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Severe Atopic Dermatitis In Spain: A Real-Life Observational Study
OBJECTIVE: To determine the epidemiology and characterize the treatment prescribed for severe atopic dermatitis (AD) in children/adults in usual clinical practice. METHODS: Observational, retrospective study made through review of medical records of Spanish patients aged ≥6 years. Patients diagnosed...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6897051/ https://www.ncbi.nlm.nih.gov/pubmed/31819466 http://dx.doi.org/10.2147/TCRM.S226456 |
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author | Sicras-Mainar, Antoni Navarro-Artieda, Ruth Armario-Hita, José C |
author_facet | Sicras-Mainar, Antoni Navarro-Artieda, Ruth Armario-Hita, José C |
author_sort | Sicras-Mainar, Antoni |
collection | PubMed |
description | OBJECTIVE: To determine the epidemiology and characterize the treatment prescribed for severe atopic dermatitis (AD) in children/adults in usual clinical practice. METHODS: Observational, retrospective study made through review of medical records of Spanish patients aged ≥6 years. Patients diagnosed with severe AD who required care between 2013 and 2017 were included. The study groups were: 6–12 years; 13–18 years; and > 18 years. Patients were followed for 5 years. The main measurements were the prevalence of AD, comorbidity and treatment duration. Statistical significance was established as p <0.05. RESULTS: We included 2323 patients with severe AD. The overall prevalence was 0.10% (95% CI: 0.09–0.11%) and was 0.39%, 0.23% and 0.07% in the 6–12 years, 13–18 years and >18 years age groups, respectively (p <0.001), the percentage of males was 58%, 48.6% and 39%, respectively, and general comorbidity was 0.1, 0.2 and 0.9 points, respectively (p <0.001).The most frequent comorbidities were asthma in 49.0%, 44.9% and 20.8%, respectively (p <0.001), and anxiety in 79.7%, 65.8% and 67.3%, respectively (p <0.001). Oral corticosteroids were administered in 97.3%, 90.9% and 81.7%, respectively (concomitant-medication). Cyclosporine (45.3%), azathioprine (15.9%) and methotrexate (9.0%) were the most frequently prescribed drugs; biologic agents were administered in 5.8% of patients (for AD). CONCLUSION: In AD the presence of comorbidities was significant, especially in the psychological, immunoallergic and cardiovascular areas. Cyclosporine was the most widely used immunosuppressant. There was a degree of variability in the use and duration of the treatments prescribed. |
format | Online Article Text |
id | pubmed-6897051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-68970512019-12-09 Severe Atopic Dermatitis In Spain: A Real-Life Observational Study Sicras-Mainar, Antoni Navarro-Artieda, Ruth Armario-Hita, José C Ther Clin Risk Manag Original Research OBJECTIVE: To determine the epidemiology and characterize the treatment prescribed for severe atopic dermatitis (AD) in children/adults in usual clinical practice. METHODS: Observational, retrospective study made through review of medical records of Spanish patients aged ≥6 years. Patients diagnosed with severe AD who required care between 2013 and 2017 were included. The study groups were: 6–12 years; 13–18 years; and > 18 years. Patients were followed for 5 years. The main measurements were the prevalence of AD, comorbidity and treatment duration. Statistical significance was established as p <0.05. RESULTS: We included 2323 patients with severe AD. The overall prevalence was 0.10% (95% CI: 0.09–0.11%) and was 0.39%, 0.23% and 0.07% in the 6–12 years, 13–18 years and >18 years age groups, respectively (p <0.001), the percentage of males was 58%, 48.6% and 39%, respectively, and general comorbidity was 0.1, 0.2 and 0.9 points, respectively (p <0.001).The most frequent comorbidities were asthma in 49.0%, 44.9% and 20.8%, respectively (p <0.001), and anxiety in 79.7%, 65.8% and 67.3%, respectively (p <0.001). Oral corticosteroids were administered in 97.3%, 90.9% and 81.7%, respectively (concomitant-medication). Cyclosporine (45.3%), azathioprine (15.9%) and methotrexate (9.0%) were the most frequently prescribed drugs; biologic agents were administered in 5.8% of patients (for AD). CONCLUSION: In AD the presence of comorbidities was significant, especially in the psychological, immunoallergic and cardiovascular areas. Cyclosporine was the most widely used immunosuppressant. There was a degree of variability in the use and duration of the treatments prescribed. Dove 2019-12-02 /pmc/articles/PMC6897051/ /pubmed/31819466 http://dx.doi.org/10.2147/TCRM.S226456 Text en © 2019 Sicras-Mainar et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Sicras-Mainar, Antoni Navarro-Artieda, Ruth Armario-Hita, José C Severe Atopic Dermatitis In Spain: A Real-Life Observational Study |
title | Severe Atopic Dermatitis In Spain: A Real-Life Observational Study |
title_full | Severe Atopic Dermatitis In Spain: A Real-Life Observational Study |
title_fullStr | Severe Atopic Dermatitis In Spain: A Real-Life Observational Study |
title_full_unstemmed | Severe Atopic Dermatitis In Spain: A Real-Life Observational Study |
title_short | Severe Atopic Dermatitis In Spain: A Real-Life Observational Study |
title_sort | severe atopic dermatitis in spain: a real-life observational study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6897051/ https://www.ncbi.nlm.nih.gov/pubmed/31819466 http://dx.doi.org/10.2147/TCRM.S226456 |
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