Characteristics and Outcomes of Infantile Hemangioma With Non, Poor, and Partial Response to Standard-Dose Systemic Beta-Blocker Therapy
Objectives: Systemic beta-blockers are highly effective for the management of infantile hemangiomas (IH), but little is known about infants who do not adequately respond. We aimed to describe the characteristics and outcomes of suboptimal responders to standard-dose systemic beta-blockers in infants with IH. Methods: This is a multicenter retrospective cohort study to evaluate demographics, IH lesion characteristics, and treatment specifics of infants with IH with suboptimal response to baseline standard-dose propranolol treatment. Clinical response was used to assess the outcome after a therapeutic change. Results: Twenty-five infants were included in this study. Seven (28%) had segmental IH, 16 (64%) focal, and 2 (8%) indeterminate. The IHs were located on the head and neck in 21 (84%) infants, with 24 (96%) having a deep or combined component. Therapy changes after standard-dose propranolol treatment failure, most commonly by escalating propranolol dose to ≥2.5 mg/kg/d (59%) or surgical interventions (29%), were associated with good therapeutic effects. Conclusion: Among suboptimal responders to standard-dose systemic propranolol, IHs with a deep or combined component and located on the head and neck were the most common. This retrospective study was largely descriptive in nature with additional exploratory analyses. However, it is still encouraging that for patients with a suboptimal clinical response, higher propranolol doses of ≥2.5–3 mg/kg/d or second-line treatments with surgical interventions or systemic steroids can be considered as potentially safe and effective alternatives. Level of evidence: Level 4 (case series).
Authors
- Gerilyn M. Olsen (ORCID: https://orcid.org/0009-0009-4843-6042)
- Mohsen Afarideh (ORCID: https://orcid.org/0000-0002-3578-5640)
- Christine T. Lauren (ORCID: https://orcid.org/0000-0002-7278-4831)
- Sonal D. Shah (ORCID: https://orcid.org/0000-0002-0336-4278)
- Denise M. Adams (ORCID: https://orcid.org/0000-0002-2892-5369)
- Brandon Newell (ORCID: https://orcid.org/0000-0002-9594-0374)
- Eulàlia Baselga (ORCID: https://orcid.org/0000-0003-1086-8439)
- Amy J. Nopper
- Kimberly A. Horii
- Ilona J. Frieden (ORCID: https://orcid.org/0000-0001-7305-5940)
- Nessa Aghazadeh (ORCID: https://orcid.org/0000-0002-4641-4626)
- Catherine McCuaïg (ORCID: https://orcid.org/0000-0003-0792-6247)
- Erin F. D. Mathes
- Maria C. Garzón (ORCID: https://orcid.org/0009-0000-7219-3356)
- Kimberly D. Morel (ORCID: https://orcid.org/0000-0003-0646-8192)
- Katinna E. Rodriguez Baisi (ORCID: https://orcid.org/0000-0002-3164-6037)
- Julie Powell
- Megha M. Tollefson
Institutions
- Children's Mercy Hospital (US)
- Mayo Clinic (US)
- Children's Hospital of Philadelphia (US)
- NewYork–Presbyterian Hospital (US)
- University of California, San Francisco (US)
- Medical College of Wisconsin (US)
- University Hospitals of Cleveland (US)
- New York Hospital Queens (US)
- Hospital de Sant Pau (ES)
- Presbyterian Hospital (US)
- North Shore Diabetes and Endocrine Associates (US)
- University School (US)
- Case Western Reserve University (US)
- Université de Montréal (CA)
- Columbia University (US)
Publication Details
- Journal
- Journal of Vascular Anomalies
- Published
- 2025-04-25
- DOI
- https://doi.org/10.1097/jova.0000000000000112
- Primary Topic
- Vascular Malformations and Hemangiomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00