EFFECT OF PHENYLEPHRINE BOLUS ADMINISTRATION ON GLOBAL LEFT-VENTRICULAR FUNCTION IN PATIENTS WITH CORONARY-ARTERY DISEASE AND PATIENTS WITHVALVULAR AORTIC-STENOSIS
Aw. Goertz et al., EFFECT OF PHENYLEPHRINE BOLUS ADMINISTRATION ON GLOBAL LEFT-VENTRICULAR FUNCTION IN PATIENTS WITH CORONARY-ARTERY DISEASE AND PATIENTS WITHVALVULAR AORTIC-STENOSIS, Anesthesiology, 78(5), 1993, pp. 834-841
Background. Although phenylephrine bolus administration is frequently
used to increase coronary perfusion pressure in patients with coronary
artery disease or valvular aortic stenosis, there are no data describ
ing its effect on left ventricular function (LVF). Methods: Twenty pat
ients scheduled for elective coronary artery bypass grafting (group 1)
and 18 patients scheduled for elective aortic valve replacement (grou
p 2) entered the study. The effect of phenylephrine was compared with
that of norepinephrine in those patients who developed a defined degre
e of arterial hypotension under general anesthesia. These patients wer
e randomized to receive an initial bolus of either phenylephrine (1 mu
g/kg) or norepinephrine (0.05 mug/kg) followed by a bolus of the other
drug after arterial pressure and heart rate (HR) had returned to base
line. Transesophageal echocardiography was used to evaluate LVF. Arter
ial pressure, HR, ejection time, and LV diameter, area, and wall thick
ness were recorded immediately before and for 3 min after bolus admini
stration. Fractional diameter shortening, fractional area change, mean
heart rate corrected velocity of circumferential fiber shortening (mV
cf(c)), and LV meridional end-systolic walt stress (ESWS) were calcula
ted. Results: Both substances effectively restored arterial pressure i
n both groups. However, in group 1, phenylephrine administration resul
ted in a reduction of fractional area change from 0.51 (median) to 0.3
9 (P = 0.0007) and a reduction of mVcf(c) from 1.16 to 0.61 circ/s (P
= 0.0001). End-systolic wall stress increased from 98 to 186 10(3) dyn
e.cm-2 (P = 0.0001). Administration of norepinephrine to group 1 and a
dministration of either substance to the group 2 patients did not caus
e any significant changes of LVF. Conclusions: The results indicate th
at phenylephrine given as an intravenous bolus to patients with CAD an
esthetized with fentanyl causes a transient impairment of LV global fu
nction and that phenylephrine bolus administration is well tolerated i
n patients with valvular aortic stenosis.