What is the recommended dose of Bactrim (trimethoprim/sulfamethoxazole) for Urinary Tract Infection (UTI) prophylaxis in children?

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Last updated: August 15, 2025View editorial policy

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Recommended Dose of Bactrim for UTI Prophylaxis in Children

For UTI prophylaxis in children, trimethoprim-sulfamethoxazole (Bactrim) should be administered at a dose of 2-3 mg/kg of trimethoprim component once daily or 5-6 mg/kg twice weekly.

Dosing Guidelines

The FDA-approved dosing for trimethoprim-sulfamethoxazole (TMP-SMX) prophylaxis in children is:

  • Recommended prophylactic dose: 2-3 mg/kg/day of trimethoprim component given as a single daily dose 1
  • Alternative dosing schedule: 5-6 mg/kg of trimethoprim component twice weekly
  • Maximum daily dose should not exceed 320 mg trimethoprim component 1
  • Not recommended for infants less than 2 months of age 1

Age-Specific Considerations

  • Infants <2 months: TMP-SMX is not recommended due to concerns about bilirubin displacement and rapidly changing drug metabolism during the first month of life 2
  • Children 2 months to 2 years: 2-3 mg/kg/day of trimethoprim component as a single daily dose
  • Children >2 years: 2-3 mg/kg/day of trimethoprim component as a single daily dose

Administration Timing

  • Administer the dose at bedtime to maximize urinary concentration during overnight hours
  • For twice-weekly regimens, administer on non-consecutive days (e.g., Monday and Thursday)

Monitoring Recommendations

  • Complete blood count with differential and platelet count should be performed:
    • At initiation of TMP-SMX prophylaxis
    • Monthly intervals thereafter to assess for hematologic toxicity 2

Efficacy Evidence

Long-term low-dose prophylaxis with TMP-SMX has proven very effective in preventing recurrent UTIs in children. In one study, only 6 of 130 children receiving prophylactic treatment developed reinfection during a total period of 2637 months of treatment 3.

Adverse Effects and Precautions

  • Common adverse effects: Rash, gastrointestinal disturbances

  • Serious but rare adverse effects:

    • Dermatologic reactions (Stevens-Johnson syndrome, exfoliative dermatitis) occur in approximately 1/200,000 courses 2
    • Hematologic reactions (leukopenia, thrombocytopenia)
    • Fatal reactions are extremely rare (<1/100,000 children) 2
  • Special considerations:

    • Patients with G6PD deficiency may rarely develop hemolytic anemia 2
    • Adjust dosage in patients with impaired renal function 1
    • Discontinue if serious adverse reactions occur (anaphylaxis, Stevens-Johnson syndrome) 2

Duration of Prophylaxis

  • Continue prophylaxis until the underlying risk factor is resolved
  • After discontinuation of prophylaxis, be aware that reinfection risk is highest within the first 3 months 3
  • Consider imaging studies (renal and bladder ultrasound) after the first febrile UTI to detect anatomical abnormalities 4

Clinical Pearls

  • TMP-SMX is preferred over other antibiotics for UTI prophylaxis due to its:

    • Proven efficacy
    • Safety profile with long-term use
    • Convenient once-daily dosing
    • Good compliance rates 3
  • Avoid using nitrofurantoin for UTI prophylaxis in children with febrile UTIs due to inadequate tissue concentrations for pyelonephritis 4

  • Remember that prophylaxis should be considered primarily in select cases with high-grade vesicoureteral reflux (grades III-IV) or recurrent infections 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Urinary Tract Infection Diagnosis and Treatment in Children

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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