首页> 美国卫生研究院文献>Drug Design Development and Therapy >Efficacy and safety of fixed-dose combination therapy with olmesartan medoxomil and rosuvastatin in Korean patients with mild to moderate hypertension and dyslipidemia: an 8-week multicenter randomized double-blind factorial-design study (OLSTA-D RCT: OLmesartan rosuvaSTAtin from Daewoong)
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Efficacy and safety of fixed-dose combination therapy with olmesartan medoxomil and rosuvastatin in Korean patients with mild to moderate hypertension and dyslipidemia: an 8-week multicenter randomized double-blind factorial-design study (OLSTA-D RCT: OLmesartan rosuvaSTAtin from Daewoong)

机译:olmesartan medoxomil和rosuvastatin固定剂量联合治疗对韩国轻至中度高血压和血脂异常患者的疗效和安全性:一项为期8周多中心随机双盲析因设计的研究(OLSTA-D RCT:OLmesartan rosuvaSTAtin (大雄)

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摘要

The pill burden of patients with hypertension and dyslipidemia can result in poor medication compliance. This study aimed to evaluate the efficacy and safety of fixed-dose combination (FDC) therapy with olmesartan medoxomil (40 mg) and rosuvastatin (20 mg) in Korean patients with mild to moderate hypertension and dyslipidemia. This multicenter, randomized, double-blind, factorial-design study included patients aged ≥20 years with mild to moderate essential hypertension and dyslipidemia. Patients were randomly assigned to receive FDC therapy (40 mg olmesartan medoxomil, 20 mg rosuvastatin), 40 mg olmesartan medoxomil, 20 mg rosuvastatin, or a placebo. The percentage change from baseline in low-density lipoprotein cholesterol levels was compared between FDC therapy and olmesartan medoxomil, and the change from baseline in diastolic blood pressure was compared between FDC therapy and rosuvastatin 8 weeks after treatment. A total of 162 patients were included. The least square mean percentage change (standard error) from baseline in low-density lipoprotein cholesterol levels 8 weeks after treatment was significantly greater in the FDC than in the olmesartan medoxomil group (−52.3% [2.8%] vs −0.6% [3.5%], P<0.0001), and the difference was −51.7% (4.1%) (95% confidence interval: −59.8% to −43.6%). The least square mean change (standard error) from baseline in diastolic blood pressure 8 weeks after treatment was significantly greater in the FDC group than in the rosuvastatin group (−10.4 [1.2] mmHg vs 0.1 [1.6] mmHg, P<0.0001), and the difference was −10.5 (1.8) mmHg (95% confidence interval: −14.1 to −6.9 mmHg). There were 50 adverse events in 41 patients (22.7%) and eight adverse drug reactions in five patients (2.8%). The study found that FDC therapy with olmesartan medoxomil and rosuvastatin is an effective, safe treatment for patients with hypertension and dyslipidemia. This combination may improve medication compliance in patients with a large pill burden.
机译:高血压和血脂异常患者的药丸负担可能导致药物依从性差。这项研究旨在评估奥美沙坦美多佐美(40 mg)和瑞舒伐他汀(20 mg)固定剂量联合治疗(FDC)在韩国轻度至中度高血压和血脂异常患者中的疗效和安全性。这项多中心,随机,双盲,析因设计研究包括年龄≥20岁的轻度至中度原发性高血压和血脂异常患者。患者被随机分配接受FDC治疗(40 mg奥美沙坦美多西米,20 mg罗苏伐他汀),40 mg奥美沙坦美多西米,20 mg罗苏伐他汀或安慰剂。比较FDC治疗和奥美沙坦medoxomil在低密度脂蛋白胆固醇水平上自基线的变化百分比,并在治疗后8周比较FDC治疗和瑞舒伐他汀在舒张压方面的基线变化。总共包括162名患者。治疗后8周,低密度脂蛋白胆固醇水平相对于基线的最小均方变化百分比(标准误)在FDC中显着大于奥美沙坦medoxomil组(-52.3%[2.8%] vs -0.6%[3.5%] ],P <0.0001),差异为−51.7%(4.1%)(95%置信区间:−59.8%至−43.6%)。 FDC组舒张压在治疗后8周相对于基线的最小均方差(标准误)显着大于瑞舒伐他汀组(-10.4 [1.2] mmHg对0.1 [1.6] mmHg,P <0.0001),差异为-10.5(1.8)mmHg(95%置信区间:-14.1至-6.9 mmHg)。 41例患者中有50例不良事件(占22.7%),五例患者中有8例药物不良反应(占2.8%)。研究发现,奥美沙坦美多西莫和瑞舒伐他汀联合FDC疗法对高血压和血脂异常患者是一种有效,安全的治疗方法。这种组合可以改善大药丸负担患者的用药依从性。

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