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dc.contributor.authorBayraktar, Adem
dc.contributor.authorAkyildiz, Arif
dc.contributor.authorDemir, Erol
dc.contributor.authorBakkaloglu, Huseyin
dc.contributor.authorUcar, Ali Riza
dc.contributor.authorDirim, Ahmet Burak
dc.contributor.authorAkgul, Sebahat
dc.contributor.authorTurkmen, Aydin
dc.contributor.authorAydin, Ali Emin
dc.contributor.authorSever, Mehmet Sukru
dc.contributor.authorOguz, Fatma Savran
dc.contributor.authorKilicaslan, Isin
dc.contributor.authorOzluk, Yasemin
dc.contributor.authorGok, Ali Fuat Kaan
dc.contributor.authorTemurhan, Sonay
dc.contributor.authorCatma, Yunus
dc.date.accessioned2021-03-02T23:18:40Z
dc.date.available2021-03-02T23:18:40Z
dc.identifier.citationBayraktar A., Catma Y., Akyildiz A., Demir E., Bakkaloglu H., Ucar A. R. , Dirim A. B. , Akgul S., Temurhan S., Gok A. F. K. , et al., "Infectious Complications of Induction Therapies in Kidney Transplantation.", Annals of transplantation, cilt.24, ss.412-417, 2019
dc.identifier.issn1425-9524
dc.identifier.othervv_1032021
dc.identifier.otherav_11be3fc7-f3d1-4cf8-b6d0-b21744cad69e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/17380
dc.identifier.urihttps://doi.org/10.12659/aot.915885
dc.description.abstractBackground: Cytomegalovirus (CMV) and BK virus (BKV) are post-transplant opportunistic viral infections that affect patientand graft survival. This study was designed to evaluate the risk of BKV nephropathy and CMV disease in kidneytransplant recipients who received induction therapy with ATG or basiliximab.Material/Methods: We retrospectively analyzed information on 257 adult patients who underwent kidney transplantation betweenJanuary 2007 and 2017. Patients were categorized into 3 groups according to the induction therapies. The primaryendpoint was the onset of CMV disease or biopsy-confirmed BKV nephropathy. The secondary endpointswere biopsy-proven rejection episodes, graft loss, loss to follow-up, and death.Results: We followed 257 patients for a median of 55.5 months. The incidence of CMV disease was significantly higherin the only ATG group compared to the group without induction treatment (p<0.001). There was no significantdifference in the incidence of BKV nephropathy among groups (p>0.05). The dosage of ATG (OR, 10.685; 95%CI, 1.343 5 to 85.009; P=0.025) was independent risk factor for death.Conclusions: This study demonstrated that a higher dosage of ATG in high-risk patients is associated with an increased riskof CMV disease and patient death, also, reducing the dosage may be a rational strategy for increasing graftand patient’s survival.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectCERRAHİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTRANSPLANTASYON
dc.subjectTıp
dc.subjectCerrahi Tıp Bilimleri
dc.titleInfectious Complications of Induction Therapies in Kidney Transplantation.
dc.typeMakale
dc.relation.journalAnnals of transplantation
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Cerrahi Tıp Bilimleri Bölümü
dc.identifier.volume24
dc.identifier.startpage412
dc.identifier.endpage417
dc.contributor.firstauthorID2520376


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