There are five reasons why I believe this to be true. #inthisessayiwill
Need anaerobic coverage? Add it! If you don’t, you’re not stuck with broader than necessary therapy.
Don’t need PsAr coverage? Drop to ceftriaxone.
VCM also allows for easier tailoring of therapy later during admission.
While PT has some activity against ESBLs, for *most* ESBLs a carbapenem will likely be utilized for empiric therapy in patients with a history of ESBL.
*Always consult your hospital’s antibiogram.
Studies showed adding M to PT for additional anaerobic coverage in intra-abdominal infections is both redundant and inferior to combinations with CM.
PT *DOES NOT* penetrate the CNS. If CNS is missed as a source in the differential, patients will have a significant coverage gap.
C has better penetration to lung AND bone than PT(‼️).
Critically ill patients with healthcare-associated risk factors commonly present or develop AKI during hospitalization.
Combinations including VPT can further increase the chance of AKI in these patients.
1. Greater incidence of Cdiff
2. No Enterococcus coverage
3. Cefepime-associated neurotoxicity (very rare)
Please feel free to chime in, disagree, post literature, and share your perspectives 💊