Suppr超能文献

一项评估 0.05%维 A 酸乳膏用于胸部年轻化的疗效、安全性和患者满意度的前瞻性、随机、双盲、对照研究。

A Prospective, Randomized, Double-Blind, Vehicle-Controlled Study Evaluating the Efficacy, Safety, and Patient Satisfaction of Tretinoin 0.05% Lotion for Chest Rejuvenation.

出版信息

J Drugs Dermatol. 2022 Jun 1;21(6):645-652. doi: 10.36849/JDD.6658.

Abstract

BACKGROUND

There is increasing interest in non-invasive options for chest rejuvenation with minimal to no downtime. Topical retinoids have long been used to correct photoaging due to their ability to promote epidermal hyperplasia, matrix metalloproteinase inhibition, collagen synthesis, and dispersion of melanin granules. Topical retinoid use is often limited by the ensuing irritation that occurs with initial use and resolves after about one month. Vehicle of delivery is a key factor to consider in order to minimize irritation and increase patient satisfaction. Micronized tretinoin 0.05% suspended in a polymer emulsion of hydrating ingredients (sodium hyaluronate, soluble collagen, and glycerin) is designed to aid in reducing irritation while ensuring uniform drug delivery.

OBJECTIVE

The primary objective of our study is to evaluate the safety, efficacy, and patient satisfaction of tretinoin 0.05% lotion for nonprocedural photorejuvenation of the chest.

RESULTS

A total of 29 patients completed the trial, average age of 54.42 years (37-66 years old), Fitzpatrick II-IV skin types. Both the active and vehicle groups showed 30-40% improvement at day 180 according to the blinded evaluator mean percent improvement. Investigator global aesthetic improvement scale also trended towards improvement in both groups, with most patients exhibiting "improvement." Both the active and vehicle groups showed a significant change over time according to the nine-point photodamage and wrinkling scale, P<0.001 and P=0.007 (single factor ANOVA), respectively. The Fabi Bolton Wrinkle Scale also demonstrated improvement from screening to day 180; however, there was no statistical significance at any time point. At day 90, the active group had statistically significantly more erythema than the vehicle group (P<0.001), although both groups were only mild. At day 180, erythema decreased in both groups with the active group being similar to the vehicle group, 0.50±0.73 versus 0.09±0.30, respectively. Subjects in both the active and vehicle groups were equally satisfied at day 180, (2.38±1.15 in the active group versus 2.30±1.16 in the treatment group), with most subjects feeling "satisfied" with their results by day 180. This was also reflected in the subject global aesthetic improvement scale with most subjects noting noticeable improvement in the appearance of their chest from day 30 to day 180.

CONCLUSION

Tretinoin 0.05% lotion delivered in a proprietary blend of hydrating ingredients offers a safe and efficacious option that has minimal downtime for patients seeking non-procedural photo-rejuvenation of the chest. The proprietary vehicle, containing hyaluronic acid, glycerin, and collagen, was crucial in minimizing irritation and producing at least a one-point improvement according to the 9 point photodamage scale and 30-40% improvement in photodamage as noted by the blinded evaluator percent improvement score in both the vehicle and active groups. J Drugs Dermatol. 2022;21(6):645-652. doi:10.36849/JDD.6658.

摘要

背景

人们对微创或非手术的胸部年轻化方法越来越感兴趣,希望其具有最小的恢复期。局部维 A 酸类药物因其能够促进表皮增生、抑制基质金属蛋白酶、促进胶原蛋白合成和分散黑色素颗粒的作用,长期以来一直被用于纠正光老化。但由于初始使用时会出现随之而来的刺激反应,通常会限制其使用,且该反应在大约一个月后会消退。为了尽量减少刺激并提高患者满意度,药物的输送载体是需要考虑的一个关键因素。将 0.05%的微粉化维 A 酸悬浮于水合成分(透明质酸钠、可溶性胶原和甘油)的聚合物乳液中,旨在帮助减少刺激,同时确保药物的均匀输送。

目的

本研究的主要目的是评估 0.05%维 A 酸乳液在非手术性胸部光老化治疗中的安全性、疗效和患者满意度。

结果

共有 29 名患者完成了试验,平均年龄 54.42 岁(37-66 岁),皮肤类型为 Fitzpatrick II-IV 型。根据盲法评估者的平均百分比改善,活性组和载体组在第 180 天均显示出 30-40%的改善。研究者整体美学改善量表也表明两组均有改善趋势,大多数患者表现出“改善”。两组均根据 9 分光损伤和皱纹量表显示出随时间的显著变化,P<0.001 和 P=0.007(单因素方差分析)。Fabi Bolton 皱纹量表也显示出从筛查到第 180 天的改善;然而,在任何时间点均无统计学意义。第 90 天时,活性组的红斑比载体组更明显(P<0.001),尽管两组均为轻度。第 180 天时,两组的红斑均减少,活性组与载体组相似,分别为 0.50±0.73 与 0.09±0.30。第 180 天时,活性组和载体组的患者满意度相当(活性组为 2.38±1.15,治疗组为 2.30±1.16),大多数患者在第 180 天对结果感到“满意”。这也反映在受试者的整体美学改善量表中,大多数受试者在第 30 天至第 180 天注意到胸部外观有明显改善。

结论

含有透明质酸、甘油和胶原的专有配方的 0.05%维 A 酸乳液为寻求微创胸部光老化治疗的患者提供了一种安全有效的选择,其恢复期很短。专有载体在减少刺激方面至关重要,根据 9 分光损伤量表和盲法评估者的百分比改善评分,活性组和载体组均显示出至少 1 分的改善,以及 30-40%的光损伤改善。J 皮肤病学杂志。2022;21(6):645-652。doi:10.36849/JDD.6658.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验