Department of Otolaryngology-Head and Neck Surgery, Medical University of South Carolina, Charleston, SC, USA.
Ann Otol Rhinol Laryngol. 2023 Mar;132(3):332-340. doi: 10.1177/00034894221089758. Epub 2022 Apr 25.
Although propranolol has been established as the gold standard when treatment is sought for infantile hemangioma, concerns over its side effect profile have led to increasing usage of atenolol, a beta-1 selective blocker.
A systematic review of PubMed, Scopus, CINAHL, Google Scholar, and Cochrane was conducted following PRISMA guidelines using MeSH terms and keywords for the terms propranolol, atenolol, and infantile hemangioma, including alternative spellings. All randomized control trials (RCTs) or cohort studies directly comparing outcomes of hemangioma treatment with atenolol and propranolol were included. A meta-analysis with pooled mean differences, pooled odds ratios, and analysis of proportions was performed.
A total of 669 participants in 7 studies (3 RCTs and 4 cohort) were included. Propranolol showed a significantly higher rate of complete response compared to atenolol (73.3% vs 85.4%, = .0004). The pooled mean difference of 0.07 (95% CI -0.12, 0.27) in Hemangioma Activity Score (HAS) was not statistically significant. In terms of side effects, there were significantly more agitation and bronchial hyperreactivity events in the propranolol group ( = .0245 and < .0001, respectively). Overall, there was a significantly greater number of adverse events in the propranolol group compared to the atenolol group (185 vs 117, < .00001). The overall pooled odds ratio was 2.70 (95% CI 1.90, 3.84), indicating that there is 2.7 times higher odds of adverse events in the propranolol group.
Propranolol treatment leads to a significantly higher rate of complete response than atenolol. However, its use must be weighed against its greater side effect profile.
虽然普萘洛尔已被确立为治疗婴儿血管瘤的金标准,但由于对其副作用的担忧,越来越多的人开始使用β-1 选择性阻滞剂阿替洛尔。
按照 PRISMA 指南,使用 PubMed、Scopus、CINAHL、Google Scholar 和 Cochrane 进行了系统评价,使用了 MeSH 术语和“普萘洛尔”、“阿替洛尔”和“婴儿血管瘤”的关键词,包括替代拼写。所有直接比较阿替洛尔和普萘洛尔治疗血管瘤结局的随机对照试验(RCT)或队列研究均被纳入。采用合并均数差、合并优势比和比例分析进行荟萃分析。
共有 7 项研究(3 项 RCT 和 4 项队列研究)的 669 名参与者被纳入。与阿替洛尔相比,普萘洛尔的完全缓解率显著更高(73.3% vs 85.4%,= 0.0004)。在血管瘤活动评分(HAS)方面,0.07 的合并均数差值(95%CI -0.12,0.27)无统计学意义。在副作用方面,普萘洛尔组出现激惹和支气管高反应性的事件明显更多(= 0.0245 和 < 0.0001)。总体而言,普萘洛尔组的不良事件明显多于阿替洛尔组(185 例 vs 117 例,< 0.00001)。普萘洛尔组的总体汇总优势比为 2.70(95%CI 1.90,3.84),表明普萘洛尔组不良事件的发生几率高 2.7 倍。
与阿替洛尔相比,普萘洛尔治疗可显著提高完全缓解率。然而,必须权衡其更大的副作用谱。