Early rehabilitation in cardiology - heart failure: The ERIC-HF protocol, a novel intervention to decompensated heart failure patients rehabilitation

被引:16
作者
Delgado, Bruno Miguel [1 ,2 ,3 ]
Lopes, Ivo [4 ]
Gomes, Barbara [5 ]
Novo, Andre [3 ,6 ]
机构
[1] Univ Porto, Inst Ciencias Biomed Abel Salazar, Porto, Portugal
[2] CHUP, Cardiol Dept, Porto, Portugal
[3] Cintesis, NursID, Porto, Portugal
[4] Hosp St Antonio Largo, Cardiol Dept, Ctr Hospitalar Porto, P-4099001 Porto, Portugal
[5] Escola Super Enfermagem Porto, Rehabil Dept, Porto, Portugal
[6] Inst Politecn Braganca, Nursing Dept, Braganca, Portugal
关键词
Heart failure; exercise; functional capacity; safety; rehabilitation nurse; CLINICALLY IMPORTANT DIFFERENCE; LONDON CHEST ACTIVITY; DAILY LIVING SCALE; 6-MINUTE WALK TEST; CARDIAC REHABILITATION; CARDIOVASCULAR PREVENTION; EUROPEAN ASSOCIATION; DISTANCE;
D O I
10.1177/1474515120913806
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Decompensated heart failure patients are characterised by functional dependence and low exercise tolerance. Aerobic exercise can improve symptoms, functional capacity and an increase in exercise tolerance. However, the benefits of early rehabilitation have not yet been validated. Objective: To evaluate the safety and feasibility of an aerobic exercise training programme in functional capacity of decompensated heart failure patients. Methodology: A single centre, parallel, randomised controlled, open label trial, with 100 patients. The training group (TG, n=50) performed the training protocol and the control group (CG, n=50) performed the usual rehabilitation procedures. The London chest activity of daily living (LCADL) scale, the Barthel index (BI) and the 6 minute walking test (6MWT) at discharge were used to evaluate the efficacy of the protocol. Safety was measured by the existence of adverse events. Results: The mean age of the patients was 70 years, 20% were New York Heart Association (NYHA) class IV and 80% NYHA class III at admission. The major heart failure aetiology was ischaemic (35 patients) and valvular disease (25 patients). There were no significant differences between groups at baseline in terms of sociodemographic or pathophysiological characteristics. There was a statistically significant difference of 54.2 meters for the training group (P=0.026) in the 6MWT and at LCADL 12 versus 16 (P=0.003), but the BI did not: 96 versus 92 (P=0.072). No major adverse events occurred. Conclusions: The training protocol demonstrated safety and efficacy, promoting functional capacity. This study elucidated about the benefits of a systematised implementation of physical exercise during the patient's clinical stabilisation phase, which had not yet been demonstrated. Trial registration: NCT03838003, URL: https://clinicaltrials.gov/ct2/show/NCT03838003.
引用
收藏
页码:592 / 599
页数:8
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