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<art>
   <ui>cc7001</ui>
   <ji>CCJ</ji>
   <fm>
      <dochead>Commentary</dochead>
      <bibl>
         <title>
            <p>Gastrointestinal dysfunction in the critically ill: can we measure it?</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Khadaroo</snm>
               <mi>G</mi>
               <fnm>Rachel</fnm>
               <insr iid="I1"/>
            </au>
            <au ca="yes" id="A2">
               <snm>Marshall</snm>
               <mi>C</mi>
               <fnm>John</fnm>
               <insr iid="I1"/>
               <email>marshallj@smh.toronto.on.ca</email>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Departments of Surgery and Critical Care Medicine, and the Li Ka Shing Knowledge Institute, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada, M5B 1W8</p>
            </ins>
         </insg>
         <source>Critical Care</source>
         <issn>1364-8535</issn>
         <pubdate>2008</pubdate>
         <volume>12</volume>
         <issue>5</issue>
         <fpage>180</fpage>
         <url>http://ccforum.com/content/12/5/180</url>
         <note>See related research by Reintam <it>et al.</it>, <url>http://ccforum.com/content/12/4/R90</url>, and related letter by Berger <it>et al.</it>, <url>http://ccforum.com/content/12/6/436</url></note>
         <xrefbib>
            <pubidlist>
               <pubid idtype="pmpid">18828891</pubid>
               <pubid idtype="doi">10.1186/cc7001</pubid>
            </pubidlist>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>24</day>
               <month>9</month>
               <year>2008</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2008</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
      <abs>
         <sec>
            <st>
               <p>Abstract</p>
            </st>
            <p>Gastrointestinal dysfunction is an intuitively important, yet descriptively elusive component of the multiple organ dysfunction syndrome. Reintam and colleagues have attempted to quantify this dimension using a combination of intolerance of enteral feeding, and the development of intra-abdominal hypertension. While they show that both parameters are associated with an increased risk of death (and therefore that, in combination, the risk of death is even greater), they fall short in developing a novel descriptor of gastrointestinal dysfunction. Nonetheless, and even with its shortcomings, their effort is a welcome contribution to the surprisingly complex process of describing the morbidity of critical illness.</p>
         </sec>
      </abs>
   </fm>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>In the previous issue of <it>Critical Care</it>, Reintam and colleagues <abbrgrp><abbr bid="B1">1</abbr></abbrgrp> report a novel scale for measuring gastrointestinal dysfunction, using as descriptors, feeding intolerance and intra-abdominal hypertension. They demonstrate convincingly that their Gastrointestinal Failure Score correlates in a graded manner with mortality, and adds prognostic power to the Sepsis-related Organ Failure Assessment (SOFA) score. But while the use of intra-abdominal hypertension as a measure of gastrointestinal dysfunction is novel, and reflects morbidity that was underappreciated 10 years ago, their scale falls short in providing a comprehensive measure of gastrointestinal dysfunction in critical illness.</p>
         <p>The concept that the morbidity of critical illness arises through the development of potentially reversible physiologic failure of multiple organ systems was first articulated by Arthur Baue more than 30 years ago <abbrgrp><abbr bid="B2">2</abbr></abbrgrp>. It was further refined by the ACCP/SCCM consensus conference of 1991, which suggested that the process involved graded degrees of organ system dysfunction, and proposed the terminology 'multiple organ dysfunction syndrome' (MODS) to describe it <abbrgrp><abbr bid="B3">3</abbr></abbrgrp>. The concept embodies several key features. First, it recognizes that it is not a single event that jeopardizes the recovery of the critically ill patient, but rather an evolving state of physiologic insufficiency, often affecting organs remote to the site of the initial insult and necessitating the use of exogenous support to ensure survival. Second, it reflects the clinical reality that the process is variable in its expression, with differing systems being involved in different patients. Finally, and of most pragmatic importance, the process is potentially reversible, and survival is possible, though strongly and inversely correlated with the aggregate severity of the process.</p>
