Meropenem body fluid and tissue concentration data from both published
studies and samples obtained during efficacy evaluation have been com
piled and presented according to a consistent format to facilitate com
parison. The concentration data have been compared with the mode MIC d
ata available for the pathogens isolated during the clinical evaluatio
n of meropenem. These data support the widespread and rapid penetratio
n of meropenem into the interstitial fluid of those tissues not protec
ted by a tight epithelial barrier. Furthermore, they suggest that the
proposed dosages of meropenem 500 mg or 1 g tds would provide an adequ
ate duration of cover at tissue sites for the treatment of a range of
commonly occurring pathogens. A higher dosage of 40 mg/kg or 2 g in ad
ults given tds would be recommended for meningitis based on the penetr
ation of meropenem into CSF. Overall, the tissue and body fluid data p
resented confirm the expectation, based on the plasma concentrations a
nd theoretical arguments, that meropenem is rapidly and readily distri
buted into the interstitial fluid, thereby producing concentrations in
tissues likely to be clinically effective. This is consistent with th
e available clinical data on the therapeutic efficacy of meropenem.