What are the dosing guidelines for Bactrim (trimethoprim‑sulfamethoxazole) in adults and children for common infections, PCP prophylaxis/treatment, and how should the dose be adjusted for renal impairment?

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Bactrim Dosing Guidelines

For adults with normal renal function, use 1 double-strength (DS) tablet (160 mg TMP/800 mg SMX) every 12 hours for most common infections, while children over 2 months require 8 mg/kg/day of trimethoprim divided every 12 hours. 1

Standard Adult Dosing

Common Infections

  • Urinary tract infections and shigellosis: 1 DS tablet every 12 hours for 10-14 days (UTI) or 5 days (shigellosis) 1
  • Acute exacerbations of chronic bronchitis: 1 DS tablet every 12 hours for 14 days 1
  • Traveler's diarrhea: 1 DS tablet every 12 hours for 5 days 1
  • MRSA skin and soft tissue infections: 2 DS tablets (320 mg TMP/1600 mg SMX) every 12 hours for 7-10 days 2

Severe Infections

  • PCP treatment: 15-20 mg/kg/day of trimethoprim (75-100 mg/kg/day sulfamethoxazole) divided every 6 hours for 14-21 days 1
    • For an 80 kg adult, this equals approximately 2-2.5 DS tablets every 6 hours 1
  • MRSA CNS infections (meningitis, brain abscess): 5 mg/kg/dose every 8-12 hours of trimethoprim component 3
  • MRSA osteomyelitis: 3.5-4.0 mg/kg/dose every 8-12 hours of trimethoprim, typically combined with rifampin for >6 weeks 3

Prophylaxis

  • PCP prophylaxis: 1 DS tablet daily 1
  • Alternative prophylaxis schedule: 1 DS tablet three times weekly on consecutive days 3

Pediatric Dosing (>2 months of age)

Standard Treatment Dosing

  • Most infections: 8 mg/kg/day trimethoprim (40 mg/kg/day sulfamethoxazole) divided every 12 hours 1, 2
  • Serious infections: 10-12 mg/kg/day trimethoprim divided every 12 hours 2
  • Life-threatening infections: Up to 15-20 mg/kg/day trimethoprim divided every 6-8 hours 2

Weight-Based Dosing Table for Standard Treatment

Weight Dose (every 12 hours)
10 kg (22 lbs) ½ tablet
20 kg (44 lbs) 1 tablet
30 kg (66 lbs) 1½ tablets
40 kg (88 lbs) 2 tablets or 1 DS tablet
[1]

PCP Treatment in Children

  • Dosing: 15-20 mg/kg/day trimethoprim (75-100 mg/kg/day sulfamethoxazole) divided every 6 hours for 14-21 days 1

PCP Prophylaxis in Children

  • Standard regimen: 150 mg/m²/day trimethoprim with 750 mg/m²/day sulfamethoxazole, divided twice daily, given 3 consecutive days per week (maximum 320 mg TMP/1600 mg SMX daily) 1, 3, 4
  • Alternative daily dosing: 8 mg/kg/day trimethoprim divided into two doses 4

HIV-Exposed/Infected Infants

  • Initiation: Start prophylaxis at 4-6 weeks of age for all HIV-exposed infants 4
  • Continue throughout first year until HIV infection definitively ruled out 4
  • HIV-infected children: Continue based on age-specific CD4+ thresholds 4

Renal Impairment Adjustments

Prophylaxis Dosing

  • CrCl 15-30 mL/min: Reduce dose by 50% (½ of standard dose) 3
  • CrCl <15 mL/min: Reduce dose by 50% or use alternative agent 3

Treatment Dosing for PCP

  • CrCl 10-50 mL/min: 3-5 mg/kg trimethoprim every 12 hours (instead of every 6-8 hours) 3, 2
  • CrCl <10 mL/min: 3-5 mg/kg trimethoprim every 24 hours 3, 2

FDA-Approved Renal Dosing

  • CrCl >30 mL/min: Use standard regimen 1
  • CrCl 15-30 mL/min: Use ½ the usual regimen 1
  • CrCl <15 mL/min: Use not recommended per FDA label, though clinical guidelines support reduced dosing 1, 3

Important consideration: In critically ill patients on continuous renal replacement therapy (CVVH), standard renal dosing may result in sub-therapeutic levels; higher doses (up to 640/3,200 mg three times daily) may be required with therapeutic drug monitoring 5

Special Populations and Monitoring

Hemodialysis Patients

  • Prophylaxis: Low-dose regimens (<6 single-strength tablets/week) are effective and better tolerated than standard dosing 6
  • Treatment: Dosing interval should be increased to 12 times the serum creatinine level in mg/dL (maximum 48 hours) 7

Monitoring Requirements

  • Baseline: Complete blood count with differential and platelet count 2
  • During therapy: Monthly CBC for prolonged therapy (>1 month) 2, 8
  • Renal function: Monitor creatinine clearance and electrolytes, especially during high-dose therapy 3
  • G6PD screening: Perform before initiating therapy due to hemolytic anemia risk 2

Hydration

  • Maintain adequate fluid intake of at least 1.5 liters daily to prevent crystalluria, particularly important with high-dose therapy 3, 2

Important Drug Interactions and Contraindications

Contraindications

  • Age <2 months: Not recommended 1
  • Severe hepatic impairment: Avoid use 2
  • G6PD deficiency: Use with extreme caution due to hemolytic anemia risk 2

Significant Drug Interactions

  • Methotrexate: Increased toxicity risk 2
  • Warfarin and other anticoagulants: Enhanced anticoagulant effect 2
  • Oral hypoglycemics: Increased hypoglycemia risk 2

Formulation Considerations

Pediatric Patients

  • Use liquid formulation for children weighing <16 kg to ensure accurate dosing 2
  • Liquid suspension: Contains 40 mg TMP/200 mg SMX per 5 mL 8

Tablet Strengths

  • Single-strength (SS): 80 mg TMP/400 mg SMX 1
  • Double-strength (DS): 160 mg TMP/800 mg SMX 1

Common Pitfalls to Avoid

  • Inadequate treatment duration: Using <7 days for febrile UTIs or pyelonephritis leads to treatment failure 8
  • Inappropriate renal dose reduction: Failing to adjust for CrCl <30 mL/min increases toxicity risk 3, 1
  • Nitrofurantoin substitution for febrile UTI: Does not achieve adequate tissue concentrations for pyelonephritis 8
  • Ignoring local resistance patterns: Always consider antimicrobial susceptibility when selecting empiric therapy 8
  • Inadequate monitoring: Failure to perform monthly CBCs during prolonged therapy may miss hematologic toxicity 2
  • Insufficient hydration: Increases crystalluria risk, especially with high-dose therapy 3

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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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