Diabetes Care
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Diabetes Care 30:403-409, 2007
DOI: 10.2337/dc06-1679
© 2007 by the American Diabetes Association
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dungan, K.
Right arrow Articles by Buse, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dungan, K.
Right arrow Articles by Buse, J.
Social Bookmarking
 Add to CiteULike   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Reviews/Commentaries/ADA Statements
Review

Glucose Measurement: Confounding Issues in Setting Targets for Inpatient Management

Kathleen Dungan, MD1, John Chapman, PHD2, Susan S. Braithwaite, MD3 and John Buse, MD, PHD3

1 Division of Endocrinology, Ohio State University School of Medicine, Columbus, Ohio
2 Department of Pathology and Laboratory Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina
3 Division of Endocrinology, University of North Carolina School of Medicine, Chapel Hill, North Carolina

Address correspondence and reprint requests to John Buse, MD, PhD, CB# 7110, Old Clinic 5039, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7110. E-mail: jbuse@med.unc.edu

Abbreviations: ADA, American Diabetes Association • CAP, College of American Pathologists • GD, glucose-1-dehydrogenase • ICU, intensive care unit • POC, point of care

The first 300 words of the full text of this article appear below.


    INTRODUCTION
 
Van den Berghe et al. (1) reported a significant reduction in mortality with normoglycemia (target value 80–110 mg/dl) in patients whose medical intensive care unit (ICU) stay was >72 h and reduced morbidity in all patients, regardless of the duration of ICU stay. Although severe hypoglycemia did not occur in the Van den Berghe et al. study, 18.7% of patients in the intensive treatment group compared with 3.1% of those who received conventional therapy did experience hypoglycemia (defined as glucose <40 mg/dl), albeit with no adverse consequences reported. However, altered consciousness is common in the ICU, and even severe hypoglycemia may be unrecognized. Other studies (2,3) examining intensive insulin protocols in various inpatient settings have suggested benefits in clinical outcomes associated with improved glycemic control. In a mixed ICU population, Van den Berghe et al. (2) previously demonstrated reduced morbidity and mortality with three- to fourfold less hypoglycemia than the medical ICU population (2). Thus, careful assessment of glucose measurement and how it may impact the targets selected in the hospital are critical safety issues in intensive management of hyperglycemia. As a result of increasing evidence that tight glycemic control is beneficial in the management of inpatients with diabetes, the American Diabetes Association (ADA) currently recommends a glucose target "as close to 110 mg/dl as possible and generally <180 mg/dl" for critically ill patients (4). The American Association of Clinical Endocrinologists recommends the "upper limits for glycemic targets" of 110 mg/dl in critically ill patients (5).

In practice, it may be difficult to obtain the level of glycemic control (average glucose 111 mg/dl in the intensively managed group) achieved by Van den Berghe et al. Though a wider range of glucose values has been targeted, rarely . . . [Full Text of this Article]


    ASSAY PRINCIPLES—
 
Enzymatic reaction
Detection method
POC techniques
Interstitial fluid glucose monitoring

    PATIENT VARIABLES WITHIN A POPULATION
 
Patient factors
Hypotension.
Hematocrit.
Oxygenation.
pH.
Temperature.
Interfering substances
Drugs.
Other substances.

    SOURCES OF SYSTEMATIC DIFFERENCE BETWEEN INSTITUTIONS—
 
Standards for comparison
Performance of POC devices
Operator error
Source of sample
Arterial samples compared with capillary samples.
Venous samples compared with capillary samples.
Postprandial state.
Differences between plasma and whole blood (specimen matrix)
Arterial whole blood compared with arterial plasma.
Venous whole blood compared with venous plasma.
Capillary whole blood compared with venous plasma.
Ramifications for the clinician

    CONCLUSIONS—
 

Add to CiteULike CiteULike   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Diabetes CareHome page
J. Mahoney and J. Ellison
Glucose Measurement: Confounding Issues in Setting Targets for Inpatient Management: Response to Dungan et al.
Diabetes Care, July 1, 2007; 30(7): e71 - e71.
[Full Text] [PDF]


Home page
Diabetes CareHome page
K. M. Dungan
Glucose Measurement: Confounding Issues in Setting Targets for Inpatient Management: Response to Mahoney and Ellison
Diabetes Care, July 1, 2007; 30(7): e72 - e72.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Diabetes Diabetes Care Clinical Diabetes Diabetes Spectrum
Copyright © 2007 by the American Diabetes Association.