Department of Dermatology and Venerology, Ibn Rochd University Hospital of Casablanca, Morocco.
Department of Dermatology and Venerology, Ibn Rochd University Hospital of Casablanca, Morocco.
Arch Pediatr. 2023 Oct;30(7):455-457. doi: 10.1016/j.arcped.2023.06.004. Epub 2023 Jun 30.
Propranolol is the first-line treatment for infantile hemangiomas (IH). Cases of propranolol-resistant infantile hemangiomas are rarely reported. The purpose of our study was to investigate the predictive factors for poor response to propranolol.
A prospective analytical study was conducted between January 2014 and January 2022 including all patients with IH who received oral propranolol therapy at a dose of 2-3 mg/kg/day maintained for at least 6 months.
A total of 135 patients with IH were treated with oral propranolol. Poor response was reported in 18 (13.4%) of the patients: 72% were girls and 28% were boys. Overall, 84% of the IH were mixed, and hemangiomas were multiple in three cases (16%), nasal tip hemangiomas accounted for four cases (22%), and 15 patients (83%) had segmental hemangiomas. There was no significant association between the age or sex of the children and type of response to treatment (p > 0.05). No significant association was found between the type of hemangioma and the therapeutic outcome as well as the recurrence after treatment discontinuation (p > 0.05). Multivariate logistic regression analysis revealed that nasal tip hemangiomas, multiple hemangiomas, and segmental hemangiomas were at greater risk of poor response to beta-blockers (p < 0.05).
Poor response to propranolol therapy has rarely been reported in the literature. In our series, it was approximately 13.4%. To our knowledge, no previous publications have focused on the predictive factors of poor response to beta-blockers. However, the reported risk factors for recurrence are discontinuation of treatment before 12 months of age, mixed or deep type IH, and female gender. In our study, the predictive factors for poor response were multiple type IH, segmental type IH, and location on the nasal tip.
普萘洛尔是治疗婴幼儿血管瘤(IH)的一线药物。普萘洛尔耐药性婴幼儿血管瘤的病例很少见报道。本研究旨在探讨普萘洛尔治疗反应不良的预测因素。
这是一项 2014 年 1 月至 2022 年 1 月进行的前瞻性分析研究,纳入了所有接受 2-3mg/kg/天剂量的口服普萘洛尔治疗、至少持续 6 个月的 IH 患者。
共 135 例 IH 患儿接受口服普萘洛尔治疗,18 例(13.4%)患儿治疗反应不佳:女孩占 72%,男孩占 28%。总体而言,84%的 IH 为混合性,3 例(16%)为多发性,鼻尖部血管瘤 4 例(22%),15 例(83%)为节段性血管瘤。儿童年龄或性别与治疗反应类型之间无显著相关性(p>0.05)。血管瘤类型与治疗结果以及治疗停止后复发之间也无显著相关性(p>0.05)。多变量逻辑回归分析显示,鼻尖部血管瘤、多发性血管瘤和节段性血管瘤对β受体阻滞剂的反应不良风险更高(p<0.05)。
文献中很少有报道普萘洛尔治疗反应不良。在我们的系列中,约为 13.4%。据我们所知,以前没有文献专门针对β受体阻滞剂治疗反应不良的预测因素进行研究。然而,报告的复发的预测因素为 12 个月前停药、混合或深部型 IH 以及女性。在本研究中,反应不良的预测因素为多发性、节段性和鼻尖部血管瘤。