Endoscopy 2013; 45(05): 362-369
DOI: 10.1055/s-0032-1326225
Original article
© Georg Thieme Verlag KG Stuttgart · New York

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

S. Doi
1   First Department of Internal Medicine, Gifu University Hospital, Gifu, Japan
,
I. Yasuda
1   First Department of Internal Medicine, Gifu University Hospital, Gifu, Japan
,
H. Kawakami
2   Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan
,
T. Hayashi
3   Fourth Department of Internal Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan
,
H. Hisai
4   Department of Gastroenterology, Japan Red Cross Date General Hospital, Date, Japan
,
A. Irisawa
5   Department of Gastroenterology, Fukushima Medical University Hospital, Fukushima, Japan
,
T. Mukai
6   Department of Gastroenterology, Gifu Municipal Hospital, Gifu, Japan
,
A. Katanuma
7   Center for Gastroenterology, Teine-Keijinkai Hospital, Sapporo, Japan
,
K. Kubota
8   Division of Gastroenterology, Yokohama City University Graduate School of Medicine, Yokohama, Japan
,
T. Ohnishi
9   Department of Gastroenterology, Gifu Prefectural General Medical Center, Gifu, Japan
,
S. Ryozawa
10   Digestive Disease Center, Showa University Northern Yokohama Hospital, Yokohama, Japan
,
K. Hara
11   Department of Gastroenterology, Aichi Cancer Center Hospital, Nagoya, Japan
,
T. Itoi
12   Department of Gastroenterology and Hepatology, Tokyo Medical University, Tokyo, Japan
,
K. Hanada
13   Center for Gastroendoscopy, Onomichi General Hospital, Onomichi, Japan, Japan
,
K. Yamao
11   Department of Gastroenterology, Aichi Cancer Center Hospital, Nagoya, Japan
› Author Affiliations
Further Information

Publication History

submitted 08 August 2012

accepted after revision 11 December 2012

Publication Date:
24 April 2013 (online)

Preview

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)