Mehta Shamir R, Yusuf Salim, Díaz Rafael, Zhu Jun, Pais Prem, Xavier Denis, Paolasso Ernesto, Ahmed Rashid, Xie Changchun, Kazmi Khawar, Tai Javed, Orlandini Andrés, Pogue Janice, Liu Lisheng
Department of Medicine, McMaster University, and Population Health Research Institute, Hamilton Health Sciences, Hamilton, Ontario, Canada.
JAMA. 2005 Jan 26;293(4):437-46. doi: 10.1001/jama.293.4.437.
Glucose-insulin-potassium (GIK) infusion is a widely applicable, low-cost therapy that has been postulated to improve mortality in patients with acute ST-segment elevation myocardial infarction (STEMI). Given the potential global importance of GIK infusion, a large, adequately powered randomized trial is required to determine the effect of GIK on mortality in patients with STEMI.
To determine the effect of high-dose GIK infusion on mortality in patients with STEMI.
DESIGN, SETTING, AND PARTICIPANTS: Randomized controlled trial conducted in 470 centers worldwide among 20,201 patients with STEMI who presented within 12 hours of symptom onset. The mean age of patients was 58.6 years, and evidence-based therapies were commonly used.
Patients were randomly assigned to receive GIK intravenous infusion for 24 hours plus usual care (n = 10,091) or to receive usual care alone (controls; n = 10,110).
Mortality, cardiac arrest, cardiogenic shock, and reinfarction at 30 days after randomization.
At 30 days, 976 control patients (9.7%) and 1004 GIK infusion patients (10.0%) died (hazard ratio [HR], 1.03; 95% confidence interval [CI], 0.95-1.13; P = .45). There were no significant differences in the rates of cardiac arrest (1.5% [151/10 107] in control and 1.4% [139/10,088] in GIK infusion; HR, 0.93; 95% CI, 0.74-1.17; P = .51), cardiogenic shock (6.3% [640/10 107] vs 6.6% [667/10 088]; HR, 1.05; 95% CI, 0.94-1.17; P = .38), or reinfarction (2.4% [246/10,107] vs 2.3% [236/10,088]; HR, 0.98; 95% CI, 0.82-1.17; P = .81). The rates of heart failure at 7 days after randomization were also similar between the groups (16.9% [1711/10,107] vs 17.1% [1721/10,088]; HR, 1.01; 95% CI, 0.95-1.08; P = .72). The lack of benefit of GIK infusion on mortality was consistent in prespecified subgroups, including in those with and without diabetes, in those presenting with and without heart failure, in those presenting early and later after symptom onset, and in those receiving and not receiving reperfusion therapy (thrombolysis or primary percutaneous coronary intervention).
In this large, international randomized trial, high-dose GIK infusion had a neutral effect on mortality, cardiac arrest, and cardiogenic shock in patients with acute STEMI.
葡萄糖-胰岛素-钾(GIK)输注是一种广泛适用且成本低廉的治疗方法,据推测可改善急性ST段抬高型心肌梗死(STEMI)患者的死亡率。鉴于GIK输注在全球范围内的潜在重要性,需要开展一项大规模、有足够统计学效力的随机试验来确定GIK对STEMI患者死亡率的影响。
确定大剂量GIK输注对STEMI患者死亡率的影响。
设计、地点和参与者:在全球470个中心对20201例症状发作后12小时内就诊的STEMI患者进行的随机对照试验。患者的平均年龄为58.6岁,且普遍采用了循证治疗。
患者被随机分配接受24小时GIK静脉输注加常规治疗(n = 10091)或仅接受常规治疗(对照组;n = 10110)。
随机分组后30天的死亡率、心脏骤停、心源性休克和再梗死。
在30天时,976例对照患者(9.7%)和1004例GIK输注患者(10.0%)死亡(风险比[HR],1.03;95%置信区间[CI],0.95 - 1.13;P = 0.45)。心脏骤停发生率(对照组为1.5%[151/10107],GIK输注组为1.4%[139/10088];HR,0.93;95%CI,0.74 - 1.17;P = 0.51)、心源性休克发生率(6.3%[640/10107]对6.6%[667/10088];HR,1.05;95%CI,0.94 - 1.17;P = 0.38)或再梗死发生率(2.4%[246/10107]对2.3%[236/10088];HR,0.98;95%CI,0.82 - 1.17;P = 0.81)均无显著差异。随机分组后7天的心力衰竭发生率在两组间也相似(16.9%[1711/10107]对17.1%[1721/10088];HR,1.01;95%CI,0.95 - 1.08;P = 0.72)。在预先设定的亚组中,包括有糖尿病和无糖尿病患者、有心力衰竭和无心力衰竭患者、症状发作早和晚的患者以及接受和未接受再灌注治疗(溶栓或直接经皮冠状动脉介入治疗)的患者中,GIK输注对死亡率均无益处。
在这项大型国际随机试验中,大剂量GIK输注对急性STEMI患者的死亡率、心脏骤停和心源性休克具有中性作用。