This guideline does not cover CA-UTI in pregnant patients or CA-UTI in children. These are considered complicated cases and should be referred to secondary care.
✔ Should be based on a full clinical assessment.
✔ Consider CA-UTI in the presence of 1 or more of:
✘ Cloudy urine is NOT an indicator of CA-UTI in the absence of symptoms and signs of a UTI
✘ Foul-smelling urine is NOT an indicator of CA-UTI in the absence of symptoms and signs of a UTI
✘ Dipstick Urinalysis is not useful in assessing for evidence of UTIs in patients with catheters. For further information please see details in the national Position Statements Dipstick Urinalysis for UTIs in Adults
Send urine to the lab only in patients where CA-UTI is suspected on clinical grounds. A urine specimen for culture should be obtained if possible prior to initiating antimicrobial therapy for presumed CA-UTI. The results can be used to guide treatment should the patient fail to respond to empiric choice antibiotic. Refer to guidance on obtaining a urine sample from a urinary catheter. Urinary catheters are often colonised with bacteria. Laboratory microscopy should not be used to diagnose a CA-UTI as urine white cells are often elevated due to the presence of the catheter. A positive urine culture result in a catheterised patient does not always indicate infection and should not be treated unless there are signs or symptoms suggestive of CA-UTI (such as suprapubic/ flank pain, fever).
In the presence of a urinary catheter, antibiotics will not eradicate bacteriuria.
✘ Long-term antibiotic prophylaxis is generally not appropriate for the prevention of UTI in catheterised patients due to the risk of antibiotic-associated harm to the patient such as adverse events and antimicrobial resistance.
Antibiotic prophylaxis for urinary catheter changes is NOT appropriate unless there is a definite history of UTIs due to catheter change.
| LOWER CA-UTI (NOT SYSTEMICALLY UNWELL) EMPIRIC TREATMENT TABLE | |||
| Drug | Dose | Duration | Notes |
| 1st Choice Options | |||
|
Nitrofurantoin Immediate release Capsules |
50 mg every 6 hours
|
7 days
|
Nitrofurantoin is NOT a suitable antibiotic choice in Upper CA-UTI or if patient systemically unwell. Nitrofurantoin poorly penetrates the prostate. Consider prostatitis as a diagnosis in males if symptoms persist. Contraindicated in patients with eGFR <30 mL/min/1.73 m2 Immediate/ prolonged release should be stated on the prescription (see note below on formulation difference)
|
| OR | |||
|
Nitrofurantoin Prolonged release Capsules |
100 mg every 12 hours
|
7 days
|
|
| 2nd Choice Options (Only use when nitrofurantoin is unsuitable) | |||
|
Cefalexin
|
500 mg every 12 hours
|
7 days
|
Cephalosporins should not be used in severe penicillin allergy.
|
|
OR |
|||
|
Trimethoprim
|
200 mg every 12 hours
|
7 days
|
Use only when risk of resistance is low i.e. where previous culture suggests susceptibility (but trimethoprim was not used) or in younger patients without a significant antibiotic exposure history. Risk of resistance is more likely in older people in residential facilities. |
| UPPER CA-UTI (SYSTEMICALLY UNWELL) EMPIRIC TREATMENT TABLE | |||
| Drug | Dose | Duration* | Notes |
| 1st Choice Option | |||
|
Cefalexin
|
500 mg every 8 hours (can increase to 1 g every 6 hours in severe infection) |
7-10 days*
|
Cephalosporins should not be used in severe penicillin allergy.
|
| 2nd Choice Option | |||
|
Co-Amoxiclav
|
875/125mg every 8 hours**
|
7-10 days*
|
Avoid in penicillin allergy. Use only when risk of resistance is low i.e. where previous culture suggests susceptibility (but co-amoxiclav was not used) or in younger patients without a significant antibiotic exposure history. Risk of resistance is more likely in older people in residential care facilities.
|
| Penicillin Allergy | |||
|
Trimethoprim
|
200 mg every 12 hours
|
14 days
|
Use only when risk of resistance is low i.e. where previous culture suggests susceptibility (but trimethoprim was not used) or in younger patients without a significant antibiotic exposure history. Risk of resistance is more likely in older people in residential care facilities.
|
|
Ciprofloxacin
|
500 mg every 12 hours
|
7 days*
|
Reserve for severe penicillin allergy or where other antibiotics not suitable. Avoid ciprofloxacin in pregnancy. |
*10 to 14 days treatment may be necessary if there is a delayed response to treatment and the organism is susceptible.
** A higher dose of co-amoxiclav (875/125 mg) every 8 hours is recommended for treatment of upper CA-UTI (875/125 mg = 875 mg amoxicillin plus 125 mg clavulanic acid)
Provided it is not contra-indicated, nitrofurantoin is the preferred first choice for lower CA-UTI where patient is not systemically unwell. Nitrofurantoin resistance rates remain low in community E. coli UTIs throughout Ireland (including in ESBL-producing isolates) despite increasing resistance to other antibiotics.
Nitrofurantoin precautions
There is data to indicate that the rate of trimethoprim resistance in E. coli in community urinary samples is high in particular in older people in residential care facilities. Empiric trimethoprim is therefore no longer recommended except where nitrofurantoin is unsuitable and the risk of resistance is low (e.g. where a previous urine culture has had a trimethoprim-susceptible isolate and trimethoprim has not been used, or in a young patient without a significant antibiotic exposure history).
Amoxicillin is not recommended as empiric therapy, as resistance rates in community E. coli UTIs are extremely high. Only use if amoxicillin susceptibility known.
Co-amoxiclav resistance in E. coli in community urine samples is high. In addition, it is a systemic agent and should be avoided in uncomplicated CA-UTI if a locally acting agent (e.g. nitrofurantoin) could be used instead.
Ciprofloxacin is a broad-spectrum antibiotic, associated with C. difficile infection and multiple adverse effects. It is not recommended for the empiric treatment of uncomplicated lower CA-UTI where patient is systemically well. It may be considered for targeted therapy of multi-resistant infections, where there are no other appropriate options.
Reviewed July 2023, minor edit September 2025, October 2025