Al. Daly et al., DOBUTAMINE PHARMACOKINETICS DURING DOBUTAMINE STRESS ECHOCARDIOGRAPHY, The American journal of cardiology, 79(10), 1997, pp. 1381-1386
Many patients fail to achieve target heart rate during dobutamine stre
ss echocardiography (DSE). We evaluated the pharmacokinetics of dobuta
mine during DSE to determine whether patients with an impaired chronot
ropic response have higher races of dobutamine clearance and consequen
tly relatively lower plasma dobutamine levels. Plasma dobutamine level
s, heart rate, and left ventricular (LV) ejection fraction (EF) were m
easured in 13 mole patients referred for DSE at baseline and at the en
d of stepped 3-minute dobutamine infusions of 5, 10, 20, and 30 mu g/k
g/min. Dobutamine levels increased with doses: 27 +/- 10, 111 +/- 17,
275 +/- 17, and 403 +/- 28 ng/ml (mean +/- SEM). There was no relation
observed between the plasma dobutamine level achieved at the 30-mu g
infusion dose and the increase in heart rate from baseline (r = 0.066;
p = 0.83). Baseline LVEF and a measure of chronotropic beta responsiv
ity were identified as independent predictors of dobutamine clearance,
together accounting for 73% of the variance in dobutamine clearance.
In conclusion, (1) there is a dose-dependent increase in plasma dobuta
mine levels during DSE, (2) dobutamine clearance is positively related
to baseline LVEF and is partially mediated by a beta-receptor mechani
sm, and (3) an impaired chronotropic response during DSE is not due to
failure to achieve a sufficiently high dobutamine level. We conclude
that in patients who lack an adequate heart rate response during the e
arly stages of DSE (e.g., up to 20 mu g/kg/min infusion), administrati
on of atropine rather than progressively higher amounts of dobutamine
may provide a more effective strategy to achieve target heart rate. (C
) 1997 by Excerpta Medica, Inc.