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Published on: August 1, 2018
Cirrhotic Cardiomyopathy After Transplantation: Neither the Transient Nor Innocent Bystander
Manhal Izzy1, Jae Oh2, Kymberly D Watt1
1Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.
Insights
Cirrhotic cardiomyopathy in end-stage liver disease shows limited evidence of reversal after liver transplantation (LT). Updated diagnostic criteria are needed to better evaluate post-LT outcomes and risks.
Area of Science:
- Cardiology
- Hepatology
- Transplantation Medicine
Background:
- Cirrhotic cardiomyopathy (CC) is defined by impaired cardiac function in end-stage liver disease without other cardiac causes.
- Established in 2005, CC diagnostic criteria have been extensively studied regarding pathophysiology and pre-transplant course.
- Post-transplant data on CC are limited, necessitating a review of its impact after liver transplantation (LT).
Purpose of the Study:
- To review the post-transplant course and prognosis of cirrhotic cardiomyopathy elements following liver transplantation.
- To assess the reversibility of CC after LT.
- To highlight the need for updated diagnostic criteria for CC.
Main Methods:
- Literature review focusing on studies examining cirrhotic cardiomyopathy post-liver transplantation.
- Analysis of existing data on the pathophysiology and clinical course of CC.
- Evaluation of echocardiographic advancements in assessing cardiac dysfunction.
Main Results:
- Limited evidence suggests CC is not readily reversible after LT.
- CC may elevate the risk of post-transplant complications.
- Significant advancements in echocardiography warrant refinement of CC diagnostic criteria.
Conclusions:
- The reversibility of cirrhotic cardiomyopathy after liver transplantation remains poorly demonstrated.
- Updated diagnostic criteria for CC are crucial for accurate assessment of post-transplant outcomes.
- Refined criteria will improve the evaluation of CC-related risks and complications in liver transplant recipients.
Abstract:
Cirrhotic cardiomyopathy in end-stage liver disease is currently characterized by blunted contractile systolic response to stress with or without diastolic dysfunction in the absence of known heart disease. Since the establishment of the diagnostic criteria of cirrhotic cardiomyopathy in 2005, there have been multiple studies regarding its pathophysiology and pretransplant clinical course. The data regarding the post-transplant course of this entity are sparse. This review addresses the course and prognosis of the elements of cirrhotic cardiomyopathy after liver transplantation (LT). To this end, there is limited compelling evidence demonstrating the reversibility of this entity post-LT. Cirrhotic cardiomyopathy may, in fact, increase the risk of post-transplant complications. This review reveals a need to refine the diagnostic criteria of cirrhotic cardiomyopathy in view of the remarkable progress in the sphere of echocardiographic evaluation of systolic and diastolic dysfunction. The post-transplant course and outcomes related to cirrhotic cardiomyopathy may be better evaluated in the setting of updated diagnostic criteria.
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