Boyce Steven W, Bartels Claus, Bolli Roberto, Chaitman Bernard, Chen John C, Chi Eric, Jessel Andreas, Kereiakes Dean, Knight John, Thulin Lars, Theroux Pierre
Washington Hospital Center, 106 Irving Street NW, Suite 316, South Tower, Washington, DC 20010, USA.
J Thorac Cardiovasc Surg. 2003 Aug;126(2):420-7. doi: 10.1016/s0022-5223(03)00209-5.
To evaluate the effects of cariporide on all-cause mortality or myocardial infarction at 36 days in patients at risk of myocardial necrosis after coronary artery bypass graft surgery.
In the coronary artery bypass graft cohort of the GUARD During Ischemia Against Necrosis trial, patients > or =18 years who required urgent coronary artery bypass graft, repeat coronary artery bypass graft, or had a history of unstable angina and > or =2 risk factors (age >65 years, female gender, diabetes mellitus, ejection fraction <35%, or left main or 3-vessel disease) were randomized to placebo (n = 743) or cariporide 20 mg (n = 736), 80 mg (n = 705), or 120 mg (n = 734). A 1-hour intravenous infusion was initiated shortly before surgery and administered every 8 hours for 2 to 7 days. Patients were followed up for 6 months. A nonparametric covariance analysis was used to calculate the primary efficacy endpoint.
Baseline characteristics were similar between treatment groups. The cariporide 20- and 80-mg groups had event rates similar to placebo. The endpoint of all-cause mortality or myocardial infarction at day 36 was significant with cariporide 120 mg versus placebo (event rate 12.2% vs 16.2%; P =.027). The risk reduction was evident on postoperative day 1 (3.3% vs 6.5%; P =.005) and was maintained at 6 months (event rate 15.0% vs 18.6%; P =.033). Cariporide was well tolerated, and most adverse events were mild and transient in this high-risk population.
Clinical benefit with cariporide 120 mg was observed early after treatment initiation and continued for 6 months postsurgery, suggesting that sodium-hydrogen exchange inhibition with cariporide is cardioprotective in patients undergoing high-risk coronary artery bypass graft surgery.
评估在冠状动脉搭桥手术后有心肌坏死风险的患者中,卡里波罗ide对36天时全因死亡率或心肌梗死的影响。
在“缺血时保护心肌坏死”试验的冠状动脉搭桥手术队列中,年龄≥18岁、需要紧急冠状动脉搭桥手术、再次冠状动脉搭桥手术或有不稳定型心绞痛病史且有≥2个危险因素(年龄>65岁、女性、糖尿病、射血分数<35%或左主干或三支血管病变)的患者被随机分为安慰剂组(n = 743)或卡里波罗ide 20毫克组(n = 736)、80毫克组(n = 705)或120毫克组(n = 734)。在手术前不久开始1小时静脉输注,并每8小时给药一次,持续2至7天。对患者进行6个月的随访。采用非参数协方差分析计算主要疗效终点。
各治疗组的基线特征相似。卡里波罗ide 20毫克组和80毫克组的事件发生率与安慰剂组相似。与安慰剂相比,卡里波罗ide 120毫克组在第36天时全因死亡率或心肌梗死这一终点有显著差异(事件发生率12.2%对16.2%;P = 0.027)。术后第1天风险降低明显(3.3%对6.5%;P = 0.005),并在6个月时维持(事件发生率15.0%对18.6%;P = 0.033)。卡里波罗ide耐受性良好,在这个高危人群中,大多数不良事件为轻度且短暂。
在开始治疗后早期即观察到卡里波罗ide 120毫克有临床益处,并在术后6个月持续存在,这表明卡里波罗ide抑制钠氢交换对接受高危冠状动脉搭桥手术的患者具有心脏保护作用。