Table 3.
Clinical situation | Antibiotic regimen |
---|---|
Sepsis without a defined focus | Ceftriaxone |
Sepsis without a defined focus of nosocomial origin | Associate vancomycin |
Neonates | Ampicillin + third generation cephalosporin (cefotaxime) + acyclovir (if suspicion of HSV infection) |
Suspected genitourinary source | Associate aminoglycoside (e.g., gentamicin) |
Suspected atypical pneumonia | Associate azithromycin |
Suspected staphylococcal toxic shock syndrome | Associate clindamycin |
Suspected encephalitis | Associate acyclovir |
Suspected intra-abdominal source | Associate piperacillin with tazobactam, clindamycin, or metronidazole |
Suspected COVID-19-related illness (PIMS-TS/MIS-C) | Ceftriaxone. Associate clindamycin if shock |
Central venous catheter | Vancomycin + anti-pseudomonal cephalosporin (e.g., cefepime) or piperacillin-tazobactam) or meropenem |
Immunocompromise or at risk for infection with Pseudomonas species |
Anti-pseudomonal cephalosporin (e.g., cefepime) or meropenem in settings where bacterial organisms with extended-spectrum beta-lactamase (ESBL) resistance are prevalent or for patients who have been recently (within 2 weeks) treated with broad-spectrum antibiotics (e.g. third-generation cephalosporin or fluoroquinolone) Associate vancomycin if risk factors for MRSA are present |
Increased risk of fungal infection (e.g. immunocompromised with persistent fever on broad-spectrum antibiotics): | Associate liposomal amphotericin B or an echinocandin (e.g., caspofungin and micafungin) |
Risk factors for rickettsial infection (e.g. travel to or reside in an endemic region): | Associate tetracycline antibiotic (e.g., doxycycline) |
Allergic to penicillin or recently received broad-spectrum antibiotics |
Meropenem Associate vancomycin if risk factors for MRSA are present |