Propranolol in infantile haemangioma: simplifying pretreatment monitoring

Oumama El Ezzi1, Judith Hohlfeld, Anthony de Buys Roessingh

  • 1Department of Pediatric Surgery, University Hospital Center of the Canton of Vaud (CHUV), Lausanne, Switzerland.

Swiss Medical Weekly
|March 11, 2014
PubMed

Insights

Propranolol is a safe and effective treatment for infantile haemangiomas (IHs). A 48-hour hospital monitoring period may be unnecessary, simplifying treatment initiation for IH patients.

Area of Science:

  • Pediatric Dermatology
  • Vascular Biology
  • Pharmacology

Background:

  • Infantile haemangiomas (IHs) are common vascular tumors in infants.
  • Propranolol is the established first-line therapy for problematic IH.
  • Current Swiss protocols mandate 48-hour inpatient monitoring for propranolol initiation.

Purpose of the Study:

  • To evaluate the safety and efficacy of propranolol for infantile haemangiomas.
  • To assess the necessity of a 48-hour hospital monitoring period for propranolol treatment.
  • To advocate for a simplified pretreatment monitoring process.

Main Methods:

  • Retrospective analysis of 29 infants with problematic IH treated with propranolol (Sept 2009-Sept 2012).
  • Patients received 1 mg/kg/day propranolol on day 1, then 2 mg/kg/day.
  • Inclusion criteria involved 48-hour hospitalisation with continuous monitoring and measurements.

Main Results:

  • 86.2% of infants showed immediate response to propranolol.
  • No severe adverse reactions were reported.
  • Transient side effects (bradycardia, hypotension, hypoglycemia) occurred after the first dose in 6 patients; none after the second dose. Treatment was not interrupted.

Conclusions:

  • Propranolol is a safe treatment for problematic infantile haemangiomas.
  • Side effects are typically transient and occur after the initial dose.
  • Strict 48-hour inpatient monitoring may be unnecessary if contraindications are respected, potentially reducing healthcare costs.
Abstract

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