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Infectious Complications of Induction Therapies in Kidney Transplantation

BACKGROUND: Cytomegalovirus (CMV) and BK virus (BKV) are post-transplant opportunistic viral infections that affect patient and graft survival. This study was designed to evaluate the risk of BKV nephropathy and CMV disease in kidney transplant recipients who received induction therapy with ATG or b...

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Detalles Bibliográficos
Autores principales: Bayraktar, Adem, Catma, Yunus, Akyildiz, Arif, Demir, Erol, Bakkaloglu, Huseyin, Ucar, Ali Riza, Dirim, Ahmet Burak, Akgul, Sebahat Usta, Temurhan, Sonay, Gok, Ali Fuat Kaan, Ozluk, Yasemin, Kilicaslan, Isin, Oguz, Fatma Savran, Sever, Mehmet Sukru, Aydin, Ali Emin, Turkmen, Aydin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6652377/
https://www.ncbi.nlm.nih.gov/pubmed/31296835
http://dx.doi.org/10.12659/AOT.915885
Descripción
Sumario:BACKGROUND: Cytomegalovirus (CMV) and BK virus (BKV) are post-transplant opportunistic viral infections that affect patient and graft survival. This study was designed to evaluate the risk of BKV nephropathy and CMV disease in kidney transplant recipients who received induction therapy with ATG or basiliximab. MATERIAL/METHODS: We retrospectively analyzed information on 257 adult patients who underwent kidney transplantation between January 2007 and 2017. Patients were categorized into 3 groups according to the induction therapies. The primary endpoint was the onset of CMV disease or biopsy-confirmed BKV nephropathy. The secondary endpoints were 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 higher in the only ATG group compared to the group without induction treatment (p<0.001). There was no significant difference 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 risk of CMV disease and patient death, also, reducing the dosage may be a rational strategy for increasing graft and patient’s survival.