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The power of data mining in diagnosis of childhood pneumonia
Childhood pneumonia is the leading cause of death of children under the age of 5 years globally. Diagnostic information on the presence of infection, severity and aetiology (bacterial versus viral) is crucial for appropriate treatment. However, the derivation of such information requires advanced eq...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971218/ https://www.ncbi.nlm.nih.gov/pubmed/27466436 http://dx.doi.org/10.1098/rsif.2016.0266 |
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author | Naydenova, Elina Tsanas, Athanasios Howie, Stephen Casals-Pascual, Climent De Vos, Maarten |
author_facet | Naydenova, Elina Tsanas, Athanasios Howie, Stephen Casals-Pascual, Climent De Vos, Maarten |
author_sort | Naydenova, Elina |
collection | PubMed |
description | Childhood pneumonia is the leading cause of death of children under the age of 5 years globally. Diagnostic information on the presence of infection, severity and aetiology (bacterial versus viral) is crucial for appropriate treatment. However, the derivation of such information requires advanced equipment (such as X-rays) and clinical expertise to correctly assess observational clinical signs (such as chest indrawing); both of these are often unavailable in resource-constrained settings. In this study, these challenges were addressed through the development of a suite of data mining tools, facilitating automated diagnosis through quantifiable features. Findings were validated on a large dataset comprising 780 children diagnosed with pneumonia and 801 age-matched healthy controls. Pneumonia was identified via four quantifiable vital signs (98.2% sensitivity and 97.6% specificity). Moreover, it was shown that severity can be determined through a combination of three vital signs and two lung sounds (72.4% sensitivity and 82.2% specificity); addition of a conventional biomarker (C-reactive protein) further improved severity predictions (89.1% sensitivity and 81.3% specificity). Finally, we demonstrated that aetiology can be determined using three vital signs and a newly proposed biomarker (lipocalin-2) (81.8% sensitivity and 90.6% specificity). These results suggest that a suite of carefully designed machine learning tools can be used to support multi-faceted diagnosis of childhood pneumonia in resource-constrained settings, compensating for the shortage of expensive equipment and highly trained clinicians. |
format | Online Article Text |
id | pubmed-4971218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-49712182016-08-04 The power of data mining in diagnosis of childhood pneumonia Naydenova, Elina Tsanas, Athanasios Howie, Stephen Casals-Pascual, Climent De Vos, Maarten J R Soc Interface Life Sciences–Engineering interface Childhood pneumonia is the leading cause of death of children under the age of 5 years globally. Diagnostic information on the presence of infection, severity and aetiology (bacterial versus viral) is crucial for appropriate treatment. However, the derivation of such information requires advanced equipment (such as X-rays) and clinical expertise to correctly assess observational clinical signs (such as chest indrawing); both of these are often unavailable in resource-constrained settings. In this study, these challenges were addressed through the development of a suite of data mining tools, facilitating automated diagnosis through quantifiable features. Findings were validated on a large dataset comprising 780 children diagnosed with pneumonia and 801 age-matched healthy controls. Pneumonia was identified via four quantifiable vital signs (98.2% sensitivity and 97.6% specificity). Moreover, it was shown that severity can be determined through a combination of three vital signs and two lung sounds (72.4% sensitivity and 82.2% specificity); addition of a conventional biomarker (C-reactive protein) further improved severity predictions (89.1% sensitivity and 81.3% specificity). Finally, we demonstrated that aetiology can be determined using three vital signs and a newly proposed biomarker (lipocalin-2) (81.8% sensitivity and 90.6% specificity). These results suggest that a suite of carefully designed machine learning tools can be used to support multi-faceted diagnosis of childhood pneumonia in resource-constrained settings, compensating for the shortage of expensive equipment and highly trained clinicians. The Royal Society 2016-07 /pmc/articles/PMC4971218/ /pubmed/27466436 http://dx.doi.org/10.1098/rsif.2016.0266 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Engineering interface Naydenova, Elina Tsanas, Athanasios Howie, Stephen Casals-Pascual, Climent De Vos, Maarten The power of data mining in diagnosis of childhood pneumonia |
title | The power of data mining in diagnosis of childhood pneumonia |
title_full | The power of data mining in diagnosis of childhood pneumonia |
title_fullStr | The power of data mining in diagnosis of childhood pneumonia |
title_full_unstemmed | The power of data mining in diagnosis of childhood pneumonia |
title_short | The power of data mining in diagnosis of childhood pneumonia |
title_sort | power of data mining in diagnosis of childhood pneumonia |
topic | Life Sciences–Engineering interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4971218/ https://www.ncbi.nlm.nih.gov/pubmed/27466436 http://dx.doi.org/10.1098/rsif.2016.0266 |
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