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      Propranolol for Treatment of Infantile Hemangioma: Efficacy and Effect on Pediatric Growth and Development

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          Abstract

          Purpose

          Propranolol has been successful in treating problematic infantile hemangiomas (IH) but concerns regarding its effect on normal growth and development have been raised. This study examines physical growth, developmental milestones, and human growth hormone (hGH) levels in infants receiving propranolol for problematic IH.

          Method

          Monthly heights and weights of children undergoing propranolol therapy for IH were prospectively collected and tabulated. Data analysis and comparison to World Health Organization (WHO) weight-for-age and weight-to-length z-scores was performed. Questionnaires regarding milestones, efficacy, and guardian satisfaction were performed, and a combination of both chart results and phone conducted surveys was tabulated. Serum from a small representative cohort of age-matched children with IH treated and not treated with propranolol was collected.

          Results

          A total of 185 children receiving propranolol therapy between 2008 and 2013 for IH were assigned to this study. The children were divided into two cohorts based on the presence of comorbidities or risk factors that may affect growth and development ( n = 142 no comorbidities, n = 43 with comorbidities). Neither cohort demonstrated deviation from normal weight in comparison to WHO normative data. There was a significant deviation for BMI-for-age and weight-for-age z-scores in our population, especially in patients on propranolol for more than 7 months. Based on data from participants, via either completed questionnaires or chart results, most children met their developmental milestones at or before target ages, regardless of the presence of comorbidities. Eighty percent of guardians noticed clinical improvement of the IH, with 91% either happy about or neutral to using the medication. hGH levels were higher in patients receiving propranolol therapy, but not significantly different.

          Conclusion

          Propranolol therapy is effective and well tolerated in the treatment of infantile hemangiomas. This study suggests that propranolol does not impair growth and has no impact on normal pediatric development.

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          Most cited references36

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          A randomized, controlled trial of oral propranolol in infantile hemangioma.

          Oral propranolol has been used to treat complicated infantile hemangiomas, although data from randomized, controlled trials to inform its use are limited.
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            • Abstract: not found
            • Article: not found

            Propranolol for severe hemangiomas of infancy.

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              Initiation and use of propranolol for infantile hemangioma: report of a consensus conference.

              Infantile hemangiomas (IHs) are common neoplasms composed of proliferating endothelial-like cells. Despite the relative frequency of IH and the potential severity of complications, there are currently no uniform guidelines for treatment. Although propranolol has rapidly been adopted, there is significant uncertainty and divergence of opinion regarding safety monitoring, dose escalation, and its use in PHACE syndrome (PHACE = posterior fossa, hemangioma, arterial lesions, cardiac abnormalities, eye abnormalities; a cutaneous neurovascular syndrome characterized by large, segmental hemangiomas of the head and neck along with congenital anomalies of the brain, heart, eyes and/or chest wall). A consensus conference was held on December 9, 2011. The multidisciplinary team reviewed existing data on the pharmacologic properties of propranolol and all published reports pertaining to the use of propranolol in pediatric patients. Workgroups were assigned specific topics to propose protocols on the following subjects: contraindications, special populations, pretreatment evaluation, dose escalation, and monitoring. Consensus protocols were recorded during the meeting and refined after the meeting. When appropriate, protocol clarifications and revision were made and agreed upon by the group via teleconference. Because of the absence of high-quality clinical research data, evidence-based recommendations are not possible at present. However, the team agreed on a number of recommendations that arose from a review of existing evidence, including when to treat complicated IH; contraindications and pretreatment evaluation protocols; propranolol use in PHACE syndrome; formulation, target dose, and frequency of propranolol; initiation of propranolol in infants; cardiovascular monitoring; ongoing monitoring; and prevention of hypoglycemia. Where there was considerable controversy, the more conservative approach was selected. We acknowledge that the recommendations are conservative in nature and anticipate that they will be revised as more data are made available.
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                Author and article information

                Contributors
                Journal
                Int J Pediatr
                Int J Pediatr
                IJPEDI
                International Journal of Pediatrics
                Hindawi
                1687-9740
                1687-9759
                2021
                7 April 2021
                : 2021
                : 6669383
                Affiliations
                1Department of Surgery, Division of Otolaryngology-Head and Neck Surgery, University of Texas Rio Grande Valley School of Medicine, 1201 W University Dr, Edinburg, TX, Canada 78539
                2Department of Otolaryngology-Head and Neck Surgery, University of Arkansas of the Medical Sciences, 4301 W, St Little Rock, Markham, AR, Canada 72205
                3Morsani College of Medicine, Department of Pediatrics, Health Informatics Institute, University of South Florida, 3650 Spectrum Blvd, Tampa, FL 33612, USA
                Author notes

                Academic Editor: Samuel Menahem

                Author information
                https://orcid.org/0000-0003-2234-7649
                https://orcid.org/0000-0001-9273-5415
                https://orcid.org/0000-0002-5421-718X
                https://orcid.org/0000-0003-3423-1213
                Article
                10.1155/2021/6669383
                8049833
                c9f2979a-dda7-4a1e-b446-f3552d7c5e16
                Copyright © 2021 Rachel A. Giese et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 January 2021
                : 10 March 2021
                Categories
                Research Article

                Pediatrics
                Pediatrics

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