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使用血管紧张素转换酶抑制剂卡托普利控制原发性高血压。

Control of essential hypertension with captopril, an angiotensin converting enzyme inhibitor.

作者信息

el-Mehairy M M, Shaker A, Ramadan M, Hamza S, Tadros S S

出版信息

Br J Clin Pharmacol. 1981 May;11(5):469-75. doi: 10.1111/j.1365-2125.1981.tb01152.x.

Abstract

1 Captopril, an orally active angiotensin converting enzyme inhibitor, was compared with hydrochlorothiazide (HCT) in the treatment of mild and moderate essential hypertension. 2 Twenty outpatients received no antihypertensive therapy for 2 weeks, after which they were given placebo for 8 weeks. Since their diastolic blood pressure remained above 100 mm Hg, they were then randomized to receive either captopril (twelve patients) or HCT (eight patients) for a 4-week titration period. If the supine diastolic blood pressure (SDBP) was normalized, (less than or equal to 90 mm Hg) by the end of titration period, the established regimen was continued for an 8-week maintenance period; if not, the alternate drug was added in increasing doses for up to 4 weeks and the combined therapy was maintained for the remaining 4 weeks. 3 After the first 4 weeks of therapy, both groups showed a statistically significant decrease in both systolic and diastolic blood pressure. Normalization of SDBP occurred in 75% of patients treated with captopril alone, and the addition of HCT produced normalization in the remainder. HCT alone resulted in normalization of SDBP in 50% of patients and the blood pressure of the remaining patients was normalized after the addition of captopril. 4 Captopril given orally, either alone or in conjunction with HCT, is an effective agent for the control of mild and moderate essential hypertension. 5 In our series the main side effects encountered were vertigo and dizziness, transient eosinophilia, a rise of BUN and or/a rise of SGPT or SGOT.

摘要
  1. 卡托普利是一种口服有效的血管紧张素转换酶抑制剂,将其与氢氯噻嗪(HCT)用于治疗轻、中度原发性高血压进行比较。2. 20名门诊患者先接受2周无抗高血压治疗,之后服用8周安慰剂。由于他们的舒张压仍高于100mmHg,然后将他们随机分为接受卡托普利治疗(12名患者)或氢氯噻嗪治疗(8名患者),进行为期4周的滴定期。如果在滴定期结束时仰卧舒张压(SDBP)恢复正常(小于或等于90mmHg),则继续既定方案进行为期8周的维持期治疗;如果未恢复正常,则增加另一种药物剂量最多4周,并在剩余4周维持联合治疗。3. 治疗的前4周后,两组的收缩压和舒张压均有统计学显著下降。仅接受卡托普利治疗的患者中75%的SDBP恢复正常,其余患者加用氢氯噻嗪后恢复正常。仅使用氢氯噻嗪治疗的患者中50%的SDBP恢复正常,其余患者加用卡托普利后血压恢复正常。4. 口服卡托普利,单独使用或与氢氯噻嗪联合使用,是控制轻、中度原发性高血压的有效药物。5. 在我们的系列研究中,主要出现的副作用有眩晕、头晕、短暂性嗜酸性粒细胞增多、尿素氮升高和/或谷丙转氨酶或谷草转氨酶升高。

相似文献

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Evaluation of cilazapril versus captopril in patients with mild to moderate essential hypertension.
Clin Exp Hypertens. 1994 Mar;16(2):179-96. doi: 10.3109/10641969409067948.
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Captopril or atenolol in essential hypertension.
Acta Med Scand Suppl. 1983;677:115-8. doi: 10.1111/j.0954-6820.1984.tb08644.x.

本文引用的文献

2
Captopril-associated agranulocytosis.卡托普利相关性粒细胞缺乏症。
Lancet. 1980 Jan 19;1(8160):150. doi: 10.1016/s0140-6736(80)90629-7.
3
Risks of mild hypertension: a ten-year report.轻度高血压的风险:十年报告
Br Heart J. 1971;33(Suppl):Suppl:116-21. doi: 10.1136/hrt.33.suppl.116.
6
[Angiotensin II inhibitors for the diagnosis and treatment of hypertension].
Schweiz Med Wochenschr. 1976 Dec 11;106(50):1791-8.
7
Angiotensin I converting enzyme.
Circ Res. 1975 Feb;36(2):247-55. doi: 10.1161/01.res.36.2.247.

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