Cardiac contractility modulation in HFrEF patients with QRS duration 120-149 ms: reduction in heart failure hospitalizations and improvement in functional outcome.
CCM-REG
device therapy
heart failure
quality of life
reduced left ventricular ejection fraction
Journal
Heart rhythm
ISSN: 1556-3871
Titre abrégé: Heart Rhythm
Pays: United States
ID NLM: 101200317
Informations de publication
Date de publication:
19 Sep 2024
19 Sep 2024
Historique:
received:
16
03
2024
revised:
11
09
2024
accepted:
15
09
2024
medline:
22
9
2024
pubmed:
22
9
2024
entrez:
21
9
2024
Statut:
aheadofprint
Résumé
A subset of heart failure (HF) patients qualifies for cardiac resynchronization therapy (CRT). However, a 30% CRT non-responder rate persists, with patients with narrower QRS durations (i.e., QRSd 120-149 ms) receiving less or inconsistent benefit. CCM may be an important alternative therapy option but has largely been evaluated only in HF patients with QRSd <120 ms. Primarily to evaluate the impact of cardiac contractility modulation (CCM) on HF-related hospitalizations and secondarily on left ventricular EF (LVEF) as well as quality of life in HF patients with QRSd 120-149 ms, compared to QRSd <120 ms. CCM-REG enrolled 503 HF patients with a follow-up of up to 2 yrs. Hospitalization rates were available for 1 yr pre-implant. Safety was assessed by comparison of actual versus MAGGIC score- or SHFM-predicted mortality. Among 111/455 subjects with QRSd 120-149 ms (mean QRSd 130±8 ms, age 68±10 yrs, 20% female, LVEF 29±9%, 82% NYHA class III), CCM diminished HF-related hospitalization rate by 72% (pre- vs. post-implant 0.90 vs. 0.25 events/per patient-yr over 2 yrs; p<0.001). LVEF improved by 7±8% (p=0.01 vs. baseline), MLWHFQ score by 10±23 pts (p=0.01 vs. baseline), and NYHA class by 0.5±0.7 classes (<0.001 vs. baseline). The effect size was similar to that in the QRSd <120 ms patients. Mortality within first year was 19% in QRSd 120-149 ms patients, i.e., not significantly different from the MAGGIC score or SHFM prediction. CCM significantly improved HF control in NYHA III HFrEF patients with moderately prolonged QRSd 120-149 ms. The effect was similar to patients with QRSd <120ms.
Sections du résumé
BACKGROUND
BACKGROUND
A subset of heart failure (HF) patients qualifies for cardiac resynchronization therapy (CRT). However, a 30% CRT non-responder rate persists, with patients with narrower QRS durations (i.e., QRSd 120-149 ms) receiving less or inconsistent benefit. CCM may be an important alternative therapy option but has largely been evaluated only in HF patients with QRSd <120 ms.
OBJECTIVES
OBJECTIVE
Primarily to evaluate the impact of cardiac contractility modulation (CCM) on HF-related hospitalizations and secondarily on left ventricular EF (LVEF) as well as quality of life in HF patients with QRSd 120-149 ms, compared to QRSd <120 ms.
METHODS
METHODS
CCM-REG enrolled 503 HF patients with a follow-up of up to 2 yrs. Hospitalization rates were available for 1 yr pre-implant. Safety was assessed by comparison of actual versus MAGGIC score- or SHFM-predicted mortality.
RESULTS
RESULTS
Among 111/455 subjects with QRSd 120-149 ms (mean QRSd 130±8 ms, age 68±10 yrs, 20% female, LVEF 29±9%, 82% NYHA class III), CCM diminished HF-related hospitalization rate by 72% (pre- vs. post-implant 0.90 vs. 0.25 events/per patient-yr over 2 yrs; p<0.001). LVEF improved by 7±8% (p=0.01 vs. baseline), MLWHFQ score by 10±23 pts (p=0.01 vs. baseline), and NYHA class by 0.5±0.7 classes (<0.001 vs. baseline). The effect size was similar to that in the QRSd <120 ms patients. Mortality within first year was 19% in QRSd 120-149 ms patients, i.e., not significantly different from the MAGGIC score or SHFM prediction.
CONCLUSIONS
CONCLUSIONS
CCM significantly improved HF control in NYHA III HFrEF patients with moderately prolonged QRSd 120-149 ms. The effect was similar to patients with QRSd <120ms.
Identifiants
pubmed: 39306264
pii: S1547-5271(24)03366-6
doi: 10.1016/j.hrthm.2024.09.038
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024. Published by Elsevier Inc.