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OWL model of clinical trial eligibility criteria compatible with partially-known information
Clinical trials are important for patients, for researchers and for companies. One of the major bottlenecks is patient recruitment. This task requires the matching of a large volume of information about the patient with numerous eligibility criteria, in a logically-complex combination. Moreover, som...
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Published in: | Journal of biomedical semantics 2013-09, Vol.4 (1), p.17-17 |
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creator | Dameron, Olivier Besana, Paolo Zekri, Oussama Bourdé, Annabel Burgun, Anita Cuggia, Marc |
description | Clinical trials are important for patients, for researchers and for companies. One of the major bottlenecks is patient recruitment. This task requires the matching of a large volume of information about the patient with numerous eligibility criteria, in a logically-complex combination. Moreover, some of the patient's information necessary to determine the status of the eligibility criteria may not be available at the time of pre-screening.
We showed that the classic approach based on negation as failure over-estimates rejection when confronted with partially-known information about the eligibility criteria because it ignores the distinction between a trial for which patient eligibility should be rejected and trials for which patient eligibility cannot be asserted. We have also shown that 58.64% of the values were unknown in the 286 prostate cancer cases examined during the weekly urology multidisciplinary meetings at Rennes' university hospital between October 2008 and March 2009.We propose an OWL design pattern for modeling eligibility criteria based on the open world assumption to address the missing information problem. We validate our model on a fictitious clinical trial and evaluate it on two real clinical trials. Our approach successfully distinguished clinical trials for which the patient is eligible, clinical trials for which we know that the patient is not eligible and clinical trials for which the patient may be eligible provided that further pieces of information (which we can identify) can be obtained.
OWL-based reasoning based on the open world assumption provides an adequate framework for distinguishing those patients who can confidently be rejected from those whose status cannot be determined. The expected benefits are a reduction of the workload of the physicians and a higher efficiency by allowing them to focus on the patients whose eligibility actually require expertise. |
doi_str_mv | 10.1186/2041-1480-4-17 |
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We showed that the classic approach based on negation as failure over-estimates rejection when confronted with partially-known information about the eligibility criteria because it ignores the distinction between a trial for which patient eligibility should be rejected and trials for which patient eligibility cannot be asserted. We have also shown that 58.64% of the values were unknown in the 286 prostate cancer cases examined during the weekly urology multidisciplinary meetings at Rennes' university hospital between October 2008 and March 2009.We propose an OWL design pattern for modeling eligibility criteria based on the open world assumption to address the missing information problem. We validate our model on a fictitious clinical trial and evaluate it on two real clinical trials. Our approach successfully distinguished clinical trials for which the patient is eligible, clinical trials for which we know that the patient is not eligible and clinical trials for which the patient may be eligible provided that further pieces of information (which we can identify) can be obtained.
OWL-based reasoning based on the open world assumption provides an adequate framework for distinguishing those patients who can confidently be rejected from those whose status cannot be determined. The expected benefits are a reduction of the workload of the physicians and a higher efficiency by allowing them to focus on the patients whose eligibility actually require expertise.</description><identifier>ISSN: 2041-1480</identifier><identifier>EISSN: 2041-1480</identifier><identifier>DOI: 10.1186/2041-1480-4-17</identifier><identifier>PMID: 24034867</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Automation ; Bioinformatics ; Clinical trials ; Computer Science ; Criteria ; Diabetes ; Life Sciences ; Mediation ; Medical informatics ; Medical records ; Medical research ; Medicine ; Medicine, Experimental ; Metastasis ; Patients ; Physicians ; Practice ; Prostate ; Prostate cancer ; Quantitative Methods ; Research data management ; Semantics ; Temporal logic ; Urology ; Workload</subject><ispartof>Journal of biomedical semantics, 2013-09, Vol.4 (1), p.17-17</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013. This work is licensed under http://creativecommons.org/licenses/by/2.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2013 Dameron et al.; licensee BioMed Central Ltd. 2013 Dameron et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b580t-80e01e04971d8a935c406c1dd95740d36406c934351452f9cdf7aec3c2333b313</citedby><cites>FETCH-LOGICAL-b580t-80e01e04971d8a935c406c1dd95740d36406c934351452f9cdf7aec3c2333b313</cites><orcidid>0000-0001-6855-4366</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852288/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2398450951?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24034867$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://inserm.hal.science/inserm-00874968$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Dameron, Olivier</creatorcontrib><creatorcontrib>Besana, Paolo</creatorcontrib><creatorcontrib>Zekri, Oussama</creatorcontrib><creatorcontrib>Bourdé, Annabel</creatorcontrib><creatorcontrib>Burgun, Anita</creatorcontrib><creatorcontrib>Cuggia, Marc</creatorcontrib><title>OWL model of clinical trial eligibility criteria compatible with partially-known information</title><title>Journal of biomedical semantics</title><addtitle>J Biomed Semantics</addtitle><description>Clinical trials are important for patients, for researchers and for companies. One of the major bottlenecks is patient recruitment. This task requires the matching of a large volume of information about the patient with numerous eligibility criteria, in a logically-complex combination. Moreover, some of the patient's information necessary to determine the status of the eligibility criteria may not be available at the time of pre-screening.
