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https://ahro.austin.org.au/austinjspui/handle/1/26007
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DC Field | Value | Language |
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dc.contributor.author | Kennedy, Jessica | - |
dc.contributor.author | Walker, Anne | - |
dc.contributor.author | Ellender, Claire M | - |
dc.contributor.author | Steinfort, Kate | - |
dc.contributor.author | Martin, Catherine | - |
dc.contributor.author | Smith, Catherine | - |
dc.contributor.author | Snell, Gregory | - |
dc.contributor.author | Whitford, Helen | - |
dc.date | 2021 | - |
dc.date.accessioned | 2021-03-09T05:05:05Z | - |
dc.date.available | 2021-03-09T05:05:05Z | - |
dc.date.issued | 2021-03-03 | - |
dc.identifier.citation | Internal Medicine Journal 2021; online first: 3 March | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/26007 | - |
dc.description.abstract | Lung 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.iso | eng | - |
dc.subject | Bronchiectasis | en |
dc.subject | lung transplantation | en |
dc.subject | morbidity | en |
dc.subject | respiratory tract diseases | en |
dc.title | Outcomes Of Non-Cystic Fibrosis Related Bronchiectasis Post Lung Transplantation. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Internal Medicine Journal | en |
dc.identifier.affiliation | Pubic Health and Preventative Medicine, Monash University, Melbourne, Australia | en |
dc.identifier.affiliation | Respiratory and Sleep Medicine | en |
dc.identifier.affiliation | Department of Thoracic Medicine, Royal Adelaide Hospital, South Australia, Australia | en |
dc.identifier.affiliation | Department of Respiratory & Sleep Medicine, Princess Alexandra Hospital, Brisbane, Australia | en |
dc.identifier.affiliation | Department of Allergy, Immunology and Respiratory Medicine, Alfred Hospital, Melbourne, Australia | en |
dc.identifier.affiliation | School of Medicine, Dentistry and Health Science, Melbourne University, Melbourne, Australia | en |
dc.identifier.doi | 10.1111/imj.15256 | en |
dc.type.content | Text | en |
dc.identifier.orcid | 0000-0003-2086-743X | en |
dc.identifier.pubmedid | 33656222 | - |
item.openairetype | Journal Article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.languageiso639-1 | en | - |
Appears in Collections: | Journal articles |
Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.