Background
The primary goal of fluid therapy is to maintain fluid homeostasis. Commonly used isotonic crystalloids are only marginally effective and contribute to fluid excess syndrome. In patients with decreased cardiovascular reserve, fluid therapy alone is not sufficient to maintain end-organ perfusion. Therefore, inotropes or vasoactive drugs are used to supplement fluid infusion. Recent animal data suggests that co-infusion of adrenergic agents modulate the distribution of fluid between the vascular and extravascular/interstitial compartments after a fluid bolus. We sought to determine if this effect would translate in humans by co-administering a beta (β)-adrenergic agonist with fluid.
Methods
Nine healthy volunteers (age 21–50 yrs) were randomly paired and received either a continuous isoproterenol infusion (ISO:0.05μg/kg/min) or 0.9% saline (control(CON)) 30min prior to a 25mL/kg 0.9% NaCl fluid bolus. Hemodynamics, ventricular volume and function and microcirculatory determinants (capillary filtration coefficient (CFC) and oncotic pressure) were measured. Vascular and extra-vascular volume (EVV) and fluid balance were determined.
Results
Compared to CON, ISO significantly increased heart rate (CON:64.2 ±4.1 bpm vs. ISO:97.4±5.7 bpm) and cardiac output (CON 4.4±0.7L/min vs. ISO:10.2±0.9) before fluid bolus. ISO significantly increased urinary output (ISO: 10.86±1.95 vs Control: 6.53±1.45 mL/kg) and reduced EVV (7.98±2.0 vs 14.15±1.1mL/kg). ISO prevented an increase in CFC (1.74±0.4 vs 3.21±0.4 mL/min/mmHg•10−3).
Conclusion
Isoproterenol, a non-selective β-adrenergic agonist, augments vascular volume expansion and eliminates EVV via enhanced diuresis, which may in part be due to enhanced endothelial barrier function.