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一项关于小凝胶颗粒透明质酸丰唇效果和安全性的随机、评估者盲法、对照研究。

A randomized, evaluator-blinded, controlled study of the effectiveness and safety of small gel particle hyaluronic acid for lip augmentation.

机构信息

San Francisco Dermatology, 350 Parnassus Ave, Suite 400, San Francisco, CA 94117, USA.

出版信息

Dermatol Surg. 2012 Jul;38(7 Pt 2):1180-92. doi: 10.1111/j.1524-4725.2012.02473.x.

Abstract

OBJECTIVES

To assess the effectiveness and safety of small gel particle hyaluronic acid (SGP-HA) for lip augmentation.

METHODS

Adults (n = 180; aged 18-65) scoring 1 (very thin) to 2 (thin) on the 5-point validated Medicis Lip Fullness Scale (MLFS) for the upper or lower lip were randomized (3:1) to SGP-HA (≤1.5 mL/lip) or no treatment. Co-primary effectiveness end points were blinded-evaluator MLFS score for upper or lower lip at week 8. Secondary end points (MLFS score, independent photographic review, Global Aesthetic Improvement Scale [GAIS], safety assessments) were measured throughout the study.

RESULTS

Statistically significantly more MLFS responders (≥1 grades of MLFS improvement at week 8) received SGP-HA (93% combined upper and lower lip responders [95% upper lip; 94% lower lip]) than no treatment (29% combined; p < .001). SGP-HA improved self-assessed combined lip GAIS (97% week 8; 74% week 24) significantly more than no treatment (0% throughout; p < .001). The SGP-HA group reported anticipated swelling (58%) and bruising (44%), 88% mild or 11% moderate severity, without unanticipated device adverse events.

CONCLUSIONS

SGP-HA is highly effective and well tolerated for lip augmentation. Statistically significant improvement was evident based on the MLFS at 8 weeks, with visible results reported in the majority of participants 6 months after treatment.

摘要

目的

评估小凝胶颗粒透明质酸(SGP-HA)用于丰唇的效果和安全性。

方法

成人(n=180;年龄 18-65 岁)的上唇或下唇经 Medis 唇部丰满度评分(MLFS)评估为 1(非常薄)至 2(薄)的患者,按 3:1 随机分组接受 SGP-HA(≤1.5mL/唇)或不治疗。主要疗效终点为第 8 周时上唇或下唇盲法评估者的 MLFS 评分。次要终点(MLFS 评分、独立照片评估、整体美观改善评分[GAIS]、安全性评估)在整个研究期间进行测量。

结果

在第 8 周时,更多的 MLFS 应答者(MLFS 改善≥1 级)接受了 SGP-HA 治疗(93%的上唇和下唇联合应答者[95%的上唇;94%的下唇]),而非不治疗(29%的联合应答者;p<0.001)。与不治疗组相比(整个研究过程中均为 0%),SGP-HA 显著改善了自我评估的联合唇部 GAIS(97%在第 8 周;74%在第 24 周)(p<0.001)。SGP-HA 组报告预期肿胀(58%)和瘀伤(44%),88%为轻度或 11%为中度,没有意外的器械不良事件。

结论

SGP-HA 用于丰唇效果显著且耐受性良好。在第 8 周时基于 MLFS 显示出明显的改善,治疗后 6 个月大多数患者报告了可见的效果。

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