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基于透明质酸的真皮填充剂在眶周区域常规使用、疗效及安全性的真实世界证据。

Real-World Evidence on the Routine Use, Efficacy, and Safety of a Hyaluronic Acid-Based Dermal Filler in the Periorbital Region.

作者信息

Bhojani-Lynch Tahera, Shah-Desai Sabrina, Bichet Jean-Christophe, Magalhães Bárbara, Poupard Kevin

机构信息

The Laser and Light Clinic, Loughborough, UK.

Perfect Eyes Ltd., London, UK.

出版信息

Aesthetic Plast Surg. 2025 May 29. doi: 10.1007/s00266-025-04809-9.

Abstract

BACKGROUND

The appearance of the periorbital region is essential in facial aesthetic perception and is a frequent concern of patients seeking rejuvenation. TEOSYAL® PureSense Redensity 2 (R2) has a 10-year track record of effectively and safely treating the under-eye area, specifically the tear trough.

METHODS

A prospective, observational study aimed to investigate the efficacy and safety of R2 in a real-world setting for aesthetic indications. Participants received at least one treatment injection with R2, and investigators followed their routine injection techniques and indications. The primary endpoint was the Global Aesthetic Improvement Scale (GAIS) score recorded 3 months post-injection. Secondary efficacy outcomes included subject and investigator satisfaction, as well as GAIS scores at later timepoints. Safety was monitored by documenting common treatment responses (CTRs) and adverse events (AEs).

RESULTS

The 136 subjects enrolled in EYELIGHT received 958 initial injections, of which 451 (47.1%) were performed with R2: 89 (35.3%) tear trough, 61 (24.2%) palpebromalar groove, 45 (17.9%) outer canthus, 38 (15.1%) crow's feet, and 19 (7.5%) brow. A GAIS improvement of more than 70% was achieved for the tear trough and remaining periorbital indications, with most subjects reporting satisfaction with treatment (84.3%). Treatment effect was observed up to 12 months post-injection. All CTRs were mild or moderate and resolved within a month. No severe AEs were reported.

CONCLUSION

Real-world evidence confirmed the 10-year long success of R2 as an effective and safe treatment of the tear trough. Based on this evidence, its use extends beyond the tear trough, showing effectiveness and safety in the whole periorbital area.

LEVEL OF EVIDENCE III

This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .

摘要

背景

眶周区域的外观在面部美学感知中至关重要,也是寻求面部年轻化的患者经常关注的问题。瑞蓝唯瑅水光2号(R2)在有效且安全地治疗眼周区域,特别是泪沟方面已有10年的记录。

方法

一项前瞻性观察性研究旨在调查R2在实际应用中用于美学适应症的疗效和安全性。参与者接受至少一次R2治疗注射,研究者遵循常规注射技术和适应症。主要终点是注射后3个月记录的全球美学改善量表(GAIS)评分。次要疗效结果包括受试者和研究者的满意度,以及后期时间点的GAIS评分。通过记录常见治疗反应(CTR)和不良事件(AE)来监测安全性。

结果

EYELIGHT研究中纳入的136名受试者接受了958次初始注射,其中451次(47.1%)使用R2进行:泪沟89次(35.3%)、睑颊沟61次(24.2%)、外眦45次(17.9%)、鱼尾纹38次(15.1%)、眉部19次(7.5%)。泪沟和其余眶周适应症的GAIS改善率超过70%,大多数受试者对治疗表示满意(84.3%)。注射后12个月内观察到治疗效果。所有CTR均为轻度或中度,且在一个月内消退。未报告严重AE。

结论

实际应用证据证实了R2在有效且安全地治疗泪沟方面长达10年的成功。基于这一证据,其应用范围超出了泪沟,在整个眶周区域均显示出有效性和安全性。

证据水平III:本刊要求作者为每篇文章指定证据水平。有关这些循证医学评级的完整描述,请参阅目录或在线作者指南www.springer.com/00266

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