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首页> 外文期刊>The Lancet >Valsartan in a Japanese population with hypertension and other cardiovascular disease (Jikei Heart Study): a randomised, open-label, blinded endpoint morbidity-mortality study.
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Valsartan in a Japanese population with hypertension and other cardiovascular disease (Jikei Heart Study): a randomised, open-label, blinded endpoint morbidity-mortality study.

机译:日本患有高血压和其他心血管疾病的人群中的缬沙坦(Jikei心脏研究):一项随机,开放标签,盲目的终点病死率研究。

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BACKGROUND: Drugs that inhibit the renin-angiotensin-aldosterone system benefit patients at risk for or with existing cardiovascular disease. However, evidence for this effect in Asian populations is scarce. We aimed to investigate whether addition of an angiotensin receptor blocker, valsartan, to conventional cardiovascular treatment was effective in Japanese patients with cardiovascular disease. METHODS: We initiated a multicentre, prospective, randomised controlled trial of 3081 Japanese patients, aged 20-79 years, (mean 65 [SD 10] years) who were undergoing conventional treatment for hypertension, coronary heart disease, heart failure, or a combination of these disorders. In addition to conventional treatment, patients were assigned either to valsartan (40-160 mg per day) or to other treatment without angiotensin receptor blockers. Our primary endpoint was a composite of cardiovascular morbidity and mortality. Analysis was by intention to treat. The study was registered at clintrials.gov with the identifier NCT00133328. FINDINGS: After a median follow-up of 3.1 years (range 1-3.9) the primary endpoint was recorded in fewer individuals given valsartan than in controls (92 vs 149; absolute risk 21.3 vs 34.5 per 1000 patient years; hazard ratio 0.61, 95% CI 0.47-0.79, p=0.0002). This difference was mainly attributable to fewer incidences of stroke and transient ischaemic attack (29 vs 48; 0.60, 0.38-0.95, p=0.028), angina pectoris (19 vs 53; 0.35, 0.20-0.58, p<0.0001), and heart failure (19 vs 36; 0.53, 0.31-0.94, p=0.029) in those given valsartan than in the control group. Mortality or tolerability did not differ between groups. INTERPRETATION: The addition of valsartan to conventional treatment prevented more cardiovascular events than supplementary conventional treatment. These benefits cannot be entirely explained by a difference in blood pressure control.
机译:背景:抑制肾素-血管紧张素-醛固酮系统的药物可使处于或患有现有心血管疾病的患者受益。然而,在亚洲人群中缺乏这种效果的证据。我们的目的是研究在传统的心血管疾病治疗中添加血管紧张素受体阻滞剂缬沙坦对日本心血管疾病患者是否有效。方法:我们启动了一项针对3081名年龄在20-79岁(平均65 [SD 10]岁)的日本患者的多中心,前瞻性,随机对照试验,这些患者正在接受高血压,冠心病,心力衰竭或联合治疗的常规治疗这些疾病。除常规治疗外,患者还被分配接受缬沙坦(每天40-160 mg)或其他无血管紧张素受体阻滞剂的治疗。我们的主要终点指标是心血管疾病的发病率和死亡率的综合指标。分析是按意向进行的。该研究已在clintrials.gov上注册,标识为NCT00133328。结果:在中位随访3.1年(范围1-3.9)之后,与对照组相比,接受缬沙坦治疗的患者的主要终点记录更少(92 vs 149;绝对风险每1000患者年21.3 vs 34.5;危险比0.61、95 %CI 0.47-0.79,p = 0.0002)。这种差异主要归因于中风和短暂性脑缺血发作的发生率较低(29 vs 48; 0.60,0.38-0.95,p = 0.028),心绞痛(19 vs 53; 0.35,0.20-0.58,p <0.0001)和心脏与对照组相比,给予缬沙坦治疗者的治疗失败率(19 vs 36; 0.53,0.31-0.94,p = 0.029)。两组间的死亡率或耐受性无差异。解释:常规治疗中加入缬沙坦比常规辅助治疗可预防更多的心血管事件。这些好处不能完全通过血压控制的差异来解释。

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