Thirty-Day Outcomes of Transcatheter Mitral Valve Replacement for Degenerated Mitral Bioprostheses (Valve-in-Valve), Failed Surgical Rings (Valve-in-Ring), and Native Valve With Severe Mitral Annular Calcification (Valve-in-Mitral Annular Calcification) in the United States: Data From the Society of Thoracic Surgeons/American College of Cardiology/Transcatheter Valve Therapy Registry.


Journal

Circulation. Cardiovascular interventions
ISSN: 1941-7632
Titre abrégé: Circ Cardiovasc Interv
Pays: United States
ID NLM: 101499602

Informations de publication

Date de publication:
03 2020
Historique:
entrez: 7 3 2020
pubmed: 7 3 2020
medline: 11 11 2020
Statut: ppublish

Résumé

Transcatheter mitral valve replacement using aortic transcatheter heart valves has recently become an alternative for patients with degenerated mitral bioprostheses, failed surgical repairs with annuloplasty rings or severe mitral annular calcification who are poor surgical candidates. Outcomes of these procedures are collected in the Society of Thoracic Surgeons/American College of Cardiology/Transcatheter Valve Therapy Registry. A comprehensive analysis of mitral valve-in-valve (MViV), mitral valve-in-ring (MViR), and valve-in-mitral annular calcification (ViMAC) outcomes has not been performed. We sought to evaluate short-term outcomes of early experience with MViV, MViR, and ViMAC in the United States. Retrospective analysis of data from the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry. Nine hundred three high-risk patients (median Society of Thoracic Surgeons score 10%) underwent MViV (n=680), MViR (n=123), or ViMAC (n=100) between March 2013 and June 2017 at 172 hospitals. Median age was 75 years, 59.2% female. Technical and procedural success were higher in MViV. Left ventricular outflow tract obstruction occurred more frequently with ViMAC (ViMAC=10%, MViR=4.9%, MViV=0.7%; MViV using aortic balloon-expandable transcatheter heart valves is associated with a low complication rate, a 30-day mortality lower than predicted by the Society of Thoracic Surgeons score, and superior short-term outcomes than MViR and ViMAC. At 30 days, patients in all groups experienced improvement of symptoms, and valve performance remained stable. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02245763.

Sections du résumé

BACKGROUND
Transcatheter mitral valve replacement using aortic transcatheter heart valves has recently become an alternative for patients with degenerated mitral bioprostheses, failed surgical repairs with annuloplasty rings or severe mitral annular calcification who are poor surgical candidates. Outcomes of these procedures are collected in the Society of Thoracic Surgeons/American College of Cardiology/Transcatheter Valve Therapy Registry. A comprehensive analysis of mitral valve-in-valve (MViV), mitral valve-in-ring (MViR), and valve-in-mitral annular calcification (ViMAC) outcomes has not been performed. We sought to evaluate short-term outcomes of early experience with MViV, MViR, and ViMAC in the United States.
METHODS
Retrospective analysis of data from the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry.
RESULTS
Nine hundred three high-risk patients (median Society of Thoracic Surgeons score 10%) underwent MViV (n=680), MViR (n=123), or ViMAC (n=100) between March 2013 and June 2017 at 172 hospitals. Median age was 75 years, 59.2% female. Technical and procedural success were higher in MViV. Left ventricular outflow tract obstruction occurred more frequently with ViMAC (ViMAC=10%, MViR=4.9%, MViV=0.7%;
CONCLUSIONS
MViV using aortic balloon-expandable transcatheter heart valves is associated with a low complication rate, a 30-day mortality lower than predicted by the Society of Thoracic Surgeons score, and superior short-term outcomes than MViR and ViMAC. At 30 days, patients in all groups experienced improvement of symptoms, and valve performance remained stable. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02245763.

