A Cardiac Computed Tomography-Based Score to Categorize Mitral Annular Calcification Severity and Predict Valve Embolization.


Journal

JACC. Cardiovascular imaging
ISSN: 1876-7591
Titre abrégé: JACC Cardiovasc Imaging
Pays: United States
ID NLM: 101467978

Informations de publication

Date de publication:
09 2020
Historique:
received: 19 12 2019
revised: 02 03 2020
accepted: 06 03 2020
pubmed: 18 5 2020
medline: 13 8 2021
entrez: 18 5 2020
Statut: ppublish

Résumé

This study aims to establish a computed tomography (CT)-based scoring system for grading mitral annular calcification (MAC) severity and potentially aid in predicting valve embolization during transcatheter mitral valve (MV) replacement using balloon-expandable aortic transcatheter heart valves. Transcatheter MV replacement is emerging as an alternative treatment for patients with severe MAC who are not surgical candidates. Although cardiac CT is the imaging modality of choice in the evaluation of candidates for valve-in-MAC (ViMAC), a standardized grading system to quantify MAC severity has not been established. We performed a multicenter retrospective review of cardiac CT and clinical outcomes of patients undergoing ViMAC. A CT-based MAC score was created using the following features: average calcium thickness (mm), degrees of annulus circumference involved, calcification at one or both fibrous trigones, and calcification of one or both leaflets. Features were assigned points according to severity (total maximum score = 10) and severity grade was assigned based on total points (mild ≤3, moderate 4 to 6, and severe ≥7 points). The association between MAC score and device migration/embolization was evaluated. Of 117 patients in the TMVR in MAC registry, 87 had baseline cardiac CT of adequate quality. Of these, 15 were treated with transatrial access and were not included. The total cohort included 72 (trans-septal = 37, transapical = 35). Mean patient age was 74 ± 12 years, 66.7% were female, and the mean Society of Thoracic Surgery risk score was 15.4 ± 10.5%. The mean MAC score was 7.7 ± 1.4. Embolization/migration rates were lower in higher scores: Patients with a MAC score of 7 had valve embolization/migration rate of 12.5%, MAC score ≥8 had a rate of 8.7%, and a MAC score of ≥9 had zero (p = 0.023). Patients with a MAC score of ≤6 had 60% embolization/migration rate versus 9.7% in patients with a MAC score ≥7 (p < 0.001). In multivariable analysis, a MAC score ≤6 was in independent predictor of valve embolization/migration (odds ratio [OR]: 5.86 [95% CI: 1.00 to 34.26]; p = 0.049). This cardiac CT-based score provides a systematic method to grade MAC severity which may assist in predicting valve embolization/migration during trans-septal or transapical ViMAC procedures.

Sections du résumé

OBJECTIVES
This study aims to establish a computed tomography (CT)-based scoring system for grading mitral annular calcification (MAC) severity and potentially aid in predicting valve embolization during transcatheter mitral valve (MV) replacement using balloon-expandable aortic transcatheter heart valves.
BACKGROUND
Transcatheter MV replacement is emerging as an alternative treatment for patients with severe MAC who are not surgical candidates. Although cardiac CT is the imaging modality of choice in the evaluation of candidates for valve-in-MAC (ViMAC), a standardized grading system to quantify MAC severity has not been established.
METHODS
We performed a multicenter retrospective review of cardiac CT and clinical outcomes of patients undergoing ViMAC. A CT-based MAC score was created using the following features: average calcium thickness (mm), degrees of annulus circumference involved, calcification at one or both fibrous trigones, and calcification of one or both leaflets. Features were assigned points according to severity (total maximum score = 10) and severity grade was assigned based on total points (mild ≤3, moderate 4 to 6, and severe ≥7 points). The association between MAC score and device migration/embolization was evaluated.
RESULTS
Of 117 patients in the TMVR in MAC registry, 87 had baseline cardiac CT of adequate quality. Of these, 15 were treated with transatrial access and were not included. The total cohort included 72 (trans-septal = 37, transapical = 35). Mean patient age was 74 ± 12 years, 66.7% were female, and the mean Society of Thoracic Surgery risk score was 15.4 ± 10.5%. The mean MAC score was 7.7 ± 1.4. Embolization/migration rates were lower in higher scores: Patients with a MAC score of 7 had valve embolization/migration rate of 12.5%, MAC score ≥8 had a rate of 8.7%, and a MAC score of ≥9 had zero (p = 0.023). Patients with a MAC score of ≤6 had 60% embolization/migration rate versus 9.7% in patients with a MAC score ≥7 (p < 0.001). In multivariable analysis, a MAC score ≤6 was in independent predictor of valve embolization/migration (odds ratio [OR]: 5.86 [95% CI: 1.00 to 34.26]; p = 0.049).
CONCLUSIONS
This cardiac CT-based score provides a systematic method to grade MAC severity which may assist in predicting valve embolization/migration during trans-septal or transapical ViMAC procedures.

