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The effect of strict blood glucose control on biliary sludge and cholestasis in critically ill patients.

Authors :
Mesotten D
Wauters J
Van den Berghe G
Wouters PJ
Milants I
Wilmer A
Source :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2009 Jul; Vol. 94 (7), pp. 2345-52. Date of Electronic Publication: 2009 Apr 14.
Publication Year :
2009

Abstract

Background and Aims: Cholestatic liver dysfunction and biliary sludge are common problems in critically ill patients. No specific strategies have been described to prevent cholestasis and biliary sludge in the intensive care unit (ICU). We examined liver dysfunction and biliary sludge prospectively in a large medical long-stay ICU population and hypothesized that tight glycemic control with intensive insulin therapy (IIT) reduces cholestasis and biliary sludge.<br />Methods: This study was a preplanned subanalysis of 658 long-stay (at least a fifth day) ICU patients out of a large randomized controlled trial (n = 1200), studying the effects of IIT on the outcome of medical critical illness. Patients were allocated to either IIT (glycemia 80-110 mg/dl) or conventional insulin therapy (CIT) requiring insulin above a glycemia of 215 mg/dl. Different patterns of liver dysfunction were studied based on daily blood sample analysis, and biliary sludge was evaluated by ultrasonography.<br />Results: On admission, cholestasis was present in 17% of patients (n = 649), increasing to 20% on d 10 (n = 347), whereas ischemic hepatitis decreased from 3.4% (n = 588) to less than 1% (n = 328). IIT significantly decreased biliary sludge on d 5 (50.4 vs. 66.4%, P = 0.01; n = 250). The difference did not remain significant on d 10 (57.4 vs. 66.2%, P = 0.29; n = 136). IIT also lowered the cumulative risk of cholestasis (P = 0.03).<br />Conclusions: Cholestatic liver dysfunction and biliary sludge are very common during prolonged critical illness but are significantly reduced by IIT.

Details

Language :
English
ISSN :
1945-7197
Volume :
94
Issue :
7
Database :
MEDLINE
Journal :
The Journal of clinical endocrinology and metabolism
Publication Type :
Academic Journal
Accession number :
19366849
Full Text :
https://doi.org/10.1210/jc.2008-2579