FRI0469 Measuring Outcome in Psoriatic Arthritis (MOPSA), A New Web-Based Tool for Assessment of Psoriatic Arthritis Showing Initiation of Treatment Change in Patients Achieving Minimal Disease Activity
BackgroundPsoriatic arthritis (PsA) is a heterogeneous disease that includes features of peripheral arthritis, spondylitis, dactylitis, enthesitis, and skin and nail disease. PsA affects about 30% of patients with psoriasis.1Minimal Disease Activity (MDA) is defined as a patient acceptable disease s...
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description | BackgroundPsoriatic arthritis (PsA) is a heterogeneous disease that includes features of peripheral arthritis, spondylitis, dactylitis, enthesitis, and skin and nail disease. PsA affects about 30% of patients with psoriasis.1Minimal Disease Activity (MDA) is defined as a patient acceptable disease state which is validated and increasingly recognised as a treatment target. MDA is defined when a patient has 5 of the following 7 criteria: tender joint count ≤1, swollen joint count ≤1, tender entheseal point ≤1, PASI ≤1 or body surface area ≤3%, Pain Visual analogue score (VAS) ≤15, patient global ≤20, Health Assessment Questionnaire ≤0.5.2Composite Psoriatic Disease Activity Index (CPDAI) assesses the five domains in PsA. Within each domain a score (range 0–3) is assigned according to predefined cut-offs. The scores for each domain are then added together to give a final score range of 0–15, 0 for no disease and 15 for severe disease.3Recently, Measuring Outcome in Psoriatic Arthritis (MOPsA), a new web-based tool for assessment of PsA was developed and is freely available to use (see https://mopsa.ie). MOPSA will calculate all the scores and determine both MDA and CPDAI. MOPSA provides a graphic representation of CPDAI in the form of a spidergram that can be compared with subsequent visits.ObjectivesOur aim was to assess, (1) disease activity using CPDAI and the percentage of patients reaching MDA, in consecutive cohort of established PsA patients attending our unit; and (2) whether treatment change was initiated based on MDA state.Methods137 patients with PsA, fulfilling CASPAR criteria, were included in this study. 68 tender joint counts (TJC) and 66 swollen joint counts (SJC) were recorded. Skin scores included Dermatology Quality of Life Index (DLQI), Body Surface Area (BSA) and Psoriasis Area Severity Index (PASI). Patient reported outcome measures (PROMs) included: Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Health Assessment Questionnaire (HAQ), Ankylosing Spondylitis Quality of Life (ASQoL). CPDAI was calculated and MDA status was assessed.ResultsThe mean age was 46.1 (± 11.6) and 72 (52.6%) were females. Clinical outcome measures and PROMs are shown in table 1. The mean CPDAI score was 3.75 (± 2.94); 52 (37%) patients reached MDA. Of the 85 patients not in MDA, CPDAI was 5.94 ± 3 in the 37 who had a treatment change and 4.54 ± 2.49 in the 48 who did not. Of those undergoing treatment changes, 7 patients started on biologics, 4 switc |
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PsA affects about 30% of patients with psoriasis.1Minimal Disease Activity (MDA) is defined as a patient acceptable disease state which is validated and increasingly recognised as a treatment target. MDA is defined when a patient has 5 of the following 7 criteria: tender joint count ≤1, swollen joint count ≤1, tender entheseal point ≤1, PASI ≤1 or body surface area ≤3%, Pain Visual analogue score (VAS) ≤15, patient global ≤20, Health Assessment Questionnaire ≤0.5.2Composite Psoriatic Disease Activity Index (CPDAI) assesses the five domains in PsA. Within each domain a score (range 0–3) is assigned according to predefined cut-offs. The scores for each domain are then added together to give a final score range of 0–15, 0 for no disease and 15 for severe disease.3Recently, Measuring Outcome in Psoriatic Arthritis (MOPsA), a new web-based tool for assessment of PsA was developed and is freely available to use (see https://mopsa.ie). MOPSA will calculate all the scores and determine both MDA and CPDAI. MOPSA provides a graphic representation of CPDAI in the form of a spidergram that can be compared with subsequent visits.ObjectivesOur aim was to assess, (1) disease activity using CPDAI and the percentage of patients reaching MDA, in consecutive cohort of established PsA patients attending our unit; and (2) whether treatment change was initiated based on MDA state.Methods137 patients with PsA, fulfilling CASPAR criteria, were included in this study. 