Friday, September 3, 2010

Using Benzoyl Peroxide and Clindamycin

Quality of life is significantly improved in patients who are treated with a benzoyl peroxide 5% plus clindamycin 1% (BPO/C) gel, compared with those receiving adapalene 0.1% (AP) gel for mild to moderate acne, researchers reported here at the 18th Congress of the European Academy of Dermatology and Venereology (EADV).

In addition, BPO/C treatment resulted in a greater reduction in the number of both inflammatory and total lesions, beginning at 2 weeks of treatment.

Aurora Guerra-Tapia, MD, Hospital Universitario, Madrid, Spain, reported the results of a comparative, multicentre, investigator-blinded, randomised, parallel-group study here on October 9.

Researchers compared the improvement in quality-of-life scores of patients who received BPO/C and those who received AP gel for treatment of mild to moderate facial acne using the Skindex-29, which evaluates 3 domains: emotional, functional, and symptomatic.

Secondary endpoints included lesion reduction, tolerability, and safety.

The study included 168 patients who were randomised to receive either BPO/C gel or AP gel.

Beginning in the second week of the study, the change from baseline in the mean global Skindex-29 score was -4.9 in the BPO/C arm, compared with -0.9 for the AP group (P = .001). At week 12, the change in Skindex-29 score was -7.25 in the BPO/C arm as compared with -2.4 for the AP group (P = .001).

Total lesion number was more reduced in every time point favouring BPO/C treatment over AP (P <= .01).

The proportion of patients with an overall tolerance score of “excellent” was higher in the BPO/C group. Overall tolerance was significantly better at week 12 in the BPO/C group (P <= .01). However, the majority of adverse events were reported by patients in the AP group.

The authors concluded that a significantly better quality-of-life trend began at week 2 and continued throughout the study that was documented in subjects treated with topical BPO/C gel. This improvement in quality of life was likely the result of the superior efficacy and tolerability profiles seen with BPO/C treatment and also due to the more rapid onset of activity of BPO/C.

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