Michelson E L, Frishman W H, Lewis J E, Edwards W T, Flanigan W J, Bloomfield S S, Johnson B F, Lucas C, Freis E D, Finnerty F A
Am J Med. 1983 Oct 17;75(4A):68-80. doi: 10.1016/0002-9343(83)90138-9.
The long-term efficacy and safety of labetalol, an antihypertensive agent with combined beta- and alpha-blocking activity, were evaluated alone (number = 193) and in combination with a diuretic (number = 144) in an open-label multicenter trial of 337 hypertensive patients aged 21 to 75 years, including initially 205 (61 percent) men and 219 (65 percent) Caucasians. There were 219 (65 percent) mild, 85 (25 percent) moderate, and 33 (10 percent) severe hypertensive patients. Labetalol (100 to 1,200 mg twice a day) alone or in combination with a diuretic reduced the mean standing blood pressure by 13/11 and 25/16 mm Hg to 135/88 and 130/91 mm Hg, respectively (p less than 0.01), and supine blood pressure by 6/7 and 18/13 mm Hg to 141/86 and 138/90 mm Hg (p less than 0.01), respectively. Blood pressure reductions observed at one month were maintained after one year; 206 (62 percent) patients had 10 mm Hg or greater reductions and 184 (56 percent) patients were maintained at diastolic blood pressures less than 90 mm Hg. Most frequently reported drug-related side effects included fatigue (14 percent), dizziness (12 percent), nausea (11 percent), nasal stuffiness (8 percent), headache (4 percent), and male sexual dysfunction (14 percent). Side effects were generally of mild to moderate intensity and often transient. In addition, in 27 (8 percent) patients reversible asymptomatic transaminase elevations to greater than twice normal developed at some time during the study. In 13 (4 percent) patients these alterations resolved during continued labetalol therapy, but in five (2 percent) patients these marked elevations led to discontinuation of the drug. A total of 32 (9.5 percent) patients were terminated prematurely due to side effects (most commonly genitourinary or gastrointestinal) possibly attributable to the drug. These findings indicate that labetalol with or without a diuretic is a potentially effective, safe, and relatively well-tolerated long-term antihypertensive therapy.
在一项开放标签的多中心试验中,对337例年龄在21至75岁的高血压患者单独(n = 193)及联合利尿剂(n = 144)使用具有β和α受体阻滞联合活性的抗高血压药物拉贝洛尔,评估其长期疗效和安全性。患者最初包括205例(61%)男性和219例(65%)白种人。有219例(65%)轻度、85例(25%)中度和33例(10%)重度高血压患者。单独使用拉贝洛尔(每日两次,每次100至1200 mg)或联合利尿剂分别使平均站立血压降低13/11和25/16 mmHg,降至135/88和130/91 mmHg(p<0.01),仰卧血压分别降低6/7和18/13 mmHg,降至141/86和138/90 mmHg(p<0.01)。1个月时观察到的血压降低在1年后得以维持;206例(62%)患者血压降低10 mmHg或更多,184例(56%)患者舒张压维持在90 mmHg以下。最常报告的与药物相关的副作用包括疲劳(14%)、头晕(12%)、恶心(11%)、鼻塞(8%)、头痛(4%)和男性性功能障碍(14%)。副作用一般为轻度至中度,且通常为一过性。此外,在27例(8%)患者中,研究期间某些时候出现可逆性无症状转氨酶升高至正常上限两倍以上。在13例(4%)患者中,这些改变在继续使用拉贝洛尔治疗期间消退,但在5例(2%)患者中,这些显著升高导致停药。共有32例(9.5%)患者因可能归因于该药物的副作用(最常见的是泌尿生殖系统或胃肠道副作用)而提前终止治疗。这些发现表明,无论是否联合利尿剂,拉贝洛尔都是一种潜在有效、安全且耐受性相对良好的长期抗高血压治疗药物。