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Tytuł pozycji:

An open-label efficacy pilot study with pimecrolimus cream 1% in adults with facial seborrhoeic dermatitis infected with HIV.

Tytuł:
An open-label efficacy pilot study with pimecrolimus cream 1% in adults with facial seborrhoeic dermatitis infected with HIV.
Autorzy:
de Moraes AP; São José Hospital of Infectious Diseases, Ceará, Brazil. />de Arruda EA
Vitoriano MA
de Moraes Filho MO
Bezerra FA
de Magalhães Holanda E
de Moraes ME
Źródło:
Journal of the European Academy of Dermatology and Venereology : JEADV [J Eur Acad Dermatol Venereol] 2007 May; Vol. 21 (5), pp. 596-601.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Publication: Oxford : Wiley-Blackwell
Original Publication: Amsterdam ; New York : Elsevier Science Publishers, c1992-
MeSH Terms:
Dermatitis, Seborrheic/*drug therapy
Dermatologic Agents/*therapeutic use
Facial Dermatoses/*drug therapy
HIV Infections/*complications
Tacrolimus/*analogs & derivatives
Administration, Topical ; Adult ; Dermatitis, Seborrheic/complications ; Dermatologic Agents/administration & dosage ; Facial Dermatoses/complications ; Female ; Humans ; Male ; Middle Aged ; Ointments ; Pilot Projects ; Recurrence ; Tacrolimus/administration & dosage ; Tacrolimus/therapeutic use ; Treatment Outcome
Substance Nomenclature:
0 (Dermatologic Agents)
0 (Ointments)
7KYV510875 (pimecrolimus)
WM0HAQ4WNM (Tacrolimus)
Entry Date(s):
Date Created: 20070424 Date Completed: 20070628 Latest Revision: 20141120
Update Code:
20240104
DOI:
10.1111/j.1468-3083.2006.01923.x
PMID:
17447972
Czasopismo naukowe
Background: Seborrhoeic dermatitis (SD) is a common dermatosis in human immunodeficiency virus (HIV)-positive patients, many of whom do not respond satisfactorily to conventional topical treatments such as corticosteroids and antifungals.
Objective: A pilot study to investigate the efficacy and tolerability of pimecrolimus cream 1% in HIV-positive patients with facial SD.
Methods: In a single-centre study, 21 HIV-infected patients with mild to severe SD were treated twice daily with pimecrolimus cream 1% for 14 days. Thereafter, treatment was discontinued and patients followed up for 5 weeks. Skin involvement at baseline and on days 7, 14, 21, 35 and 49 was assessed using a four-point clinical score and digital photography.
Main Outcome Measures: Efficacy and safety of pimecrolimus cream 1% treatment and incidence of relapse in the follow-up phase. Results Marked improvement was seen in clinical parameters at day 7, with >or= 90% patients clear of symptoms at day 14. Relapse was observed at day 35 but signs were milder than at baseline. All patients responded to therapy, despite their immunological status. Pimecrolimus did not alter CD4(+) and CD8(+) T-cell counts or viral load during the treatment period.
Conclusion: Pimecrolimus cream represents a new, effective therapeutic option for facial SD in HIV patients.

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