Centre for Heart Valve Innovation, University of British Columbia, Vancouver, British Columbia, Canada.
Centre for Heart Valve Innovation, University of British Columbia, Vancouver, British Columbia, Canada.
JACC Cardiovasc Interv. 2019 Mar 11;12(5):459-469. doi: 10.1016/j.jcin.2018.12.020.
The authors sought to prospectively determine the safety and efficacy of next-day discharge using the Vancouver 3M (Multidisciplinary, Multimodality, but Minimalist) Clinical Pathway.
Transfemoral transcatheter aortic valve replacement (TAVR) is an alternative to surgery in high- and intermediate-risk patients; however, hospital stays average at least 6 days in most trials. The Vancouver 3M Clinical Pathway is focused on next-day discharge, made possible by the use of objective screening criteria as well as streamlined peri- and post-procedural management guidelines.
Patients were enrolled from 6 low-volume (<100 TAVR/year), 4 medium-volume, and 3 high-volume (>200 TAVR/year) centers in Canada and the United States. The primary outcomes were a composite of all-cause death or stroke by 30 days and the proportion of patients successfully discharged home the day following TAVR.
Of 1,400 screened patients, 411 were enrolled at 13 centers and received a SAPIEN XT (58.2%) or SAPIEN 3 (41.8%) valve (Edwards Lifesciences, Irvine, California). In centers enrolling exclusively in the study, 55% of screened patients were enrolled. The median age was 84 years (interquartile range: 78 to 87 years) with a median STS score of 4.9% (interquartile range: 3.3% to 6.8%). Next-day discharge home was achieved in 80.1% of patients, and within 48 h in 89.5%. The composite of all-cause mortality or stroke by 30 days occurred in 2.9% (95% confidence interval: 1.7% to 5.1%), with neither component of the primary outcome affected by hospital TAVR volume (p = 0.51). Secondary outcomes at 30 days included major vascular complication 2.4% (n = 10), readmission 9.2% (n = 36), cardiac readmission 5.7% (n = 22), new permanent pacemaker 5.7% (n = 23), and >mild paravalvular regurgitation 3.8% (n = 15).
Adherence to the Vancouver 3M Clinical Pathway at low-, medium-, and high-volume TAVR centers allows next-day discharge home with excellent safety and efficacy outcomes.
作者旨在前瞻性地评估使用温哥华 3M(多学科、多模式、但简约)临床路径实现次日出院的安全性和有效性。
经股动脉经导管主动脉瓣置换术(TAVR)是高危和中危患者替代手术的一种选择;然而,大多数试验中的平均住院时间至少为 6 天。温哥华 3M 临床路径专注于次日出院,这得益于使用客观的筛选标准以及简化的围手术期和术后管理指南。
研究对象招募自加拿大和美国的 6 家低容量(每年<100 例 TAVR)、4 家中容量和 3 家高容量(每年>200 例 TAVR)中心。主要结局是 30 天内全因死亡或卒中和 TAVR 次日成功出院回家的患者比例的复合指标。
在 1400 例筛选患者中,有 411 例在 13 家中心接受了 SAPIEN XT(58.2%)或 SAPIEN 3(41.8%)瓣膜(爱德华兹生命科学公司,加利福尼亚州欧文市)治疗。在仅纳入研究患者的中心,55%的筛选患者被纳入。中位年龄为 84 岁(四分位距:78 至 87 岁),中位 STS 评分 4.9%(四分位距:3.3%至 6.8%)。80.1%的患者实现了次日出院回家,89.5%的患者在 48 小时内出院。30 天内全因死亡率或卒中的复合指标发生率为 2.9%(95%置信区间:1.7%至 5.1%),主要终点的任何组成部分均不受医院 TAVR 量的影响(p=0.51)。30 天的次要结局包括大血管并发症 2.4%(n=10)、再入院 9.2%(n=36)、心脏再入院 5.7%(n=22)、新植入永久性起搏器 5.7%(n=23)和>中度瓣周漏 3.8%(n=15)。
在低、中、高容量 TAVR 中心遵循温哥华 3M 临床路径可以实现次日出院回家,且安全性和有效性结果优异。