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拉贝洛尔与氢氯噻嗪相比在高血压黑人患者中的疗效。

The effectiveness of labetalol compared to hydrochlorothiazide in hypertensive black patients.

作者信息

Lucas C, Jenkins P, Mendels J, Due D, Forbes W P, Sirgo M A

机构信息

Division of Preventive and Nutritional Medicine, William Beaumont Hospital, Birmingham, Michigan.

出版信息

J Natl Med Assoc. 1991 Oct;83(10):866-71.

Abstract

Labetalol and hydrochlorothiazide (HCTZ) were compared for their efficacy in controlling hypertension of blacks in a prospective, double-blind study. Sixty-one adult patients with mild to moderate hypertension (standing diastolic blood pressure greater than or equal to 95 mm Hg and less than or equal to 114 mm Hg) were randomly selected to receive either labetalol 100 mg twice daily (n = 30) or HCTZ 25 mg twice daily (n = 31). The study was divided into two phases: a 4-week placebo run-in phase, during which all previous antihypertensive medication was discontinued, and a 12-week drug treatment phase. Labetalol and HCTZ doses were titrated to 400 mg twice and 50 mg twice daily, respectively, during the first 6 weeks of the drug treatment phase for those patients not achieving blood pressure control (standing diastolic blood pressure less than 90 mm Hg and a decrease of 10 mm Hg from baseline) on initial dosages. By the end of the 12 weeks of drug administration, patients on labetalol experienced a mean decrease of 10 mm Hg in standing diastolic blood pressure compared to a mean decrease of 10.1 mm Hg in patients on HCTZ. No differences were observed between the two treatment groups in reductions of either standing blood pressure or heart rate. While 19 of 30 patients on labetalol (63%) achieved blood pressure control at some point during the study with a mean daily dose of 568 mg, 18 of 31 (58%) HCTZ-treated patients achieved control with a mean daily dose of 72 mg.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项前瞻性双盲研究中,对拉贝洛尔和氢氯噻嗪(HCTZ)控制黑人高血压的疗效进行了比较。随机选择61例轻度至中度高血压成年患者(站立位舒张压大于或等于95 mmHg且小于或等于114 mmHg),分别接受每日两次100 mg拉贝洛尔治疗(n = 30)或每日两次25 mg HCTZ治疗(n = 31)。该研究分为两个阶段:为期4周的安慰剂导入期,在此期间停用所有先前的抗高血压药物;以及为期12周的药物治疗期。对于初始剂量治疗后未实现血压控制(站立位舒张压小于90 mmHg且较基线下降10 mmHg)的患者,在药物治疗期的前6周内,拉贝洛尔和HCTZ的剂量分别滴定至每日两次400 mg和每日两次50 mg。到药物治疗12周结束时,服用拉贝洛尔的患者站立位舒张压平均下降10 mmHg,而服用HCTZ的患者平均下降10.1 mmHg。两个治疗组在站立位血压或心率降低方面未观察到差异。在研究期间,30例服用拉贝洛尔的患者中有19例(63%)在平均每日剂量568 mg时的某个时间点实现了血压控制,而31例接受HCTZ治疗的患者中有18例(58%)在平均每日剂量72 mg时实现了控制。(摘要截断于250字)

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Am J Med. 1981 Apr;70(4):762-8. doi: 10.1016/0002-9343(81)90530-1.
2
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Clin Pharmacol Ther. 1982 Sep;32(3):307-12. doi: 10.1038/clpt.1982.165.

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