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Diabetic status and the relation of the three domains of glycemic control to mortality in critically ill patients: an international multicenter cohort study

Identifieur interne : 004753 ( Main/Exploration ); précédent : 004752; suivant : 004754

Diabetic status and the relation of the three domains of glycemic control to mortality in critically ill patients: an international multicenter cohort study

Auteurs : James S. Krinsley [États-Unis] ; Moritoki Egi [Japon] ; Alex Kiss [Canada] ; Amin N. Devendra [États-Unis] ; Philipp Schuetz [Suisse] ; Paula M. Maurer [États-Unis] ; Marcus J. Schultz [Pays-Bas] ; Roosmarijn Tm Van Hooijdonk [Pays-Bas] ; Morita Kiyoshi [Japon] ; Iain Mj Mackenzie [Royaume-Uni] ; Djillali Annane [France] ; Peter Stow [Australie] ; Stanley A. Nasraway [États-Unis] ; Sharon Holewinski [États-Unis] ; Ulrike Holzinger [Autriche] ; Jean-Charles Preiser [Belgique] ; Jean-Louis Vincent [Belgique] ; Rinaldo Bellomo [Australie]

Source :

RBID : PMC:3733432

Abstract

Introduction

Hyperglycemia, hypoglycemia, and increased glycemic variability have each been independently associated with increased risk of mortality in critically ill patients. The role of diabetic status on modulating the relation of these three domains of glycemic control with mortality remains uncertain. The purpose of this investigation was to determine how diabetic status affects the relation of hyperglycemia, hypoglycemia, and increased glycemic variability with the risk of mortality in critically ill patients.

Methods

This is a retrospective analysis of prospectively collected data involving 44,964 patients admitted to 23 intensive care units (ICUs) from nine countries, between February 2001 and May 2012. We analyzed mean blood glucose concentration (BG), coefficient of variation (CV), and minimal BG and created multivariable models to analyze their independent association with mortality. Patients were stratified according to the diagnosis of diabetes.

Results

Among patients without diabetes, mean BG bands between 80 and 140 mg/dl were independently associated with decreased risk of mortality, and mean BG bands >140 mg/dl, with increased risk of mortality. Among patients with diabetes, mean BG from 80 to 110 mg/dl was associated with increased risk of mortality and mean BG from 110 to 180 mg/dl with decreased risk of mortality. An effect of center was noted on the relation between mean BG and mortality. Hypoglycemia, defined as minimum BG <70 mg/dl, was independently associated with increased risk of mortality among patients with and without diabetes and increased glycemic variability, defined as CV >20%, was independently associated with increased risk of mortality only among patients without diabetes. Derangements of more than one domain of glycemic control had a cumulative association with mortality, especially for patients without diabetes.

Conclusions

Although hyperglycemia, hypoglycemia, and increased glycemic variability is each independently associated with mortality in critically ill patients, diabetic status modulates these relations in clinically important ways. Our findings suggest that patients with diabetes may benefit from higher glucose target ranges than will those without diabetes. Additionally, hypoglycemia is independently associated with increased risk of mortality regardless of the patient's diabetic status, and increased glycemic variability is independently associated with increased risk of mortality among patients without diabetes.

See related commentary by Krinsley, http://ccforum.com/content/17/2/131

See related commentary by Finfer and Billot, http://ccforum.com/content/17/2/134


Url:
DOI: 10.1186/cc12547
PubMed: 23452622
PubMed Central: 3733432


Affiliations:


