Infective endocarditis follows a structural vulnerability gradient (prosthetic > aortic > mitral > tricuspid > pulmonary) where anatomical determinants drive surgical complexity and outcomes.
A proposed valve-specific structural vulnerability framework for infective endocarditis highlights that anatomical determinants drive surgical complexity and clinical prognosis, with prosthetic and aortic valves being the most vulnerable.
Abstract Background Infective endocarditis (IE) carries in-hospital mortality of 15–20% and 1-year mortality approaching 40%, with surgery required in 40–50% of cases. IE is not uniformly distributed across cardiac valves aortic 30–45%, mitral 25–30%, tricuspid 5–10%, pulmonary aortic > mitral > tricuspid > pulmonary) is proposed as a conceptual model of valve-specific disease behaviour. Aortic IE carries maximal vulnerability through peri-annular extension, 30–40% of cases, requiring radical root reconstruction with elevated operative mortality. Mitral IE exhibits conditional vulnerability; repair yields superior outcomes over replacement. Tricuspid IE is predominantly IVDU-associated with comparatively lower operative mortality. PVE carries the highest operative risk, with prolonged operative times and significant reoperation rates. Conclusions IE is best understood as a valve- and substrate-specific disease in which anatomical determinants drive surgical complexity and clinical prognosis. This proposed vulnerability hierarchy may enable preoperative risk stratification, inform valve-specific surgical planning, and provide a mechanistic framework for understanding differential outcomes across valve types. Prospective outcome registries and standardised complexity metrics are needed to validate and refine this conceptual model.
Rani et al. (Fri,) conducted a review in Infective endocarditis. Cardiac valve surgery was evaluated on Surgical complexity, perioperative outcomes, and re-surgery risk across cardiac valve types. Infective endocarditis follows a structural vulnerability gradient (prosthetic > aortic > mitral > tricuspid > pulmonary) where anatomical determinants drive surgical complexity and outcomes.