Literature DB >> 30515761

Efficacy and safety of oral atenolol for the treatment of infantile haemangioma: A systematic review.

Qi Wang1, Bo Xiang1, Siyuan Chen2, Yi Ji1.   

Abstract

Recently, several studies have reported their experience in using oral atenolol in patients with infantile haemangioma (IH), especially as an alternative to propranolol, but the efficacy and safety of oral atenolol has not been evaluated. We searched PubMed (Medline), Central, Embase, Web of Science and EBSCOhost (until May 2018) for the eligible studies reporting more than 10 IH patients who were treated with oral atenolol with detailed original data, including outcomes, regimens and adverse events (AEs). The data was standardised and analysed by using R software with meta-package. A total of 9 of 141 identified articles, including 341 infantile haemangioma patients treated with oral atenolol therapy, were included. The pooled response rate of atenolol was 0.90 (95% CI: 0.85-0.93), and the rebound rate was 0.11 (95% CI: 0.08-0.16). Among the 341 patients, 44 patients were switched to atenolol therapy from propranolol due to adverse events. The response rate of subsequent atenolol treatment was 90.9% (40/44). Regarding AEs, 141 patients reported 177 episodes of AEs, and the pooled rate was 0.26 (95% CI: 0.12-0.47). Gastrointestinal symptoms (e.g. constipation, diarrhoea and vomiting) were the most frequent AEs (22.6%). Widely known propranolol-related AEs, including hypoglycaemia, bronchospasm, bradycardia and hypotension, were not recorded. Overall, atenolol appears to be an effective and safe therapy for the treatment of IH and may be a promising alternative to propranolol.
© 2018 The Australasian College of Dermatologists.

Entities:  

Keywords:  atenolol; efficacy; infantile hemangioma; safety; β-blockers

Mesh:

Substances:

Year:  2018        PMID: 30515761     DOI: 10.1111/ajd.12966

Source DB:  PubMed          Journal:  Australas J Dermatol        ISSN: 0004-8380            Impact factor:   2.875


  5 in total

1.  Atenolol use for infantile hemangiomas.

Authors:  Rosalia Ballona; Felipe Velásquez'; Iris Kikushima; Jean Pierre Zevallos; Jeanette Nuñez; Consuelo Apagüeño
Journal:  Indian J Dermatol Venereol Leprol       Date:  2021 Mar-Apr       Impact factor: 2.545

2.  Using Esterase Selectivity to Determine the In Vivo Duration of Systemic Availability and Abolish Systemic Side Effects of Topical β-Blockers.

Authors:  Jillian G Baker; Christophe Fromont; Marjorie Bruder; Kevin S J Thompson; Barrie Kellam; Stephen J Hill; Sheila M Gardiner; Peter M Fischer
Journal:  ACS Pharmacol Transl Sci       Date:  2020-07-01

3.  An ulcerated giant segmental hemangioma resulting in contracture of the left elbow.

Authors:  Alexander K C Leung; Kin Fon Leong; Joseph M Lam
Journal:  Paediatr Child Health       Date:  2020-04-24       Impact factor: 2.253

4.  Non-beta blocker enantiomers of propranolol and atenolol inhibit vasculogenesis in infantile hemangioma.

Authors:  Caroline T Seebauer; Matthew S Graus; Lan Huang; Alex McCann; Jill Wylie-Sears; Frank Fontaine; Tara Karnezis; David Zurakowski; Steven J Staffa; Frédéric Meunier; John B Mulliken; Joyce Bischoff; Mathias Francois
Journal:  J Clin Invest       Date:  2022-02-01       Impact factor: 14.808

5.  Celecoxib induces adipogenic differentiation of hemangioma-derived mesenchymal stem cells through the PPAR-γ pathway in vitro and in vivo.

Authors:  Yuan Wang; Liangliang Kong; Buhao Sun; Jie Cui; Weimin Shen
Journal:  Exp Ther Med       Date:  2022-04-07       Impact factor: 2.447

  5 in total

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