Infectious Diseases II
Answer: C
The prophylactic regimen for a patient without a
Ξ²-lactam allergy who is undergoing cardiac surgery
should be cephalosporin administered within 60 min-
utes of incision time, administered every 4 hours during
surgery, and continued for no more than 48 hours. In this
case, the patient has obesity disorder and weighs more
than 120 kg; hence, the patient requires an initial dose of
cefazolin 3 g (Answer C is correct). Given the patientβs
weight, administering cefazolin 2 g initially is inappro-
priate (Answers A and D are incorrect). Vancomycin
is usually reserved for patients with a Ξ²-lactam allergy
(Answer B is incorrect).
Although critical care pharmacists may not officially be
part of many antimicrobial stewardship teams, many
of their daily clinical activities constitute antimicro-
bial stewardship activities. These may include selecting
the most appropriate treatment regimen and advocat-
ing the early de-escalation of antimicrobials. Even in
the presence of a formalized antimicrobial steward-
ship team, these activities are often complementary to
the formalized activities of the team (Answer C is cor-
rect). Given the wide variations in clinical practice, it
may not be feasible to include an infectious diseasesβ
trained pharmacist with every stewardship team. In
that case, the activities and involvement of a critical
care pharmacist may be even more crucial (Answer A
is incorrect). Antimicrobial cycling has not consistently
demonstrated beneficial effect on antimicrobial resis-
tance. (Answer B is incorrect). Studies have shown that
antimicrobial stewardship efforts in critically ill patients
do not worsen outcomes. Given the aggressive empiric
antimicrobial regimens commonly used in critically ill
patients, antimicrobial stewardship should be instituted
to minimize adverse effects and the emergence of resis-
tance (Answer D is incorrect).
Answer: D
This patient presents with a health careβassociated CNS
infection, given the post-neurosurgical and device-
related etiology of the infection. The most common
pathogens include MRSA and multidrug-resistant
gram-negative organisms. In addition to neurosurgical
management of the device (e.g., removal or revision),
empiric antibiotic therapy is indicated, including therapy
with agents having empiric activity against suspected
pathogens and the ability to safely achieve relevant
CSF concentrations. Cefepime and vancomycin are the
most appropriate options listed with consideration of
CNS-specific dosing (Answer D is correct). Ceftriaxone
does not cover nosocomial-acquired gram negatives
such as Pseudomonas (Answers A and B are incorrect).
Piperacillin/tazobactam would be reasonable according
to the spectrum of antibacterial activity; however, poor
CNS penetration of tazobactam limits the utility of this
agent for meningitis and other CNS infections (Answer
C is incorrect).
Answer: D
The presence of the CTX-M gene detected on E. coli by
rapid diagnostic testing usually signifies the presence of
ESBL. This may be why the patient has not yet responded
to piperacillin/tazobactam. The most appropriate action
at this point is to broaden the coverage to cover for
potential ESBL-producing E. coli. Carbapenems remain
the drug of choice for ESBL-producing organisms, par-
ticularly in a patient who is hemodynamically unstable
(Answer D is correct). Extended-spectrum Ξ²-lactamases
are usually encoded on genes that carry resistance
against other classes of antimicrobials; hence, resistance
to other antimicrobials is common; therefore, adding
either aminoglycosides or fluoroquinolones may not be
appropriate (Answers B and C are incorrect). Although
at times ESBLs may be covered by cefepime, it must be
determined by final AST (Answer A is incorrect).
Answer: C
E.
cloacae
are
AmpC
Ξ²-lactamaseβproducing
Enterobacterales. The use of ceftriaxone or extended-
spectrum penicillins (e.g., piperacillin and ticarcillin)
may select out derepressed mutants, which are capable
of causing the hyperproduction of AmpC Ξ²-lactamases.
Derepressed mutants are capable of producing resistance
against third-generation cephalosporins, monobactams,
and extended-spectrum penicillins. In this case, the
patient was taking 10 days of ceftriaxone before
a new blood culture was growing lactose-positive
gram-negative bacilli. Because lactose-positive gram-
negative bacilli are usually Enterobacterales, growing
multidrug-resistant pathogens such as P. aeruginosa