Ivleva A Ia, Moiseev V S, Antiia I D
Ter Arkh. 1993;65(4):52-8.
A clinical trial of 75 hypertensive subjects in stage II of the disease receiving ramipril monotherapy has established a marked efficacy of the above treatment. Individually adjusted single doses varied from 2.5 mg to 7.5 mg/day. The drug was well tolerated and had mild adverse effects (dry cough) in 2% of the patients. Long-term 12-week ramipril treatment in effective for hypertension doses is able to reduce myocardial mass without inhibition of the pumping capacity in the patients with left ventricular hypertrophy of the myocardium. In primary signs of nephroangiosclerosis hypertension correction was associated with improvement of filtration function and an increase in effective renal flow of plasma. The above pharmacodynamic effects make it possible to consider ramipril an effective hypotensive agent with organ-protective properties.
一项针对75名处于疾病二期的高血压患者接受雷米普利单药治疗的临床试验证实了上述治疗具有显著疗效。个体化调整后的单剂量范围为每日2.5毫克至7.5毫克。该药物耐受性良好,2%的患者出现轻度不良反应(干咳)。对心肌肥厚患者进行为期12周的有效剂量雷米普利长期治疗能够在不抑制泵血能力的情况下减轻心肌质量。在肾血管性硬化高血压的主要症状方面,血压纠正与滤过功能改善及有效肾血浆流量增加相关。上述药效学作用使得可以将雷米普利视为一种具有器官保护特性的有效降压药。