Transcatheter edge‐to‐edge repair for secondary mitral regurgitation with third‐generation devices in heart failure patients – results from the Global EXPAND Post‐Market study

Author:

Orban Mathias12ORCID,Rottbauer Wolfgang3,Williams Mathew4,Mahoney Paul5,von Bardeleben Ralph Stephan6,Price Matthew J.7,Grasso Carmelo8,Lurz Philipp9,Zamorano Jose L.10,Asch Federico M.11,Maisano Francesco12,Kar Saibal13,Hausleiter Jörg12

Affiliation:

1. Medizinische Klinik I Ludwig‐Maximilians Universität Munich Germany

2. Munich Heart Alliance Partner site German Centre for Cardiovascular Research (DZHK) Munich Germany

3. Department of Internal Medicine II Ulm University Medical Center Ulm Germany

4. Heart Valve Center New York University Langone Health New York NY USA

5. Sentera Heart and Valve and Structural Disease Center Norfolk VA USA

6. Department of Cardiology University Medical Center of Mainz Mainz Germany

7. Division of Cardiovascular Diseases, Scripps Clinic La Jolla CA USA

8. Department of Cardiology, Ferrarotto Hospital University of Catania Catania Italy

9. Department of Cardiology Heart Center Leipzig – University Hospital Leipzig Germany

10. Hospital Ramon y Cajal Madrid Spain

11. Cardiovascular Core Laboratories MedStar Health Research Institute Washington DC USA

12. San Raffaele University Hospital Milan Italy

13. Los Robles Regional Medical Center Thousand Oaks CA USA

Abstract

ABSTRACTAimsMitral valve transcatheter edge‐to‐edge repair is a guideline‐recommended treatment option for patients with secondary mitral regurgitation (SMR). The purpose of this analysis was to report contemporary real‐world outcomes in SMR patients treated with third‐generation MitraClip systems.Methods and resultsEXPAND is a prospective, multicentre, international, single‐arm study with 1041 patients treated for mitral regurgitation (MR) with MitraClip NTR/XTR, with 30‐day and 1‐year follow‐up. All echocardiograms were analysed by an independent echocardiographic core lab. Study outcomes included procedural outcomes, durability of MR reduction, and major adverse events including all‐cause mortality and heart failure hospitalizations (HFH). A subgroup of 413 symptomatic patients (age 74.7 ± 10.1 years, 58% male) with severe SMR were included. MR reduction to MR ≤ 1+ and MR ≤ 2+ was achieved in 93.0% and 98.5% of patients, respectively, which was sustained at 1‐year follow‐up. All‐cause mortality was 17.7% at 1‐year‐ follow‐up, and the combined endpoint of all‐cause mortality or first HFH occurred in 34% of patients. This combined endpoint was significantly less frequently observed in MR ≤ 1+ patients (Kaplan–Maier estimates: 29.7% vs. 69.6% for MR ≤ 1+ vs. MR  ≥ 2 +; p < 0.0001). New York Heart Association (NYHA) functional class improved significantly from baseline (NYHA ≤ II: 17%) to 1‐year follow‐up (NYHA ≤ II: 78%) (p < 0.0001). While MR reduction was comparable between NTR‐only vs. XTR‐only treated patients, less XTR clips were required for achieving MR reduction.ConclusionsUnder real‐world conditions, optimal sustained MR reduction to MR ≤ 1+ was achieved in a high percentage of patients with third‐generation MitraClip, which translated into symptomatic improvement and low event rates. These results appear to be comparable with recent randomized clinical trials.

Funder

Abbott Laboratories

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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