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己酮可可碱联合卡托普利治疗原发性高血压的疗效观察:一项随机临床试验

Effects of Adding Pentoxifylline to Captopril on Primary Hypertension: A Pilot Randomized Clinical Trial.

机构信息

Cardiovascular Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Faculty of Pharmacy, Department of Clinical Pharmacy, Ardabil University of Medical Sciences, Ardabil, Iran.

出版信息

J Clin Pharmacol. 2020 Feb;60(2):181-187. doi: 10.1002/jcph.1516. Epub 2019 Sep 5.

Abstract

Because of the key role blood viscosity plays in the regulation of blood pressure (BP) and the hemorheological effects of pentoxifylline (PTX), this study was conducted to evaluate whether PTX can reduce BP when added to captopril in patients with stage 1 hypertension. In this randomized clinical trial 62 patients with stage 1 hypertension were entered. The intervention group (n = 30) received 1200 mg PTX in 3 divided doses plus 25 mg captopril 3 times a day, whereas the control group (n = 32) received only 75 mg captopril in 3 divided doses. Measurements of BP were done at baseline and in the first and second months after entering the study. Major adverse cardiac events during this period were recorded. When the systolic BP levels in the intervention and the control groups were compared, no significant differences at baseline (150.4 ± 6.03 versus 150.4 ± 6.2, P = .98) or first (138.4 ± 9.4 versus 142.3 ± 5.6, P = .08) or second (134.6  ± 8.9 versus 137.4 ± 6.0, P = .20) month of the study were noted. Similarly no significant difference was observed in the diastolic BP at baseline (91.7 ± 3.9 versus 92.0 ± 3.7, P = .84) or first (85.5 ± 5.1 versus 86.9  ± 3.8, P = .27) or second (82.6  ± 5.7 versus 84.0  ± 3.5, P = .31) month. Based on the results of present study, adding PTX as a hemorheological agent to captopril could not significantly reduce blood pressure in the patients with stage 1 hypertension.

摘要

由于血液粘度在调节血压(BP)和己酮可可碱的血液流变学效应中起着关键作用,因此进行了这项研究,以评估在 1 期高血压患者中添加己酮可可碱是否可以降低血压。在这项随机临床试验中,纳入了 62 名 1 期高血压患者。干预组(n=30)接受 1200 毫克己酮可可碱分 3 次服用,每天 3 次,每次 25 毫克卡托普利,而对照组(n=32)仅接受 75 毫克卡托普利分 3 次服用。在基线和研究进入后的第一个和第二个月测量血压。记录这段时间内的主要不良心脏事件。当比较干预组和对照组的收缩压水平时,在基线(150.4±6.03 与 150.4±6.2,P=0.98)或第一个(138.4±9.4 与 142.3±5.6,P=0.08)或第二个(134.6±8.9 与 137.4±6.0,P=0.20)月均无显著差异。同样,在基线(91.7±3.9 与 92.0±3.7,P=0.84)或第一个(85.5±5.1 与 86.9±3.8,P=0.27)或第二个(82.6±5.7 与 84.0±3.5,P=0.31)月时,舒张压也没有显著差异。基于本研究结果,添加己酮可可碱作为血液流变学药物不能显著降低 1 期高血压患者的血压。

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