Clinical Insights into Risk Factors for Infantile Hemangioma and Propranolol Treatment Outcomes
Ioana Roșca1,2, Raluca-Gabriela Miulescu1,3, Alexandra-Maria Roman1,4
1Faculty of Medicine, University of Medicine and Pharmacy "Carol Davila", 020021 Bucharest, Romania.
Insights
Infantile hemangioma (IH) is linked to preterm birth and low birth weight. Early diagnosis and propranolol treatment are effective for IH, with few side effects.
Area of Science:
- Pediatrics
- Dermatology
- Neonatology
Background:
- Infantile hemangioma (IH) is a common neonatal vascular tumor with multifactorial origins.
- Prenatal and perinatal factors may influence IH development and clinical presentation.
- Understanding risk factors is crucial for early detection and management.
Purpose of the Study:
- Identify risk factors for infantile hemangioma in infants and mothers.
- Correlate risk factors with clinical characteristics and severity.
- Evaluate the efficacy and outcomes of propranolol therapy for IH.
Main Methods:
- Retrospective observational study of 43 infants (<12 months) with IH.
- Analysis of maternal and neonatal data, including gestational age, birth weight, and Apgar scores.
- Utilized the Infantile Hemangioma Referral Score (IHReS) for risk stratification.
Main Results:
- IH showed a female predominance and was associated with preterm birth (50%) and low birth weight (51.16%).
- Maternal anemia and gestational hypertension were noted but not significantly linked to IH severity.
- Propranolol therapy demonstrated high efficacy with significant lesion regression; common side effects included sleep disturbances and diarrhea.
Conclusions:
- Infantile hemangioma is prevalent in preterm and low-birth-weight infants.
- Early diagnosis, risk stratification using tools like IHReS, and prompt propranolol treatment are key to favorable outcomes.
- Further research is warranted to explore long-term effects and potential rebound phenomena associated with propranolol therapy.
Abstract:
Background/Objectives: Infantile hemangioma (IH) is a common vascular tumor in neonates, influenced by multiple prenatal and perinatal factors. This study aimed to identify risk factors in both infants and mothers, assess their link to clinical characteristics and severity, and evaluate treatment outcomes when systemic propranolol therapy was administered. Methods: We conducted a retrospective observational study analyzing 43 infants under 12 months, including 11 neonates (<28 days) diagnosed with IH. Maternal and neonatal factors, diagnostic timelines, clinical presentation, and treatment efficacy were examined. Data analysis included descriptive statistics, focusing on gestational age, birth weight, Apgar scores, and the Infantile Hemangioma Referral Score (IHReS). Results: The study found a female predominance and a correlation between IH and pre-term birth (50%) and low birth weight (<2760 g, 51.16%). Maternal anemia (23%) and gestational hypertension (9%) were present in the cohort, but no statistical association with IH severity was found. A significant number (44.18%) were diagnosed within the first two weeks postpartum. The IHReS was inversely correlated with Apgar scores, with newborns scoring above 8 having a lower IHReS. Treatment with propranolol (1-3 mg/kg/day) was highly effective, resulting in significant lesion regression in most patients. Mild complications included sleep disturbances (12%) and diarrhea (9%). The most affected areas were the face/eyelid (32.55%), limbs (18.6%), and anterior thorax. Additionally, 42% of cases had an IHReS above 4, with multiple hemangiomas increasing severity. Conclusions: IH was common in pre-term and low-birth-weight infants, whereas the maternal comorbidities observed in this small cohort did not show a definitive association, underscoring the need for controlled studies. Early diagnosis, risk stratification, and timely propranolol therapy are crucial in achieving favorable outcomes. Further research is needed to assess long-term effects and evaluate risks of treatment rebound.
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