The importance of beta-lactamase resistance in surgical infections

Surg Infect (Larchmt). 2001:2 Suppl 1:S13-22. doi: 10.1089/10962960152742187.

Abstract

Substantial costs are associated with the treatment of nosocomial infections, 2 million cases of which occur annually in the United States. Hospital-acquired, gram-negative infection has become an increasing problem, particularly in the intensive care unit where up to 40% of the most frequently isolated strains of Enterobacteriaceae are resistant to standard beta-lactam antibiotics. Among several mechanisms of acquisition of resistance, beta-lactamase production accounts for a high percentage of treatment failures and relapses. By the end of the 1980s, some 10-30% of all nosocomial infections were caused by type-1 beta-lactamase-producing gram-negative isolates, and Enterobacter species had emerged as a major resistant pathogen. The beta-lactam/beta-lactamase inhibitor combinations, such as ampicillin/sulbactam, represent an innovative approach to the problem of beta-lactamase-mediated resistance. Clinical use of these agents has been associated with low rates of resistance and new data suggest they may have a specific role in controlling the emergence and spread of nosocomial infections.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Cross Infection / drug therapy*
  • Cross Infection / epidemiology
  • Cross Infection / prevention & control
  • Female
  • Gram-Negative Bacteria / drug effects
  • Gram-Positive Bacteria / drug effects
  • Humans
  • Male
  • Microbial Sensitivity Tests
  • Postoperative Complications / drug therapy*
  • Postoperative Complications / microbiology
  • Risk Assessment
  • Sensitivity and Specificity
  • Surgical Procedures, Operative / adverse effects
  • Surgical Procedures, Operative / methods
  • Surgical Wound Infection / drug therapy*
  • Surgical Wound Infection / microbiology
  • Treatment Outcome
  • United States / epidemiology
  • beta-Lactam Resistance*
  • beta-Lactamases / pharmacology
  • beta-Lactamases / therapeutic use*

Substances

  • beta-Lactamases