TY - JOUR
T1 - Acute and 12-month results with catheter-based mitral valve leaflet repair
T2 - The EVEREST II (Endovascular Valve Edge-to-Edge Repair) High Risk Study
AU - Whitlow, Patrick L.
AU - Feldman, Ted
AU - Pedersen, Wes R.
AU - Lim, D. Scott
AU - Kipperman, Robert
AU - Smalling, Richard
AU - Bajwa, Tanvir
AU - Herrmann, Howard C.
AU - Lasala, John
AU - Maddux, James T.
AU - Tuzcu, Murat
AU - Kapadia, Samir
AU - Trento, Alfredo
AU - Siegel, Robert J.
AU - Foster, Elyse
AU - Glower, Donald
AU - Mauri, Laura
AU - Kar, Saibal
N1 - Funding Information:
The study is sponsored by Abbott Vascular (formerly Evalve Inc.) All authors received research support from Abbott Vascular for enrolling patients in the EVEREST trials. Dr. Feldman is a consultant for and has received research grants from Abbott Vascular , Boston Scientific , and Edwards Lifesciences . Dr. Kipperman is a consultant for Cardiokinetix. Dr. Lim is a consultant for Abbott Vascular. Dr. Smalling has received a research grant from E-Valve Co. Dr. Herrmann has received research funding from Edwards LifeSciences; is a consultant for Micro-Interventional Devices Inc. and St. Jude Medical; and has equity in Micro-Interventional Inc. Dr. Siegel is on the Speaker's Bureau of Philips Ultrasound; and is a consultant for Abbott Vascular and Edwards LifeSciences. Dr. Foster has received grant support from Boston Scientific and GD Systems ; and is a consultant for Maquet Actelion. Dr. Glower has received research grants from Edwards LifeSciences and St. Jude Medical. Dr. Mauri is a consultant for Abbott Vascular, Cordis, and Medtronic; and her institution has received grant support from Abbott Vascular , Cordis , Medtronic , Boston Scientific , Eli Lilly , Daiichi Sankyo , Bristol-Myers Squibb , and Sanofi-Aventis . Dr. Kar is a consultant for Abbott Vascular, Medtronic, QuantumCor, and Guided Delivery Systems.
PY - 2012/1/10
Y1 - 2012/1/10
N2 - Objectives: The EVEREST II (Endovascular Valve Edge-to-Edge Repair) High Risk Study (HRS) assessed the safety and effectiveness of the MitraClip device (Abbott Vascular, Santa Clara, California) in patients with significant mitral regurgitation (MR) at high risk of surgical mortality rate. Background: Patients with severe MR (3 to 4+) at high risk of surgery may benefit from percutaneous mitral leaflet repair, a potentially safer approach to reduce MR. Methods: Patients with severe symptomatic MR and an estimated surgical mortality rate of ≥12% were enrolled. A comparator group of patients screened concurrently but not enrolled were identified retrospectively and consented to compare survival in patients treated by standard care. Results: Seventy-eight patients underwent the MitraClip procedure. Their mean age was 77 years, >50% had previous cardiac surgery, and 46 had functional MR and 32 degenerative MR. MitraClip devices were successfully placed in 96% of patients. Protocol-predicted surgical mortality rate in the HRS and concurrent comparator group was 18.2% and 17.4%, respectively, and Society of Thoracic Surgeons calculator estimated mortality rate was 14.2% and 14.9%, respectively. The 30-day procedure-related mortality rate was 7.7% in the HRS and 8.3% in the comparator group (p = NS). The 12-month survival rate was 76% in the HRS and 55% in the concurrent comparator group (p = 0.047). In surviving patients with matched baseline and 12-month data, 78% had an MR grade of ≤2+. Left ventricular end-diastolic volume improved from 172 ml to 140 ml and end-systolic volume improved from 82 ml to 73 ml (both p = 0.001). New York Heart Association functional class improved from III/IV at baseline in 89% to class I/II in 74% (p < 0.0001). Quality of life was improved (Short Form-36 physical component score increased from 32.1 to 36.1 [p = 0.014] and the mental component score from 45.5 to 48.7 [p = 0.065]) at 12 months. The annual rate of hospitalization for congestive heart failure in surviving patients with matched data decreased from 0.59 to 0.32 (p = 0.034). Conclusions: The MitraClip device reduced MR in a majority of patients deemed at high risk of surgery, resulting in improvement in clinical symptoms and significant left ventricular reverse remodeling over 12 months. (Pivotal Study of a Percutaneous Mitral Valve Repair System [EVEREST II]; NCT00209274).
AB - Objectives: The EVEREST II (Endovascular Valve Edge-to-Edge Repair) High Risk Study (HRS) assessed the safety and effectiveness of the MitraClip device (Abbott Vascular, Santa Clara, California) in patients with significant mitral regurgitation (MR) at high risk of surgical mortality rate. Background: Patients with severe MR (3 to 4+) at high risk of surgery may benefit from percutaneous mitral leaflet repair, a potentially safer approach to reduce MR. Methods: Patients with severe symptomatic MR and an estimated surgical mortality rate of ≥12% were enrolled. A comparator group of patients screened concurrently but not enrolled were identified retrospectively and consented to compare survival in patients treated by standard care. Results: Seventy-eight patients underwent the MitraClip procedure. Their mean age was 77 years, >50% had previous cardiac surgery, and 46 had functional MR and 32 degenerative MR. MitraClip devices were successfully placed in 96% of patients. Protocol-predicted surgical mortality rate in the HRS and concurrent comparator group was 18.2% and 17.4%, respectively, and Society of Thoracic Surgeons calculator estimated mortality rate was 14.2% and 14.9%, respectively. The 30-day procedure-related mortality rate was 7.7% in the HRS and 8.3% in the comparator group (p = NS). The 12-month survival rate was 76% in the HRS and 55% in the concurrent comparator group (p = 0.047). In surviving patients with matched baseline and 12-month data, 78% had an MR grade of ≤2+. Left ventricular end-diastolic volume improved from 172 ml to 140 ml and end-systolic volume improved from 82 ml to 73 ml (both p = 0.001). New York Heart Association functional class improved from III/IV at baseline in 89% to class I/II in 74% (p < 0.0001). Quality of life was improved (Short Form-36 physical component score increased from 32.1 to 36.1 [p = 0.014] and the mental component score from 45.5 to 48.7 [p = 0.065]) at 12 months. The annual rate of hospitalization for congestive heart failure in surviving patients with matched data decreased from 0.59 to 0.32 (p = 0.034). Conclusions: The MitraClip device reduced MR in a majority of patients deemed at high risk of surgery, resulting in improvement in clinical symptoms and significant left ventricular reverse remodeling over 12 months. (Pivotal Study of a Percutaneous Mitral Valve Repair System [EVEREST II]; NCT00209274).
KW - high surgical risk
KW - mitral valve insufficiency
KW - percutaneous
UR - http://www.scopus.com/inward/record.url?scp=84855383997&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2011.08.067
DO - 10.1016/j.jacc.2011.08.067
M3 - Article
C2 - 22222076
AN - SCOPUS:84855383997
SN - 0735-1097
VL - 59
SP - 130
EP - 139
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 2
ER -