<?xml version='1.0'?>
<!DOCTYPE art SYSTEM 'http://www.biomedcentral.com/xml/article.dtd'>
<art>
   <ui>cc312</ui>
   <ji>CCJ</ji>
   <fm>
      <dochead>Meeting abstract</dochead>
      <bibl>
         <title>
            <p>Effects of blood viscosity on renal function during cardiopulmonary bypass - investigations in infants and experimental setting in pig kidneys</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Dittrich</snm>
               <fnm>S</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A2">
               <snm>Priesemann</snm>
               <fnm>M</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A3">
               <snm>Schuth</snm>
               <fnm>A</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A4">
               <snm>M&#252;ller</snm>
               <fnm>C</fnm>
               <insr iid="I2"/>
            </au>
            <au id="A5">
               <snm>Fischer</snm>
               <fnm>T</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A6">
               <snm>Alexi-Meskishvili</snm>
               <fnm>V</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A7">
               <snm>Lang</snm>
               <fnm>PE</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Deutsches Herzzentrum Berlin, Augustenburger Platz 1, 13353 Berlin, Germany</p>
            </ins>
            <ins id="I2">
               <p>Departement of Clinical Chemistry and Biochemistry, Charit&#233;, Humboldt University, Berlin, Germany</p>
            </ins>
         </insg>
         <source>Critical Care</source>
         <supplement>
            <title>
               <p>International Symposium on the Pathophysiology of Cardiopulmonary Bypass</p>
            </title>
            <note>Meeting abstracts</note>
         </supplement>
         <conference>
            <title>
               <p>International Symposium on the Pathophysiology of Cardiopulmonary Bypass</p>
            </title>
            <location>Aachen, Germany</location>
            <date-range>12 December 1998</date-range>
         </conference>
         <issn>1364-8535</issn>
         <pubdate>1999</pubdate>
         <volume>3</volume>
         <issue>Suppl A</issue>
         <fpage>P01</fpage>
         <xrefbib>
            <pubidlist>
               <pubid idtype="pmpid">17005033</pubid>
               <pubid idtype="doi">10.1186/cc312</pubid>
            </pubidlist>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>2</day>
               <month>3</month>
               <year>1999</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>1999</year>
         <collab>Current Science Ltd</collab>
      </cpyrt>
   </fm>
   <meta>
      <classifications>
         <classification type="BMC" subtype="old_arx_id">cc-3-2-p001-p01</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p>Objectives</p>
         </st>
         <p>Acute renal failure (ARF) is a common complication following open heart surgery especially in infants. Effects of blood viscosity on renal function are well known, but have not been investigated in cardiopulmonary bypass (CPS) as yet.</p>
      </sec>
      <sec>
         <st>
            <p>Material and methods</p>
         </st>
         <p>We investigated blood viscosity and different markers of glomerular and tubular renal function in a group of 37 infants below 18 month of age, receiving CPS surgery for different diagnoses.</p>
         <p>In an experimental setting, we investigated 28 isolated pig-kidneys with different hematocrits in an autologous blood perfused model.</p>
      </sec>
      <sec>
         <st>
            <p>Results</p>
         </st>
         <p>In infants, creatinine clearance decreased and urinary excretion of albumin and &#946;-NAG increased during the aortic cross clamp time (AT) and during the first hours following operation, indicating moderate glomerular and tubular damage. During AT, blood was hemodiluted to a hemoglobin of 8.4 &#177; 0.4 g/dl. Thus, blood viscosity during AT and hypothermia was slightly below pre-CPB values. Lower blood viscosity was related to less renal damage (<it>P</it> &lt; 0.01).</p>
         <p>In isolated pig-kidneys, group I (<it>n</it> = 14) was perfused with a hemoglobin of 10.2 &#177; 0.3 g/dl and group II (<it>n</it> = 14) was hemodiluted to 6.5 &#177; 0.9 g/dl. Group II kidneys showed lower vascular resistance, elevated creatinine clearance, elevated oxygen consumption and elevated sodium reabsorption (<it>P</it> &lt; 0.05).</p>
      </sec>
      <sec>
         <st>
            <p>Conclusions</p>
         </st>
         <p>Reducing blood viscosity below physiological values improves tubular as well as glomerular function under CPB conditions. Thus we hold hemodilution to be an appropriate method for optimizing CPB procedures.</p>
      </sec>
   </bdy>
</art>
