Rn. Jones et al., Cefditoren in vitro activity and spectrum: A review of international studies using reference methods, DIAG MICR I, 41(1-2), 2001, pp. 1-14
Cefditoren, a broad-spectrum orally administered cephalosporin ester, has d
ocumented in vitro efficacy against many Gram-positive and -negative pathog
ens and stability against clinically important beta -lactamases. We have re
viewed the microbiology and the pharmacokinetic/pharmacodynamic literature
regarding the spectrum and potency of this newer agent against the major et
iologic agents of community-acquired respiratory infection, (Streptococcus
pneumoniae, Hemophilus influenzae and Moraxella catarrhalis), as well as th
e Enterobacteriaceae and non-enteric Grain-negative bacilli, staphylococci,
and other anerobic and anaerobic Gram-positive cocci. The level of cefdito
ren activity against S. pneumoniae (MIC90, 0.5 mug/mL) was superior to all
marketed oral cephalosporins and at least equal to amoxicillin +/- clavulan
ate. H. influenzae (MIC90, 0.016-0.03 mug/mL) and M. catarrhalis (MIC90, 0.
06-0.5 mug/mL) were also very susceptible to cefditoren. In contrast to cef
ixime and ceftibuten, cefditoren was active against oxacillin-susceptible s
taphylococci (MIC90, less than or equal to 1 mug/mL) at a level comparable
to cefuroxime axetil, cefaclor or cefprozil. Enterococci, Pseudomonas aerug
inosa and most anaerobes (Gram-negative) were not cefditoren-susceptible, b
ut most Enterobacteriaceae, beta -haemolytic and viridans group streptococc
i were highly susceptible. Furthermore, an overview of key in vitro suscept
ibility testing methods and issues including disk diffusion testing and Ete
st (AB BIODISK, Solna, Sweden) method accuracy, interpretive criteria, and
pharmacodynamic considerations for the selection of a breakpoint concentrat
ion are provided. The rapid bactericidal nature of the antibacterial activi
ty of cefditoren, its post antibiotic effect, penicillin binding protein ta
rgets, and extent of beta -lactamase stability are all favorable qualities.
In conclusion, this orally administered (BID))beta -lactam possesses promi
se for use against commonly isolated problematic respiratory tract pathogen
s such as penicillin-non-susceptible pneumococci and beta -lactamase-positi
ve M. catarrhalis or H. influenzae. Success in the clinical trials will fur
ther define the role of cefditoren in this era of emerging resistant bacter
ial pathogens. (C) 2001 Elsevier Science Inc. All rights reserved.