Sg. Dehert et al., INOTROPIC EFFECTS OF SODIUM-NITROPRUSSIDE - A CLINICAL-STUDY ON CORONARY SURGERY PATIENTS, Acta cardiologica, 52(4), 1997, pp. 347-357
Objective. Sodium nitroprusside (SNP) induces release of nitric oxide
and is widely used as a vasoactive drug. Recent research analyzed effe
cts of SNP on cardiac muscle and described variable inotropic effects.
The present study evaluated effects of SNP on left ventricular (LV) f
unction in patients undergoing coronary artery surgery. Methods. The s
tudy was performed in 100 patients with a preoperative ejection fracti
on >40%. LV pressures were measured with a fluid-filled catheter in th
e LV cavity. Hearts were placed in AV sequential mode at a rate of 90
beats/min. Measurements were obtained at end-expiration and consisted
of a control tracing and a tracing obtained after a 5 min infusion of
SNP 0.5 mu g.kg(-1).min(-1). These measurements were obtained before a
nd after cardiopulmonary bypass (CPB). An average of 5 consecutive bea
ts was obtained for analysis. Ventricular function was assessed with L
V pressure and dP/dt. Data were analyzed suing two factor analysis of
variance for repeated measurements. Results. 1. Baseline patient data
(n=80). Before CPB, a variable inotropic response to SNP was observed.
The direction of the inotropic response was related to preoperative b
eta-blocking medication. LVP and dP/dt(max) increased with SNP in pati
ents without preoperative beta-blocking medication. In patients on pre
operative beta-blocking medication, SNP dit not alter LVP and dP/dt(ma
x). After CPB, a positive inotropic response was not observed in any o
f the patients. 2. Postoperative patient data under dobutamine (n=20).
Data of these separate observations were similar to baseline data bef
ore CPB. After CPB and under dobutamine administration (5 mu g.kg(-1).
min(-1)) all 20 patients developed a positive inotropic response to SN
P. Conclusions. In coronary surgery patients, SNP induced a variable i
notropic effect. The direction of the inotropic response appeared to b
e modulated by the beta-adrenergic drive.