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Venovenous bypass in adult liver transplant recipients: A single-center observational case series

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dc.contributor.authorWeinberg, Laurence-
dc.contributor.authorCaragata, Rebecca-
dc.contributor.authorHazard, Riley-
dc.contributor.authorLudski, Jarryd-
dc.contributor.authorLee, Dong-Kyu-
dc.contributor.authorSlifirski, Hugh-
dc.contributor.authorNugraha, Patrick-
dc.contributor.authorDo, Daniel-
dc.contributor.authorZhang, Wendell-
dc.contributor.authorNicolae, Robert-
dc.contributor.authorKaldas, Peter-
dc.contributor.authorFink, Michael A.-
dc.contributor.authorPerini, Marcos V.-
dc.date.accessioned2024-08-08T13:00:36Z-
dc.date.available2024-08-08T13:00:36Z-
dc.date.issued2024-05-
dc.identifier.issn1932-6203-
dc.identifier.issn1932-6203-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/22281-
dc.description.abstractBackground Very little information is currently available on the use and outcomes of venovenous bypass (VVB) in liver transplantation (LT) in adults in Australia. In this study, we explored the indications, intraoperative course, and postoperative outcomes of patients who underwent VVB in a high-volume LT unit. Methods The study was a single-center, retrospective observational case series of adult patients who underwent VVB during LT at Austin Health in Melbourne, Australia between March 2008 and March 2022. Information on baseline preoperative status and intraoperative variables, including specific VVB characteristics as well as postoperative and VVB-related complications was collected. The lengths of intensive care unit and hospital stays as well as intraoperative and in-hospital mortality were recorded. Results Of the 900 LTs performed at this center during the aforementioned 14-year period, 27 (3%) included a VVB procedure. VVB was performed electively in 16 of these 27 patients (59.3%) and as a rescue technique to control massive bleeding in the other 11 (40.1%). The median (interquartile range [IQR]) age of those who underwent VVB procedures was 48 (39–55) years; the median age was 56 (47–62) years in the non-VVB group (p<0.0001). The median model for end-stage liver disease (MELD) scores were similar between the two patient groups. Complete blood data was available for 622 non-VVB patients. Twenty-six VVB (96.3%) and 603 non-VVB (96.9%) patients required intraoperative blood transfusions. The median (IQR) number of units of packed red blood cells transfused was 7 (4.8–12.5) units in the VVB group compared to 3.0 units (1.0–6.0) in the non-VVB group (p<0.0001). Inpatient mortality was 18.5% and 1.1% for the VVB and non-VVB groups, respectively (p<0.0001). There were no significant differences in length of hospital stay or incidence of acute kidney injury, primary graft dysfunction, or long-term graft failure between the two groups. Patients in the VVB group experienced a higher rate of postoperative non-anastomotic biliary stricture compared to patients in the non-VVB group (33% and 7.9%, respectively; p = 0.0003). Conclusions VVB continues to play a vital role in LT. This case series highlights the heightened risk of major complications linked to VVB. However, the global transition to selective use of VVB underscores the urgent need for collaborative multi-center studies designed to address outstanding questions and parameters related to the safe implementation of this procedure. © 2024 Weinberg et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.-
dc.format.extent16-
dc.language영어-
dc.language.isoENG-
dc.publisherPublic Library of Science-
