Intravenous omega-3 fatty acids are associated with better clinical outcome and less inflammation in patients with predicted severe acute pancreatitis: A randomised double blind controlled trial.


Journal

Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603

Informations de publication

Date de publication:
09 2020
Historique:
received: 15 08 2017
revised: 08 02 2018
accepted: 02 04 2018
entrez: 14 9 2020
pubmed: 15 9 2020
medline: 7 8 2021
Statut: ppublish

Résumé

Omega-3 fatty acids (FA) can ameliorate the hyper-inflammatory response that occurs in conditions such as severe acute pancreatitis (SAP) and this may improve clinical outcome. We tested the hypothesis that parenteral omega-3 FA from a lipid emulsion that includes fish oil could be beneficial in patients with predicted SAP by reducing C-reactive protein (CRP) concentration (primary outcome), and modulating the inflammatory response and improving clinical outcome (secondary outcomes). In a phase II randomized double-blind single-centre controlled trial, patients with predicted SAP were randomised to receive a daily infusion of fish oil containing lipid emulsion (Lipidem® 20%, BBraun) for 7 days (n = 23) or a daily infusion of a lipid emulsion without fish oil (Lipofundin® MCT 20%, BBraun) (n = 22). On admission, both groups had comparable pancreatitis predicted severity and APACHE II scores. Administration of fish oil resulted in lower total blood leukocyte number (P = 0.04), CRP (P = 0.013), interleukin-8 (P = 0.05) and intercellular adhesion molecule 1 (P = 0.01) concentrations, multiple organ dysfunction score, sequential organ failure assessment score (P = 0.004), early warning score (P = 0.01), and systemic inflammatory response syndrome (P = 0.03) compared to the control group. The fish oil group had fewer new organ failures (P = 0.07), lower critical care admission rate (P = 0.06), shorter critical care stay (P = 0.03) and shorter total hospital stay (P = 0.04). It is concluded that intravenous administration of a fish oil containing lipid emulsion, a source of omega-3 FA, improves clinical outcomes in patients with predicted SAP, benefits that may be linked to reduced inflammation. CLINICALTRIALS. NCT01745861. EudraCT (2010-018660-16).

Sections du résumé

BACKGROUND AND AIMS
Omega-3 fatty acids (FA) can ameliorate the hyper-inflammatory response that occurs in conditions such as severe acute pancreatitis (SAP) and this may improve clinical outcome. We tested the hypothesis that parenteral omega-3 FA from a lipid emulsion that includes fish oil could be beneficial in patients with predicted SAP by reducing C-reactive protein (CRP) concentration (primary outcome), and modulating the inflammatory response and improving clinical outcome (secondary outcomes).
METHODS
In a phase II randomized double-blind single-centre controlled trial, patients with predicted SAP were randomised to receive a daily infusion of fish oil containing lipid emulsion (Lipidem® 20%, BBraun) for 7 days (n = 23) or a daily infusion of a lipid emulsion without fish oil (Lipofundin® MCT 20%, BBraun) (n = 22).
RESULTS
On admission, both groups had comparable pancreatitis predicted severity and APACHE II scores. Administration of fish oil resulted in lower total blood leukocyte number (P = 0.04), CRP (P = 0.013), interleukin-8 (P = 0.05) and intercellular adhesion molecule 1 (P = 0.01) concentrations, multiple organ dysfunction score, sequential organ failure assessment score (P = 0.004), early warning score (P = 0.01), and systemic inflammatory response syndrome (P = 0.03) compared to the control group. The fish oil group had fewer new organ failures (P = 0.07), lower critical care admission rate (P = 0.06), shorter critical care stay (P = 0.03) and shorter total hospital stay (P = 0.04).
CONCLUSIONS
It is concluded that intravenous administration of a fish oil containing lipid emulsion, a source of omega-3 FA, improves clinical outcomes in patients with predicted SAP, benefits that may be linked to reduced inflammation. CLINICALTRIALS.
GOV NUMBER
NCT01745861.
EU CLINICAL TRIALS REGISTER
EudraCT (2010-018660-16).

Identifiants

pubmed: 32921364
pii: S0261-5614(18)30132-8
doi: 10.1016/j.clnu.2018.04.003
pii:
doi:

Substances chimiques

Fat Emulsions, Intravenous 0
Fatty Acids, Omega-3 0
Fish Oils 0
C-Reactive Protein 9007-41-4

Banques de données

ClinicalTrials.gov
['NCT01745861']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

2711-2719

Informations de copyright

Copyright © 2018. Published by Elsevier Ltd.

Auteurs

D Al-Leswas (D)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK. Electronic address: dhya@doctros.org.uk.

A M Eltweri (AM)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.

W-Y Chung (WY)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.

A Arshad (A)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.

J A Stephenson (JA)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.

O Al-Taan (O)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.

C Pollard (C)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.

H L Fisk (HL)

Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.

P C Calder (PC)

Human Development and Health Academic Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK; NIHR Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust and University of Southampton, Southampton SO16 6YD, UK.

G Garcea (G)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK; Department of Cancer Studies, University of Leicester, Leicester, LE1 7RH, UK.

M S Metcalfe (MS)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK; Department of Cancer Studies, University of Leicester, Leicester, LE1 7RH, UK.

A R Dennison (AR)

Department of Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK; Department of Cancer Studies, University of Leicester, Leicester, LE1 7RH, UK.

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Classifications MeSH