Wang Yanwei, Zhou Yijiang, Zhang Li, Zhu Jianhua
Department of Cardiology, Ningbo Medical Treatment Center Lihuili Hospital, Ningbo, PR China.
Department of Cardiology, The First Affiliated Hospital, Zhejiang University, School of Medicine, Hangzhou, PR China.
J Cardiol. 2018 Jun;71(6):534-539. doi: 10.1016/j.jjcc.2017.10.020.
Current guidelines recommend transcatheter aortic valve replacement (TAVR) in patients with severe symptomatic aortic stenosis (AS) who are not suitable for conventional surgical aortic valve replacement (SAVR). In light of the recent trend in performing TAVR in patients with lower risk profile, we assessed the midterm outcome comparing TAVR and SAVR for the treatment of patients with severe AS at low to intermediate risk.
PubMed, EBSCO, and Cochrane CENTRAL were systematically searched for randomized controlled trials that reported the clinical outcomes of TAVR versus SAVR in patients at low to intermediate surgical risk with at least 2 years of follow-up. Clinical endpoints including death, acute kidney injury, myocardial infarction, stroke, permanent pacemaker implantation, and life-threatening bleeding events were assessed.
From 2000 to 2017, 4 clinical studies comprising 4355 patients were identified. At 2-year follow-up, TAVR was associated with similar rate of death from any cause (RR 0.86; 95%CI: 0.67-1.10), cardiovascular death (RR 0.88; 95%CI: 0.73-1.06), and stroke (RR 0.97; 95%CI: 0.81-1.15). TAVR reduced incidence of bleeding events (RR 0.45; 95%CI: 0.28-0.73) and acute kidney injury (RR 0.48; 95%CI: 0.25-0.93). However, TAVR was associated with higher rate of permanent pacemaker implantation (RR 3.01; 95%CI: 1.04-8.72).
In patients at low to intermediate surgical risk, midterm clinical outcomes of TAVR were similar to SAVR in survival and stroke rate, superior in reducing life-threatening bleeding, acute kidney injury, and new-onset atrial fibrillation, but inferior in increasing permanent pacemaker implantation.
当前指南推荐,对于不适合传统外科主动脉瓣置换术(SAVR)的严重症状性主动脉瓣狭窄(AS)患者,可采用经导管主动脉瓣置换术(TAVR)。鉴于近期在低风险患者中进行TAVR的趋势,我们评估了TAVR与SAVR治疗低至中度风险严重AS患者的中期结果。
系统检索PubMed、EBSCO和Cochrane CENTRAL,查找报告低至中度手术风险患者TAVR与SAVR临床结局且随访至少2年的随机对照试验。评估包括死亡、急性肾损伤、心肌梗死、中风、永久性起搏器植入和危及生命的出血事件在内的临床终点。
2000年至2017年,共确定4项临床研究,涉及4355例患者。在2年随访时,TAVR组全因死亡率(RR 0.86;95%CI:0.67 - 1.10)、心血管死亡率(RR 0.88;95%CI:0.73 - 1.06)和中风发生率(RR 0.97;95%CI:0.81 - 1.15)与SAVR组相似。TAVR降低了出血事件发生率(RR 0.45;95%CI:0.28 - 0.73)和急性肾损伤发生率(RR 0.48;95%CI:0.25 - 0.93)。然而,TAVR组永久性起搏器植入率较高(RR 3.01;95%CI:1.04 - 8.72)。
对于低至中度手术风险的患者,TAVR的中期临床结局在生存率和中风发生率方面与SAVR相似,在降低危及生命的出血、急性肾损伤和新发房颤方面更具优势,但在增加永久性起搏器植入方面则较差。