Cardiac Disease Burden and Risk of Mortality in Hospitalized Muscular Dystrophy Patients
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Updated: Mar 19, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
Published on: January 12, 2019
Ann R Punnoose1,2, Jonathan R Kaltman3, William Pastor4
1Division of Cardiology, Lurie Children's Hospital of Chicago, 225 E Chicago Avenue, Chicago, IL, 60611, USA. apunnoose@chw.org.
Insights
Cardiac disease, including heart failure and ventricular tachycardia, significantly increases the risk of death in males with muscular dystrophy (MD). These conditions also lead to longer hospital stays and higher costs for MD patients.
Area of Science:
- Cardiology
- Neuromuscular Disorders
Background:
- Improved management of extra-cardiac issues in muscular dystrophy (MD) increases the likelihood of cardiac complications in affected males.
- The specific impact of cardiomyopathy/heart failure (HF) and ventricular tachycardia (VT) on hospitalization and in-hospital mortality in MD patients remains unclear.
Purpose of the Study:
- To investigate the association between cardiac disease (cardiomyopathy/HF, VT) and in-hospital mortality or cardiac arrest in male patients with MD.
- To compare hospital resource utilization (charges, length of stay) in MD patients with and without cardiac disease.
Main Methods:
- Analysis of inpatient admission data from the Pediatric Health Information System database (2003-2013).
- Inclusion of males aged 6 years and older with MD and cardiac disease diagnoses (cardiomyopathy/HF, VT).
- Logistic regression modeling to identify predictors of cardiac arrest or death; comparison of hospital charges and length of stay.
Main Results:
- Ventricular tachycardia (VT) and cardiomyopathy/heart failure (HF) were identified as significant risk factors for cardiac arrest or death in MD patients.
- Cardiac disease accounted for 58% of cardiac arrests or deaths in the analyzed MD patient cohort.
- MD patients with VT experienced significantly longer hospital stays and higher hospital charges compared to those without cardiac disease or with only cardiomyopathy/HF.
Conclusions:
- Cardiac disease represents a substantial burden for hospitalized patients with muscular dystrophy.
- Ventricular tachycardia and cardiomyopathy/heart failure are associated with a heightened risk of adverse cardiac events, including death, in MD patients.
Abstract:
As treatments of the extra-cardiac complications of muscular dystrophy (MD) improve, males with MD are more likely to develop cardiac disease. The impact of cardiomyopathy or heart failure (HF) and ventricular tachycardia (VT) on hospitalizations and in hospital mortality are not known. We performed an analysis of inpatient admission data for patients with MD using the Pediatric Health Information System database. We selected males who were 6 years or older with diagnosis codes of MD and cardiac disease including cardiomyopathy/HF and VT between 2003 and 2013. We created a logistic regression model to identify predictors of subsequent cardiac arrest or death in MD patients. We also compared hospital charges, lengths of stay and ages among MD patients with or without cardiac disease. Our logistic regression model showed that VT (OR 5.41, 95 % CI 2.83, 10.34) and cardiomyopathy/HF (OR 1.79, 95 % CI 1.05, 3.04) were risk factors for cardiac arrest or death. Of the 84 cardiac arrests or deaths in 3363 MD patients, 49 (58 %) were related to cardiac disease. Nineteen (39 %) of these events occurred in MD patients with VT. The mean hospital charges and the mean length of stay were greater and longer in MD patients with VT compared to those without cardiac disease and those with only cardiomyopathy/HF (p < 0.05). Cardiac disease is a significant burden in hospitalized MD patients. Our results suggest that VT and cardiomyopathy/HF are associated with an increased risk of cardiac arrest or death in MD patients.
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