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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 | 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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