Inage Terunaga, Fujino Kosuke, Motooka Yamato, Ishiwata Tsukasa, Ujiie Hideki, Gregor Alexander, Bernards Nicholas, Chan Harley H L, Chen Zhenchian, Aragaki Masato, Kinoshita Tomonari, Effat Andrew, Yoshino Ichiro, Yasufuku Kazuhiro
Division of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, Canada.
Department of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
J Thorac Dis. 2022 Feb;14(2):238-246. doi: 10.21037/jtd-21-1242.
Current massive pulmonary embolism (PE) animal models use central venous access to deliver blood clots, which have features of random clot distribution and potentially fatal hemodynamic compromise. A clinically relevant preclinical model for generating pulmonary emboli in a more controlled fashion would be of value for a variety of research studies, including initial evaluation of novel therapeutic approaches. Endobronchial ultrasound-guided transbronchial needle injection (EBUS-TBNI) is a newly established approach for peri-tracheal/bronchial targets. The purpose of the present work was to establish a minimally invasive PE model in swine via a transbronchial approach.
In anesthetized Yorkshire pigs, a 21-G EBUS-guided transbronchial needle aspiration (EBUS-TBNA) needle was introduced into the pulmonary artery under EBUS guidance. Autologous blood clots were administered into the right and left lower pulmonary arteries sequentially (PE1 and PE2, respectively). Hemodynamic and biochemical responses were evaluated.
Ten pigs were evaluated; all 20 blood clots (6.3±1.9 mL) were successfully injected. After injection, mean pulmonary artery pressure (mPAP; mmHg) increased (baseline: 16.6±5.6 PE1: 24.5±7.6, P<0.0001 PE2: 26.9±6.7, P<0.0001), and a positive correlation was observed between clot volume and change in mPAP (PE1: r=0.69, P=0.025; PE1 + PE2: r=0.60, P=0.063). Mean arterial pressure (MAP; mmHg) (baseline: 57.5±5.1 PE1: 59.0±9.1, P=0.918 PE2: 60.9±9.6, P=0.664) remained stable. No complications were observed.
EBUS allows minimally invasive, precise, and reliable generation of pulmonary emboli in pigs. This model may serve as an important tool for new PE-related diagnostic and therapeutic research.
目前的大面积肺栓塞(PE)动物模型采用中心静脉通路来输送血栓,这些模型具有血栓分布随机和潜在致命性血流动力学损害的特点。一种以更可控方式生成肺栓塞的临床相关临床前模型对于包括新型治疗方法的初步评估在内的各种研究具有重要价值。支气管内超声引导下经支气管针注射(EBUS-TBNI)是一种针对气管周围/支气管靶点的新方法。本研究的目的是通过经支气管途径建立猪的微创PE模型。
在麻醉的约克夏猪中,在EBUS引导下将21G EBUS引导的经支气管针吸活检(EBUS-TBNA)针插入肺动脉。将自体血栓依次注入右、左下肺动脉(分别为PE1和PE2)。评估血流动力学和生化反应。
对10头猪进行了评估;所有20个血栓(6.3±1.9 mL)均成功注射。注射后,平均肺动脉压(mPAP;mmHg)升高(基线:16.6±5.6,PE1:24.5±7.6,P<0.0001;PE2:26.9±6.7,P<0.0001),并且观察到血栓体积与mPAP变化之间存在正相关(PE1:r=0.69,P=0.025;PE1+PE2:r=0.60,P=0.063)。平均动脉压(MAP;mmHg)(基线:57.5±5.1,PE1:59.0±9.1,P=0.918;PE2:60.9±9.6,P=0.664)保持稳定。未观察到并发症。
EBUS能够以微创、精确且可靠的方式在猪中生成肺栓塞。该模型可作为新的PE相关诊断和治疗研究的重要工具。