From the Department of Anaesthesia and Perioperative Medicine, Groote Schuur Hospital and University of Cape Town, Cape Town, South Africa.
Anesth Analg. 2018 Sep;127(3):678-687. doi: 10.1213/ANE.0000000000002837.
The global rate of major noncardiac surgical procedures is increasing annually, and of those patients presenting for surgery, increasing numbers are taking either an angiotensin-converting enzyme inhibitor (ACE-I) or an angiotensin receptor blocker (ARB). The current recommendations of whether to continue or withhold ACE-I and ARB in the perioperative period are conflicting. Previous meta-analyses have linked preoperative ACE-I/ARB therapy to the increased incidence of postinduction hypotension; however, they have failed to correlate this with adverse patient outcomes. The aim of this meta-analysis was to determine whether continuation or withholding ACE-I or ARB therapy in the perioperative period is associated with mortality and major morbidity.
This meta-analysis was prospectively registered on PROSPERO (CRD42017055291). A comprehensive search of MEDLINE (PubMed), CINAHL (EBSCO host), ProQuest, Cochrane database, Scopus, and Web of Science was conducted on December 6, 2016. We included adult patients >18 years of age on chronic ACE-I or ARB therapy who underwent noncardiac surgery in which ACE-I or ARB was either withheld or continued on the morning of surgery. Primary outcomes included all-cause mortality and major cardiac events (MACE). Secondary outcomes included the risk of congestive heart failure, acute kidney injury, stroke, intraoperative/postoperative hypotension, and the length of hospital stay.
After abstract review, the full text of 25 studies was retrieved, of which 9 fulfilled the inclusion criteria: 5 were randomized control trials, and 4 were cohort studies. These studies included a total of 6022 patients on chronic ACE-I/ARB therapy before noncardiac surgery. A total of 1816 patients withheld treatment the morning of surgery and 4206 continued their ACE-I/ARB. Preoperative demographics were similar between the 2 groups. Withholding ACE-I/ARB therapy was not associated with a difference in mortality (odds ratio [OR], 0.97; 95% confidence interval [CI], 0.62-1.52; I = 0%) or MACE (OR, 1.12; 95% CI, 0.82-1.52; I = 0%). However, withholding therapy was associated with significantly less intraoperative hypotension (OR, 0.63; 95% CI, 0.47-0.85; I = 71%). No effect estimate could be pooled concerning length of hospital stay and congestive heart failure.
This meta-analysis did not demonstrate an association between perioperative administration of ACE-I/ARB and mortality or MACE. It did, however, confirm the current observation that perioperative continuation of ACE-I/ARBs is associated with an increased incidence of intraoperative hypotension. A large randomized control trial is necessary to determine the appropriate perioperative management of ACE-I and ARBs.
全球非心脏手术的比例正在逐年增加,而在接受手术的患者中,越来越多的人正在服用血管紧张素转换酶抑制剂(ACE-I)或血管紧张素受体阻滞剂(ARB)。目前关于围手术期继续或停止使用 ACE-I 和 ARB 的建议存在冲突。先前的荟萃分析将术前 ACE-I/ARB 治疗与诱导后低血压的发生率增加联系起来;然而,他们未能将这与不良的患者结局相关联。本荟萃分析的目的是确定围手术期继续或停止 ACE-I 或 ARB 治疗是否与死亡率和主要发病率相关。
本荟萃分析在 PROSPERO(CRD42017055291)上进行了前瞻性注册。于 2016 年 12 月 6 日对 MEDLINE(PubMed)、CINAHL(EBSCO 主机)、ProQuest、Cochrane 数据库、Scopus 和 Web of Science 进行了全面检索。我们纳入了正在服用慢性 ACE-I 或 ARB 治疗且年龄大于 18 岁的成年患者,这些患者接受了非心脏手术,在手术当天早上停用或继续使用 ACE-I 或 ARB。主要结局包括全因死亡率和主要心脏事件(MACE)。次要结局包括充血性心力衰竭、急性肾损伤、中风、术中/术后低血压和住院时间的风险。
经过摘要审查,共检索到 25 篇研究的全文,其中 9 篇符合纳入标准:5 项为随机对照试验,4 项为队列研究。这些研究共纳入了 6022 例在非心脏手术前接受慢性 ACE-I/ARB 治疗的患者。共有 1816 例患者在手术当天早晨停止治疗,4206 例继续使用 ACE-I/ARB。两组术前人口统计学特征相似。停用 ACE-I/ARB 治疗与死亡率(比值比 [OR],0.97;95%置信区间 [CI],0.62-1.52;I = 0%)或 MACE(OR,1.12;95% CI,0.82-1.52;I = 0%)无关。然而,停用治疗与术中低血压的发生率显著降低相关(OR,0.63;95% CI,0.47-0.85;I = 71%)。关于住院时间和充血性心力衰竭,无法汇总效果估计值。
本荟萃分析未显示围手术期 ACE-I/ARB 给药与死亡率或 MACE 之间存在关联。然而,它确实证实了目前的观察结果,即围手术期继续使用 ACE-I/ARB 与术中低血压的发生率增加有关。需要一项大型随机对照试验来确定 ACE-I 和 ARB 的适当围手术期管理。