
|
作者
Diop, Michelle S. [1 ,2 ]
Rudolph, James L. [2 ,3 ,4 ]
Zimmerman, Kristin M. [5 ]
Richter, Mary A. [6 ]
Skarf, L. Michal [7 ,8 ]
机构
[1] Brown Univ, Warren Alpert Med Sch, Primary Care & Populat Med Program, Providence, RI 02912 USA
[2] Providence VAMC, Ctr Innovat Long Term Serv & Supports, Providence, RI USA
[3] Brown Univ, Dept Med, Warren Alpert Med Sch Brown, Providence, RI 02912 USA
[4] Brown Univ, Sch Publ Hlth, Ctr Gerontol, Providence, RI 02912 USA
[5] Virginia Commonwealth Univ, Dept Pharmacotherapy & Outcomes, Richmond, VA USA
[6] Tulane Univ, Sch Med, Dept Obstet & Gynecol, 1430 Tulane Ave, New Orleans, LA 70112 USA
[7] VA Boston Healthcare Syst, Div Geriatr & Palliat Care, Boston, MA USA
[8] Harvard Med Sch, Boston, MA USA
关键词
cultural care; heart failure; palliative care; quality of life; symptoms; utilization; QUALITY-OF-LIFE; RANDOMIZED CONTROLLED-TRIAL; MEDICINE CONSULTATION; CANCER-PATIENTS; HEALTH-CARE; OUTCOMES; HOSPICE; DISEASE; IMPACT; SATISFACTION;
D O I
10.1089/jpm.2016.0330
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
Objective: To systematically characterize interventions and effectiveness of palliative care for advanced heart failure (HF) patients. Background: Patients with advanced heart failure experience a high burden of distressing symptoms and diminished quality of life. Palliative care expertise with symptom management and healthcare decision-making benefits HF patients. Methods: A systematic PubMed search was conducted from inception to June 2016 for studies of palliative care interventions for HF patients. Studies of humans with a HF diagnosis who underwent a palliative care intervention were included. Data were extracted on study design, participant characteristics, intervention components, and in three groups of outcomes: patient-centered outcomes, quality-of-death outcomes, and resource utilization. Study characteristics were examined to determine if meta-analysis was possible. Results: The fifteen identified studies varied in design (prospective, n = 10; retrospective, n = 5). Studies enrolled older patients, but greater variability was found for race, sex, and marital status. A majority of studies measuring patient-centered outcomes demonstrated improvements including quality of life and satisfaction. Quality-of-death outcomes were mixed with a majority of studies reporting clarification of care preferences, but less improvement in death at home and hospice enrollment. A meta-analysis in three studies found that home-based palliative care consults in HF patients lower the risk of rehospitalization by 42% (RR = 0.58; 95% Confidence Interval 0.44, 0.77). Discussion: Available evidence suggests that home and team-based palliative interventions for HF patients improve patient-centered outcomes, documentation of preferences, and utilization. Increased high quality studies will aid the determination of the most effective palliative care approaches for the HF population.
引用
收藏
页码:84 / 92
页数:9
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