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Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium
Efinaconazole is a topical antifungal drug approved in Japan for tinea unguium. Although topical treatments generally have low cure rates with a prolonged therapy period, a Cochrane review confirmed that high‐quality evidence supports the effectiveness of efinaconazole for the complete cure of tinea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453900/ https://www.ncbi.nlm.nih.gov/pubmed/34028842 http://dx.doi.org/10.1111/1346-8138.15973 |
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author | Noguchi, Hiromitsu Kubo, Masahide Kashiwada‐Nakamura, Kayo Makino, Katsunari Aoi, Jun Fukushima, Satoshi |
author_facet | Noguchi, Hiromitsu Kubo, Masahide Kashiwada‐Nakamura, Kayo Makino, Katsunari Aoi, Jun Fukushima, Satoshi |
author_sort | Noguchi, Hiromitsu |
collection | PubMed |
description | Efinaconazole is a topical antifungal drug approved in Japan for tinea unguium. Although topical treatments generally have low cure rates with a prolonged therapy period, a Cochrane review confirmed that high‐quality evidence supports the effectiveness of efinaconazole for the complete cure of tinea unguium. Combination therapy is a way to improve the cure rate of onychomycosis. In this study, topical efinaconazole was administrated to 12 patients who had been treated with oral terbinafine (125 mg daily) for more than 20 weeks with little expected effect. Because terbinafine accumulates for a long time in the nail, treatment immediately followed by other drugs can be considered sequential combination therapy. During terbinafine monotherapy, the percentage involvement decreased from 53.5% to 44.0% after 37.4 weeks and the effective and cure rates were 16.7% and 0%, respectively. During sequential topical efinaconazole therapy combined with lasting terbinafine in the nail, the percentage involvement decreased from 44.0% to 18.7% after 28.4 weeks, and the effective and cure rates were 66.7% and 16.7%, respectively. The improvement rate per month of combination therapy (12.6%) was higher than that with monotherapy (2.1%) (p = 0.002). There were no serious side‐effects. This sequential combination therapy with efinaconazole was effective in poor terbinafine responders, making it a promising regimen for improving the cure rate of tinea unguium. |
format | Online Article Text |
id | pubmed-8453900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84539002021-09-27 Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium Noguchi, Hiromitsu Kubo, Masahide Kashiwada‐Nakamura, Kayo Makino, Katsunari Aoi, Jun Fukushima, Satoshi J Dermatol Concise Communications Efinaconazole is a topical antifungal drug approved in Japan for tinea unguium. Although topical treatments generally have low cure rates with a prolonged therapy period, a Cochrane review confirmed that high‐quality evidence supports the effectiveness of efinaconazole for the complete cure of tinea unguium. Combination therapy is a way to improve the cure rate of onychomycosis. In this study, topical efinaconazole was administrated to 12 patients who had been treated with oral terbinafine (125 mg daily) for more than 20 weeks with little expected effect. Because terbinafine accumulates for a long time in the nail, treatment immediately followed by other drugs can be considered sequential combination therapy. During terbinafine monotherapy, the percentage involvement decreased from 53.5% to 44.0% after 37.4 weeks and the effective and cure rates were 16.7% and 0%, respectively. During sequential topical efinaconazole therapy combined with lasting terbinafine in the nail, the percentage involvement decreased from 44.0% to 18.7% after 28.4 weeks, and the effective and cure rates were 66.7% and 16.7%, respectively. The improvement rate per month of combination therapy (12.6%) was higher than that with monotherapy (2.1%) (p = 0.002). There were no serious side‐effects. This sequential combination therapy with efinaconazole was effective in poor terbinafine responders, making it a promising regimen for improving the cure rate of tinea unguium. John Wiley and Sons Inc. 2021-05-24 2021-09 /pmc/articles/PMC8453900/ /pubmed/34028842 http://dx.doi.org/10.1111/1346-8138.15973 Text en © 2021 The Authors. The Journal of Dermatology published by John Wiley & Sons Australia, Ltd on behalf of Japanese Dermatological Association https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Concise Communications Noguchi, Hiromitsu Kubo, Masahide Kashiwada‐Nakamura, Kayo Makino, Katsunari Aoi, Jun Fukushima, Satoshi Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium |
title | Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium |
title_full | Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium |
title_fullStr | Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium |
title_full_unstemmed | Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium |
title_short | Topical efinaconazole: A sequential combination therapy with oral terbinafine for refractory tinea unguium |
title_sort | topical efinaconazole: a sequential combination therapy with oral terbinafine for refractory tinea unguium |
topic | Concise Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453900/ https://www.ncbi.nlm.nih.gov/pubmed/34028842 http://dx.doi.org/10.1111/1346-8138.15973 |
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