Why the study?
Does intravenous nisoldipine compared to nifedipine improve acute haemodynamic profiles in male patients with stable angina treated with atenolol?
Does intravenous nisoldipine compared to nifedipine improve acute haemodynamic profiles in male patients with stable angina treated with atenolol?
Intravenous nisoldipine provides a more complementary haemodynamic profile than nifedipine when combined with atenolol in patients with stable angina.
Answers are grounded in this paper and cite their sources.
Favors nisoldipine over nifedipine for acute afterload reduction in atenolol-treated angina; extends head-to-head dihydropyridine haemodynamic comparisons.
The acute haemodynamic effects of intravenous nisoldipine (1, 2, 4 microg kg(-1)) and nifedipine (2.5, 5, 10 microg kg(-1)) were compared in a randomised, within-patient crossover study. Fifteen male patients with stable angina pectoris treated with atenolol were studied after undergoing routine cardiac catheterisation. 2. Nisoldipine caused a dose-related fall in systemic vascular resistance (maximum 22%) associated with an increase in heart rate and cardiac index (18%) and a fall in mean arterial pressure (7%). 3. By contrast, nifedipine was associated with a significant increase in heart rate but systemic vascular resistance, cardiac index and mean arterial pressure remained unaltered. 4. At doses with equivalent effects on heart rate (2 microg kg(-1) nisoldipine; 10 microg kg(-1) nifedipine) acute dosing with nisoldipine caused a significantly greater fall in systemic vascular resistance and increase in cardiac index, whilst nifedipine caused a greater reduction in stroke volume index and left ventricular stroke work index. 5. The results suggest that, when combined with atenolol, acute dosing with nisoldipine may have a more complementary haemodynamic profile than nifedipine. The implications of this finding for chronic oral dosing in patients with impaired left ventricular function should be evaluated.
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Donaldson et al. (1993) studied this question.
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