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. 2014 Feb;70(2):369-73.
doi: 10.1016/j.jaad.2013.07.044.

Systematic review of randomized controlled trials on interventions for melasma: an abridged Cochrane review

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Systematic review of randomized controlled trials on interventions for melasma: an abridged Cochrane review

Gurpreet Singh Jutley et al. J Am Acad Dermatol. 2014 Feb.

Abstract

Background: Multiple treatments exist for melasma; they are often substandard and associated with side effects.

Objectives: We sought to assess the effectiveness of interventions used in the management of all types of melasma.

Methods: We undertook a systematic review using the methodology of the Cochrane Collaboration.

Results: We included 20 studies with a total of 2125 participants covering 23 different treatments. A meta-analysis was not possible because of the heterogeneity of treatments. Triple-combination cream (hydroquinone, tretinoin, and fluocinolone acetonide) was more effective at lightening melasma than hydroquinone alone (relative risk 1.58, 95% confidence interval 1.26-1.97) or any of the agents in a dual-combination cream. Azelaic acid (20%) was significantly more effective than 2% hydroquinone (relative risk 1.25, 95% confidence interval 1.06-1.48) at lightening melasma. In 2 studies where tretinoin was compared with placebo, objective measures demonstrated significant reductions in the severity. However, only in 1 study did participants rate a significant improvement (relative risk 13, 95% confidence interval 1.88-89.74).

Limitations: There was poor methodology, a lack of standardized outcome assessments, and short duration of studies.

Conclusions: The current limited evidence supports the efficacy of multiple interventions. Randomized controlled trials on well-defined participants with long-term outcomes are needed.

Keywords: ascorbic acid; azelaic acid; chloasma; glycolic acid; hydroquinone; melasma; pigment; tretinoin; triple combination; vitamin C.

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Republished from

  • Interventions for melasma.
    Rajaratnam R, Halpern J, Salim A, Emmett C. Rajaratnam R, et al. Cochrane Database Syst Rev. 2010 Jul 7;(7):CD003583. doi: 10.1002/14651858.CD003583.pub2. Cochrane Database Syst Rev. 2010. PMID: 20614435

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