The Impact of Mitral Disease Etiology on Operative Mortality After Mitral Valve Operations.

Published

Journal Article

BACKGROUND: The pathoetiology of mitral regurgitation (MR) has been suggested as a mediator of outcomes after mitral valve (MV) operations, particularly in ischemic functional mitral regurgitation (IMR). This study examined the independent association of MV etiology with mortality. METHODS: The Society of Thoracic Surgeons Database was utilized to assess all patients undergoing MV replacement or repair from 2011 to 2014. Patients who underwent concomitant surgical ablation, septal defect closure, tricuspid valve repair, or coronary artery bypass grafting were included. All other concomitant operations were excluded, producing a final cohort of 89,085 patients. A hierarchical etiology decision tree was developed to categorize the population into eight etiology groups: endocarditis, reoperation, acute IMR, rheumatic, uncommon etiologies (hypertrophic obstructive cardiomyopathy, trauma, tumor, or congenital), degenerative primary MR, chronic IMR, and pure annular dilatation. The statistical association of etiology with unadjusted and risk-adjusted operative mortality was evaluated by logistic regression and supplemented by sensitivity analyses using established risk models. RESULTS: The decision tree showed that etiology categories appeared clinically aligned with published population distributions, baseline characteristics, and unadjusted outcomes. Unadjusted operative mortality ranged from 1.2% for degenerative MV repair to 15.1% for MV replacement in acute IMR. After risk adjustment, MV etiologies per se exhibited insignificant independent associations with risk-adjusted operative mortality. CONCLUSIONS: Mortality after mitral operations is determined primarily by standard clinical risk factors. Mitral etiology does not appear to add independent predictive value.

Full Text

Duke Authors

Cited Authors

  • Rankin, JS; Grau-Sepulveda, M; Shahian, DM; Gillinov, AM; Suri, R; Gammie, JS; Bolling, SF; McCarthy, PM; Thourani, VH; Ad, N; O'Brien, SM; Jacobs, JP; Badhwar, V

Published Date

  • November 2018

Published In

Volume / Issue

  • 106 / 5

Start / End Page

  • 1406 - 1413

PubMed ID

  • 29777670

Pubmed Central ID

  • 29777670

Electronic International Standard Serial Number (EISSN)

  • 1552-6259

Digital Object Identifier (DOI)

  • 10.1016/j.athoracsur.2018.04.053

Language

  • eng

Conference Location

  • Netherlands