Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26007
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dc.contributor.authorKennedy, Jessica-
dc.contributor.authorWalker, Anne-
dc.contributor.authorEllender, Claire M-
dc.contributor.authorSteinfort, Kate-
dc.contributor.authorMartin, Catherine-
dc.contributor.authorSmith, Catherine-
dc.contributor.authorSnell, Gregory-
dc.contributor.authorWhitford, Helen-
dc.date2021-
dc.date.accessioned2021-03-09T05:05:05Z-
dc.date.available2021-03-09T05:05:05Z-
dc.date.issued2021-03-03-
dc.identifier.citationInternal Medicine Journal 2021; online first: 3 Marchen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26007-
dc.description.abstractLung transplantation is a recognised treatment for end-stage lung disease due to bronchiectasis. Non-CF bronchiectasis and CF are often combined into one cohort, however outcomes for non-CF bronchiectasis patients varies between centres, and in comparison to those for CF. To compare lung transplantation mortality and morbidity of bronchiectasis (non-CF) patients to those with CF and other indications. Retrospective analysis of patients undergoing lung transplantation between 01 January 2008-31 December 2013. Time to and cause of lung allograft loss was censored on 01 April 2018. A case-note review was conducted on a sub-group of 78 patients, to analyse hospital admissions as a marker of morbidity. 341 patients underwent lung transplantation, 22 (6%) had bronchiectasis compared to 69 (20%) with CF. The 5-year survival for the bronchiectasis group was 32%, compared to CF 69%, obstructive lung disease (OLD) 64%, pulmonary hypertension 62% and ILD 55% (p = 0.008). Lung allograft loss due to CLAD with predominant infection was significantly higher in the bronchiectasis group at 2 years. The rate of acute admissions was 2.24 higher in the bronchiectasis group when compared to OLD (p = 0.01). Patients with bronchiectasis spent 45.81 days in hospital per person year after transplantation compared with 18.21 days for CF. Bronchiectasis patients in this study had a lower 5-year survival and poorer outcomes in comparison to other indications including CF. Bronchiectasis should be considered a separate entity to CF in survival analysis. This article is protected by copyright. All rights reserved.en
dc.language.isoeng-
dc.subjectBronchiectasisen
dc.subjectlung transplantationen
dc.subjectmorbidityen
dc.subjectrespiratory tract diseasesen
dc.titleOutcomes Of Non-Cystic Fibrosis Related Bronchiectasis Post Lung Transplantation.en
dc.typeJournal Articleen
dc.identifier.journaltitleInternal Medicine Journalen
dc.identifier.affiliationPubic Health and Preventative Medicine, Monash University, Melbourne, Australiaen
dc.identifier.affiliationRespiratory and Sleep Medicineen
dc.identifier.affiliationDepartment of Thoracic Medicine, Royal Adelaide Hospital, South Australia, Australiaen
dc.identifier.affiliationDepartment of Respiratory & Sleep Medicine, Princess Alexandra Hospital, Brisbane, Australiaen
dc.identifier.affiliationDepartment of Allergy, Immunology and Respiratory Medicine, Alfred Hospital, Melbourne, Australiaen
dc.identifier.affiliationSchool of Medicine, Dentistry and Health Science, Melbourne University, Melbourne, Australiaen
dc.identifier.doi10.1111/imj.15256en
dc.type.contentTexten
dc.identifier.orcid0000-0003-2086-743Xen
dc.identifier.pubmedid33656222-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
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