G. Bonfiglio et al., IN-VITRO ACTIVITY OF PIPERACILLIN TAZOBACTAM AGAINST 615 PSEUDOMONAS-AERUGINOSA STRAINS ISOLATED IN INTENSIVE-CARE UNITS/, Chemotherapy, 44(5), 1998, pp. 305-312
From May 1996 to September 1997, 615 Pseudomonas aeruginosa strains is
olated from patients in intensive care units collected from different
Italian laboratories were studied. The susceptibility of piperacillin/
tazobactam, in comparison with other antipseudomonal antibiotics, to t
heir NCCLS breakpoints was evaluated: amikacin 79.6%, carbenicillin 67
.0%, ceftazidime 73.4%, ciprofloxacin 55.8%, imipenem 64.1%, piperacil
lin 88.1%, piperacillin/tazobactam 92.4% and ticarcillin/clavulanic ac
id 69.0%. Seventy-three strains were selected because of their resista
nce to piperacillin and the mechanisms underlying such a resistance we
re investigated. Isoelectric focusing and hydrolysis assays revealed t
he presence of 15 plasmid-mediated p-lactamases. Chromosomal beta-lact
amase derepression was demonstrated in 34 isolates. The remaining 24 p
iperacillin-resistant strains did not produce beta-lactamases and an '
intrinsic mechanism' of resistance was inferred. The piperacillin/tazo
bactam combination restored resistance in 25 piperacillin strains. Nin
e of these were derepressed for chromosomal beta-lactamase, 8 showed i
mpermeability and 8 showed plasmid enzymes.