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Halometasone monohydrate (0.05%) in occupational contact dermatitis

OBJECTIVE: The impact of occupational contact dermatitis (OCD) is often underestimated because of underreporting, and its management is also inadequate, especially in developing countries. Topical corticosteroids have remained the first line treatment but till date, there is no study on efficacy and...

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Autores principales: Maiti, Rituparna, Sirka, Chandra Sekhar, Shaju, Noel, Hota, Debasish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825427/
https://www.ncbi.nlm.nih.gov/pubmed/27127314
http://dx.doi.org/10.4103/0253-7613.178823
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author Maiti, Rituparna
Sirka, Chandra Sekhar
Shaju, Noel
Hota, Debasish
author_facet Maiti, Rituparna
Sirka, Chandra Sekhar
Shaju, Noel
Hota, Debasish
author_sort Maiti, Rituparna
collection PubMed
description OBJECTIVE: The impact of occupational contact dermatitis (OCD) is often underestimated because of underreporting, and its management is also inadequate, especially in developing countries. Topical corticosteroids have remained the first line treatment but till date, there is no study on efficacy and safety of halometasone in OCD, and there is a paucity of data on its comparative efficacy in allergic and irritant variety. This study aims to evaluate the efficacy and safety of halometasone in OCD and to compare its effect in allergic and irritant types of OCD. METHODS: The present study is a prospective, interventional, single arm clinical study conducted on 150 patients of OCD. Detailed history and clinical examination was done at baseline, and all enrolled patients underwent patch test with the Indian Standard Battery of allergens. Eczema severity was assessed by the Investigator's Global Assessment (IGA) scale, SCORing Atopic Dermatitis (SCORAD) index, and patient-oriented eczema measure (POEM). Change in quality of life was assessed by using the Dermatology Life Quality Index (DLQI). After baseline assessments, they were prescribed halometasone 0.05% ointment and were followed up after 4 weeks, and efficacy variables were evaluated. RESULTS: At follow-up, 19 patients were lost, and data of 131 patients were analyzed. After 4 weeks of halometasone therapy, there was statistically significant (P < 0.001) improvement in SCORAD index, IGA, POEM, and DLQI. Considering improvement in IGA as treatment success criteria, treatment was found to be successful in 87.8%. Subgroup analysis revealed no significant difference in effect of halometasone in allergic and irritant OCD. CONCLUSIONS: Halometasone is efficacious with a good safety profile in patients with OCD, and there is no significant difference in efficacy of the drug in allergic and irritant OCD.
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spelling pubmed-48254272016-04-28 Halometasone monohydrate (0.05%) in occupational contact dermatitis Maiti, Rituparna Sirka, Chandra Sekhar Shaju, Noel Hota, Debasish Indian J Pharmacol Research Article OBJECTIVE: The impact of occupational contact dermatitis (OCD) is often underestimated because of underreporting, and its management is also inadequate, especially in developing countries. Topical corticosteroids have remained the first line treatment but till date, there is no study on efficacy and safety of halometasone in OCD, and there is a paucity of data on its comparative efficacy in allergic and irritant variety. This study aims to evaluate the efficacy and safety of halometasone in OCD and to compare its effect in allergic and irritant types of OCD. METHODS: The present study is a prospective, interventional, single arm clinical study conducted on 150 patients of OCD. Detailed history and clinical examination was done at baseline, and all enrolled patients underwent patch test with the Indian Standard Battery of allergens. Eczema severity was assessed by the Investigator's Global Assessment (IGA) scale, SCORing Atopic Dermatitis (SCORAD) index, and patient-oriented eczema measure (POEM). Change in quality of life was assessed by using the Dermatology Life Quality Index (DLQI). After baseline assessments, they were prescribed halometasone 0.05% ointment and were followed up after 4 weeks, and efficacy variables were evaluated. RESULTS: At follow-up, 19 patients were lost, and data of 131 patients were analyzed. After 4 weeks of halometasone therapy, there was statistically significant (P < 0.001) improvement in SCORAD index, IGA, POEM, and DLQI. Considering improvement in IGA as treatment success criteria, treatment was found to be successful in 87.8%. Subgroup analysis revealed no significant difference in effect of halometasone in allergic and irritant OCD. CONCLUSIONS: Halometasone is efficacious with a good safety profile in patients with OCD, and there is no significant difference in efficacy of the drug in allergic and irritant OCD. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4825427/ /pubmed/27127314 http://dx.doi.org/10.4103/0253-7613.178823 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Research Article
Maiti, Rituparna
Sirka, Chandra Sekhar
Shaju, Noel
Hota, Debasish
Halometasone monohydrate (0.05%) in occupational contact dermatitis
title Halometasone monohydrate (0.05%) in occupational contact dermatitis
title_full Halometasone monohydrate (0.05%) in occupational contact dermatitis
title_fullStr Halometasone monohydrate (0.05%) in occupational contact dermatitis
title_full_unstemmed Halometasone monohydrate (0.05%) in occupational contact dermatitis
title_short Halometasone monohydrate (0.05%) in occupational contact dermatitis
title_sort halometasone monohydrate (0.05%) in occupational contact dermatitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4825427/
https://www.ncbi.nlm.nih.gov/pubmed/27127314
http://dx.doi.org/10.4103/0253-7613.178823
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