Mitral Annulus Calcium Score.


Journal

Circulation. Cardiovascular imaging
ISSN: 1942-0080
Titre abrégé: Circ Cardiovasc Imaging
Pays: United States
ID NLM: 101479935

Informations de publication

Date de publication:
12 2019
Historique:
entrez: 15 1 2019
pubmed: 15 1 2019
medline: 29 10 2019
Statut: ppublish

Résumé

The risk of conduction system abnormalities (CSA) after transcatheter aortic valve implantation remains high. We aimed to evaluate the impact of mitral annular calcium (MAC) score on the development of CSA after transcatheter aortic valve implantation. Consecutive patients (n=168), with severe AoV stenosis, without prior CSA, underwent computed tomography transcatheter AoV implantation followed by device implantation; CoreValve (n=72) and SAPIEN (n=96). MAC, AoV, and left ventricular outflow tract calcium (Ca++) scores were quantitated from noncontrast ECG-gated computed tomography using Agatston method. The primary end point was a combination of complete left bundle branch block or high-degree atrioventricular block. Logistic regression was used to analyze the predictive value of Ca++ scores of different locations. The primary end point was documented in 62% of the fourth quartile MAC score (>2700) patients as compared with 31% of the first quartile (<140); P=0.03. Logistic regression analysis documented MAC score as an independent predictor either of primary end point as a continuous variable (odds ratio: 1.02, 95% [CI]: 1.00 - 1.03, p = 0.021) or as quartile cutoffs, whereas Q4 was a strong and independent predictor (odds ratio: 3.69, 95% [CI]: 1.37 - 9.95, p = 0.010). MAC score was found to be an independent predictor of CSA in patients undergoing transcatheter aortic valve implantation without preexisting CSA. Therefore, the current study suggests that patients with high MAC score category (fourth MAC score quartile) should be considered at high risk for CSA, warranting closer monitoring. URL: https://www.clinicaltrials.gov. Unique identifier: NCT02023060.

Sections du résumé

BACKGROUND
The risk of conduction system abnormalities (CSA) after transcatheter aortic valve implantation remains high. We aimed to evaluate the impact of mitral annular calcium (MAC) score on the development of CSA after transcatheter aortic valve implantation.
METHODS
Consecutive patients (n=168), with severe AoV stenosis, without prior CSA, underwent computed tomography transcatheter AoV implantation followed by device implantation; CoreValve (n=72) and SAPIEN (n=96). MAC, AoV, and left ventricular outflow tract calcium (Ca++) scores were quantitated from noncontrast ECG-gated computed tomography using Agatston method. The primary end point was a combination of complete left bundle branch block or high-degree atrioventricular block. Logistic regression was used to analyze the predictive value of Ca++ scores of different locations.
RESULTS
The primary end point was documented in 62% of the fourth quartile MAC score (>2700) patients as compared with 31% of the first quartile (<140); P=0.03. Logistic regression analysis documented MAC score as an independent predictor either of primary end point as a continuous variable (odds ratio: 1.02, 95% [CI]: 1.00 - 1.03, p = 0.021) or as quartile cutoffs, whereas Q4 was a strong and independent predictor (odds ratio: 3.69, 95% [CI]: 1.37 - 9.95, p = 0.010).
CONCLUSIONS
MAC score was found to be an independent predictor of CSA in patients undergoing transcatheter aortic valve implantation without preexisting CSA. Therefore, the current study suggests that patients with high MAC score category (fourth MAC score quartile) should be considered at high risk for CSA, warranting closer monitoring.
CLINICAL TRIAL REGISTRATION
URL: https://www.clinicaltrials.gov. Unique identifier: NCT02023060.

Identifiants

pubmed: 30636515
doi: 10.1161/CIRCIMAGING.117.007508
doi:

Banques de données

ClinicalTrials.gov
['NCT02023060']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e007508

Commentaires et corrections

Type : CommentIn

Auteurs

Yafim Brodov (Y)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.
Department of Diagnostic Imaging (Y.B., E.K., M.D.S., D.S.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Eli Konen (E)

Department of Diagnostic Imaging (Y.B., E.K., M.D.S., D.S.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Mattia Di Segni (M)

Department of Diagnostic Imaging (Y.B., E.K., M.D.S., D.S.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

David Samoocha (D)

Department of Diagnostic Imaging (Y.B., E.K., M.D.S., D.S.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Fernando Chernomordik (F)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Israel Barbash (I)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Ehud Regev (E)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Ehud Raanani (E)

Department of Cardiac Surgery (E. Raanani), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Victor Guetta (V)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Amit Segev (A)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Paul Fefer (P)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

Michael Glikson (M)

Leviev Heart Center (Y.B., F.C., I.B., E.R., V.G., A.S., P.F., M.G.), Sheba Medical Center, Tel Hashomer, Tel-Aviv University, Israel.

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Classifications MeSH