<?xml version="1.0" encoding="utf-8"?>
<export-example>
  <doc>
    <id>5803</id>
    <completedYear/>
    <publishedYear>2020</publishedYear>
    <thesisYearAccepted/>
    <language>eng</language>
    <pageFirst>922</pageFirst>
    <pageLast>928</pageLast>
    <pageNumber/>
    <edition/>
    <issue>8</issue>
    <volume>66</volume>
    <type>article</type>
    <publisherName>Lippincott Williams &amp; Wilkins</publisherName>
    <publisherPlace/>
    <creatingCorporation/>
    <contributingCorporation/>
    <belongsToBibliography>0</belongsToBibliography>
    <completedDate>2023-02-13</completedDate>
    <publishedDate>--</publishedDate>
    <thesisDateAccepted>--</thesisDateAccepted>
    <title language="eng">Analysis of Thrombotic Deposits in Extracorporeal Membrane Oxygenators by High-resolution Microcomputed Tomography: A Feasibility Study</title>
    <abstract language="eng">Coagulative disorders, especially clotting during extracorporeal membrane oxygenation, are frequent complications. Direct visualization and analysis of deposits in membrane oxygenators using computed tomography (CT) may provide an insight into the underlying mechanisms causing thrombotic events. However, the already established multidetector CT1 (MDCT) method shows major limitations. Here, we demonstrate the feasibility of applying industrial micro-CT (μCT) to circumvent these restrictions. Three clinically used membrane oxygenators were investigated applying both MDCT and μCT.&#13;
The scans were analyzed in terms of clot volume and local clot distribution. As validation, the clot volume was also determined from the fluid volume, which could be filled into the respective used oxygenator compared to a new device. In addition, cross-sectional CT images were compared with crosscut oxygenators. Based on the μCT findings, a morphological measure (sphericity) for assessing clot structures in membrane oxygenators is introduced. Furthermore, by comparing MDCT and μCT results, an augmentation of the MDCT method is proposed, which allows for improved clot volume determination in a clinical setting.</abstract>
    <parentTitle language="eng">ASAIO Journal / American Society for Artificial Internal Organs</parentTitle>
    <identifier type="doi">10.1097/MAT.0000000000001089</identifier>
    <identifier type="issn">1538-943X</identifier>
    <enrichment key="opus.source">publish</enrichment>
    <enrichment key="BegutachtungStatus">peer-reviewed</enrichment>
    <licence>Keine Lizenz - Es gilt das deutsche Urheberrecht: § 53 UrhG</licence>
    <author>Clemens Birkenmaier</author>
    <author>Christian Dornia</author>
    <author>Karla Lehle</author>
    <author>Thomas Müller</author>
    <author>Michael Gruber</author>
    <author>Alois Philipp</author>
    <author>Lars Krenkel</author>
    <collection role="institutes" number="FAKMB">Fakultät Maschinenbau</collection>
    <collection role="institutes" number="RCBE">Research Center of Biomedical Engineering - RCBE</collection>
    <collection role="institutes" number="RCHST">Research Center of Health Sciences and Technology - RCHST</collection>
    <collection role="institutes" number="RCAI">Research Center for Artificial Intelligence - RCAI</collection>
    <collection role="institutes" number="">Labor Biofluidmechanik</collection>
    <collection role="persons" number="krenkellbfmpub">Krenkel, Lars (Prof. Dr.), Publikationen - Labor Biofluidmechanik</collection>
    <collection role="othforschungsschwerpunkt" number="">Gesundheit und Soziales</collection>
  </doc>
</export-example>