We showed that the classic approach based on negation as failure over-estimates rejection when confronted with partially-known information about the eligibility criteria because it ignores the distinction between a trial for which patient eligibility should be rejected and trials for which patient eligibility cannot be asserted. We have also shown that 58.64% of the values were unknown in the 286 prostate cancer cases examined during the weekly urology multidisciplinary meetings at Rennes' university hospital between October 2008 and March 2009.We propose an OWL design pattern for modeling eligibility criteria based on the open world assumption to address the missing information problem. We validate our model on a fictitious clinical trial and evaluate it on two real clinical trials. Our approach successfully distinguished clinical trials for which the patient is eligible, clinical trials for which we know that the patient is not eligible and clinical trials for which the patient may be eligible provided that further pieces of information (which we can identify) can be obtained.
OWL-based reasoning based on the open world assumption provides an adequate framework for distinguishing those patients who can confidently be rejected from those whose status cannot be determined. The expected benefits are a reduction of the workload of the physicians and a higher efficiency by allowing them to focus on the patients whose eligibility actually require expertise.</description><subject>Automation</subject><subject>Bioinformatics</subject><subject>Clinical trials</subject><subject>Computer Science</subject><subject>Criteria</subject><subject>Diabetes</subject><subject>Life Sciences</subject><subject>Mediation</subject><subject>Medical informatics</subject><subject>Medical records</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine, Experimental</subject><subject>Metastasis</subject><subject>Patients</subject><subject>Physicians</subject><subject>Practice</subject><subject>Prostate</subject><subject>Prostate cancer</subject><subject>Quantitative Methods</subject><subject>Research data management</subject><subject>Semantics</subject><subject>Temporal logic</subject><subject>Urology</subject><subject>Workload</subject><issn>2041-1480</issn><issn>2041-1480</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp1ks1vFCEYxidGY5vaq0dD4sWDU2GAGbiYbBq1Jpv0ovFiQhiG2X0rAyuwbfa_l3Hr2tYKCR8vP54XeKiqlwSfESLadw1mpCZM4JrVpHtSHR8CT--Mj6rTlK5wKZQSLOjz6qhhmDLRdsfV98tvSzSFwToURmQceDDaoRyhtNbBCnpwkHfIRMi2RJEJ00Zn6J1FN5DXaKNjLrDb1T98uPEI_BjiVIjgX1TPRu2SPb3tT6qvHz98Ob-ol5efPp8vlnXPBc61wBYTi5nsyCC0pNww3BoyDJJ3DA-0naeSMsoJ480ozTB22hpqGkppTwk9qd7vdTfbfrKDsT5H7dQmwqTjTgUN6v6Kh7VahWtFBW8aIYrA273A-sG2i8VSgU82Tgpj0THZius532KP9xD-k-_-SnkzNfuhZj8UU6QrGm9uzxzDz61NWU2QjHVOexu2qZBcEs4obgr6-gF6FbbRlxdVDZWCcSw5-UuttLNqdqGkNrOoWvDiNhHiN3X2CFXqYCcwwdsRSvyxDSaGlKIdD9ckWM2_8N-LvbprxgH_8-foL_7l1cw</recordid><startdate>20130913</startdate><enddate>20130913</enddate><creator>Dameron, Olivier</creator><creator>Besana, Paolo</creator><creator>Zekri, Oussama</creator><creator>Bourdé, Annabel</creator><creator>Burgun, Anita</creator><creator>Cuggia, Marc</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6855-4366</orcidid></search><sort><creationdate>20130913</creationdate><title>OWL model of clinical trial eligibility criteria compatible with partially-known information</title><author>Dameron, Olivier ; 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One of the major bottlenecks is patient recruitment. This task requires the matching of a large volume of information about the patient with numerous eligibility criteria, in a logically-complex combination. Moreover, some of the patient's information necessary to determine the status of the eligibility criteria may not be available at the time of pre-screening.
We showed that the classic approach based on negation as failure over-estimates rejection when confronted with partially-known information about the eligibility criteria because it ignores the distinction between a trial for which patient eligibility should be rejected and trials for which patient eligibility cannot be asserted. We have also shown that 58.64% of the values were unknown in the 286 prostate cancer cases examined during the weekly urology multidisciplinary meetings at Rennes' university hospital between October 2008 and March 2009.We propose an OWL design pattern for modeling eligibility criteria based on the open world assumption to address the missing information problem. We validate our model on a fictitious clinical trial and evaluate it on two real clinical trials. Our approach successfully distinguished clinical trials for which the patient is eligible, clinical trials for which we know that the patient is not eligible and clinical trials for which the patient may be eligible provided that further pieces of information (which we can identify) can be obtained.
OWL-based reasoning based on the open world assumption provides an adequate framework for distinguishing those patients who can confidently be rejected from those whose status cannot be determined. The expected benefits are a reduction of the workload of the physicians and a higher efficiency by allowing them to focus on the patients whose eligibility actually require expertise.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>24034867</pmid><doi>10.1186/2041-1480-4-17</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6855-4366</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Automation Bioinformatics Clinical trials Computer Science Criteria Diabetes Life Sciences Mediation Medical informatics Medical records Medical research Medicine Medicine, Experimental Metastasis Patients Physicians Practice Prostate Prostate cancer Quantitative Methods Research data management Semantics Temporal logic Urology Workload |
title | OWL model of clinical trial eligibility criteria compatible with partially-known information |
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