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Safety of Prior Propranolol Therapy for Infantile Hemangioma
1School of Medicine, West Virginia University, Morgantown, West Virginia, USA.
Insights
Propranolol treatment for infantile hemangioma (IH) in infancy showed no increased risk of growth impairment, sleep disorders, learning disabilities, or diabetes mellitus up to age 17. This study confirms the safety of propranolol for IH patients long-term.
Area of Science:
- Pediatric pharmacology
- Dermatology
- Clinical research
Background:
- Propranolol is the standard treatment for infantile hemangioma (IH) since 2008.
- Previous research explored short-term effects of infant propranolol therapy for IH.
- Long-term adverse effects of propranolol for IH require further investigation.
Purpose of the Study:
- To assess the long-term risk of specific adverse effects in children treated with propranolol for IH.
- To evaluate the association between infant propranolol therapy for IH and later-life health outcomes.
Main Methods:
- Retrospective cohort study using the TrinetX database.
- Included children aged 10-17 years who received propranolol for IH in infancy.
- Analyzed risks of growth impairment, sleep disorders, learning disabilities, and diabetes mellitus.
Main Results:
- No statistically significant increased risk of growth impairment was observed.
- No statistically significant increased risk of sleep disorders was observed.
- No statistically significant increased risk of learning disabilities or diabetes mellitus was observed.
Conclusions:
- Infant propranolol therapy for IH is not associated with increased long-term risks up to age 17.
- Findings support the established safety profile of propranolol for infantile hemangioma treatment.
- This study provides evidence for the continued safe use of propranolol in managing IH.
Abstract:
Propranolol has been the primary treatment for infantile hemangioma (IH) since 2008. Prior studies have investigated the effects in late childhood of propranolol therapy given in infancy for IH, including neurocognitive dysfunction, sleep disorders, and hypoglycemia. However, few studies have determined the risk of these adverse effects later in life. Using the TrinetX database, we studied the risk of growth impairment, sleep disorders, learning disabilities, and diabetes mellitus in children aged 10-17 years who had received propranolol for IH in infancy. The maximum age of 17 years was chosen for the study, as propranolol was established as a treatment for IH in 2008. The results showed no statistically significant risk of growth impairment, sleep disorders, learning disabilities, or diabetes mellitus in IH patients treated with propranolol. These findings support existing evidence that propranolol therapy given in infancy for IH is not associated with long-term adverse effects up to age 17 years in the studied patient population.
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