Department of Clinical Sciences, Division of Cardiology, Karolinska Institutet, Danderyd Hospital, Stockholm, Sweden
Department of Medical Sciences, Cardiology, Uppsala University, Sweden.
Circulation. 2018 Dec 11;138(24):2754-2762. doi: 10.1161/CIRCULATIONAHA.118.036220.
In the DETO2X-AMI trial (Determination of the Role of Oxygen in Suspected Acute Myocardial Infarction), we compared supplemental oxygen with ambient air in normoxemic patients presenting with suspected myocardial infarction and found no significant survival benefit at 1 year. However, important secondary end points were not yet available. We now report the prespecified secondary end points cardiovascular death and the composite of all-cause death and hospitalization for heart failure.
In this pragmatic, registry-based randomized clinical trial, we used a nationwide quality registry for coronary care for trial procedures and evaluated end points through the Swedish population registry (mortality), the Swedish inpatient registry (heart failure), and cause of death registry (cardiovascular death). Patients with suspected acute myocardial infarction and oxygen saturation of ≥90% were randomly assigned to receive either supplemental oxygen at 6 L/min for 6 to 12 hours delivered by open face mask or ambient air.
A total of 6629 patients were enrolled. Acute heart failure treatment, left ventricular systolic function assessed by echocardiography, and infarct size measured by high-sensitive cardiac troponin T were similar in the 2 groups during the hospitalization period. All-cause death or hospitalization for heart failure within 1 year after randomization occurred in 8.0% of patients assigned to oxygen and in 7.9% of patients assigned to ambient air (hazard ratio, 0.99; 95% CI, 0.84–1.18; P=0.92). During long-term follow-up (median [range], 2.1 [1.0–3.7] years), the composite end point occurred in 11.2% of patients assigned to oxygen and in 10.8% of patients assigned to ambient air (hazard ratio, 1.02; 95% CI, 0.88–1.17; P=0.84), and cardiovascular death occurred in 5.2% of patients assigned to oxygen and in 4.8% assigned to ambient air (hazard ratio, 1.07; 95% CI, 0.87–1.33; P=0.52). The results were consistent across all predefined subgroups.
Routine use of supplemental oxygen in normoxemic patients with suspected myocardial infarction was not found to reduce the composite of all-cause mortality and hospitalization for heart failure, or cardiovascular death within 1 year or during long-term follow-up.
URL: https://www.clinicaltrials.gov. Unique identifier: NCT01787110.
在 DETO2X-AMI 试验(确定疑似急性心肌梗死患者中氧气的作用)中,我们比较了补充氧气与正常氧合的疑似心肌梗死患者吸入环境空气,未发现 1 年时的生存获益有显著差异。然而,重要的次要终点尚未公布。我们现在报告预先指定的次要终点心血管死亡和全因死亡及心力衰竭住院的复合终点。
在这项基于实践的、基于全国性冠状动脉护理质量登记的随机临床试验中,我们使用了一个全国性的冠状动脉护理质量登记来进行试验程序,并通过瑞典人群登记(死亡率)、瑞典住院病人登记(心力衰竭)和死因登记(心血管死亡)来评估终点。氧饱和度≥90%的疑似急性心肌梗死患者被随机分配接受 6 L/min 的补充氧气治疗 6 至 12 小时,通过开放面罩输送,或吸入环境空气。
共有 6629 例患者入选。在住院期间,两组的急性心力衰竭治疗、超声心动图评估的左心室射血分数和高敏心肌肌钙蛋白 T 测量的梗死面积相似。随机分组后 1 年内全因死亡或心力衰竭住院的发生率在接受氧气治疗的患者中为 8.0%,在接受环境空气治疗的患者中为 7.9%(风险比,0.99;95%CI,0.84–1.18;P=0.92)。在长期随访期间(中位数[范围],2.1[1.0–3.7]年),接受氧气治疗的患者中有 11.2%发生了复合终点事件,接受环境空气治疗的患者中有 10.8%发生了复合终点事件(风险比,1.02;95%CI,0.88–1.17;P=0.84),接受氧气治疗的患者中有 5.2%发生心血管死亡,接受环境空气治疗的患者中有 4.8%发生心血管死亡(风险比,1.07;95%CI,0.87–1.33;P=0.52)。所有预先设定的亚组结果一致。
在疑似心肌梗死且氧合正常的患者中常规使用补充氧气并未降低 1 年内及长期随访期间全因死亡率和心力衰竭住院的复合终点事件、或心血管死亡的发生风险。
网址:https://www.clinicaltrials.gov。唯一标识符:NCT01787110。