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Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales
Journal of Neurology, Neurosurgery and Psychiatry, Volume: 95, Issue: 11, Pages: 1032 - 1035
Swansea University Authors: James Witts , Elaine Craig, Sarah Knowles, Rod Middleton
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DOI (Published version): 10.1136/jnnp-2024-333532
Abstract
Background: Identification of multiple sclerosis (MS) cases in routine healthcare data repositories remains challenging. MS can have a protracted diagnostic process and is rarely identified as a primary reason for admission to the hospital. Difficulties in identification are compounded in systems th...
Published in: | Journal of Neurology, Neurosurgery and Psychiatry |
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ISSN: | 0022-3050 1468-330X |
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2024
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<?xml version="1.0" encoding="utf-8"?><rfc1807 xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:xsd="http://www.w3.org/2001/XMLSchema"><bib-version>v2</bib-version><id>66529</id><entry>2024-05-29</entry><title>Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales</title><swanseaauthors><author><sid>c8d1e374a823863aae5d0dfaec19c7b5</sid><ORCID>0009-0008-3386-2965</ORCID><firstname>James</firstname><surname>Witts</surname><name>James Witts</name><active>true</active><ethesisStudent>false</ethesisStudent></author><author><sid>99f62fa657546df3f118c712d18e5595</sid><firstname>Elaine</firstname><surname>Craig</surname><name>Elaine Craig</name><active>true</active><ethesisStudent>false</ethesisStudent></author><author><sid>6c4c4acf0f27a0964f6f4b36c2a4ffac</sid><firstname>Sarah</firstname><surname>Knowles</surname><name>Sarah Knowles</name><active>true</active><ethesisStudent>false</ethesisStudent></author><author><sid>005518f819ef1a2a13fdf438529bdfcd</sid><ORCID>0000-0002-2130-4420</ORCID><firstname>Rod</firstname><surname>Middleton</surname><name>Rod Middleton</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2024-05-29</date><deptcode>MEDS</deptcode><abstract>Background: Identification of multiple sclerosis (MS) cases in routine healthcare data repositories remains challenging. MS can have a protracted diagnostic process and is rarely identified as a primary reason for admission to the hospital. Difficulties in identification are compounded in systems that do not include insurance or payer information concerning drug treatments or non-notifiable disease. Aim: To develop an algorithm to reliably identify MS cases within a national health data bank. Method: Retrospective analysis of the Secure Anonymised Information Linkage (SAIL) databank was used to identify MS cases using a novel algorithm. Sensitivity and specificity were tested using two existing independent MS datasets, one clinically validated and population-based and a second from a self-registered MS national registry. Results: From 4 757 428 records, the algorithm identified 6194 living cases of MS within Wales on 31 December 2020 (prevalence 221.65 (95% CI 216.17 to 227.24) per 100 000). Case-finding sensitivity and specificity were 96.8% and 99.9% for the clinically validated population-based cohort and sensitivity was 96.7% for the self-declared registry population. Discussion: The algorithm successfully identified MS cases within the SAIL databank with high sensitivity and specificity, verified by two independent populations and has important utility in large-scale epidemiological studies of MS.</abstract><type>Journal Article</type><journal>Journal of Neurology, Neurosurgery and Psychiatry</journal><volume>95</volume><journalNumber>11</journalNumber><paginationStart>1032</paginationStart><paginationEnd>1035</paginationEnd><publisher>BMJ</publisher><placeOfPublication/><isbnPrint/><isbnElectronic/><issnPrint>0022-3050</issnPrint><issnElectronic>1468-330X</issnElectronic><keywords/><publishedDay>16</publishedDay><publishedMonth>10</publishedMonth><publishedYear>2024</publishedYear><publishedDate>2024-10-16</publishedDate><doi>10.1136/jnnp-2024-333532</doi><url/><notes>Short report</notes><college>COLLEGE NANME</college><department>Medical School</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>MEDS</DepartmentCode><institution>Swansea University</institution><apcterm>SU Library paid the OA fee (TA Institutional Deal)</apcterm><funders>This study was funded by Multiple Sclerosis Society (147).