Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/123249
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Domingo, Christian | en_US |
dc.contributor.author | Sogo, Ana | en_US |
dc.contributor.author | Casado, Enrique | en_US |
dc.contributor.author | Martínez-Moragón, Eva | en_US |
dc.contributor.author | Blanco-Aparicio, Marina | en_US |
dc.contributor.author | Carrillo Díaz, Teresa | en_US |
dc.contributor.author | Bañas-Conejero, David | en_US |
dc.contributor.author | Sánchez-Herrero, María Guadalupe | en_US |
dc.date.accessioned | 2023-06-05T13:23:17Z | - |
dc.date.available | 2023-06-05T13:23:17Z | - |
dc.date.issued | 2023 | en_US |
dc.identifier.issn | 1663-9812 | en_US |
dc.identifier.other | Scopus | - |
dc.identifier.uri | http://hdl.handle.net/10553/123249 | - |
dc.description.abstract | Oral corticosteroids (OCS) are commonly used for the acute management of severe asthma exacerbations or as maintenance therapy; however, chronic use is associated with significant toxicities, e.g., osteoporosis. In the REal worlD Effectiveness and Safety (REDES) study of mepolizumab in a multicentric Spanish cohort of asthma patients, mepolizumab effectively reduced clinically severe asthma exacerbations and decreased OCS dependence. This post-hoc analysis further evaluates mepolizumab’s de-escalation effect on OCS dose. Patients enrolled in REDES who had OCS consumption data available for 12 months pre- and post-mepolizumab treatment were included in this analysis. Primary outcomes were to determine the change in the proportion of patients eligible for anti-osteoporotic treatment due to the changes in OCS consumption before and after 1 year of mepolizumab treatment. All analyses are descriptive. Approximately one-third (98/318; 30.8%) of patients in REDES were on maintenance OCS at the time of mepolizumab treatment initiation. In REDES, mean cumulative OCS exposure decreased by 54.3% after 1 year of treatment. The proportion of patients on high-dose OCS (≥7.5 mg/day) fell from 57.1% at baseline to 28.9% after 12 months of mepolizumab treatment. Thus, 53.6% of OCS-dependent asthma patients treated with mepolizumab would cease to be candidates for anti-osteoporotic treatment according to guidelines thresholds. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | Frontiers in Pharmacology | en_US |
dc.source | Frontiers in Pharmacology[EISSN 1663-9812],v. 14, (Mayo 2023) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 3209 Farmacología | en_US |
dc.subject | 320903 Evaluación de medicamentos | en_US |
dc.subject.other | Anti-Resorptive Treatment | en_US |
dc.subject.other | Asthma | en_US |
dc.subject.other | Mepolizumab | en_US |
dc.subject.other | Oral Corticosteroid | en_US |
dc.subject.other | Osteoporosis Treatment | en_US |
dc.title | Potential impact of mepolizumab in stepping down anti-osteporotic treatment in corticosteroid-dependent asthma | en_US |
dc.type | info:eu-repo/semantics/Article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.3389/fphar.2023.1183156 | en_US |
dc.identifier.scopus | 85159894969 | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.orcid | NO DATA | - |
dc.contributor.authorscopusid | 55636347100 | - |
dc.contributor.authorscopusid | 35068752900 | - |
dc.contributor.authorscopusid | 55408093200 | - |
dc.contributor.authorscopusid | 7004095526 | - |
dc.contributor.authorscopusid | 6603249462 | - |
dc.contributor.authorscopusid | 7003526269 | - |
dc.contributor.authorscopusid | 57226498408 | - |
dc.contributor.authorscopusid | 55948973000 | - |
dc.identifier.eissn | 1663-9812 | - |
dc.relation.volume | 14 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.numberofpages | 6 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Mayo 2023 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 1,066 | |
dc.description.jcr | 5,6 | |
dc.description.sjrq | Q1 | |
dc.description.jcrq | Q1 | |
dc.description.scie | SCIE | |
dc.description.miaricds | 10,5 | |
item.grantfulltext | open | - |
item.fulltext | Con texto completo | - |
crisitem.author.dept | GIR IUIBS: Patología y Tecnología médica | - |
crisitem.author.dept | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0002-3047-8908 | - |
crisitem.author.parentorg | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.fullName | Carrillo Díaz, Teresa | - |
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