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新型长效血管紧张素转换酶抑制剂西拉普利治疗高血压患者的疗效及耐受性评估(初步报告)

[Evaluation of the efficacy and tolerance of the new delayed-action angiotensin-converting enzyme inhibitor cilazapril in patients with hypertension (preliminary report)].

作者信息

Vil'chinskaia M Iu, Sorokin E V, Podinovskaia Ia V, Karpov Iu A

出版信息

Ter Arkh. 1993;65(9):32-4.

PMID:8303591
Abstract

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.

摘要

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。

相似文献

1
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Ter Arkh. 1993;65(9):32-4.
2
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