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Effect of Critical Illness on Triglyceride Absorption
Authors:Yasmine Ali Abdelhamid MBBS  Caroline E. Cousins BSc   Jennifer A. Sim B Med Sci   Max S. Bellon Dip Med Tech  A Dip Nuc Med  Nam Q. Nguyen MBBS  PhD   FRACP  Michael Horowitz MBBS  PhD   FRACP  Marianne J. Chapman BMBS  PhD   FANZCA  FCICM  Adam M. Deane MBBS  PhD   FRACP  FCICM
Affiliation:1. Department of Critical Care Services, Royal Adelaide Hospital, Adelaide, Australia;2. Discipline of Acute Care Medicine, University of Adelaide, Adelaide, Australia;3. Department of Nuclear Medicine, Royal Adelaide Hospital, Adelaide, Australia;4. Discipline of Medicine, University of Adelaide, Adelaide, Australia
Abstract:Background: Adequate nutrition support for critically ill patients optimizes outcome, and enteral feeding is the preferred route of nutrition. Small intestinal glucose absorption is frequently impaired in critical illness. Despite lipid being a major constituent of liquid nutrient administered, there is little information about lipid absorption during critical illness. Objectives: To determine small intestinal lipid, as well as glucose, absorption in critical illness compared with health. Materials and Methods: Twenty‐nine mechanically ventilated critically ill patients and 16 healthy volunteers were studied. Liquid nutrient (60 mL, 1 kcal/mL), containing 200 µL 13C‐triolein and 3 g 3‐O‐methyl‐glucose (3‐OMG), was infused directly into the duodenum at a rate of 2 kcal/min. Exhaled 13CO2 and serum 3‐OMG concentrations were measured at timed intervals over 360 minutes. Lipid absorption was measured as the cumulative percentage dose (cPDR) of 13CO2 recovered at 360 minutes. Glucose absorption was measured as the area under the 3‐OMG concentration curve. Data are median (range) and analyzed using the Mann‐Whitney U and Pearson correlation tests. Results: Lipid absorption was markedly less in the critically ill (cPDR13CO2: patients, 22.6% [0%–100%] vs healthy participants, 40.7% [5.3%–84.7%]; P = .018). While glucose absorption was less at 60 minutes in the critically ill (3‐OMG60: 13.2 [3.5–29.5] vs 21.1 [9.3–31.9] mmol/L·min; P = .003), this was not apparent at 360 minutes (3‐OMG360: 92.7 [54.5–147.9] vs 107.9 [64.0–168.7] mmol/L·min; P = .126). There was no relationship between lipid and glucose absorption. Conclusion: Small intestinal absorption of lipid is diminished during critical illness.
Keywords:lipids  nutrition  critical care  research and diseases  enteral nutrition
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