GAS-EXCHANGE AND PULMONARY HEMODYNAMIC-RESPONSES TO FAT EMULSIONS IN ACUTE RESPIRATORY-DISTRESS SYNDROME

Citation
Jr. Masclans et al., GAS-EXCHANGE AND PULMONARY HEMODYNAMIC-RESPONSES TO FAT EMULSIONS IN ACUTE RESPIRATORY-DISTRESS SYNDROME, Intensive care medicine, 24(9), 1998, pp. 918-923
Citations number
20
Categorie Soggetti
Emergency Medicine & Critical Care
Journal title
ISSN journal
03424642
Volume
24
Issue
9
Year of publication
1998
Pages
918 - 923
Database
ISI
SICI code
0342-4642(1998)24:9<918:GAPHTF>2.0.ZU;2-E
Abstract
Objective:To investigate the gas exchange and pulmonary haemodynamic r esponses to two different intravenous fat emulsions in patients with a cute respiratory distress syndrome (ARDS). Design: Prospective, random ized, double-blind, placebo-controlled study. Setting: Intensive care unit in a university-affiliated hospital. Patients: 21 patients with A RDS [mean age, 57 +/- 3 (SEM) years; Acute Physiology and Chronic Heal th Evaluation II, 20 +/- 3; Murray's score, 2.85 +/- 0.12] consecutive ly admitted. Interventions: Patients were assigned to three groups (n = 7 each): group A (LCT) received long-chain triglycerides (20 % LCT), group B (MCT/LCT), medium-chain trigly cerides/long-chain triglycerid es (20 % MCT/LCT: 50/50) and group C placebo (0.9 % sodium chloride, N aCl). The infusion was always given at the rate of 2 mg/kg min over a total period of 12 h, with a volume infusion of 500 mi in each group. Measurements: Data were collected before, immediately after and 12 h a fter infusion ceased. Pulmonary and systemic haemodynamic and gas exch ange variables were measured at each time point. Serum triglyceride ch olesterol, and non-esterified fatty acids levels were measured. Result s: During LCT infusion, cardiac output, oxygen consumption and oxygen delivery increased tall p < 0.05), whereas pulmonary haemodynamics, ar terial oxygen tension, mixed venous partial pressure of oxygen and ven ous admixture ratio remained essentially unaltered. No changes were ob served following MCT/LCT infusion. Conclusions: The administration of LCT emulsion given at a slow rate did not alter arterial oxygenation b ecause of the beneficial effect of a high cardiac output, hence offset ting the detrimental effect of increased O-2 consumption.