Wijeysundera Duminda N, Bender Jennifer S, Beattie W Scott
Department of Anesthesia, Toronto General Hospital and University of Toronto, EN 3-450, Toronto General Hospital,, 200 Elizabeth Street, Toronto, Ontario, Canada, M5G 2C4.
Cochrane Database Syst Rev. 2009 Oct 7(4):CD004126. doi: 10.1002/14651858.CD004126.pub2.
The surgical stress response plays an important role on the pathogenesis of perioperative cardiac complications. Alpha-2 adrenergic agonists attenuate this response and may thereby prevent cardiac complications.
This review assessed the efficacy and safety of preoperative (within 24 hours), intraoperative, and postoperative (first 48 hours) alpha-2 adrenergic agonists for preventing mortality and cardiac complications after surgery performed under either general or neuraxial anaesthesia, or both.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2008, Issue 3), MEDLINE (1950 to August week 4 2008), EMBASE (1980 to week 36 2008), the Science Citation Index, and reference lists of articles.
We included randomized controlled trials that compared alpha-2 adrenergic agonists (clonidine, dexmedetomidine, or mivazerol) against placebo or non-alpha-2 adrenergic agonists. Included studies had to report on mortality, myocardial infarction, myocardial ischaemia, or supraventricular tachyarrhythmia.
Three authors independently assessed trial quality and extracted data. Two authors independently performed computer entry of abstracted data. We contacted study authors for additional information. Adverse event data were gathered from the trials.
We included 31 studies (4578 participants). Study quality was generally inadequate, with only six studies clearly reporting methods for blinding and allocation concealment. Overall, alpha-2 adrenergic agonists reduced mortality (relative risk (RR) 0.66; 95% CI 0.44 to 0.98; P = 0.04) and myocardial ischaemia (RR 0.68; 95% CI 0.57 to 0.81; P < 0.0001). However, their effects appeared to vary with the surgical procedure. The most encouraging data pertained to vascular surgery, where they reduced mortality (RR 0.47; 95% CI 0.25 to 0.90; P = 0.02), cardiac mortality (RR 0.36; 95% CI 0.16 to 0.79; P = 0.01), and myocardial infarction (RR 0.66; 95% CI 0.46 to 0.94; P = 0.02). With regard to adverse effects, alpha-2 adrenergic agonists significantly increased perioperative hypotension (RR 1.32; 95% CI 1.07 to 1.62; P = 0.009) and bradycardia (RR 1.66; 95% CI 1.14 to 2.41; P = 0.008).
AUTHORS' CONCLUSIONS: Our study provides encouraging evidence that alpha-2 adrenergic agonists may reduce cardiac risk, especially during vascular surgery. Nonetheless, these data remain insufficient to make firm conclusions about their efficacy and safety. A large randomized trial of alpha-2 adrenergic agonists is therefore warranted. Additionally, future research must determine which specific alpha-2 adrenergic agonist should be used, and whether it is safe to combine them with other perioperative interventions (for example beta-adrenergic blockade).
手术应激反应在围手术期心脏并发症的发病机制中起重要作用。α-2肾上腺素能激动剂可减轻这种反应,从而可能预防心脏并发症。
本综述评估术前(24小时内)、术中及术后(最初48小时)使用α-2肾上腺素能激动剂预防全身麻醉或椎管内麻醉或两者联合麻醉下手术后死亡和心脏并发症的有效性和安全性。
我们检索了Cochrane对照试验中心注册库(CENTRAL)(《Cochrane图书馆》2008年第3期)、MEDLINE(1950年至2008年8月第4周)、EMBASE(1980年至2008年第36周)、科学引文索引以及文章的参考文献列表。
我们纳入了比较α-2肾上腺素能激动剂(可乐定、右美托咪定或米伐唑醇)与安慰剂或非α-2肾上腺素能激动剂的随机对照试验。纳入的研究必须报告死亡率、心肌梗死、心肌缺血或室上性快速心律失常。
三位作者独立评估试验质量并提取数据。两位作者独立进行提取数据的计算机录入。我们与研究作者联系以获取更多信息。不良事件数据从试验中收集。
我们纳入了31项研究(4578名参与者)。研究质量总体不足,只有6项研究明确报告了盲法和分配隐藏方法。总体而言,α-2肾上腺素能激动剂降低了死亡率(相对危险度(RR)0.66;95%可信区间0.44至0.98;P = 0.04)和心肌缺血(RR 0.68;95%可信区间0.57至0.81;P < 0.0001)。然而,其效果似乎因手术方式而异。最令人鼓舞的数据与血管手术有关,在血管手术中它们降低了死亡率(RR 0.47;95%可信区间0.25至0.90;P = 0.02)、心脏死亡率(RR 0.36;95%可信区间0.16至0.79;P = 0.01)和心肌梗死(RR 0.66;95%可信区间0.46至0.94;P = 0.02)。关于不良反应,α-2肾上腺素能激动剂显著增加围手术期低血压(RR 1.32;95%可信区间1.07至1.62;P = 0.009)和心动过缓(RR 1.66;95%可信区间1.14至2.41;P = 0.008)。
我们的研究提供了令人鼓舞的证据,表明α-2肾上腺素能激动剂可能降低心脏风险,尤其是在血管手术期间。尽管如此,这些数据仍不足以就其有效性和安全性得出确凿结论。因此,有必要进行一项关于α-2肾上腺素能激动剂的大型随机试验。此外,未来的研究必须确定应使用哪种特定的α-2肾上腺素能激动剂,以及将它们与其他围手术期干预措施(如β-肾上腺素能阻滞剂)联合使用是否安全。