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Published on: May 28, 2019
Myocardial specific creatine phosphokinase isoenzyme elevation in children with asthma treated with intravenous
Insights
Intravenous isoproterenol for severe childhood asthma may elevate cardiac enzymes, suggesting potential myocardial injury. Monitoring creatine phosphokinase MB (CPK-MB) is recommended during this treatment.
Area of Science:
- Pediatric Critical Care
- Cardiology
- Pulmonology
Background:
- Severe childhood asthma (status asthmaticus) is a critical condition requiring intensive care.
- Intravenous (IV) isoproterenol has been used in managing severe asthma.
- Potential cardiac side effects of asthma medications require careful evaluation.
Purpose of the Study:
- To investigate the association between IV isoproterenol use and cardiac enzyme elevation in children with severe asthma.
- To determine if elevated cardiac enzymes indicate myocardial injury during this therapy.
Main Methods:
- Retrospective review of intensive care unit admissions for severe childhood status asthmaticus.
- Analysis of serum creatine phosphokinase MB (CPK-MB) levels in patients receiving IV isoproterenol.
- Comparison of CPK-MB levels before and after discontinuation of IV isoproterenol.
Main Results:
- Elevated CPK-MB levels were observed in 15 out of 19 admissions (79%).
- Mean peak CPK-MB elevation was 204 IU/L with a mean peak MB band of 6.05%.
- CPK-MB levels normalized in all 9 patients after IV isoproterenol was stopped, even with continued other asthma therapies.
Conclusions:
- Elevated serum CPK-MB levels in children treated with IV isoproterenol for severe asthma may indicate myocardial injury.
- Caution and serial monitoring of CPK-MB levels are recommended when using IV isoproterenol in pediatric asthma management.
Abstract:
We retrospectively reviewed admissions that required intravenous (IV) isoproterenol in an intensive care unit setting for management of severe childhood status asthmaticus. Elevation of the cardiac-specific serum creatine phosphokinase MB (CPK-MB) isoenzyme was noted in 15 of 19 admissions. The mean peak elevation of serum CPK in those 15 admissions was 204 IU/L with a mean peak MB band of 6.05%. Nine of the 15 admissions with elevated CPK-MB level had follow-up levels measured after IV isoproterenol had been stopped. In all nine cases, the follow-up serum CPK-MB level was 0%. In six of those nine cases, follow-up serum with undetectable CPK-MB level was obtained while the patients continued to receive IV aminophylline and corticosteroids, and inhaled but not intravenous beta-adrenergic agonist medications. These observations suggest that elevated serum CPK-MB levels that may be indicative of myocardial injury are associated with IV isoproterenol therapy of severe childhood asthma. Therefore, we recommend caution along with serial monitoring of serum CPK-MB levels when IV isoproterenol is administered in the therapy of childhood asthma.
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