医学
射血分数
心力衰竭
康复
随机对照试验
物理疗法
干预(咨询)
置信区间
临床试验
射血分数保留的心力衰竭
内科学
护理部
作者
Hasnain Dalal,Chim C. Lang,Karen Smith,Jennifer Wingham,Victoria Eyre,Colin Greaves,Fiona C Warren,Colin Green,Kate Jolly,Russell Davis,Patrick Doherty,Jackie Austin,Nicholas Britten,Charles Abraham,Robin van Lingen,Sally Singh,Kevin Paúl,Melvyn Hillsdon,Susannah Sadler,Christopher Hayward,Rod S Taylor
标识
DOI:10.3399/bjgp18x697013
摘要
Background Home-based models of cardiac rehabilitation may overcome suboptimal rates of participation. Aim This study sought to assess the feasibility and acceptability of a novel healthcare professional facilitated home-based comprehensive self-management REACH-HF rehabilitation intervention for patients with heart failure with preserved ejection fraction (HFpEF) and their caregivers. Method Patients were randomised 1 to the REACH-HF intervention plus usual care (intervention group) or usual care alone (control group). Outcomes were collected at baseline, 3 and 6 months post-randomisation. Outcomes were also collected in caregivers. Results We enrolled 50 symptomatic patients with a left ventricular ejection fraction ≥ 45% (mean age: 73.9 years, 54% female: 96% in NYHA II/III) and 21 caregivers. Study retention (90%) and intervention uptake (92%) were excellent. At 6 months, a number of patient outcomes showed a potential direction of effect in favour of the intervention group, including the primary outcome of Minnesota Living with Heart Failure Questionnaire total score (between group mean difference: −11.5, 95% confidence interval: −22.8 to 0.3). A total of 11 (4 intervention, 7 control) patients experienced a hospital admission over the 6 months follow up with 4 (all control patients) of these admissions being HF-related. Improvements were seen in a number intervention caregiver mental health and burden compared to control. Conclusion Our findings support the feasibility and rationale for the delivering the REACH-HF facilitated home-based rehabilitation intervention for patients with HFpEF and their caregivers and progression to a full multicentre randomised clinical trial to test the clinical and cost-effectiveness of this novel intervention.
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