# A Systematic Review and Meta‐Analysis of the Efficacy and Safety of Propranolol Versus Other Drugs in the Treatment of Infantile Hemangioma

**Authors:** Jiahua Hu, Lisha Pan, Hong Kong, Jiaqi Lou

PMC · DOI: 10.1111/jocd.70750 · Journal of Cosmetic Dermatology · 2026-02-17

## TL;DR

This study compares propranolol with other drugs for treating infantile hemangioma and finds it more effective for complete remission.

## Contribution

The study provides a meta-analysis showing propranolol's significant advantage in complete remission for infantile hemangioma.

## Key findings

- Propranolol showed a significantly higher complete remission rate compared to other drugs.
- No significant differences were found in overall response rates or adverse event incidence between propranolol and control groups.
- Atenolol is suggested as an effective alternative for patients with specific tolerability concerns.

## Abstract

This study aimed to systematically evaluate and compare the efficacy and safety of propranolol versus atenolol, corticosteroids, timolol, and other therapies in the treatment of infantile hemangioma (IH) through a meta‐analysis, thereby providing evidence‐based guidance for clinical practice.

A comprehensive literature search was conducted across PubMed, Cochrane Library, EMBASE, Web of Science, CNKI, and Wanfang databases from inception to December 2025. The protocol was prospectively registered with PROSPERO (CRD420261294316). Randomized controlled trials (RCTs) or clinical controlled trials (CCTs) comparing oral propranolol with other active drugs in IH patients aged ≤ 12 years were included. Primary outcomes were overall response rate (≥ 50% reduction), complete remission rate, and incidence of adverse events. Two reviewers independently performed study selection, data extraction, and quality assessment using the Cochrane RoB 2.0 tool and Newcastle‐Ottawa Scale. Pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using R software. Heterogeneity was assessed using the I
2 statistic.

Eight studies involving 900 patients (propranolol: 464; control: 436) were included. Meta‐analysis revealed no statistically significant difference in overall response rate between propranolol and control groups (pooled OR = 1.29, 95% CI: 0.80–2.09, p = 0.30). However, propranolol demonstrated a significantly higher complete remission rate (OR = 1.35, 95% CI: 1.01–1.82, p = 0.045). Subgroup analyses by control drug type (atenolol, corticosteroids, timolol, combination therapy) showed no significant differences in efficacy (all p > 0.05). Safety analysis indicated no significant difference in adverse event incidence between groups (OR = 0.76, 95% CI: 0.38–1.55, p = 0.45), albeit with moderate heterogeneity (I
2 = 56%). Heterogeneity was low for efficacy outcomes (I
2 = 0%). Funnel plot symmetry and a non‐significant Egger's test suggested a low risk of publication bias.

Propranolol offers a statistically significant advantage in achieving complete remission of infantile hemangioma compared to other active agents, while maintaining comparable overall response rates and a similar overall safety profile. These findings support propranolol as a first‐line therapy when complete lesion resolution is the primary goal. Atenolol represents an effective alternative, particularly for patients with specific tolerability concerns, underscoring the need for individualized treatment selection.

## Linked entities

- **Chemicals:** propranolol (PubChem CID 4946), atenolol (PubChem CID 2249), timolol (PubChem CID 5478)
- **Diseases:** infantile hemangioma (MONDO:0002407)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, IGKV5-2 (immunoglobulin kappa variable 5-2) [NCBI Gene 28907] {aka B2, IGKV52}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}
- **Diseases:** vascular tumor (MESH:D009369), sleep disruption (MESH:D019958), asthma (MESH:D001249), anxiety (MESH:D001007), sleep disturbances (MESH:D012893), pain (MESH:D010146), growth retardation (MESH:D006130), hypotension (MESH:D007022), bronchospasm (MESH:D001986), bradycardia (MESH:D001919), bleeding (MESH:D006470), infection (MESH:D007239), hypoglycemia (MESH:D007003), gastrointestinal upset (MESH:D005767), capillary hemangioma (MESH:D018324), visual axis obstruction (MESH:C566610), facial lesions (MESH:D005155), strawberry hemangioma (MESH:D006392), hypertension (MESH:D006973), IHs (MESH:C535746), vascular anomalies (MESH:D020785), facial hemangiomas (MESH:D006391), functional impairment (MESH:D003072), reactive airway disease (MESH:D000275), IH (MESH:C535860)
- **Chemicals:** Atenolol (MESH:D001262), Timolol (MESH:D013999), nitric oxide (MESH:D009569), Propranolol (MESH:D011433), Prednisolone (MESH:D011239), steroids (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12910639/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12910639/full.md

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Source: https://tomesphere.com/paper/PMC12910639