Empiric therapy
Carbapenem Resistant Enterobacterales (K. pneumoniae, E. coli)
Treatment options when carbapenemase testing result is available are given in Table.
- Polymyxins (Do-not use polymyxin B for UTI) plus other agent to which organism has demonstrated susceptible MIC (like tigecycline, aminoglycosides, IV fosfomycin) or high dose carbapenems if MIC < 16
- Tigecycline (approved for intra-abdominal infection and skin –soft tissue infection)- DO-NOT use for blood stream infection or pneumonia as a standalone agent
- Aminoglycosides (for uncomplicated infections like UTI, any other infection for which source reduction has been done)
- Polymyxins (do-not use polymyxin B for UTI) plus other agent to which organism has demonstrated susceptible MIC (like tigecycline, aminoglycosides, IV fosfomycin) or high dose carbapenems if MIC < 16
- Tigecycline (approved for intra-abdominal infection and skin –soft tissue infection)- DO-NOT use for blood stream infection or pneumonia as a standalone agent
- Aminoglycosides (for uncomplicated infections like UTI, any other infection for which source reduction has been done)
- Polymyxins (do-not use polymyxin B for UTI) plus other agent to which organism has demonstrated susceptible MIC (like tigecycline, aminoglycosides, IV fosfomycin) or high dose carbapenems if MIC < 16
- Tigecycline (approved for intra-abdominal infection and skin –soft tissue infection)- DO-NOT use for blood stream infection or pneumonia as a standalone agent
- Aminoglycosides (for uncomplicated infections like UTI, any other infection for which source reduction has been done)
- Polymyxins (do-not use polymyxin B for UTI) plus other agent to which organism has demonstrated susceptible MIC (like tigecycline, aminoglycosides, IV fosfomycin) or high dose carbapenems if MIC < 16
- Tigecycline (approved for intra-abdominal infection and skin –soft tissue infection)- DO-NOT use for blood stream infection or pneumonia as a standalone agent
- Aminoglycosides (for uncomplicated infections like UTI, any other infection for which source reduction has been done)
Treatment options when Carbapenemase testing result is not available
- Polymyxins (do-not use polymyxin B for UTI) plus other agent to which organism has demonstrated susceptible MIC (like tigecycline, aminoglycosides, IV fosfomycin) or high dose carbapenems if MIC < 16
- Ceftazidime-avibactam alone if in-vitro susceptibility has been demonstrated or in combination with aztreonam if synergy test is demonstrating zone of inhibition.
- Tigecycline (approved for intra-abdominal infection and skin –soft tissue infection)- DO-NOT use for blood stream infection or pneumonia as a standalone agent
- Polymyxins (do-not use polymyxin B for UTI) as a single agent (for uncomplicated infections like UTI, any other infection for which source reduction has been done and patient is hemodynamically stable)
- Aminoglycosides (for uncomplicated infections like UTI, any other infection for which source reduction has been done)
Available treatment options for carbapenem resistant enterobacterales in India
Carbapenemase | |
---|---|
Metallo-β-lactamase (eg. NDM) | 1st Choice: Prolonged infusion of ceftazidime-avibactam and aztreonam (over 3 hours)* Other options: |
Metallo-β-lactamase (eg. NDM) + OXA-48 | 1st Choice: Prolonged infusion of ceftazidime-avibactam and aztreonam (over 3 hours)* Other options: |
OXA-48 like | 1st Choice: Prolonged Infusion of ceftazidime-avibactam** Other options: |
KPC | 1st Choice: Prolonged Infusion of ceftazidime-avibactam ** Other options: |
*Ceftazidime-avibactam + aztreonam: Perform a synergy test and demonstrate zone of inhibition. Prolonged infusion over 3 hours yields best result. This combination is not well studied in pediatric situations, de-ranged creatinine clearance and CNS infections. (Consultation with an Infectious Disease Physician or a physician having experience in treating such infection is advised)
** Ceftazidime-avibactam alone: Apart from carbapenemase test; in-vitro susceptibility testing is recommended prior to use.