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PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care
BACKGROUND: Clinical phenotype information greatly facilitates genetic diagnostic interpretations pipelines in disease. While post-hoc extraction using natural language processing on unstructured clinical notes continues to improve, there is a need to improve point-of-care collection of patient phen...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335954/ https://www.ncbi.nlm.nih.gov/pubmed/35902925 http://dx.doi.org/10.1186/s12911-022-01927-1 |
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author | Havrilla, James M. Singaravelu, Anbumalar Driscoll, Dennis M. Minkovsky, Leonard Helbig, Ingo Medne, Livija Wang, Kai Krantz, Ian Desai, Bimal R. |
author_facet | Havrilla, James M. Singaravelu, Anbumalar Driscoll, Dennis M. Minkovsky, Leonard Helbig, Ingo Medne, Livija Wang, Kai Krantz, Ian Desai, Bimal R. |
author_sort | Havrilla, James M. |
collection | PubMed |
description | BACKGROUND: Clinical phenotype information greatly facilitates genetic diagnostic interpretations pipelines in disease. While post-hoc extraction using natural language processing on unstructured clinical notes continues to improve, there is a need to improve point-of-care collection of patient phenotypes. Therefore, we developed “PheNominal”, a point-of-care web application, embedded within Epic electronic health record (EHR) workflows, to permit capture of standardized phenotype data. METHODS: Using bi-directional web services available within commercial EHRs, we developed a lightweight web application that allows users to rapidly browse and identify relevant terms from the Human Phenotype Ontology (HPO). Selected terms are saved discretely within the patient’s EHR, permitting reuse both in clinical notes as well as in downstream diagnostic and research pipelines. RESULTS: In the 16 months since implementation, PheNominal was used to capture discrete phenotype data for over 1500 individuals and 11,000 HPO terms during clinic and inpatient encounters for a genetic diagnostic consultation service within a quaternary-care pediatric academic medical center. An average of 7 HPO terms were captured per patient. Compared to a manual workflow, the average time to enter terms for a patient was reduced from 15 to 5 min per patient, and there were fewer annotation errors. CONCLUSIONS: Modern EHRs support integration of external applications using application programming interfaces. We describe a practical application of these interfaces to facilitate deep phenotype capture in a discrete, structured format within a busy clinical workflow. Future versions will include a vendor-agnostic implementation using FHIR. We describe pilot efforts to integrate structured phenotyping through controlled dictionaries into diagnostic and research pipelines, reducing manual effort for phenotype documentation and reducing errors in data entry. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12911-022-01927-1. |
format | Online Article Text |
id | pubmed-9335954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-93359542022-07-30 PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care Havrilla, James M. Singaravelu, Anbumalar Driscoll, Dennis M. Minkovsky, Leonard Helbig, Ingo Medne, Livija Wang, Kai Krantz, Ian Desai, Bimal R. BMC Med Inform Decis Mak Research BACKGROUND: Clinical phenotype information greatly facilitates genetic diagnostic interpretations pipelines in disease. While post-hoc extraction using natural language processing on unstructured clinical notes continues to improve, there is a need to improve point-of-care collection of patient phenotypes. Therefore, we developed “PheNominal”, a point-of-care web application, embedded within Epic electronic health record (EHR) workflows, to permit capture of standardized phenotype data. METHODS: Using bi-directional web services available within commercial EHRs, we developed a lightweight web application that allows users to rapidly browse and identify relevant terms from the Human Phenotype Ontology (HPO). Selected terms are saved discretely within the patient’s EHR, permitting reuse both in clinical notes as well as in downstream diagnostic and research pipelines. RESULTS: In the 16 months since implementation, PheNominal was used to capture discrete phenotype data for over 1500 individuals and 11,000 HPO terms during clinic and inpatient encounters for a genetic diagnostic consultation service within a quaternary-care pediatric academic medical center. An average of 7 HPO terms were captured per patient. Compared to a manual workflow, the average time to enter terms for a patient was reduced from 15 to 5 min per patient, and there were fewer annotation errors. CONCLUSIONS: Modern EHRs support integration of external applications using application programming interfaces. We describe a practical application of these interfaces to facilitate deep phenotype capture in a discrete, structured format within a busy clinical workflow. Future versions will include a vendor-agnostic implementation using FHIR. We describe pilot efforts to integrate structured phenotyping through controlled dictionaries into diagnostic and research pipelines, reducing manual effort for phenotype documentation and reducing errors in data entry. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12911-022-01927-1. BioMed Central 2022-07-28 /pmc/articles/PMC9335954/ /pubmed/35902925 http://dx.doi.org/10.1186/s12911-022-01927-1 Text en © The Author(s) 2022 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 | Research Havrilla, James M. Singaravelu, Anbumalar Driscoll, Dennis M. Minkovsky, Leonard Helbig, Ingo Medne, Livija Wang, Kai Krantz, Ian Desai, Bimal R. PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care |
title | PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care |
title_full | PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care |
title_fullStr | PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care |
title_full_unstemmed | PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care |
title_short | PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care |
title_sort | phenominal: an ehr-integrated web application for structured deep phenotyping at the point of care |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9335954/ https://www.ncbi.nlm.nih.gov/pubmed/35902925 http://dx.doi.org/10.1186/s12911-022-01927-1 |
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