Volume 8 Issue 5
Sep.  2017
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Li Zhibin, Zhang Geng, Liu Kepu, et al. Clinical study of early infection of multi-drug resistant organisms after renal transplantation from organ donation after citizen's death[J]. ORGAN TRANSPLANTATION, 2017, 8(5): 386-391. doi: 10.3969/j.issn.1674-7445.2017.05.010
Citation: Li Zhibin, Zhang Geng, Liu Kepu, et al. Clinical study of early infection of multi-drug resistant organisms after renal transplantation from organ donation after citizen's death[J]. ORGAN TRANSPLANTATION, 2017, 8(5): 386-391. doi: 10.3969/j.issn.1674-7445.2017.05.010
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Clinical study of early infection of multi-drug resistant organisms after renal transplantation from organ donation after citizen's death

doi: 10.3969/j.issn.1674-7445.2017.05.010

  • Department of Urology Surgery, Xijing Hospital of the Forth Military Medical University, Xi'an 710032, China

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  • Corresponding author: Yuan Jianlin, Email: jianliny@fmmu.edu.cn
  • Received Date: 2017-06-30
    Available Online: 2021-01-19
  • Publish Date: 2017-09-15
    Abstract
  •   Objective  To investigate the clinical characteristics, prevention and treatment of multi-drug resistant organisms (MDROs) infection early after renal transplantation from donation after citizen's death.  Methods  Clinical data of 166 patients undergoing allogeneic renal transplantation and regular follow-up in Xijing Hospital from November 2011 to September 2016 were retrospectively analyzed. General conditions were statistically compared between the recipients undergoing renal transplantation from donation after cardiac death (DCD) and their counterparts receiving living related donor renal transplantation. The incidence of MDROs infection, onset time, course of diseases, complications, infection site and etiological type were observed. The therapeutic methods and clinical prognosis were summarized.  Results  The incidence of MDROs infection early after renal transplantation in the recipients undergoing DCD renal transplantation was 14%, significantly higher than 2% in those receiving living related donor renal transplantation, and 13% and 2% for the incidence of delayed graft function with statistical significance (both P < 0.05). The incidence of renal graft loss was 8% and 2%, and 5% and 1% for the mortality rate without statistical significance between two groups (both P < 0.05). MDROs infection occurred in 11 patients after DCD renal transplantation. The most common infection site was urinary system (n=6) and the most prevalent pathogenic bacterium was Escherichia coli (n=4). All patients infected with MDROs were treated with a sufficient dosage of effective antibiotics according to the outcomes of bacterial culture and drug sensitivity test. Eight patients obtained favorable clinical prognosis, one underwent nephrectomy and two died.  Conclusions  The incidence of MDROs infection early after DCD renal transplantation is higher than that after living related-donor renal transplantation. Strict donor screening, early detection, intimate monitoring and timely treatment can effectively reduce the risk of MDROs and enhance clinical prognosis.

     

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