Division of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Pediatric Nephrology Unit, Dana-Dwek Children's Hospital, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Dermatol Ther. 2022 Nov;35(11):e15870. doi: 10.1111/dth.15870. Epub 2022 Oct 11.
Treating infantile hemangiomas with oral propranolol may be initiated in accordance with various protocols some require hospitalization. However, different adverse events have been reported during treatment, thus it is of special importance to find a protocol which is both safe and feasible. We performed a retrospective cohort study of all cases of infantile hemangiomas treated with oral propranolol at our institute between January 2010 and February 2020. Pretreatment evaluation consisted of pediatric cardiologist evaluation including electrocardiography and echocardiography. The propranolol starting dosage was 0.5 mg/kg bid; 2 weeks later the dosage was escalated to 1 mg/kg bid. During the initiation and escalation visits, heart rate and blood pressure were measured before and every hour for a total of 3 h, and blood glucose level was measured within the first hour of treatment. A total of 131 children were treated during the study period. Scalp, facial and genital region infantile hemangiomas were more prevalent in regard to their relative body surface area. No symptomatic bradycardia, hypotension, hypoglycemia, or any other adverse events were documented; few patients had asymptomatic bradycardia and hypotension, which were more common in infants below 6-months of age. Only one patient had asymptomatic hypoglycemia, not requiring any intervention. Initiation and escalation of propranolol treatment for infantile hemangiomas proved to be safe, and without symptomatic adverse effects. However, considering the young age of the patients and the possible asymptomatic adverse reactions, we recommend the following simple protocol as presented, for pretreatment evaluation and short monitoring during treatment initiation and dose escalation.
采用口服普萘洛尔治疗婴儿血管瘤,可依据不同方案进行,部分方案可能需要住院。然而,在治疗过程中已报道了不同的不良反应,因此,找到既安全又可行的方案尤为重要。我们对 2010 年 1 月至 2020 年 2 月期间在我院接受口服普萘洛尔治疗的所有婴儿血管瘤病例进行了回顾性队列研究。治疗前评估包括儿科心脏病专家评估,包括心电图和超声心动图。普萘洛尔起始剂量为 0.5mg/kg,bid;2 周后剂量增至 1mg/kg,bid。在起始和递增就诊期间,在治疗前和每小时测量一次心率和血压,共 3 小时,并在治疗的第一个小时内测量血糖水平。研究期间共治疗了 131 例儿童。头皮、面部和生殖器区域的婴儿血管瘤,就其相对体表面积而言更为常见。未记录到有症状的心动过缓、低血压、低血糖或任何其他不良反应;少数患者有无症状的心动过缓及低血压,这在 6 个月以下的婴儿中更为常见。仅有 1 例患者出现无症状性低血糖,无需任何干预。婴儿血管瘤普萘洛尔起始和递增治疗是安全的,无有症状的不良反应。然而,考虑到患者年龄较小,以及可能出现无症状的不良反应,我们建议采用如下简化方案,用于治疗前评估和治疗起始及剂量递增期间的短期监测。