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<art>
   <ui>cc2550</ui>
   <ji>CCJ</ji>
   <fm>
      <dochead>Poster presentation</dochead>
      <bibl>
         <title>
            <p>Efficacy of levosimendan in shock</p>
         </title>
         <aug>
            <au id="A1">
               <snm>McLean</snm>
               <fnm>A</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A2">
               <snm>Huang</snm>
               <fnm>S</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A3">
               <snm>Stewart</snm>
               <fnm>D</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A4">
               <snm>Nalos</snm>
               <fnm>M</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A5">
               <snm>Tang</snm>
               <fnm>B</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Nepean Hospital, Kingswood, Australia</p>
            </ins>
         </insg>
         <source>Critical Care</source>
         <supplement>
            <title>
               <p>24th International Symposium on Intensive Care and Emergency Medicine</p>
            </title>
            <note>Meeting abstracts</note>
            <url>http://ccforum.com/supplements/notes/cc-8-s1-info.pdf</url>
         </supplement>
         <conference>
            <title>
               <p>24th International Symposium on Intensive Care and Emergency Medicine</p>
            </title>
            <location>Brussels, Belgium</location>
            <date-range>30 March &#8211; 2 April 2004</date-range>
            <url>http://www.intensive.org</url>
         </conference>
         <issn>1364-8535</issn>
         <pubdate>2004</pubdate>
         <volume>8</volume>
         <issue>Suppl 1</issue>
         <fpage>P83</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/cc2550</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>15</day>
               <month>3</month>
               <year>2004</year>
            </date>
         </pub>
      </history>
   </fm>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>Levosimendan is used intravenously for the management of heart failure. At the therapeutic dose, levosimendan acts predominantly as a calcium sensitizer and ATP-sensitive K<sup>+</sup>-channel (KATP-channel) opener. It binds directly to the calcium-dependent site on troponin C, stabilizing the calcium-induced conformational change and enhances the calcium sensitivity of the cardiac myofilaments. The advantages of a calcium sensitizer over dobutamine is the lack of intracellular calcium overload and that it acts without increasing the energy demand for handling intracellular calcium.</p>
      </sec>
      <sec>
         <st>
            <p>Method</p>
         </st>
         <p>Fifteen patients with cardiogenic, septic or mixed cardiogenic/septic shock were administered a loading dose of 12 &#956;g/kg/min levosimendan, followed by a continuous infusion of 0.1 &#956;g/kg/min for 24 hours. Five patients were diagnosed with septic shock, six with cardiogenic shock and four with mixed septic and cardiogenic shock. The mean APACHE II score was 21.3 &#177; 6.4 The arterial blood pressures of the patients were monitored closely via arterial catheters. Intravenous noradrenaline was administered, where necessary, to maintain mean arterial pressure > 65 mmHg. Echocardiographic left ventricular ejection fraction (LVEF) (Simpson's method) and plasma B-type natriuretic peptide (Biosite Triage method) were measured before and after (within 1 hour) levosimendan infusion.</p>
      </sec>
      <sec>
         <st>
            <p>Results</p>
         </st>
         <p>The LVEF showed a significantly but relatively small improvement in response to levosimendan infusion (pre, 25.7 &#177; 11.0% vs post, 29.8 &#177; 8.6%), representing an absolute change of 4.1 &#177; 8.4% (<it>P </it>= 0.039). The plasma B-type natriuretic peptide concentrations demonstrated a significant decrease, from 993 &#177; 389 to 644 &#177; 408 pg/ml, before and after levosimendan infusion (<it>P </it>= 0.001).</p>
      </sec>
      <sec>
         <st>
            <p>Conclusion</p>
         </st>
         <p>The use of levosimendan in shock patients proved to be feasible, and holds promise as a potential alternative to catecholamine inotropes.</p>
      </sec>
   </bdy>
</art>
