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西帕胺与氯噻酮降压活性的比较:一项双盲、随机、交叉试验。

Comparison of the antihypertensive activities of xipamide and chlorthalidone: a double-blind, randomized, crossover trial.

作者信息

Bonaduce D, Ferrara N, Petretta M, Canonico V, Romango E, Rengo F

出版信息

Curr Med Res Opin. 1981;7(4):247-52. doi: 10.1185/03007998109114270.

DOI:10.1185/03007998109114270
PMID:7014105
Abstract

The effectiveness of a new potent diuretic, xipamide, was evaluated in the treatment of patients with mild to moderate essential hypertension. The effects of daily doses of 40 mg xipamide were compared with those of 100 mg chlorthalidone with respect to systolic and diastolic blood pressure, using a double-blind crossover design. Patients received each drug for 6 weeks, the order of treatments being at random and the periods being separated by a 'washout' period of 7 days. The results showed that xipamide was as effective as chlorthalidone in controlling blood pressure, both in the upright and supine positions, and when administered after chlorthalidone produced a further reduction. No such further reduction occurred when chlorthalidone was given after xipamide. Serum electrolyte changes induced by the two diuretics were comparable. Both drugs were well tolerated and caused few side-effects.

摘要

对一种新型强效利尿剂西帕胺治疗轻至中度原发性高血压患者的疗效进行了评估。采用双盲交叉设计,比较了每日40毫克西帕胺剂量与100毫克氯噻酮剂量对收缩压和舒张压的影响。患者每种药物服用6周,治疗顺序随机,各阶段间隔7天的“洗脱期”。结果显示,西帕胺在控制直立位和仰卧位血压方面与氯噻酮同样有效,且在氯噻酮之后给药时能进一步降低血压。而在西帕胺之后给予氯噻酮则不会出现这种进一步降低的情况。两种利尿剂引起的血清电解质变化相当。两种药物耐受性良好,副作用较少。

相似文献

1
Comparison of the antihypertensive activities of xipamide and chlorthalidone: a double-blind, randomized, crossover trial.西帕胺与氯噻酮降压活性的比较:一项双盲、随机、交叉试验。
Curr Med Res Opin. 1981;7(4):247-52. doi: 10.1185/03007998109114270.
2
[Evaluation of the hypotensive efficacy in a double-blind study of xipamide versus chlorthalidone].[在一项关于氯磺丙脲与氯噻酮的双盲研究中对降压疗效的评估]
Clin Ter. 1985 Jun 15;113(5):379-83.
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A randomized double-blind clinical trial of xipamid and hydrochlorothiazide in essential hypertension.西帕胺与氢氯噻嗪治疗原发性高血压的随机双盲临床试验
Int J Clin Pharmacol Ther Toxicol. 1984 Oct;22(10):549-51.
4
Double-blind crossover study of fenquizone compared to chlorthalidone in essential hypertension.非洛地平与氯噻酮治疗原发性高血压的双盲交叉研究。
Int J Clin Pharmacol Ther Toxicol. 1985 Sep;23(9):501-5.
5
Hypotensive effects of xipamide in essential hypertension. Crossover comparison with hydrochlorothiazide.
J Clin Pharmacol. 1981 Jul;21(7):316-22. doi: 10.1002/j.1552-4604.1981.tb01773.x.
6
Studies covering combined treatments with xipamide. Results of a long-term antihypertensive treatment.
Int J Clin Pharmacol Biopharm. 1977 Jun;15(6):260-6.
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Comparison of two combined diuretics in the treatment of essential hypertension.两种联合利尿剂治疗原发性高血压的比较。
Int J Clin Pharmacol Ther Toxicol. 1989 Jul;27(7):342-5.
8
Mathematical model of the time-course of essential hypertension blood pressure changes during chronic xipamide treatment.
Curr Med Res Opin. 1980;6(8):523-7. doi: 10.1185/03007998009109481.
9
Xipamide and cyclopenthiazide in essential hypertension--comparative effects on blood pressure and plasma potassium.氯磺水杨胺和环戊噻嗪治疗原发性高血压——对血压和血钾的比较效果
Br J Clin Pharmacol. 1982 Jun;13(6):859-63. doi: 10.1111/j.1365-2125.1982.tb01879.x.
10
Clinical trial of xipamide in the treatment of hypertension.氯噻嗪治疗高血压的临床试验。
J Int Med Res. 1980;8(1):38-43. doi: 10.1177/030006058000800107.

引用本文的文献

1
Blood pressure-lowering efficacy of loop diuretics for primary hypertension.襻利尿剂对原发性高血压的降压疗效
Cochrane Database Syst Rev. 2015 May 22;2015(5):CD003825. doi: 10.1002/14651858.CD003825.pub4.
2
Xipamide: no advantage over bendrofluazide in hypertension.氯噻嗪:在治疗高血压方面并不比苄氟噻嗪更具优势。
Br J Clin Pharmacol. 1984 Oct;18(4):616-8. doi: 10.1111/j.1365-2125.1984.tb02514.x.
3
Xipamide. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy.氯噻嗪。对其药效学、药代动力学特性及治疗效果的综述。
Drugs. 1985 Oct;30(4):313-32. doi: 10.2165/00003495-198530040-00002.
4
Selective alpha 1-adrenoreceptor blockers in the treatment of hypertension: should we be using them more?选择性α1肾上腺素能受体阻滞剂在高血压治疗中的应用:我们是否应更多地使用它们?
Clin Auton Res. 1991 Sep;1(3):251-8. doi: 10.1007/BF01824996.