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Real-world outcomes of long-term prednisone and deflazacort use in patients with Duchenne muscular dystrophy: experience at a single, large care center
To assess outcomes among patients with Duchenne muscular dystrophy receiving deflazacort or prednisone in real-world practice. Clinical data for 435 boys with Duchenne muscular dystrophy from Cincinnati Children’s Hospital Medical Center were studied retrospectively using time-to-event and regressio...
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Published in: | Journal of comparative effectiveness research 2020-02, Vol.9 (3), p.177-189 |
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description | To assess outcomes among patients with Duchenne muscular dystrophy receiving deflazacort or prednisone in real-world practice.
Clinical data for 435 boys with Duchenne muscular dystrophy from Cincinnati Children’s Hospital Medical Center were studied retrospectively using time-to-event and regression analyses.
Median ages at loss of ambulation were 15.6 and 13.5 years among deflazacort- and prednisone-initiated patients, respectively. Deflazacort was also associated with a lower risk of scoliosis and better ambulatory function, greater % lean body mass, shorter stature and lower weight, after adjusting for age and steroid duration. No differences were observed in whole body bone mineral density or left ventricular ejection fraction.
This single center study adds to the real-world evidence associating deflazacort with improved clinical outcomes.
This retrospective study described outcomes for boys with Duchenne muscular dystrophy treated at Cincinnati Children’s Hospital Medical Center with the glucocorticoids deflazacort (∼95% daily dosing) or prednisone (∼68% daily dosing). Patients receiving deflazacort had lower risk of losing ambulation, lost ambulation at older ages than those receiving prednisone, and had lower risk of scoliosis. Across clinic visits, deflazacort was associated with greater preservation of ambulatory and pulmonary function, shorter stature, lower bodyweight and greater % lean body mass. This study adds to the evidence associating real-world dosing of deflazacort with improved outcomes for patients with Duchenne muscular dystrophy. |
doi_str_mv | 10.2217/cer-2019-0170 |
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Clinical data for 435 boys with Duchenne muscular dystrophy from Cincinnati Children’s Hospital Medical Center were studied retrospectively using time-to-event and regression analyses.
Median ages at loss of ambulation were 15.6 and 13.5 years among deflazacort- and prednisone-initiated patients, respectively. Deflazacort was also associated with a lower risk of scoliosis and better ambulatory function, greater % lean body mass, shorter stature and lower weight, after adjusting for age and steroid duration. No differences were observed in whole body bone mineral density or left ventricular ejection fraction.
This single center study adds to the real-world evidence associating deflazacort with improved clinical outcomes.
This retrospective study described outcomes for boys with Duchenne muscular dystrophy treated at Cincinnati Children’s Hospital Medical Center with the glucocorticoids deflazacort (∼95% daily dosing) or prednisone (∼68% daily dosing). Patients receiving deflazacort had lower risk of losing ambulation, lost ambulation at older ages than those receiving prednisone, and had lower risk of scoliosis. Across clinic visits, deflazacort was associated with greater preservation of ambulatory and pulmonary function, shorter stature, lower bodyweight and greater % lean body mass. This study adds to the evidence associating real-world dosing of deflazacort with improved outcomes for patients with Duchenne muscular dystrophy.</description><identifier>ISSN: 2042-6305</identifier><identifier>EISSN: 2042-6313</identifier><identifier>DOI: 10.2217/cer-2019-0170</identifier><identifier>PMID: 31922454</identifier><language>eng</language><publisher>England: Future Medicine Ltd</publisher><subject>Adolescent ; Age ; Bone Density ; Cardiac function ; Child ; Child, Preschool ; deflazacort ; Duchenne muscular dystrophy ; Electronic health records ; FDA approval ; Humans ; Male ; Muscular dystrophy ; Muscular Dystrophy, Duchenne - drug therapy ; Muscular Dystrophy, Duchenne - physiopathology ; Patients ; prednisone ; Prednisone - therapeutic use ; Pregnenediones - therapeutic use ; real-world data ; Retrospective Studies ; Scoliosis ; Steroids ; Stroke Volume ; Ventricular Function, Left ; Walking</subject><ispartof>Journal of comparative effectiveness research, 2020-02, Vol.9 (3), p.177-189</ispartof><rights>2020 Analysis Group, Inc.</rights><rights>2020. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-8282bfdc88ef247bdd07f46bcd2896d89eed771667731cc03d8ce49f098729603</citedby><cites>FETCH-LOGICAL-c410t-8282bfdc88ef247bdd07f46bcd2896d89eed771667731cc03d8ce49f098729603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31922454$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marden, Jessica R</creatorcontrib><creatorcontrib>Freimark, Jonathan</creatorcontrib><creatorcontrib>Yao, Zhiwen</creatorcontrib><creatorcontrib>Signorovitch, James</creatorcontrib><creatorcontrib>Tian, Cuixia</creatorcontrib><creatorcontrib>Wong, Brenda L</creatorcontrib><title>Real-world outcomes of long-term prednisone and deflazacort use in patients with Duchenne muscular dystrophy: experience at a single, large care center</title><title>Journal of comparative effectiveness research</title><addtitle>J Comp Eff Res</addtitle><description>To assess outcomes among patients with Duchenne muscular dystrophy receiving deflazacort or prednisone in real-world practice.
