Randomized, placebo-controlled, double-blind study of oral tranexamic acid in the treatment of moderate-to-severe melasma

被引:105
作者
Del Rosario, Eunice [1 ]
Florez-Pollack, Stephanie [1 ]
Zapata, Lucio, Jr. [1 ]
Hernandez, Katia [1 ]
Tovar-Garza, Andrea [1 ]
Rodrigues, Michelle [5 ,6 ,7 ]
Hynan, Linda S. [2 ,3 ,4 ]
Pandya, Amit G. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Dermatol, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Clin Sci, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr Dallas, Dept Biostat, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Psychiat, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[5] St Vincents Hosp, Dept Dermatol, Melbourne, Vic, Australia
[6] Skin & Canc Fdn Inc, Melbourne, Vic, Australia
[7] Royal Childrens Hosp, Melbourne, Vic, Australia
关键词
evidence-based medicine; Hispanic; melanin; melasma; pigmentation; randomized controlled trial; tranexamic acid; MELANOGENESIS; VALIDATION; EFFICACY; TRIAL;
D O I
10.1016/j.jaad.2017.09.053
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Background: Melasma is a common pigmentary disorder that is often difficult to treat. Tranexamic acid (TA) has emerged as a promising treatment for melasma; however, few controlled studies exist. Objective: To determine the efficacy of oral TA in patients with moderate-to-severe melasma. Methods: Patients with moderate-to-severe melasma were treated with 250 mg of TA or placebo capsules twice daily for 3 months and sunscreen followed by 3 months of treatment with sunscreen only. The primary outcome measure was the modified Melasma Area and Severity Index (mMASI) score. Results: A total of 44 patients were enrolled and 39 completed the study. At 3 months, there was a 49% reduction in mMASI score in the TA group versus 18% in the control group. Patients with severe melasma improved more than those with moderate melasma. Three months after treatment was stopped, there was a 26% reduction in mMASI score in the TA group compared with the baseline visit versus a 19% reduction in the placebo arm. No serious adverse events were noted in either group. Limitations: Single-center study enrolling predominantly Hispanic women. Conclusions: Oral TA appears to be an effective treatment for moderate-to-severe melasma with minimal side effects.
引用
收藏
页码:363 / 369
页数:7
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