Publications

The hemodynamic response to controlled oxygen administration was investigated in 35 patients who presented with acute decompensation of chronic obstructive pulmonary disease. Gasometric and hemodynamic data were successively measured under inspiratory fractions in oxygen of 0.21 (room air) and 0.28. Response to oxygen therapy was characterized by a decrease in cardiac output and an increase in oxygen delivery because of a sharp increase in arterial oxygen content. The coefficient of oxygen delivery (oxygen delivery/oxygen consumption) increased in each patient. All these changes were highly significant (p les than 0.001). Somewhat unexpectedly, there was no change in pulmonary artery pressures, so that pulmonary arteriolar resistance even increased (p less than 0.05). Further analysis individualized 2 types of hemodynamic response to oxygen therapy. In 15 patients who presented with severe hypoxemia, oxygen therapy resulted in a significant increase in oxygen delivery without change in cardiac output. By contrast, in 20 patients with moderate hypoxemia, oxygen therapy induced a significant decrease in cardiac output (p less than 0.001) without change in oxygen delivery. Patients in whom cardiac output was unaffected by oxygen administration presented with a lower mixed venous oxygen tension (less than 35 mmHg) and a lower coefficient of oxygen delivery (less than 3.5). This study demonstrated that oxygen therapy does not always increase oxygen delivery in acute decompensation of chronic obstructive pulmonary disease.

SOCIETY OF CRITICAL CARE MEDICINE 32ND CRITICAL CARE CONGRESS SAN ANTONIO, TEXAS, USA JANUARY 28-FEBRUARY 2, 2003: ORAL/SANDWICH PRESENTATIONS: Poster Presentation: Clinical Science: Cardiovascular Monitoring: Oxygenation: PDF Only

We compared the effects of a new compound (TV7130) with those of activated protein C (APC) in a large animal model of septic shock. Thirty-two fasted, anesthetized, invasively monitored, mechanically ventilated female sheep received 1.5 g/kg body weight of feces into the abdomen to induce sepsis. Immediately after feces injection, all animals received a bolus followed by a continuous infusion of saline (n = 8, bolus 1.5 mL for 15 min, infusion 1.5 mL/[kg·h]), low-dose TV7130 (n = 8; 0.4 mg/kg bolus, 0.4 mg/[kg·h] infusion), high-dose TV7130 (n = 8; 0.8 mg/kg bolus, 0.8 mg/[kg·h] infusion), or APC (n = 8; saline bolus, APC infusion of 0.024 mg/[kg·h]). Experiments were pursued until each sheep's spontaneous death. There were no significant differences among groups in heart rate or cardiac index, but mean arterial pressure, systemic vascular resistance index, and left ventricular stroke work index decreased less in the high-dose TV7130 and APC groups than in the other groups. Gas exchange was preserved better in the high-dose TV7130 and APC groups. Interleukin 6 and lactate concentrations were lower in the high-dose TV7130 and APC groups than in the other groups. Functional capillary density and proportion of perfused vessels, evaluated in the sublingual region using sidestream dark-field videomicroscopy, were significantly higher in the TV7130 and APC groups than in the vehicle group at 16 h. Survival time was significantly longer in the high-dose TV7130 and APC groups than in the other groups (log-rank test, P = 0.0002). TV7130 has similar effects to APC and may be a promising agent for the management of severe sepsis.