Are We Able to Suppress Disease Activity Adequately in Patients With Established Rheumatoid Arthritis? An Observational and Cross-Sectional Study
This study aims to explore current disease activity status and simultaneous pharmacological therapies in patients with established rheumatoid arthritis (RA) to determine the extent to which treatment targets are achieved. One hundred patients (7 males, 93 females; median age 57 years; range 31 to 76...
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Veröffentlicht in: | Archives of rheumatology 2016-06, Vol.31 (2), p.127-132 |
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creator | Şengül, İlker Akçay Yalbuzdağ, Seniz Ince, Buğra Karatepe, Altınay Göksel Kaya, Taciser |
description | This study aims to explore current disease activity status and simultaneous pharmacological therapies in patients with established rheumatoid arthritis (RA) to determine the extent to which treatment targets are achieved.
One hundred patients (7 males, 93 females; median age 57 years; range 31 to 76 years) with established RA receiving any conventional synthetic disease modifying anti-rheumatic drug (DMARD) and/or biological DMARD for at least three months were enrolled. Disease activity was determined by using the Simplified Disease Activity Index. First, patients were categorized into four groups as remission, low disease activity, moderate disease activity, and high disease activity. Then, they were divided into two subgroups, namely a remission/low disease activity subgroup and moderate disease activity/high disease activity subgroup.
Fifty-one percent of the patients had remission or low disease activity. The most frequently used conventional synthetic DMARDs were methotrexate (50%) and leflunomide (34%). Forty-five percent of patients were receiving glucocorticoid therapy. In patients receiving only conventional synthetic DMARDs, the proportion of remission and low disease activity was 54% (42/78). Forty-two percent (8/19) of the patients receiving biological DMARDs were in remission or had low disease activity. A comparison of subgroups revealed that median age and sulfasalazine use were significantly higher in the moderate disease activity/high disease activity subgroup.
The results of this study demonstrated that half of patients with established RA had moderate or high disease activity in our local outpatient clinic. Some barriers might be responsible for the difficulties in controlling disease activity. Determining such barriers might result in a better clinical response during the management of patients with established RA in real-life practice. |
doi_str_mv | 10.5606/ArchRheumatol.2016.5704 |
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One hundred patients (7 males, 93 females; median age 57 years; range 31 to 76 years) with established RA receiving any conventional synthetic disease modifying anti-rheumatic drug (DMARD) and/or biological DMARD for at least three months were enrolled. Disease activity was determined by using the Simplified Disease Activity Index. First, patients were categorized into four groups as remission, low disease activity, moderate disease activity, and high disease activity. Then, they were divided into two subgroups, namely a remission/low disease activity subgroup and moderate disease activity/high disease activity subgroup.
Fifty-one percent of the patients had remission or low disease activity. The most frequently used conventional synthetic DMARDs were methotrexate (50%) and leflunomide (34%). Forty-five percent of patients were receiving glucocorticoid therapy. In patients receiving only conventional synthetic DMARDs, the proportion of remission and low disease activity was 54% (42/78). Forty-two percent (8/19) of the patients receiving biological DMARDs were in remission or had low disease activity. A comparison of subgroups revealed that median age and sulfasalazine use were significantly higher in the moderate disease activity/high disease activity subgroup.
