首页> 外文OA文献 >Ambulatory blood pressure parameters after canrenone addition to existing treatment regimens with maximum tolerated dose of angiotensin-converting enzyme inhibitors/angiotensin II type 1 receptor blockers plus hydrochlorothiazide in uncontrolled hypertensive patients
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Ambulatory blood pressure parameters after canrenone addition to existing treatment regimens with maximum tolerated dose of angiotensin-converting enzyme inhibitors/angiotensin II type 1 receptor blockers plus hydrochlorothiazide in uncontrolled hypertensive patients

机译:加入现有治疗后犬的动态血压参数,最大耐受剂量的血管紧张素转换酶抑制剂/血管紧张素II 1型受体阻滞剂加氢氯噻嗪治疗未控制的高血压患者

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摘要

Background: Blockade of the reninâ\u80\u93angiotensinâ\u80\u93aldosterone system is a cornerstone in cardiovascular disease prevention and hypertension treatment. The relevance of ambulatory blood pressure monitoring (ABPM) has been widely confirmed for both increasing the accuracy of blood pressure (BP) measurements, particularly in pharmacological trials, and focusing on 24 h BP prognostic parameters. The aim of this study was to assess the effects of canrenone addition on ambulatory BP in uncontrolled hypertensive patients already treated with the highest tolerated dose of angiotensin-converting enzyme (ACE) inhibitors or angiotensin II type 1 receptor (AT1R) antagonists plus hydrochlorothiazide (HCT). Methods: ABPM was performed at baseline and after 3 months of combination therapy in 158 outpatients with stage 1 or 2 hypertension who were randomized to add canrenone (50 or 100 mg) to the pre-existing therapy with ACE inhibitors or AT1R antagonists plus HCT. Twenty-four-hour systolic and diastolic BPs were considered normalized when the values were,130 and,80 mmHg, respectively. Results: The addition of canrenone was associated with a reduction in systolic and diastolic BPs (24 h and daytime and nighttime; P,0.001), mean arterial pressures (P,0.001), and pulse pressures (P,0.01). The Î\u94 24 h systolic/diastolic BPs were -13.5±11.2/-8±8 mmHg and -16.1±13.5/-11.2±8.3 mmHg (50 and 100 mg/day, respectively). In the 50 mg arm, the 24 h systolic and diastolic BPs were normalized in 67.5% and 74% of the patients, respectively, and in 61.6% and 68.5% of the patients in the 100 mg arm, respectively (P,0.05; P= not significant for 50 vs 100 mg). The percentage of patients whose nocturnal decrease was.10% with respect to diurnal values did not change during combination therapy. Conclusion: Canrenone addition to ACE inhibitors or AT1R antagonists plus HCT was associated with a significant reduction of 24 h BP and to an increased number of patients meeting 24 h ABPM targets in a clinical setting of uncontrolled stage 1 or 2 hypertension.
机译:背景:肾素,血管紧张素,醛固酮系统的封锁是预防心血管疾病和治疗高血压的基石。动态血压监测(ABPM)的相关性已被广泛证实,既可以提高血压(BP)测量的准确性,尤其是在药理试验中,也可以关注24 h BP的预后参数。这项研究的目的是评估已接受最高耐受剂量的血管紧张素转换酶(ACE)抑制剂或血管紧张素II 1型受体(AT1R)拮抗剂加氢氯噻嗪(HCT)治疗的非控制性高血压患者中,肾上腺素的添加对动态BP的影响)。方法:ABPM是在158例1或2期高血压门诊患者的基线治疗和联合治疗3个月后进行的,这些患者被随机分配在既往使用ACE抑制剂或AT1R拮抗剂加HCT的治疗中添加肾上腺素(50或100 mg)。当分别为130和80 mmHg时,二十四小时收缩压和舒张压被认为是正常的。结果:肾上腺素的添加与收缩压和舒张压降低(24小时以及白天和夜晚; P,0.001),平均动脉压(P,0.001)和脉压(P,0.01)有关。 u94 24小时收缩压/舒张压BPs为-13.5±11.2 / -8±8 mmHg和-16.1±13.5 / -11.2±8.3 mmHg(分别为50和100 mg /天)。在50 mg组中,分别在67.5%和74%的患者中以及在100 mg组中分别在61.6%和68.5%的患者中使24 h收缩压和舒张压标准化(P,0.05; P =对50毫克与100毫克无关)。在联合治疗期间,夜间值下降10%的患者百分比相对于昼夜值没有变化。结论:在不受控制的1或2期高血压临床环境中,将ACER或AT1R拮抗剂加HCT添加烯睾丙内酯与24 h BP显着降低和达到24 h ABPM目标的患者数量增加相关。

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