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[钙拮抗剂在高血压治疗中的应用]

[Calcium antagonists in the therapy of hypertension].

作者信息

Heidland A, Heidbreder E, Hörl W H, Schäfer R M

出版信息

Klin Wochenschr. 1983 Jul 1;61(13):633-40. doi: 10.1007/BF01487579.

Abstract

Calcium antagonists (nifedipine, verapamil, diltiazem) are potent vascular smooth muscle relaxants. Experimental and clinical investigations provide growing evidence that they are effective in acute and (sub)chronic therapy of arterial hypertension by lowering peripheral vascular resistance and improvement of altered hemodynamics--independent from pathogenesis of hypertension. Due to its prompt and profound hypotensive action, sublingual or oral nifedipine has been used successfully in hypertensive crises. The hypotensive effect usually correlated closely with the severity of hypertension and is nearly absent in normotensive controls. Since the blood pressure drop may occasionally results in absolute or relative hypotension, the initial dose should be as low as possible. The activation of the adrenergic and renin angiotension systems seen after nifedipine administration is less pronounced after chronic administration of the drug and is nearly absent after verapamil and diltiazem. Plasma aldosterone concentrations remain constant or are slightly decreased. In contrast to classic vasodilators, the long-term administration of calcium antagonists usually does not result in tachycardia (nifedipine), but slight sinus bradycardia (verapamil, diltiazem). Peripheral edema may occasionally occur after nifedipine. A tolerance has been observed during long-term treatment of hypertension. Combining these drugs (verapamil, diltiazem) with betablockers is not recommended due to the negative inotropic and bathmotropic effects. Simultaneous administration of nifedipine and beta-blockers enhances the hypotensive action, but favours the development of peripheral edema and in rare cases (especially in severe coronary heart disease) results in a dramatic drop in blood pressure and/or congestive heart failure. Further clinical evaluation and long-term trials of calcium antagonists as antihypertensive agents will be needed before definite conclusions can be drawn.

摘要

钙拮抗剂(硝苯地平、维拉帕米、地尔硫䓬)是强效的血管平滑肌松弛剂。实验和临床研究越来越多地证明,它们通过降低外周血管阻力和改善血流动力学改变,对动脉高血压的急性和(亚)慢性治疗有效——与高血压的发病机制无关。由于硝苯地平具有迅速而显著的降压作用,舌下含服或口服硝苯地平已成功用于高血压危象。降压效果通常与高血压的严重程度密切相关,在血压正常的对照者中几乎没有降压效果。由于血压下降偶尔可能导致绝对或相对低血压,初始剂量应尽可能低。硝苯地平给药后出现的肾上腺素能和肾素血管紧张素系统激活在长期给药后不太明显,而在维拉帕米和地尔硫䓬给药后几乎不存在。血浆醛固酮浓度保持不变或略有下降。与经典血管扩张剂不同,长期服用钙拮抗剂通常不会导致心动过速(硝苯地平),而是轻微的窦性心动过缓(维拉帕米、地尔硫䓬)。硝苯地平治疗后偶尔可能出现外周水肿。在高血压的长期治疗中已观察到耐受性。由于其负性肌力和变力作用,不建议将这些药物(维拉帕米、地尔硫䓬)与β受体阻滞剂联合使用。同时服用硝苯地平和β受体阻滞剂可增强降压作用,但有利于外周水肿的发生,在极少数情况下(尤其是严重冠心病)会导致血压急剧下降和/或充血性心力衰竭。在得出明确结论之前,需要对钙拮抗剂作为抗高血压药物进行进一步的临床评估和长期试验。

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