The results of this study demonstrated that half of patients with established RA had moderate or high disease activity in our local outpatient clinic. Some barriers might be responsible for the difficulties in controlling disease activity. Determining such barriers might result in a better clinical response during the management of patients with established RA in real-life practice.</description><identifier>ISSN: 2148-5046</identifier><identifier>ISSN: 1309-0291</identifier><identifier>EISSN: 1309-0283</identifier><identifier>DOI: 10.5606/ArchRheumatol.2016.5704</identifier><identifier>PMID: 29900932</identifier><language>eng</language><publisher>Turkey: Turkish League Against Rheumatism</publisher><subject>Analysis ; Antirheumatic agents ; Arthritis ; Care and treatment ; Corticosteroids ; Medical research ; Medicine, Experimental ; Rheumatoid factor ; Sulfasalazine</subject><ispartof>Archives of rheumatology, 2016-06, Vol.31 (2), p.127-132</ispartof><rights>COPYRIGHT 2016 Turkish League Against Rheumatism</rights><rights>Copyright Prof Sebnem Ataman, President Turkish League Against Rheumatism 2016</rights><rights>Copyright © 2016, Turkish League Against Rheumatism 2016 Turkish League Against Rheumatism</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827827/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827827/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29900932$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Şengül, İlker</creatorcontrib><creatorcontrib>Akçay Yalbuzdağ, Seniz</creatorcontrib><creatorcontrib>Ince, Buğra</creatorcontrib><creatorcontrib>Karatepe, Altınay Göksel</creatorcontrib><creatorcontrib>Kaya, Taciser</creatorcontrib><title>Are We Able to Suppress Disease Activity Adequately in Patients With Established Rheumatoid Arthritis? An Observational and Cross-Sectional Study</title><title>Archives of rheumatology</title><addtitle>Arch Rheumatol</addtitle><description>This study aims to explore current disease activity status and simultaneous pharmacological therapies in patients with established rheumatoid arthritis (RA) to determine the extent to which treatment targets are achieved.
One hundred patients (7 males, 93 females; median age 57 years; range 31 to 76 years) with established RA receiving any conventional synthetic disease modifying anti-rheumatic drug (DMARD) and/or biological DMARD for at least three months were enrolled. Disease activity was determined by using the Simplified Disease Activity Index. First, patients were categorized into four groups as remission, low disease activity, moderate disease activity, and high disease activity. Then, they were divided into two subgroups, namely a remission/low disease activity subgroup and moderate disease activity/high disease activity subgroup.
Fifty-one percent of the patients had remission or low disease activity. The most frequently used conventional synthetic DMARDs were methotrexate (50%) and leflunomide (34%). Forty-five percent of patients were receiving glucocorticoid therapy. In patients receiving only conventional synthetic DMARDs, the proportion of remission and low disease activity was 54% (42/78). Forty-two percent (8/19) of the patients receiving biological DMARDs were in remission or had low disease activity. A comparison of subgroups revealed that median age and sulfasalazine use were significantly higher in the moderate disease activity/high disease activity subgroup.
The results of this study demonstrated that half of patients with established RA had moderate or high disease activity in our local outpatient clinic. Some barriers might be responsible for the difficulties in controlling disease activity. Determining such barriers might result in a better clinical response during the management of patients with established RA in real-life practice.</description><subject>Analysis</subject><subject>Antirheumatic agents</subject><subject>Arthritis</subject><subject>Care and treatment</subject><subject>Corticosteroids</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Rheumatoid factor</subject><subject>Sulfasalazine</subject><issn>2148-5046</issn><issn>1309-0291</issn><issn>1309-0283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNptUl1r2zAUNWNjDV3_wiYYjL44k2Rbtl42TNZ9QKFj2eijkOWrWkWxUkkO5GfsH0-madeMIYHg3nPO_dDJsjcELyuG2fvWq-HHANNGRmeXFBO2rGpcPssWpMA8x7QpnmcLSsomr3DJTrKzEG4xxqSsGcPFy-yEco4xL-gi-916QNeA2s4Cig6tp-3WQwjokwkgQ0qoaHYm7lHbw90kI9g9MiP6LqOBMQZ0beKALkKUnTVhgB49dGZ61Po4eBNN-IjaEV11Afwu8dwoLZJjj1behZCvQR1i6zj1-1fZCy1tgLPDe5r9-nzxc_U1v7z68m3VXuaqbHjMpS5YX9WE9TXjSpcAwDqpFaEca8q17rqil7hmVYcVJVwrrsqqI1AUugHQxWn24V53O3Ub6FWaxksrtt5spN8LJ404zoxmEDduJ6qG1ukmgfODgHd3E4QoNiYosFaO4KYgKK4qRhjlTYK-_Qd66yafRg6C1JyVdZqD_kXdSAvCjNqlumoWFW1ZsVSXsyqhlv9BpdPDxig3gjYpfkR494QwgLRxCM5O89LDMbC-B6r5Xzzox2UQLGbniSPnidl5YnZeYr5-ustH3oPPij-PMdn7</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Şengül, İlker</creator><creator>Akçay