
Vol. 22, No. 2-3, 2006
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Original Paper
A Randomised, Controlled Pilot Study to Investigate the Potential Benefit of Intervention with Insulin in Hyperglycaemic Acute Ischaemic Stroke Patients
M.R. Walters, C.J. Weir, K.R. Lees
University Department of Medicine and Therapeutics, Western Infirmary, Glasgow, UK
Address of Corresponding Author
Cerebrovasc Dis 2006;22:116-122 (DOI: 10.1159/000093239)
Key Words
- Hyperglycaemia
- Insulin treatment
- Acute ischaemic stroke
Abstract
Background: Hyperglycaemia on presentation with acute ischaemic stroke (AIS) is associated with poor outcome, but intervention is unproven. We investigated the safety and tolerability of one method of glycaemic control. Methods: Patients within 24 h of AIS and plasma glucose 8-20 mmol/l were randomised to receive either rigorous glycaemic control (RC) or standard management (SM) for 48 h. RC comprised i.v. insulin at a variable rate adjusted for target glucose concentration of 5-8 mmol/l, and intravenous crystalloid. The SM group received intravenous crystalloid alone in an open-label design. Results: Thirteen patients were randomised to RC and 12 to SM (age 75 ± 6.2 years; 40% male; 20% lacunar stroke; time to treatment 8 ± 6.1 h; plasma glucose 10.6 ± 0.9 mmol/l; known diabetes 52%; NIHSS 8, range 2-28). The glucose concentration-time curve was reduced in the RC group (AUC 324 ± 15 versus 385 ± 28 h·mmol/l, p = 0.04). By 48 h, plasma glucose in both groups was 6.8 ± 1.1 and 7.5 ± 1.3 mmol/l respectively, but mean hourly insulin requirements in the RC group had dropped from 3.25 ± 0.32 units to 1.25 ± 0.5 units (p < 0.01). One transient episode of hypoglycaemic symptoms occurred in the RC group. Conclusion: Glycaemic control with sliding scale insulin for 48 h is feasible and well-tolerated after AIS. Treatment after 48 h may be unnecessary. Copyright © 2006 S. Karger AG, Basel
Author Contacts
M.R. Walters University Department of Medicine and Therapeutics Western Infirmary Glasgow, G11 6NT (UK) Tel. +44 141 211 2821, Fax +44 141 211 6319, E-Mail m.walters@clinmed.gla.ac.uk
Article Information
Received: August 15, 2005
Accepted: January 30, 2006
Published online: May 9, 2006
Number of Print Pages : 7
Number of Figures : 2, Number of Tables : 2, Number of References : 23 |
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