Luther R R, Glassman H N, Jordan D C, Klepper M J
J Int Med Res. 1986;14(4):167-74. doi: 10.1177/030006058601400401.
Seventy-two patients entered the treatment phase of an open, long-term, dose-ranging trial of carteolol in stable, exercise-induced angina pectoris. Patients were to be treated with progressive doses of carteolol (2.5, 5, 10, 20, 40, and 60 mg), given as a single daily oral dose. Thirty of the patients (42%) completed one year of treatment with carteolol as the sole antianginal therapy. The most frequent final carteolol doses were 20 mg and 40 mg once daily. Statistically significant improvements from baseline in exercise tolerance as reflected in time to onset of angina, time to the endpoint of exercise and time to the onset of 1 mm S-T segment change on ECG were observed in carteolol-treated patients. Exercise-induced increases in heart rate and double-product were significantly suppressed, compared to baseline, throughout the study. Resting heart rate and double-product were modestly decreased. Carteolol was shown to be effective and safe when administered on a long-term basis to patients with angina pectoris.
72例患者进入了一项卡替洛尔治疗稳定型运动诱发心绞痛的开放性、长期、剂量范围试验的治疗阶段。患者将接受递增剂量的卡替洛尔(2.5、5、10、20、40和60毫克)治疗,每日口服一次。其中30例患者(42%)完成了以卡替洛尔作为唯一抗心绞痛治疗的一年疗程。最常用的最终卡替洛尔剂量是每日一次20毫克和40毫克。在接受卡替洛尔治疗的患者中,观察到从基线开始,在心绞痛发作时间、运动终点时间和心电图上出现1毫米ST段改变的时间等方面,运动耐量有统计学意义的改善。与基线相比,在整个研究过程中,运动诱发的心率和双乘积增加得到了显著抑制。静息心率和双乘积略有下降。结果表明,卡替洛尔长期应用于心绞痛患者时是有效且安全的。