68 tender joint counts (TJC) and 66 swollen joint counts (SJC) were recorded. Skin scores included Dermatology Quality of Life Index (DLQI), Body Surface Area (BSA) and Psoriasis Area Severity Index (PASI). Patient reported outcome measures (PROMs) included: Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Health Assessment Questionnaire (HAQ), Ankylosing Spondylitis Quality of Life (ASQoL). CPDAI was calculated and MDA status was assessed.ResultsThe mean age was 46.1 (± 11.6) and 72 (52.6%) were females. Clinical outcome measures and PROMs are shown in table 1. The mean CPDAI score was 3.75 (± 2.94); 52 (37%) patients reached MDA. Of the 85 patients not in MDA, CPDAI was 5.94 ± 3 in the 37 who had a treatment change and 4.54 ± 2.49 in the 48 who did not. Of those undergoing treatment changes, 7 patients started on biologics, 4 switched to another biologic and 3 had their dose increased. 6 were started on synthetic DMARD, 2 had a second DMARD added to their regimen, and 8 had their dose increased. 6 patients had a short course of systemic steroids while 12 patients had intra-articular steroids injections.ConclusionsMOPsA gives a comprehensive assessment of psoriatic disease that can be followed longitudinally. One third of patients in our cohort achieved MDA. CPDAI was higher in those patients not achieving MDA status where treatment was changed.ReferencesMease PJ, et al. J Am Acad Dermatol. 2013, 69(5):729–35Coates LC, et al. Ann Rheum Dis. 2010, 69:48–53Mumtaz A, et al. Ann Rheum Dis. 2011, 70(2):272–7Disclosure of InterestM. Elmamoun: None declared, A. Szentpetery: None declared, P. Gallagher: None declared, O. FitzGerald Grant/research support from: Pfizer, AbbVie, BMS, UCB, Consultant for: Pfizer, AbbVie, Janssen, MSD, Cellgene, Novartis, Speakers bureau: Pfizer, AbbVie, Janssen, Cellgene</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2016-eular.3694</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><ispartof>Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.607-607</ispartof><rights>2016, 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</rights><rights>Copyright: 2016 (c) 2016, 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</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b1852-f30e5a00854b62bc6a35b6751aedd5bb82be78c09f86848cb0ee44d6f53c8da63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/75/Suppl_2/607.2.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/75/Suppl_2/607.2.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids></links><search><creatorcontrib>Elmamoun, M.</creatorcontrib><creatorcontrib>Szentpetery, A.</creatorcontrib><creatorcontrib>Gallagher, P.</creatorcontrib><creatorcontrib>FitzGerald, O.</creatorcontrib><title>FRI0469 Measuring Outcome in Psoriatic Arthritis (MOPSA), A New Web-Based Tool for Assessment of Psoriatic Arthritis Showing Initiation of Treatment Change in Patients Achieving Minimal Disease Activity</title><title>Annals of the rheumatic diseases</title><description>BackgroundPsoriatic arthritis (PsA) is a heterogeneous disease that includes features of peripheral arthritis, spondylitis, dactylitis, enthesitis, and skin and nail disease. PsA affects about 30% of patients with psoriasis.1Minimal Disease Activity (MDA) is defined as a patient acceptable disease state which is validated and increasingly recognised as a treatment target. MDA is defined when a patient has 5 of the following 7 criteria: tender joint count ≤1, swollen joint count ≤1, tender entheseal point ≤1, PASI ≤1 or body surface area ≤3%, Pain Visual analogue score (VAS) ≤15, patient global ≤20, Health Assessment Questionnaire ≤0.5.2Composite Psoriatic Disease Activity Index (CPDAI) assesses the five domains in PsA. Within each domain a score (range 0–3) is assigned according to predefined cut-offs. The scores for each domain are then added