Davidov M E, Moir G D, Poland M P, Maloy J, Medakovic M
Am J Med. 1983 Oct 17;75(4A):47-53. doi: 10.1016/0002-9343(83)90136-5.
The antihypertensive effects of oral labetalol compared with placebo were evaluated in 74 mildly hypertensive patients (standing diastolic blood pressure 95 to 110 mm Hg) in a bicentric double-blind parallel group study. Following a four-week placebo phase, 36 patients were randomly assigned to receive labetalol and 38 to receive placebo. A five-week titration phase followed during which the dose of labetalol was increased weekly from 100 mg twice a day to 600 mg twice a day to achieve a standing diastolic blood pressure of less than 90 mm Hg and decreased 10 mm Hg or more from baseline. A matching number of placebo capsules for each dose of labetalol was dispensed for blinding purposes. Patients then entered a two-month maintenance phase. A thiazide diuretic could be added when the standing diastolic blood pressure was 100 mm Hg or greater at the highest dose of the study drug. At the end of this phase, the administration of labetalol (or placebo) was abruptly discontinued and patients were given the same number of placebo capsules twice a day taken during maintenance. Blood pressure and heart rate in the supine and standing position were measured eight to 10 hours after a dose at each visit. This study demonstrated that labetalol (median daily doses of 600 mg) was significantly more effective than placebo (p less than 0.05) in lowering the supine and standing blood pressures. Significantly more (p less than 0.001) placebo-treated patients than labetalol-treated patients (six versus 20) required the addition of a thiazide diuretic. Control of hypertension (that is, standing diastolic blood pressure less than 90 mm Hg) was achieved in significantly (p less than 0.001) more labetalol-treated patients than placebo-treated patients at the monotherapy endpoint (26 of 36; 72 percent versus six of 38; 16 percent). Blood pressure overshoot did not occur when labetalol was abruptly discontinued. Not one labetalol-treated patient discontinued the study because of adverse experiences. Labetalol is a safe and effective treatment for patients with mild hypertension.
在一项双中心双盲平行组研究中,对74例轻度高血压患者(站立位舒张压95至110毫米汞柱)评估了口服拉贝洛尔与安慰剂相比的降压效果。在为期四周的安慰剂阶段后,36例患者被随机分配接受拉贝洛尔治疗,38例接受安慰剂治疗。随后是为期五周的滴定阶段,在此期间拉贝洛尔的剂量从每日两次,每次100毫克每周增加至每日两次,每次600毫克,以使站立位舒张压降至90毫米汞柱以下且较基线下降10毫米汞柱或更多。为了实现盲法,为每剂拉贝洛尔配给了相应数量的安慰剂胶囊。患者随后进入为期两个月的维持阶段。当在研究药物的最高剂量下站立位舒张压为100毫米汞柱或更高时,可以加用噻嗪类利尿剂。在该阶段结束时,突然停用拉贝洛尔(或安慰剂),并给予患者与维持期相同数量的安慰剂胶囊,每日两次。每次访视时,在给药8至10小时后测量仰卧位和站立位的血压及心率。该研究表明,拉贝洛尔(中位日剂量600毫克)在降低仰卧位和站立位血压方面明显比安慰剂更有效(p<0.05)。需要加用噻嗪类利尿剂的安慰剂治疗患者显著多于拉贝洛尔治疗患者(6例对20例,p<0.001)。在单药治疗终点时,实现高血压控制(即站立位舒张压低于90毫米汞柱)的拉贝洛尔治疗患者显著多于安慰剂治疗患者(36例中的26例;72%对38例中的6例;16%,p<0.001)。突然停拉拉贝洛尔时未出现血压反跳。没有一名拉贝洛尔治疗患者因不良事件而退出研究。拉贝洛尔是轻度高血压患者的一种安全有效的治疗方法。