Clinical data for 435 boys with Duchenne muscular dystrophy from Cincinnati Children’s Hospital Medical Center were studied retrospectively using time-to-event and regression analyses.
Median ages at loss of ambulation were 15.6 and 13.5 years among deflazacort- and prednisone-initiated patients, respectively. Deflazacort was also associated with a lower risk of scoliosis and better ambulatory function, greater % lean body mass, shorter stature and lower weight, after adjusting for age and steroid duration. No differences were observed in whole body bone mineral density or left ventricular ejection fraction.
This single center study adds to the real-world evidence associating deflazacort with improved clinical outcomes.
This retrospective study described outcomes for boys with Duchenne muscular dystrophy treated at Cincinnati Children’s Hospital Medical Center with the glucocorticoids deflazacort (∼95% daily dosing) or prednisone (∼68% daily dosing). Patients receiving deflazacort had lower risk of losing ambulation, lost ambulation at older ages than those receiving prednisone, and had lower risk of scoliosis. Across clinic visits, deflazacort was associated with greater preservation of ambulatory and pulmonary function, shorter stature, lower bodyweight and greater % lean body mass. This study adds to the evidence associating real-world dosing of deflazacort with improved outcomes for patients with Duchenne muscular dystrophy.</description><subject>Adolescent</subject><subject>Age</subject><subject>Bone Density</subject><subject>Cardiac function</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>deflazacort</subject><subject>Duchenne muscular dystrophy</subject><subject>Electronic health records</subject><subject>FDA approval</subject><subject>Humans</subject><subject>Male</subject><subject>Muscular dystrophy</subject><subject>Muscular Dystrophy, Duchenne - drug therapy</subject><subject>Muscular Dystrophy, Duchenne - physiopathology</subject><subject>Patients</subject><subject>prednisone</subject><subject>Prednisone - therapeutic use</subject><subject>Pregnenediones - therapeutic use</subject><subject>real-world data</subject><subject>Retrospective Studies</subject><subject>Scoliosis</subject><subject>Steroids</subject><subject>Stroke Volume</subject><subject>Ventricular Function, Left</subject><subject>Walking</subject><issn>2042-6305</issn><issn>2042-6313</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10U1rFDEcBvAgii21R68S8OLB0SSTmSTepNUqFATRc8gm_9mdkknGvNCuX8Sva9atPQjmkBf45SHkQeg5JW8Yo-KthdQxQlVHqCCP0CkjnHVjT_vHD3synKDznG9IG6PkamBP0UlPFWN84Kfo11cwvruNyTsca7FxgYzjhH0M265AWvCawIU5xwDYBIcdTN78NDamgmsGPAe8mjJDKBnfzmWHL6vdQWh6qdlWbxJ2-1xSXHf7dxjuVkgN2xZWsMF5DlsPr3FjW8DWpDa1KEjP0JPJ-Azn9-sZ-v7xw7eLT931l6vPF--vO8spKZ1kkm0mZ6WEiXGxcY6IiY8b65hUo5MKwAlBx1GInlpLeictcDURJQVTI-nP0Ktj7prijwq56GXOFrw3AWLNmvX9yIahH0SjL_-hN7Gm0F6n2UAE5Ypw2VR3VDbFnBNMek3zYtJeU6IPpelWmj6Upg-lNf_iPrVuFnAP-m9FDagjmGqpCbL98336eGo3ZjsH-E_4bweHp50</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Marden, Jessica R</creator><creator>Freimark, Jonathan</creator><creator>Yao, Zhiwen</creator><creator>Signorovitch, James</creator><creator>Tian, Cuixia</creator><creator>Wong, Brenda L</creator><general>Future Medicine Ltd</general><scope>FUMOA</scope><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>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>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></search><sort><creationdate>20200201</creationdate><title>Real-world outcomes of long-term prednisone and deflazacort use in patients with Duchenne muscular dystrophy: experience at a single, large care center</title><author>Marden, Jessica R ; Freimark, Jonathan ; Yao, Zhiwen ; Signorovitch, James ; Tian, Cuixia ; Wong, Brenda L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-8282bfdc88ef247bdd07f46bcd2896d89eed771667731cc03d8ce49f098729603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Age</topic><topic>Bone Density</topic><topic>Cardiac function</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>deflazacort</topic><topic>Duchenne muscular dystrophy</topic><topic>Electronic health records</topic><topic>FDA approval</topic><topic>Humans</topic><topic>Male</topic><topic>Muscular