Infectious Diseases I
Likely Pathogens
Recommended Empiric Antibiotic(s)a
Patients without MDRO risk factor: Single antipseudomonal agent with 90% or greater empiric activity on
local ICU antibiogram, and local MRSA prevalence is less than 10-20%
P. aeruginosa
S. pneumoniae
Haemophilus influenzae
Ξ±- and Ξ²-hemolytic Streptococcus spp.
Methicillin-sensitive S. aureus (MSSA)
Antibiotic-sensitive enteric gram-negative bacilli
(GNB) (e.g., E. coli; Klebsiella spp.; Enterobacter spp.;
Proteus spp.; Serratia spp.)
Cefepime, imipenem, levofloxacin, meropenem,
piperacillin/tazobactam
Patient without MDRO risk factor: Single antipseudomonal agent with less than 90% empiric activity on
local ICU antibiogram and/or local MRSA prevalence greater than 10-20%b
P. aeruginosa
Methicillin-resistant S. aureus (MRSA)
S. pneumoniae
Haemophilus influenzae
Ξ±- and Ξ²-hemolytic Streptococcus spp.
Methicillin-sensitive S. aureus (MSSA)
Antibiotic-sensitive enteric gram-negative bacilli
(GNB) (e.g., E. coli; Klebsiella spp.; Enterobacter spp.;
Proteus spp.; Serratia spp.)
Double Antipseudomonal Coverage
Antipseudomonal Ξ²-lactamc
(aztreonam, cefepime, ceftazidime, imipenem,
meropenem, piperacillin/tazobactam)
+
Antipseudomonal fluoroquinolone (ciprofloxacin or
levofloxacin)
OR
aminoglycosided
(amikacin or tobramycin)
MRSA
Linezolid or vancomycin
Patients with MDRO risk factor
P. aeruginosa
Methicillin-resistant S. aureus (MRSA)
Acinetobacter spp.
Antibiotic-resistant enteric GNB (e.g., extended-
spectrum Ξ²-lactamase [ESBL]-producing organisms)
Stenotrophomonas maltophilia
Antipseudomonal Ξ²-lactamc
(aztreonam, cefepime, ceftazidime, imipenem,
meropenem, piperacillin/tazobactam)
+
Antipseudomonal fluoroquinolone (ciprofloxacin or
levofloxacin)
OR
aminoglycosided
(amikacin, gentamicin, or tobramycin)
AND
Linezolid or vancomycin
aAgents/classes are listed in alphabetic order.
bThere may be situations in which a patient has no MDRO risk factors but may meet the recommendation to receive dual antipseudomonal therapy and/or MRSA
coverage.
cDoripenem is no longer available in the United States. Before being discontinued, doripenem had a U.S. Food and Drug Administration (FDA) warning against use for
treatment of ventilator-associated bacterial pneumonia.
dGuidelines suggest avoiding empiric aminoglycoside if alternative agents with activity are available. New CLSI guidance have lowered MIC breakpoints and no longer
recommend the use of gentamicin in the treatment of P. aeruginosa infections.