Ravid D, Lishner M, Lang R, Ravid M
Sackler Faculty of Medicine, Tel Aviv University, Israel.
J Clin Pharmacol. 1994 Nov;34(11):1116-20. doi: 10.1002/j.1552-4604.1994.tb01989.x.
Angiotensin-converting enzyme inhibitors (ACE-I) have become the mainstem of antihypertensive therapy and first-choice agents for vasodilatation in congestive heart failure (CHF). A typical dry cough is the main cause for discontinuation of ACE-I therapy. Data about the incidence, course, and clinical significance of this side effect are conflicting. This study determined the incidence of cough in ACE-I treated patients with hypertension and with CHF and to appreciate its clinical significance; 268 ACE-I treated patients, 164 with hypertension and 104 with CHF were prospectively followed for at least 1 year and specifically questioned about cough and other side effects. In those in whom cough developed, a second and then a third ACE-I were tried. Cough developed in 50 (18.6%) of the 268 patients; 23 patients with hypertension (14%) had coughs 24.7 +/- 17.1 (SD) weeks after initiation of therapy; 27 patients with CHF (26%) had coughs 12.3 +/- 12 (SD) weeks after the start of ACE-I therapy (P = 0.005). All but three patients had coughs also on the second and third ACE-I. The time from the beginning of therapy to the onset of cough was significantly shorter with the second than the first drug. ACE-I agents had to be discontinued in 50% of the patients in whom coughs developed, most of them in the CHF group. In the others, cough was well tolerated or disappeared during subsequent months. The incidence of cough, which necessitated discontinuation of ACE-I treatment, was 4% among patients with hypertension and 18% among patients with CHF (P < 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)
血管紧张素转换酶抑制剂(ACE-I)已成为抗高血压治疗的主流药物以及充血性心力衰竭(CHF)血管扩张治疗的首选药物。典型的干咳是停用ACE-I治疗的主要原因。关于这种副作用的发生率、病程及临床意义的数据存在矛盾。本研究确定了接受ACE-I治疗的高血压患者和CHF患者咳嗽的发生率,并评估其临床意义;对268例接受ACE-I治疗的患者进行了前瞻性随访,其中164例为高血压患者,104例为CHF患者,随访至少1年,并专门询问了咳嗽及其他副作用情况。对于出现咳嗽的患者,尝试换用第二种然后第三种ACE-I。268例患者中有50例(18.6%)出现咳嗽;23例高血压患者(14%)在开始治疗后24.7±17.1(标准差)周出现咳嗽;27例CHF患者(26%)在开始ACE-I治疗后12.3±12(标准差)周出现咳嗽(P = 0.005)。除3例患者外,所有患者在使用第二种和第三种ACE-I时也出现咳嗽。从开始治疗到咳嗽发作的时间,使用第二种药物比第一种药物明显缩短。出现咳嗽的患者中有50%不得不停用ACE-I药物,其中大多数在CHF组。在其他患者中,咳嗽耐受性良好或在随后几个月内消失。因咳嗽而必须停用ACE-I治疗的发生率,高血压患者为4%,CHF患者为18%(P < 0.001)。(摘要截选至250字)