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曲匹地尔与硝酸异山梨酯治疗稳定型心绞痛疗效的双盲随机多中心研究

Double-blind randomized multicenter study on the efficacy of trapidil versus isosorbide dinitrate in stable angina pectoris.

作者信息

Raubach K H, Vlahov V, Wolter K, Bussmann W D

机构信息

Medical Academy Sofia, Bulgaria.

出版信息

Clin Cardiol. 1997 May;20(5):483-8. doi: 10.1002/clc.4960200516.

Abstract

BACKGROUND

Trapidil is an inhibitor of phosphodiesterase I-IV with resulting positive lusitropic, vasodilating, and antiplatelet effects.

HYPOTHESIS

This study was undertaken to compare the antianginal efficacy of trapidil with that of isosorbide dinitrate (ISDN) in patients with stable angina pectoris.

METHODS

We studied 95 patients with stable angina pectoris who were randomized into a double-blind parallel group study with either oral trapidil or ISDN. After a 1-week run-in period and a 2-week wash-out phase, the patients received either trapidil 200 mg t.i.d. (n = 48) or ISDN 20 mg t.i.d. (n = 47) for 12 weeks. All antianginal medication, except sublingual glyceryl trinitrate (GTN), was discontinued during the study. Patients underwent an exercise electrocardiogram on an ergometer bicycle according to a modified Bruce protocol before and at 6 and 12 weeks during treatment.

RESULTS

The workload capacity increased from 583 +/- 281 W.min before treatment to 833 +/- 444 W.min after 12 weeks of treatment in the trapidil group (p < 0.01) and from 555 +/- 276 W.min to 827 +/- 361 W.min in the ISDN group (p < 0.01). The anginal attacks per week as well as the use of GTN decreased significantly in both groups. After 12 weeks of therapy, the cumulative ST-segment depression during exercise decreased by 67% in the trapidil patients and by 23% in the ISDN patients. Compared with baseline, the double product at the 75 W level was reduced in both groups after 12 weeks of treatment. Blood pressure and heart rate at rest remained nearly unchanged. Overall, no statistical difference was found between the two study groups. The tolerability was good.

CONCLUSION

Oral trapidil therapy is safe and effective in stable angina pectoris and is equivalent to standard therapy with ISDN.

摘要

背景

曲匹地尔是一种磷酸二酯酶I-IV抑制剂,具有正性变松弛、血管舒张和抗血小板作用。

假设

本研究旨在比较曲匹地尔与硝酸异山梨酯(ISDN)对稳定型心绞痛患者的抗心绞痛疗效。

方法

我们研究了95例稳定型心绞痛患者,将其随机分为口服曲匹地尔或ISDN的双盲平行组研究。经过1周的导入期和2周的洗脱期后,患者接受曲匹地尔200mg每日三次(n = 48)或ISDN 20mg每日三次(n = 47)治疗12周。在研究期间,除舌下硝酸甘油(GTN)外,所有抗心绞痛药物均停用。患者在治疗前以及治疗期间的第6周和第12周,按照改良的Bruce方案在测力计自行车上进行运动心电图检查。

结果

曲匹地尔组治疗前的工作量能力为583±281W·min,治疗12周后增加至833±444W·min(p < 0.01);ISDN组从555±276W·min增加至827±361W·min(p < 0.01)。两组每周的心绞痛发作次数以及GTN的使用量均显著减少。治疗12周后,曲匹地尔组患者运动期间的累积ST段压低减少了67%,ISDN组减少了23%。与基线相比,治疗12周后两组在75W水平的双乘积均降低。静息血压和心率几乎保持不变。总体而言,两个研究组之间未发现统计学差异。耐受性良好。

结论

口服曲匹地尔治疗稳定型心绞痛安全有效,且与ISDN标准治疗等效。

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