Remote patient management of heart failure across the ejection fraction spectrum: A pre‐specified analysis of the TIM‐HF2 trial

Author:

Kerwagen Fabian12ORCID,Koehler Kerstin34,Vettorazzi Eik5,Stangl Verena46,Koehler Magdalena78,Halle Martin8,Koehler Friedrich34,Störk Stefan12

Affiliation:

1. Department of Clinical Research and Epidemiology, Comprehensive Heart Failure Center University Hospital Würzburg Würzburg Germany

2. Department of Medicine I, Cardiology University Hospital Würzburg Würzburg Germany

3. Centre for Cardiovascular Telemedicine, Campus Charité Mitte German Heart Center Charité Berlin Germany

4. German Center for Cardiovascular Research (DZHK) Berlin Germany

5. Institute of Medical Biometry and Epidemiology University Medical Center Hamburg‐Eppendorf Hamburg Germany

6. Department of Cardiology, Angiology and Intensive Care Campus Charité Mitte, German Heart Center Charité Berlin Germany

7. Ludwig‐Maximilians Universität München Munich Germany

8. Department of Preventive Sports Medicine and Sports Cardiology, University Hospital ‘Klinikum rechts der Isar’, School of Medicine Technical University Munich Munich Germany

Abstract

AbstractAimsThe benefit of non‐invasive remote patient management (RPM) for patients with heart failure (HF) has been demonstrated. We evaluated the effect of left ventricular ejection fraction (LVEF) on treatment outcomes in the TIM‐HF2 (Telemedical Interventional Management in Heart Failure II; NCT01878630) randomized trial.Methods and resultsTIM‐HF2 was a prospective, randomized, multicentre trial investigating the effect of a structured RPM intervention versus usual care in patients who had been hospitalized for HF within 12 months before randomization. The primary endpoint was the percentage of days lost due to all‐cause death or unplanned cardiovascular hospitalization. Key secondary endpoints were all‐cause and cardiovascular mortality. Outcomes were assessed by LVEF in guideline‐defined subgroups of ≤40% (HF with reduced EF [HFrEF]), 41–49% (HF with mildly reduced EF [HFmrEF]), and ≥50% (HF with preserved EF [HFpEF]). Out of 1538 participants, 818 (53%) had HFrEF, 224 (15%) had HFmrEF, and 496 (32%) had HFpEF. Within each LVEF subgroup, the primary endpoint was lower in the treatment group, i.e. the incidence rate ratio [IRR] remained below 1.0. Comparing intervention and control group, the percentage of days lost was 5.4% versus 7.6% for HFrEF (IRR 0.72, 95% confidence interval [CI] 0.54–0.97), 3.3% versus 5.9% for HFmrEF (IRR 0.85, 95% CI 0.48–1.50) and 4.7% versus 5.4% for HFpEF (IRR 0.93, 95% CI 0.64–1.36). No interaction between LVEF and the randomized group became apparent. All‐cause and cardiovascular mortality were also reduced by RPM in each subgroup with hazard ratios <1.0 across the LVEF spectrum for both endpoints.ConclusionIn the clinical set‐up deployed in the TIM‐HF2 trial, RPM appeared effective irrespective of the LVEF‐based HF phenotype.

Funder

Bundesministerium für Bildung und Forschung

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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