• Intensive care medicine · Jul 2001

    Clinical Trial

    Hepato-splanchnic metabolic effects of the stable prostacyclin analogue iloprost in patients with septic shock.

    • P Kiefer, I Tugtekin, H Wiedeck, H Bracht, J Vogt, U Wachter, M Weiss, C Altin, M Georgieff, and P Radermacher.
    • Department of Anesthesiology, University Clinic Ulm, Germany. peter.kiefer@medizin.uni-ulm.de
    • Intensive Care Med. 2001 Jul 1;27(7):1179-86.

    ObjectiveTo evaluate the effects of the stable prostacyclin analogue iloprost on hepato-splanchnic blood flow, oxygen exchange and metabolism in patients with septic shock.DesignProspective clinical study.SettingIntensive care unit in a university clinic.PatientsEleven patients with septic shock requiring norepinephrine to maintain mean arterial pressure above 70 mmHg.InterventionsIloprost was incrementally infused to increase cardiac index by 15%.Measurements And Main ResultsSplanchnic blood flow (Qspl) was measured using the steady-state indocyanine-green infusion technique and endogenous glucose production rate (EGP) using a stable isotope approach. Systemic and splanchnic oxygen consumption (VO2), the hepato-splanchnic uptake rates of the glucose precursors lactate, pyruvate, alanine and glutamine, the hepatic venous redox state and gastric mucosal-arterial PCO2 gradients were determined. After a baseline measurement, iloprost infusion was started. After 90 min all measurements were repeated and a third measurement was obtained after another 90 min following iloprost withdrawal. Qspl (baseline I: 0.82/0.75-1.08 l x min x m2; iloprost: 0.94/0.88-1.29 l x min x m2; baseline II: 0.87/0.74-1.09 l x min x m2) and splanchnic oxygen delivery (baseline I: 122/103-166 ml x min x m2; iloprost: 134/117-203 ml x min x m2; baseline II: 130/98-158 ml x min x m2) significantly increased. While systemic VO2 significantly increased (baseline I: 139/131-142 ml x min x m2; iloprost: 147/136-164 ml x min x m2; baseline II: 143/133-154 ml x min x m2) splanchnic VO2 increased in 9 of 11 patients which, however, did not reach statistical significance. EGP significantly decreased (baseline I: 23/16-26 micromol x kg x min; iloprost: 16/14-21 micromol x kg x min; baseline II: 18/12-20 micromol x kg x min), whereas all other parameters of energy metabolism remained unchanged.ConclusionIn patients with septic shock an iloprost-induced increase in cardiac index increased splanchnic blood flow and shifted oxygen utilization from the energy requiring de novo glucose production rate to other oxygen-demanding metabolic pathways.

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