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dc.contributor.authorCristeto Porras, Martaes_ES
dc.contributor.authorMora Cuesta, Víctor Manueles_ES
dc.contributor.authorIturbe Fernández, David es_ES
dc.contributor.authorTello Mena, Sandraes_ES
dc.contributor.authorAlonso Lecue, Pilares_ES
dc.contributor.authorSánchez Moreno, Laura es_ES
dc.contributor.authorMiñambres García, Eduardo es_ES
dc.contributor.authorNaranjo Gozalo, Sara es_ES
dc.contributor.authorIzquierdo Cuervo, Sheilaes_ES
dc.contributor.authorCifrián Martínez, José Manuel es_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-02-24T15:15:47Z
dc.date.available2023-02-24T15:15:47Z
dc.date.issued2022-10es_ES
dc.identifier.issn0902-0063es_ES
dc.identifier.issn1399-0012es_ES
dc.identifier.urihttps://hdl.handle.net/10902/27880
dc.description.abstractIntroduction: Azithromycin (AZI) may be an effective immune modulator in lung transplant (LT) recipients, and can decrease chronic lung allograft dysfunction (CLAD) rates, the leading cause of mortality after the first year post-LT. The aim of the study is to assess the effect of AZI initiation and its timing on the incidence and severity of CLAD in LT recipients. Methods: Single-center retrospective study, including LT recipients from 01/01/2011 to 30/06/2020. Four groups were established: those who started AZI at the 3rd week post-LT (group A), those who received AZI later than the 3rd week post-LT and had preserved FEV1 (B), those who did not receive AZI (C) and those who started AZI due to a decline in FEV1 (D). The dosage of AZI prescribed was 250 mg three times per week. CLAD was defined and graduated according to the 2019 ISHLT criteria. Results: We included 358 LT recipients: 139 (38.83%) were in group A, 94 (26.25%) in group B, 91 (25.42%) in group C, and 34 (9.50%) in group D. Group A experienced the lowest CLAD incidence and severity at 1 (p = 0.01), 3 (p < 0.001), and 5 years post-LT, followed by Group B. Groups C and D experienced a higher incidence and severity of CLAD (p = 0.015). Initiation of AZI prior to FEV1 decline (groups A and B) proved to be protective against CLAD after adjusting for differences between the treatment groups. Conclusions: Early initiation of AZI in LT recipients could have a role in decreasing the incidence and severity of CLAD. In addition, as long as FEV1 is preserved, initiating AZI at any time could also be useful to prevent the incidence of CLAD and reduce its severity. This article is protected by copyright. All rights reserved.es_ES
dc.description.sponsorshipFunding Sources: This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.es_ES
dc.format.extent27 p.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rights© John Wiley & Sons. This is the peer reviewed version of the following article: Clinical transplantation 2022 Oct 11; e14832, which has been published in final form at https://doi.org/10.1111/ctr.14832. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.es_ES
dc.sourceClinical transplantation 2022 Oct 11; e14832es_ES
dc.subject.otherAzithromycines_ES
dc.subject.otherChronic Lung Allograft Dysfunctiones_ES
dc.subject.otherLung transplantationes_ES
dc.titleEarly onset of azithromycin to prevent clad in lung transplantation: promising results of a retrospective single centre experiencees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1111/ctr.14832es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1111/ctr.14832es_ES
dc.type.versionacceptedVersiones_ES


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