Yalbuzdağ, Seniz</creator><creator>Ince, Buğra</creator><creator>Karatepe, Altınay Göksel</creator><creator>Kaya, Taciser</creator><general>Turkish League Against Rheumatism</general><general>Prof Sebnem Ataman, President Turkish League Against Rheumatism</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>EDSIH</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201606</creationdate><title>Are We Able to Suppress Disease Activity Adequately in Patients With Established Rheumatoid Arthritis? An Observational and Cross-Sectional Study</title><author>Şengül, İlker ; Akçay Yalbuzdağ, Seniz ; Ince, Buğra ; Karatepe, Altınay Göksel ; Kaya, Taciser</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-af36d5716d769cf4eee6bafc1290f29ffbb3da0765b0c219fc9c45b1e33f8eef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Analysis</topic><topic>Antirheumatic agents</topic><topic>Arthritis</topic><topic>Care and treatment</topic><topic>Corticosteroids</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Rheumatoid factor</topic><topic>Sulfasalazine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Şengül, İlker</creatorcontrib><creatorcontrib>Akçay Yalbuzdağ, Seniz</creatorcontrib><creatorcontrib>Ince, Buğra</creatorcontrib><creatorcontrib>Karatepe, Altınay Göksel</creatorcontrib><creatorcontrib>Kaya, Taciser</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Turkey Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Archives of rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Şengül, İlker</au><au>Akçay Yalbuzdağ, Seniz</au><au>Ince, Buğra</au><au>Karatepe, Altınay Göksel</au><au>Kaya, Taciser</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Are We Able to Suppress Disease Activity Adequately in Patients With Established Rheumatoid Arthritis? An Observational and Cross-Sectional Study</atitle><jtitle>Archives of rheumatology</jtitle><addtitle>Arch Rheumatol</addtitle><date>2016-06</date><risdate>2016</risdate><volume>31</volume><issue>2</issue><spage>127</spage><epage>132</epage><pages>127-132</pages><issn>2148-5046</issn><issn>1309-0291</issn><eissn>1309-0283</eissn><abstract>This study aims to explore current disease activity status and simultaneous pharmacological therapies in patients with established rheumatoid arthritis (RA) to determine the extent to which treatment targets are achieved.
One hundred patients (7 males, 93 females; median age 57 years; range 31 to 76 years) with established RA receiving any conventional synthetic disease modifying anti-rheumatic drug (DMARD) and/or biological DMARD for at least three months were enrolled. Disease activity was determined by using the Simplified Disease Activity Index. First, patients were categorized into four groups as remission, low disease activity, moderate disease activity, and high disease activity. Then, they were divided into two subgroups, namely a remission/low disease activity subgroup and moderate disease activity/high disease activity subgroup.
Fifty-one percent of the patients had remission or low disease activity. The most frequently used conventional synthetic DMARDs were methotrexate (50%) and leflunomide (34%). Forty-five percent of patients were receiving glucocorticoid therapy. In patients receiving only conventional synthetic DMARDs, the proportion of remission and low disease activity was 54% (42/78). Forty-two percent (8/19) of the patients receiving biological DMARDs were in remission or had low disease activity. A comparison of subgroups revealed that median age and sulfasalazine use were significantly higher in the moderate disease activity/high disease activity subgroup.
The results of this study demonstrated that half of patients with established RA had moderate or high disease activity in our local outpatient clinic. Some barriers might be responsible for the difficulties in controlling disease activity. Determining such barriers might result in a better clinical response during the management of patients with established RA in real-life practice.</abstract><cop>Turkey</cop><pub>Turkish League Against Rheumatism</pub><pmid>29900932</pmid><doi>10.5606/ArchRheumatol.2016.5704</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Antirheumatic agents Arthritis Care and treatment Corticosteroids Medical research Medicine, Experimental Rheumatoid factor Sulfasalazine |
title | Are We Able to Suppress Disease Activity Adequately in Patients With Established Rheumatoid Arthritis? An Observational and Cross-Sectional Study |
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