Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1988 Feb;32(2):180-5.
doi: 10.1128/AAC.32.2.180.

National collaborative study of the prevalence of antimicrobial resistance among clinical isolates of Haemophilus influenzae

Affiliations

National collaborative study of the prevalence of antimicrobial resistance among clinical isolates of Haemophilus influenzae

G V Doern et al. Antimicrob Agents Chemother. 1988 Feb.

Abstract

A total of 2,811 clinical isolates of Haemophilus influenzae were obtained during 1986 from 30 medical centers and one nationwide private independent laboratory in the United States. Among these, 757 (26.9%) were type b strains. The overall rate of beta-lactamase-mediated ampicillin resistance was 20.0%. Type b strains were approximately twice as likely as non-type b strains to produce beta-lactamase (31.7 versus 15.6%). The MICs of 12 antimicrobial agents were determined for all isolates. Ampicillin resistance among strains that lacked beta-lactamase activity was extremely uncommon (0.1%). Percentages of study isolates susceptible to cefamandole, cefaclor, cephalothin, and cephalexin were 98.7, 94.5, 87.3, and 43.3%, respectively. For 14 strains (0.5% of the total), chloramphenicol MICs were greater than or equal to 8.0 micrograms, and thus the strains were considered resistant. All of these resistant strains produced chloramphenicol acetyltransferase. In addition, all 14 strains were resistant to tetracycline; 11 produced beta-lactamase. The percentage of isolates susceptible to tetracycline was 97.7%. In contrast, erythromycin and sulfisoxazole were relatively inactive. The combination of erythromycin-sulfisoxazole (1/64) was more active than erythromycin alone but essentially equivalent in activity to sulfisoxazole alone. Finally, small numbers of clinical isolates of H. influenzae were resistant to trimethoprim-sulfamethoxazole and rifampin.

PubMed Disclaimer

References

    1. J Gen Microbiol. 1976 Mar;93(1):9-62 - PubMed
    1. J Clin Microbiol. 1979 Feb;9(2):205-7 - PubMed
    1. Antimicrob Agents Chemother. 1980 Oct;18(4):610-5 - PubMed
    1. Antimicrob Agents Chemother. 1981 Aug;20(2):168-70 - PubMed
    1. J Infect Dis. 1982 Jun;145(6):815-21 - PubMed

Publication types

MeSH terms