Treatment of Uncomplicated Cystitis in Females
Nitrofurantoin monohydrate/macrocrystals 100 mg twice daily for 5 days is the preferred first-line treatment for uncomplicated cystitis in women, offering excellent efficacy (88-93% clinical cure rates) with minimal resistance and limited collateral damage to normal flora. 1, 2
First-Line Treatment Options
The choice among first-line agents depends primarily on local resistance patterns and patient-specific factors:
Nitrofurantoin (Preferred)
- Dose: 100 mg twice daily for 5 days 1, 2
- Clinical cure rates: 88-93% 1
- Bacterial cure rates: 81-92% 1, 2
- Advantages: Minimal resistance, limited collateral damage to gut flora, maintains efficacy even in areas with high resistance to other agents 1
- Do NOT use if pyelonephritis is suspected (inadequate renal tissue concentrations) 2
- Contraindicated if creatinine clearance <30 mL/min due to risk of peripheral neuropathy 2
- Most common side effects: nausea and headache (5.6-34% adverse event rate) 2
Trimethoprim-Sulfamethoxazole (TMP-SMX)
- Dose: 160/800 mg (one double-strength tablet) twice daily for 3 days 3
- Clinical cure rates: 90-100% when organisms are susceptible 3
- CRITICAL LIMITATION: Only use if local E. coli resistance is <20% 4, 3, 1
- When organisms are resistant, cure rates plummet to only 41-54% 3
- Avoid in patients who used TMP-SMX in the preceding 3-6 months or traveled outside the United States recently (independent predictors of resistance) 3
- Avoid in last trimester of pregnancy 3
Fosfomycin Trometamol
- Dose: 3 g single dose 4, 1
- Clinical cure rates: approximately 90% 1
- Advantages: Single-dose convenience, minimal resistance, minimal collateral damage 4
- May have slightly inferior efficacy compared to nitrofurantoin and TMP-SMX (microbiological cure rates 78% vs 86% for nitrofurantoin) 1
Alternative Agents (When First-Line Cannot Be Used)
Fluoroquinolones (Reserve for More Serious Infections)
- Ciprofloxacin 250 mg twice daily for 3 days 3, 5
- Bacteriologic eradication rates: 93-97% when susceptible 3
- Should be reserved as alternatives due to propensity for collateral damage and promotion of resistance 4, 1
- These agents are needed for pyelonephritis and other serious infections 1
Beta-Lactams (Use Only When Other Options Unavailable)
- Options include: amoxicillin-clavulanate, cefdinir, cefaclor, cefpodoxime-proxetil for 3-7 days 4, 1
- Generally have inferior efficacy and more adverse effects compared to first-line agents 4, 1
- Cephalexin is less well studied but may be appropriate in certain settings 4
Agents to AVOID
- Amoxicillin or ampicillin should NOT be used empirically due to poor efficacy and very high worldwide resistance rates 4, 1
Special Considerations for Allergies
For Sulfa Allergy (Cannot Use TMP-SMX)
- First choice: Nitrofurantoin 100 mg twice daily for 5 days 1, 2
- Second choice: Fosfomycin 3 g single dose 1
- If both unavailable: Consider fluoroquinolones (ciprofloxacin 250 mg twice daily for 3 days), recognizing their limitations 1
For Penicillin Allergy
- Nitrofurantoin or fosfomycin remain excellent options 1
- Cephalosporins may be used if no cross-reactivity, though they have inferior efficacy 1
Common Pitfalls to Avoid
- Using TMP-SMX empirically without knowing local resistance rates - if >20% resistance, expect treatment failure in majority of cases 4, 3
- Using fluoroquinolones as first-line therapy - despite high efficacy, this promotes resistance to agents needed for serious infections 1
- Prescribing nitrofurantoin for suspected pyelonephritis - it does not achieve adequate renal tissue concentrations 2
- Using nitrofurantoin in patients with CrCl <30 mL/min - increased risk of serious toxicity 2
- Relying on hospital antibiograms for community UTI treatment - these often overestimate community resistance rates 3
Treatment Duration Rationale
The 5-day nitrofurantoin regimen and 3-day TMP-SMX regimen represent the shortest effective durations that balance efficacy with minimizing antibiotic exposure and adverse effects 3, 2. Each additional day beyond recommended duration carries a 5% increased risk of antibiotic-associated adverse events without additional benefit 3.