Cited 9 times in
Preclinical evaluation of endoscopic placement of a steroid-eluting metal stent in an in vivo porcine benign biliary stricture model
DC Field | Value | Language |
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dc.contributor.author | 남지해 | - |
dc.contributor.author | 이동기 | - |
dc.contributor.author | 장성일 | - |
dc.contributor.author | 조재희 | - |
dc.contributor.author | 황성순 | - |
dc.contributor.author | 도민영 | - |
dc.date.accessioned | 2022-07-08T03:04:54Z | - |
dc.date.available | 2022-07-08T03:04:54Z | - |
dc.date.issued | 2022-05 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/188653 | - |
dc.description.abstract | Treatment of benign biliary strictures (BBS) using fully covered self-expandable metal stents (FCSEMS) has a high success rate, but recurrence can occur. Corticosteroids may be useful based on their anti-fibrotic and anti-inflammatory effects. We investigated the safety and efficacy of corticosteroid-eluting FCSEMS in an animal model. BBSs were created by radiofrequency ablation in 12 mini-pigs. Four weeks later, FCSEMS coated with 0 mg (control), 15 mg (steroid 1 × group), or 30 mg (steroid 2 × group) triamcinolone were inserted endoscopically. The in vitro drug release assay revealed that the optimal stent had 15 mg of triamcinolone and a hydrophilic membrane. No transmural necrosis or perforation occurred in any animal. Fibrous wall thickness tended to decrease macroscopically and microscopically in a triamcinolone dose-dependent manner (control vs. steroid 2 × group: 773.1 vs. 468.5 µm, P = 0.037). Thickness also decreased over time in the steroid 2 × group (3 days vs. 4 weeks: 907.9 vs. 468.5 µm, P = 0.025). Blood parameters tended to improve after stent insertion. In a porcine BBS model, steroid-eluting FCSEMS showed potential as a safe and effective treatment modality to reduce fibrotic tissue. Studies are required to confirm their safety and efficacy in humans with refractory BBS. | - |
dc.description.statementOfResponsibility | open | - |
dc.format | application/pdf | - |
dc.language | English | - |
dc.publisher | Nature Publishing Group | - |
dc.relation.isPartOf | SCIENTIFIC REPORTS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Cholangiopancreatography, Endoscopic Retrograde* | - |
dc.subject.MESH | Cholestasis* / therapy | - |
dc.subject.MESH | Constriction, Pathologic / surgery | - |
dc.subject.MESH | Device Removal | - |
dc.subject.MESH | Stents / adverse effects | - |
dc.subject.MESH | Steroids | - |
dc.subject.MESH | Swine | - |
dc.subject.MESH | Swine, Miniature | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Triamcinolone | - |
dc.title | Preclinical evaluation of endoscopic placement of a steroid-eluting metal stent in an in vivo porcine benign biliary stricture model | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Pathology (병리학교실) | - |
dc.contributor.googleauthor | Sung Ill Jang | - |
dc.contributor.googleauthor | Sungsoon Fang | - |
dc.contributor.googleauthor | Ji Hae Nahm | - |
dc.contributor.googleauthor | Jae Hee Cho | - |
dc.contributor.googleauthor | Min Young Do | - |
dc.contributor.googleauthor | Su Yeon Lee | - |
dc.contributor.googleauthor | Seok Jeong | - |
dc.contributor.googleauthor | Don Haeng Lee | - |
dc.contributor.googleauthor | Dong Ki Lee | - |
dc.identifier.doi | 10.1038/s41598-022-12957-0 | - |
dc.contributor.localId | A05120 | - |
dc.contributor.localId | A02723 | - |
dc.contributor.localId | A03441 | - |
dc.contributor.localId | A03902 | - |
dc.contributor.localId | A05443 | - |
dc.relation.journalcode | J02646 | - |
dc.identifier.eissn | 2045-2322 | - |
dc.identifier.pmid | 35614115 | - |
dc.contributor.alternativeName | Nahm, Ji Hae | - |
dc.contributor.affiliatedAuthor | 남지해 | - |
dc.contributor.affiliatedAuthor | 이동기 | - |
dc.contributor.affiliatedAuthor | 장성일 | - |
dc.contributor.affiliatedAuthor | 조재희 | - |
dc.contributor.affiliatedAuthor | 황성순 | - |
dc.citation.volume | 12 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 8864 | - |
dc.identifier.bibliographicCitation | SCIENTIFIC REPORTS, Vol.12(1) : 8864, 2022-05 | - |
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