together to give a final score range of 0–15, 0 for no disease and 15 for severe disease.3Recently, Measuring Outcome in Psoriatic Arthritis (MOPsA), a new web-based tool for assessment of PsA was developed and is freely available to use (see https://mopsa.ie). MOPSA will calculate all the scores and determine both MDA and CPDAI. MOPSA provides a graphic representation of CPDAI in the form of a spidergram that can be compared with subsequent visits.ObjectivesOur aim was to assess, (1) disease activity using CPDAI and the percentage of patients reaching MDA, in consecutive cohort of established PsA patients attending our unit; and (2) whether treatment change was initiated based on MDA state.Methods137 patients with PsA, fulfilling CASPAR criteria, were included in this study. 68 tender joint counts (TJC) and 66 swollen joint counts (SJC) were recorded. Skin scores included Dermatology Quality of Life Index (DLQI), Body Surface Area (BSA) and Psoriasis Area Severity Index (PASI). Patient reported outcome measures (PROMs) included: Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Health Assessment Questionnaire (HAQ), Ankylosing Spondylitis Quality of Life (ASQoL). CPDAI was calculated and MDA status was assessed.ResultsThe mean age was 46.1 (± 11.6) and 72 (52.6%) were females. Clinical outcome measures and PROMs are shown in table 1. The mean CPDAI score was 3.75 (± 2.94); 52 (37%) patients reached MDA. Of the 85 patients not in MDA, CPDAI was 5.94 ± 3 in the 37 who had a treatment change and 4.54 ± 2.49 in the 48 who did not. Of those undergoing treatment changes, 7 patients started on biologics, 4 switched to another biologic and 3 had their dose increased. 6 were started on synthetic DMARD, 2 had a second DMARD added to their regimen, and 8 had their dose increased. 6 patients had a short course of systemic steroids while 12 patients had intra-articular steroids injections.ConclusionsMOPsA gives a comprehensive assessment of psoriatic disease that can be followed longitudinally. One third of patients in our cohort achieved MDA. CPDAI was higher in those patients not achieving MDA status where treatment was changed.ReferencesMease PJ, et al. J Am Acad Dermatol. 2013, 69(5):729–35Coates LC, et al. Ann Rheum Dis. 2010, 69:48–53Mumtaz A, et al. Ann Rheum Dis. 2011, 70(2):272–7Disclosure of InterestM. Elmamoun: None declared, A. Szentpetery: None declared, P. Gallagher: None declared, O. FitzGerald Grant/research support from: Pfizer, AbbVie, BMS, UCB, Consultant for: Pfizer, AbbVie, Janssen, MSD, Cellgene, Novartis, Speakers bureau: Pfizer, AbbVie, Janssen, Cellgene</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqVUcFu1DAQtRBILIV_sNQLSKTYceJ1xCkstKzU7VZ0EUfLTiaNVxu7tZ1WvfXSv-tX8CU4XQ49cOE0mnnvzTzNQ-iQkiNKGf-krPU9jENrQpYTyjMYd8ofMV4VL9CMFlykMScv0YwQwrKi4vPX6E0I29QSQcUMPR7_WJKCV7_vH1agwuiNvcTrMTZuAGwsPg_OGxVNg2sfe2-iCfj9an1-UX_4iGt8Brf4F-jsiwrQ4o1zO9w5j-sQIIQBbMSu--eOi97dTqeWNrUJc3Zibjyo-CRb9Mpe7h0kNE0CrpvewM0kWhlrBrXDX01IniEh0dyYePcWverULsC7v_UA_Tz-tll8z07XJ8tFfZppKso86xiBUqUHlIXmuW64YqXm85IqaNtSa5FrmIuGVJ3gohCNJgBF0fKuZI1oFWcH6HC_98q76xFClFs3eptOSloRKihjNE-sz3tW410IHjp55ZNtfycpkVN88ll8copPPsUnp_iSmu_Vetj-l_APnNKqDA</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Elmamoun, M.</creator><creator>Szentpetery, A.</creator><creator>Gallagher, P.</creator><creator>FitzGerald, O.</creator><general>BMJ Publishing Group LTD</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201606</creationdate><title>FRI0469 Measuring Outcome in Psoriatic Arthritis (MOPSA), A New Web-Based Tool for Assessment of Psoriatic Arthritis Showing Initiation of Treatment Change in Patients Achieving Minimal Disease Activity</title><author>Elmamoun, M. ; Szentpetery, A. ; Gallagher, P. ; FitzGerald, O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1852-f30e5a00854b62bc6a35b6751aedd5bb82be78c09f86848cb0ee44d6f53c8da63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elmamoun, M.</creatorcontrib><creatorcontrib>Szentpetery, A.</creatorcontrib><creatorcontrib>Gallagher, P.</creatorcontrib><creatorcontrib>FitzGerald, O.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Family Health Database (Proquest)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elmamoun, M.