Santos-A-C. Pedersen-H. Sallusto-J-A. Johnson-H-V Morishima-H-
O. Finster-M. Arthur-G-R. Covino-B-G. Pharmacokinetics of ropivacaine in
nonpregnant and pregnant ewes.
Anesth-Analg. 1990 Mar. 70(3). P 262-6.
The pharmacokinetics of ropivacaine were studied in
chronically instrumented nonpregnant and pregnant ewes. On the
day of study, the urinary bladder was catheterized.
Ropivacaine (2.5 or 3.0 mg/kg) was administered by
intravenous infusion over 2 or 4 min. Serial samples of
arterial blood and urine were collected over 5 h, and drug
concentrations were determined using a gas chromatographic
technique. Total clearance of ropivacaine was lower in
the pregnant animals (21.6 +/- 4.5 mL.min-1.kg-1) compared with
the nonpregnant animals (45.1 +/- 6.7 mL.min-1.kg-1). There was
a tendency toward a decrease in the volume of distribution
during the terminal exponential phase of drug elimination of
2.03 +/- 0.36 L/kg in the pregnant and 4.32 +/- 1.03 L/kg in
the nonpregnant sheep. Thus the difference in the elimination
half-life was only minimal: 74.7 +/- 10.7 min in the pregnant
and 64.4 +/- 7.4 min in the nonpregnant animals. It is
concluded that ovine pregnancy is accompanied by changes in the
pharmacokinetics of ropivacaine. Inadvertent intravenous
injections of similar drug doses to pregnant and nonpregnant
women might result in higher plasma concentrations of
ropivacaine in the former. However, the rate of decline
in plasma levels of the drug would be similar in both.