Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Poostchi Ophthalmology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Ophthalmic Plast Reconstr Surg. 2019 Sep/Oct;35(5):484-486. doi: 10.1097/IOP.0000000000001336.
To evaluate the clinical and ultrasonographic response of periocular infantile capillary hemangioma during treatment with oral propranolol.
Patients with infantile periocular hemangioma and visual or cosmetic concerns were enrolled in this prospective interventional case series. Propranolol was given at a dose of 2 mg/kg per day for at least 6 months. Evaluation of treatment response was performed at month 3 (time point 1) and month 6 (time point 2). Gray scale ultrasonography and color Doppler imaging were performed at baseline and month 3.
Thirty-one patients with mean age of 4.1 ± 2.3 months were eligible for analysis. Complete or near complete clinical resolution was observed in 4 patients (12.9%) at time point 1 and 21 patients (67.7%) at time point 2. Longitudinal diameter, transverse diameter, thickness, arterial peak systolic velocity, and end diastolic velocity reduced significantly from baseline to 3-month follow up. Complete clinical response at time point 2 was significantly higher in patients with peak systolic velocity reduction >50% from baseline to month 3 than patients with peak systolic velocity reduction of 10% to 50% and <10%.
Propranolol is safe and effective for infantile periocular hemangioma. Ultrasonography and color Doppler imaging are useful modalities to monitor and predict the treatment response.
评估口服普萘洛尔治疗眼周婴幼儿毛细血管瘤的临床和超声反应。
本前瞻性干预性病例系列研究纳入了有眼周婴幼儿血管瘤且存在视力或美容问题的患者。普萘洛尔的剂量为 2mg/kg/天,至少治疗 6 个月。在第 3 个月(时间点 1)和第 6 个月(时间点 2)进行治疗反应评估。在基线和第 3 个月进行灰阶超声和彩色多普勒成像。
31 名平均年龄为 4.1±2.3 个月的患者符合分析条件。4 名患者(12.9%)在时间点 1 和 21 名患者(67.7%)在时间点 2观察到完全或接近完全的临床消退。从基线到 3 个月随访时,纵向直径、横向直径、厚度、动脉收缩期峰值速度和舒张末期速度均显著降低。与收缩期峰值速度降低 10%至 50%和<10%的患者相比,收缩期峰值速度降低>50%的患者在时间点 2达到完全临床缓解的比例显著更高。
普萘洛尔治疗眼周婴幼儿血管瘤安全有效。超声和彩色多普勒成像可用于监测和预测治疗反应。