Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2213
Title: Centralised versus outreach models of cystic fibrosis care should be tailored to the needs of the individual patient
Authors: Reid, D. W.
O'Rourke, P.
Wainwright, Claire 
Bell, S. C.
Geake, J.
Ballard, E.
Issue Date: 2020
Source: 50, (2), 2020, p. 232-235
Pages: 232-235
Journal: Internal Medicine Journal
Abstract: Cystic fibrosis (CF) is a common life-limiting genetic condition. As the disease progresses access to specialist tertiary multi-disciplinary care services may become necessary. For patients living in regional/remote Australia, accessing such services may be a challenge. Here, we describe long-term outcomes for CF patients according to their access to specialist CF centre care in childhood.L20042344502020-02-17
2020-02-20
DOI: 10.1111/imj.14724
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L2004234450&from=exporthttp://dx.doi.org/10.1111/imj.14724 |
Keywords: mortality;outcome assessment;patient care;priority journal;Pseudomonas infection;respiratory failure;spirometry;human;health status;health care need;lung function;lung transplantation;forced expiratory volume;cystic fibrosis;articlebody mass;health care access
Type: Article
Appears in Sites:Children's Health Queensland Publications

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