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血管扩张剂MDL - 899用于原发性高血压患者的临床评估。

Clinical evaluation of the vasodilator MDL-899 in patients with essential hypertension.

作者信息

Elliott H L, Campbell L, Sumner D J, Reid J L

出版信息

J Cardiovasc Pharmacol. 1985 Sep-Oct;7(5):948-52. doi: 10.1097/00005344-198509000-00021.

Abstract

In this study of 10 patients with essential hypertension inadequately controlled by standard beta-blocker-diuretic combination therapy, the addition of 5 mg of MDL-899, a peripheral arteriolar vasodilator, resulted in significant reductions in blood pressure, both supine and standing, which was maximal 4-8 h after dosing, with no additional orthostatic component. There were associated small rises in heart rate but no evidence of significant activation of the sympathetic or renin-angiotensin systems. Six patients continued for 4 weeks receiving MDL-899 twice daily with significant improvement in their blood pressure control--from a mean of 182/95 to 146/77 mm Hg (supine) and from 161/93 to 138/79 mm Hg (erect). These six patients experienced no significant side effects, but four patients were unable to proceed with the study as a result of adverse effects, particularly headache, following the first few doses. It seems likely that these side effects are dose related. In a combined drug regimen, MDL-899 is an effective vasodilator drug that significantly improved the blood pressure control of patients with essential hypertension.

摘要

在这项针对10例原发性高血压患者的研究中,这些患者采用标准β受体阻滞剂-利尿剂联合治疗后血压控制不佳,添加外周小动脉血管扩张剂MDL-899 5毫克后,仰卧位和站立位血压均显著降低,给药后4至8小时降至最大降幅,且无额外的直立性成分。心率有相关小幅升高,但无交感神经或肾素-血管紧张素系统明显激活的证据。6例患者持续4周每天两次服用MDL-899,血压控制有显著改善——仰卧位平均血压从182/95毫米汞柱降至146/77毫米汞柱,直立位从161/93毫米汞柱降至138/79毫米汞柱。这6例患者未出现明显副作用,但4例患者在最初几次给药后因不良反应(尤其是头痛)而无法继续该研究。这些副作用似乎与剂量有关。在联合用药方案中,MDL-899是一种有效的血管扩张剂,可显著改善原发性高血压患者的血压控制。

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