Publication:
Lung transplantation for cystic fibrosis: differential characteristics and outcomes between children and adults.

dc.contributor.authorMoreno, Paula
dc.contributor.authorAlvarez, Antonio
dc.contributor.authorCarrasco, Guadalupe
dc.contributor.authorRedel, Javier
dc.contributor.authorGuaman, Hugo Dario
dc.contributor.authorBaamonde, Carlos
dc.contributor.authorAlgar, Francisco Javier
dc.contributor.authorCerezo, Francisco
dc.contributor.authorSalvatierra, Angel
dc.date.accessioned2023-01-25T08:30:12Z
dc.date.available2023-01-25T08:30:12Z
dc.date.issued2015-09-10
dc.description.abstractThe survival benefit of lung transplantation (LTx) for cystic fibrosis (CF) patients is well demonstrated. We aim to compare children and adult CF recipients to assess whether there are differences in survival and clinical outcomes, and to identify risk factors for mortality. A retrospective analysis of 442 consecutive LTx performed at our institution in a 20-year period was conducted. CF patients were distributed into two groups: children (age The study group included 120 consecutive CF patients: 50 children (13 ± 3 years) and 70 adults (25 ± 6 years) undergoing 111 bilateral, 4 lobar, 4 combined and 1 unilateral LTx. Comparative analysis (children versus adults): survival (overall; 5, 10 and 15 years) 57, 45, 35% vs 67, 55, 43% (P = 0.32); survival (1-year survivors; 5, 10 and 15 years): 75, 64, 46% vs 90, 75, 59% (P = 0.09); 30-day mortality: 14 vs 16% (P = 0.27); urgent LTx: 32 vs 17% (P = 0.04); use of cardiopulmonary bypass (CPB): 56 vs 28% (P = 0.002); intensive care unit stay: 20 ± 19 vs 10 ± 9 days (P = 0.006); AR episodes (n): 1.4 ± 0.7 vs 1.2 ± 0.8 (P = 0.004). Incidence of PGD and freedom from CLAD did not differ between groups. Predictors of mortality were: use of CPB (HR 3.12; 95% CI 1.33-7.35; P Paediatric CF patients usually present with poorer pre-transplant status, require CPB more frequently and have a higher incidence of post-LTx diabetes and infections. This might explain the trend towards a better long-term survival observed in adult CF patients.
dc.description.versionSi
dc.identifier.citationMoreno P, Alvarez A, Carrasco G, Redel J, Guaman HD, Baamonde C, et al. Lung transplantation for cystic fibrosis: differential characteristics and outcomes between children and adults. Eur J Cardiothorac Surg. 2016 May;49(5):1334-43
dc.identifier.doi10.1093/ejcts/ezv377
dc.identifier.essn1873-734X
dc.identifier.pmid26530270
dc.identifier.unpaywallURLhttps://academic.oup.com/ejcts/article-pdf/49/5/1334/7912685/ezv377.pdf
dc.identifier.urihttp://hdl.handle.net/10668/9611
dc.issue.number5
dc.journal.titleEuropean journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
dc.journal.titleabbreviationEur J Cardiothorac Surg
dc.language.isoen
dc.organizationHospital Universitario Reina Sofía
dc.organizationInstituto Maimónides de Investigación Biomédica de Córdoba-IMIBIC
dc.page.number1334-43
dc.provenanceRealizada la curación de contenido 20/08/2024
dc.publisherOxford University Press
dc.pubmedtypeJournal Article
dc.relation.publisherversionhttps://academic.oup.com/ejcts/article/49/5/1334/2570828?login=false
dc.rights.accessRightsopen access
dc.subjectAdults
dc.subjectCystic fibrosis
dc.subjectLung transplantation
dc.subjectOutcomes
dc.subjectPaediatrics
dc.subject.decsAnálisis de supervivencia
dc.subject.decsEstudios retrospectivos
dc.subject.decsFibrosis quística
dc.subject.decsNiño
dc.subject.decsResultado del tratamiento
dc.subject.decsTrasplante de pulmón
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshChild
dc.subject.meshCystic fibrosis
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshLung transplantation
dc.subject.meshMale
dc.subject.meshRetrospective studies
dc.subject.meshRisk factors
dc.subject.meshSurvival analysis
dc.subject.meshTreatment outcome
dc.subject.meshYoung adult
dc.titleLung transplantation for cystic fibrosis: differential characteristics and outcomes between children and adults.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number49
dspace.entity.typePublication

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