AI Article Synopsis

  • This study investigates the effects of converting hepatitis C-positive kidney transplant recipients to everolimus (EVR) as there is no established immunosuppressive protocol for this group.
  • Participants were randomly assigned to either switch to EVR or continue with calcineurin inhibitors, with a total of 30 patients involved, and 28 followed up for one year.
  • Results indicated that while viral loads remained stable across both groups, those on EVR experienced higher rates of dyslipidemia and proteinuria, with no significant changes in kidney function or other complications.

Article Abstract

Introduction: Currently, there is no specific immunosuppressive protocol for hepatitis C (HCV)-positive renal transplants recipients. Thus, the aim of this study was to evaluate the conversion effect to everolimus (EVR) on HCV in adult kidney recipients.

Method: This is an exploratory single-center, prospective, randomized, open label controlled trial with renal allograft recipients with HCV-positive serology. Participants were randomized for conversion to EVR or maintenance of calcineurin inhibitors.

Results: Thirty patients were randomized and 28 were followed-up for 12 months (conversion group, Group 1 =15 and control group, Group 2 =13). RT-PCR HCV levels reported in log values were comparable in both groups and among patients in the same group. The statistical analysis showed no interaction effect between time and group (p value G*M= 0.852), overtime intra-groups (p-value M=0.889) and between group (p-value G=0.286). Group 1 showed a higher incidence of dyslipidemia (p=0.03) and proteinuria events (p=0.01), while no difference was observed in the incidence of anemia (p=0.17), new onset of post-transplant diabetes mellitus (p=1.00) or urinary tract infection (p=0.60). The mean eGFR was similar in both groups.

Conclusion: Our study did not show viral load decrease after conversion to EVR with maintenance of antiproliferative therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533980PMC
http://dx.doi.org/10.1590/2175-8239-JBN-3860DOI Listing

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