A randomized clinical trial was carried out between January 2004 and October 2006. In total, 283 patients admitted to hospital with a diagnosis of heart failure were randomly allocated to a home-based intervention (intervention group) or usual care (control group). The primary end-point was the combination of allcause mortality and hospital readmission for worsening heart failure at 1-year follow-up.
The primary end-point was observed in 41.7 % of patients in the intervention group and in 54.3 % in the control group. The hazard ratio was 0.70 (95 % confidence interval [CI], 0.55-0.99). Taking significant clinical variables into account slightly reduced the hazard ratio to 0.62 (95 % CI, 0.50-0.87). At the end of the study, the quality of life of patients in the intervention group was better than in the control group (18.57 vs 31.11; P<.001).
A home-based intervention for patients with heart failure reduced the aggregate of mortality and hospital readmissions and improved quality of life.