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   <ui>1546-0096-6-S1-P40</ui>
   <ji>1546-0096</ji>
   <fm>
      <dochead>Poster presentation</dochead>
      <bibl>
         <title>
            <p>When and how to stop etanercept after successful treatment of patients with juvenile idiopathic arthritis</p>
         </title>
         <aug>
            <au id="A1" ca="yes">
               <snm>Prince</snm>
               <fnm>FHM</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A2">
               <snm>Twilt</snm>
               <fnm>M</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A3">
               <snm>Simon</snm>
               <fnm>SCM</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A4">
               <snm>van Rossum</snm>
               <fnm>MAJ</fnm>
               <insr iid="I3"/>
            </au>
            <au id="A5">
               <snm>Armbrust</snm>
               <fnm>W</fnm>
               <insr iid="I4"/>
            </au>
            <au id="A6">
               <snm>Hoppenreijs</snm>
               <fnm>EPAH</fnm>
               <insr iid="I5"/>
            </au>
            <au id="A7">
               <snm>Kamphuis</snm>
               <fnm>SSM</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A8">
               <snm>van Santen-Hoeufft</snm>
               <fnm>M</fnm>
               <insr iid="I6"/>
            </au>
            <au id="A9">
               <snm>Koopman-Keemink</snm>
               <fnm>Y</fnm>
               <insr iid="I7"/>
            </au>
            <au id="A10">
               <snm>Wulffraat</snm>
               <fnm>N</fnm>
               <insr iid="I8"/>
            </au>
            <au id="A11">
               <snm>ten Cate</snm>
               <fnm>R</fnm>
               <insr iid="I2"/>
            </au>
            <au id="A12">
               <snm>van Suijlekom-Smit</snm>
               <fnm>LWA</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands</p>
            </ins>
            <ins id="I2">
               <p>Leiden University Medical Centre, Leiden, Netherlands</p>
            </ins>
            <ins id="I3">
               <p>AMC Emma Children's Hospital, Amsterdam, Netherlands</p>
            </ins>
            <ins id="I4">
               <p>UMCG Beatrix Children's Hospital, Groningen, Netherlands</p>
            </ins>
            <ins id="I5">
               <p>Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands</p>
            </ins>
            <ins id="I6">
               <p>Academic Hospital Maastricht, Maastricht, Netherlands</p>
            </ins>
            <ins id="I7">
               <p>Hagaziekenhuis Juliana Children's Hospital, Den Haag, Netherlands</p>
            </ins>
            <ins id="I8">
               <p>Utrecht MC Wilhelmina Children's Hospital, Utrecht, Netherlands</p>
            </ins>
         </insg>
         <source>Pediatric Rheumatology</source>
         <supplement>
            <title>
               <p>15<sup>th </sup>Paediatric Rheumatology European Society (PreS) Congress</p>
            </title>
            <editor>Wietse Kuis, Patricia Woo, Angelo Ravelli, Hermann Girschick, Micha&#235;l Hofer, Johannes Roth, Rotraud K Saurenmann, Alberto Martini, Pavla Dolezova, Janjaap van der Net, Pierre Quartier, Lucy Wedderburn and Jan Scott</editor>
            <note>Meeting abstracts &#8211; A single PDF containing all abstracts in this Supplement is available <a href="http://www.biomedcentral.com/content/files/PDF/1546-0096-6-S1-full.pdf">here</a>.</note>
         </supplement>
         <conference>
            <title>
               <p>15<sup>th </sup>Paediatric Rheumatology European Society (PreS) Congress</p>
            </title>
            <location>London, UK</location>
            <date-range>14&#8211;17 September 2008</date-range>
            <url>http://www.pres.org.uk</url>
         </conference>
         <issn>1546-0096</issn>
         <pubdate>2008</pubdate>
         <volume>6</volume>
         <issue>Suppl 1</issue>
         <fpage>P40</fpage>
         <url>http://www.ped-rheum.com/content/6/S1/P40</url>
         <xrefbib>
            <pubid idtype="doi">10.1186/1546-0096-6-S1-P40</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>15</day>
               <month>9</month>
               <year>2008</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2008</year>
         <collab>Prince et al; licensee BioMed Central Ltd.</collab>
      </cpyrt>
   </fm>
   <bdy>
      <sec>
         <st>
            <p>Objective</p>
         </st>
         <p>The aim of etanercept therapy in juvenile idiopathic arthritis (JIA) is to achieve disease remission. However, little is known about when or how to stop etanercept when this aim is reached. Our objective was to describe characteristics and disease course of JIA patients who discontinued etanercept because of a sustained good clinical response.</p>
      </sec>
      <sec>
         <st>
            <p>Methods</p>
         </st>
         <p>The "Arthritis and Biologicals in Children" (ABC)-project is the Dutch national register on biologicals in JIA, in which data are collected prospectively. All patients from this register who discontinued etanercept because of a good clinical response were selected. For evaluation of the disease course we used the criteria for clinical remission on medication and off medication by Wallace et al.</p>
      </sec>
      <sec>
         <st>
            <p>Results</p>
         </st>
         <p>Of the 210 patients in the ABC-register, 17 patients discontinued etanercept because of a good clinical response. After discontinuation nine patients (53%), with a mean follow-up of 1.4 years, did not develop a disease flare. They showed a longer mean period of clinical remission on medication (1.9 vs. 0.3 years, <it>p </it>&lt; 0.01) and used etanercept longer (3.7 vs. 2.4 years, <it>p </it>= 0.16) compared to patients who flared. Three out of the 17 patients discontinued etanercept instantaneously and flared within one year, all other patients tapered the etanercept dose before discontinuation. All seven patients who resumed etanercept use after flaring recovered soon.</p>
      </sec>
      <sec>
         <st>
            <p>Conclusion</p>
         </st>
         <p>Patients who meet the clinical remission criteria on etanercept for a longer period have a better chance of retaining remission after etanercept discontinuation. Tapering of etanercept dose before discontinuation is favourable.</p>
      </sec>
   </bdy>
</art>

