Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts
Background Typically, algorithms to classify phenotypes using electronic medical record (EMR) data were developed to perform well in a specific patient population. There is increasing interest in analyses which can allow study of a specific outcome across different diseases. Such a study in the EMR...
Main Authors: | , , , , , , , , , , , , , , , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | en_US |
Published: |
Public Library of Science
2015
|
Online Access: | http://hdl.handle.net/1721.1/99879 https://orcid.org/0000-0001-8411-6403 |
_version_ | 1826215257677234176 |
---|---|
author | Liao, Katherine P. Ananthakrishnan, Ashwin N. Kumar, Vishesh Xia, Zongqi Cagan, Andrew Gainer, Vivian S. Goryachev, Sergey Chen, Pei Savova, Guergana K. Agniel, Denis Churchill, Susanne Lee, Jaeyoung Murphy, Shawn N. Plenge, Robert M. Szolovits, Peter Kohane, Isaac Shaw, Stanley Y. Karlson, Elizabeth W. Cai, Tianxi |
author2 | Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory |
author_facet | Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory Liao, Katherine P. Ananthakrishnan, Ashwin N. Kumar, Vishesh Xia, Zongqi Cagan, Andrew Gainer, Vivian S. Goryachev, Sergey Chen, Pei Savova, Guergana K. Agniel, Denis Churchill, Susanne Lee, Jaeyoung Murphy, Shawn N. Plenge, Robert M. Szolovits, Peter Kohane, Isaac Shaw, Stanley Y. Karlson, Elizabeth W. Cai, Tianxi |
author_sort | Liao, Katherine P. |
collection | MIT |
description | Background
Typically, algorithms to classify phenotypes using electronic medical record (EMR) data were developed to perform well in a specific patient population. There is increasing interest in analyses which can allow study of a specific outcome across different diseases. Such a study in the EMR would require an algorithm that can be applied across different patient populations. Our objectives were: (1) to develop an algorithm that would enable the study of coronary artery disease (CAD) across diverse patient populations; (2) to study the impact of adding narrative data extracted using natural language processing (NLP) in the algorithm. Additionally, we demonstrate how to implement CAD algorithm to compare risk across 3 chronic diseases in a preliminary study.
Methods and Results
We studied 3 established EMR based patient cohorts: diabetes mellitus (DM, n = 65,099), inflammatory bowel disease (IBD, n = 10,974), and rheumatoid arthritis (RA, n = 4,453) from two large academic centers. We developed a CAD algorithm using NLP in addition to structured data (e.g. ICD9 codes) in the RA cohort and validated it in the DM and IBD cohorts. The CAD algorithm using NLP in addition to structured data achieved specificity >95% with a positive predictive value (PPV) 90% in the training (RA) and validation sets (IBD and DM). The addition of NLP data improved the sensitivity for all cohorts, classifying an additional 17% of CAD subjects in IBD and 10% in DM while maintaining PPV of 90%. The algorithm classified 16,488 DM (26.1%), 457 IBD (4.2%), and 245 RA (5.0%) with CAD. In a cross-sectional analysis, CAD risk was 63% lower in RA and 68% lower in IBD compared to DM (p<0.0001) after adjusting for traditional cardiovascular risk factors.
