From Baylor Scott and White Health, Plano, TX (M.J.M., D.L.B.); Columbia University Irving Medical Center and New York-Presbyterian Hospital (M.B.L., S.K.K., R.T.H., M.C.A., C.R.S.) and New York University Langone Medical Center (M.R.W.) - both in New York; Medstar Heart and Vascular Institute, Georgetown University, Washington, DC (V.H.T.); Cedars-Sinai Heart Institute, Los Angeles (R.M.); Robert Wood Johnson Medical School, Rutgers University, New Brunswick (M.R.), and Gagnon Cardiovascular Institute, Morristown Medical Center, Morristown (P.G.) - both in New Jersey; Cleveland Clinic, Cleveland (S.R.K.); Feinberg School of Medicine, Northwestern University, Chicago (S.C.M.); Saint Luke's Mid America Heart Institute, Kansas City, MO (D.J.C.); Quebec Heart and Lung Institute, Laval University, Quebec, QC (P.P.), and St. Paul's Hospital, University of British Columbia, Vancouver (J.L., P.B., J.G.W.) - both in Canada; University of Washington, Seattle (J.M.M.); Emory University Hospital, Atlanta (V.B.); Lankenau Medical Center, Wynnewood (S.G.), and the Hospital of the University of Pennsylvania, Philadelphia (W.Y.S.) - both in Pennsylvania; Banner University Medical Center, Phoenix, AZ (A.P.); and the London School of Hygiene and Tropical Medicine, London (S.J.P.).
N Engl J Med. 2019 May 2;380(18):1695-1705. doi: 10.1056/NEJMoa1814052. Epub 2019 Mar 16.
Among patients with aortic stenosis who are at intermediate or high risk for death with surgery, major outcomes are similar with transcatheter aortic-valve replacement (TAVR) and surgical aortic-valve replacement. There is insufficient evidence regarding the comparison of the two procedures in patients who are at low risk.
We randomly assigned patients with severe aortic stenosis and low surgical risk to undergo either TAVR with transfemoral placement of a balloon-expandable valve or surgery. The primary end point was a composite of death, stroke, or rehospitalization at 1 year. Both noninferiority testing (with a prespecified margin of 6 percentage points) and superiority testing were performed in the as-treated population.
At 71 centers, 1000 patients underwent randomization. The mean age of the patients was 73 years, and the mean Society of Thoracic Surgeons risk score was 1.9% (with scores ranging from 0 to 100% and higher scores indicating a greater risk of death within 30 days after the procedure). The Kaplan-Meier estimate of the rate of the primary composite end point at 1 year was significantly lower in the TAVR group than in the surgery group (8.5% vs. 15.1%; absolute difference, -6.6 percentage points; 95% confidence interval [CI], -10.8 to -2.5; P<0.001 for noninferiority; hazard ratio, 0.54; 95% CI, 0.37 to 0.79; P = 0.001 for superiority). At 30 days, TAVR resulted in a lower rate of stroke than surgery (P = 0.02) and in lower rates of death or stroke (P = 0.01) and new-onset atrial fibrillation (P<0.001). TAVR also resulted in a shorter index hospitalization than surgery (P<0.001) and in a lower risk of a poor treatment outcome (death or a low Kansas City Cardiomyopathy Questionnaire score) at 30 days (P<0.001). There were no significant between-group differences in major vascular complications, new permanent pacemaker insertions, or moderate or severe paravalvular regurgitation.
Among patients with severe aortic stenosis who were at low surgical risk, the rate of the composite of death, stroke, or rehospitalization at 1 year was significantly lower with TAVR than with surgery. (Funded by Edwards Lifesciences; PARTNER 3 ClinicalTrials.gov number, NCT02675114.).
对于手术死亡风险为中高危的主动脉瓣狭窄患者,经导管主动脉瓣置换术(TAVR)与外科主动脉瓣置换术的主要结局相似。对于低风险患者,两种手术方式的比较证据不足。
我们将严重主动脉瓣狭窄且手术风险低的患者随机分为 TAVR 组(经股动脉入路植入球囊扩张瓣膜)和手术组。主要终点是 1 年时死亡、卒中和再住院的复合终点。在治疗人群中进行了非劣效性检验(预设 6 个百分点的边界)和优效性检验。
在 71 个中心,1000 名患者被随机分组。患者的平均年龄为 73 岁,平均胸外科医生协会风险评分 1.9%(评分范围为 0 至 100%,评分越高表示术后 30 天内死亡的风险越高)。Kaplan-Meier 估计 TAVR 组 1 年时主要复合终点的发生率明显低于手术组(8.5% vs. 15.1%;绝对差异-6.6 个百分点;95%置信区间-10.8 至-2.5;P<0.001 表示非劣效性;风险比 0.54;95%置信区间 0.37 至 0.79;P=0.001 表示优效性)。术后 30 天,TAVR 组的卒中发生率低于手术组(P=0.02),死亡或卒中和新发心房颤动发生率也低于手术组(P<0.001)。TAVR 组的住院时间也短于手术组(P<0.001),术后 30 天不良治疗结局(死亡或低堪萨斯城心肌病问卷评分)的风险也低于手术组(P<0.001)。两组间主要血管并发症、新的永久性起搏器植入或中重度瓣周漏的发生率无显著差异。
对于手术风险低的严重主动脉瓣狭窄患者,TAVR 组 1 年时死亡、卒中和再住院的复合终点发生率明显低于手术组。(由爱德华兹生命科学公司资助;PARTNER 3 临床试验.gov 编号,NCT02675114.)