HOSPITAL OUTBREAK OF KLEBSIELLA-PNEUMONIAE RESISTANT TO BROAD-SPECTRUM CEPHALOSPORINS AND BETA-LACTAM-BETA-LACTAMASE INHIBITOR COMBINATIONSBY HYPERPRODUCTION OF SHV-5 BETA-LACTAMASE
Gl. French et al., HOSPITAL OUTBREAK OF KLEBSIELLA-PNEUMONIAE RESISTANT TO BROAD-SPECTRUM CEPHALOSPORINS AND BETA-LACTAM-BETA-LACTAMASE INHIBITOR COMBINATIONSBY HYPERPRODUCTION OF SHV-5 BETA-LACTAMASE, Journal of clinical microbiology, 34(2), 1996, pp. 358-363
AN aminoglycoside- and ceftazidime-resistant stain of Klebsiella pneum
oniae K2 producing the extended-spectrom beta-lactamase SHV-5 infected
or colonized 14 pediatric patients at Guy's Hospital. The patients we
re mostly neonates recovering from cardiac surgery for congenital defe
cts. The organism was also isolated from a nurse and from the father o
f one of the children. Four patients had septicemia, and two septicemi
c neonates with postoperative renal failure died. Aminoglycoside and c
ephalosporin resistance transferred to Escherichia coli in vitro on a
160-kb plasmid, and a similar resistant E. coli strain was isolated fr
om the stools of one of the affected children. The epidemic organism c
olonized the bowel and skin and was probably transmitted via staff han
ds. Five wards were involved because of extensive patient movements. T
he outbreak was controlled by patient isolation and attention to handw
ashing. All of the isolates of the outbreak strain were identical by p
hage typing, ribotyping, plasmid profiling, and biochemical and serolo
gical testing, but they varied in their production of SHV-5. Some isol
ates produced normal amounts of SHV-5 and were susceptible to beta-lac
tam-beta-lactamase inhibitor combinations. Others, including the singl
e isolate of multiresistant E. coli, produced up to five times as much
enzyme as ''normal'' isolates. This hyperproduction resulted in incre
ased resistance to several penicillins and cephalosporins and to the b
eta-lactam-beta-lactamase inhibitor combinations amoxicillin-clavulani
c acid, ampicillin-sulbactam, piperacillin-tazobactam, and ceftazidime
-clavulanic acid. The hyperproduction of SHV-5 by K. pneumoniae and E.
coli seen in this outbreak suggests that beta-lactam-beta-lactamase i
nhibitor combinations may be unreliable for the treatment of organisms
producing extended-spectrum beta-lactamases.