Endomyocardial Biopsy Using Rigid Bioptome Technique and the Risk of Tricuspid Regurgitation after Heart Transplantation.

Arquivos brasileiros de cardiologia Pub Date : 2024-10-28 eCollection Date: 2024-01-01 DOI:10.36660/abc.20240223
Luís Beck-da-Silva, Leonardo Hennig Bridi, Bruno S Matte, Felipe Homem Valle
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Abstract

Endomyocardial biopsy (EB) is the preferred procedure for post-heart transplant rejection diagnosis. The rigid bioptome technique has been used due to its greater simplicity and has been criticized for the potential risk of tricuspid regurgitation (TR). We aimed to review all the EBs performed by this technique in a tertiary center and estimate the rate of complications and/or aggravation of TR. Cross-sectional, retrospective, anterograde study. Data were collected from 729 EBs performed in 55 post-heart transplant patients with a rigid Scholten Novatome™ bioptome between September 2012 to March 2022. All EBs were performed via the right jugular vein under local anesthesia and through micro-puncture and ultrasound guidance. A total of 729 procedures had an echocardiography performed before and after the procedures. The estimate of TR was categorized as absent, minimal, mild, moderate, and severe. McNemar's chi-square test was used to analyze the degree of pre- and post-EB TR. There was a worsening enough to become moderate or severe post-biopsy TR in two (0.27%) procedures, and there was a slight change in TR from minimal to mild TR in 25 (3.42%) procedures. In 729 percutaneous EBs performed with a rigid bioptome, there was no myocardial perforation, cardiac tamponade or pneumothorax. One death occurred within 24 hours after the procedure for an unknown reason. EB using a rigid bioptome is safe and has not been associated with worsening TR in a follow-up of 729 EBs performed after cardiac transplantation. The overall complication rate, including moderate to severe TR, was 0.81%. The mortality rate was 0.14%.

使用刚性生物光束技术进行心内膜活检与心脏移植后三尖瓣反流的风险
心内膜活检(EB)是诊断心脏移植后排斥反应的首选方法。硬质生物透视技术因其更为简便而被广泛使用,但也因三尖瓣反流(TR)的潜在风险而受到批评。我们的目的是回顾一个三级中心使用该技术进行的所有 EB,并估计并发症和/或 TR 恶化的发生率。横断面、回顾性、前向研究。研究收集了 2012 年 9 月至 2022 年 3 月期间使用硬质 Scholten Novatome™ 生物光罩对 55 名心脏移植术后患者进行的 729 例 EB 的数据。所有 EB 都是在局部麻醉、微穿刺和超声引导下通过右颈静脉进行的。共有 729 例手术在手术前后进行了超声心动图检查。对 TR 的估计分为无、轻微、轻度、中度和重度。采用 McNemar's chi-square 检验分析手术前后 TR 的程度。有2例(0.27%)手术活检后TR恶化至中度或重度,有25例(3.42%)手术TR从极小变为轻微。在使用硬质生物光罩进行的 729 例经皮 EB 中,没有发生心肌穿孔、心脏填塞或气胸。有一人在术后 24 小时内死亡,原因不明。在对心脏移植术后进行的 729 例 EB 的随访中,使用硬质生物光器进行 EB 是安全的,并且与 TR 的恶化无关。包括中度至重度TR在内的总体并发症发生率为0.81%。死亡率为 0.14%。
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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