dEBM, Klinik für Dermatologie, Charité-Universitätsmedizin, Berlin, Germany.
J Eur Acad Dermatol Venereol. 2010 Jan;24 Suppl 1:1-14. doi: 10.1111/j.1468-3083.2009.03475.x.
Azzalure (Galderma) is a newly approved European botulinum neurotoxin type A (BoNT-A) specifically designed for aesthetic usages. It is sourced from Dysport (Ipsen Ltd.), which has a 20-year product consistency and has been used widely for various therapeutic and aesthetic applications. Azzalure and Dysport are collectively referred to as BoNT-A (Speywood Unit; s.U) (or abobotulinumtoxinA in the U.S.) after their biological activity unit, which is unique and not interchangeable with units of other commercial BoNT-A preparations. Azzalure is approved for the treatment of moderate-to-severe glabellar lines, with a total dose of 50 s.U distributed evenly among 5 injection points. To ensure optimal treatment outcomes with BoNT-A (s.U), it is crucial for injectors to adopt proper methods of reconstitution and injection, which can be acquired through training. We review here the method of reconstitution for BoNT-A (s.U), as well as the injection dose, points and techniques for glabellar line treatment. We also review the efficacy and safety results of BoNT-A (s.U) demonstrated in 11 clinical studies, most of which were randomized, double-blind and placebo-controlled. The studies included assessments after single injections as well as after up to 6 repeated treatment sessions. We summarize the clinical efficacy results, which include the responder rate 1 month post-injection, onset of response and duration of action, as well as safety results, which include incidence of treatment-emergent adverse events and specifically eyelid ptosis. The efficacy and safety profiles reported here are unique to BoNT-A (s.U) and cannot be generalized to other BoNT-A products.
吉适(高德美)是一种新批准的欧洲型 A 型肉毒毒素(BoNT-A),专门用于美容用途。它源自丽舒妥(益普生有限公司),具有 20 年的产品一致性,已广泛用于各种治疗和美容应用。阿泽拉和丽舒妥统称为 BoNT-A(斯佩伍德单位;s.U)(在美国称为 abobotulinumtoxinA),这是因为它们的生物学活性单位是独特的,不能与其他商业 BoNT-A 制剂的单位互换。阿泽拉获准用于治疗中度至重度眉间纹,总剂量为 50s.U,均匀分布在 5 个注射点。为了确保 BoNT-A(s.U)的最佳治疗效果,注射者采用适当的复溶和注射方法至关重要,这些方法可以通过培训获得。我们在此回顾 BoNT-A(s.U)的复溶方法,以及眉间线治疗的注射剂量、注射点和技术。我们还回顾了 11 项临床研究中展示的 BoNT-A(s.U)的疗效和安全性结果,其中大多数是随机、双盲和安慰剂对照研究。这些研究包括单次注射后的评估以及最多 6 次重复治疗后的评估。我们总结了临床疗效结果,包括注射后 1 个月的应答率、起效时间和作用持续时间,以及安全性结果,包括治疗中出现的不良事件发生率和特发性眼睑下垂。这里报告的疗效和安全性概况是 BoNT-A(s.U)所特有的,不能推广到其他 BoNT-A 产品。