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<nlm:aff id="I9">Critical Care Department, Service de Réanimation, Hopital Raymond Poincaré, Université de Versailles SQY, 104 Boulevard Raymond Poincare, 92830, Garches, France</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>Critical Care Department, Service de Réanimation, Hopital Raymond Poincaré, Université de Versailles SQY, 104 Boulevard Raymond Poincare, 92830, Garches</wicri:regionArea>
<placeName>
<region type="region" nuts="2">Île-de-France</region>
<settlement type="city">Garches</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Stow, Peter" sort="Stow, Peter" uniqKey="Stow P" first="Peter" last="Stow">Peter Stow</name>
<affiliation wicri:level="1">
<nlm:aff id="I10">Intensive Care Unit, The Geelong Hospital, Barwon Health, Ryrie Street, Geelong, Victoria, 3220, Australia</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Intensive Care Unit, The Geelong Hospital, Barwon Health, Ryrie Street, Geelong, Victoria, 3220</wicri:regionArea>
<wicri:noRegion>3220</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Nasraway, Stanley A" sort="Nasraway, Stanley A" uniqKey="Nasraway S" first="Stanley A" last="Nasraway">Stanley A. Nasraway</name>
<affiliation wicri:level="2">
<nlm:aff id="I11">Surgical Intensive Care Units, Tufts Medical Center, 800 Washington Street, NEMC 4360, Boston, MA 02111, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Surgical Intensive Care Units, Tufts Medical Center, 800 Washington Street, NEMC 4360, Boston, MA 02111</wicri:regionArea>
<placeName>
<region type="state">Massachusetts</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Holewinski, Sharon" sort="Holewinski, Sharon" uniqKey="Holewinski S" first="Sharon" last="Holewinski">Sharon Holewinski</name>
<affiliation wicri:level="2">
<nlm:aff id="I11">Surgical Intensive Care Units, Tufts Medical Center, 800 Washington Street, NEMC 4360, Boston, MA 02111, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Surgical Intensive Care Units, Tufts Medical Center, 800 Washington Street, NEMC 4360, Boston, MA 02111</wicri:regionArea>
<placeName>
<region type="state">Massachusetts</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Holzinger, Ulrike" sort="Holzinger, Ulrike" uniqKey="Holzinger U" first="Ulrike" last="Holzinger">Ulrike Holzinger</name>
<affiliation wicri:level="3">
<nlm:aff id="I12">Medical Intensive Care Unit, Department of Medicine III, Division of Gastroenterology and Hepatology, ICU 13H1, Medical University of Vienna, Waehringer Guertel 18-20, Vienna, 1090, Austria</nlm:aff>
<country xml:lang="fr">Autriche</country>
<wicri:regionArea>Medical Intensive Care Unit, Department of Medicine III, Division of Gastroenterology and Hepatology, ICU 13H1, Medical University of Vienna, Waehringer Guertel 18-20, Vienna, 1090</wicri:regionArea>
<placeName>
<region type="land" nuts="2">Vienne (Autriche)</region>
<settlement type="city">Vienne (Autriche)</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Preiser, Jean Charles" sort="Preiser, Jean Charles" uniqKey="Preiser J" first="Jean-Charles" last="Preiser">Jean-Charles Preiser</name>
<affiliation wicri:level="3">
<nlm:aff id="I13">Department of Intensive Care, Erasme University Hospital, Université Libre de Bruxelles, Route de Lennik 808, Brussels, 1070, Belgium</nlm:aff>
<country xml:lang="fr">Belgique</country>
<wicri:regionArea>Department of Intensive Care, Erasme University Hospital, Université Libre de Bruxelles, Route de Lennik 808, Brussels, 1070</wicri:regionArea>
<placeName>
<region type="land" nuts="2">Vienne (Autriche)</region>
<settlement type="city">Vienne (Autriche)</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Vincent, Jean Louis" sort="Vincent, Jean Louis" uniqKey="Vincent J" first="Jean-Louis" last="Vincent">Jean-Louis Vincent</name>
<affiliation wicri:level="3">
<nlm:aff id="I13">Department of Intensive Care, Erasme University Hospital, Université Libre de Bruxelles, Route de Lennik 808, Brussels, 1070, Belgium</nlm:aff>
<country xml:lang="fr">Belgique</country>
<wicri:regionArea>Department of Intensive Care, Erasme University Hospital, Université Libre de Bruxelles, Route de Lennik 808, Brussels, 1070</wicri:regionArea>
<placeName>
<region type="land" nuts="2">Vienne (Autriche)</region>
<settlement type="city">Vienne (Autriche)</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Bellomo, Rinaldo" sort="Bellomo, Rinaldo" uniqKey="Bellomo R" first="Rinaldo" last="Bellomo">Rinaldo Bellomo</name>
<affiliation wicri:level="1">
<nlm:aff id="I14">Department of Intensive Care, Austin Hospital and Monash University, Studley Road, Heidelberg, Victoria, 3084, Australia</nlm:aff>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Intensive Care, Austin Hospital and Monash University, Studley Road, Heidelberg, Victoria, 3084</wicri:regionArea>
<wicri:noRegion>3084</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Critical Care</title>
<idno type="ISSN">1364-8535</idno>
<idno type="eISSN">1466-609X</idno>
<imprint>
<date when="2013">2013</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<sec>
<title>Introduction</title>
<p>Hyperglycemia, hypoglycemia, and increased glycemic variability have each been independently associated with increased risk of mortality in critically ill patients. The role of diabetic status on modulating the relation of these three domains of glycemic control with mortality remains uncertain. The purpose of this investigation was to determine how diabetic status affects the relation of hyperglycemia, hypoglycemia, and increased glycemic variability with the risk of mortality in critically ill patients.</p>
</sec>
<sec>
<title>Methods</title>
<p>This is a retrospective analysis of prospectively collected data involving 44,964 patients admitted to 23 intensive care units (ICUs) from nine countries, between February 2001 and May 2012. We analyzed mean blood glucose concentration (BG), coefficient of variation (CV), and minimal BG and created multivariable models to analyze their independent association with mortality. Patients were stratified according to the diagnosis of diabetes.</p>
</sec>
<sec>
<title>Results</title>
<p>Among patients without diabetes, mean BG bands between 80 and 140 mg/dl were independently associated with decreased risk of mortality, and mean BG bands
<underline>></underline>
140 mg/dl, with increased risk of mortality. Among patients with diabetes, mean BG from 80 to 110 mg/dl was associated with increased risk of mortality and mean BG from 110 to 180 mg/dl with decreased risk of mortality. An effect of center was noted on the relation between mean BG and mortality. Hypoglycemia, defined as minimum BG <70 mg/dl, was independently associated with increased risk of mortality among patients with and without diabetes and increased glycemic variability, defined as CV
<underline>></underline>
20%, was independently associated with increased risk of mortality only among patients without diabetes. Derangements of more than one domain of glycemic control had a cumulative association with mortality, especially for patients without diabetes.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>Although hyperglycemia, hypoglycemia, and increased glycemic variability is each independently associated with mortality in critically ill patients, diabetic status modulates these relations in clinically important ways. Our findings suggest that patients with diabetes may benefit from higher glucose target ranges than will those without diabetes. Additionally, hypoglycemia is independently associated with increased risk of mortality regardless of the patient's diabetic status, and increased glycemic variability is independently associated with increased risk of mortality among patients without diabetes.</p>
<p>See related commentary by Krinsley,
<ext-link ext-link-type="uri" xlink:href="http://ccforum.com/content/17/2/131">http://ccforum.com/content/17/2/131</ext-link>
</p>
<p>See related commentary by Finfer and Billot,
<ext-link ext-link-type="uri" xlink:href="http://ccforum.com/content/17/2/134">http://ccforum.com/content/17/2/134</ext-link>
</p>
</sec>
</div>
</front>
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