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A method for controlling complex confounding effects in the detection of adverse drug reactions using electronic health records
Electronic health records (EHRs) contain information to detect adverse drug reactions (ADRs), as they contain comprehensive clinical information. A major challenge of using comprehensive information involves confounding. We propose a novel data-driven method to identify ADR signals accurately by adj...
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Published in: | Journal of the American Medical Informatics Association : JAMIA 2014-03, Vol.21 (2), p.308-314 |
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creator | Li, Ying Salmasian, Hojjat Vilar, Santiago Chase, Herbert Friedman, Carol Wei, Ying |
description | Electronic health records (EHRs) contain information to detect adverse drug reactions (ADRs), as they contain comprehensive clinical information. A major challenge of using comprehensive information involves confounding. We propose a novel data-driven method to identify ADR signals accurately by adjusting for confounders.
We focused on two serious ADRs, rhabdomyolysis and pancreatitis, and used information in 264,155 unique patient records. We identified an ADR using established criteria, selected potential confounders, and then used penalized logistic regressions to estimate confounder-adjusted ADR associations. A reference standard was created to evaluate and compare the precision of the proposed method and four others.
Precision was 83.3% for rhabdomyolysis and 60.8% for pancreatitis when using the proposed method, and we identified several drug safety signals that are interesting for further clinical review.
The proposed method effectively estimated ADR associations after adjusting for confounders. A main cause of error was probably due to the nature of the dataset in that a substantial number of patients had a single visit only and, therefore, it was not possible to determine correctly the appropriate sequence of events for them. It is likely that performance will be improved with use of EHR data that contain more longitudinal records.
This data-driven method is effective in controlling for confounding, resulting in either a higher or similar precision when compared with four comparators, has the unique ability to provide insight into confounders for each specific medication-ADR pair, and can be easily adapted to other EHR systems. |
doi_str_mv | 10.1136/amiajnl-2013-001718 |
format | article |
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We focused on two serious ADRs, rhabdomyolysis and pancreatitis, and used information in 264,155 unique patient records. We identified an ADR using established criteria, selected potential confounders, and then used penalized logistic regressions to estimate confounder-adjusted ADR associations. A reference standard was created to evaluate and compare the precision of the proposed method and four others.
Precision was 83.3% for rhabdomyolysis and 60.8% for pancreatitis when using the proposed method, and we identified several drug safety signals that are interesting for further clinical review.
The proposed method effectively estimated ADR associations after adjusting for confounders. A main cause of error was probably due to the nature of the dataset in that a substantial number of patients had a single visit only and, therefore, it was not possible to determine correctly the appropriate sequence of events for them. It is likely that performance will be improved with use of EHR data that contain more longitudinal records.
This data-driven method is effective in controlling for confounding, resulting in either a higher or similar precision when compared with four comparators, has the unique ability to provide insight into confounders for each specific medication-ADR pair, and can be easily adapted to other EHR systems.</description><identifier>ISSN: 1067-5027</identifier><identifier>EISSN: 1527-974X</identifier><identifier>DOI: 10.1136/amiajnl-2013-001718</identifier><identifier>PMID: 23907285</identifier><language>eng</language><publisher>England: BMJ Publishing Group</publisher><subject>Adult ; Adverse Drug Reaction Reporting Systems ; Aged ; Confounding Factors (Epidemiology) ; Drug-Related Side Effects and Adverse Reactions - diagnosis ; Electronic Health Records ; Female ; Humans ; Knowledge Bases ; Male ; Middle Aged ; Pancreatitis - diagnosis ; Research and Applications ; Rhabdomyolysis - diagnosis</subject><ispartof>Journal of the American Medical Informatics Association : JAMIA, 2014-03, Vol.21 (2), p.308-314</ispartof><rights>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-101399faf0fd76e80b741c471b3d6de84bbd7c086936afd69f5beaf73a98605a3</citedby><cites>FETCH-LOGICAL-c471t-101399faf0fd76e80b741c471b3d6de84bbd7c086936afd69f5beaf73a98605a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932454/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932454/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23907285$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Ying</creatorcontrib><creatorcontrib>Salmasian, Hojjat</creatorcontrib><creatorcontrib>Vilar, Santiago</creatorcontrib><creatorcontrib>Chase, Herbert</creatorcontrib><creatorcontrib>Friedman, Carol</creatorcontrib><creatorcontrib>Wei, Ying</creatorcontrib><title>A method for controlling complex confounding effects in the detection of adverse drug reactions using electronic health records</title><title>Journal of the American Medical Informatics Association : JAMIA</title><addtitle>J Am Med Inform Assoc</addtitle><description>Electronic health records (EHRs) contain information to detect adverse drug reactions (ADRs), as they contain comprehensive clinical information. A major challenge of using comprehensive information involves confounding. We propose a novel data-driven method to identify ADR signals accurately by adjusting for confounders.
We focused on two serious ADRs, rhabdomyolysis and pancreatitis, and used information in 264,155 unique patient records. We identified an ADR using established criteria, selected potential confounders, and then used penalized logistic regressions to estimate confounder-adjusted ADR associations. A reference standard was created to evaluate and compare the precision of the proposed method and four others.
Precision was 83.3% for rhabdomyolysis and 60.8% for pancreatitis when using the proposed method, and we identified several drug safety signals that are interesting for further clinical review.
The proposed method effectively estimated ADR associations after adjusting for confounders. A main cause of error was probably due to the nature of the dataset in that a substantial number of patients had a single visit only and, therefore, it was not possible to determine correctly the appropriate sequence of events for them. It is likely that performance will be improved with use of EHR data that contain more longitudinal records.