dystrophy</topic><topic>Muscular Dystrophy, Duchenne - drug therapy</topic><topic>Muscular Dystrophy, Duchenne - physiopathology</topic><topic>Patients</topic><topic>prednisone</topic><topic>Prednisone - therapeutic use</topic><topic>Pregnenediones - therapeutic use</topic><topic>real-world data</topic><topic>Retrospective Studies</topic><topic>Scoliosis</topic><topic>Steroids</topic><topic>Stroke Volume</topic><topic>Ventricular Function, Left</topic><topic>Walking</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marden, Jessica R</creatorcontrib><creatorcontrib>Freimark, Jonathan</creatorcontrib><creatorcontrib>Yao, Zhiwen</creatorcontrib><creatorcontrib>Signorovitch, James</creatorcontrib><creatorcontrib>Tian, Cuixia</creatorcontrib><creatorcontrib>Wong, Brenda L</creatorcontrib><collection>Future Medicine (Open Access)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>PHMC-Proquest健康医学期刊库</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)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</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><jtitle>Journal of comparative effectiveness research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marden, Jessica R</au><au>Freimark, Jonathan</au><au>Yao, Zhiwen</au><au>Signorovitch, James</au><au>Tian, Cuixia</au><au>Wong, Brenda L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-world outcomes of long-term prednisone and deflazacort use in patients with Duchenne muscular dystrophy: experience at a single, large care center</atitle><jtitle>Journal of comparative effectiveness research</jtitle><addtitle>J Comp Eff Res</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>9</volume><issue>3</issue><spage>177</spage><epage>189</epage><pages>177-189</pages><issn>2042-6305</issn><eissn>2042-6313</eissn><abstract>To assess outcomes among patients with Duchenne muscular dystrophy receiving deflazacort or prednisone in real-world practice.
Clinical data for 435 boys with Duchenne muscular dystrophy from Cincinnati Children’s Hospital Medical Center were studied retrospectively using time-to-event and regression analyses.
Median ages at loss of ambulation were 15.6 and 13.5 years among deflazacort- and prednisone-initiated patients, respectively. Deflazacort was also associated with a lower risk of scoliosis and better ambulatory function, greater % lean body mass, shorter stature and lower weight, after adjusting for age and steroid duration. No differences were observed in whole body bone mineral density or left ventricular ejection fraction.
This single center study adds to the real-world evidence associating deflazacort with improved clinical outcomes.
This retrospective study described outcomes for boys with Duchenne muscular dystrophy treated at Cincinnati Children’s Hospital Medical Center with the glucocorticoids deflazacort (∼95% daily dosing) or prednisone (∼68% daily dosing). Patients receiving deflazacort had lower risk of losing ambulation, lost ambulation at older ages than those receiving prednisone, and had lower risk of scoliosis. Across clinic visits, deflazacort was associated with greater preservation of ambulatory and pulmonary function, shorter stature, lower bodyweight and greater % lean body mass. This study adds to the evidence associating real-world dosing of deflazacort with improved outcomes for patients with Duchenne muscular dystrophy.</abstract><cop>England</cop><pub>Future Medicine Ltd</pub><pmid>31922454</pmid><doi>10.2217/cer-2019-0170</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Age Bone Density Cardiac function Child Child, Preschool deflazacort Duchenne muscular dystrophy Electronic health records FDA approval Humans Male Muscular dystrophy Muscular Dystrophy, Duchenne - drug therapy Muscular Dystrophy, Duchenne - physiopathology Patients prednisone Prednisone - therapeutic use Pregnenediones - therapeutic use real-world data Retrospective Studies Scoliosis Steroids Stroke Volume Ventricular Function, Left Walking |
title | Real-world outcomes of long-term prednisone and deflazacort use in patients with Duchenne muscular dystrophy: experience at a single, large care center |
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