Five-year outcomes of transcatheter reduction of significant mitral regurgitation in high-surgical-risk patients

Saibal Kar(Cedars-Sinai Medical Center), Ted Feldman(NorthShore University HealthSystem), Atif Qasim(University of California, San Francisco), Alfredo Trento(Cedars-Sinai Medical Center), Samir Kapadia(Cleveland Clinic), Wesley Pedersen(Minneapolis Heart Institute Foundation), D. Scott Lim(University of Virginia), Robert Kipperman(Oklahoma Heart Hospital), Richard W. Smalling(Memorial Hermann), Tanvir Bajwa(Aurora St. Luke's Medical Center), H Hermann(University of Pennsylvania), James Hermiller(St. Vincent Hospital), John M. Lasala(Washington University in St. Louis), Mark Reisman(University of Washington Medical Center), Donald D. Glower(Duke Medical Center), Laura Mauri(Brigham and Women's Hospital), Patrick L. Whitlow(Cleveland Clinic)
Heart
August 4, 2018
Cited by 65

Abstract

OBJECTIVES: This study evaluates the 5-year clinical outcomes of transcatheter mitral valve (MV) repair with the MitraClip device in patients at high risk for MV surgery treated in the Endovascular Valve Edge-to-Edge Repair (EVEREST) II High Risk Study (HRS). METHODS: Patients with mitral regurgitation (MR) 3+ or 4+ and predicted surgical mortality risk ≥12% or surgeon assessment based on prespecified high-risk factors were enrolled. Patients prospectively consented to 5 years of follow-up. RESULTS: At 5 years, clinical follow-up was achieved in 90% of 78 enrolled patients. The rate of postprocedural adverse events declined from 30 days to 1 year follow-up and was stable thereafter through 5 years. Two patients (2.6%) developed mitral stenosis (MS). Two patients underwent MV surgery, including one due to MS. A total of 42 deaths were reported through 5 years. Effectiveness measures at 5 years showed reductions in MR severity to ≤2+ in 75% of patients (p=0.0107), left ventricular (LV) end-diastolic volume (-38.2 mL; 95% CI -55.0 to -21.4; p<0.0001) and LV end-systolic volume (-14.6 mL; 95% CI -27.7 to -1.5; p=0.0303) compared with baseline. The New York Heart Association (NYHA) functional class improved from baseline to 5 years (p<0.005), and septal-lateral annular dimensions remained stable with no indication of mitral annular dilation through 5 years. CONCLUSIONS: The EVEREST II HRS demonstrated long-term safety and efficacy of MitraClip in high-surgical-risk patients through 5 years. The observed mortality was most likely a consequence of the advanced age and comorbidity profile of the enrolled patients, while improvements in NYHA class in surviving patients were durable through long-term follow-up. TRIAL REGISTRATION NUMBER: NCT01940120.


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