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Cirrhotic cardiomyopathy in children: A comprehensive assessment using ECG, echocardiography, and NT-Pro-BNP
Ataollahi Maryam1, Amir Naghshzan2, Haghighat Mahmood3
1Shiraz Transplant Center, Abu-Ali Sina Hospital, Shiraz University of Medical Science, Shiraz, Iran; Gastroenterohepatology Research Center, Nemazee Teaching Hospital, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Insights
Cirrhotic cardiomyopathy (CCMP) affects over 30% of children with portal hypertension, often silently. Elevated PELD/MELD scores and ascites are key predictors, necessitating routine cardiac screening in pediatric liver disease patients.
Area of Science:
- Pediatric Cardiology
- Hepatology
- Clinical Medicine
Background:
- Cirrhotic cardiomyopathy (CCMP) is a cardiac dysfunction associated with cirrhosis.
- Portal hypertension (PHTN) is a common complication in children with liver disease.
- Early identification of CCMP in pediatric patients is crucial for management and prognosis.
Purpose of the Study:
- To determine the prevalence and diagnostic criteria of CCMP in pediatric patients with PHTN.
- To identify predictive factors for CCMP in this population.
- To evaluate the utility of ECG, echocardiography, and NT-proBNP in diagnosing CCMP.
Main Methods:
- A cross-sectional study involving 54 children with PHTN (45 with cirrhosis) and 54 healthy controls.
- Participants underwent ECG, echocardiography, and NT-proBNP testing.
- Logistic regression analysis was used to identify CCMP predictors, including PELD/MELD and Child-Pugh scores.
Main Results:
- CCMP was present in 31.1% of cirrhotic children, with both symptomatic and silent cases.
- Ascites and higher PELD/MELD scores were significantly associated with CCMP.
- QTc prolongation and reduced ejection fraction were key diagnostic findings; PELD/MELD score was a significant predictor (OR 1.19, p=0.01).
Conclusions:
- CCMP is a prevalent complication in pediatric cirrhosis with PHTN, often asymptomatic.
- Elevated PELD/MELD scores and ascites are significant predictive factors for CCMP.
- Routine cardiac evaluation is recommended for early detection and risk stratification in children with PHTN.
Objective:
To evaluate the prevalence, diagnostic criteria, and predictive factors of cirrhotic cardiomyopathy (CCMP) in pediatric patients with portal hypertension (PHTN), using electrocardiography (ECG), echocardiography, and NT-proBNP levels.
Methods:
This cross-sectional study included 54 children with portal hypertension (45 with cirrhosis and 9 without), and 54 age- and sex-matched healthy controls. All participants underwent ECG, echocardiography, and NT-proBNP testing. CCMP was diagnosed based on the Møller-Henriksen criteria. Demographic, clinical, and laboratory variables, including PELD/MELD and Child-Pugh scores, were analyzed. Logistic regression was used to identify predictors of CCMP.
Results:
CCMP was identified in 14 cirrhotic patients (31.1 %), with 9 symptomatic and 5 silent cases. No cases were observed among non-cirrhotic patients or controls. The presence of ascites and higher PELD/MELD scores were significantly associated with CCMP. QTc prolongation and reduced ejection fraction were key diagnostic findings. Systolic dysfunction was present in 3 patients, and 4 patients with CCMP died before or shortly after liver transplantation. Multivariate analysis confirmed PELD/MELD score as a significant predictor of CCMP (OR 1.19; 95 % CI 1.038-1.367; p=0.01).
Conclusion:
Cirrhotic cardiomyopathy is a prevalent but often silent complication in children with cirrhosis and PHTN. Elevated PELD/MELD scores and the presence of ascites are important predictive factors. Routine cardiac evaluation using ECG, echocardiography, and biomarkers like NT-proBNP is recommended for early detection and risk stratification in this population.
Main Points:
Cirrhotic cardiomyopathy (CCMP) is an uncommon yet serious condition in children with liver disease. Current diagnostic criteria require reassessment for pediatric use, particularly considering regional genetic and environmental differences.
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