</au><au>Szentpetery, A.</au><au>Gallagher, P.</au><au>FitzGerald, O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>FRI0469 Measuring Outcome in Psoriatic Arthritis (MOPSA), A New Web-Based Tool for Assessment of Psoriatic Arthritis Showing Initiation of Treatment Change in Patients Achieving Minimal Disease Activity</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2016-06</date><risdate>2016</risdate><volume>75</volume><issue>Suppl 2</issue><spage>607</spage><epage>607</epage><pages>607-607</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>BackgroundPsoriatic arthritis (PsA) is a heterogeneous disease that includes features of peripheral arthritis, spondylitis, dactylitis, enthesitis, and skin and nail disease. PsA affects about 30% of patients with psoriasis.1Minimal Disease Activity (MDA) is defined as a patient acceptable disease state which is validated and increasingly recognised as a treatment target. MDA is defined when a patient has 5 of the following 7 criteria: tender joint count ≤1, swollen joint count ≤1, tender entheseal point ≤1, PASI ≤1 or body surface area ≤3%, Pain Visual analogue score (VAS) ≤15, patient global ≤20, Health Assessment Questionnaire ≤0.5.2Composite Psoriatic Disease Activity Index (CPDAI) assesses the five domains in PsA. Within each domain a score (range 0–3) is assigned according to predefined cut-offs. The scores for each domain are then added together to give a final score range of 0–15, 0 for no disease and 15 for severe disease.3Recently, Measuring Outcome in Psoriatic Arthritis (MOPsA), a new web-based tool for assessment of PsA was developed and is freely available to use (see https://mopsa.ie). MOPSA will calculate all the scores and determine both MDA and CPDAI. MOPSA provides a graphic representation of CPDAI in the form of a spidergram that can be compared with subsequent visits.ObjectivesOur aim was to assess, (1) disease activity using CPDAI and the percentage of patients reaching MDA, in consecutive cohort of established PsA patients attending our unit; and (2) whether treatment change was initiated based on MDA state.Methods137 patients with PsA, fulfilling CASPAR criteria, were included in this study. 68 tender joint counts (TJC) and 66 swollen joint counts (SJC) were recorded. Skin scores included Dermatology Quality of Life Index (DLQI), Body Surface Area (BSA) and Psoriasis Area Severity Index (PASI). Patient reported outcome measures (PROMs) included: Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Health Assessment Questionnaire (HAQ), Ankylosing Spondylitis Quality of Life (ASQoL). CPDAI was calculated and MDA status was assessed.ResultsThe mean age was 46.1 (± 11.6) and 72 (52.6%) were females. Clinical outcome measures and PROMs are shown in table 1. The mean CPDAI score was 3.75 (± 2.94); 52 (37%) patients reached MDA. Of the 85 patients not in MDA, CPDAI was 5.94 ± 3 in the 37 who had a treatment change and 4.54 ± 2.49 in the 48 who did not. Of those undergoing treatment changes, 7 patients started on biologics, 4 switched to another biologic and 3 had their dose increased. 6 were started on synthetic DMARD, 2 had a second DMARD added to their regimen, and 8 had their dose increased. 6 patients had a short course of systemic steroids while 12 patients had intra-articular steroids injections.ConclusionsMOPsA gives a comprehensive assessment of psoriatic disease that can be followed longitudinally. One third of patients in our cohort achieved MDA. CPDAI was higher in those patients not achieving MDA status where treatment was changed.ReferencesMease PJ, et al. J Am Acad Dermatol. 2013, 69(5):729–35Coates LC, et al. Ann Rheum Dis. 2010, 69:48–53Mumtaz A, et al. Ann Rheum Dis. 2011, 70(2):272–7Disclosure of InterestM. Elmamoun: None declared, A. Szentpetery: None declared, P. Gallagher: None declared, O. FitzGerald Grant/research support from: Pfizer, AbbVie, BMS, UCB, Consultant for: Pfizer, AbbVie, Janssen, MSD, Cellgene, Novartis, Speakers bureau: Pfizer, AbbVie, Janssen, Cellgene</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/annrheumdis-2016-eular.3694</doi><tpages>1</tpages></addata></record> |
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