Oral Atenolol versus Propranolol in the Treatment of Infantile Hemangioma

Infantile hemangiomas (IH) are the most common benign vascular tumors of infancy. Propranolol has been established as the first-line therapy; however, its adverse effects have prompted the search for safer alternatives. Atenolol, a selective β-1 blocker, has been suggested to offer similar efficacy with fewer side effects. This study compared the efficacy and safety of propranolol and atenolol in treating problematic IHs in Pakistani infants. Objective: To evaluate and compare the therapeutic efficacy and safety profiles of oral propranolol and atenolol in infants with IH. Methods: A randomized controlled trial was conducted at the Department of Pediatric Surgery, Sheikh Zayed Hospital, Rahim Yar Khan, from December 2024 to May 2025. A total of 120 infants with problematic IHs were randomly assigned to propranolol (n=60) or atenolol (n=60). Propranolol was initiated at 1 mg/kg/day in two divided doses and subsequently increased to 2 mg/kg/day. Atenolol was started at 0.5 mg/kg/day once daily and subsequently increased to 1 mg/kg/day. Treatment duration was six months. The primary outcome was complete/near-complete involution (PGA-5: ≥90% improvement). Secondary outcomes included time to PGA-5 and incidence of adverse events. Data were analyzed using SPSS v25, employing chi-square and t-tests, with p < 0.05 considered significant. Results: Of the 120 infants (mean age 5.2 ± 2.1 months; 56.7% females), 70% in the propranolol group and 63.3% in the atenolol group achieved PGA-5 (p=0.41). The mean time to PGA-5 was 14.2 ± 3.5 weeks for propranolol and 15.0 ± 3.7 weeks for atenolol (p=0.23). Adverse events were significantly higher in the propranolol group (18.3%) compared with the atenolol group (6.7%) (p = 0.048). Most adverse events were mild and manageable, with no life-threatening complications. Conclusion: Both propranolol and atenolol were effective for treating infantile hemangiomas. While propranolol showed slightly higher rates of complete involution and faster response, atenolol demonstrated a safer profile with fewer adverse effects. Atenolol may serve as a viable alternative for infants at risk of propranolol-related complications.

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Publication Details

Journal
Biological and Clinical Sciences Research Journal
Published
2025-06-30
DOI
https://doi.org/10.54112/bcsrj.v6i6.1938
Primary Topic
Image Processing and 3D Reconstruction
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article
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article

Oral Atenolol versus Propranolol in the Treatment of Infantile Hemangioma

Biological and Clinical Sciences Research Journal
Image Processing and 3D Reconstruction
article

Oral Atenolol versus Propranolol in the Treatment of Infantile Hemangioma

article en

Abstract

Infantile hemangiomas (IH) are the most common benign vascular tumors of infancy. Propranolol has been established as the first-line therapy; however, its adverse effects have prompted the search for safer alternatives. Atenolol, a selective β-1 blocker, has been suggested to offer similar efficacy with fewer side effects. This study compared the efficacy and safety of propranolol and atenolol in treating problematic IHs in Pakistani infants. Objective: To evaluate and compare the therapeutic efficacy and safety profiles of oral propranolol and atenolol in infants with IH. Methods: A randomized controlled trial was conducted at the Department of Pediatric Surgery, Sheikh Zayed Hospital, Rahim Yar Khan, from December 2024 to May 2025. A total of 120 infants with problematic IHs were randomly assigned to propranolol (n=60) or atenolol (n=60). Propranolol was initiated at 1 mg/kg/day in two divided doses and subsequently increased to 2 mg/kg/day. Atenolol was started at 0.5 mg/kg/day once daily and subsequently increased to 1 mg/kg/day. Treatment duration was six months. The primary outcome was complete/near-complete involution (PGA-5: ≥90% improvement). Secondary outcomes included time to PGA-5 and incidence of adverse events. Data were analyzed using SPSS v25, employing chi-square and t-tests, with p < 0.05 considered significant. Results: Of the 120 infants (mean age 5.2 ± 2.1 months; 56.7% females), 70% in the propranolol group and 63.3% in the atenolol group achieved PGA-5 (p=0.41). The mean time to PGA-5 was 14.2 ± 3.5 weeks for propranolol and 15.0 ± 3.7 weeks for atenolol (p=0.23). Adverse events were significantly higher in the propranolol group (18.3%) compared with the atenolol group (6.7%) (p = 0.048). Most adverse events were mild and manageable, with no life-threatening complications. Conclusion: Both propranolol and atenolol were effective for treating infantile hemangiomas. While propranolol showed slightly higher rates of complete involution and faster response, atenolol demonstrated a safer profile with fewer adverse effects. Atenolol may serve as a viable alternative for infants at risk of propranolol-related complications.

Biological and Clinical Sciences Research JournalVol. 6(6)
Shaikh Zayed Medical College and Hospital (PK)
Good health and well-being
Openalex Percentile: Top 47%
Image Processing and 3D Reconstruction
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Oral Atenolol versus Propranolol in the Treatment of Infantile Hemangioma · Biological and Clinical Sciences Research Journal (2025) | TGRS Research Map | TGRS