Navookarasu N T, Rahman A R, Abdullah I
Kuching General Hospital, Sarawak.
Int J Clin Pract. 1999 Jan-Feb;53(1):25-30.
Despite their proven value in reducing morbidity and mortality in different grades of heart failure, angiotensin converting enzyme (ACE) inhibitors continue to be underused. One reason for this is clinicians' apprehension of first-dose hypotension. We conducted a double-blind, randomised, placebo-controlled parallel group study to investigate the effect of various ACE inhibitors on first-dose hypotension. Eighty unselected patients were randomised into five treatment groups: placebo, captopril 6.25 mg, enalapril 2.5 mg, perindopril 2 mg and lisinopril 2.5 mg. Blood pressure was measured at baseline, half hourly for two hours and hourly for three hours after drug treatment. The maximum drops in mean arterial pressure (in mmHg +/- SD) were placebo 5.89 +/- 2.65, perindopril 5.29 +/- 2.49, enalapril 13.28 +/- 3.31, lisinopril 15.04 +/- 5.74 and captopril 16.76 +/- 5.74 (all p < 0.05 vs placebo except for perindopril). Perindopril, unlike the other ACE inhibitors studied, did not produce first-dose hypotension following its initiation in patients with congestive heart failure.
尽管血管紧张素转换酶(ACE)抑制剂在降低不同程度心力衰竭的发病率和死亡率方面已被证实具有价值,但仍未得到充分使用。原因之一是临床医生担心首剂低血压。我们进行了一项双盲、随机、安慰剂对照的平行组研究,以调查各种ACE抑制剂对首剂低血压的影响。80名未经挑选的患者被随机分为五个治疗组:安慰剂组、卡托普利6.25毫克组、依那普利2.5毫克组、培哚普利2毫克组和赖诺普利2.5毫克组。在基线时测量血压,药物治疗后两小时内每半小时测量一次,之后三小时每小时测量一次。平均动脉压的最大降幅(以mmHg±SD表示)分别为:安慰剂组5.89±2.65,培哚普利组5.29±2.49,依那普利组13.28±3.31,赖诺普利组15.