首页> 外文期刊>Canadian journal of surgery: Journal canadien de chirurgie >CAGS and ACS Evidence Based Reviews in Surgery. 34: effects of ss-blockers in patients undergoing noncardiac surgery.
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CAGS and ACS Evidence Based Reviews in Surgery. 34: effects of ss-blockers in patients undergoing noncardiac surgery.

机译:CAGS和ACS循证医学评论。 34:ss阻滞剂在非心脏手术患者中的作用。

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QUESTION: Do ss-blockers have an effect on the 30-day risk of major cardiovascular events in patients with or at risk of atherosclerotic disease undergoing noncardiac surgery? DESIGN: Randomized controlled trial. SETTING: Multicentre trial in 190 hospitals in 23 countries. PATIENTS: In total, 8351 patients with or at risk of atherosclerotic disease undergoing noncardiac surgery. INTERVENTION: Patients were randomly assigned by a computerized 24-hour phone service to receive extended-release metoprolol succinate 200 mg (n = 4174) or placebo (n = 4177). Treatment was started 2-4 hours before surgery and continued for 30 days. MAIN OUTCOME: Cardiovascular death, nonfatal myocardial infarction (MI) and nonfatal cardiac arrest. RESULTS: Of those randomized, 8331 (99.8%) patients completed the 30-day follow-up. Fewer patients in the metoprolol group than in the placebo group had an MI (176 [4.2%] v. 239 [5.7%] patients; hazard ratio [HR] 0.73, 95% confidence interval [CI] 0.60-0.089, p = 0.0017). However, there were more deaths in the metoprolol group than in the placebo group (129 [3.1%] v. 97 [2.3%] patients; HR 1.33, 95% CI 1.03-1.74, p = 0.0317). More patients in the metoprolol group than in the placebo group had a stroke (41 [1.0%] v. 19 [0.5%] patients; HR 2.17, 95% CI 1.26-3.74, p = 0.0053). CONCLUSION: A perioperative ss-blocker regimen results in fewer MIs but is associated with an increased risk of stroke and perioperative death in patients with or at risk for atherosclerotic disease undergoing noncardiac surgery. Patients are unlikely to accept the risks associated with perioperative extended-release metoprolol use.
机译:问题:接受非心脏手术的患有动脉粥样硬化性疾病或有动脉粥样硬化性疾病风险的患者中,ss受体阻滞剂是否对发生重大心血管事件的30天风险有影响?设计:随机对照试验。地点:在23个国家/地区的190家医院进行了多中心试验。患者:总共有8351名患有或有动脉粥样硬化疾病风险的患者接受了非心脏手术。干预措施:通过计算机化的24小时电话服务将患者随机分配,以接受200 mg琥珀酸美托洛尔缓释剂(n = 4174)或安慰剂(n = 4177)。在手术前2-4小时开始治疗,并持续30天。主要观察指标:心血管死亡,非致命性心肌梗塞(MI)和非致命性心脏骤停。结果:在随机分组的患者中,有8331(99.8%)位患者完成了30天的随访。美托洛尔组的患者发生心梗的比例低于安慰剂组(176 [4.2%] vs. 239 [5.7%];危险比[HR] 0.73,95%置信区间[CI] 0.60-0.089,p = 0.0017) )。然而,美托洛尔组的死亡人数高于安慰剂组(129 [3.1%] vs. 97 [2.3%]患者; HR 1.33,95%CI 1.03-1.74,p = 0.0317)。美托洛尔组的中风患者比安慰剂组的多(41 [1.0%] vs. 19 [0.5%]患者; HR 2.17,95%CI 1.26-3.74,p = 0.0053)。结论:围手术期的ss受体阻滞剂治疗方案可减少心梗,但伴有或有动脉粥样硬化性疾病的非心脏手术风险的中风和围手术期死亡的风险增加。患者不太可能接受围手术期使用美托洛尔的相关风险。

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