Systolic hypertension

  • 文章类型: Journal Article
    这项III期研究评估了沙库巴曲/缬沙坦与奥美沙坦在日本原发性高血压患者中的疗效和安全性。轻度至中度高血压(平均坐位收缩压[msSBP]≥150至<180mmHg)的患者(n=1161,年龄≥20岁)随机接受沙库巴曲/缬沙坦200mg(n=387),沙库必曲/缬沙坦400毫克(n=385),或奥美沙坦20毫克(n=389),每日一次,持续8周。主要评估是沙库比曲/缬沙坦200mg与msSBP从基线降低奥美沙坦20毫克在第8周。次要评估包括沙库巴曲/缬沙坦400mg与msSBP降低第8周时奥美沙坦和平均坐位舒张压(msDBP)降低,平均坐位脉压(msPP),在第8周,所有治疗组的总体血压(BP)控制率。在第8周时,Sacubitril/缬沙坦200mg与奥美沙坦相比,msSBP从基线的下降幅度明显大于奥美沙坦(治疗间差异:-5.01mmHg[95%置信区间:-6.95至-3.06mmHg,非劣效性和优越性P<0.001)。沙库巴曲/缬沙坦400mg与msSBP的减少更大奥美沙坦,以及在msDBP和msPP中两种剂量的沙库必曲/缬沙坦与奥美沙坦(均P<0.05),也被观察到了。用沙库巴曲/缬沙坦治疗的患者总体血压控制率较高。沙库巴曲/缬沙坦的安全性和耐受性通常与奥美沙坦相当。沙库巴曲/缬沙坦的不良事件发生率不是剂量依赖性的。沙库必曲/缬沙坦治疗是有效的,并提供优越的血压降低,在日本轻中度原发性高血压患者中,达到目标BP目标的患者比例高于奥美沙坦治疗。
    This phase III study assessed the efficacy and safety of sacubitril/valsartan compared with those of olmesartan in Japanese patients with essential hypertension. Patients (n = 1161, aged ≥20 years) with mild to moderate hypertension (mean sitting systolic blood pressure [msSBP] ≥150 to <180 mmHg) were randomized to receive sacubitril/valsartan 200 mg (n = 387), sacubitril/valsartan 400 mg (n = 385), or olmesartan 20 mg (n = 389) once daily for 8 weeks. The primary assessment was a reduction in msSBP from baseline with sacubitril/valsartan 200 mg vs. olmesartan 20 mg at Week 8. Secondary assessments included msSBP reduction with sacubitril/valsartan 400 mg vs. olmesartan at Week 8 and reductions in mean sitting diastolic blood pressure (msDBP), mean sitting pulse pressure (msPP), and overall blood pressure (BP) control rate for all treatment groups at Week 8. Sacubitril/valsartan 200 mg provided a significantly greater reduction in msSBP from baseline than olmesartan at Week 8 (between-treatment difference: -5.01 mmHg [95% confidence interval: -6.95 to -3.06 mmHg, P < 0.001 for noninferiority and superiority]). Greater reductions in msSBP with sacubitril/valsartan 400 mg vs. olmesartan, as well as in msDBP and msPP with both doses of sacubitril/valsartan vs. olmesartan (P < 0.05 for all), were also observed. Patients treated with sacubitril/valsartan achieved an overall higher BP control rate. The safety and tolerability profiles of sacubitril/valsartan were generally comparable to those of olmesartan. The adverse event rate with sacubitril/valsartan was not dose-dependent. Treatment with sacubitril/valsartan was effective and provided superior BP reduction, with a higher proportion of patients achieving target BP goals than treatment with olmesartan in Japanese patients with mild to moderate essential hypertension.