</funders><projectreference/><lastEdited>2024-10-17T15:37:16.5903452</lastEdited><Created>2024-05-29T17:03:30.6928179</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Health Data Science</level></path><authors><author><firstname>Richard</firstname><surname>Nicholas</surname><orcid>0000-0003-0414-1225</orcid><order>1</order></author><author><firstname>Emma Clare</firstname><surname>Tallantyre</surname><orcid>0000-0002-3760-6634</orcid><order>2</order></author><author><firstname>James</firstname><surname>Witts</surname><orcid>0009-0008-3386-2965</orcid><order>3</order></author><author><firstname>Ruth Ann</firstname><surname>Marrie</surname><orcid>0000-0002-1855-5595</orcid><order>4</order></author><author><firstname>Elaine</firstname><surname>Craig</surname><order>5</order></author><author><firstname>Sarah</firstname><surname>Knowles</surname><order>6</order></author><author><firstname>Owen Rhys</firstname><surname>Pearson</surname><orcid>0000-0002-2712-0200</orcid><order>7</order></author><author><firstname>Katherine</firstname><surname>Harding</surname><order>8</order></author><author><firstname>Karim</firstname><surname>Kreft</surname><order>9</order></author><author><firstname>J</firstname><surname>Hawken</surname><order>10</order></author><author><firstname>Gillian</firstname><surname>Ingram</surname><order>11</order></author><author><firstname>Bethan</firstname><surname>Morgan</surname><order>12</order></author><author><firstname>Rod</firstname><surname>Middleton</surname><orcid>0000-0002-2130-4420</orcid><order>13</order></author><author><firstname>Neil</firstname><surname>Robertson</surname><order>14</order></author><author><firstname>UKMS Register Research</firstname><surname>Group</surname><order>15</order></author></authors><documents><document><filename>66529__30487__88a72cf17813481dbcb835d60fa511e6.pdf</filename><originalFilename>66529.VoR.pdf</originalFilename><uploaded>2024-05-29T17:08:04.5357246</uploaded><type>Output</type><contentLength>618712</contentLength><contentType>application/pdf</contentType><version>Version of Record</version><cronfaStatus>true</cronfaStatus><documentNotes>This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY- NC 4.0) license.</documentNotes><copyrightCorrect>true</copyrightCorrect><language>eng</language><licence>http://creativecommons.org/licenses/by-nc/4.0/</licence></document></documents><OutputDurs/></rfc1807> |
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v2 66529 2024-05-29 Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales c8d1e374a823863aae5d0dfaec19c7b5 0009-0008-3386-2965 James Witts James Witts true false 99f62fa657546df3f118c712d18e5595 Elaine Craig Elaine Craig true false 6c4c4acf0f27a0964f6f4b36c2a4ffac Sarah Knowles Sarah Knowles true false 005518f819ef1a2a13fdf438529bdfcd 0000-0002-2130-4420 Rod Middleton Rod Middleton true false 2024-05-29 MEDS Background: Identification of multiple sclerosis (MS) cases in routine healthcare data repositories remains challenging. MS can have a protracted diagnostic process and is rarely identified as a primary reason for admission to the hospital. Difficulties in identification are compounded in systems that do not include insurance or payer information concerning drug treatments or non-notifiable disease. Aim: To develop an algorithm to reliably identify MS cases within a national health data bank. Method: Retrospective analysis of the Secure Anonymised Information Linkage (SAIL) databank was used to identify MS cases using a novel algorithm. Sensitivity and specificity were tested using two existing independent MS datasets, one clinically validated and population-based and a second from a self-registered MS national registry. Results: From 4 757 428 records, the algorithm identified 6194 living cases of MS within Wales on 31 December 2020 (prevalence 221.65 (95% CI 216.17 to 227.24) per 100 000). Case-finding sensitivity and specificity were 96.8% and 99.9% for the clinically validated population-based cohort and sensitivity was 96.7% for the self-declared registry population. Discussion: The algorithm successfully identified MS cases within the SAIL databank with high sensitivity and specificity, verified by two independent populations and has important utility in large-scale epidemiological studies of MS. Journal Article Journal of Neurology, Neurosurgery and Psychiatry 95 11 1032 1035 BMJ 0022-3050 1468-330X 16 10 2024 2024-10-16 10.1136/jnnp-2024-333532 Short report COLLEGE NANME Medical School COLLEGE CODE MEDS Swansea University SU Library paid the OA fee (TA Institutional Deal) This study was funded by Multiple Sclerosis Society (147). 2024-10-17T15:37:16.5903452 2024-05-29T17:03:30.6928179 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Health Data Science Richard Nicholas 0000-0003-0414-1225 1 Emma Clare Tallantyre 0000-0002-3760-6634 2 James Witts 0009-0008-3386-2965 3 Ruth Ann Marrie 0000-0002-1855-5595 4 Elaine Craig 5 Sarah Knowles 6 Owen Rhys Pearson 0000-0002-2712-0200 7 Katherine Harding 8 Karim Kreft 9 J Hawken 10 Gillian Ingram 11 Bethan Morgan 12 Rod Middleton 0000-0002-2130-4420 13 Neil Robertson 14 UKMS Register Research Group 15 66529__30487__88a72cf17813481dbcb835d60fa511e6.pdf 66529.VoR.pdf 2024-05-29T17:08:04.5357246 Output 618712 application/pdf Version of Record true This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY- NC 4.0) license. true eng http://creativecommons.org/licenses/by-nc/4.0/ |
