The prevalence of cirrhotic cardiomyopathy according to different diagnostic criteria

Marcel Razpotnik1, Simona Bota1, Philipp Wimmer2

  • 1Department of Internal Medicine and Gastroenterology (IMuG), Hepatology, Endocrinology, Rheumatology, Nephrology and Emergency Medicine (ZAE), Klinikum Klagenfurt am Wörthersee, Klagenfurt, Austria.

Insights

Cirrhotic cardiomyopathy affects about 60% of patients. The 2019 Cirrhotic Cardiomyopathy Consortium (CCC) criteria identify more cases of systolic dysfunction in cirrhosis compared to older guidelines.

Area of Science:

  • Cardiology
  • Hepatology
  • Medical Diagnostics

Background:

  • Cirrhotic cardiomyopathy (CC) is a complex condition affecting cardiac function in patients with liver cirrhosis.
  • Recent diagnostic criteria, such as the 2019 Cirrhotic Cardiomyopathy Consortium (CCC) guidelines, have updated thresholds for systolic dysfunction and incorporated advanced imaging techniques.
  • Discrepancies exist between various diagnostic criteria, necessitating an evaluation of their prevalence in cirrhotic populations.

Purpose of the Study:

  • To assess and compare the prevalence of cirrhotic cardiomyopathy using different diagnostic criteria.
  • To evaluate the impact of the 2019 CCC criteria on the diagnosis of systolic and diastolic dysfunction in cirrhotic patients.

Main Methods:

  • The study enrolled 122 cirrhotic patients meeting specific inclusion criteria, excluding those with other cardiac conditions or complications.
  • Speckle-tracking echocardiography was performed by certified investigators.
  • Prevalence of CC was determined using the 2005 Montreal recommendations, 2009 ASE/EACVI guidelines, and 2019 CCC criteria.

Main Results:

  • The overall prevalence of CC was similar between the 2005 Montreal (67.2%) and 2019 CCC (55.7%) criteria.
  • However, CC prevalence was significantly higher with both sets of criteria compared to the 2009 ASE/EACVI guidelines (35.2%).
  • The 2019 CCC criteria identified a significantly higher prevalence of systolic dysfunction (53.3%) compared to the 2005 Montreal (16.4%) and 2009 ASE/EACVI (4.9%) criteria.

Conclusions:

  • Cirrhotic cardiomyopathy is highly prevalent, affecting approximately 60% of patients when assessed by hepatological criteria.
  • The 2019 CCC criteria reveal a substantially higher prevalence of systolic dysfunction in cirrhotic patients.
  • Further longitudinal studies are required to validate the prognostic significance of these updated diagnostic criteria for cirrhotic cardiomyopathy.
Abstract

Related Concept Videos

Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
249
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
232
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
164
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
177
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
127
Myocarditis II: Clinical Features and Diagnostic Tests01:27

Myocarditis II: Clinical Features and Diagnostic Tests

Myocarditis is an inflammation of the heart muscle. The symptoms vary widely, encompassing asymptomatic presentations to severe, acute manifestations.Clinical PresentationAsymptomatic cases: In some instances, myocarditis may be asymptomatic, with the infection resolving without intervention. These cases often go undetected unless discovered incidentally through diagnostic imaging or tests conducted for other reasons.General Early Symptoms: Early symptoms of myocarditis are non-specific and can...
109