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希鲁洛肽治疗不稳定型心绞痛。心肌缺血凝血酶抑制(TIMI)7试验结果。

Hirulog in the treatment of unstable angina. Results of the Thrombin Inhibition in Myocardial Ischemia (TIMI) 7 trial.

作者信息

Fuchs J, Cannon C P

机构信息

Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Boston, MA 02115, USA.

出版信息

Circulation. 1995 Aug 15;92(4):727-33. doi: 10.1161/01.cir.92.4.727.

Abstract

BACKGROUND

Direct thrombin inhibitors are a new class of drugs that may offer a more effective and potentially simpler alternative to heparin. Hirulog is a synthetic peptide based on the leech-derived compound hirudin and, like hirudin, is a highly specific, direct inhibitor of free and clot-bound thrombin.

METHODS AND RESULTS

TIMI 7 was a randomized, double-blind study of Hirulog, given with 325 mg/d aspirin to 410 patients with unstable angina. Patients received a constant infusion of Hirulog for 72 hours at one of four doses: 0.02 (n = 160), 0.25 (n = 81), 0.5 (n = 88), and 1.0 (n = 81) mg.kg-1.h-1. The primary efficacy end point was "unsatisfactory outcome," defined as death, nonfatal myocardial infarction (MI), rapid clinical deterioration, or recurrent ischemic pain at rest with ECG changes by 72 hours. Unsatisfactory outcome was not different among the four dose groups: 8.1%, 6.2%, 11.4%, and 6.2% (P = NS). However, the secondary end point of death or nonfatal MI through hospital discharge occurred in 10.0% of patients treated with 0.02 mg.kg-1.h-1 compared with 3.2% of patients treated with the three higher doses of Hirulog (0.25, 0.5, and 1.0 mg.kg-1.h-1, P = .008). Only 2 of 410 patients (0.5%) experienced a major hemorrhage attributed to Hirulog.

CONCLUSIONS

The direct thrombin inhibitor Hirulog is a promising new antithrombotic agent that deserves further study. The results of TIMI 7 lend support to the use of an antithrombin agent with aspirin in patients with unstable angina.

摘要

背景

直接凝血酶抑制剂是一类新型药物,可能为肝素提供更有效且可能更简便的替代方案。希美加群是一种基于水蛭素衍生化合物合成的肽,与水蛭素一样,是游离和结合于凝块的凝血酶的高度特异性直接抑制剂。

方法与结果

TIMI 7是一项针对410例不稳定型心绞痛患者的随机双盲研究,给予希美加群联合325 mg/d阿司匹林治疗。患者以四种剂量之一持续输注希美加群72小时:0.02(n = 160)、0.25(n = 81)、0.5(n = 88)和1.0(n = 81)mg·kg⁻¹·h⁻¹。主要疗效终点为“不满意结局”,定义为死亡、非致命性心肌梗死(MI)、临床快速恶化或72小时时静息时出现复发性缺血性疼痛且伴有心电图改变。四个剂量组的不满意结局无差异:分别为8.1%、6.2%、11.4%和6.2%(P =无显著性差异)。然而,至出院时死亡或非致命性MI的次要终点在接受0.02 mg·kg⁻¹·h⁻¹治疗的患者中发生率为10.0%,而接受三种较高剂量希美加群(0.25、0.5和1.0 mg·kg⁻¹·h⁻¹)治疗的患者中发生率为3.2%(P = 0.008)。410例患者中仅2例(0.5%)发生了归因于希美加群的严重出血。

结论

直接凝血酶抑制剂希美加群是一种有前景的新型抗血栓药物,值得进一步研究。TIMI 7的结果支持在不稳定型心绞痛患者中使用抗凝血酶药物联合阿司匹林。

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