Identifiants

pubmed: 32138529
doi: 10.1161/CIRCINTERVENTIONS.119.008425
doi:

Banques de données

ClinicalTrials.gov
['NCT02245763', 'NCT02245763']

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e008425

Commentaires et corrections

Type : CommentIn

Auteurs

Mayra Guerrero (M)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, MN (M.G., M.E., A.K.C., G.S., D.H., C.R.).

Sreekanth Vemulapalli (S)

Duke Clinical Research Institute, Durham, NC (S.V., Q.X.).

Qun Xiang (Q)

Duke Clinical Research Institute, Durham, NC (S.V., Q.X.).

Dee Dee Wang (DD)

Center for Structural Heart Disease, Henry Ford Hospital (D.D.W., W.O.).

Mackram Eleid (M)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, MN (M.G., M.E., A.K.C., G.S., D.H., C.R.).

Allison K Cabalka (AK)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, MN (M.G., M.E., A.K.C., G.S., D.H., C.R.).

Gurpreet Sandhu (G)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, MN (M.G., M.E., A.K.C., G.S., D.H., C.R.).

Michael Salinger (M)

Division of Cardiology, Froedtert Medical College of Wisconsin, Milwaukee (M.S.).

Hyde Russell (H)

Division of Cardiovascular Surgery (H.R.), NorthShore University Health System, Evanston, IL.

Adam Greenbaum (A)

Structural Heart and Valve Center, Emory University, Atlanta, GA (A.G., V.B.).

Susheel Kodali (S)

Division of Cardiology (S.K., M.L.).

Isaac George (I)

Department of Surgery, Columbia University Medical Center, New York (I.G., V.B.).

Danny Dvir (D)

Division of Cardiology, University of Washington Medical Center, Seattle (D.D.).

Brian Whisenant (B)

Division of Cardiology, Intermountain Heart Institute, Salt Lake City, UT (B.W.).

Mark J Russo (MJ)

Department of Surgery, Rutgers Robert Wood Johnson Medical School in New Brunswick, NJ (M.J.R.).

Ashish Pershad (A)

Division of Cardiology (A.P.), Banner University Medical Center, Phoenix, AZ.

Kenith Fang (K)

Department of Surgery (K.F.), Banner University Medical Center, Phoenix, AZ.

Megan Coylewright (M)

Division of Cardiology, Dartmouth-Hitchcock Medical Center, Lebanon, NH (M.C.).

Pinak Shah (P)

Division of Cardiology, Brigham and Women's Hospital, Brighton, MA (P.S.).

Vasilis Babaliaros (V)

Structural Heart and Valve Center, Emory University, Atlanta, GA (A.G., V.B.).

Jaffar M Khan (JM)

Cardiovascular and Pulmonary Branch, Division of Intramural Research, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD (J.M.K.).

Carl Tommaso (C)

Division of Cardiology (C.T., T.F.), NorthShore University Health System, Evanston, IL.

Saibal Kar (S)

Division of Cardiology, Cedar's Sinai Medical Center, Los Angeles, CA (S.K., R.M.).

Rajj Makkar (R)

Division of Cardiology, Cedar's Sinai Medical Center, Los Angeles, CA (S.K., R.M.).

Michael Mack (M)

Department of Surgery, Heart Hospital Baylor Plano, Baylor Healthcare System, TX (M.M.).

David Holmes (D)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, MN (M.G., M.E., A.K.C., G.S., D.H., C.R.).

Martin Leon (M)

Division of Cardiology (S.K., M.L.).

Vinayak Bapat (V)

Department of Surgery, Columbia University Medical Center, New York (I.G., V.B.).

Vinod H Thourani (VH)

Department of Cardiovascular Surgery, Marcus Valve Center, Piedmont Heart Institute, Atlanta, GA (V. H.T.).

Charanjit Rihal (C)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, MN (M.G., M.E., A.K.C., G.S., D.H., C.R.).

William O'Neill (W)

Center for Structural Heart Disease, Henry Ford Hospital (D.D.W., W.O.).

Ted Feldman (T)

Division of Cardiology (C.T., T.F.), NorthShore University Health System, Evanston, IL.

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Classifications MeSH