Management of tinea capitis in Israel: A comparative study.


Journal

Pediatric dermatology
ISSN: 1525-1470
Titre abrégé: Pediatr Dermatol
Pays: United States
ID NLM: 8406799

Informations de publication

Date de publication:
Jul 2021
Historique:
pubmed: 18 5 2021
medline: 1 9 2021
entrez: 17 5 2021
Statut: ppublish

Résumé

Tinea capitis is a common fungal infection in Israel, most commonly caused by the dermatophyte Trichophyton tonsurans. To investigate the effectiveness of oral antifungal monotherapy in producing clinical or complete cure. We also evaluated the impact of topical therapy (bifonazole 1% shampoo and/or betamethasone valerate 0.1% solution), prior to oral treatment, on patients' likelihood of clinical or complete cure. A retrospective chart review was conducted. Patients with mycologically confirmed tinea capitis were treated with one of four regimens: (1) terbinafine (greater than 40 kg: 250 mg/day, 20 to 40 kg: 125 mg/day, less than 20 kg: 62.5 mg/day), (2) itraconazole 5 mg/kg daily, (3) fluconazole 6 mg/kg daily, or (4) griseofulvin 20 mg/kg daily. We used generalized linear models (GLM) to determine whether there was a significant association between the odds of cure and choice of treatment. The causative species was Trichophyton tonsurans in all but 6 cases that grew T violaceum. For pediatric patients, the odds of having complete or clinical cure within 6 weeks was greater if they used terbinafine compared to itraconazole, fluconazole, or griseofulvin (odds ratio [OR] = 9.06, P = .047). The likelihood of complete or clinical cure within 8 weeks of oral therapy was lower if topical steroids were previously used compared to if topical antifungals were used prior to systemic treatment (OR = 0.29, P = .046). Our findings substantiate prior literature demonstrating that terbinafine is non-inferior to griseofulvin, itraconazole, and fluconazole in the therapy of pediatric tinea capitis caused by T tonsurans.

Sections du résumé

BACKGROUND BACKGROUND
Tinea capitis is a common fungal infection in Israel, most commonly caused by the dermatophyte Trichophyton tonsurans.
OBJECTIVES OBJECTIVE
To investigate the effectiveness of oral antifungal monotherapy in producing clinical or complete cure. We also evaluated the impact of topical therapy (bifonazole 1% shampoo and/or betamethasone valerate 0.1% solution), prior to oral treatment, on patients' likelihood of clinical or complete cure.
METHODS METHODS
A retrospective chart review was conducted. Patients with mycologically confirmed tinea capitis were treated with one of four regimens: (1) terbinafine (greater than 40 kg: 250 mg/day, 20 to 40 kg: 125 mg/day, less than 20 kg: 62.5 mg/day), (2) itraconazole 5 mg/kg daily, (3) fluconazole 6 mg/kg daily, or (4) griseofulvin 20 mg/kg daily. We used generalized linear models (GLM) to determine whether there was a significant association between the odds of cure and choice of treatment.
RESULTS RESULTS
The causative species was Trichophyton tonsurans in all but 6 cases that grew T violaceum. For pediatric patients, the odds of having complete or clinical cure within 6 weeks was greater if they used terbinafine compared to itraconazole, fluconazole, or griseofulvin (odds ratio [OR] = 9.06, P = .047). The likelihood of complete or clinical cure within 8 weeks of oral therapy was lower if topical steroids were previously used compared to if topical antifungals were used prior to systemic treatment (OR = 0.29, P = .046).
CONCLUSIONS CONCLUSIONS
Our findings substantiate prior literature demonstrating that terbinafine is non-inferior to griseofulvin, itraconazole, and fluconazole in the therapy of pediatric tinea capitis caused by T tonsurans.

Identifiants

pubmed: 33998709
doi: 10.1111/pde.14572
doi:

Substances chimiques

Antifungal Agents 0
Naphthalenes 0
Itraconazole 304NUG5GF4
Griseofulvin 32HRV3E3D5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

806-811

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

Avner Shemer (A)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Aditya K Gupta (AK)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Mediprobe Research Inc., London, ON, Canada.
Division of Dermatology, Department of Medicine, University of Toronto School of Medicine, Toronto, ON, Canada.

Eran Galili (E)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Ralph Daniel (R)

University of Mississippi Medical Center and University of Alabama, Birmingham, AL, USA.

Riad Kassem (R)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Renata Farhi (R)

Hospital Nossa Senhora da Saude, University Fundação Tecnico Educacional Souza Marques, Rio de Janeiro, Brazil.

Hadas Grunwald (H)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Mary A Bamimore (MA)

Mediprobe Research Inc., London, ON, Canada.

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Classifications MeSH