Gelişmiş Arama

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dc.contributor.authorAnilir E.
dc.contributor.authorOral A.
dc.contributor.authorSahin T.
dc.contributor.authorTurker F.
dc.contributor.authorYuzer Y.
dc.contributor.authorTokat Y.
dc.date.accessioned2024-02-04T13:30:16Z
dc.date.available2024-02-04T13:30:16Z
dc.date.issued2023
dc.identifier.issn21484902
dc.identifier.urihttps://doi.org/10.14744/NCI.2023.49354
dc.identifier.urihttp://hdl.handle.net/11446/4880
dc.description.abstractOBJECTIVE: Factor 2 and Factor 5 mutations are among the most common procoagulant genetic disorders and are routinely evaluated in donor preparation. Homozygous mutations are contraindicated for surgery, but heterozygous mutations cannot be said to be an impediment. We aimed to investigate the effect of heterozygous gene mutation of F2 and/or F5 on complications. METHODS: In our study, 210 living liver donors were examined. The available data of Factor 2 and 5 heterozygous positive donors were evaluated in terms of 21 donor patients and 30 liver recipients. The heterozygous positive group and the control group were statistically compared in terms of age, gender, length of hospital stay, post-operative deep vein thrombosis, pulmonary embolism, portal vein thrombosis, bile duct stenosis and bile leakage complications, lung infection and atelectasis, and wound infection. In addition, these patients were statistically compared in terms of laboratory tests. In addition, complications in recipients implanted with mutant grafts were evaluated statistically and numerically. RESULTS: Hospital staying was longer statistically in the donor group with heterozygous mutations than in the control group. Hemoglobin and albumin blood levels were lower (p=0.031, p=0.016); INR and ALT levels were higher (p=0.005, p=0.047) statistically in the control group than in the donor group with heterozygous mutations. There was no statistically significant dif-ference between heterozygous mutant groups in terms of biliary tract complications and hepatic vessel thrombosis in recipients. CONCLUSION: Considering the longer hospital stay in the presence of these mutations, the increased need for treatment in this process and the close follow-up of liver functions should be considered. © 2023 by Istanbul Provincial Directorate of Health.en_US
dc.language.isoengen_US
dc.publisherKare Publishingen_US
dc.relation.ispartofNorthern Clinics of Istanbulen_US
dc.identifier.doi10.14744/NCI.2023.49354
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFactor 2en_US
dc.subjectFactor 5en_US
dc.subjectheterozygousen_US
dc.subjectliveren_US
dc.subjectmutationen_US
dc.subjecttransplanten_US
dc.titleFactor 5 and Factor 2 heterozygous positivity and complications in living donor liver transplant donorsen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue5en_US
dc.identifier.volume10en_US
dc.identifier.startpage550en_US
dc.identifier.endpage555en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempAnilir, E., Liver Transplantation Center, Demiroglu Bilim University Group, Florence Nightingale Hospitals, Istanbul, Turkey; Oral, A., Department of Internal Medicine, Demiroglu Bilim University Group, Florence Nightingale Hospitals, Istanbul, Turkey; Sahin, T., Department of Hepatology and Liver Transplantation, Demiroglu Bilim University Group, Florence Nightingale Hospitals, Istanbul, Turkey; Turker, F., Department of Internal Medicine, Haseki Training and Research Hospital, Istanbul, Turkey; Yuzer, Y., Liver Transplantation Center, Demiroglu Bilim University Group, Florence Nightingale Hospitals, Istanbul, Turkey; Tokat, Y., Department of Hepatobiliary and Liver Surgery, Acibadem Fulya Hospital, Istanbul, Turkeyen_US
dc.identifier.scopus2-s2.0-85174161641en_US
dc.authorscopusid57192542622
dc.authorscopusid56545328700
dc.authorscopusid57209820899
dc.authorscopusid57189240325
dc.authorscopusid6602304915
dc.authorscopusid7004609201


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