Key result
AKI and cardiac arrest are major risk factors for ~9% inpatient mortality in pediatric cardiomyopathy.
Why the study?
Therapies for children with congenital heart disease and cardiomyopathy continue to be introduced with large practice variability and questionable outcomes.
Do various medications (diuretics, steroids, ACE inhibitors, calcium channel blockers, beta blockers) improve intensive care unit length of stay, total length of stay, billed charges, and mortality in paediatric patients with congenital heart disease and cardiomyopathy?
Case-Control (n=10,376)
Yes
Do various medications (diuretics, steroids, ACE inhibitors, calcium channel blockers, beta blockers) improve intensive care unit length of stay, total length of stay, billed charges, and mortality in paediatric patients with congenital heart disease and cardiomyopathy?
Specific medications including methylprednisolone, captopril, enalapril, furosemide, and amlodipine are associated with improved admission outcomes in pediatric patients with congenital heart disease and cardiomyopathy.
INTRODUCTION: Children with congenital heart disease and cardiomyopathy are a unique patient population. Different therapies continue to be introduced with large practice variability and questionable outcomes. The purpose of this study is to determine the impact of various medications on intensive care unit length of stay, total length of stay, billed charges, and mortality for admissions with congenital heart disease and cardiomyopathy. MATERIALS AND METHODS: We identified admissions of paediatric patients with cardiomyopathy using the Pediatric Health Information System database. The admissions were then separated into two groups: those with and without inpatient mortality. Univariate analyses were conducted between the groups and the significant variables were entered as independent variables into the regression analyses. RESULTS: A total of 10,376 admissions were included these analyses. Of these, 904 (8.7%) experienced mortality. Comparing patients who experienced mortality with those who did not, there was increased rate of acute kidney injury with an odds ratio (OR) of 5.0 [95% confidence interval (CI) 4.3 to 5.8, p < 0.01], cardiac arrest with an OR 7.5 (95% CI 6.3 to 9.0, p < 0.01), and heart transplant with an OR 0.3 (95% CI 0.2 to 0.4, p < 0.01). The medical interventions with benefit for all endpoints after multivariate regression analyses in this cohort are methylprednisolone, captopril, enalapril, furosemide, and amlodipine. CONCLUSIONS: Diuretics, steroids, angiotensin-converting enzyme inhibitors, calcium channel blockers, and beta blockers all appear to offer beneficial effects in paediatric cardiomyopathy admission outcomes. Specific agents within each group have varying effects.
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Loomba et al. (2020) conducted a case-control in Congenital heart disease and cardiomyopathy (n=10,376). Medical interventions (methylprednisolone, captopril, enalapril, furosemide, amlodipine) vs. Admissions without inpatient mortality was evaluated on Intensive care unit length of stay, total length of stay, billed charges, and mortality. Acute kidney injury (OR 5.0; 95% CI 4.3-5.8) and cardiac arrest (OR 7.5; 95% CI 6.3-9.0) were significant risk factors for the 8.7% inpatient mortality rate in pediatric cardiomyopathy admissions.
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