What antibiotics are effective against Extended-Spectrum Beta-Lactamase (ESBL) producing bacteria in urine?

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From the Guidelines

For treating ESBL-producing bacteria in urinary tract infections, intravenous fosfomycin is a recommended treatment option, especially for patients without septic shock, with or without bacteraemia, as shown in the ZEUS and FOREST trials 1.

Treatment Options

  • Intravenous fosfomycin can be used as an alternative to carbapenems, with high-certainty evidence supporting its effectiveness in treating complicated urinary tract infections (cUTI) caused by ESBL-producing Enterobacterales 1.
  • Aminoglycosides, such as amikacin, can also be considered for short durations of therapy, but with moderate certainty of evidence and a higher risk of nephrotoxicity 1.
  • Carbapenems, such as meropenem or ertapenem, are still recommended as first-line treatment options for severe infections or septic shock, with strong recommendations for use and moderate certainty of evidence 1.

Important Considerations

  • Treatment should always be guided by susceptibility testing, as resistance patterns can vary 1.
  • Patients should complete the full course of antibiotics, even if symptoms improve quickly, to ensure eradication of the infection.
  • Increased fluid intake can help flush bacteria from the urinary tract, and follow-up urine cultures may be necessary to confirm eradication of the infection.
  • Healthcare providers should consider risk factors for ESBL infections, including recent hospitalization, prior antibiotic use, and advanced age, when selecting empiric therapy 1.

From the FDA Drug Label

Among Gram-negative uropathogens from both arms of Trial 2, genotypic testing identified certain ESBL groups (e.g., TEM-1, SHV-12, CTX-M-15, CTX-M-27, KPC-2, KPC-3, OXA-48) and AmpC beta-lactamases expected to be inhibited by avibactam in isolates from 273/281 (97.2%) patients in the mMITT population.

ESBL-producing organisms in urine can be treated with avibactam, as it has been shown to inhibit certain ESBL groups, including TEM-1, SHV-12, CTX-M-15, and others. The clinical and microbiological cure rates in patients with ESBL-producing organisms were similar to the overall results, suggesting that avibactam is effective against these organisms 2.

From the Research

ESBL in Urine Antibiotics

  • The use of different antibiotics to treat urinary tract infections (UTIs) can lead to the development of antimicrobial resistance, including the production of extended-spectrum beta-lactamases (ESBL) by Enterobacteriaceae 3.
  • ESBL-producing Enterobacteriaceae are often multidrug resistant, making treatment challenging, but studies have shown that certain antibiotics such as pivmecillinam, fosfomycin, and nitrofurantoin may be effective against these organisms 3, 4.
  • A study found that more than 95% of ESBL-producing Enterobacteriaceae were sensitive to pivmecillinam, fosfomycin, and nitrofurantoin, making these antibiotics potential treatment options for uncomplicated UTIs caused by these organisms 3.
  • Amoxicillin-clavulanic acid (AMC) has also been shown to be effective in treating UTIs caused by ESBL-producing organisms, particularly those with low minimum inhibitory concentrations (MICs) of AMC 5.
  • However, the development of resistance to AMC during therapy is a concern, particularly in organisms with high AMC MICs 5.
  • The duration of treatment for complicated UTIs caused by ESBL-producing Enterobacteriaceae is also an important consideration, with studies suggesting that short courses of antimicrobial treatment (≤ 7 days) may be effective in some cases 6.
  • In cases where intravenous antibiotics are initially required, switching to oral antibiotics such as AMC may be a viable option, as shown in a study where two children with ESBL-UTI were successfully treated with AMC after initial intravenous therapy 7.

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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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