Cefuroxime for UTI in Dialysis Patients
Cefuroxime can effectively cover UTIs in dialysis patients, but requires dose adjustment to 750 mg every 24 hours with an additional dose administered after each dialysis session. 1
Dosing Recommendations for Dialysis Patients
The FDA-approved dosing for cefuroxime in patients with creatinine clearance <10 mL/min (including those on hemodialysis) is 750 mg every 24 hours, with a supplemental dose given at the end of each dialysis session. 1
- Cefuroxime is dialyzable, meaning significant drug is removed during hemodialysis, necessitating post-dialysis supplementation 1
- The standard dose should not be reduced below 750 mg, as smaller doses are explicitly not recommended even in severe renal impairment 1
- Post-dialysis administration prevents premature drug removal and facilitates directly observed therapy 1
Pharmacokinetic Considerations in Severe Renal Impairment
The elimination half-life of cefuroxime increases dramatically with declining renal function:
- In patients with creatinine clearance of 23 mL/min, the half-life extends to 4.2 hours 2
- In patients with creatinine clearance of 5 mL/min, the half-life extends to 22.3 hours 2
- Despite prolonged half-life, urinary concentrations remain adequate for treating UTIs, as cephalosporins routinely achieve urinary concentrations exceeding 1000 mg/L even with reduced dosing 3
Clinical Efficacy in Dialysis Patients
Cefuroxime demonstrates good clinical efficacy for UTIs in patients with severe renal insufficiency, with symptoms typically resolving within 3-4 days and pathogen eradication achieved in clinical trials. 2
- In a study of patients with creatinine clearance ≤23 mL/min, cefuroxime 750 mg once or twice daily (depending on degree of impairment) successfully eradicated urinary pathogens with no relapses observed during 3-month follow-up 2
- The drug was well tolerated with no nephrotoxicity observed, even with concomitant furosemide use 2
Coverage Spectrum and Limitations
Cefuroxime provides adequate coverage for most common uropathogens in dialysis patients:
- Effective against most gram-negative organisms causing UTIs, including E. coli (the predominant pathogen accounting for 61% of UTI isolates) 4
- Active against beta-lactamase producing bacteria 5
- However, cefuroxime lacks activity against Pseudomonas aeruginosa, Enterococcus species, and ESBL-producing organisms 6
Critical Monitoring Parameters
Renal function evaluation during therapy is recommended, especially in seriously ill patients receiving maximum doses, though cefuroxime rarely produces alterations in kidney function. 1
- Monitor for superinfection during prolonged therapy, as broad-spectrum antibiotics can result in overgrowth of non-susceptible organisms 1
- Prothrombin time should be monitored in patients with renal impairment receiving protracted courses, as cephalosporins may be associated with decreased prothrombin activity 1
Common Pitfalls to Avoid
- Do not administer cefuroxime before dialysis sessions, as this leads to premature drug removal and subtherapeutic levels 1
- Do not reduce the milligram dose below 750 mg even in severe renal impairment; instead, increase the dosing interval 1
- Do not use cefuroxime empirically if local resistance rates to cephalosporins exceed 20% or if ESBL-producing organisms or Pseudomonas are suspected 6
- Ensure the supplemental post-dialysis dose is not omitted, as dialysis removes significant drug 1