![]() |
|
|
-Ketoglutarate Administration in Burn Patients
Manuscript received 29 October 1996. Initial reviews completed 16 December 1996. Revision accepted 18 May 1997.
,
,
* Laboratoire de Biochimie A and
Service des Brûlés, Hôpital Saint Antoine, 75571 Paris Cedex 12, France
To investigate appropriate mode and daily dose of enteral ornithine
-ketoglutarate (OKG) administration, 54 burn patients (total burn surface area: 20-50%) were included in a randomized controlled trial and assigned to receive either a supplement of OKG (10, 20 or 30 g/d) as bolus or continuous infusion, or a continuous infusion of an isonitrogenous amount of a soy protein mixture (Protil-1: 10, 20 or 30 g/d) in addition to their enteral diet. The influence of these treatments on clinical outcome and biological indices was evaluated. OKG administration significantly improved nitrogen balance and reduced 3-methylhistidine and hydroxyproline urinary elimination. This was associated with a gradual rise in plasma glutamine over time. Given as a bolus, OKG significantly improved wound healing, assessed both clinically [day of last graft: (mean ± SEM) OKG bolus 23.7 ± 2.1 d versus Protil-1, 39.9 ± 9.9 d; P < 0.05] and by hydroxyproline excretion, and biological markers of nitrogen metabolism, and tended to reduce duration of enteral nutrition (P = 0.12). The higher catabolic status in the patients administered 20 g OKG/d at the onset of the study, despite randomization, precludes any definite conclusion (concerning the dose-effect relationship). However, based on 3-methylhistidine elimination, our data indicate a benefit of 30 g OKG/d administration over 10 g/d. This study further supports OKG supplementation in burn patients. In addition, this is the first trial based on objective data that favors bolus over continuous infusion of OKG in critically ill patients.
-ketoglutarate,
burn injury,
enteral nutrition,
humans.
The Journal of Nutrition Vol. 128 No. 3 March 1998,
pp. 563-569
Copyright ©1998 by the American Society for Nutritional Sciences
This article has been cited by other articles:
![]() |
L. A Cynober Clinical nutrition: commercially or clinically essential? Am. J. Clinical Nutrition, July 1, 2002; 76(1): 255 - 256. [Full Text] [PDF] |
||||
![]() |
A. L Buchman Reply to LA Cynober Am. J. Clinical Nutrition, July 1, 2002; 76(1): 256 - 257. [Full Text] [PDF] |
||||
![]() |
V. R. Young and A. M. Ajami Glutamine: The Emperor or His Clothes? J. Nutr., September 1, 2001; 131(9): 2449S - 2459. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Bruce, D. Constantin-Teodosiu, P. L. Greenhaff, L. H. Boobis, C. Williams, and J. L. Bowtell Glutamine supplementation promotes anaplerosis but not oxidative energy delivery in human skeletal muscle Am J Physiol Endocrinol Metab, April 1, 2001; 280(4): E669 - E675. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Ushmorov, V. Hack, and W. Droge Differential Reconstitution of Mitochondrial Respiratory Chain Activity and Plasma Redox State by Cysteine and Ornithine in a Model of Cancer Cachexia Cancer Res., July 1, 1999; 59(14): 3527 - 3534. [Abstract] [Full Text] [PDF] |
||||