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Endoscopic ultrasound-guided celiac ganglia neurolysis vsceliac plexus neurolysis: A randomized multicenter trial

机译:内镜超声引导下的腹腔神经节神经溶解与神经丛神经溶解:一项随机的多中心试验

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Background and study aims: No prospective comparison of endoscopic ultrasonography-guided direct celiac ganglia neurolysis (EUS - CGN) vs. EUS-guided celiac plexus neurolysis (EUS - CPN) has been reported. The aim of the current study was to compare the effectiveness of EUS - CGN and EUS - CPN in providing pain relief from upper abdominal cancer pain in a multicenter randomized controlled trial. Patients and methods: Patients with upper abdominal cancer pain were randomly assigned to treatment using either EUS - CGN or EUS - CPN. Evaluation was performed at Day 7 postoperatively using a pain scale of 0 to 10. Patients for whom pain decreased to ≤ 3 were considered to have a positive response, and those experiencing a decrease in pain to ≤ 1 were considered to be completely responsive. Comparison between the two groups was performed using intention-to-treat analysis. The primary endpoint was the difference in treatment response rates between EUS - CGN and EUS - CPN at postoperative Day 7. Secondary endpoints included differences in complete response rates, pain scores, duration of pain relief, and incidence of adverse effects. Results: A total of 34 patients were assigned to each group. Visualization of ganglia was possible in 30 cases (88 %) in the EUS - CGN group. The positive response rate was significantly higher in the EUS - CGN group (73.5 %) than in the EUS - CPN group (45.5 %; P = 0.026). The complete response rate was also significantly higher in the EUS - CGN group (50.0 %) than in the EUS - CPN group (18.2 %; P = 0.010). There was no difference in adverse events or duration of pain relief between the two groups. Conclusions: EUS - CGN is significantly superior to conventional EUS - CPN in cancer pain relief. Clinical trial registration: http://www.umin.ac.jp/ctr/index.htm (ID: UMIN-000002536).
机译:背景和研究目的:尚无内镜超声引导下的直接腹腔神经节神经溶解(EUS-CGN)与EUS引导的腹腔神经丛神经溶解(EUS-CPN)的前瞻性比较。本研究的目的是在多中心随机对照试验中比较EUS-CGN和EUS-CPN在缓解上腹部癌痛方面的有效性。患者和方法:上腹部癌痛患者被随机分配使用EUS-CGN或EUS-CPN治疗。术后第7天以0到10的疼痛评分进行评估。疼痛降低至≤3的患者被视为阳性,而疼痛降低至≤1的患者被认为是完全缓解。两组之间的比较使用意向性治疗进行。主要终点是术后第7天EUS-CGN和EUS-CPN之间的治疗缓解率差异。次要终点包括完全缓解率,疼痛评分,缓解疼痛的持续时间以及不良反应发生率的差异。结果:每组共分配34名患者。在EUS-CGN组中,有30例(88%)的神经节可视化。 EUS-CGN组的阳性反应率(73.5%)明显高于EUS-CPN组的45.5%; P = 0.026。 EUS-CGN组的完全缓解率(50.0%)也比EUS-CPN组的完全缓解率(18.2%; P = 0.010)。两组之间的不良事件或疼痛缓解时间无差异。结论:EUS-CGN在缓解癌症疼痛方面显着优于常规EUS-CPN。临床试验注册:http://www.umin.ac.jp/ctr/index.htm(ID:UMIN-000002536)。

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