Conclusions
We developed and validated a CAD algorithm that performed well across diverse patient populations. The addition of NLP into the CAD algorithm improved the sensitivity of the algorithm, particularly in cohorts where the prevalence of CAD was low. Preliminary data suggest that CAD risk was significantly lower in RA and IBD compared to DM. |
first_indexed | 2024-09-23T16:21:30Z |
format | Article |
id | mit-1721.1/99879 |
institution | Massachusetts Institute of Technology |
language | en_US |
last_indexed | 2024-09-23T16:21:30Z |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | dspace |
spelling | mit-1721.1/998792022-09-29T19:37:59Z Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts Liao, Katherine P. Ananthakrishnan, Ashwin N. Kumar, Vishesh Xia, Zongqi Cagan, Andrew Gainer, Vivian S. Goryachev, Sergey Chen, Pei Savova, Guergana K. Agniel, Denis Churchill, Susanne Lee, Jaeyoung Murphy, Shawn N. Plenge, Robert M. Szolovits, Peter Kohane, Isaac Shaw, Stanley Y. Karlson, Elizabeth W. Cai, Tianxi Massachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratory Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Szolovits, Peter Background Typically, algorithms to classify phenotypes using electronic medical record (EMR) data were developed to perform well in a specific patient population. There is increasing interest in analyses which can allow study of a specific outcome across different diseases. Such a study in the EMR would require an algorithm that can be applied across different patient populations. Our objectives were: (1) to develop an algorithm that would enable the study of coronary artery disease (CAD) across diverse patient populations; (2) to study the impact of adding narrative data extracted using natural language processing (NLP) in the algorithm. Additionally, we demonstrate how to implement CAD algorithm to compare risk across 3 chronic diseases in a preliminary study. Methods and Results We studied 3 established EMR based patient cohorts: diabetes mellitus (DM, n = 65,099), inflammatory bowel disease (IBD, n = 10,974), and rheumatoid arthritis (RA, n = 4,453) from two large academic centers. We developed a CAD algorithm using NLP in addition to structured data (e.g. ICD9 codes) in the RA cohort and validated it in the DM and IBD cohorts. The CAD algorithm using NLP in addition to structured data achieved specificity >95% with a positive predictive value (PPV) 90% in the training (RA) and validation sets (IBD and DM). The addition of NLP data improved the sensitivity for all cohorts, classifying an additional 17% of CAD subjects in IBD and 10% in DM while maintaining PPV of 90%. The algorithm classified 16,488 DM (26.1%), 457 IBD (4.2%), and 245 RA (5.0%) with CAD. In a cross-sectional analysis, CAD risk was 63% lower in RA and 68% lower in IBD compared to DM (p<0.0001) after adjusting for traditional cardiovascular risk factors. Conclusions We developed and validated a CAD algorithm that performed well across diverse patient populations. The addition of NLP into the CAD algorithm improved the sensitivity of the algorithm, particularly in cohorts where the prevalence of CAD was low. Preliminary data suggest that CAD risk was significantly lower in RA and IBD compared to DM. National Institutes of Health (U.S.). Informatics for Integrating Biology and the Bedside Project (U54LM008748) 2015-11-10T16:23:06Z 2015-11-10T16:23:06Z 2015-08 2014-09 Article http://purl.org/eprint/type/JournalArticle 1932-6203 http://hdl.handle.net/1721.1/99879 Liao, Katherine P., Ashwin N. Ananthakrishnan, Vishesh Kumar, Zongqi Xia, Andrew Cagan, Vivian S. Gainer, Sergey Goryachev, et al. “Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts.” Edited by Giorgos Bamias. PLOS ONE 10, no. 8 (August 24, 2015): e0136651. https://orcid.org/0000-0001-8411-6403 en_US http://dx.doi.org/10.1371/journal.pone.0136651 PLOS ONE Creative Commons Attribution http://creativecommons.org/licenses/by/4.0/ application/pdf Public Library of Science Public Library of Science |
spellingShingle | Liao, Katherine P. Ananthakrishnan, Ashwin N. Kumar, Vishesh Xia, Zongqi Cagan, Andrew Gainer, Vivian S. Goryachev, Sergey Chen, Pei Savova, Guergana K. Agniel, Denis Churchill, Susanne Lee, Jaeyoung Murphy, Shawn N. Plenge, Robert M. Szolovits, Peter Kohane, Isaac Shaw, Stanley Y. Karlson, Elizabeth W. Cai, Tianxi Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts |
title | Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts |
title_full | Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts |
title_fullStr | Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts |
title_full_unstemmed | Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts |
title_short | Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts |
title_sort | methods to develop an electronic medical record phenotype algorithm to compare the risk of coronary artery disease across 3 chronic disease cohorts |
url | http://hdl.handle.net/1721.1/99879 https://orcid.org/0000-0001-8411-6403 |
work_keys_str_mv | AT liaokatherinep methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT ananthakrishnanashwinn methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT kumarvishesh methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT xiazongqi methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT caganandrew methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT gainervivians methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT goryachevsergey methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT chenpei methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT savovaguerganak methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT agnieldenis methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT churchillsusanne methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT leejaeyoung methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT murphyshawnn methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT plengerobertm methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT szolovitspeter methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT kohaneisaac methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT shawstanleyy methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT karlsonelizabethw methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts AT caitianxi methodstodevelopanelectronicmedicalrecordphenotypealgorithmtocomparetheriskofcoronaryarterydiseaseacross3chronicdiseasecohorts |