Shah Sonal D, Baselga Eulalia, McCuaig Catherine, Pope Elena, Coulie Julien, Boon Laurence M, Garzon Maria C, Haggstrom Anita N, Adams Denise, Drolet Beth A, Newell Brandon D, Powell Julie, García-Romero Maria Teresa, Chute Carol, Roe Esther, Siegel Dawn H, Grimes Barbara, Frieden Ilona J
Departments of Dermatology and
Department of Dermatology, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain;
Pediatrics. 2016 Apr;137(4). doi: 10.1542/peds.2015-1754. Epub 2016 Mar 7.
Propranolol is first-line therapy for problematic infantile hemangiomas (IHs). Rebound growth after propranolol discontinuation is noted in 19% to 25% of patients. Predictive factors for rebound are not completely understood and may alter the management approach. The goal of the study was to describe a cohort of patients with IHs treated with propranolol and to identify predictors for rebound growth.
A multicenter retrospective cohort study was conducted in patients with IHs treated with propranolol. Patient demographic characteristics, IH characteristics, and specifics of propranolol therapy were obtained. Episodes of rebound growth were recorded. Patients' responses to propranolol were evaluated through a visual analog scale.
A total of 997 patients were enrolled. The incidence of rebound growth was 231 of 912 patients (25.3%). Mean age at initial rebound was 17.1 months. The odds of rebound among those who discontinued therapy at <9 months was 2.4 (odds ratio [OR]: 2.4; 95% confidence interval [CI]: 1.3 to 4.5; P = .004) compared with those who discontinued therapy between 12 to 15 months of life. Female gender, location on head and neck, segmental pattern, and deep or mixed skin involvement were associated with rebound on univariate analysis. With multivariate analysis, only deep IHs (OR: 3.3; 95% CI: 1.9 to 6.0; P < .001) and female gender (OR: 1.7; 95% CI: 1.1 to 2.6; P = .03) were associated. Of those with rebound growth, 83% required therapeutic modification including 62% of patients with modifications in their propranolol therapy.
Rebound growth occurred in 25% of patients, requiring modification of systemic therapy in 15%. Predictive factors for rebound growth included age of discontinuation, deep IH component, and female gender. Patients with these predictive factors may require a prolonged course of therapy.
普萘洛尔是治疗婴幼儿血管瘤(IHs)的一线药物。19%至25%的患者在停用普萘洛尔后出现反弹性生长。反弹性生长的预测因素尚未完全明确,可能会改变治疗方法。本研究的目的是描述一组接受普萘洛尔治疗的IHs患者,并确定反弹性生长的预测因素。
对接受普萘洛尔治疗的IHs患者进行了一项多中心回顾性队列研究。获取了患者的人口统计学特征、IH特征以及普萘洛尔治疗的具体情况。记录反弹性生长的发作情况。通过视觉模拟量表评估患者对普萘洛尔的反应。
共纳入997例患者。912例患者中反弹性生长的发生率为231例(25.3%)。首次反弹性生长时的平均年龄为17.1个月。与在12至15个月龄时停药的患者相比,在9个月龄前停药的患者反弹性生长的几率为2.4(比值比[OR]:2.4;95%置信区间[CI]:1.3至4.5;P = 0.004)。单因素分析显示,女性、头颈部位置、节段性模式以及深部或混合性皮肤受累与反弹性生长相关。多因素分析显示,仅深部IHs(OR:3.3;95%CI:1.9至6.0;P < 0.001)和女性(OR:1.7;95%CI:1.1至2.6;P = 0.03)与反弹性生长相关。在出现反弹性生长的患者中,83%需要调整治疗,其中62%的患者调整了普萘洛尔治疗。
25%的患者出现反弹性生长,15%的患者需要调整全身治疗。反弹性生长的预测因素包括停药年龄、深部IH成分和女性。具有这些预测因素的患者可能需要延长治疗疗程。