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A randomised clinical trial to assess the effect of total enteral and total parenteral nutritional support on metabolic, inflammatory and oxidative markers in patients with predicted severe acute pancreatitis (APACHE II ?6)

A randomised clinical trial to assess the effect of total enteral and total parenteral nutritional support on metabolic, inflammatory and oxidative markers in patients with predicted severe acute pancreatitis (APACHE II ?6)
A randomised clinical trial to assess the effect of total enteral and total parenteral nutritional support on metabolic, inflammatory and oxidative markers in patients with predicted severe acute pancreatitis (APACHE II ?6)
Background: Total enteral nutrition (TEN) within 48 h of admission has recently been shown to be safe and efficacious as part of the management of severe acute pancreatitis. Our aim was to ascertain the safety of immediate TEN in these patients and the effect of TEN on systemic inflammation, psychological state, oxidative stress, plasma glutamine levels and endotoxaemia.
Methods: Patients admitted with predicted severe acute pancreatitis (APACHE II score >5) were randomised to total enteral (TEN; n = 8) or total parenteral nutrition (TPN; n = 9). Measurements of systemic inflammation (C-reactive protein), fatigue (visual analogue scale), oxidative stress (plasma thiobarbituric acid-reactive substances), plasma glutamine and anti-endotoxin IgG and IgM antibody concentrations were made on admission and repeated on days 3 and 7 thereafter. Clinical progress was monitored using APACHE II score. Organ failure and complications were recorded.
Results: All patients tolerated the feeding regime well with few nutrition-related complications. Fatigue improved in both groups but more rapidly in the TEN group. Oxidative stress was high on admission and rose by similar amounts in both groups. Plasma glutamine concentrations did not change significantly in either group. In the TPN group, 3 patients developed respiratory failure and 3 developed non-respiratory single organ failure. There were no such complications in the TEN group. Hospital stay was shorter in the TEN group [7 (4-14) vs. 10 (7-26) days; p = 0.05] as was time to passing flatus and time to opening bowels [1 (0-2) vs. 2 (1-5) days; p = 0.01]. The cost of TEN was considerably less than of TPN.
Conclusion: Immediate institution of nutritional support in the form of TEN is safe in predicted severe acute pancreatitis. It is as safe and as efficacious as TPN and may be beneficial in the clinical course of this disease.
total enteral nutrition, total parenteral nutrition, predicted severe acute pancreatitis
1424-3903
406-413
Gupta, R.
619ee4fe-3929-46b6-911e-d42188b490f5
Patel, K.
4abba9fd-ff3d-42f1-a4fe-c43e0f22367f
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Yaqoob, P.
eb74426f-4486-41ca-bb29-2e3ce3e65b68
Primrose, J.N.
d85f3b28-24c6-475f-955b-ec457a3f9185
Johnson, C.D.
e50aa9cd-8c61-4fe3-a0b3-f51cc3a6c74a
Gupta, R.
619ee4fe-3929-46b6-911e-d42188b490f5
Patel, K.
4abba9fd-ff3d-42f1-a4fe-c43e0f22367f
Calder, P.C.
1797e54f-378e-4dcb-80a4-3e30018f07a6
Yaqoob, P.
eb74426f-4486-41ca-bb29-2e3ce3e65b68
Primrose, J.N.
d85f3b28-24c6-475f-955b-ec457a3f9185
Johnson, C.D.
e50aa9cd-8c61-4fe3-a0b3-f51cc3a6c74a

Gupta, R., Patel, K., Calder, P.C., Yaqoob, P., Primrose, J.N. and Johnson, C.D. (2003) A randomised clinical trial to assess the effect of total enteral and total parenteral nutritional support on metabolic, inflammatory and oxidative markers in patients with predicted severe acute pancreatitis (APACHE II ?6). Pancreatology, 3 (5), 406-413. (doi:10.1159/000073657).

Record type: Article

Abstract

Background: Total enteral nutrition (TEN) within 48 h of admission has recently been shown to be safe and efficacious as part of the management of severe acute pancreatitis. Our aim was to ascertain the safety of immediate TEN in these patients and the effect of TEN on systemic inflammation, psychological state, oxidative stress, plasma glutamine levels and endotoxaemia.
Methods: Patients admitted with predicted severe acute pancreatitis (APACHE II score >5) were randomised to total enteral (TEN; n = 8) or total parenteral nutrition (TPN; n = 9). Measurements of systemic inflammation (C-reactive protein), fatigue (visual analogue scale), oxidative stress (plasma thiobarbituric acid-reactive substances), plasma glutamine and anti-endotoxin IgG and IgM antibody concentrations were made on admission and repeated on days 3 and 7 thereafter. Clinical progress was monitored using APACHE II score. Organ failure and complications were recorded.
Results: All patients tolerated the feeding regime well with few nutrition-related complications. Fatigue improved in both groups but more rapidly in the TEN group. Oxidative stress was high on admission and rose by similar amounts in both groups. Plasma glutamine concentrations did not change significantly in either group. In the TPN group, 3 patients developed respiratory failure and 3 developed non-respiratory single organ failure. There were no such complications in the TEN group. Hospital stay was shorter in the TEN group [7 (4-14) vs. 10 (7-26) days; p = 0.05] as was time to passing flatus and time to opening bowels [1 (0-2) vs. 2 (1-5) days; p = 0.01]. The cost of TEN was considerably less than of TPN.
Conclusion: Immediate institution of nutritional support in the form of TEN is safe in predicted severe acute pancreatitis. It is as safe and as efficacious as TPN and may be beneficial in the clinical course of this disease.

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More information

Published date: 2003
Additional Information: Original Paper
Keywords: total enteral nutrition, total parenteral nutrition, predicted severe acute pancreatitis

Identifiers

Local EPrints ID: 25573
URI: http://eprints.soton.ac.uk/id/eprint/25573
ISSN: 1424-3903
PURE UUID: df725c4e-365c-4dc4-b917-27b0ab1466f8
ORCID for P.C. Calder: ORCID iD orcid.org/0000-0002-6038-710X
ORCID for J.N. Primrose: ORCID iD orcid.org/0000-0002-2069-7605

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Date deposited: 19 Apr 2006
Last modified: 16 Mar 2024 02:51

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Contributors

Author: R. Gupta
Author: K. Patel
Author: P.C. Calder ORCID iD
Author: P. Yaqoob
Author: J.N. Primrose ORCID iD
Author: C.D. Johnson

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