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Role of Aminoglycosides in Face of Introduction of New Beta-Lactam Antibiotics in Treatment of Nosocomial Infection

Published online by Cambridge University Press:  02 January 2015

John E. McGowan Jr.*
Affiliation:
Departments of Pathology and Laboratory Medicine and Medicine (Infectious Diseases), Emory University School of Medicine and the Clinical Microbiology Laboratory, Grady Memorial Hospital, Atlanta, Georgia
David B. McClellan
Affiliation:
Departments of Pathology and Laboratory Medicine and Medicine (Infectious Diseases), Emory University School of Medicine and the Clinical Microbiology Laboratory, Grady Memorial Hospital, Atlanta, Georgia
Paula S. Irwin
Affiliation:
Departments of Pathology and Laboratory Medicine and Medicine (Infectious Diseases), Emory University School of Medicine and the Clinical Microbiology Laboratory, Grady Memorial Hospital, Atlanta, Georgia
*
Clinical Microbiology (Box 248), Grady Memorial Hospital, 80 Butler Street, Atlanta, GA30335

Abstract

Aminoglycosides often are employed for empiric therapy of nosocomial infection because of their activity against a wide spectrum of gram-negative aerobic bacilli (GNAB). New beta-lactam antimicrobials also are active against many GNAB. As toxicity appears less likely for the beta-lactams than for aminoglycosides, their use might be preferable if susceptibility profiles were equivalent.

We studied susceptibility of 90 GNAB recovered from blood culture during a three-month period. All were susceptible to aminoglycosides; 93% were susceptible to at least one of the following: ampicillin, carbenicillin, ticarcillin, cephalothin, chloramphenicol or trimethoprim-sulfamethoxazole. All were susceptible to at least one of our newer beta-lactams (cefamandole, cefoxitin, cefotaxime, moxalactam, piperacillin), but the percentage susceptible to any single beta-lactam was lower than that for any of the aminoglycosides tested. All of the isolates were susceptible to combinations of two beta-lactam drugs.

In our hospital, beta-lactams may be reasonable alternatives to aminoglycosides in selected cases where susceptibility has been demonstrated. However, aminoglycosides continue to provide the broadest single-drug coverage for empiric therapy of known or suspected sepsis with GNAB. The utility of combinations of beta-lactam drugs for empiric therapy requires further assessment by clinical trials.

Type
Original Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 1983

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References

1.Phillips, I: Aminoglycosides. Lancet 1982;2:311315.CrossRefGoogle ScholarPubMed
2.Wilkowske, CJ, Hermans, PE: General principles of antimicrobial therapy. Mayo Clin Proc 1983;58:613.Google ScholarPubMed
3.Platt, R: Diagnosis and empiric therapy of urinary tract infection in the seriously ill patient. Rev Infect Dis 1983; 5(suppl 1):S65S71.CrossRefGoogle ScholarPubMed
4.Neu, HC: The new beta-lactamase-stable cephalosporins. Ann Intern Med 1982;97:408419.CrossRefGoogle ScholarPubMed
5.Brooks, GF, Barriere, SL: Clinical use of the new beta-lactam antimicrobial drugs. Practical considerations for physicians, microbiology laboratories, pharmacists, and formulary committees. Ann Intern Med 1983;98:530535.CrossRefGoogle ScholarPubMed
6.Haley, RW, Schaberg, DR, McClish, DK, et al: The accuracy of retrospective chart review in measuring nosocomial infection rates: Results of validation studies in pilot hospitals. Am J Epidemiol 1980;111:516523.CrossRefGoogle ScholarPubMed
7.National Committee for Clinical Laboratory Standards: Performance Standards for Antimicrobic Disk Susceptibility Tests, ed 2, NCCLS Standard M2-A2. Villanova, Pennsylvania, NCCLS, 1982.Google Scholar
8.Finland, M: Empiric therapy for bacterial infections: The historical perspective. Rev Infect Dis 1983; 5(suppl 1):S2S8.CrossRefGoogle ScholarPubMed
9.McGowan, JE Jr: Antimicrobial resistance in hospital organisms and its relationship to antibiotic use. Rev Infect Dis 1983;5:10331048.CrossRefGoogle ScholarPubMed
10.Klastersky, J: Empiric treatment of infections in neutropenic patients with cancer. Rev Infect Dis 1983; 5(suppl 1):S21S31.CrossRefGoogle ScholarPubMed
11.Sanders, CC: Novel resistance selected by the new expanded spectrum cephalosporins: A concern. J Infect Dis 1983;147:585589.CrossRefGoogle ScholarPubMed