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Adverse effects of systemic glucocorticosteroid therapy in infants with hemangiomas
Manju E George1, Vidya Sharma, Jill Jacobson
1Section of Dermatology, Children's Mercy Hospital, Kansas City, MO, USA. mgeorge@kumc.edu
Insights
Systemic glucocorticosteroids (GS) for infantile hemangiomas can cause behavioral changes and gastrointestinal issues. Long-term use frequently leads to hypertension and adrenal suppression, requiring careful infant monitoring.
Area of Science:
- Pediatric Dermatology
- Neonatal Medicine
- Pharmacology
Background:
- Infantile hemangiomas are common vascular tumors in infants.
- Systemic glucocorticosteroids (GS) are a primary treatment for problematic hemangiomas.
- Evaluating the safety profile of GS therapy in this population is crucial.
Purpose of the Study:
- To assess the short- and long-term adverse effects of systemic glucocorticosteroid (GS) therapy in infants diagnosed with hemangiomas.
- To identify common complications and monitor physiological changes associated with GS treatment.
Main Methods:
- Retrospective chart review of 22 infants treated with GS for hemangiomas over a 3-year period.
- Analysis included demographic data, GS dosage and duration, parental concerns, hemangioma complications, and hormonal assessments (cortisol levels, corticotropin stimulation tests).
Main Results:
- Common parental concerns included irritability, fussiness, and insomnia (73%).
- Hypertension was observed in 45% of patients.
- Adrenal suppression was frequent, with abnormal morning cortisol levels in 87% and abnormal corticotropin stimulation tests in 2 of 3 infants.
Conclusions:
- Systemic glucocorticosteroid therapy for infantile hemangiomas is generally tolerated but associated with significant adverse effects.
- Hypertension and hypothalamic-pituitary-adrenal axis suppression are common findings.
- Close monitoring for these adverse effects is recommended for infants receiving long-term GS treatment.
Objective:
To evaluate the short- and long-term adverse effects of systemic glucocorticosteroid (GS) therapy in infants with hemangiomas.
Design:
Retrospective chart review of infants treated with GSs for hemangiomas during a 3-year period.
Setting:
Tertiary care children's hospital.
Patients:
Of 141 patients identified with hemangiomas, 22 were treated with GSs.
Interventions:
Minimum of 1-month GS therapy at a minimum starting dose of 0.5 mg/kg per day.
Outcome Measures:
Demographic and anthropometric measurements, starting dose and duration of GS therapy, subjective parental concerns, complications related to hemangioma, adjunctive treatment, and morning cortisol levels and/or results of corticotropin stimulation tests.
Results:
The average starting dose was 2.23 mg/kg per day; average length of therapy was 28.1 weeks. Complaints of irritability, fussiness, or insomnia were identified in 16 patients (73%). Hypertension, defined as 3 or more episodes of systolic blood pressure higher than 105 mm Hg, was observed in 10 patients (45%). Morning cortisol levels were abnormal in 13 (87%) of the 15 patients evaluated. Low-dose corticotropin stimulation test results were abnormal in 2 of the 3 infants tested.
Conclusions:
While GS therapy for infantile hemangiomas was tolerated well overall, changes in behavior, insomnia, and gastrointestinal symptoms were common parental concerns. Hypertension and hypothalamic-pituitary-adrenal axis suppression were observed frequently. Infants undergoing long-term GS treatment of hemangiomas should be monitored carefully for these potential adverse effects.
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