| pubmed-article:8195380 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8195380 | lifeskim:mentions | umls-concept:C0014834 | lld:lifeskim |
| pubmed-article:8195380 | lifeskim:mentions | umls-concept:C0001699 | lld:lifeskim |
| pubmed-article:8195380 | lifeskim:mentions | umls-concept:C0080194 | lld:lifeskim |
| pubmed-article:8195380 | lifeskim:mentions | umls-concept:C0597979 | lld:lifeskim |
| pubmed-article:8195380 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
| pubmed-article:8195380 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:8195380 | pubmed:dateCreated | 1994-6-30 | lld:pubmed |
| pubmed-article:8195380 | pubmed:abstractText | Plasmids encoding extended-spectrum beta-lactamases of the TEM, SHV, and AmpC families were introduced into common Escherichia coli and Klebsiella pneumoniae hosts to create a homogeneous panel for evaluating the abilities of five test systems to detect resistance to eight beta-lactam antibiotics. Although MICs, as determined by agar dilution or E test strips, were increased and disk diffusion zone diameters were diminished, breakpoints for resistance were often not reached, and neither approach was sensitive in detecting resistance to oxyimino-beta-lactams. The MicroScan 18-h microdilution or Vitek rapid automated procedures were similarly insensitive. Ceftazidime was the best single test antibiotic for detecting extended-spectrum beta-lactamase production. beta-Lactamases TEM-7 and TEM-12 were particularly difficult to detect. Because of such difficulties, the prevalence of extended-spectrum beta-lactamases is likely to be greater than is currently appreciated. | lld:pubmed |
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| pubmed-article:8195380 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8195380 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8195380 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8195380 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8195380 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:8195380 | pubmed:issn | 0095-1137 | lld:pubmed |
| pubmed-article:8195380 | pubmed:author | pubmed-author:JacobyG AGA | lld:pubmed |
| pubmed-article:8195380 | pubmed:author | pubmed-author:SuttonLL | lld:pubmed |
| pubmed-article:8195380 | pubmed:author | pubmed-author:FerraroM JMJ | lld:pubmed |
| pubmed-article:8195380 | pubmed:author | pubmed-author:SpargoJJ | lld:pubmed |
| pubmed-article:8195380 | pubmed:author | pubmed-author:KatsanisG PGP | lld:pubmed |
| pubmed-article:8195380 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8195380 | pubmed:volume | 32 | lld:pubmed |
| pubmed-article:8195380 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8195380 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8195380 | pubmed:pagination | 691-6 | lld:pubmed |
| pubmed-article:8195380 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:8195380 | pubmed:year | 1994 | lld:pubmed |
| pubmed-article:8195380 | pubmed:articleTitle | Detection of Klebsiella pneumoniae and Escherichia coli strains producing extended-spectrum beta-lactamases. | lld:pubmed |
| pubmed-article:8195380 | pubmed:affiliation | Infectious Disease Unit, Massachusetts General Hospital, Boston 02114. | lld:pubmed |
| pubmed-article:8195380 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8195380 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8195380 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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