Sepsis & infection

Population pharmacokinetics of prophylactic cefoxitin in elective bariatric surgery patients: a prospective monocentric study

Anaesth Crit Care Pain MedPublished Prospective population pharmacokinetic study

Authors' conclusion

Intermittent dosing regimens resulted in optimal FTAs against susceptible MIC distributions of S. aureus and E. coli when simulating with 50% cefoxitin protein binding. Continuous infusion of cefoxitin may improve FTA regardless of protein binding.

Study context

Population
Obese patients undergoing elective bariatric surgery receiving prophylactic cefoxitin381 concentration values
Participants
123 patients
Exposure
Cefoxitin dosing regimens for target attainment
Outcome
Population PK of cefoxitin and probability of target attainment (cefoxitin fu above MIC from surgical incision to wound closure)
Methodological detailsmonocentric, dosing simulations
  • Monocentric
  • Dosing simulations

Main finding

As reported in the abstract

Cefoxitin population PK
Mean clearance (L/h)
10.9 ± 6.1
Mean volume of distribution (L)
23.4 ± 10.5
Surgery <2 h: 2 g dose sufficient for minimum inhibitory concentrations (MIC) up to 4 mg/L (fu 50%)
4
Surgery <2 h: 4 g dose sufficient for MIC up to 8 mg/L (fu 50%)
8
Prolonged surgery (2-4 h): only continuous infusion enabled optimal probability of target attainment (PTA) for MIC up to 16 mg/L
16

Observational data: associations, not effects.

Further findings

Fractional target attainment (FTA) against S. aureus and E. coli MIC distributions

Optimal FTAs only with 50% protein binding (intermittent regimen) and regardless of protein binding for continuous infusion

Original publication

Population pharmacokinetics of prophylactic cefoxitin in elective bariatric surgery patients: a prospective monocentric study. Anaesth Crit Care Pain Med. Published 15 March 2024. doi:10.1016/j.accpm.2024.101376

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