LAB WORK
TREATMENT OPTIONS
CLINICAL NOTES
- Gram (-), non-fermenter, oxidase (-)
TREATMENT OPTIONS
- Carbapenems
- DO NOT USE ERTAPENEM
- Susceptibility to meropenem DOES NOT predict susceptiblity to imipenem or doripenem (or vice versa), different resistance mechanisms
- Unasyn
- Sulbactam is the agent with activity, not ampicillin
- Polymyxin B, Polymyxin E (Colistin)
- Reserved as last option against MDR strains
- Polymyxin B more favorable PK/PD over colistin
- Use loading doses
- Aminoglycosides
- Tobramycin and amikacin more active than gentamicin
- Usually used in combo with another active agent, not recommended as monotherapy for severe infections
- Tigecycline and Tetracyclines
- Doxycycline and minocycline more active than tetracycline
- Tetracycline sensitivity DOES NOT indicate minocycline or doxycycline sensitivity
- Other agents such as anti-pseudomonal cephalosporins, anti-pseudomonal penicillins, aztreonam, Bactrim, or fluoroquinolones can still be used if cultures confirm sensitivity
CLINICAL NOTES
- Able to acquire resistance to multiple antibiotics faster than other gram negative organisms
- Combination therapy
- Conflicting results, even for same agents being tested
- Some experts favor colistin + carbapenem combination
- Respiratory tract infections are most common site
- Bacteremia second most common site
- Vascular catheters and respiratory tract most common source
- May also be implicated in skin/soft tissue infections (indwelling catheters, wounds, burns, incisions), genitourinary (but rarely invasive), and rarely meningitis, endocarditis, osteomyelitis, endopthalmitis, or liver/pancreatic abscess
- May be a contaminant occasionally (colonizes skin, wounds, respiratory tract, GI tract)