Antibiotics Effective Against Klebsiella pneumoniae
For non-resistant Klebsiella pneumoniae infections, third and fourth-generation cephalosporins (ceftriaxone, cefotaxime, cefepime), carbapenems (meropenem, imipenem, ertapenem), or fluoroquinolones (levofloxacin, ciprofloxacin) are the most effective treatment options. 1
First-line Treatment Options for Susceptible K. pneumoniae
- Third and fourth-generation cephalosporins such as ceftriaxone, cefotaxime, and cefepime are effective first-line treatments for susceptible K. pneumoniae infections 1
- Carbapenems including ertapenem, meropenem (1g every 8h), and imipenem (500mg every 6h or 1g every 8h) offer broad-spectrum activity against K. pneumoniae 2
- Fluoroquinolones such as levofloxacin (750mg daily) and ciprofloxacin (400mg every 8h) may be used in patients with beta-lactam allergies, though resistance rates are increasing 2, 1
- Piperacillin-tazobactam (4.5g every 6h) can be effective against susceptible strains 2
Treatment for Resistant K. pneumoniae Strains
ESBL-Producing K. pneumoniae
- Carbapenems remain the most reliable choice for ESBL-producing K. pneumoniae 2
- Cefepime at high doses may be effective against some ESBL strains, but carbapenems are preferred 2
Carbapenem-Resistant K. pneumoniae (CRE)
- For KPC-producing (Klebsiella pneumoniae carbapenemase) strains, newer agents such as ceftazidime-avibactam or meropenem-vaborbactam should be the first-line treatment options 2
- Ceftazidime-avibactam has shown significantly lower 28-day mortality (18.3% vs 40.8%) compared to other regimens in patients with KPC-producing K. pneumoniae bloodstream infections 2
- For OXA-48-like producing CRE, ceftazidime-avibactam is the recommended first-line treatment 2
- For metallo-β-lactamase (MBL) producing strains, ceftazidime-avibactam plus aztreonam or cefiderocol may be considered 2, 3
Treatment Based on Infection Site
For Pneumonia
- For hospital-acquired pneumonia with suspected K. pneumoniae, an antipseudomonal cephalosporin (cefepime, ceftazidime), carbapenem, or β-lactam/β-lactamase inhibitor plus an aminoglycoside or fluoroquinolone is recommended 2
- Meropenem-vaborbactam may be particularly effective for respiratory infections as it achieves good epithelial lining fluid concentrations 2
For Intra-abdominal Infections
- AVYCAZ (ceftazidime-avibactam) plus metronidazole has demonstrated clinical cure rates of 78.4% against K. pneumoniae in complicated intra-abdominal infections 4
- For healthcare-associated intra-abdominal infections with risk of MDR organisms, meropenem, doripenem, imipenem/cilastatin, or piperacillin/tazobactam plus tigecycline are recommended 2
For Urinary Tract Infections
- AVYCAZ (ceftazidime-avibactam) has shown 75% microbiological cure rates against K. pneumoniae in complicated UTIs 4
- For ceftazidime non-susceptible strains, AVYCAZ demonstrated superior combined clinical and microbiological cure rates (70.1%) compared to best available therapy (54.0%) 4
Combination Therapy Considerations
- For severely ill patients with suspected carbapenem-resistant K. pneumoniae, combination therapy may be beneficial 2
- Polymyxin or tigecycline-based combinations with a second in vitro active drug may improve outcomes in severe infections 2
- High-dose extended-infusion meropenem-polymyxin combination therapy may be beneficial even when MICs are elevated (≤16 mg/L) 2
Important Clinical Considerations
- Early appropriate antibiotic therapy is crucial - delays in appropriate antimicrobial treatment are associated with increased mortality 2
- Local antibiotic resistance patterns should guide empiric therapy choices 2
- Rapid diagnostic methods to detect carbapenemase production can help guide timely and targeted treatment 3
- Monotherapy is as effective as combination therapy for susceptible K. pneumoniae strains when using newer agents with good activity 5
- Emergence of ceftazidime-avibactam resistance in KPC-producing isolates (0-12.8%) should be considered when selecting therapy 2
Remember that K. pneumoniae can rapidly develop resistance, so antimicrobial susceptibility testing is essential to guide definitive therapy and ensure optimal patient outcomes.