Takano Yuichi, Tamai Naoki, Yamawaki Masataka, Noda Jun, Azami Tetsushi, Niiya Fumitaka, Nishimoto Fumiya, Maruoka Naotaka, Yamagami Tatsuya, Nagahama Masatsugu
Division of Gastroenterology, Department of Internal Medicine, Showa University Fujigaoka Hospital, Yokohama, Japan.
Showa Daigaku Fujigaoka Byoin, Yokohama, Japan.
Endosc Int Open. 2024 Nov 18;12(11):E1309-E1314. doi: 10.1055/a-2427-2427. eCollection 2024 Nov.
In patients with ascites, percutaneous liver biopsy is generally contraindicated. Because endoscopic ultrasound-guided tissue acquisition (EUS-TA) allows tissue sample obtention from the digestive tract lumen, a biopsy without the intervention of ascites may prevent adverse events (AEs). This study aimed to evaluate the safety of EUS-TA for focal liver lesions in the presence of ascites. A retrospective study was conducted using medical records of cases in which EUS-TA was performed on focal liver lesions between 2016 and 2022. Study participants were classified into two groups: those with ascites and those without it, and the outcomes were compared. The primary outcome was AEs. We included 109 cases of EUS-TA for focal liver lesions. Ascites was present in 20.1% of cases (22/109) and absent in 79.8% of cases (87/109). There were no significant differences between the two groups in clinical backgrounds and EUS-TA procedure, although fine-needle biopsy needles were significantly more frequently used in patients without ascites. In the ascites group, puncture without intervening ascites was successful in 90.9% of cases (20/22). The incidence of AEs was 4.5% (1/22) in the ascites group and 1.1% (1/87) in the non-ascites group, showing no significant difference. The two AEs were mild self-limiting abdominal pain. In focal liver lesions with ascites, EUS-TA allows biopsy without the intervention of ascites in most cases. The incidence of AEs did not differ significantly between patients with and without ascites.
对于腹水患者,经皮肝活检通常是禁忌的。由于内镜超声引导下组织获取(EUS-TA)可从消化道管腔获取组织样本,无需腹水干预的活检可能会预防不良事件(AE)。本研究旨在评估在存在腹水的情况下,EUS-TA对肝脏局灶性病变的安全性。使用2016年至2022年期间对肝脏局灶性病变进行EUS-TA的病例的医疗记录进行了一项回顾性研究。研究参与者分为两组:有腹水组和无腹水组,并比较了结果。主要结局是不良事件。我们纳入了109例肝脏局灶性病变的EUS-TA病例。20.1%的病例(22/109)存在腹水,79.8%的病例(87/109)无腹水。两组在临床背景和EUS-TA操作方面无显著差异,尽管无腹水患者更频繁地使用细针活检针。在腹水组中,90.9%的病例(20/22)成功在不干预腹水的情况下进行了穿刺。腹水组的不良事件发生率为4.5%(1/22),无腹水组为1.1%(1/87),无显著差异。这两例不良事件均为轻度自限性腹痛。在伴有腹水的肝脏局灶性病变中,EUS-TA在大多数情况下可在不干预腹水的情况下进行活检。有腹水和无腹水患者的不良事件发生率无显著差异。