Keflex Dosing for UTI in Dialysis Patients
For patients on hemodialysis with UTI, administer Cephalexin (Keflex) 250-500 mg after each dialysis session, as the drug is significantly removed during dialysis and achieves adequate urinary concentrations even in anephric patients. 1
Dosing Rationale and Pharmacokinetics
Cephalexin remains effective for UTI treatment in dialysis patients because:
- Even in anephric patients, urinary concentrations of cephalexin remain adequate for treating most common UTI pathogens including E. coli, Klebsiella, and Proteus mirabilis 1
- Single doses of 250-500 mg produce high, prolonged serum concentrations in patients without kidney function, with peak levels typically occurring within 1 hour (though delayed absorption up to 6-12 hours can occur in some patients) 1
- Hemodialysis removes approximately 58% of serum cephalexin over a 6-hour session, necessitating post-dialysis administration 1
Specific Dosing Algorithm
For patients on hemodialysis:
- Administer 250-500 mg orally after each dialysis session 1
- Always give the medication after dialysis, never before, to prevent premature drug removal and maintain therapeutic levels 2
- On non-dialysis days, extend the dosing interval rather than reducing the dose, as is standard practice for patients with creatinine clearance <30 mL/min 2
Treatment Duration
- For complicated UTIs, treat for 7-14 days, adjusting based on clinical response 2
- The drug maintains full antimicrobial activity in urine against common uropathogens 3
Critical Pitfalls to Avoid
- Do not administer before dialysis - this leads to subtherapeutic levels due to drug removal during the session 2
- Do not use standard dosing regimens designed for patients with normal renal function, as this causes drug accumulation and potential toxicity 2
- Avoid nephrotoxic drug combinations to protect any residual renal function, which is particularly important as some patients may regain kidney function 4
- Be aware that 2 out of 6 anephric patients in one study showed delayed absorption (6-12 hours), so if clinical response is suboptimal, consider this pharmacokinetic variability 1