Price A, Rai S, Mcleod R W J, Birchall J C, Elhassan H A
Wound Healing Research Unit, Cardiff University, Cardiff, UK.
School of Medicine, Cardiff University, Cardiff, UK.
J Eur Acad Dermatol Venereol. 2018 Dec;32(12):2083-2089. doi: 10.1111/jdv.14963. Epub 2018 May 3.
Infantile haemangiomas are the most common tumour of infancy. Whilst the majority are left untreated to involute spontaneously, residual skin changes commonly occur, particularly in superficial haemangiomas. The current first-line treatment for problematic lesions is oral propranolol; however due to the risk of systemic adverse effects, the use of off-label topical preparations has recently been investigated. Our systematic review was conducted in accordance with PRISMA guidelines. Four databases were searched to identify original articles evaluating the use of topical propranolol as the primary therapy for infantile haemangiomas. Twelve articles with a total of 597 patients and 632 haemangiomas were included. Three topical propranolol preparations were used, creams, ointments and gels and were all prepared by local pharmaceutical laboratories. The concentration of propranolol ranged from 0.5% to 5%. Treatment duration ranged from two weeks to 16.5 months. Overall, 90% of lesions improved following the initiation of topical propranolol. A good or excellent response, defined as a reduction in the size of at least 50%, was seen in 59% of lesions. Earlier initiation of treatment (less than 3 months of age) was associated with improved outcomes. No systemic adverse effects were reported. Minor local reactions were seen in 1.3% of patients. Topical propranolol is safer than oral propranolol, though may be less effective. Topical propranolol may be more suitable for patients with small, superficial haemangiomas at risk of cosmetic sequelae, where the cosmetic or symptomatic impact does not warrant oral propranolol treatment.
婴儿血管瘤是婴儿期最常见的肿瘤。虽然大多数血管瘤无需治疗即可自行消退,但通常会留下皮肤改变,尤其是浅表性血管瘤。目前,针对有问题的病变,一线治疗方法是口服普萘洛尔;然而,由于存在全身不良反应的风险,最近人们对使用非标签外用制剂进行了研究。我们的系统评价是按照PRISMA指南进行的。检索了四个数据库,以确定评估外用普萘洛尔作为婴儿血管瘤主要治疗方法的原始文章。纳入了12篇文章,共597例患者和632个血管瘤。使用了三种外用普萘洛尔制剂,乳膏、软膏和凝胶,均由当地制药实验室配制。普萘洛尔的浓度范围为0.5%至5%。治疗持续时间为两周至16.5个月。总体而言,外用普萘洛尔治疗后90%的病变有所改善。59%的病变出现了良好或极佳的反应,即尺寸至少缩小50%。早期开始治疗(年龄小于3个月)与更好的治疗效果相关。未报告全身不良反应。1.3%的患者出现轻微局部反应。外用普萘洛尔比口服普萘洛尔更安全,尽管效果可能较差。外用普萘洛尔可能更适合那些有美容后遗症风险的小型浅表性血管瘤患者,其美容或症状影响不足以进行口服普萘洛尔治疗。