title |
Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales |
spellingShingle |
Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales James Witts Elaine Craig Sarah Knowles Rod Middleton |
title_short |
Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales |
title_full |
Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales |
title_fullStr |
Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales |
title_full_unstemmed |
Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales |
title_sort |
Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales |
author_id_str_mv |
c8d1e374a823863aae5d0dfaec19c7b5 99f62fa657546df3f118c712d18e5595 6c4c4acf0f27a0964f6f4b36c2a4ffac 005518f819ef1a2a13fdf438529bdfcd |
author_id_fullname_str_mv |
c8d1e374a823863aae5d0dfaec19c7b5_***_James Witts 99f62fa657546df3f118c712d18e5595_***_Elaine Craig 6c4c4acf0f27a0964f6f4b36c2a4ffac_***_Sarah Knowles 005518f819ef1a2a13fdf438529bdfcd_***_Rod Middleton |
author |
James Witts Elaine Craig Sarah Knowles Rod Middleton |
author2 |
Richard Nicholas Emma Clare Tallantyre James Witts Ruth Ann Marrie Elaine Craig Sarah Knowles Owen Rhys Pearson Katherine Harding Karim Kreft J Hawken Gillian Ingram Bethan Morgan Rod Middleton Neil Robertson UKMS Register Research Group |
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Journal of Neurology, Neurosurgery and Psychiatry |
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95 |
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1032 |
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2024 |
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Swansea University |
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0022-3050 1468-330X |
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10.1136/jnnp-2024-333532 |
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BMJ |
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Faculty of Medicine, Health and Life Sciences |
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Faculty of Medicine, Health and Life Sciences |
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Swansea University Medical School - Health Data Science{{{_:::_}}}Faculty of Medicine, Health and Life Sciences{{{_:::_}}}Swansea University Medical School - Health Data Science |
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description |
Background: Identification of multiple sclerosis (MS) cases in routine healthcare data repositories remains challenging. MS can have a protracted diagnostic process and is rarely identified as a primary reason for admission to the hospital. Difficulties in identification are compounded in systems that do not include insurance or payer information concerning drug treatments or non-notifiable disease. Aim: To develop an algorithm to reliably identify MS cases within a national health data bank. Method: Retrospective analysis of the Secure Anonymised Information Linkage (SAIL) databank was used to identify MS cases using a novel algorithm. Sensitivity and specificity were tested using two existing independent MS datasets, one clinically validated and population-based and a second from a self-registered MS national registry. Results: From 4 757 428 records, the algorithm identified 6194 living cases of MS within Wales on 31 December 2020 (prevalence 221.65 (95% CI 216.17 to 227.24) per 100 000). Case-finding sensitivity and specificity were 96.8% and 99.9% for the clinically validated population-based cohort and sensitivity was 96.7% for the self-declared registry population. Discussion: The algorithm successfully identified MS cases within the SAIL databank with high sensitivity and specificity, verified by two independent populations and has important utility in large-scale epidemiological studies of MS. |
published_date |
2024-10-16T15:37:14Z |
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1813172280048484352 |
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11.036815 |