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dc.contributor.authorLópez-Vilella, R.
dc.contributor.authorGómez Bueno, M.
dc.contributor.authorGonzález Vílchez, Francisco Jesús 
dc.contributor.authorSole Jover, A.
dc.contributor.authorLaporta Hernández, R.
dc.contributor.authorVicente Guillén, R.
dc.contributor.authorGonzález Román, A. I.
dc.contributor.authorSánchez-Lázaro, I.
dc.contributor.authorHernández Pérez, F.
dc.contributor.authorSales Badfa, G.
dc.contributor.authorCórdoba Peláez, M. D. M.
dc.contributor.authorTorregrosa Puerta, S.
dc.contributor.authorForteza Gil, A.
dc.contributor.authorMartínez Dolz, L.
dc.contributor.authorSegovia Cubero, J.
dc.contributor.authorAlmenar Bonet, L.
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-04-03T17:03:18Z
dc.date.available2025-04-03T17:03:18Z
dc.date.issued2022
dc.identifier.issn2008-6490
dc.identifier.issn2008-6482
dc.identifier.urihttps://hdl.handle.net/10902/36189
dc.description.abstractBackground: This study aims to evaluate the entire experience in heart-lung transplantation (HLTx) in a country of the European Union with 47 million inhabitants according to the etiologies that motivated the procedure. Methods: A retrospective study on 1,751 consecutive transplants (HLTx: 78) was performed from 1990 to 2020 in two centers. Overall survival, adjusted for clinical profile and etiological subgroups, was compared. 7 subgroups were considered: 1) Cardiomyopathy with pulmonary hypertension (CM + PH). 2) Eisenmenger syndrome. 3) Congenital heart disease (CHD). 4) Idiopathic pulmonary arterial hypertension (IPAH). 5) Cystic fibrosis. 6) Chronic obstructive pulmonary disease (COPD)/Emphysema. 7) Diffuse interstitial lung disease (ILD). Results: Early mortality was 44% and that of the rest of the follow-up was 31%. There were differences between HTLx and HTx in survival, also comparing groups with a similar clinical profile with propensity score (p= 0.04). Median survival was low in CM + PH (18 days), ILD (29 days) and CHD (114 days), intermediate in Eisenmenger syndrome (600 days), and longer in IPAH, COPD/Emphysema and cystic fibrosis. Conclusion: HLTx has a high mortality. The etiological analysis is of the utmost interest to make the most of the organs and improve survival.es_ES
dc.format.extent13 p.es_ES
dc.language.isoenges_ES
dc.publisherAvicenna Organ Transplant Institutees_ES
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.sourceInternational Journal of Organ Transplantation Medicine, 2022, 13(2), 51-62es_ES
dc.subject.otherHeart-lung transplantationes_ES
dc.subject.otherHeart transplantationes_ES
dc.subject.otherSurvivales_ES
dc.subject.otherEtiologyes_ES
dc.titleCurrent situation and prognostic evolution of combined heart-lung transplantation in a European Union countryes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10460527/es_ES
dc.rights.accessRightsopenAccesses_ES
dc.type.versionpublishedVersiones_ES


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Attribution-NonCommercial-ShareAlike 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial-ShareAlike 4.0 International