Next-Day Discharge After Transcatheter Aortic Valve Implantation With the ACURATE neo/neo2 Self-Expanding Aortic Bioprosthesis

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
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Abstract

Previous studies have shown the safety of early discharge pathways in selected patients and using selected transcatheter heart valves. Hence, we sought to evaluate the safety of next-day discharge (NDD) in patients who underwent transfemoral transcatheter aortic valve implantation (TF-TAVI) with the ACURATE neo/neo2 (Boston Scientific, Marlborough, Massachusetts) self-expanding aortic bioprosthesis. Patients who underwent TF-TAVI between January 2018 and April 2023 were prospectively included. Patients were stratified into 3 groups according to discharge times within 24 hours (NDD), between 24 and 48 hours, and those discharged >48 hours after TAVI. The primary outcome was the first unplanned readmission at 30 days after TAVI. Log-rank test was used to assess the differences in the outcome of interest between the groups. A total of 368 all-comers were included in this study. According to discharge times, 204 patients followed NDD, 69 patients 24 to 48 hours discharge, and 95 patients >48 hours discharge after TAVI. The mean age was 84 ± 6.3 years and 61% were women, without differences between the groups. The mean Society of Thoracic Surgeons score was lower in those with NDD versus 24 to 48 hours and >48 hours (2.9 ± 1.0, 3.2 ± 1.2, and 3.4 ± 1.4, respectively, p = 0.014). There were no differences between the groups in terms of preprocedural right bundle branch block or pacemaker. The need for new permanent pacemaker implantation was the leading postprocedural complication; it occurred more frequently in the >48 hours group than the 24 to 48 hours, and <24 hours groups (24% vs 8.6% and 2.2%, p <0.001). There were 5 strokes (1.4%) and all of them occurred in the >48 hours group (p = 0.005). At 30 days after discharge, there were no deaths and no differences in all-cause readmissions (9.3% in <24 hours, 8.6% in 24 to 48 hours, and 19% in >48 hours, log-rank p = 0.087). The readmission rates for new permanent pacemaker implantation requirement were 3.3% (n = 6) in NDD, 0% in 24 to 48 hours, and 1.6% (n = 5) in the >48 hours groups (p = 0.27). In conclusion, in unselected patients who underwent TF-TAVI with the ACURATE neo/neo2 self-expanding bioprosthesis, the NDD pathway is feasible and appears to be safe, without an increased risk of death or all-cause rehospitalization through 30 days after hospital discharge.

使用 Acurate neo/neo2 自扩张主动脉瓣生物假体进行经导管主动脉瓣植入术后的次日出院。
先前的研究表明,在选定的患者和使用选定的经导管心脏瓣膜时,提前出院(ED)途径是安全的。因此,我们试图评估使用 Acurate neo/neo2 (Boston Scientific, Marlborough, MA) 自扩张主动脉生物瓣膜接受经股动脉经导管主动脉瓣植入术(TF-TAVI)的患者次日出院(NDD)的安全性。前瞻性地纳入了在 2018 年 1 月至 2023 年 4 月期间接受 TF-TAVI 的患者。根据 TAVI 术后 24 小时(NDD)内出院时间、24-48 小时出院时间和 48 小时以上出院时间将患者分为 3 组。主要结果是TAVI术后30天内首次非计划再入院。采用对数秩检验评估各组间相关结果的差异。本研究共纳入了 368 名所有患者。根据出院时间,204 名患者遵循 NDD,69 名患者遵循 24-48 小时出院,95 名患者遵循 >48 小时出院。平均年龄为(84±6.3)岁,61%为女性,组间无差异。NDD 患者的平均 STS 评分低于 24-48h 和 >48h 患者(分别为 2.9±1.0、3.2±1.2 和 3.4±1.4,P=0.014)。在术前右束支传导阻滞或起搏器方面,各组之间没有差异。需要植入新的永久起搏器(PPI)是术后最主要的并发症;与24-48小时组和48小时组相比,48小时以上组的发生率更高(P=0.005)。出院后 30 天内,无死亡病例,全因再入院率也无差异(48 小时内为 9.3%,对数秩 P=0.087)。新需要 PPI 的再入院率在 NDD 组为 3.3%(n=6),在 24-48h 组为 0%,在 >48h 组为 1.6%(n=5)(P=0.27)。总之,在使用Acurate neo/neo2自扩张生物前列腺假体进行TF-TAVI的非选择性患者中,NDD途径是可行的,而且似乎是安全的,不会增加出院后30天内的死亡或全因再住院风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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