         <p>Some 15 to 20 years ago, there emerged a spate of efforts to provide robust and reproducible criteria for the objective measurement of organ dysfunction <abbrgrp><abbr bid="B4">4</abbr><abbr bid="B5">5</abbr><abbr bid="B6">6</abbr><abbr bid="B7">7</abbr></abbrgrp>. These are strikingly similar in their architecture, a reflection not only of an emerging consensus on what organ dysfunction is, but also of the substantial intellectual collaboration of those who developed the scores. Although the final products vary in specific details, they reflect an implicit consensus that a valid descriptor of organ dysfunction should meet certain criteria (Table <tblr tid="T1">1</tblr>).</p>
         <tbl id="T1">
            <title>
               <p>Table 1</p>
            </title>
            <caption>
               <p>Characteristics of an optimal descriptor of organ dysfunction</p>
            </caption>
            <tblbdy cols="1">
               <r>
                  <c ca="left">
                     <p>Specific for the function of the organ system of interest</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Comprehensive measure of function in that system</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Sensitive to clinically important change in function</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Recognizable to clinician</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Increasing abnormality associated with increasing risk of adverse outcome</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Not readily reversed by resuscitation</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Objective</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Measure of physiologic derangement, rather than treatment decision</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Reliably, readily, and reproducibly measured</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Inexpensive</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Abnormal in one direction only</p>
                  </c>
               </r>
               <r>
                  <c ca="left">
                     <p>Single, continuous variable</p>
                  </c>
               </r>
            </tblbdy>
            <tblfn>
               <p>Adapted from <abbrgrp><abbr bid="B4">4</abbr></abbrgrp>.</p>
            </tblfn>
         </tbl>
         <p>The rationale for quantifying organ dysfunction is not to provide another tool to predict the outcome of critically ill patients; dedicated prognostic scores such as the Simplified Acute Physiology Score (SAPS) and Acute Physiology and Chronic Health Evaluation (APACHE) do this more than adequately. Rather, their purpose is to measure the evolution over time of a multi-dimensional process, to enable response to specific unmet needs. First, an organ dysfunction scale can serve as a measure of intensive care unit-related morbidity, and so reflect important, but non-mortal, outcomes in a complex patient population. Second, it can provide an aggregate measure of whether an individual patient is improving or deteriorating over time &#8211; a common challenge in an illness characterized by improvement in some dimensions, and deterioration in others. Third, it can measure new morbidity arising in a patient whose risk of dying at the time of intensive care unit admission is quantifiable, but unalterable, and for whom the real goal of care is to prevent <it>de novo </it>morbidity. Finally, it can serve as a more sensitive and informative outcome measure for a population of patients for whom mortality risk is heavily influenced by pre-morbid conditions, and survival <it>per se </it>is of variable importance.</p>
         <p>Gastrointestinal failure was a classic feature in early descriptions of MODS, and invariably measured as bleeding from acute stress ulceration of the stomach <abbrgrp><abbr bid="B8">8</abbr><abbr bid="B9">9</abbr></abbrgrp>. But stress ulceration has become distinctly uncommon <abbrgrp><abbr bid="B10">10</abbr></abbrgrp>, and so other metrics have been sought, including tolerance of enteral feeds, ileus and nasogastric drainage, intestinal ischemia, acalculous cholecystitis, and diarrhea <abbrgrp><abbr bid="B11">11</abbr></abbrgrp>. None of these have satisfactorily met criteria for face validity and utility as summarized in Table <tblr tid="T1">1</tblr>, and for this reason, gut dysfunction was omitted from the available organ dysfunction scales.</p>
         <p>The work of Reintam and colleagues has several limitations. First, tolerance of enteral feeding is subjective, and reflects a clinical decision &#8211; to withhold feeds &#8211; more than it does an intrinsic characteristic of the patient. One would want to know how reproducible these criteria were when measured by different observers, and whether they showed a graded correlation with mortality risk; the simple measure of nasogastric output does not.</p>
         <p>Second, intra-abdominal hypertension is not strictly a measure of gastrointestinal dysfunction, but rather of the combination of increased intra-abdominal pressure and decreased compliance of the abdominal wall, and its risk factors are conditions characterized by a need to administer large amounts of fluid in the setting of significantly increased capillary permeability <abbrgrp><abbr bid="B12">12</abbr></abbrgrp>.</p>
