Bravo Bruna S F, Calvacante Thamires, Nobre Camila Silveira, Bravo Leonardo G, Zafra Maria Carolina, Elias Mariana Calomeni
Department of Dermatology, Bravo Private Clinic, Rio de Janeiro, Brazil.
J Cosmet Dermatol. 2025 Feb;24(2):e16723. doi: 10.1111/jocd.16723. Epub 2024 Dec 12.
Esthetic medicine has shifted significantly toward non-surgical procedures, with the collagen biostimulator poly-l-lactic acid (PLLA) becoming increasingly popular for facial rejuvenation. However, the safety and patient satisfaction associated with PLLA facial treatments remain largely unexplored.
This study aimed to evaluate the safety profile of PLLA treatment and assess patient mid- and long-term satisfaction with the outcome.
This prospective single-center study was conducted at Bravo Clinic in Rio de Janeiro from August 2023 to August 2024. The patients' mid and lower face was treated by injecting Rennova Elleva (a collagen biostimulator containing 210 mg of PLLA) into the zygomatic and pre-masseteric regions. All patients underwent monthly clinical evaluations for the first 150 days and kept diaries to self-record any adverse effects during the first 30 days. Patient satisfaction was measured using the Global Aesthetic Improvement Scale (GAIS) on days 90 and 150 post-injection.
The study included 52 female patients [mean age: 49.87 ± 10.7 years; mean body mass index (BMI): 23.99 ± 3.5 kg/m]. Patients reported mild to moderate injection site reactions, including redness, pain, hardening, swelling, lumps, bruises, and skin discoloration, with most symptoms resolving within a few days. Clinically, no major adverse events were noted, except for one small, painless nodulation that resolved without intervention. On post-injection Day 90, the average GAIS was rated at 2.32 ± 1.0. This rating remained stable at Day 150, with an average GAIS of 2.32 ± 0.8 (p = 0.862). Inverse correlations were identified between the duration of mild pain and GAIS (r = -0.546, p = 0.035), as well as between the duration of mild bruises and GAIS (r = -0.598, p = 0.019). The duration of moderate pain was significantly associated with age (r = -0.894, p = 0.041).
Rennova Elleva, a PLLA-based collagen biostimulator, is safe and well-tolerated with a low incidence of adverse effects. It provides long-lasting, satisfactory results for patients with mild to moderate facial sagging, rendering it an effective non-surgical option for enhancing facial esthetics.
美容医学已显著转向非手术程序,胶原蛋白生物刺激剂聚左旋乳酸(PLLA)在面部年轻化方面越来越受欢迎。然而,与PLLA面部治疗相关的安全性和患者满意度在很大程度上仍未得到充分探索。
本研究旨在评估PLLA治疗的安全性,并评估患者对治疗结果的中长期满意度。
这项前瞻性单中心研究于2023年8月至2024年8月在里约热内卢的布拉沃诊所进行。通过将Rennova Elleva(一种含有210毫克PLLA的胶原蛋白生物刺激剂)注射到颧骨和咬肌前区域来治疗患者的中下面部。所有患者在最初的150天内每月接受临床评估,并在最初的30天内记日记以自我记录任何不良反应。在注射后第90天和第150天使用全球美学改善量表(GAIS)测量患者满意度。
该研究纳入了52名女性患者[平均年龄:49.87±10.7岁;平均体重指数(BMI):23.99±3.5kg/m]。患者报告了轻度至中度的注射部位反应,包括发红、疼痛、硬结、肿胀、肿块、瘀斑和皮肤变色,大多数症状在几天内消退。临床上,除了一个小的、无痛的结节在未干预的情况下自行消退外,未观察到重大不良事件。在注射后第90天,平均GAIS评分为2.32±1.0。在第150天,该评分保持稳定,平均GAIS为2.32±0.8(p = 0.862)。轻度疼痛持续时间与GAIS之间存在负相关(r = -0.546,p = 0.035),轻度瘀斑持续时间与GAIS之间也存在负相关(r = -0.598,p = 0.019)。中度疼痛持续时间与年龄显著相关(r = -0.894,p = 0.041)。
基于PLLA的胶原蛋白生物刺激剂Rennova Elleva安全且耐受性良好,不良反应发生率低。它为轻度至中度面部松弛的患者提供了持久、令人满意的效果,使其成为增强面部美学的一种有效的非手术选择。