Evaluation of the Impact of Elexacaftor/Tezacaftor/Ivacaftor on Aerobic Capacity in Children With Cystic Fibrosis Aged 6–11 Years: Actual Observations and Clinical Perspectives.
| dc.contributor.author | Pérez Ruiz, Margarita | |
| dc.contributor.author | Bos, Mats te | |
| dc.contributor.author | Fernández García, Patricia | |
| dc.contributor.author | Manuel, Cristina de | |
| dc.contributor.author | Morales Tirado, Ana | |
| dc.contributor.author | López Neyra, Alejandro | |
| dc.contributor.author | Ruiz de Valbuena, Marta | |
| dc.contributor.author | Rubio Alonso, Margarita | |
| dc.contributor.author | Sanz Santiago, Verónica | |
| dc.date.accessioned | 2025-10-20T08:04:53Z | |
| dc.date.available | 2025-10-20T08:04:53Z | |
| dc.date.issued | 2025 | |
| dc.description.abstract | Cystic fibrosis causes exercise limitation due to impaired lung function and other complications, which in turn increases the chance of mortality. CFTR modulators, particularly the elexacaftor/tezacaftor/ivacaftor (ETI) combination, improve lung function in children older than 6 years in real-life studies. This study aimed to assess the impact of ETI on aerobic capacity in children with CF aged 6–11 years under real-life conditions and to evaluate whether prior CFTR modulator treatment affects these outcomes. | |
| dc.description.filiation | UEM | |
| dc.description.impact | 9.2 Q1 JCR 2024 | spa |
| dc.description.impact | 0.466 Q3 SJR 2024 | spa |
| dc.description.impact | No data IDR 2023 | spa |
| dc.description.sponsorship | Sn financiación | |
| dc.identifier.citation | Pérez-Ruiz, M., Te Bos, M., Fernández-García, P., Manuel, C. D., Morales-Tirado, A., López-Neyra, A., Valbuena, M. R. D., Rubio, M., & Sanz-Santiago, V. (2025). Evaluation of the impact of elexacaftor/tezacaftor/ivacaftor on aerobic capacity in children with cystic fibrosis aged 6–11 years: Actual observations and clinical perspectives. Archivos de Bronconeumología, S0300289625000717. https://doi.org/10.1016/j.arbres.2025.02.010 | |
| dc.identifier.doi | 10.1016/j.arbres.2025.02.010 | |
| dc.identifier.issn | 0300-2896 | |
| dc.identifier.uri | https://hdl.handle.net/11268/16408 | |
| dc.language.iso | eng | |
| dc.peerreviewed | Si | |
| dc.relation.publisherversion | http://doi.org/10.1016/j.arbres.2025.02.010 | |
| dc.rights | Sin licencia Creative Commons | eng |
| dc.rights.accessRights | open access | |
| dc.subject.other | Niño | |
| dc.subject.other | Fibrosis Quística | |
| dc.subject.other | Calidad de vida | |
| dc.subject.sdg | Goal 3: Ensure healthy lives and promote well-being for all at all ages | |
| dc.subject.unesco | Salud | |
| dc.subject.unesco | Aparato respiratorio | |
| dc.subject.unesco | Salud materno-infantil | |
| dc.title | Evaluation of the Impact of Elexacaftor/Tezacaftor/Ivacaftor on Aerobic Capacity in Children With Cystic Fibrosis Aged 6–11 Years: Actual Observations and Clinical Perspectives. | |
| dc.type | journal article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | a5c08444-aa82-4924-a71e-de56086bcd7c | |
| relation.isAuthorOfPublication | 0413b5c5-4ebf-4116-b5d7-829f891a6e9c | |
| relation.isAuthorOfPublication.latestForDiscovery | a5c08444-aa82-4924-a71e-de56086bcd7c |
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