Advanced Search

Home > Journals > Giornale Italiano di Dermatologia e Venereologia > Archive > Giornale Italiano di Dermatologia e Venereologia 2012 October;147(5) > Giornale Italiano di Dermatologia e Venereologia 2012 October;147(5):491-7

CURRENT ISSUE   ARCHIVE   EPUB AHEAD OF PRINT   MOST READ


GIORNALE ITALIANO DI DERMATOLOGIA E VENEREOLOGIA

Giornale Italiano di Dermatologia e Venereologia 2012 October;147(5):491-7

 

    ORIGINAL ARTICLES

Efficacy and tolerability of topical 0.2% Myrtacine® and 4% vitamin PP for prevention and treatment of retinoid dermatitis in patients with mild to moderate acne

Veraldi S. 1, Giovene G. L. 2, Guerriero C. 3, Bettoli V. 4

1 Department of Anesthesiology, Intensive Care and Dermatological Sciences, University of Milan, Milan, Italy;
2 Private Practioner, Perugia, Italy;
3 Clinic of Dermatology, Sacro Cuore Catholic University, Rome, Italy;
4 Department of Clinic and Specialistic Medicine, S. Anna University Hospital, Ferrara, Italy

AIM:The aim of the present study was to evaluate the efficacy and tolerability of an emulsion of 0.2% Myrtacine® and 4% vitamin PP, compared with a simple emollient cream, in the treatment of retinoid dermatitis in patients with mild-to-moderate acne.
METHODS:This was a prospective, multicenter, open-label, non-randomised, parallel-group study. Patients (age 12-49 years; skin phototype I-IV) with mild-to-moderate acne, who were treated with a topical retinoid for at least one month and had developed skin irritation were assigned to one of the two following treatments: 0.2% Myrtacine® and 4% vitamin PP (N.=116) or a simple emollient cream (N.=48). Both treatments were administered twice daily, 1-1.5 hours after the application of the topical retinoid. Study endpoints were improvement in signs and symptoms of retinoid dermatitis, global efficacy, reduction in acne severity, overall clinical outcome, patient satisfaction and tolerability.
RESULTS: At day 28, compared with the simple emollient cream, 0.2% Myrtacine® and 4% vitamin PP significantly decreased signs (erythema, dryness/scaling, oedema, and roughness) and symptoms (itching, stinging, burning sensation and discomfort) of retinoid dermatitis (P<0.01). In addition, compared with the simple emollient cream, 0.2% Myrtacine® and 4% vitamin PP decreased acne severity in a significantly greater proportion of patients (P=0.023) and was associated with a better clinical outcome (mild, intermediate, clinically relevant or global improvement; P<0.001). 0.2% Myrtacine® and 4% vitamin PP was also associated with greater patient satisfaction and was better tolerated than the simple emollient cream.
CONCLUSION: 0.2% Myrtacine® and 4% vitamin PP was effective and well tolerated in the treatment of retinoid dermatitis in patients with mild-to-moderate acne and significantly improved acne severity and overall clinical outcome.

language: English


FULL TEXT  REPRINTS

top of page