This data-driven method is effective in controlling for confounding, resulting in either a higher or similar precision when compared with four comparators, has the unique ability to provide insight into confounders for each specific medication-ADR pair, and can be easily adapted to other EHR systems.</description><subject>Adult</subject><subject>Adverse Drug Reaction Reporting Systems</subject><subject>Aged</subject><subject>Confounding Factors (Epidemiology)</subject><subject>Drug-Related Side Effects and Adverse Reactions - diagnosis</subject><subject>Electronic Health Records</subject><subject>Female</subject><subject>Humans</subject><subject>Knowledge Bases</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pancreatitis - diagnosis</subject><subject>Research and Applications</subject><subject>Rhabdomyolysis - diagnosis</subject><issn>1067-5027</issn><issn>1527-974X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpVUd1KwzAUDqK4OX0CQfIC1aRpk-ZGGMM_GHij4F1Im2TNaJuRtEOvfHXTbQ69ysn3dzh8AFxjdIsxoXeytXLdNUmKMEkQwgwXJ2CK85QlnGUfp3FGlCU5StkEXISwjhqakvwcTFLCEUuLfAq-57DVfe0UNM7DynW9d01ju1Wc202jP0fMuKFTI6aN0VUfoO1gX2uodB-_1nXQGSjVVvsQQT-soNdyRwQ4hJ2xiULvOlvBWsumr6Oicl6FS3BmZBP01eGdgffHh7fFc7J8fXpZzJdJlTHcJzjeyLmRBhnFqC5QyTI8UiVRVOkiK0vFKlRQTqg0inKTl1oaRiQvKMolmYH7fe5mKFutKh0PlY3YeNtK_yWctOI_09larNxWEE7SLM9iANkHVN6F4LU5ejESYx_i0IcY-xD7PqLr5u_ao-e3APID382Npw</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Li, Ying</creator><creator>Salmasian, Hojjat</creator><creator>Vilar, Santiago</creator><creator>Chase, Herbert</creator><creator>Friedman, Carol</creator><creator>Wei, Ying</creator><general>BMJ Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20140301</creationdate><title>A method for controlling complex confounding effects in the detection of adverse drug reactions using electronic health records</title><author>Li, Ying ; Salmasian, Hojjat ; Vilar, Santiago ; Chase, Herbert ; Friedman, Carol ; Wei, Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-101399faf0fd76e80b741c471b3d6de84bbd7c086936afd69f5beaf73a98605a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Adverse Drug Reaction Reporting Systems</topic><topic>Aged</topic><topic>Confounding Factors (Epidemiology)</topic><topic>Drug-Related Side Effects and Adverse Reactions - diagnosis</topic><topic>Electronic Health Records</topic><topic>Female</topic><topic>Humans</topic><topic>Knowledge Bases</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pancreatitis - diagnosis</topic><topic>Research and Applications</topic><topic>Rhabdomyolysis - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Ying</creatorcontrib><creatorcontrib>Salmasian, Hojjat</creatorcontrib><creatorcontrib>Vilar, Santiago</creatorcontrib><creatorcontrib>Chase, Herbert</creatorcontrib><creatorcontrib>Friedman, Carol</creatorcontrib><creatorcontrib>Wei, Ying</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Medical Informatics Association : JAMIA</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Ying</au><au>Salmasian, Hojjat</au><au>Vilar, Santiago</au><au>Chase, Herbert</au><au>Friedman, Carol</au><au>Wei, Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A method for controlling complex confounding effects in the detection of adverse drug reactions using electronic health records</atitle><jtitle>Journal of the American Medical Informatics Association : JAMIA</jtitle><addtitle>J Am Med Inform Assoc</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>21</volume><issue>2</issue><spage>308</spage><epage>314</epage><pages>308-314</pages><issn>1067-5027</issn><eissn>1527-974X</eissn><abstract>Electronic health records (EHRs) contain information to detect adverse drug reactions (ADRs), as they contain comprehensive clinical information. A major challenge of using comprehensive information involves confounding. We propose a novel data-driven method to identify ADR signals accurately by adjusting for confounders.
We focused on two serious ADRs, rhabdomyolysis and pancreatitis, and used information in 264,155 unique patient records. We identified an ADR using established criteria, selected potential confounders, and then used penalized logistic regressions to estimate confounder-adjusted ADR associations. A reference standard was created to evaluate and compare the precision of the proposed method and four others.
Precision was 83.3% for rhabdomyolysis and 60.8% for pancreatitis when using the proposed method, and we identified several drug safety signals that are interesting for further clinical review.
The proposed method effectively estimated ADR associations after adjusting for confounders. A main cause of error was probably due to the nature of the dataset in that a substantial number of patients had a single visit only and, therefore, it was not possible to determine correctly the appropriate sequence of events for them. It is likely that performance will be improved with use of EHR data that contain more longitudinal records.
This data-driven method is effective in controlling for confounding, resulting in either a higher or similar precision when compared with four comparators, has the unique ability to provide insight into confounders for each specific medication-ADR pair, and can be easily adapted to other EHR systems.</abstract><cop>England</cop><pub>BMJ Publishing Group</pub><pmid>23907285</pmid><doi>10.1136/amiajnl-2013-001718</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Adverse Drug Reaction Reporting Systems Aged Confounding Factors (Epidemiology) Drug-Related Side Effects and Adverse Reactions - diagnosis Electronic Health Records Female Humans Knowledge Bases Male Middle Aged Pancreatitis - diagnosis Research and Applications Rhabdomyolysis - diagnosis |
title | A method for controlling complex confounding effects in the detection of adverse drug reactions using electronic health records |
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