Cited by 2Cystic Fibrosis Research AdvancesMobile Health and mHealth ApplicationsChronic Obstructive Pulmonary Disease (COPD) Research

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Regarding the article entitled “A smartphone application for reporting symptoms in adults with cystic fibrosis improves the detection of exacerbations: Results of a randomised controlled trial”

Open access
Hoo, Zhe Hui, Wildman, Martin J·2020·Journal of Cystic Fibrosis

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Integrity signals

Registry

Crossref · 10.1016/j.jcf.2019.09.017

Cites

3 of 3 references verified0 citation errors · 0 not checkable

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  • Trials using objective recorded measures suggest that adherence to inhaled therapies in people with CF is around 31% to 36% in adults.

    “Trials using objective recorded measures suggest that adherence to inhaled therapies in people with CF is around 31% to 36% in adults (Daniels 2011;Hoo 2019;Hoo 2020;Hoo 2021)”

    From Psychological interventions for improving adherence to inhaled therapies in people with cystic fibrosis (2023) · cites this paper as Hoo 2020

    The Dear Editor section says adherence to preventative therapies in CF may be as low as 35–50%, supporting the general point that adherence can be low. It does not give the claimed 31–36% range or specify that the estimate comes from trials using objective recorded measures in adults receiving inhaled therapies. (LLM, conf=0.87)

    Experimental — accuracy not yet measured

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Citations

Cites

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Research works printed but not linked: 6

  1. Wood, 2019, A smartphone application for reporting symptoms in adults with cystic fibrosis improves the detection of exacerbations: results of a randomised controlled trial, J Cyst Fibros
  2. Bell, 2017, Early intervention of cystic fibrosis pulmonary exacerbations based on home monitoring. eICE through the looking glass, Am J Respir Crit Care Med, 196, 1090, 10.1164/rccm.201706-1207ED · DOI
  3. Wood, 2018, A smartphone application for reporting symptoms in adults with cystic fibrosis: protocol of a randomised controlled trial, BMJ Open, 8, 10.1136/bmjopen-2017-021136 · DOI
  4. Somayaji, 2017, Lung function recovery in cystic fibrosis following a pulmonary exacerbation treated with intravenous and oral antibiotics: analysis of the eICE trial, Pediatr Pulmonol, 52, S383
  5. Hoo, 2019, Intravenous antibiotic use and exacerbation events in an adult cystic fibrosis centre: A prospective observational study, Respir Med, 154, 109, 10.1016/j.rmed.2019.06.017 · DOI
  6. Edmondson, 2019, CLInical Monitoring and Biomarkers to stratify severity and predict outcomes in children with cystic fibrosis (CLIMB-CF): results from the feasibility study, J Cyst Fibros, 18, S52, 10.1016/S1569-1993(19)30285-1 · DOI

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Metadata

Authors
Hoo, Z. H., & Wildman, M. J.
Affiliations
Northern General Hospital (GB)
Corresponding author
  • Hoo, Zhe Hui
  • Wildman, Martin J
Venue
Journal of Cystic Fibrosis
Publisher
Elsevier BV
Published
2020-03
Volume
19
Issue
2
Pages
e9
ISSN
1569-1993 (ISSN-L)
OpenAlex
W2982573304
Cited by
2
References
3
Citations by year
2023: 2
Type
journal article
Language
en
Open access
Locations
  • Journal of Cystic Fibrosis (publishedVersion)
  • PubMed (publishedVersion)
  • White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
Funders
National Institute for Health and Care Research (DRF-2014-07-092)
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
  • Health Sciences › Health Professions › General Health Professions › Mobile Health and mHealth Applications
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
Keywords
exacerbation detection, mobile application, symptom monitoring, adults
MeSH terms
Smartphone, Adult, Cystic Fibrosis, Forced Expiratory Volume, Humans

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