# Impact of Late ARNI Initiation on Quality of Life and Functional Capacity in CRT-Treated HFrEF Patients: A Single-Centre Cohort Study

**Authors:** Oana Patru, Silvia Luca, Dragos Cozma, Cristina Vacarescu, Simina Crisan, Andreea Bena, Mirela Virtosu, Adrian Sebastian Zus, Constantin Tudor Luca, Simona Ruxanda Dragan

PMC · DOI: 10.3390/jcm15041617 · 2026-02-19

## TL;DR

Starting ARNI therapy later in patients with long-term CRT improves quality of life, exercise ability, and heart function.

## Contribution

This study shows that late initiation of ARNI in CRT-treated HFrEF patients still provides significant clinical benefits.

## Key findings

- Quality of life improved significantly with 89.5% achieving a meaningful improvement.
- Heart function and structure improved, with reduced diuretic use and fewer arrhythmias.
- Higher ARNI doses were linked to better outcomes, though longer CRT duration limited structural benefits.

## Abstract

Background/Objectives: Cardiac resynchronization therapy (CRT) is a cornerstone treatment for heart failure with reduced ejection fraction (HFrEF), yet many patients remain symptomatic despite long-term electrical optimization. Although sacubitril/valsartan (ARNI) is central to guideline-directed medical therapy (GDMT), data on its late initiation in patients with chronic CRT are scarce. This study evaluated the impact of delayed ARNI initiation on clinical status, functional capacity, and cardiac remodelling in a real-world CRT population. Methods: We performed a single-centre, retrospective observational study including 76 HFrEF patients with chronic CRT who started ARNI between 2022 and late 2024. Patients underwent standardized assessment at baseline (T0) and after 12 ± 3 months (T1), including clinical evaluation, 12-item Kansas City Cardiomyopathy Questionnaire (KCCQ-12), symptom-limited bicycle exercise testing, and comprehensive echocardiography. The primary endpoint was change in quality of life (QoL). Secondary endpoints included exercise capacity, echocardiographic reverse remodelling, NYHA class, loop diuretic dose, and device-detected arrhythmias. Dose–response and multidimensional response patterns were explored. Results: KCCQ-12 increased from 52.96 ± 16.33 to 75.55 ± 18.12 (Δ +22.59 ± 13.22, p < 0.001), with 89.5% achieving a clinically meaningful improvement. Exercise duration and peak workload improved significantly. LVEF increased from 35.08 ± 6.96% to 43.18 ± 8.42% (Δ +8.11%, p < 0.001), with reductions in left ventricular and atrial volumes. Loop diuretic dose decreased (median −10 mg/day furosemide equivalent, p < 0.001), and 26.3% discontinued diuretics. A lower prevalence of device-detected arrhythmias was observed at follow-up, from 34.2% to 6.6% (p < 0.001). Higher ARNI doses were associated with greater likelihood of clinical, functional, and structural response. Longer CRT duration reduced the probability of structural remodelling but not symptomatic or functional benefit. Conclusions: In patients with long-standing CRT, delayed ARNI initiation was associated with improvements in QoL, exercise capacity, cardiac remodelling, congestion status, and electrical stability. These findings suggest that CRT is not a therapeutic ceiling and that late ARNI initiation remains a valuable component of comprehensive GDMT.

## Linked entities

- **Chemicals:** sacubitril/valsartan (PubChem CID 24755620), furosemide (PubChem CID 3440)
- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** Cardiomyopathy (MESH:D009202), fatigue (MESH:D005221), Arrhythmia (MESH:D001145), tachycardia (MESH:D013610), frailty (MESH:D000073496), Arrhythmic (OMIM:212500), electrical dyssynchrony (MESH:D004556), hypotension (MESH:D007022), myocardial remodelling (MESH:D064752), injury to (MESH:D014947), angina (MESH:D000787), ischemic (MESH:D002545), valvular disease (MESH:D006349), dyspnea (MESH:D004417), cardiac remodelling (MESH:D020257), heart failure (MESH:D006333), renal dysfunction (MESH:D007674), musculoskeletal limitations (MESH:D009140), HFrEF (MESH:D054143), ventricular tachycardia (MESH:D017180), atrial fibrillation (MESH:D001281), GDMT (MESH:D016609), myocardial infarction (MESH:D009203), Cardiovascular Diseases (MESH:D002318), congestion (MESH:D002311)
- **Chemicals:** HF (MESH:D006195), spironolactone (MESH:D013148), Sacubitril (MESH:C000717211), valsartan (MESH:D000068756), potassium (MESH:D011188), ARNI (-), sacubitril/valsartan (MESH:C549068), furosemide (MESH:D005665)
- **Species:** HF [taxon 2008765], Homo sapiens (human, species) [taxon 9606]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941977/full.md

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Source: https://tomesphere.com/paper/PMC12941977