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Published on: November 4, 2010
Use of intravenous isoproterenol for status asthmaticus in children
Insights
Low-dose intravenous isoproterenol effectively treats severe pediatric asthma by lowering carbon dioxide levels and preventing respiratory failure. Careful monitoring is essential due to potential complications like arrhythmias and rebound bronchospasm.
Area of Science:
- Pediatric Pulmonology
- Critical Care Medicine
- Pharmacology
Background:
- Severe asthma in children (status asthmaticus) can lead to respiratory failure.
- Standard treatments like aminophylline, corticosteroids, and aerosolized medications may be insufficient.
- Intravenous (IV) isoproterenol has been explored for managing severe asthma exacerbations.
Purpose of the Study:
- To evaluate the efficacy and indications of low-dose continuous drip IV isoproterenol in children with severe asthma.
- To determine optimal dosing and administration parameters for IV isoproterenol in this population.
Main Methods:
- Thirty-seven pediatric patients (6 months-16 years) with severe asthma (asthma score ≥6 or PCO2 ≥55 torr) unresponsive to other therapies received IV isoproterenol.
- Initial dose was 0.05 mcg/kg/min, increased incrementally as needed, with continuous IV aminophylline and oxygen.
- Infusion continued until PCO2 ≤40 torr, maintained, then tapered.
Main Results:
- Complete response was observed in 34 patients (89%) with a mean isoproterenol dose of 0.2 mcg/kg/min and mean response time of 1.3 hours.
- One patient had a partial response due to arrhythmia, and another experienced rebound bronchospasm upon abrupt discontinuation.
- The treatment effectively reversed hypercapnia and averted impending respiratory failure.
Conclusions:
- Low-dose IV isoproterenol is an effective treatment for reversing hypercapnia in pediatric status asthmaticus.
- Careful monitoring for limitations and potential complications, such as arrhythmias and rebound bronchospasm, is crucial for safe and effective use.
Abstract:
The use of continuous drip iv isoproterenol was studied to determine its efficacy and indications in lower doses in severe asthma. Thirty-seven patients (6 months to 16 yr) received iv isoproterenol with asthma score of 6 (mean 6.8) or greater indicating PCO2 of 60 torr or higher or a PCO2 of 55 (mean 58.4) torr or greater without response to therapeutic levels of aminophylline, corticosteroids, and aerosolized isoetharine as well as appropriate oxygen. The initial dose of isoproterenol was 0.05 microgram/kg X min; if there was no response in PCO2, the continuous drip was increased by increments of not more than 0.05 microgram/kg X min every 15-20 min; iv aminophylline was continued by continuous infusion at therapeutic levels. The isoproterenol was infused until the PCO2 less than or equal to 40 torr and maintained at that dose for an equal time, then decreased over an interval equal to the response and maintenance time. There was complete response in 34 patients (mean dose 0.2 microgram/kg X min; mean response time 1.3 h, range 0.2-3.2 h). One patient had a partial response but the isoproterenol was discontinued with reversal of an arrhythmia; a 2nd patient had initial resolution but had rebound bronchospasm when the isoproterenol was abruptly discontinued. Thus, iv isoproterenol at lower initial and responding dose is effective for reversing increased PCO2 and impending respiratory failure in status asthmaticus in children, but the limitations and complications must be closely monitored.
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