Vil'chinskaia M Iu, Sorokin E V, Podinovskaia Ia V, Karpov Iu A
Ter Arkh. 1993;65(9):32-4.
Cilazapril [correction of Silazapril], a new inhibitor of long-acting angiotensin-converting enzyme, was given to 39 hypertensive subjects aged 24-68 with initial diastolic pressure 95-120 mm Hg. Of them 16 were females and 23 were males. The course of the treatment lasted 8 weeks, the drug being taken daily in a single dose 2.5 mg in the morning. Checkups, measurements of arterial pressure (AP), blood counts, urinalyses were made before the treatment, on the treatment week 4 and 8. In one patient the drug was discontinued 4 weeks after the treatment start because the AP fall to 110/63, in 23 patients the dose was raised to 5 mg, the rest continued on 2.5 mg/day. The treatment ended in the systolic pressure decrease by 14.9% (from 161.0 +/- 2.9 to 137.8 +/- 2.8 mm Hg, p < 0.0001) and diastolic pressure fall by 13.5% (from 104.5 +/- 1.4 to 90.1 +/- 1.7 mm Hg, p < 0.005). No side effects causing the drug withdrawal were registered. It is concluded that the drug is effective in essential hypertension stage IIA-IIB as monotherapy.
西拉普利(纠正:昔拉普利),一种新型长效血管紧张素转换酶抑制剂,被给予39名年龄在24至68岁之间、初始舒张压为95至120毫米汞柱的高血压患者。其中16名是女性,23名是男性。治疗疗程持续8周,药物每天早晨单次服用2.5毫克。在治疗前、治疗第4周和第8周进行检查、测量动脉血压(AP)、血细胞计数、尿液分析。1名患者在治疗开始4周后因血压降至110/63而停药,23名患者剂量增至5毫克,其余患者继续服用2.5毫克/天。治疗结束时,收缩压下降14.9%(从161.0±2.9降至137.8±2.8毫米汞柱,p<0.0001),舒张压下降13.5%(从104.5±1.4降至90.1±1.7毫米汞柱,p<0.005)。未记录到导致停药的副作用。结论是该药物作为单一疗法对IIA-IIB期原发性高血压有效。