dc.titleVenovenous bypass in adult liver transplant recipients: A single-center observational case series-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1371/journal.pone.0303631-
dc.identifier.scopusid2-s2.0-85195004035-
dc.identifier.wosid001237119600148-
dc.identifier.bibliographicCitationPLoS ONE, v.19, no.5, pp 1 - 16-
dc.citation.titlePLoS ONE-
dc.citation.volume19-
dc.citation.number5-
dc.citation.startPage1-
dc.citation.endPage16-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusTEMPORARY PORTACAVAL-SHUNT-
dc.subject.keywordPlusVENA-CAVA PRESERVATION-
dc.subject.keywordPlusVENOUS BYPASS-
dc.subject.keywordPlusSELECTIVE USE-
dc.subject.keywordPlusPIGGYBACK-
dc.subject.keywordPlusCOMPLICATIONS-
dc.subject.keywordPlusREQUIREMENTS-
dc.subject.keywordPlusTRANSFUSION-
dc.subject.keywordPlusADVANTAGES-
dc.subject.keywordPlusCANNULA-
dc.subject.keywordAuthorFentanyl-
dc.subject.keywordAuthorIsoflurane-
dc.subject.keywordAuthorMidazolam-
dc.subject.keywordAuthorPropofol-
dc.subject.keywordAuthorSevoflurane-
dc.subject.keywordAuthorTranexamic Acid-
dc.subject.keywordAuthorGraphpad Prism Version 10.2.2-
dc.subject.keywordAuthorFentanyl-
dc.subject.keywordAuthorIsoflurane-
dc.subject.keywordAuthorMidazolam-
dc.subject.keywordAuthorPropofol-
dc.subject.keywordAuthorSevoflurane-
dc.subject.keywordAuthorTranexamic Acid-
dc.subject.keywordAuthorAdult-
dc.subject.keywordAuthorAged-
dc.subject.keywordAuthorAll Cause Mortality-
dc.subject.keywordAuthorArticle-
dc.subject.keywordAuthorAxillary Vein-
dc.subject.keywordAuthorBlood Clotting Time-
dc.subject.keywordAuthorBlood Transfusion-
dc.subject.keywordAuthorBody Mass-
dc.subject.keywordAuthorCase Study-
dc.subject.keywordAuthorClinical Outcome-
dc.subject.keywordAuthorClinical Trial-
dc.subject.keywordAuthorData Analysis-
dc.subject.keywordAuthorEchocardiography-
dc.subject.keywordAuthorElectronic Medical Record-
dc.subject.keywordAuthorElectronic Medical Record System-
dc.subject.keywordAuthorGraft Recipient-
dc.subject.keywordAuthorHematothorax-
dc.subject.keywordAuthorHepatectomy-
dc.subject.keywordAuthorHospital Mortality-
dc.subject.keywordAuthorHospitalization-
dc.subject.keywordAuthorHuman-
dc.subject.keywordAuthorHypoxia-
dc.subject.keywordAuthorIn-hospital Mortality-
dc.subject.keywordAuthorIntensive Care Unit-
dc.subject.keywordAuthorKidney Transplantation-
dc.subject.keywordAuthorLength Of Stay-
dc.subject.keywordAuthorLiver Graft-
dc.subject.keywordAuthorLiver Transplantation-
dc.subject.keywordAuthorMiddle Aged-
dc.subject.keywordAuthorMortality-
dc.subject.keywordAuthorObservational Study-
dc.subject.keywordAuthorOutcome Assessment-
dc.subject.keywordAuthorPerioperative Period-
dc.subject.keywordAuthorPostoperative Care-
dc.subject.keywordAuthorPostoperative Period-
dc.subject.keywordAuthorPrevalence-
dc.subject.keywordAuthorRetrospective Study-
dc.subject.keywordAuthorTransesophageal Echocardiography-
dc.subject.keywordAuthorVascular Access-
dc.subject.keywordAuthorVein Bypass-
dc.subject.keywordAuthorVenovenous Bypass-
dc.subject.keywordAuthorAdverse Event-
dc.subject.keywordAuthorAustralia-
dc.subject.keywordAuthorEpidemiology-
dc.subject.keywordAuthorEtiology-
dc.subject.keywordAuthorFemale-
dc.subject.keywordAuthorMale-
dc.subject.keywordAuthorPostoperative Complication-
dc.subject.keywordAuthorAdult-
dc.subject.keywordAuthorFemale-
dc.subject.keywordAuthorHospital Mortality-
dc.subject.keywordAuthorHumans-
dc.subject.keywordAuthorLength Of Stay-
dc.subject.keywordAuthorLiver Transplantation-
dc.subject.keywordAuthorMale-
dc.subject.keywordAuthorMiddle Aged-
dc.subject.keywordAuthorPostoperative Complications-
dc.subject.keywordAuthorRetrospective Studies-
dc.subject.keywordAuthorTransplant Recipients-
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