Feasibility and Safety of 1.1-mm Cryobiopsy for Acute Rejection Surveillance in Lung Transplant Recipients: A Comparative Study and Review of the Literature.

IF 2.1 Q3 RESPIRATORY SYSTEM
Alanna Barrios-Ruiz, Alejandra Yu Lee-Mateus, Bryan F Vaca-Cartagena, Paola Gutierrez-Gallegos, Rodrigo Funes-Ferrada, Prasanth Balasubramanian, Andras Khoor, Sadia Z Shah, Francisco G Alvarez, Maher Baz, Tathagat Narula, Remzi Bag, Kelly S Robertson, Sebastian Fernandez-Bussy, David Abia-Trujillo
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引用次数: 0

Abstract

Background: Identifying graft rejection after lung transplantation remains challenging, and no consensus exists on the optimal surveillance strategy. Transbronchial forceps biopsy (FBx) is the conventional method but is limited by small sample size and crush artifacts. Sheath-guided cryobiopsy (CBx) using a novel 1.1-mm probe has emerged as a promising alternative. This study evaluates the feasibility and safety of the 1.1-mm cryoprobe and provides a focused review of current literature.

Methods: We conducted a retrospective observational single-center study between October 2022 and January 2023 of adult lung transplant recipients who underwent transbronchial biopsies for surveillance. Procedures were performed using either standard FBx or the 1.1-mm cryoprobe. Descriptive analyses compared feasibility and safety between groups.

Results: We identified 72 lung transplant recipients who underwent 109 surveillance biopsies. A total of n = 56 CBx and n = 53 FBx procedures were performed. The median procedure time was 20 min (IQR 17-26) in the CBx group versus 22 min (IQR 15-33) in the FBx group. We found a statistically higher median sample area for CBx compared with FBx (11 vs. 6 mm2, p < 0.01). No pneumothorax or postprocedural respiratory failure occurred in either group.

Conclusion: CBx with a 1.1-mm probe provides larger histological samples than FBx, with comparable safety and potentially shorter procedural times. These findings support its feasibility for lung transplant surveillance.

1.1 mm低温活检用于肺移植受者急性排斥反应监测的可行性和安全性:比较研究和文献综述。
背景:识别肺移植后的移植排斥反应仍然具有挑战性,并且在最佳监测策略上没有达成共识。经支气管钳活检(FBx)是传统的方法,但受样本量小和挤压伪影的限制。鞘引导冷冻活检(CBx)使用一种新颖的1.1毫米探针已经成为一种很有前途的替代方法。本研究评估了1.1 mm冷冻探针的可行性和安全性,并对现有文献进行了重点综述。方法:我们在2022年10月至2023年1月期间对接受经支气管活检监测的成人肺移植受者进行了回顾性观察性单中心研究。使用标准FBx或1.1 mm冷冻探针进行手术。描述性分析比较了两组间的可行性和安全性。结果:我们确定了72名肺移植受者,他们接受了109次监测活检。共进行了n = 56例CBx和n = 53例FBx手术。CBx组的中位手术时间为20分钟(IQR 17-26),而FBx组为22分钟(IQR 15-33)。我们发现与FBx相比,CBx的中位样本面积在统计学上更高(11比6 mm2, p < 0.01)。两组均未发生气胸或术后呼吸衰竭。结论:与FBx相比,使用1.1 mm探针的CBx提供了更大的组织学样本,安全性相当,并且可能缩短手术时间。这些发现支持了其用于肺移植监测的可行性。
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
Pulmonary Medicine
Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
10.20
自引率
0.00%
发文量
4
审稿时长
14 weeks
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