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Chelation therapy for ischemic heart disease: a randomized controlled trial.

机译:螯合疗法治疗缺血性心脏病:一项随机对照试验。

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CONTEXT: Chelation therapy using EDTA is an unproven but widely used alternative therapy for ischemic heart disease. OBJECTIVE: To determine if current EDTA protocols have a favorable impact on exercise ischemia threshold and quality of life measures in patients with stable ischemic heart disease. DESIGN: Double-blind, randomized, placebo-controlled trial conducted between January 1996 and January 2000. SETTING: Participants were recruited from a cohort of cardiac catheterization patients and the practices of cardiologists in Calgary, Alberta. PARTICIPANTS: We screened 3140 patients, performed a qualifying treadmill test in 171, and enrolled 84. Entry criteria included age at least 21 years with coronary artery disease proven by angiography or a documented myocardial infarction and stable angina while receiving optimal medical therapy. The required treadmill test used a gradual ramping protocol and patients had to demonstrate at least 1-mm ST depression. INTERVENTIONS: Patients were randomly assigned to receive infusion with either weight-adjusted (40 mg/kg) EDTA chelation therapy (n = 41) or placebo (n = 43) for 3 hours per treatment, twice weekly for 15 weeks and once per month for an additional 3 months. Patients in both groups took oral multivitamin therapy as well. MAIN OUTCOME MEASURE: Change from baseline to 27-week follow-up in time to ischemia (1-mm ST depression). RESULTS: Thirty-nine patients in each group completed the 27-week protocol. One chelation patient had therapy discontinued for a transient rise in serum creatinine. The mean (SD) baseline exercise time to ischemia was 572 (172) and 589 (176) seconds in the placebo and chelation groups, respectively. The corresponding mean changes in time to ischemia at 27 weeks were 54 seconds (95% confidence interval [CI], 23-84 seconds; P<.001) and 63 seconds (95% CI, 29-95 seconds; P<.001), for a difference of 9 seconds (95% CI, -36 to 53 seconds; P =.69). Exercise capacity and quality of life scores improved by similar degrees in both groups. CONCLUSION: Based on exercise time to ischemia, exercise capacity, and quality of life measurements, there is no evidence to support a beneficial effect of chelation therapy in patients with ischemic heart disease, stable angina, and a positive treadmill test for ischemia.
机译:背景:使用EDTA的螯合疗法是一种未经证实但广泛使用的缺血性心脏病替代疗法。目的:确定目前的EDTA方案是否对稳定型缺血性心脏病患者的运动缺血阈值和生活质量指标产生有利影响。设计:在1996年1月至2000年1月之间进行的双盲,随机,安慰剂对照试验。地点:参与者选自一组心脏导管插入患者和阿尔伯塔省卡尔加里的心脏病专家。参与者:我们筛查了3140例患者,在171例中进行了合格的跑步机测试,并入组84例。入选标准包括年龄至少21岁,经血管造影证实为冠状动脉疾病或有证据证明心肌梗塞和稳定型心绞痛,同时接受最佳药物治疗。必需的跑步机测试使用了逐渐倾斜的方案,患者必须证明至少有1毫米的ST凹陷。干预措施:患者被随机分配接受重量调整(40 mg / kg)EDTA螯合疗法(n = 41)或安慰剂(n = 43)输注,每次治疗3小时,每周两次,连续15周,每月一次再延长3个月。两组患者均接受口服多种维生素治疗。主要观察指标:从基线到27周的随访时间变化为缺血(1-mm ST凹陷)。结果:每组中有39名患者完成了27周的治疗方案。一名螯合患者因血清肌酐的短暂升高而停止治疗。安慰剂和螯合组的平均(SD)基线缺血运动时间分别为572(172)和589(176)秒。 27周时缺血时间的相应平均变化为54秒(95%置信区间[CI],23-84秒; P <.001)和63秒(95%CI,29-95秒; P <.001) ),相差9秒(95%CI,-36至53秒; P = .69)。两组的运动能力和生活质量得分均有相似程度的提高。结论:基于运动至缺血的时间,运动能力和生活质量的测量,尚无证据支持螯合疗法对缺血性心脏病,稳定型心绞痛和踏车试验阳性的患者的有益作用。

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