Gurfinkel E P, Manos E J, Mejaíl R I, Cerdá M A, Duronto E A, García C N, Daroca A M, Mautner B
Institute of Cardiology and Cardiovascular Surgery, Favaloro Foundation, Buenos Aires, Argentina.
J Am Coll Cardiol. 1995 Aug;26(2):313-8. doi: 10.1016/0735-1097(95)80001-w.
This study was designed to test the hypothesis that low molecular weight heparin may lessen the severity of ischemic events in patients with unstable angina.
Unstable angina is a thrombotic process that requires intensive medical treatment. Although current treatments can reduce the number of complications, serious bleeding continues to occur. Nadroparin calcium, a low molecular weight heparin, seems to be a safe therapeutic agent that does not require laboratory monitoring.
A total of 219 patients with unstable angina entered the study at a mean time of 6.17 h after the last episode of rest pain. Patients were randomized to receive aspirin (200 mg/day [group A]), aspirin plus regular heparin (400 IU/kg body weight per day intravenously and titered by activated partial thromboplastin time [group B]) and aspirin plus low molecular weight heparin (214 UIC/kg anti-Xa twice daily subcutaneously [group C]). The major end points determined for the in-hospital period were 1) recurrent angina, 2) myocardial infarction, 3) urgent revascularization, 4) major bleeding, and 5) death. Minor end points were 1) silent myocardial ischemia, and 2) minor bleeding. Event rates were tested by chi-square analysis.
Recurrent angina occurred in 37%, 44% and 21% of patients in groups A, B and C, respectively, and was significantly less frequent in group C than in either group A (odds ratio 2.26, 95% confidence interval [CI] 1 to 5.18, p = 0.03) or group B (odds ratio, 3.07, 95% CI 1.36 to 7.00, p = 0.002). Nonfatal myocardial infarction was present in seven patients in group A, four in group B and none in group C (group B vs. A, p = 0.5; group C vs. A, p = 0.01). Urgent revascularization was performed in nine patients in group A, seven in group B and one in group C (C vs. A, p = 0.01). Two episodes of major bleeding occurred in group B. Silent myocardial ischemia was present in 38%, 41% and 25% of patients in groups A, B and C, respectively, and was significantly less frequent in group C than group B (odds ratio 2.12, 95% CI 0.97 to 4.69, p = 0.04). Minor bleeding was detected in 10 patients in group B, 1 patient in group C (B vs. C, p = 0.01) and no patient in group A (A vs. B, p = 0.003).
In this study, treatment with aspirin plus a high dose of low molecular weight heparin during the acute phase of unstable angina was significantly better than treatment with aspirin alone or aspirin plus regular heparin.
本研究旨在验证低分子量肝素可减轻不稳定型心绞痛患者缺血事件严重程度这一假说。
不稳定型心绞痛是一个需强化药物治疗的血栓形成过程。尽管当前治疗可减少并发症数量,但严重出血仍会发生。那屈肝素钙,一种低分子量肝素,似乎是一种无需实验室监测的安全治疗药物。
共219例不稳定型心绞痛患者在最后一次静息性疼痛发作后平均6.17小时进入研究。患者被随机分为接受阿司匹林(200毫克/天[甲组])、阿司匹林加普通肝素(每天静脉注射400国际单位/千克体重,并根据活化部分凝血活酶时间调整剂量[乙组])以及阿司匹林加低分子量肝素(每天皮下注射214抗Xa国际单位/千克,分两次给药[丙组])。确定的住院期间主要终点为:1)复发性心绞痛;2)心肌梗死;3)紧急血运重建;4)严重出血;5)死亡。次要终点为:1)无症状性心肌缺血;2)轻微出血。事件发生率通过卡方分析进行检验。
甲组、乙组和丙组患者复发性心绞痛的发生率分别为37%、44%和21%,丙组复发性心绞痛的发生率显著低于甲组(优势比2.26,95%置信区间[CI]1至5.18,p = 0.03)或乙组(优势比3.07,95%CI 1.36至7.00,p = 0.002)。甲组有7例患者发生非致命性心肌梗死,乙组有4例,丙组无(乙组与甲组比较,p = 0.5;丙组与甲组比较,p = 0.01)。甲组有9例患者接受紧急血运重建,乙组有7例,丙组有1例(丙组与甲组比较,p =