首页> 外文期刊>Journal of the American College of Cardiology >Intensive multifactorial intervention for stable coronary artery disease: optimal medical therapy in the COURAGE (Clinical Outcomes Utilizing Revascularization and Aggressive Drug Evaluation) trial.
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Intensive multifactorial intervention for stable coronary artery disease: optimal medical therapy in the COURAGE (Clinical Outcomes Utilizing Revascularization and Aggressive Drug Evaluation) trial.

机译:强化多因素干预以稳定冠状动脉疾病:在COURAGE(利用血运重建和积极药物评估的临床结果)试验中的最佳药物治疗。

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OBJECTIVES: This paper describes the medical therapy used in the COURAGE (Clinical Outcomes Utilizing Revascularization and Aggressive Drug Evaluation) trial and its effect on risk factors. BACKGROUND: Most cardiovascular clinical trials test a single intervention. The COURAGE trial tested multiple lifestyle and pharmacologic interventions (optimal medical therapy) with or without percutaneous coronary intervention in patients with stable coronary disease. METHODS: All patients, regardless of treatment assignment, received equivalent lifestyle and pharmacologic interventions for secondary prevention. Most medications were provided at no cost. Therapy was administered by nurse case managers according to protocols designed to achieve predefined lifestyle and risk factor goals. RESULTS: The patients (n = 2,287) were followed for 4.6 years. There were no significant differences between treatment groups in proportion of patients achieving therapeutic goals. The proportion of smokers decreased from 23% to 19% (p = 0.025), those who reported <7% of calories from saturated fat increased from 46% to 80% (p < 0.001), and those who walked >or=150 min/week increased from 58% to 66% (p < 0.001). Body mass index increased from 28.8 +/- 0.13 kg/m(2) to 29.3 +/- 0.23 kg/m(2) (p < 0.001). Appropriate medication use increased from pre-randomization to 5 years as follows: antiplatelets 87% to 96%; beta-blockers 69% to 85%; renin-angiotensin-aldosterone system inhibitors 46% to 72%; and statins 64% to 93%. Systolic blood pressure decreased from a median of 131 +/- 0.49 mm Hg to 123 +/- 0.88 mm Hg. Low-density lipoprotein cholesterol decreased from a median of 101 +/- 0.83 mg/dl to 72 +/- 0.88 mg/dl. CONCLUSIONS: Secondary prevention was applied equally and intensively to both treatment groups in the COURAGE trial by nurse case managers with treatment protocols and resulted in significant improvement in risk factors. Optimal medical therapy in the COURAGE trial provides an effective model for secondary prevention among patients with chronic coronary disease. (Clinical Outcomes Utilizing Revascularization and Aggressive Drug Evaluation; NCT00007657).
机译:目的:本文描述了COURAGE(利用血运重建和积极药物评估的临床结果)试验中使用的药物治疗及其对危险因素的影响。背景:大多数心血管临床试验仅对单一干预进行测试。 COURAGE试验测试了稳定型冠心病患者是否接受经皮冠状动脉介入治疗的多种生活方式和药物干预(最佳药物治疗)。方法:所有患者,无论治疗方案如何,均接受相同的生活方式和药物干预以进行二级预防。大多数药物都是免费提供的。护理病例经理根据旨在实现预定的生活方式和危险因素目标的方案进行治疗。结果:患者(n = 2287)被随访了4。6年。治疗组之间达到治疗目标的患者比例没有显着差异。吸烟者的比例从23%下降到19%(p = 0.025),那些报告了<7%的饱和脂肪热量从46%上升到80%(p <0.001),并且步行>或= 150分钟的人/周从58%增加到66%(p <0.001)。体重指数从28.8 +/- 0.13 kg / m(2)增加到29.3 +/- 0.23 kg / m(2)(p <0.001)。适当的药物使用从随机分配前增加到5年,具体方法如下:抗血小板药物的使用率从87%提高到96%; β-受体阻滞剂69%至85%;肾素-血管紧张素-醛固酮系统抑制剂46%至72%;他汀类药物占64%至93%。收缩压从中位数131 +/- 0.49毫米汞柱降至123 +/- 0.88毫米汞柱。低密度脂蛋白胆固醇从中位数101 +/- 0.83 mg / dl降至72 +/- 0.88 mg / dl。结论:在COURAGE试验中,由护理案例管理者根据治疗方案对两个治疗组均进行了二级预防,且强化了二级预防措施,并显着改善了危险因素。 COURAGE试验中的最佳药物治疗为慢性冠心病患者提供了二级预防的有效模型。 (利用血运重建和积极药物评估的临床结果; NCT00007657)。

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