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dc.contributor.authorOkada, Hirokazuen
dc.contributor.authorUza, Norimitsuen
dc.contributor.authorMatsumori, Tomoakien
dc.contributor.authorYamazaki, Hajimeen
dc.contributor.authorYasuda, Munejien
dc.contributor.authorKuwada, Takeshien
dc.contributor.authorNishikawa, Yoshihiroen
dc.contributor.authorMaruno, Takahisaen
dc.contributor.authorShiokawa, Masahiroen
dc.contributor.authorTakai, Atsushien
dc.contributor.authorTakahashi, Kenen
dc.contributor.authorFukuda, Akihisaen
dc.contributor.authorHatano, Etsuroen
dc.contributor.authorMinamiguchi, Sachikoen
dc.contributor.authorSeno, Hiroshien
dc.date.accessioned2025-03-18T02:35:20Z-
dc.date.available2025-03-18T02:35:20Z-
dc.date.issued2025-03-
dc.identifier.urihttp://hdl.handle.net/2433/292550-
dc.description.abstractBackground/Aims: Pathological evaluation is crucial for diagnosing biliary lesions and determining appropriate treatment strategies. However, tissue sampling via the transpapillary route can be difficult. In this study, we aimed to assess the efficacy and safety of a novel tapered-tip sheath system for tissue sampling from biliary strictures. Methods: This single-center, randomized, parallel-group clinical trial included patients aged 20 to 85 years admitted to Kyoto University Hospital for biliary strictures. The patients were randomly assigned (1:1) to a new or conventional method group. The primary outcome was technical success of biopsy at the target bile duct using the assigned method, as determined in accordance with the intention-to-treat principle. Adverse events were assessed in all eligible patients. Results: Fifty-six patients were assessed for eligibility between September 2020 and March 2023; 50 patients were enrolled. The patients were randomly divided into the new (n=25) method group and the conventional (n=25) method group. Technical success was achieved in 96.0% (24/25) and 48.0% (12/25) of patients in the new and conventional method groups, respectively (risk ratio, 2.00; 95% confidence interval [CI], 1.32 to 3.03; risk difference, 48.0%; 95% CI, 27.0% to 69.0%; p<0.001). Adverse events occurred in 4.0% (1/25) and 36.0% (9/25) of patients in the new and conventional method groups, respectively (risk ratio, 0.11; 95% CI, 0.02 to 0.81; risk difference, –32.0%; 95% CI, –52.3% to –11.7%; p=0.005). Conclusions: The novel tapered-tip sheath system is a promising option for precisely and safely delivering biopsy forceps to target sites, thereby facilitating the diagnosis of biliary strictures.en
dc.language.isoeng-
dc.publisherThe Editorial Office of Gut and Liveren
dc.rightsThis is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0-
dc.subjectBile ductsen
dc.subjectBile duct neoplasmsen
dc.subjectBiopsyen
dc.subjectCholestasisen
dc.subjectIntention to treat analysisen
dc.titleEfficacy and Safety of a Novel Tapered-Tip Sheath System for Biliary-Lesion Tissue Sampling: A Randomized Controlled Trialen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleGut and liveren
dc.identifier.volume19-
dc.identifier.issue1-
dc.identifier.spage136-
dc.identifier.epage144-
dc.relation.doi10.5009/gnl240349-
dc.textversionpublisher-
dc.identifier.pmid39778881-
dcterms.accessRightsopen access-
dc.identifier.pissn1976-2283-
dc.identifier.eissn2005-1212-
出現コレクション:学術雑誌掲載論文等

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