Utility of dedicated bougie dilator for a 0.018-inch guidewire during EUS-guided biliary drainage: A multi-center retrospective cohort study.


Journal

Journal of hepato-biliary-pancreatic sciences
ISSN: 1868-6982
Titre abrégé: J Hepatobiliary Pancreat Sci
Pays: Japan
ID NLM: 101528587

Informations de publication

Date de publication:
Jul 2022
Historique:
revised: 04 06 2021
received: 12 04 2021
accepted: 08 07 2021
pubmed: 18 7 2021
medline: 26 7 2022
entrez: 17 7 2021
Statut: ppublish

Résumé

During endoscopic ultrasound-guided biliary drainage (EUS-BD), a combination of a 19-gauge needle and a 0.025-inch guidewire is generally used. However, a 19-gauge needle has poor maneuverability because of their stiffness and rigidity and might have poor penetrability in non-dilated bile ducts because of their large bore. In contrast, the application of a 22-gauge needle is expected to have improved maneuverability. However, only a 0.018-inch guidewire, which has less supportability, is applicable in the subsequent guidewire selection. This study aimed to evaluate the feasibility and safety of a dedicated bougie dilator for a 0.018-inch guidewire. From September 2019 to May 2020, 26 patients underwent fistula dilation using the dilator after accessing the bile duct using a 22-gauge needle and a 0.018-inch guidewire during EUS-BD. The success and adverse event rates of EUS-BD were evaluated. Biliary access with a combination of a 22-gauge needle and a 0.018-inch guidewire was successful in all with a median bile duct diameter of 5 mm. Dilation of the fistula using the dedicated dilator was also successful in all cases. Subsequently, the dilator was successfully exchanged to an ERCP catheter that allowed for exchange to a 0.025-inch guidewire, except in one case where the catheter did not cross the fistula and a dilation balloon was inserted for an exchange to a 0.025-inch guidewire. The technical success rate of the EUS-BD was 100%. The adverse event rate was 19%. The application of the dedicated dilator for a 0.018-inch guidewire was considered feasible and safe for EUS-BD.

Sections du résumé

BACKGROUND BACKGROUND
During endoscopic ultrasound-guided biliary drainage (EUS-BD), a combination of a 19-gauge needle and a 0.025-inch guidewire is generally used. However, a 19-gauge needle has poor maneuverability because of their stiffness and rigidity and might have poor penetrability in non-dilated bile ducts because of their large bore. In contrast, the application of a 22-gauge needle is expected to have improved maneuverability. However, only a 0.018-inch guidewire, which has less supportability, is applicable in the subsequent guidewire selection. This study aimed to evaluate the feasibility and safety of a dedicated bougie dilator for a 0.018-inch guidewire.
METHODS METHODS
From September 2019 to May 2020, 26 patients underwent fistula dilation using the dilator after accessing the bile duct using a 22-gauge needle and a 0.018-inch guidewire during EUS-BD. The success and adverse event rates of EUS-BD were evaluated.
RESULTS RESULTS
Biliary access with a combination of a 22-gauge needle and a 0.018-inch guidewire was successful in all with a median bile duct diameter of 5 mm. Dilation of the fistula using the dedicated dilator was also successful in all cases. Subsequently, the dilator was successfully exchanged to an ERCP catheter that allowed for exchange to a 0.025-inch guidewire, except in one case where the catheter did not cross the fistula and a dilation balloon was inserted for an exchange to a 0.025-inch guidewire. The technical success rate of the EUS-BD was 100%. The adverse event rate was 19%.
CONCLUSION CONCLUSIONS
The application of the dedicated dilator for a 0.018-inch guidewire was considered feasible and safe for EUS-BD.

Identifiants

pubmed: 34272831
doi: 10.1002/jhbp.1021
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

810-816

Informations de copyright

© 2021 Japanese Society of Hepato-Biliary-Pancreatic Surgery.

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Auteurs

Takuji Iwashita (T)

First Department of Internal Medicine, Gifu University Hospital, Gifu, Japan.

Takeshi Ogura (T)

Second Department of Internal Medicine, Osaka Medical College, Osaka, Japan.

Hirotoshi Ishiwatari (H)

Division of Endoscopy, Shizuoka Cancer Center, Shizuoka, Japan.

Yousuke Nakai (Y)

Department of Endoscopy and Endoscopic Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Keisuke Iwata (K)

Department of Gastroenterology, Gifu Prefectural General Medical Center, Gifu, Japan.

Tsuyoshi Mukai (T)

Department of Gastroenterology, Gifu Municipal Hospital, Gifu, Japan.

Masahito Shimizu (M)

First Department of Internal Medicine, Gifu University Hospital, Gifu, Japan.

Hiroyuki Isayama (H)

Department of Gastroenterology, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Ichiro Yasuda (I)

Third Department of Internal Medicine, University of Toyama, Toyama, Japan.

Takao Itoi (T)

Department of Gastroenterology and Hepatology, Tokyo Medical University, Tokyo, Japan.

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