Cardiac dysfunction in patients with cirrhosis and acute decompensation

Author:

Gananandan Kohilan1ORCID,Wiese Signe23,Møller Søren24ORCID,Mookerjee Rajeshwar P.15ORCID

Affiliation:

1. Liver Failure Group Institute for Liver and Digestive Health, University College London London UK

2. Centre of Functional Imaging and Research, Department of Clinical Physiology and Nuclear Medicine University of Copenhagen Copenhagen Denmark

3. Gastroenterology Unit, Medical Division, Faculty of Health Sciences University of Copenhagen Copenhagen Denmark

4. Department of Clinical Medicine, Faculty of Health Sciences University of Copenhagen Copenhagen Denmark

5. Department of Hepatology and Gastroenterology Aarhus University Hospital Aarhus Denmark

Abstract

AbstractThe prevalence of cirrhotic cardiomyopathy (CCM) has been reported as high as 60%–70% in patients with liver cirrhosis and is associated with various negative outcomes. There has been a growing understanding of CCM over recent years. Indeed, the development of imaging techniques has enabled new diagnostic criteria to be proposed by the Cirrhotic Cardiomyopathy Consortium. However, important unanswered questions remain over pathophysiological mechanisms, optimal diagnostic modalities and potential treatment options. While there has been an increasing volume of literature evaluating CCM, there is a lack of clarity on its implications in acute decompensation, acute‐on‐chronic liver failure and following interventions such as transjugular intrahepatic portosystemic shunt insertion and liver transplantation. This review aims to summarise the literature in these challenging domains and suggest where future research should focus. We conclude that systemic inflammation and structural myocardial changes are likely to be crucial in the pathophysiology of the disease, but the relative contribution of different components remains elusive. Furthermore, future studies need to use standardised diagnostic criteria for CCM as well as incorporate newer imaging techniques assessing both myocardial structure and function. Finally, while specific treatments are currently lacking, therapeutics targeting systemic inflammation, microbial dysbiosis and bacterial translocation are promising targets and warrant further research.

Publisher

Wiley

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