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Laboratory Capacity to Detect Antimicrobial Resistance, 1998
JAMA. 2000;283:599-600.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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MMWR. 1999;48:1167-1171
2 tables omitted
Emerging mechanisms of antimicrobial resistance have clinical, microbiologic, and infection-control implications for health-care providers. Antimicrobial resistant organisms include Staphylococcus aureus with reduced susceptibility to vancomycin (minimum inhibitory concentration [MIC] 4 µg/mL), including vancomycin intermediate S. aureus (VISA; vancomycin MIC = 8-16 µg/mL)1-4 and Enterobacteriaceae that produce extended spectrum -lactamases (ESBLS), which result in resistance to a broad range of -lactam antibiotics.5 Detecting VISA and ESBLs-producing gram-negative pathogens can be difficult for clinical microbiology laboratories. Although CDC1-3,6 and the National Committee for Clinical Laboratory Standards (NCCLS)7-9 have published screening and confirmatory methods for these pathogens, the extent of use of these methods is unknown. This report summarizes results from a survey of microbiology laboratories that participate in the Active Bacterial Core Surveillance (ABCs)/Emerging Infections Program (EIP) Network to assess the capacity of clinical microbiology laboratories to detect VISA and ESBL-producing pathogens; findings indicate that despite adequate . . . [Full Text of this Article]
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