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Published on: May 10, 2024
Effects of nebulized corticosteroids therapy on hypothalamic-pituitary-adrenal axis in young children with recurrent
Feyzullah Cetinkaya1, Petek Kayiran, Nihal Memioglu
1Sisli Etfal Education and Research Hospital, Istanbul, Turkey. feyzulkaya@mynet.com
Insights
Nebulized budesonide and fluticasone propionate demonstrate safety for infant asthma treatment. Periodic adrenal function testing is recommended during long-term use of these inhaled corticosteroids.
Area of Science:
- Pediatric Pulmonology
- Pediatric Endocrinology
Background:
- Inhaled corticosteroids (ICS) are standard for childhood asthma but safety data in infants is limited.
- Recurrent or persistent wheeze in infants necessitates safe and effective treatment options.
Purpose of the Study:
- To evaluate the safety and efficacy of nebulized budesonide (BUD) and fluticasone propionate (FP) on the hypothalamic-pituitary-adrenal (HPA) axis in infants.
- To assess the impact of these inhaled corticosteroids on adrenal function in young children.
Main Methods:
- A randomized study involving 31 infants (6-24 months) with recurrent/persistent wheeze.
- Patients received either nebulized BUD or FP (0.25 mg twice daily for 6 weeks, then half dose for 6 weeks).
- Adrenal function was assessed via basal and cosyntropin-stimulated plasma cortisol levels, alongside glucose, HbA1c, and electrolytes.
Main Results:
- All patients except one maintained adequate adrenal function post-treatment.
- Cortisol levels remained above 500 nmol/l or showed an incremental rise >200 nmol/l after stimulation.
- Nebulized corticosteroid treatment showed no significant adverse effects on the HPA axis in this cohort.
Conclusions:
- Nebulized budesonide and fluticasone propionate appear safe for treating wheezing illnesses in infants.
- Long-term therapy with nebulized steroids in infancy warrants periodic monitoring of adrenal function.
Abstract:
Inhaled corticosteroids (ICS) are preferred drugs for the long-term treatment of all severities of asthma in children. However, data about the safety of ICS in infants is lacking. So, it is essential to do further clinical studies to examine the safety and efficacy of ICS in this population. In this study, the effects of nebulized budesonide and nebulized fluticasone propionate suspensions on hypothalamic-pituitary-adrenal axis is examined in infants with recurrent or persistent wheeze. Thirty-one children aged 6-24 months admitted to our hospital between January and December 2005 with symptoms of recurrent or persistent wheeze were included in the study. The patients were randomly allocated to receive 0.25 mg BUD or 0.25 mg fluticasone propionate twice daily for 6 wk and half dose for another 6 wk with a jet nebulizer at home. Blood samples for basal cortisol concentration, adrenocarticotropic hormone, glucose, HbA1c and electrolytes were obtained at the beginning and at the end of the study. Adrenal function assessment was based on changes in cosyntropin-stimulated plasma cortisol levels. The study was completed with 31 patients, 16 of whom received BUD and 15 FP. All patients except one had plasma cortisol concentrations above 500 nmol/l (18 microg/dl) or had an incremental rise in cortisol of >200 nmol/l after stimulation. Although nebulized steroids seem to be safe in infancy, we recommend that adrenal functions should be tested periodically during long-term treatment with nebulized steroids.
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