Riva E, Cavalli A, Abbondati G, Cedrini M C, Schleman M, Fuccella L M
Smith Kline and French, Clinical Research and Development, Milan, Italy.
Int J Clin Pharmacol Res. 1989;9(1):21-8.
Ibopamine is a new orally active dopamine analogue with positive inotropic and vasodilating activity. The tolerability of the drug administered at the dose of 100 mg thrice daily for 12 months was studied in 302 patients with congestive heart failure, New York Heart Association (NYHA) class II and III. Of the 302 patients, 198 completed the study (65%); 59 patients (19%) were withdrawn for clinical events; 27 of them died (9%); 35 patients (12%) did not complete the study for non-compliance and 10 (3%) for protocol violations. Clinical events were generally related to the cardiovascular system and 85% of deaths were from cardiovascular causes. None of the deaths was considered related to treatment by the investigators. Clinically significant laboratory abnormalities were observed during the study in four patients only. This trial suggests that ibopamine is well tolerated in patients with congestive heart failure, NYHA class II and III, at the dose of 100 mg thrice daily for up to one year.
异波帕明是一种新型的具有口服活性的多巴胺类似物,具有正性肌力和血管舒张活性。对302例纽约心脏病协会(NYHA)心功能II级和III级的充血性心力衰竭患者进行了研究,观察每日三次、每次100 mg剂量的该药连续服用12个月的耐受性。302例患者中,198例(65%)完成了研究;59例(19%)因临床事件退出研究,其中27例(9%)死亡;35例(12%)因未遵守方案未完成研究,10例(3%)因违反方案未完成研究。临床事件一般与心血管系统有关,85%的死亡由心血管原因导致。研究者认为无一例死亡与治疗有关。研究期间仅4例患者观察到具有临床意义的实验室异常。该试验表明,对于NYHA心功能II级和III级的充血性心力衰竭患者,每日三次、每次100 mg剂量服用该药长达一年耐受性良好。