         <p>These shortcomings notwithstanding, however, the authors are to be complimented on their continuing efforts to improve our ability to describe a common, frustratingly elusive, but intuitively important element of the MODS. In an earlier publication, they found that the development of gastrointestinal failure reflected in a diverse group of gastrointestinal signs and symptoms was associated with an eightfold increase in mortality <abbrgrp><abbr bid="B13">13</abbr></abbrgrp>; clearly, this is a problem that we need to understand better.</p>
      </sec>
      <sec>
         <st>
            <p>Abbreviations</p>
         </st>
         <p>MODS: multiple organ dysfunction syndrome.</p>
      </sec>
      <sec>
         <st>
            <p>Competing interests</p>
         </st>
         <p>The authors declare that they have no competing interests.</p>
      </sec>
   </bdy>
   <bm>
      <refgrp>
         <bibl id="B1">
            <title>
               <p>Gastrointestinal Failure score in critically ill patients: a prospective observational study</p>
            </title>
            <aug>
               <au>
                  <snm>Reintam</snm>
                  <fnm>A</fnm>
               </au>
               <au>
                  <snm>Parm</snm>
                  <fnm>P</fnm>
               </au>
               <au>
                  <snm>Kitus</snm>
                  <fnm>R</fnm>
               </au>
               <au>
                  <snm>Starkopf</snm>
                  <fnm>J</fnm>
               </au>
               <au>
                  <snm>Kern</snm>
                  <fnm>H</fnm>
               </au>
            </aug>
            <source>Crit Care</source>
            <pubdate>2008</pubdate>
            <volume>12</volume>
            <fpage>R90</fpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1186/cc6958</pubid>
                  <pubid idtype="pmpid" link="fulltext">18625051</pubid>
                  <pubid idtype="pmcid">2575570</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B2">
            <title>
               <p>Multiple, progressive, or sequential systems failure. A syndrome of the 1970s</p>
            </title>
            <aug>
               <au>
                  <snm>Baue</snm>
                  <fnm>AE</fnm>
               </au>
            </aug>
            <source>Arch Surg</source>
            <pubdate>1975</pubdate>
            <volume>110</volume>
            <fpage>779</fpage>
            <lpage>781</lpage>
            <xrefbib>
               <pubid idtype="pmpid">1079720</pubid>
            </xrefbib>
         </bibl>
         <bibl id="B3">
            <title>
               <p>Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis</p>
            </title>
            <aug>
               <au>
                  <snm>Bone</snm>
                  <fnm>RC</fnm>
               </au>
               <au>
                  <snm>Balk</snm>
                  <fnm>RA</fnm>
               </au>
               <au>
                  <snm>Cerra</snm>
                  <fnm>FB</fnm>
               </au>
               <au>
                  <snm>Dellinger</snm>
                  <fnm>RP</fnm>
               </au>
               <au>
                  <snm>Fein</snm>
                  <fnm>AM</fnm>
               </au>
               <au>
                  <snm>Knaus</snm>
                  <fnm>WA</fnm>
               </au>
               <au>
                  <snm>Schein</snm>
                  <fnm>RM</fnm>
               </au>
               <au>
                  <snm>Sibbald</snm>
                  <fnm>WJ</fnm>
               </au>
            </aug>
            <source>Chest</source>
            <pubdate>1992</pubdate>
            <volume>101</volume>
            <fpage>1644</fpage>
            <lpage>1655</lpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1378/chest.101.6.1644</pubid>
                  <pubid idtype="pmpid" link="fulltext">1303622</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B4">
            <title>
               <p>Multiple organ dysfunction score: A reliable descriptor of a complex clinical outcome</p>
            </title>
            <aug>
               <au>
                  <snm>Marshall</snm>
                  <fnm>JC</fnm>
               </au>
               <au>
                  <snm>Cook</snm>
                  <fnm>DJ</fnm>
               </au>
               <au>
                  <snm>Christou</snm>
                  <fnm>NV</fnm>
               </au>
               <au>
                  <snm>Bernard</snm>
                  <fnm>GR</fnm>
               </au>
               <au>
                  <snm>Sprung</snm>
                  <fnm>CL</fnm>
               </au>
               <au>
                  <snm>Sibbald</snm>
                  <fnm>WJ</fnm>
               </au>
            </aug>
