Role of Cardiac Magnetic Resonance Imaging in Hypocalcemia-Induced Dilated Cardiomyopathy in Pediatric Population
Ankit Garg1, Sushil Azad1, Khemendra Kumar2
1Department of Pediatric Cardiology, Fortis Escorts Heart Institute, New Delhi, India.
Insights
Hypocalcemic dilated cardiomyopathy in children is reversible with prompt treatment. Cardiac MRI findings, specifically the absence of edema and late gadolinium enhancement, predict a favorable outcome.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Imaging
- Metabolic Disorders
Background:
- Hypocalcemia is a rare, reversible cause of pediatric dilated cardiomyopathy.
- Myocarditis presents similarly but is more common.
- Cardiac magnetic resonance imaging (CMRI) is crucial for evaluating cardiomyopathy.
Purpose of the Study:
- To identify specific Cardiac MRI (CMR) characteristics in hypocalcemic dilated cardiomyopathy.
- To correlate CMR findings with patient outcomes.
Main Methods:
- Retrospective analysis of 10 pediatric hypocalcemic dilated cardiomyopathy cases.
- CMRI analysis of 9 patients, categorized by edema and late gadolinium enhancement (LGE).
- Correlation of CMR categories with clinical outcomes and ejection fraction.
Main Results:
- Mean ejection fraction improved from 20.5% to 35.2% at discharge and 56.5% at follow-up.
- Absence of edema and LGE (Category 1) correlated with normalized ventricular function.
- Presence of edema and/or LGE indicated a worse prognosis or potential myocarditis.
Conclusions:
- Hypocalcemic dilated cardiomyopathy has a favorable prognosis with timely treatment.
- CMR aids in prognostication; absence of edema/LGE predicts good outcomes.
- Edema/LGE may suggest coexistent myocarditis, warranting further investigation.
Abstract:
Background Hypocalcemia is a rare reversible cause of dilated cardiomyopathy in pediatric population. Myocarditis is another more frequent cause of cardiomyopathy with overlapping presenting features. Cardiac magnetic resonance imaging (CMRI) is a vital modality capable of tissue characterization for the evaluation of cardiomyopathy. The present study is the first attempt to determine if any specific characteristics on CMR exist in patients with hypocalcemic dilated cardiomyopathy. Methods A retrospective analysis of 10 cases of hypocalcemic dilated cardiomyopathy (August 2012-August 2019), among which CMRI of nine patients were analyzed. Patients were categorized in to three categories; category 1 defined as absence of edema and late gadolinium enhancement (LGE), category 2 having edema only, and category 3 with presence of both edema and LGE. A diagnosis of myocarditis was considered if both edema and LGE were present. Results The mean age of the cohort was 5.5 ± 3.3 months. The mean ejection fraction of the cohort was 20.5 ± 6.85% that improved significantly to 35.22 ± 9.3% at the time of discharge. Five of nine patients had no edema or LGE (category 1), whereas two patients each were categorized into category 2 and 3. All cases in category 1 had normalized ventricular function on follow-up. One patient in category 2 had normal ejection fraction and one was lost to follow-up. Out of the two patients in category 3, there was one mortality and another was lost to follow-up. Of the six patients at follow-up (19 ± 11.0 months), the mean left ventricle ejection fraction improved to 56.5 ± 6.1%. Conclusion Hypocalcemic dilated cardiomyopathy has a favorable outcome on rapid initiation of treatment. CMR can be utilized for further prognostication of these patients. Absence of edema and LGE predicts a good outcome, whereas presence of LGE and/or edema either indicates a worse prognosis or an underlying coexistent myocarditis warranting an early myocardial biopsy.
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