A MULTICENTER STUDY OF THE ANTIMICROBIAL SUSCEPTIBILITY OF COMMUNITY-ACQUIRED LOWER RESPIRATORY-TRACT PATHOGENS IN THE UNITED-STATES, 1992-1994 - THE ALEXANDER PROJECT
Ja. Washington, A MULTICENTER STUDY OF THE ANTIMICROBIAL SUSCEPTIBILITY OF COMMUNITY-ACQUIRED LOWER RESPIRATORY-TRACT PATHOGENS IN THE UNITED-STATES, 1992-1994 - THE ALEXANDER PROJECT, Diagnostic microbiology and infectious disease, 25(4), 1996, pp. 183-190
A multicenter, collaborative study was performed over a three-year per
iod (1992-1994) to determine the antimicrobial susceptibilities of iso
lates of Haemophilus influenzae, Moraxella catarrhalis, and Streptococ
cus pneumoniae from community-acquired lower respiratory tract infecti
ons. Isolates were collected from five geographically separated medica
l centers in the United States and sent to a central laboratory for an
timicrobial susceptibility testing. Of 350, 536, and 372 isolates of H
. influenzae collected from the five centers in 1992, 1993, and 1994,
26.3%, 28.2%, and 30.1%, respectively, were beta-lactamase-positive. A
ll isolates of H. influenzae remained susceptible to ceftriaxone, doxy
cycline, ciprofloxacin, and ofloxacin over the three-year period. Betw
een 95 and 100% of isolates of H. influenzae remained susceptible to a
moxicillin-clavulanic acid cefixime, clarithromycin, and chloramphenic
ol over this same period. The prevalence of beta-lactamase-positive is
olates of M. catarrhalis increased from 92.1% in 1992 to 93.8% in 1993
and to 96.5% in 1994; however, isolates of this species were highly s
usceptible to amoxicillin-clavulanic acid, the cephalosporins, the mac
rolides, the fluoroquinolones, chloramphenicol, doxycycline, and trime
thoprim-sulfamethoxazole. The prevalence of penicillin-intermediate is
olates of S. pneumoniae decreased from 16% in 1992 to 8.2% in 1994, wh
ereas that of penicillin-resistant isolates increased from 5.6% to 10.
9% in the same period. Ceftriaxone susceptibility declined from 95.2%
to 88.4% over the three years, whereas chloramphenicol susceptibility
declined from 98.4% to 90.5% and that of trimethoprim-sulfamethoxazole
declined from 85.6% to 68.7%. Macrolide activity remained unchanged.
(C) 1996 Elsevier Science Inc.