Carlon R, Cappelletti F, Ometto R, Maiolino P, Vincenzi M
Divisione Cardiologica, Ospedale Civile, Cittadella.
Cardiologia. 1990 May;35(5):407-14.
The efficacy of a new calcium channel blocker, gallopamil, has been tested via a single blind, self-controlled versus placebo protocol in 9 consecutive patients admitted to our Coronary Care Unit because of repeated daily attacks of Prinzmetal variant angina. Exclusion criteria were age (greater than 65 years) bradycardia (less than 50 beats/min), recent myocardial infarction, heart failure, sinoatrial or atrioventricular block. After a 24 hours run-in period on saline drip, gallopamil was administered as 0.03 mg/kg bolus followed by continuous infusion at 0.02 mg/kg/h for the first 24 hours and 0.03 mg/kg/h for the last 48 hours. Treatment was then stopped and the patients were again kept on saline infusion for the next 30 hours. Holter monitoring was recorded during run-in, on third day of treatment and 6 hours after gallopamil withdrawal. Anginal attacks were significantly reduced in number by therapy (-63%, -91%, -84% in the 3 days of treatment). Holter monitoring during gallopamil infusion showed a statistically significant reduction in silent (-98%) and symptomatic (-93%) ischemic episodes (IE). During the last 24 hours of the washout period we observed a statistically significant increase in silent ischemic episodes. While no transient ST segment elevation was recorded in 3 patients, in 1 patient symptomatic IE were increased of 150% with respect to the run-in period. On the whole we observed complete suppression of IE in 7 patients (78%) at the third day of treatment with gallopamil. In 2 patients (22%) a greater than 75% reduction was observed.(ABSTRACT TRUNCATED AT 250 WORDS)
一种新型钙通道阻滞剂加洛帕米的疗效,已通过单盲、自身对照与安慰剂对照方案,在9例因每日反复发作普林兹金属变异型心绞痛而入住我们冠心病监护病房的连续患者中进行了测试。排除标准为年龄(大于65岁)、心动过缓(小于50次/分钟)、近期心肌梗死、心力衰竭、窦房或房室传导阻滞。在进行24小时生理盐水滴注的导入期后,给予加洛帕米0.03mg/kg静脉推注,随后在前24小时以0.02mg/kg/h持续输注,在最后48小时以0.03mg/kg/h持续输注。然后停止治疗,患者在接下来的30小时再次接受生理盐水输注。在导入期、治疗第三天以及加洛帕米撤药后6小时进行动态心电图监测。治疗使心绞痛发作次数显著减少(治疗的3天中分别减少-63%、-91%、-84%)。加洛帕米输注期间的动态心电图监测显示,无症状(-98%)和有症状(-93%)缺血发作(IE)在统计学上显著减少。在洗脱期的最后24小时,我们观察到无症状缺血发作在统计学上显著增加。虽然3例患者未记录到短暂ST段抬高,但1例患者有症状的IE较导入期增加了150%。总体而言,我们观察到在加洛帕米治疗第三天,7例患者(78%)的IE完全得到抑制。2例患者(22%)观察到减少超过75%。(摘要截短于250字)