Aortic stenosis in cirrhosis: Pathophysiology and management in the context of liver transplantation
Author Department
Medicine
Document Type
Article, Peer-reviewed
Publication Date
12-2025
Abstract
Aortic stenosis (AS), a progressive disease affecting aortic valve function, is common among individuals with metabolic and degenerative conditions, and is notably challenging to manage in patients with cirrhosis. Patients with cirrhosis frequently experience exacerbated AS symptoms due to the hyperdynamic circulatory state induced by portal hypertension, which masks early AS signs, resulting in delayed diagnosis. The coexistence of AS and liver disease significantly complicates management, particularly for those awaiting liver transplantation (LT), where untreated AS can increase perioperative morbidity and mortality. This review examines the pathophysiology, clinical manifestations, and management of AS in cirrhotic patients, with a focus on implications for LT candidates. Available treatment options, including surgical aortic valve replacement and transcatheter aortic valve replacement (TAVR), are discussed, with TAVR emerging as a preferred approach due to favorable outcomes in high-risk patients. We also explore the potential role of TAVR as a bridge to LT, with case reports showing promising, albeit anecdotal, success in restoring LT candidacy. Limitations in current perioperative risk assessment tools, which inadequately address the unique risks faced by cirrhotic patients undergoing cardiac procedures, highlight the need for multi-disciplinary care and further research to improve outcomes of patients with concomitant end-stage liver disease and AS.
Keywords: Aortic stenosis; Aortic valve replacement; Cardio-hepatology; End stage liver disease; Liver transplant.
Recommended Citation
Osorio B, Fox SW, Cooper KM, Chandragiri S, Mohani AF, Devuni D. Aortic stenosis in cirrhosis: Pathophysiology and management in the context of liver transplantation. World J Transplant. 2025 Dec 18;15(4):102995. doi: 10.5500/wjt.v15.i4.102995.
PMID
41357369