Smith D H, Neutel J M, Black H R, Schoenberger J A, Weber M A
Veterans Affairs Medical Center, Long Beach, CA, USA.
J Hum Hypertens. 1996 Feb;10(2):129-34.
Once-daily antihypertensive drugs that control blood pressure (BP) for the full 24-h dosing period, enhance patient compliance and may reduce the cardiovascular complications of hypertension which occur with increased frequency in the early morning. Since some once-daily agents are more effective than others in maintaining antihypertensive effects toward the end of the 24-h dosing interval this study was designed to evaluate the duration of antihypertensive action of trandolapril using 48 h ambulatory blood pressure monitoring (ABPM) in 41 patients with mild-to-moderate essential hypertension. Twenty-four hour ABPM was performed on two consecutive days (48 h) after a 4 week single blind placebo run-in period and repeated after an 8 week double-blind period during which 20 patients were randomized to treatment with trandolapril (2-4 mg once-daily) and 21 patients to matching placebo. During the second 48 h monitoring period, placebo rather than active medication was taken by both of the groups at the beginning of the second 24 h segment. Trandolapril reduced ambulatory systolic and diastolic BP by 9.4 and 6.2 mm Hg respectively (P < or = 0.01) during the first 24 h of the post treatment monitoring period while placebo increased the systolic and diastolic BPs in the same period by 3.8 and 2.6 mm Hg (P < 0.05). During the second monitoring period (hours 25-48), trandolapril reduced systolic and diastolic BP by 5.6 and 3.9 mm Hg while placebo increased BP by 2.3 and 1.6 mm Hg (P < 0.03). When compared to placebo by 2 h time blocks, throughout the 2 days of monitoring, trandolapril produced clinically significant decreases in systolic and diastolic BP for 30 and 28 h following dosing. This indicates that trandolapril can be considered a true once-daily antihypertensive agent.
每日一次的降压药物能够在整个24小时给药期间控制血压,提高患者的依从性,并可能减少清晨时高血压心血管并发症的发生频率,此类并发症出现的频率更高。由于一些每日一次的药物在24小时给药间隔末期维持降压效果方面比其他药物更有效,本研究旨在采用48小时动态血压监测(ABPM)评估41例轻至中度原发性高血压患者中群多普利的降压作用持续时间。在为期4周的单盲安慰剂导入期后,连续两天(48小时)进行24小时ABPM,并在为期8周的双盲期后重复进行,在此期间,20例患者被随机分配接受群多普利治疗(每日一次2 - 4毫克),21例患者接受匹配的安慰剂治疗。在第二个48小时监测期内,两组在第二个24小时时段开始时服用的是安慰剂而非活性药物。在治疗后监测期的第一个24小时内,群多普利使动态收缩压和舒张压分别降低了9.4和6.2毫米汞柱(P≤0.01),而安慰剂在同一时期使收缩压和舒张压分别升高了3.8和2.6毫米汞柱(P<0.05)。在第二个监测期(第25 - 48小时),群多普利使收缩压和舒张压分别降低了5.6和3.9毫米汞柱,而安慰剂使血压升高了2.3和1.6毫米汞柱(P<0.03)。在整个2天的监测期间,与安慰剂按2小时时间段进行比较时,群多普利在给药后30和28小时使收缩压和舒张压出现临床上显著的降低。这表明群多普利可被视为真正的每日一次降压药物。