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Management and Control

Detecting asthma exacerbations using daily home monitoring and machine learning

, MEng, , PhD & , PhD
Pages 1518-1527 | Received 27 Apr 2020, Accepted 24 Jul 2020, Published online: 14 Aug 2020
 

Abstract

Objective

Acute exacerbations contribute significantly to the morbidity of asthma. Recent studies have shown that early detection and treatment of asthma exacerbations leads to improved outcomes. We aimed to develop a machine learning algorithm to detect severe asthma exacerbations using easily available daily monitoring data.

Methods

We analyzed daily peak expiratory flow and symptom scores recorded by participants in the SAKURA study (NCT00839800), an international multicentre randomized controlled trial comparing budesonide/formoterol as maintenance and reliever therapy versus budesonide/formoterol maintenance plus terbutaline as reliever, in adults with persistent asthma. The dataset consisted of 728,535 records of daily monitoring data in 2010 patients, with 576 severe exacerbation events. Data post-processing techniques included normalization, standardization, calculation of differences or slopes over time and the use of smoothing filters. Principal components analysis was used to reduce the large number of derived variables to a smaller number of linearly independent components. Logistic regression, decision tree, naïve Bayes, and perceptron algorithms were evaluated. Model accuracy was assessed using stratified cross-validation. The primary outcome was the detection of exacerbations on the same day or up to three days in the future.

Results

The best model used logistic regression with input variables derived from post-processed data using principal components analysis. This had an area under the receiver operating characteristic curve of 0.85, with a sensitivity of 90% and specificity of 83% for severe asthma exacerbations.

Conclusion

Asthma exacerbations may be detected using machine learning algorithms applied to daily self-monitoring of peak expiratory flow and asthma symptoms.

Acknowledgements

The authors are grateful to AstraZeneca for providing the SAKURA dataset used in the study. AstraZeneca did not contribute to the data analysis or the decision to publish.

Declarations of interest

SG has received speaker’s fees from Teva and consultancy fees from Anaxsys and 3M. OZ and LM have no competing interests to declare.

Additional information

Funding

This paper presents independent research funded by the National Institute for Health Research (NIHR). The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health. SG was funded by an NIHR Clinical Lectureship.

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