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dfgcompare: a library to support process variant analysis through Markov models
BACKGROUND: Data-driven process analysis is an important area that relies on software support. Process variant analysis is a sort of analysis technique in which analysts compare executed process variants, a.k.a. process cohorts. This comparison can help to identify insights for improving processes....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686257/ https://www.ncbi.nlm.nih.gov/pubmed/34930223 http://dx.doi.org/10.1186/s12911-021-01715-3 |
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author | Jalali, Amin Johannesson, Paul Perjons, Erik Askfors, Ylva Rezaei Kalladj, Abdolazim Shemeikka, Tero Vég, Anikó |
author_facet | Jalali, Amin Johannesson, Paul Perjons, Erik Askfors, Ylva Rezaei Kalladj, Abdolazim Shemeikka, Tero Vég, Anikó |
author_sort | Jalali, Amin |
collection | PubMed |
description | BACKGROUND: Data-driven process analysis is an important area that relies on software support. Process variant analysis is a sort of analysis technique in which analysts compare executed process variants, a.k.a. process cohorts. This comparison can help to identify insights for improving processes. There are a few software supports to enable process cohort comparison based on the frequencies of process activities and performance metrics. These metrics are effective in cohort analysis, but they cannot support cohort comparison based on the probability of transitions among states, which is an important enabler for cohort analysis in healthcare. RESULTS: This paper defines an approach to compare process cohorts using Markov models. The approach is formalized, and it is implemented as an open-source python library, named dfgcompare. This library can be used by other researchers to compare process cohorts. The implementation is also used to compare caregivers’ behavior when prescribing drugs in the Stockholm Region. The result shows that the approach enables the comparison of process cohorts in practice. CONCLUSIONS: We conclude that dfgcompare supports identifying differences among process cohorts. |
format | Online Article Text |
id | pubmed-8686257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86862572021-12-20 dfgcompare: a library to support process variant analysis through Markov models Jalali, Amin Johannesson, Paul Perjons, Erik Askfors, Ylva Rezaei Kalladj, Abdolazim Shemeikka, Tero Vég, Anikó BMC Med Inform Decis Mak Software BACKGROUND: Data-driven process analysis is an important area that relies on software support. Process variant analysis is a sort of analysis technique in which analysts compare executed process variants, a.k.a. process cohorts. This comparison can help to identify insights for improving processes. There are a few software supports to enable process cohort comparison based on the frequencies of process activities and performance metrics. These metrics are effective in cohort analysis, but they cannot support cohort comparison based on the probability of transitions among states, which is an important enabler for cohort analysis in healthcare. RESULTS: This paper defines an approach to compare process cohorts using Markov models. The approach is formalized, and it is implemented as an open-source python library, named dfgcompare. This library can be used by other researchers to compare process cohorts. The implementation is also used to compare caregivers’ behavior when prescribing drugs in the Stockholm Region. The result shows that the approach enables the comparison of process cohorts in practice. CONCLUSIONS: We conclude that dfgcompare supports identifying differences among process cohorts. BioMed Central 2021-12-20 /pmc/articles/PMC8686257/ /pubmed/34930223 http://dx.doi.org/10.1186/s12911-021-01715-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Software Jalali, Amin Johannesson, Paul Perjons, Erik Askfors, Ylva Rezaei Kalladj, Abdolazim Shemeikka, Tero Vég, Anikó dfgcompare: a library to support process variant analysis through Markov models |
title | dfgcompare: a library to support process variant analysis through Markov models |
title_full | dfgcompare: a library to support process variant analysis through Markov models |
title_fullStr | dfgcompare: a library to support process variant analysis through Markov models |
title_full_unstemmed | dfgcompare: a library to support process variant analysis through Markov models |
title_short | dfgcompare: a library to support process variant analysis through Markov models |
title_sort | dfgcompare: a library to support process variant analysis through markov models |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686257/ https://www.ncbi.nlm.nih.gov/pubmed/34930223 http://dx.doi.org/10.1186/s12911-021-01715-3 |
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