Dakak N, Makhoul N, Merdler A, Yechiely H, Kahana L, Halon D A, Schneeweiss A, Lewis B S
Department of Cardiology, Lady Davis Carmel Hospital, Haifa, Israel.
Eur Heart J. 1993 Jun;14(6):836-44. doi: 10.1093/eurheartj/14.6.836.
The acute haemodynamic and neurohumoral effects of flosequinan, a new direct-acting vasodilator, were studied in 12 patients with severe (eight in New York Heart Association grade 3, four in grade 4) cardiac failure. Flosequinan was administered in a single oral dose of 100 mg, with haemodynamic monitoring over a 22 h period. The effects were compared with those observed during high dose intravenous nitroglycerin therapy (276 +/- 100 micrograms.min-1), given to the same patients for an identical period on the previous day. Both flosequinan and nitroglycerin produced significant haemodynamic improvement during the 22 h monitoring period. Cardiac and stroke indices increased with both drugs. However, while systemic and pulmonary vascular resistance were reduced similarly by both drugs, the decrease in right atrial and pulmonary capillary wedge pressures was greater with nitroglycerin and less with flosequinan, indicating a greater venodilator effect for nitroglycerin and a more balanced arterial and venodilator effect for flosequinan. Systemic arterial pressure and heart rate tended to increase with flosequinan and to decrease with nitroglycerin. In contrast to nitroglycerin, flosequinan did not increase plasma renin activity and serum aldosterone levels. Atrial natriuretic peptide decreased appropriately after both drugs, in keeping with the decreases in left and right heart filling pressures. The favourable haemodynamic and neurohumoral profiles of flosequinan suggest that it may be a useful vasodilating drug in the management of patients with severe heart failure.
对12例重度(纽约心脏协会分级3级8例,4级4例)心力衰竭患者研究了新型直接作用血管扩张剂氟司喹南的急性血流动力学和神经体液效应。给予氟司喹南单次口服剂量100mg,并在22小时内进行血流动力学监测。将这些效应与前一天同一批患者在相同时间段内接受大剂量静脉硝酸甘油治疗(276±100微克·分钟-1)时观察到的效应进行比较。在22小时监测期内,氟司喹南和硝酸甘油均使血流动力学显著改善。两种药物均使心脏指数和卒中指数增加。然而,虽然两种药物同样降低了体循环和肺血管阻力,但硝酸甘油使右心房和肺毛细血管楔压下降幅度更大,氟司喹南下降幅度较小,这表明硝酸甘油的静脉扩张作用更强,而氟司喹南的动脉和静脉扩张作用更均衡。氟司喹南使体循环动脉压和心率趋于升高,硝酸甘油则使其趋于降低。与硝酸甘油不同,氟司喹南不会增加血浆肾素活性和血清醛固酮水平。两种药物使用后心房利钠肽均适当下降,与左、右心充盈压下降一致。氟司喹南良好的血流动力学和神经体液特征表明,它可能是治疗重度心力衰竭患者的一种有用的血管扩张药物。