Adverse Effects of Systemic Glucocorticosteroid Therapy in Infants With Hemangiomas
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 14...
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Veröffentlicht in: | Archives of dermatology (1960) 2004-08, Vol.140 (8), p.963-969 |
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Zusammenfassung: | 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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ISSN: | 0003-987X 2168-6068 1538-3652 2168-6084 |
DOI: | 10.1001/archderm.140.8.963 |