            <source>Crit Care Med</source>
            <pubdate>1995</pubdate>
            <volume>23</volume>
            <fpage>1638</fpage>
            <lpage>1652</lpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1097/00003246-199510000-00007</pubid>
                  <pubid idtype="pmpid" link="fulltext">7587228</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B5">
            <title>
               <p>The sepsis-related organ failure assessment (SOFA) score to describe organ dysfunction/failure</p>
            </title>
            <aug>
               <au>
                  <snm>Vincent</snm>
                  <fnm>JL</fnm>
               </au>
               <au>
                  <snm>Moreno</snm>
                  <fnm>R</fnm>
               </au>
               <au>
                  <snm>Takala</snm>
                  <fnm>J</fnm>
               </au>
               <au>
                  <snm>Willatts</snm>
                  <fnm>S</fnm>
               </au>
               <au>
                  <snm>De Mendon&#231;a</snm>
                  <fnm>A</fnm>
               </au>
               <au>
                  <snm>Bruining</snm>
                  <fnm>H</fnm>
               </au>
               <au>
                  <snm>Reinhart</snm>
                  <fnm>CK</fnm>
               </au>
               <au>
                  <snm>Suter</snm>
                  <fnm>PM</fnm>
               </au>
               <au>
                  <snm>Thijs</snm>
                  <fnm>LG</fnm>
               </au>
            </aug>
            <source>Intensive Care Med</source>
            <pubdate>1996</pubdate>
            <volume>22</volume>
            <fpage>707</fpage>
            <lpage>710</lpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="pmpid">8844239</pubid>
                  <pubid idtype="doi">10.1007/BF01709751</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B6">
            <title>
               <p>The Brussels score</p>
            </title>
            <aug>
               <au>
                  <snm>Bernard</snm>
                  <fnm>G</fnm>
               </au>
            </aug>
            <source>Sepsis</source>
            <pubdate>1997</pubdate>
            <volume>1</volume>
            <fpage>43</fpage>
            <lpage>44</lpage>
            <xrefbib>
               <pubid idtype="doi">10.1023/A:1009711301483</pubid>
            </xrefbib>
         </bibl>
         <bibl id="B7">
            <title>
               <p>The logistic organ dysfunction system &#8211; a new way to assess organ dysfunction in the intensive care unit</p>
            </title>
            <aug>
               <au>
                  <snm>Le Gall</snm>
                  <fnm>JR</fnm>
               </au>
               <au>
                  <snm>Klar</snm>
                  <fnm>J</fnm>
               </au>
               <au>
                  <snm>Lemeshow</snm>
                  <fnm>S</fnm>
               </au>
               <au>
                  <snm>Saulnier</snm>
                  <fnm>F</fnm>
               </au>
               <au>
                  <snm>Alberti</snm>
                  <fnm>C</fnm>
               </au>
               <au>
                  <snm>Artigas</snm>
                  <fnm>A</fnm>
               </au>
               <au>
                  <snm>Teres</snm>
                  <fnm>D</fnm>
               </au>
            </aug>
            <source>JAMA</source>
            <pubdate>1996</pubdate>
            <volume>276</volume>
            <fpage>802</fpage>
            <lpage>810</lpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1001/jama.276.10.802</pubid>
                  <pubid idtype="pmpid">8769590</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B8">
            <title>
               <p>Respiratory failure, hypotension, sepsis, and jaundice. A clinical syndrome associated with lethal hemorrhage and acute stress ulceration in the stomach</p>
            </title>
            <aug>
               <au>
                  <snm>Skillman</snm>
                  <fnm>JJ</fnm>
               </au>
               <au>
                  <snm>Bushnell</snm>
                  <fnm>LS</fnm>
               </au>
               <au>
                  <snm>Goldman</snm>
                  <fnm>H</fnm>
               </au>
               <au>
                  <snm>Silen</snm>
                  <fnm>W</fnm>
               </au>
            </aug>
            <source>Am J Surg</source>
            <pubdate>1969</pubdate>
            <volume>117</volume>
            <fpage>523</fpage>
            <lpage>530</lpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1016/0002-9610(69)90011-7</pubid>
                  <pubid idtype="pmpid" link="fulltext">5771525</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B9">
            <title>
               <p>Multiple system organ failure. The role of uncontrolled infection</p>
