Division of Cardiology, Department of Internal Medicine, St. Marianna University School of Medicine, Japan.
Division of Cardiology, Department of Internal Medicine, St. Marianna University School of Medicine, Japan.
Cardiovasc Revasc Med. 2024 Jan;58:68-76. doi: 10.1016/j.carrev.2023.07.014. Epub 2023 Jul 21.
Aortic stenosis (AS) and chronic kidney disease (CKD) can coexist. Repeat exposure to contrast media in patients undergoing transcatheter aortic valve implantation (TAVI) has latent mortality risks and increased risk for acute kidney injury. We aimed to assess our "zero-contrast TAVI" protocol for patients with advanced CKD.
Consecutive patients with severe AS who underwent TAVI at a single center registry were enrolled. Zero-contrast TAVI group included patients who underwent TAVI without contrast and who had an estimated glomerular filtration rate <30 mL/min/1.73 m. Conventional TAVI group included patients who underwent the regular TAVI procedure. Patients using balloon-expandable valves via transfemoral approach were analyzed. Baseline clinical and procedural characteristics and clinical outcomes were compared between two groups. The primary outcome was early safety as defined by Valve Academic Research Consortium Criteria. Secondary outcomes included the presence of severe prosthesis-patient mismatch, moderate or greater perivalvular leakage, and requirement for new dialysis (within 3 months).
A total of 520 patients were analyzed. Among these, 32 (6 %) underwent zero-contrast TAVI and 488 (94 %) conventional TAVI. In the zero-contrast TAVI group, 12 patients (37.5 %) had to use 20.7 (11.0-31.2) mL of contrast media. There were no significant differences in the primary and secondary outcomes between zero-contrast TAVI and conventional TAVI groups (78.1 % vs. 86.8 %, P = 0.184 and 9.4 % vs. 8.1 %, P = 0.738 for the primary and secondary outcomes, respectively).
Zero-contrast TAVI is feasible, safe, and effective in patients with AS and stage 4 CKD.
主动脉瓣狭窄(AS)和慢性肾脏病(CKD)可共存。经导管主动脉瓣植入术(TAVI)中反复接触造影剂有潜在的死亡风险,并增加急性肾损伤的风险。我们旨在评估我们用于晚期 CKD 患者的“无对比 TAVI”方案。
连续纳入在单个中心登记处接受 TAVI 的严重 AS 患者。无对比 TAVI 组包括未使用造影剂且估计肾小球滤过率 <30 mL/min/1.73 m 的患者。常规 TAVI 组包括接受常规 TAVI 程序的患者。经股动脉途径使用球囊扩张瓣膜的患者进行分析。比较两组患者的基线临床和手术特征及临床结局。主要结局为 Valve Academic Research Consortium 标准定义的早期安全性。次要结局包括严重假体-患者不匹配、中度或更严重瓣周漏和需要新透析(3 个月内)。
共分析了 520 例患者。其中,32 例(6%)行无对比 TAVI,488 例(94%)行常规 TAVI。在无对比 TAVI 组中,12 例(37.5%)需要使用 20.7(11.0-31.2)mL 造影剂。无对比 TAVI 和常规 TAVI 组在主要和次要结局方面无显著差异(78.1% vs. 86.8%,P=0.184;主要和次要结局的 9.4% vs. 8.1%,P=0.738)。
无对比 TAVI 对 AS 和 4 期 CKD 患者是可行、安全和有效的。