Copyright: ©Author(s) 2026.
World J Nephrol. Sep 25, 2026; 15(3): 118797
Published online Sep 25, 2026. doi: 10.5527/wjn.118797
Published online Sep 25, 2026. doi: 10.5527/wjn.118797
Table 1 Key multidrug-resistant phenotypes in kidney transplant recipients - epidemiology, risk factors, and outcomes
| Phenotype | Epidemiology | Risk factors | Outcomes |
| Extended-spectrum beta-lactamase-Enterobacterales | Cause 18%-31% of post-transplant urinary tract infections. Cause 29%-71% of Gram-negative bloodstream infections. Genitourinary tract is the predominant source of bloodstream infection | Diabetes mellitus. Previous antibiotic use. Delayed graft function. Relapsing infection/previous urinary tract infection. Perianal extended-spectrum beta-lactamase carriage (rectal swab). Second kidney transplantation/induction therapy | 3 × greater risk of recurrent urinary tract infection. Increased hospitalization needs. Lower 1-year epidermal growth factor receptor. Lower long-term death-censored graft survival. High mortality in bloodstream infection |
| Carbapenem-resistant Enterobacterales | Incidence in solid organ transplant is 5 × higher than general population. Common species: Klebsiella, Enterobacter. Sites: Urinary tract infection > surgical site infection > catheter-related bloodstream infection | Colonization (21%-38% of colonized patients develop infection). Recipient age > 50 years. Lymphopenia (median 700 cells/mm3). Prior carbapenem use. Colonization by polymyxin-resistant strains | Mortality up to 42%. Higher mortality compared to carbapenem-susceptible infections |
| Difficult to treat resistant Pseudomonas aeruginosa | Accounts for up to 15% of solid organ transplant bloodstream infections. Up to 43% of isolates in solid organ transplant are multidrug-resistant-Pseudomonas aeruginosa | Prior intensive care unit admission. Nosocomial acquisition. Previous carbapenem therapy | Mortality associated with: Age, urinary catheter, high-risk source, carbapenem resistance, severity of infection. Correct empirical therapy reduces mortality |
| Carbapenem-resistant Acinetobacter baumannii | Almost exclusively nosocomial. Sites: Soft tissue, urinary tract infection, catheter bloodstream infection, ventilator-associated pneumonia | Hospital/intensive care unit exposure. Mechanical ventilation/invasive devices | Highest mortality among solid organ transplant multidrug-resistant organism infections (> 40%) |
| Vancomycin-resistant Enterococci | Enterococcus causes 19% of urinary tract infections (mostly Escherichia faecalis). Vancomycin-resistant Enterococci colonization prevalence approximately 14% in kidney transplant recipients. Escherichia faecium has higher vancomycin resistance rates | Perioperative prophylaxis targeting Gram-negatives. Previous vancomycin use. Ureteral stents | Differentiating colonization from infection is vital; colonization does not always lead to infection |
| Methicillin-resistant Staphylococcus aureus | 1.9% of kidney transplant recipients are methicillin-resistant Staphylococcusaureus carriers. Infections occur early post-transplant | Pre-operative colonization. Presence of central venous catheters. Dialysis history | Pre-operative colonization is an independent predictor of renal allograft failure at 5 years |
| Clostridioides difficile infection | Leading cause of post-transplant diarrhea. Prevalence approximately 2.4% | Antimicrobial exposure (3rd gen cephalosporins, clindamycin, imipenem) | Associated with worse outcomes in kidney transplant recipients |
- Citation: Shetty A, Shankar M. Emerging therapies and diagnostic innovations for multidrug-resistant infections in kidney allograft recipients: Challenges and future directions. World J Nephrol 2026; 15(3): 118797
- URL: https://www.wjgnet.com/2220-6124/full/v15/i3/118797.htm
- DOI: https://dx.doi.org/10.5527/wjn.118797