Penicillin G is frequently used to treat
infective endocarditis (IE) caused by streptococci,
penicillin-susceptible staphylococci and enterococci. Appropriate
antibiotic exposure is essential for survival and reduces the risk of complications and drug resistance development. We determined
penicillin G plasma concentration [p-
penicillin] once weekly in 46 IE patients. The aim was to evaluate whether
penicillin G 3 g every 6 hr (q6 h) resulted in therapeutic concentrations and to analyse potential factors that influence inter- and intra-individual variability, using linear regression and a random coefficient model. [P-
penicillin] at 3 hr and at 6 hr was compared with the minimal inhibitory concentration (MIC) of the bacteria isolated from blood cultures to evaluate the following PK/PD targets: 50% fT > MIC and 100% fT > MIC. [P-
penicillin] varied notably between patients and was associated with age, weight, p-
creatinine and estimated
creatinine clearance (eCLcr). Additionally, an increase in [p-
penicillin] during the treatment period showed strong correlation with age, a low eCLcr, a low weight and a low p-
albumin. Of the 46 patients, 96% had [p-
penicillin] that resulted in 50% fT > MIC, while 71% had [p-
penicillin] resulting in 100% fT > MIC. The majority of patients not achieving the 100% fT > MIC target were infected with enterococci. Streptococci and staphylococci isolated from blood cultures were highly susceptible to
penicillin G. Our results suggest that
penicillin G 3 g q6 h is suitable to treat IE caused by streptococci and
penicillin-susceptible staphylococci, but caution must be taken when the
infection is caused by enterococci. When treating enterococci, therapeutic
drug monitoring should be applied to optimize
penicillin G dosing and exposure.