TY - JOUR
T1 - Adrenergic drugs alter both the fluid kinetics and the hemodynamic responses to volume expansion in sheep
AU - Ewaldsson, Carl Arne
AU - Vane, Luiz A.
AU - Kramer, George C.
AU - Hahn, Robert G.
PY - 2006/3
Y1 - 2006/3
N2 - Background. Plasma volume expansion is often performed during adrenergic therapy in the intensive care unit, but little is known about their combined effects. Materials and methods. The influence of three adrenergic drugs (50 μg/kg/min of dopamine, 0.1 μg/kg/min of isoprenaline, or 3 μg/kg/min of phenylephrine) on the relationship between plasma dilution (an index of volume expansion) and the central hemodynamic responses to volume loading with 24 ml/kg of 0.9% saline were evaluated in 6 adult sheep. Kinetic analysis was also applied to the data on plasma dilution and the urinary excretion measured during and after volume loading. Results. The adrenergic agents markedly changed the baseline values for all hemodynamic parameters. The kinetic analysis showed that phenylephrine, which is an alpha-adrenergic receptor agonist, promoted renal excretion of infused fluid at the expense of fluid distribution to the periphery (P < 0.05 versus controls). Isoprenaline, which stimulates adrenergic beta-receptors, had the opposite effect. During volume expansion, cardiac atrial pressures increased by 25 to 90%, cardiac output by 13-80% and the arterial pressures by 2 to 22%. Plasma dilution during and after volume loading correlated, in a linear fashion, with these hemodynamic responses. The correlations were strong (r > 0.80) in the control and phenylephrine groups, but weaker in the dopamine and isoprenaline groups. Dopamine was associated with the most variable hemodynamic responses overall. Conclusions. Adrenergic drugs altered the hemodynamics at baseline (direct effects), changed the distribution and elimination of infused 0.9% saline (indirect effects) and, finally, modified most hemodynamic responses to plasma dilution (interaction effects).
AB - Background. Plasma volume expansion is often performed during adrenergic therapy in the intensive care unit, but little is known about their combined effects. Materials and methods. The influence of three adrenergic drugs (50 μg/kg/min of dopamine, 0.1 μg/kg/min of isoprenaline, or 3 μg/kg/min of phenylephrine) on the relationship between plasma dilution (an index of volume expansion) and the central hemodynamic responses to volume loading with 24 ml/kg of 0.9% saline were evaluated in 6 adult sheep. Kinetic analysis was also applied to the data on plasma dilution and the urinary excretion measured during and after volume loading. Results. The adrenergic agents markedly changed the baseline values for all hemodynamic parameters. The kinetic analysis showed that phenylephrine, which is an alpha-adrenergic receptor agonist, promoted renal excretion of infused fluid at the expense of fluid distribution to the periphery (P < 0.05 versus controls). Isoprenaline, which stimulates adrenergic beta-receptors, had the opposite effect. During volume expansion, cardiac atrial pressures increased by 25 to 90%, cardiac output by 13-80% and the arterial pressures by 2 to 22%. Plasma dilution during and after volume loading correlated, in a linear fashion, with these hemodynamic responses. The correlations were strong (r > 0.80) in the control and phenylephrine groups, but weaker in the dopamine and isoprenaline groups. Dopamine was associated with the most variable hemodynamic responses overall. Conclusions. Adrenergic drugs altered the hemodynamics at baseline (direct effects), changed the distribution and elimination of infused 0.9% saline (indirect effects) and, finally, modified most hemodynamic responses to plasma dilution (interaction effects).
KW - Dopamine
KW - Isoprenaline
KW - Normal saline
KW - Pharmacokinetics
KW - Phenylephrine
KW - Volume expansion
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U2 - 10.1016/j.jss.2005.09.012
DO - 10.1016/j.jss.2005.09.012
M3 - Article
C2 - 16325856
AN - SCOPUS:32444442821
SN - 0022-4804
VL - 131
SP - 7
EP - 14
JO - Journal of Surgical Research
JF - Journal of Surgical Research
IS - 1
ER -