Jin Shuan, Zhou Xueyue
Department of Anesthesia, Jinan Central Hospital Affiliated to Shandong University, Shandong Province, Jinan, 250013, China.
Medical Center Tsinghua University, Beijing, 100084, China.
Int J Clin Pharm. 2017 Aug;39(4):629-640. doi: 10.1007/s11096-017-0493-8. Epub 2017 Jun 28.
Background The cardiac protection of dexmedetomidine (Dex) in peri-operative period of patients with non-cardiac surgery is still controversial. Aim of the Review We aimed to evaluate the influence of Dex on cardiac complications in peri-operative period of non-cardiac surgery by using a meta-analysis. Methods PubMed, Embase, the Cochrane library and Springer databases were searched for relevant studies. Patients in the eligible studies were divided into Dex group and placebo group. Relative risk (RR) and the 95 % confidence interval (CI) were calculated to evaluate the outcomes including all-cause mortality, myocardial infarction, myocardial ischaemia, hypotension and bradycardia. Subgroup analysis was performed based on the dosage of Dex. Publication bias was assessed by Egger's test. Results Twenty double-blind randomized controlled trials containing 1157 patients were included in this meta-analysis. The pooled results showed no significant difference between Dex group and placebo group in peri-operative myocardial infarction, myocardial ischaemia and all-cause mortality. However, Dex group showed higher risk of hypotension (RR = 1.46, 95 % CI 1.07, 2.01) and bradycardia (RR = 1.98, 95 % CI 1.33, 2.95) than that of placebo group. In addition, significant publication bias was found among studies involving hypotension and bradycardia. In subgroup analysis, the risk of bradycardia was significantly higher in 1.0 μg/kg Dex group than that in placebo group. Besides, a higher risk of hypotension in 0.5 μg/kg Dex group than that in placebo group was found. Conclusions Dex supplement might not reduce the risk of cardiac complications but increases the risk of hypotension and bradycardia in peri-operative period of patients who underwent non-cardiac surgeries.
右美托咪定(Dex)在非心脏手术患者围手术期的心脏保护作用仍存在争议。综述目的:我们旨在通过荟萃分析评估Dex对非心脏手术围手术期心脏并发症的影响。方法:检索PubMed、Embase、Cochrane图书馆和Springer数据库中的相关研究。符合条件的研究中的患者分为Dex组和安慰剂组。计算相对风险(RR)和95%置信区间(CI)以评估包括全因死亡率、心肌梗死、心肌缺血、低血压和心动过缓在内的结局。根据Dex的剂量进行亚组分析。通过Egger检验评估发表偏倚。结果:本荟萃分析纳入了20项包含1157例患者的双盲随机对照试验。汇总结果显示,Dex组和安慰剂组在围手术期心肌梗死、心肌缺血和全因死亡率方面无显著差异。然而,Dex组的低血压风险(RR = 1.46,95%CI 1.07,2.01)和心动过缓风险(RR = 1.98,95%CI 1.33,2.95)高于安慰剂组。此外,在涉及低血压和心动过缓的研究中发现了显著的发表偏倚。亚组分析中,1.0μg/kg Dex组的心动过缓风险显著高于安慰剂组。此外,发现0.5μg/kg Dex组的低血压风险高于安慰剂组。结论:在接受非心脏手术的患者围手术期,补充Dex可能不会降低心脏并发症的风险,但会增加低血压和心动过缓的风险。