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Use of Hepatitis C Virus Antibody-Positive Donors in Kidney Transplantation
被引:0
|作者:
Ventura, Sofia
[1
]
Figueiredo, Catia
[2
]
Sousa, Ciria
[3
]
Almeida, Manuela
[4
]
Martins, La Salete
[4
]
机构:
[1] EPER, Hosp Divino Espirito Santo, Nephrol, P-9500370 Ponta Delgada, Portugal
[2] Ctr Hosp Medio Tejo, Nephrol, Torres Novas, Portugal
[3] Ctr Hosp Tras Os Montes & Alto Douro, Vila Real, Portugal
[4] Ctr Hosp Univ Porto, Nephrol, Porto, Portugal
关键词:
immunosuppresion;
post-renal transplant;
viral serology;
hepatitis c (hcv) infection;
kidney transplantation;
ORGAN DONORS;
CHRONIC HCV;
RECIPIENT;
D O I:
10.7759/cureus.51849
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background The use of kidney donors with hepatitis C virus (HCV) has been arising as a possibility to increase the donor pool. It encompasses both the use of donors with positive and negative viremia, particularly since the advent of direct antiviral agents that produce sustained virologic response. Methodology We conducted a retrospective observational study to describe the experience of our transplantation center in the use of HCV antibody -positive (HCV-Ab+) kidneys. Results We performed five transplants with HCV-Ab+ donors. The median age of kidney recipients was 63 (interquartile range (IQR) = 54-71) years, and 60% (n = 3) were males. Two recipients received a second transplant. The median dialysis vintage was 1,414 (IQR = 1,103-2,806) days. The induction immunosuppression protocol was basiliximab in most patients (60%, n = 3), and all received maintenance immunosuppression with tacrolimus, mycophenolate mofetil, and prednisolone. One of the recipients had a personal history of cured HCV infection. Seroconversion occurred in half of the remaining patients, which was sustained during the follow-up. None of the patients developed HCV viremia. At the end of follow-up, mean creatinine and proteinuria were 1.45 +/- 1.12 mg/dL and 0.099 +/- 0.045 g/g, respectively. We did not observe any rejection episodes, need for dialysis, or recipient's death. Conclusions Our work aligns with the current literature that advocates that the use of these donors is safe and costeffective and can be an effective strategy for expanding the donor pool and augmenting the transplantation volume. Seroconversion is a known risk whose mechanisms are not entirely understood, although it does not appear to be related to a higher transmission risk.
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