Presented in part to meetings of the European Society for Clinical Nutrition and Metabolism, Istanbul, Turkey, October 2006, and the Association of Coloproctology of Great Britain and Ireland, Glasgow, UK, July 2007; and published in abstract form as Colorectal Dis 2007; 9(Suppl 1): 17
Randomized Clinical Trial
Article first published online: 4 MAR 2010
Copyright © 2010 British Journal of Surgery Society Ltd. Published by John Wiley & Sons, Ltd.
British Journal of Surgery
Volume 97, Issue 4, pages 485–494, April 2010
How to Cite
Mathur, S., Plank, L. D., McCall, J. L., Shapkov, P., McIlroy, K., Gillanders, L. K., Merrie, A. E. H., Torrie, J. J., Pugh, F., Koea, J. B., Bissett, I. P. and Parry, B. R. (2010), Randomized controlled trial of preoperative oral carbohydrate treatment in major abdominal surgery. Br J Surg, 97: 485–494. doi: 10.1002/bjs.7026
The Editors have satisfied themselves that all authors have contributed significantly to this publication
- Issue published online: 4 MAR 2010
- Article first published online: 4 MAR 2010
- Manuscript Accepted: 18 DEC 2009
- Nutricia (NZ) Ltd.
- Health Research Council Clinical Training Fellowship
- Foundation New Zealand Research Fellowship
Major surgery is associated with postoperative insulin resistance which is attenuated by preoperative carbohydrate (CHO) treatment. The effect of this treatment on clinical outcome after major abdominal surgery has not been assessed in a double-blind randomized trial.
Patients undergoing elective colorectal surgery or liver resection were randomized to oral CHO or placebo drinks to be taken on the evening before surgery and 2 h before induction of anaesthesia. Primary outcomes were postoperative length of hospital stay and fatigue measured by visual analogue scale.
Sixty-nine and 73 patients were evaluated in the CHO and placebo groups respectively. The groups were well matched with respect to surgical procedure, epidural analgesia, laparoscopic procedures, fasting period before induction and duration of surgery. Postoperative changes in fatigue score from baseline did not differ between the groups. Median (range) hospital stay was 7 (2–35) days in the CHO group and 8 (2–92) days in the placebo group (P = 0·344). For patients not receiving epidural blockade or laparoscopic surgery (20 CHO, 19 placebo), values were 7 (3–11) and 9 (2–48) days respectively (P = 0·054).
Preoperative CHO treatment did not improve postoperative fatigue or length of hospital stay after major abdominal surgery. A benefit is not ruled out when epidural blockade or laparoscopic procedures are not used. Registration number: ACTRN012605000456651 (http://www.anzctr.org.au). Copyright © 2010 British Journal of Surgery Society Ltd. Published by John Wiley & Sons, Ltd.