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首页> 外文期刊>The Lancet >Effect of high-dose allopurinol on exercise in patients with chronic stable angina: a randomised, placebo controlled crossover trial.
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Effect of high-dose allopurinol on exercise in patients with chronic stable angina: a randomised, placebo controlled crossover trial.

机译:大剂量别嘌呤醇对慢性稳定型心绞痛患者运动的影响:一项随机,安慰剂对照的交叉试验。

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BACKGROUND: Experimental evidence suggests that xanthine oxidase inhibitors can reduce myocardial oxygen consumption for a particular stroke volume. If such an effect also occurs in man, this class of inhibitors could become a new treatment for ischaemia in patients with angina pectoris. We ascertained whether high-dose allopurinol prolongs exercise capability in patients with chronic stable angina. METHODS: 65 patients (aged 18-85 years) with angiographically documented coronary artery disease, a positive exercise tolerance test, and stable chronic angina pectoris (for at least 2 months) were recruited into a double-blind, randomised, placebo-controlled, crossover study in a hospital and two infirmaries in the UK. We used computer-generated randomisation to assign patients to allopurinol (600 mg per day) or placebo for 6 weeks before crossover. Our primary endpoint was the time to ST depression, and the secondary endpoints were total exercise time and time to chest pain. We did a completed case analysis. This study is registered as an International Standard Randomised Controlled Trial, number ISRCTN 82040078. FINDINGS: In the first treatment period, 31 patients were allocated to allopurinol and 28 were analysed, and 34 were allocated to placebo and 32 were analysed. In the second period, all 60 patients were analysed. Allopurinol increased the median time to ST depression to 298 s (IQR 211-408) from a baseline of 232 s (182-380), and placebo increased it to 249 s (200-375; p=0.0002). The point estimate (absolute difference between allopurinol and placebo) was 43 s (95% CI 31-58). Allopurinol increased median total exercise time to 393 s (IQR 280-519) from a baseline of 301 s (251-447), and placebo increased it to 307 s (232-430; p=0.0003); the point estimate was 58 s (95% CI 45-77). Allopurinol increased the time to chest pain from a baseline of 234 s (IQR 189-382) to 304 s (222-421), and placebo increased it to 272 s (200-380; p=0.001); the point estimate was 38 s (95% CI 17-55). No adverse effects of treatment were reported. INTERPRETATION: Allopurinol seems to be a useful, inexpensive, well tolerated, and safe anti-ischaemic drug for patients with angina. FUNDING: British Heart Foundation.
机译:背景:实验证据表明,黄嘌呤氧化酶抑制剂可以减少特定中风量的心肌耗氧量。如果这种作用也发生在人类身上,则这类抑制剂可能成为心绞痛患者局部缺血的一种新疗法。我们确定了大剂量别嘌呤醇是否可以延长慢性稳定型心绞痛患者的运动能力。方法:将65例血管造影记录的冠状动脉疾病,积极的运动耐力测试和稳定的慢性心绞痛(至少2个月)的患者(年龄在18-85岁之间)纳入双盲,随机,安慰剂对照,在英国的一家医院和两家医务室进行交叉研究。我们使用计算机生成的随机化方法,将患者在交叉前分配为别嘌呤醇(每天600 mg)或安慰剂6周。我们的主要终点是达到ST抑郁的时间,次要终点是总运动时间和到达胸痛的时间。我们完成了案例分析。该研究已注册为国际标准随机对照试验,编号ISRCTN82040078。结果:在第一个治疗期间,将31例患者分配给别嘌呤醇,分析28例,将34例分配给安慰剂,对32例进行分析。在第二阶段,对所有60例患者进行了分析。别嘌醇将ST抑郁的中位时间从232 s(182-380)的基线增加到298 s(IQR 211-408),而安慰剂将其增加到249 s(200-375; p = 0.0002)。点估计值(别嘌醇与安慰剂之间的绝对差)为43 s(95%CI 31-58)。别嘌醇将中位总运动时间从301 s(251-447)的基线增加到393 s(IQR 280-519),而安慰剂将其增加到307 s(232-430; p = 0.0003)。该点估计为58秒(95%CI 45-77)。别嘌呤醇使发生胸痛的时间从基线的234 s(IQR 189-382)增加到304 s(222-421),而安慰剂将其增加到272 s(200-380; p = 0.001)。该点估计为38秒(95%CI 17-55)。尚无治疗不良反应的报道。解释:别嘌呤醇对于心绞痛患者似乎是一种有用,便宜,耐受性好,安全的抗缺血药物。资金来源:英国心脏基金会。

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