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    <title>Herting, E.</title>
    <link>http://repub.eur.nl/res/aut/15222/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Reducing atelectasis attenuates bacterial growth and translocation in experimental pneumonia. (Article)</title>
      <link>http://repub.eur.nl/res/pub/13310/</link>
      <pubDate>2004-01-01T00:00:00Z</pubDate>
      <description>Besides being one of the mechanisms responsible for ventilator-induced
      lung injury, atelectasis also seems to aggravate the course of
      experimental pneumonia. In this study, we examined the effect of reducing
      the degree of atelectasis by natural modified surfactant and/or open lung
      ventilation on bacterial growth and translocation in a piglet model of
      Group B streptococcal pneumonia. After creating surfactant deficiency by
      whole lung lavage, intratracheal instillation of bacteria induced severe
      pneumonia with bacterial translocation into the blood stream, resulting in
      a mortality rate of almost 80%. Treatment with 300 mg/kg of exogenous
      surfactant before instillation of streptococci attenuated both bacterial
      growth and translocation and prevented clinical deterioration. This goal
      was also achieved by reversing atelectasis in lavaged animals via open
      lung ventilation. Combining both exogenous surfactant and open lung
      ventilation prevented bacterial translocation completely, comparable to
      Group B streptococci instillation into healthy animals. We conclude that
      exogenous surfactant and open lung ventilation attenuate bacterial growth
      and translocation in experimental pneumonia and that this attenuation is
      at least in part mediated by a reduction in atelectasis. These findings
      suggest that minimizing alveolar collapse by exogenous surfactant and open
      lung ventilation may reduce the risk of pneumonia and subsequent sepsis in
      ventilated patients.</description>
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