Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/32799
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dc.contributor.authorRosella, Sam-
dc.contributor.authorZorron Cheng Tao Pu, Leo-
dc.contributor.authorNg, Jonathan-
dc.contributor.authorBe, Kim Hay-
dc.contributor.authorVaughan, Rhys B-
dc.contributor.authorChandran, Sujievvan-
dc.contributor.authorEfthymiou, Marios-
dc.date2023-
dc.date.accessioned2023-05-10T23:23:28Z-
dc.date.available2023-05-10T23:23:28Z-
dc.date.issued2023-04-
dc.identifier.citationJGH Open : an Open Access Journal of Gastroenterology and Hepatology 2023; 7(4)en_US
dc.identifier.issn2397-9070-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/32799-
dc.description.abstractObtaining endoscopic biopsies from the ampulla of Vater is important for the diagnosis of lesions that are suspicious for neoplasia. The clinical safety profile is not well defined in the literature. Our aim was to evaluate the procedure-related readmission rate and complications from ampullary biopsy in patients undergoing duodenoscopy and endoscopic retrograde cholangiopancreatography (ERCP). A retrospective data analysis was performed on adult patients at Austin Hospital who underwent ampullary biopsies between 1 January 2010 and 1 March 12022. Medical records were identified using pathology databases. The electronic health record was reviewed for baseline characteristics including demographics, date, indication for ampullary biopsy, procedure type (duodenoscopy or ERCP), and procedural associated interventions during ERCP. Readmissions to the Austin Emergency Department within 30 days following the biopsy were identified, and complications were noted. A total of 506 records were reviewed and 246 episodes of ampullary biopsy met the inclusion criteria. The procedure-related readmission rate for all episodes was 6.1%, which included pain (3.3%), pancreatitis (2.0%), cholangitis (1.6%), and bleeding (0.8%). Ampullary biopsies with ERCP had a procedure-related readmission rate of 8.4%, whereas ampullary biopsies without ERCP had a rate of 2.2%. Increased readmissions and complications were associated with male sex (P = 0.01 and P = 0.05, respectively). There was no association between the number of biopsies taken and complications. Performing an ampullary biopsy without an associated ERCP carries a low rate of clinical complications and procedure-related readmissions. The combination of ERCP and ampullary biopsy increases the risk four-fold.en_US
dc.language.isoeng-
dc.subjectampulla of Vateren_US
dc.subjectampullary biopsyen_US
dc.subjectcomplication rateen_US
dc.subjectduodenoscopyen_US
dc.subjectendoscopic retrograde cholangiopancreatographyen_US
dc.subjectreadmission rateen_US
dc.titleReadmission rate and complications following biopsy of the ampulla of Vater-A retrospective data analysis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJGH Open : an Open Access Journal of Gastroenterology and Hepatologyen_US
dc.identifier.affiliationMedicine, Dentistry and Health Sciences University of Melbourne Parkville Victoria Australia.en_US
dc.identifier.affiliationGastroenterology and Hepatologyen_US
dc.identifier.affiliationMedicine, Dentistry and Health Sciences University of Melbourne Parkville Victoria Australia.en_US
dc.identifier.affiliationMedicine, Dentistry and Health Sciences University of Melbourne Parkville Victoria Australia.;Department of Gastroenterology and Hepatology Austin Health Melbourne Victoria Australia.;Department of Medicine Monash University, Peninsula Health Campus Frankston Victoria Australia.en_US
dc.identifier.doi10.1002/jgh3.12895en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-8481-9376en_US
dc.identifier.orcid0000-0003-0792-3265en_US
dc.identifier.pubmedid37125251-
dc.description.volume7-
dc.description.issue4-
dc.description.startpage299-
dc.description.endpage304-
local.name.researcherChandran, Sujievvan
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.grantfulltextnone-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptGastroenterology and Hepatology-
crisitem.author.deptGastroenterology and Hepatology-
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