Transluminal antegrade drill dilation technique for hepaticojejunostomy stricture with cholangioscopic evaluation (with video)

Author:

Kanadani Takafumi1,Ogura Takeshi2,Ueno Saori3,Okuda Atsushi4ORCID,Nishioka Nobu4,Nakamura Junichi1,Yamada Masanori5ORCID,Uba Yuki1,Tomita Mitsuki1,Hattori Nobuhiro2,Sakamoto Jun1,Nishikawa Hiroki1

Affiliation:

1. 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Takatsuki, Japan

2. 2nd Department of Internal Medicine, Osaka Medical College, Takatsuki-shi, Japan

3. 2nd Department of Internal Medicine, Osaka Medical College, Osaka, Japan

4. 2nd Department of Internal Medicine, Osaka Medical College, Takatsukishi, Japan

5. Endoscopic Center, Osaka Medical and Pharmaceutical University, Takatsuki, Japan

Abstract

Background and aim Balloon dilation and plastic stent deployment have been performed as hepaticojejunostomy stricture (HJS) treatment techniques by EUS guidance. Although these techniques have shown favorable clinical results, the treatment period can be long because stent deployment is required. In addition, HJS may recur even after treatment because the scar tissue itself remains. To overcome these challenges, we developed an EUS-guided antegrade drill dilation technique for treating HJS. The aim of this study was to evaluate the technical feasibility and safety of this technique in terms of the pre- and post-cholangioscopic findings. Method This retrospective study included consecutive patients who were complicated with symptomatic 22 HJS between November 2022 and February 2023. Transluminal antegrade drill dilation (TAD) using a novel drill dilator was attempted within 14 days after EUS-HGS. HJS was diagnosed by cholangioscopy before TAD, and resolution was evaluated after TAD using cholangioscopy. Result TAD was attempted at around 11 days after EUS-HGS. The cholangioscope was inserted successfully in all patients after this procedure. Cholangioscopy revealed stricture without evidence of malignancy in 19 patients. In the remaining three patients, stricture was not observed and these patients underwent stent exchange rather than TAD. Among the 19 patients, passage of the guidewire across the HJS into the intestine was unsuccessful in 4 patients, and the technical success rate of this procedure was 78.9%. TAD was successful in all 15 patients in whom passage of the guidewire was achieved. Conclusions In conclusion, TAD appears to be technically feasible and safe.

Publisher

Georg Thieme Verlag KG

Subject

Obstetrics and Gynecology

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