Endoscopic ultrasound-guided celiac ganglia neurolysis vs. celiac plexus neurolysis: a randomized multicenter trial

被引:86
|
作者
Doi, S. [1 ]
Yasuda, I. [1 ]
Kawakami, H. [2 ]
Hayashi, T. [3 ]
Hisai, H. [4 ]
Irisawa, A. [5 ]
Mukai, T. [6 ]
Katanuma, A. [7 ]
Kubota, K. [8 ]
Ohnishi, T. [9 ]
Ryozawa, S. [10 ]
Hara, K. [11 ]
Itoi, T. [12 ]
Hanada, K. [13 ]
Yamao, K. [11 ]
机构
[1] Gifu Univ Hosp, Dept Internal Med 1, Gifu 5011194, Japan
[2] Hokkaido Univ, Dept Gastroenterol & Hepatol, Grad Sch Med, Sapporo, Hokkaido, Japan
[3] Sapporo Med Univ, Sch Med, Dept Internal Med 4, Sapporo, Hokkaido, Japan
[4] Japan Red Cross Date Gen Hosp, Dept Gastroenterol, Date, Japan
[5] Fukushima Med Univ Hosp, Dept Gastroenterol, Fukushima, Japan
[6] Gifu Municipal Hosp, Dept Gastroenterol, Gifu, Japan
[7] Teine Keijinkai Hosp, Ctr Gastroenterol, Sapporo, Hokkaido, Japan
[8] Yokohama City Univ, Div Gastroenterol, Grad Sch Med, Yokohama, Kanagawa 232, Japan
[9] Gifu Prefectural Gen Med Ctr, Dept Gastroenterol, Gifu, Japan
[10] Showa Univ, Northern Yokohama Hosp, Ctr Digest Dis, Yokohama, Kanagawa, Japan
[11] Aichi Canc Ctr Hosp, Dept Gastroenterol, Nagoya, Aichi 464, Japan
[12] Tokyo Med Univ, Dept Gastroenterol & Hepatol, Tokyo 1608402, Japan
[13] Onomichi Gen Hosp, Ctr Gastroendoscopy, Onomichi, Japan
关键词
PAIN RELIEF; CANCER PAIN; BLOCK; VISUALIZATION;
D O I
10.1055/s-0032-1326225
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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)
引用
收藏
页码:362 / 369
页数:8
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