Why the study?
Real-world effectiveness and safety data for the Carillon Mitral Contour System (CMCS) for indirect annuloplasty in patients with heart failure and secondary mitral regurgitation needed evaluation.
Does indirect mitral annuloplasty with the Carillon Mitral Contour System improve symptoms, mitral regurgitation severity, echocardiographic parameters, and BNP levels at 3 months in patients with HFrEF or HFpEF and secondary mitral regurgitation?
Does indirect mitral annuloplasty with the Carillon Mitral Contour System improve symptoms, mitral regurgitation severity, echocardiographic parameters, and BNP levels at 3 months in patients with HFrEF or HFpEF and secondary mitral regurgitation?
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In a real-world cohort of elderly patients with secondary mitral regurgitation, indirect mitral annuloplasty with the Carillon system demonstrated high procedural success and comparable 3-month improvements in NYHA class, MR severity, cardiac remodeling, and BNP levels across both HFrEF and HFpEF phenotypes.
Aims We aim to evaluate the real-world effectiveness and safety of the Carillon Mitral Contour System (CMCS) for indirect annuloplasty in patients with heart failure (HF) and secondary mitral regurgitation (SMR). Methods and results This was a single-centre retrospective study of 204 consecutive patients (age 83 ± 6 years, 68% female, 72% HFrEF) with NYHA class II-IV HF and moderate and moderate-to-severe (grade 2 + or 3+) SMR planned for CMCS implantation between 2021 and 2024. Echocardiographic variables, B-type natriuretic peptide (BNP) and NYHA functional class were routinely assessed prior to the procedure and, in those with a successful implantation, after 3 months. The device was successfully implanted in 201 (98.5%) patients; the remaining 3 had unsuitable coronary sinus anatomy. Procedural complications occurred in 10.4% and included circumflex artery compression requiring percutaneous coronary intervention (9.5%); coronary sinus injury (1.5%); procedural mortality (0%). At 3 months, NYHA class improved by ≥1 category in 94% of patients and 98% achieved NYHA class I or II. MR decreased by ≥1 grade in 91% of patients, with all patients classified as grade 1+ or 2+ post-procedure. Vena contracta width decreased (6.43 ± 0.84 to 3.85 ± 1.19 mm; P < 0.001), and there was a reduction of LA area from 44.4 ± 6.0 to 35.4 ± 5.1 cm2 (P < 0.001). Diastolic filling was improved (change in E/E′ ratio from 20.1 ± 5.5 to 14.0 ± 3.8; P < 0.001), systolic pulmonary artery pressure was lower in follow-up (44 ± 11 to 35 ± 9 mm; P < 0.001), and there was also a clinically relevant reduction in median BNP levels from 2849 to 1390 pg/mL (P < 0.001). These changes were not different between HFrEF and HFpEF. Conclusions In this single-centre observational cohort study, CMCS implantation success was high, and associated with low complication rates, improvements in symptoms and echocardiographic variables, and clinically relevant reductions in BNP levels.
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Priebe‐Brämer et al. (2025) studied this question.
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