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  • 文章类型: Journal Article
    老年患者收缩期高血压的有效治疗仍然是主要的治疗挑战。一个多中心,双盲,沙库巴曲/缬沙坦的随机对照试验(LCZ696),一类血管紧张素受体脑啡肽酶抑制剂,进行,以确定其效果与奥美沙坦(血管紧张素受体阻滞剂)对中央主动脉压,在收缩期高血压和脉压>60mmHg的老年患者(年龄≥60岁)中,表明动脉僵硬。患者(n=454;平均年龄,67.7年;平均坐位收缩压,158.6mmHg;平均固定脉压,69.7mmHg)随机接受每日一次的沙库巴曲/缬沙坦200mg或奥美沙坦20mg,力滴定到4周后的初始剂量加倍,在12周时进行初步评估之前。这项研究延长了12至52周的双盲治疗,在此期间,氨氯地平(2.5-5mg)和随后的氢氯噻嗪(6.25-25mg)用于未达到血压目标(<140/90)的患者。在第12周,沙库巴曲/缬沙坦降低中心主动脉收缩压(主要评估)比奥美沙坦降低-3.7mmHg(P=0.010),在第12周的二级评估进一步证实(中央主动脉脉压,-2.4mmHg,P<0.012;平均24小时动态肱动脉收缩压和中央主动脉收缩压,-4.1mmHg和-3.6mmHg,分别,两者P<0.001)。睡眠期间24小时动态压力的差异很明显。52周后,不同治疗组的血压参数相似(P<0.002);然而,与沙库巴曲/缬沙坦(32%;P<0.002)相比,更多的患者需要奥美沙坦(47%)联合降压治疗.两种治疗均具有同样良好的耐受性。参数研究(血管紧张素受体脑啡肽抑制剂与血管紧张素受体阻滞剂测量老年人动脉僵硬度的前瞻性比较),第一次,在收缩期高血压和动脉僵硬的老年患者中,沙库巴曲/缬沙坦与奥美沙坦相比,在降低临床和动态中心性主动脉和肱动脉压方面具有优势。
    Effective treatment of systolic hypertension in elderly patients remains a major therapeutic challenge. A multicenter, double-blind, randomized controlled trial with sacubitril/valsartan (LCZ696), a first-in-class angiotensin receptor neprilysin inhibitor, was conducted to determine its effects versus olmesartan (angiotensin receptor blocker) on central aortic pressures, in elderly patients (aged ≥60 years) with systolic hypertension and pulse pressure >60 mm Hg, indicative of arterial stiffness. Patients (n=454; mean age, 67.7 years; mean seated systolic blood pressure, 158.6 mm Hg; mean seated pulse pressure, 69.7 mm Hg) were randomized to receive once-daily sacubitril/valsartan 200 mg or olmesartan 20 mg, force titrated to double the initial doses after 4 weeks, before primary assessment at 12 weeks. The study extended double-blind treatment for 12 to 52 weeks, during which amlodipine (2.5-5 mg) and subsequently hydrochlorothiazide (6.25-25 mg) were added-on for patients not achieving blood pressure target (<140/90). At week 12, sacubitril/valsartan reduced central aortic systolic pressure (primary assessment) greater than olmesartan by -3.7 mm Hg (P=0.010), further corroborated by secondary assessments at week 12 (central aortic pulse pressure, -2.4 mm Hg, P<0.012; mean 24-hour ambulatory brachial systolic blood pressure and central aortic systolic pressure, -4.1 mm Hg and -3.6 mm Hg, respectively, both P<0.001). Differences in 24-hour ambulatory pressures were pronounced during sleep. After 52 weeks, blood pressure parameters were similar between treatments (P<0.002); however, more patients required add-on antihypertensive therapy with olmesartan (47%) versus sacubitril/valsartan (32%; P<0.002). Both treatments were equally well tolerated. The PARAMETER study (Prospective Comparison of Angiotensin Receptor Neprilysin Inhibitor With Angiotensin Receptor Blocker Measuring Arterial Stiffness in the Elderly), for the first time, demonstrated superiority of sacubitril/valsartan versus olmesartan in reducing clinic and ambulatory central aortic and brachial pressures in elderly patients with systolic hypertension and stiff arteries.
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  • 文章类型: Journal Article
    OBJECTIVE: De novo hypertension (HTN) in liver transplantation recipients is a known entity. We investigated haemodynamic behaviour after a liver transplant to see if it can predict survival to discharge from the hospital.
    METHODS: electronic records of Haemodynamic parameters and laboratory investigations of 95 patients of living donor liver transplant (LDLT) were retrospectively analysed.
    RESULTS: Twenty-three patients were operated for acute liver failure (ALF) and 72 patients for chronic liver disease (CLD). Eight patients of CLD and four of ALF did not survive. CLD patients had statistically significant rise in systolic blood pressure from the post-operative day (POD) 1 to POD 4 and diastolic blood pressure (DBP) from POD 3 to POD 6. Heart rate (HR) significantly decreased from POD 3 to POD 5. Haemodynamic parameters returned to baseline values within 20 days. Diastolic HTN had a positive predictive value of 100% for survival with 100% sensitivity and specificity. Systolic HTN had a positive predictive value of 100% for survival (sensitivity-89%, specificity-100%). ALF patients had a significant decrease in HR from POD 2 to POD 10. Bradycardia (HR ≤60/min) had a positive predictive value of 100% for survival with a sensitivity of 45% and 58% in CLD and ALF, respectively, with a specificity of 100% in both the groups. Non-survivors had no significant change in haemodynamics. In CLD group, International Normalised Ratio had statistically significant, strong negative correlation with DBP.
    CONCLUSIONS: Haemodynamic pattern of recovery may be used for predicting survival to discharge after LDLT.
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