UTI Treatment in Hemodialysis Patients
For adult hemodialysis patients with symptomatic UTI, obtain urine culture before initiating empiric therapy with trimethoprim-sulfamethoxazole 160/800 mg once daily (adjusted for dialysis schedule) or a fluoroquinolone such as levofloxacin 250 mg once daily for 7-10 days, then adjust based on culture results and local resistance patterns. 1, 2
Critical First Steps
- Obtain urine culture before starting antibiotics to guide definitive therapy, as hemodialysis patients have higher rates of resistant organisms 1, 2
- Distinguish symptomatic UTI from asymptomatic bacteriuria (ASB), which is present in 28% of hemodialysis patients and should NOT be treated 3
- Do not treat ASB in dialysis patients - it provides no clinical benefit and promotes antimicrobial resistance 3
Empiric Antibiotic Selection Algorithm
First-Line Options (if local resistance <20%):
- Trimethoprim-sulfamethoxazole (TMP-SMX): 160/800 mg once daily (given after dialysis on dialysis days) 1, 2
- Fluoroquinolones: Levofloxacin 250 mg once daily (dose-adjusted for renal failure) 1, 4
Alternative Options:
- Ceftriaxone: 1-2g IV daily for severe infections requiring hospitalization (no dose adjustment needed for dialysis) 2, 5
- Ertapenem: 500 mg IV once daily for complicated UTI with resistant organisms (dose-adjusted for dialysis patients) 5
Avoid These Agents:
- Nitrofurantoin: Contraindicated in dialysis patients due to inadequate urinary concentrations and risk of toxicity 4, 6
- Fosfomycin: Inadequate data for dosing in dialysis patients 4, 7
Treatment Duration
- Uncomplicated cystitis: 7-10 days 1, 2
- Complicated UTI or pyelonephritis: 10-14 days, depending on clinical response 2
- Catheter-associated UTI: 7 days for prompt response, 10-14 days for delayed response 2
Special Considerations for Dialysis Patients
Dosing Adjustments:
- Administer antibiotics after dialysis sessions when possible, as most UTI antibiotics are dialyzable 1
- TMP-SMX: Give supplemental dose (half of daily dose) after each dialysis session 1
- Fluoroquinolones: Reduce dose to 250 mg levofloxacin once daily 4
- Beta-lactams: Ceftriaxone requires no adjustment; ertapenem reduced to 500 mg daily 5
Catheter Management:
- If indwelling catheter present >2 weeks, replace catheter before initiating antibiotics and obtain culture from fresh catheter 3, 2
- Never collect urine from collection bag or extension tubing - always from freshly placed catheter 1
- Consider catheter removal entirely if clinically feasible, as this is the most effective intervention to prevent recurrent CA-UTI 1
Culture-Directed Therapy
- Always adjust therapy based on susceptibility results when available 1, 2
- If symptoms persist or recur within 2 weeks, do not use the same antibiotic - this indicates treatment failure requiring alternative susceptibility-guided therapy 1
- Expect broader bacterial spectrum in dialysis patients, including Klebsiella, Proteus, and resistant organisms 4, 8
Common Pitfalls to Avoid
Critical Errors:
- Never treat asymptomatic bacteriuria in dialysis patients - this is the most common error and promotes resistance without clinical benefit 3
- Do not use nitrofurantoin in dialysis patients - inadequate urinary concentrations make it ineffective 4, 6
- Avoid empiric fluoroquinolones as first-line unless other options contraindicated, due to increasing resistance and serious adverse effects 1, 4
Diagnostic Pitfalls:
- Pyuria alone does not indicate infection - it is commonly present without infection in dialysis patients 6
- Cloudy or smelly urine alone should not trigger treatment - these are not reliable indicators of symptomatic infection 3
- Bacteriuria >10^5 CFU/mL without symptoms is ASB, not UTI, and should not be treated 3
Antimicrobial Stewardship
- Reserve carbapenems and broad-spectrum agents for culture-proven resistant organisms only 4
- Avoid prophylactic antibiotics in dialysis patients with catheters - this does not reduce symptomatic UTI and significantly increases resistance 2
- Consider local antibiogram data when selecting empiric therapy, as resistance patterns vary by institution 2, 4