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Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study
BACKGROUND: Rosacea is a chronic inflammatory disease which requires treatment to maintain remission. OBJECTIVE: Recently, the effect of Demodex mites in recurrence of rosacea has been described. Although there is limited data, previous reports have suggested that oral metronidazole demonstrated eff...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Dermatological Association; The Korean Society for Investigative Dermatology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763916/ https://www.ncbi.nlm.nih.gov/pubmed/36478427 http://dx.doi.org/10.5021/ad.22.093 |
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author | Kim, Jin Soo Seo, Byeong Hak Cha, Doo Rae Suh, Ho Seok Choi, Yu Sung |
author_facet | Kim, Jin Soo Seo, Byeong Hak Cha, Doo Rae Suh, Ho Seok Choi, Yu Sung |
author_sort | Kim, Jin Soo |
collection | PubMed |
description | BACKGROUND: Rosacea is a chronic inflammatory disease which requires treatment to maintain remission. OBJECTIVE: Recently, the effect of Demodex mites in recurrence of rosacea has been described. Although there is limited data, previous reports have suggested that oral metronidazole demonstrated efficacy in treatment of rosacea. METHODS: Fifty-eight Korean patients with rosacea who received treatment with oral minocycline (50 mg twice daily) only or with two-week of oral metronidazole (250 mg thrice daily) were evaluated retrospectively. Their responses were evaluated by Investigator’s Global Assessment (IGA), Clinician’s Erythema Assessment (CEA), and patient’s Global Assessment. The recurrence rate and odds ratio of risk factors for recurrence were also estimated. RESULTS: The combination treatment group reported earlier clinical improvement and lower mean IGA and CEA than the monotherapy group. Approximately 48% of patients with combination treatment did not show relapse within 24 weeks, which is significantly higher than that in the monotherapy group (p=0.042). CONCLUSION: Add-on therapy of oral metronidazole appeared to be a significant protective factor for recurrence of rosacea (p<0.05). This study suggests that oral metronidazole can be added to oral minocycline to reduce relapses in rosacea patients with tolerable safety. |
format | Online Article Text |
id | pubmed-9763916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Dermatological Association; The Korean Society for Investigative Dermatology |
record_format | MEDLINE/PubMed |
spelling | pubmed-97639162023-01-03 Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study Kim, Jin Soo Seo, Byeong Hak Cha, Doo Rae Suh, Ho Seok Choi, Yu Sung Ann Dermatol Original Article BACKGROUND: Rosacea is a chronic inflammatory disease which requires treatment to maintain remission. OBJECTIVE: Recently, the effect of Demodex mites in recurrence of rosacea has been described. Although there is limited data, previous reports have suggested that oral metronidazole demonstrated efficacy in treatment of rosacea. METHODS: Fifty-eight Korean patients with rosacea who received treatment with oral minocycline (50 mg twice daily) only or with two-week of oral metronidazole (250 mg thrice daily) were evaluated retrospectively. Their responses were evaluated by Investigator’s Global Assessment (IGA), Clinician’s Erythema Assessment (CEA), and patient’s Global Assessment. The recurrence rate and odds ratio of risk factors for recurrence were also estimated. RESULTS: The combination treatment group reported earlier clinical improvement and lower mean IGA and CEA than the monotherapy group. Approximately 48% of patients with combination treatment did not show relapse within 24 weeks, which is significantly higher than that in the monotherapy group (p=0.042). CONCLUSION: Add-on therapy of oral metronidazole appeared to be a significant protective factor for recurrence of rosacea (p<0.05). This study suggests that oral metronidazole can be added to oral minocycline to reduce relapses in rosacea patients with tolerable safety. The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2022-12 2022-11-17 /pmc/articles/PMC9763916/ /pubmed/36478427 http://dx.doi.org/10.5021/ad.22.093 Text en Copyright © The Korean Dermatological Association and The Korean Society for Investigative Dermatology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Jin Soo Seo, Byeong Hak Cha, Doo Rae Suh, Ho Seok Choi, Yu Sung Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study |
title | Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study |
title_full | Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study |
title_fullStr | Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study |
title_full_unstemmed | Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study |
title_short | Maintenance of Remission after Oral Metronidazole Add-on Therapy in Rosacea Treatment: A Retrospective, Comparative Study |
title_sort | maintenance of remission after oral metronidazole add-on therapy in rosacea treatment: a retrospective, comparative study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763916/ https://www.ncbi.nlm.nih.gov/pubmed/36478427 http://dx.doi.org/10.5021/ad.22.093 |
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