5种钙通道阻滞剂对高血压患者静息和运动时血流动力学影响的比较。

Annals of clinical research Pub Date : 1988-01-01
P Omvik, P Lund-Johansen
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引用次数: 0

摘要

二氢吡啶和维拉帕米样钙通道阻滞剂可降低原发性高血压(EH)患者的血压(BP),但对静息心率(HR)的影响不同。本研究比较了五组轻度和中度EH(舒张压100-120 mmHg)患者长期使用硝苯地平、尼索地平、维拉帕米、替帕米和地尔硫卓治疗后的心率和血流动力学反应。76例患者(平均年龄43岁)分别测量动脉内血压、染料稀释(Cardiogreen)心输出量和心电图HR。急性HR和心脏指数(CI)分别升高(9%和12%),BP和总外周阻力指数(TPRI)分别降低(9%和19%)。钙通道阻断一年后,静坐时动脉内压从172/105降至150/91 mmHg (13%), 100 W运动时动脉内压从205/109降至188/97 mmHg(10%)。在所有情况下,二氢吡啶组的心率保持不变(范围为+/- 3%),而在维拉帕米尔样钙阻滞剂组,心率总是下降(范围为3 - 15%)。运动时心率的下降比休息时更大(平均10% vs 6%)。使用这些药物,脑卒中体积(SV)倾向于增加(范围为1%至10%),而在二氢吡啶组中保持不变。在所有组中,TPRI在休息和运动时平均下降了15%。因此,维拉帕米尔样钙阻滞剂诱导负性变时效应,在工作时增强,但心脏泵功能通过SI代偿性增加得以保留。独立于心脏反应,两组钙阻滞剂在休息和运动时通过外周血管扩张降低血压。
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Comparison of the hemodynamic effects of five calcium channel blockers at rest and during exercise in essential hypertension.

Dihydropyridine and verapamil-like calcium channel blockers reduce blood pressure (BP) in essential hypertension (EH) but have different effects on heart rate (HR) at rest. This study compares the HR and hemodynamic responses to exercise of long-term treatment with nifedipine, nisoldipine, verapamil, tiapamil and diltiazem in five groups of patients with mild and moderate EH (diastolic BP ranging 100-120 mmHg). In a total of 76 patients (mean age 43 years) BP was measured intraarterially, cardiac output by dye dilution (Cardiogreen) and HR by electrocardiogram. Acutely HR and cardiac index (CI) rose (9 and 12%) while BP and total peripheral resistance index (TPRI) were reduced (9 and 19%). After one year calcium channel blockade intraarterial pressure at rest sitting fell from 172/105 to 150/91 mmHg (13%) and at 100 W exercise from 205/109 to 188/97 mmHg (10%). HR remained unchanged in the dihydropyridine groups (range +/- 3%) in all situations while it invariably fell (range 3 to 15%) in the groups treated with verapamil-like calcium blockers. The fall in HR was greater during exercise than at rest (mean 10% vs 6%). With these drugs stroke volume (SV) tended to increase (range 1 to 10%) while it remained unchanged in the dihydropyridine groups. Only minor changes were seen in CO. In all groups the TPRI fell, averaging 15% at rest and during exercise. Thus, the verapamil-like calcium blockers induce a negative chronotropic effect that is enhanced during work, but the cardiac pump function is preserved by a compensatory increase in SI. Independent on the cardiac responses both groups of calcium blockers lower BP by peripheral vasodilatation both at rest and during exercise.

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