            </title>
            <aug>
               <au>
                  <snm>Fry</snm>
                  <fnm>DE</fnm>
               </au>
               <au>
                  <snm>Pearlstein</snm>
                  <fnm>L</fnm>
               </au>
               <au>
                  <snm>Fulton</snm>
                  <fnm>RL</fnm>
               </au>
               <au>
                  <snm>Polk</snm>
                  <fnm>HC</fnm>
               </au>
            </aug>
            <source>Arch Surg</source>
            <pubdate>1980</pubdate>
            <volume>115</volume>
            <fpage>136</fpage>
            <lpage>140</lpage>
            <xrefbib>
               <pubid idtype="pmpid">6965449</pubid>
            </xrefbib>
         </bibl>
         <bibl id="B10">
            <title>
               <p>Risk factors for clinically important upper gastrointestinal bleeding in patients requiring mechanical ventilation</p>
            </title>
            <aug>
               <au>
                  <snm>Cook</snm>
                  <fnm>D</fnm>
               </au>
               <au>
                  <snm>Heyland</snm>
                  <fnm>D</fnm>
               </au>
               <au>
                  <snm>Griffith</snm>
                  <fnm>L</fnm>
               </au>
               <au>
                  <snm>Cook</snm>
                  <fnm>R</fnm>
               </au>
               <au>
                  <snm>Marshall</snm>
                  <fnm>J</fnm>
               </au>
               <au>
                  <snm>Pagliarello</snm>
                  <fnm>J</fnm>
               </au>
            </aug>
            <source>Crit Care Med</source>
            <pubdate>1999</pubdate>
            <volume>27</volume>
            <fpage>2812</fpage>
            <lpage>2817</lpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1097/00003246-199912000-00034</pubid>
                  <pubid idtype="pmpid" link="fulltext">10628631</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B11">
            <title>
               <p>Clinical markers of gastrointestinal dysfunction</p>
            </title>
            <aug>
               <au>
                  <snm>Marshall</snm>
                  <fnm>JC</fnm>
               </au>
            </aug>
            <source>Gut Dysfunction in Critical Illness</source>
            <publisher>Berlin: Springer-Verlag</publisher>
            <editor>Rombeau JL, Takala J</editor>
            <pubdate>1996</pubdate>
            <fpage>114</fpage>
            <lpage>128</lpage>
         </bibl>
         <bibl id="B12">
            <title>
               <p>Abdominal compartment syndrome: a concise clinical review</p>
            </title>
            <aug>
               <au>
                  <snm>An</snm>
                  <fnm>G</fnm>
               </au>
               <au>
                  <snm>West</snm>
                  <fnm>MA</fnm>
               </au>
            </aug>
            <source>Crit Care Med</source>
            <pubdate>2008</pubdate>
            <volume>36</volume>
            <fpage>1304</fpage>
            <lpage>1310</lpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1097/CCM.0b013e31816929f4</pubid>
                  <pubid idtype="pmpid" link="fulltext">18379259</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
         <bibl id="B13">
            <title>
               <p>Gastrointestinal failure in intensive care: a retrospective clinical study in three different intensive care units in Germany and Estonia</p>
            </title>
            <aug>
               <au>
                  <snm>Reintam</snm>
                  <fnm>A</fnm>
               </au>
               <au>
                  <snm>Parm</snm>
                  <fnm>P</fnm>
               </au>
               <au>
                  <snm>Redlich</snm>
                  <fnm>U</fnm>
               </au>
               <au>
                  <snm>Tooding</snm>
                  <fnm>LM</fnm>
               </au>
               <au>
                  <snm>Starkopf</snm>
                  <fnm>J</fnm>
               </au>
               <au>
                  <snm>K&#246;hler</snm>
                  <fnm>F</fnm>
               </au>
               <au>
                  <snm>Spies</snm>
                  <fnm>C</fnm>
               </au>
               <au>
                  <snm>Kern</snm>
                  <fnm>H</fnm>
               </au>
            </aug>
            <source>BMC Gastroenterol</source>
            <pubdate>2006</pubdate>
            <volume>6</volume>
            <fpage>19</fpage>
            <xrefbib>
               <pubidlist>
                  <pubid idtype="doi">10.1186/1471-230X-6-19</pubid>
                  <pubid idtype="pmpid" link="fulltext">16792799</pubid>
                  <pubid idtype="pmcid">1513588</pubid>
               </pubidlist>
            </xrefbib>
         </bibl>
      </refgrp>
   </bm>
</art>
