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EUS-guided biliary drainage with a novel electrocautery-enhanced lumen apposing metal stent as first approach for distal malignant biliary obstruction: a prospective studyopen access

Authors
Mangiavillano, BenedettoMoon, Jong HoFacciorusso, AntonioDi Matteo, FrancescoPaduano, DaniloBulajic, MilutinOfosu, AndrewAuriemma, FrancescoLamonaca, LauraYoo, Hae WonRea, RobertaMassidda, MarcoRepici, Alessandro
Issue Date
Jul-2022
Publisher
Thieme Medical Publishers
Citation
Endoscopy International Open, v.10, no.07, pp E998 - E1003
Journal Title
Endoscopy International Open
Volume
10
Number
07
Start Page
E998
End Page
E1003
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/21822
DOI
10.1055/a-1838-2683
ISSN
2196-9736
Abstract
Background and study aims Endoscopic retrograde cholangiopancreatography (ERCP) represents the gold standard for jaundice palliation in malignant biliary obstruction (MBO) patients. Biliary drainage using electrocautery lumen apposing metal stent (EC-LAMS) is currently a well-established procedure when ERCP fails. We aimed to assess the technical and clinical success of a new EC-LAMS as the first approach to the palliation of malignant jaundice due to MBO in patients unfit for surgery. Patients and methods Twenty-five consecutive patients undergoing endoscopic-guided biliary drainage with the new EC-LAMS were prospectively enrolled. Clinical success was defined as bilirubin level decrease >15% 24 hours after EC-LAMS placement. Results Mean age was 76.6 +/- 11.56 years, and male patients were 10 (40%). EC-LAMS placement was technically feasible in 24 patients (96%) and clinical success rate was 100%. Only one patient (4%) experienced a misplacement rescued by an immediate second EC-LAMS placement. The mean duration of hospital stay was 4.66 +/- 4.22 days. The median overall survival was 7 months (95% CI 1-7). Conclusions In this preliminary study, the new EC-LAMS seems to allow a single-step palliative endoscopic therapy in patients affected by jaundice due to MBO, with high technical and clinical success and low adverse events. Further large prospective studies are warranted to validate these results.
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