Identifiants

pubmed: 32417332
pii: S1936-878X(20)30308-9
doi: 10.1016/j.jcmg.2020.03.013
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1945-1957

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Auteurs

Mayra Guerrero (M)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, Minnesota. Electronic address: guerrero.mayra@mayo.edu.

Dee Dee Wang (DD)

Center for Structural Heart Disease, Henry Ford Hospital, Detroit, Michigan.

Amit Pursnani (A)

Division of Cardiology, NorthShore University HealthSystem, Evanston, Illinois.

Mackram Eleid (M)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, Minnesota.

Omar Khalique (O)

Division of Cardiology, Columbia University Medical Center, New York, New York.

Marina Urena (M)

Department of Cardiology, Bichat Hospital, Paris, France.

Michael Salinger (M)

Division of Cardiology, NorthShore University HealthSystem, Evanston, Illinois.

Susheel Kodali (S)

Division of Cardiology, Columbia University Medical Center, New York, New York.

Tatiana Kaptzan (T)

Cardiovascular Research Unit, Mayo Clinic Hospital, Rochester, Minnesota.

Bradley Lewis (B)

Department of Health Sciences Research, Mayo Clinic Hospital, Rochester, Minnesota.

Nahoko Kato (N)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, Minnesota.

Hector M Cajigas (HM)

University of Illinois College of Medicine, Chicago, Illinois.

Olaf Wendler (O)

Department of Surgery, King's College Hospital, London, United Kingdom.

David Holzhey (D)

Department of Cardiac Surgery, Leipzig Heart Center, Leipzig, Germany.

Ashish Pershad (A)

Division of Cardiology, Banner University Medical Center, Phoenix, Arizona.

Christian Witzke (C)

Division of Cardiology, Einstein Medical Center, Philadelphia, Pennsylvania.

Sami Alnasser (S)

Division of Cardiology, St. Michael's Hospital, Toronto, Ontario, Canada; Northern Ontario School of Medicine, Health Sciences North, Sudbury, Ontario.

Gilbert H L Tang (GHL)

Department of Cardiovascular Surgery, Mount Sinai Health System, New York, New York.

Kendra Grubb (K)

Division of Cardiothoracic Surgery, Emory University, Atlanta, Georgia.

Mark Reisman (M)

Division of Cardiology, University of Washington Medical Center, Seattle, Washington.

Philipp Blanke (P)

Center for Heart Valve Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.

Jonathon Leipsic (J)

Center for Heart Valve Innovation, St. Paul's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.

Eric Williamson (E)

Department of Radiology, Mayo Clinic Hospital, Rochester, Minnesota.

Patricia A Pellikka (PA)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, Minnesota.

Sorin Pislaru (S)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, Minnesota.

Juan Crestanello (J)

Department of Cardiac Surgery, Mayo Clinic Hospital, Rochester, Minnesota.

Dominique Himbert (D)

Department of Cardiology, Bichat Hospital, Paris, France.

Alec Vahanian (A)

Universite de Paris, Paris, France.

John Webb (J)

Division of Cardiology, University of Washington Medical Center, Seattle, Washington.

Rebecca T Hahn (RT)

Division of Cardiology, Columbia University Medical Center, New York, New York.

Martin Leon (M)

Division of Cardiology, Columbia University Medical Center, New York, New York.

Isaac George (I)

Division of Cardiothoracic Surgery, Columbia University Medical Center, New York, New York.

Vinayak Bapat (V)

Division of Cardiothoracic Surgery, Columbia University Medical Center, New York, New York.

William O'Neill (W)

Center for Structural Heart Disease, Henry Ford Hospital, Detroit, Michigan.

Charanjit Rihal (C)

Department of Cardiovascular Medicine, Mayo Clinic Hospital, Rochester, Minnesota.

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