Cohort study on the treatment with dapsone 5% gel of mild to moderate inflammatory acne of the face in women

Skinmed. 2014 Jan-Feb;12(1):15-21.

Abstract

Topical dapsone 5% gel for the treatment of mild to moderate acne has been shown to be effective in randomized controlled studies. A total of 101 adult women with mild to moderate facial inflammatory acne participated in a 12-week cohort study to evaluate the efficacy, tolerability, and safety of dapsone gel 5% in this specific group who often complain of sensitive skin. The women were instructed to apply dapsone 5% gel twice daily after washing their face with a standard noncomedogenic soap-free cleanser. Treatment outcome was evaluated using physician-scored Global Acne Assessment Scale (GAAS) and patient-reported facial skin condition. Ninety-three women completed the study (6 were lost to follow-up and 2 had mild skin irritation). At 12 weeks, significant physician GAAS scores (t55 = 8.85, P = .001) and patient-reported lesion reductions were shown. Treatment success (GAAS 0 or 1) at 12 weeks was achieved in 69.4% (n = 75) of women (t94 = 4.17, P = .001), improving patient-reported quality-of-life aspects. Topical dapsone gel 5% was shown to be safe, minimally irritating, and effective in the treatment of mild to moderate inflammatory facial acne in adult women with sensitive skin.

MeSH terms

  • Acne Vulgaris / drug therapy*
  • Acne Vulgaris / pathology
  • Administration, Cutaneous
  • Adolescent
  • Adult
  • Aged
  • Cohort Studies
  • Dapsone / administration & dosage
  • Dapsone / adverse effects
  • Dapsone / therapeutic use*
  • Dermatologic Agents / administration & dosage
  • Dermatologic Agents / adverse effects
  • Dermatologic Agents / therapeutic use*
  • Face
  • Female
  • Follow-Up Studies
  • Gels
  • Humans
  • Inflammation / drug therapy*
  • Inflammation / pathology
  • Middle Aged
  • Quality of Life*
  • Severity of Illness Index
  • Treatment Outcome
  • Young Adult

Substances

  • Dermatologic Agents
  • Gels
  • Dapsone