Department of Dermatology, Rambam Health Care Campus, Haifa, Israel.
Lübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Dermatol Ther. 2021 May;34(3):e14936. doi: 10.1111/dth.14936. Epub 2021 Mar 23.
Propranolol emerged as the first-line therapy for infantile hemangioma (IH). Determinants of interindividual variation in drug response and predictors of rebound growth after drug discontinuation are yet to be firmly established. We aimed to evaluate the outcomes of a relatively large cohort of patients with IH treated by propranolol and to determine predictors of (a) an excellent response to treatment (≥90 improvement) and (b) of rebound growth after drug cessation. A retrospective cohort study was conducted to follow all patients with IH receiving systemic propranolol in a referral center-based specialized clinic. Multivariate logistic regression analysis was performed to identify predictors of excellent response and rebound growth. The study included 206 patients who completed oral propranolol treatment. The mean (SD) age in which the drug was initiated was 4.8 (3.1) months. The average improvement rate was estimated at 85.5 (13.8)%. Initiation of propranolol at the age of 0 to 3 (adjusted odds ratio [OR], 3.43; 95% confidence interval [CI], 1.25-9.40; P = .016) and 3 to 6 (adjusted OR, 3.71; 95% CI, 1.50-9.19; P = .005) months was associated with an increased likelihood of excellent response. Twenty-four (11.7%) patients developed rebound growth following cessation of propranolol. No significant predictors of rebound were identified in the multivariate analysis. Eleven (5.3%) patients experienced mild adverse events, which necessitated drug discontinuation in only two (1.0%) patients. Propranolol is highly effective and safe based on the real-life experience of a referral center for IH. The current study supports early initiation of propranolol.
普萘洛尔成为治疗婴儿血管瘤(IH)的一线治疗药物。药物反应的个体间差异的决定因素和停药后反弹生长的预测因素尚未得到明确确立。我们旨在评估接受普萘洛尔治疗的相对大量 IH 患者的结果,并确定(a)治疗反应良好(≥90改善)和(b)停药后反弹生长的预测因素。进行了一项回顾性队列研究,以随访在基于转诊中心的专门诊所接受全身普萘洛尔治疗的所有 IH 患者。进行多变量逻辑回归分析以确定良好反应和反弹生长的预测因素。该研究包括 206 名完成口服普萘洛尔治疗的患者。开始使用药物的平均(SD)年龄为 4.8(3.1)个月。平均改善率估计为 85.5(13.8)%。0 至 3 个月(调整后的优势比[OR],3.43;95%置信区间[CI],1.25-9.40;P =.016)和 3 至 6 个月(调整后的 OR,3.71;95% CI,1.50-9.19;P =.005)时开始使用普萘洛尔与良好反应的可能性增加相关。24 名(11.7%)患者在停止使用普萘洛尔后出现反弹生长。在多变量分析中未发现反弹的显著预测因素。11 名(5.3%)患者出现轻度不良反应,仅两名(1.0%)患者需要停药。根据 IH 转诊中心的实际经验,普萘洛尔具有高度的有效性和安全性。目前的研究支持早期开始使用普萘洛尔。