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Using digital technology for home monitoring, adherence and self-management in cystic fibrosis: A state of the art review

Calthorpe, Rebecca J; Smith, Sherie; Gathercole, Katie; Smyth, Alan R

Using digital technology for home monitoring, adherence and self-management in cystic fibrosis: A state of the art review Thumbnail


Authors

Rebecca J Calthorpe

SHERIE SMITH sherie.smith@nottingham.ac.uk
Cochrane Systematic Reviewer

Katie Gathercole

Alan R Smyth



Abstract

Digital healthcare is a rapidly growing healthcare sector. Its importance has been recognised at both national and international level, with the WHO recently publishing its first global strategy for digital health. The use of digital technology within cystic fibrosis (CF) has also increased. CF is a chronic, life-limiting condition, in which the treatment burden is high and treatment regimens are not static. Digital technologies present an opportunity to support the lives of people with CF. We included 59 articles and protocols in this state-of-the-art review, relating to 48 studies from 1999 until 2019. This provides a comprehensive overview of the expansion and evolution of the use of digital technology. Technology has been used with the aim of increasing accessibility to healthcare, earlier detection of pulmonary exacerbations and objective electronic adherence monitoring. It may also be used to promote adherence and self-management through education, treatment management Apps and social media.

Citation

Calthorpe, R. J., Smith, S., Gathercole, K., & Smyth, A. R. (2020). Using digital technology for home monitoring, adherence and self-management in cystic fibrosis: A state of the art review. Thorax, 75(1), 72-77. https://doi.org/10.1136/thoraxjnl-2019-213233

Journal Article Type Article
Acceptance Date Sep 27, 2019
Online Publication Date Oct 8, 2019
Publication Date 2020-01
Deposit Date Oct 1, 2019
Publicly Available Date Oct 2, 2019
Journal Thorax
Print ISSN 0040-6376
Electronic ISSN 1468-3296
Publisher BMJ Publishing Group
Peer Reviewed Peer Reviewed
Volume 75
Issue 1
Pages 72-77
DOI https://doi.org/10.1136/thoraxjnl-2019-213233
Keywords Cystic Fibrosis; Psychology; Exercise
Public URL https://nottingham-repository.worktribe.com/output/2731787
Publisher URL https://thorax.bmj.com/content/early/2019/10/08/thoraxjnl-2019-213233
Additional Information This article has been accepted for publication in Thorax, 2019 following peer review, and the Version of Record can be accessed online at https://thorax.bmj.com/content/early/2019/10/08/thoraxjnl-2019-213233

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