| pubmed-article:21430102 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21430102 | lifeskim:mentions | umls-concept:C0010453 | lld:lifeskim |
| pubmed-article:21430102 | lifeskim:mentions | umls-concept:C1552130 | lld:lifeskim |
| pubmed-article:21430102 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
| pubmed-article:21430102 | lifeskim:mentions | umls-concept:C0205160 | lld:lifeskim |
| pubmed-article:21430102 | lifeskim:mentions | umls-concept:C0035899 | lld:lifeskim |
| pubmed-article:21430102 | lifeskim:mentions | umls-concept:C2348609 | lld:lifeskim |
| pubmed-article:21430102 | lifeskim:mentions | umls-concept:C1294313 | lld:lifeskim |
| pubmed-article:21430102 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:21430102 | pubmed:dateCreated | 2011-4-28 | lld:pubmed |
| pubmed-article:21430102 | pubmed:abstractText | PCR-hybridization was compared to culture methods for evaluating suspected blood infections. A total of 231 clinical samples from blood culture bottles that were flagged positive by the BacT/Alert system or were negative 1 week after inoculation were tested. When the PCR-hybridization and culture method results were compared, the positive and negative concordance rates were 99.2% (122/123) and 89.5% (94/105), respectively. Of the negative blood cultures, 10.5% (11/105) were positive by PCR-hybridization. Supplemental testing of negative blood cultures may identify bacterial pathogens that are undetectable by culture methods. | lld:pubmed |
| pubmed-article:21430102 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21430102 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21430102 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21430102 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21430102 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21430102 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21430102 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21430102 | pubmed:month | May | lld:pubmed |
| pubmed-article:21430102 | pubmed:issn | 1098-660X | lld:pubmed |
| pubmed-article:21430102 | pubmed:author | pubmed-author:MasonWilbert... | lld:pubmed |
| pubmed-article:21430102 | pubmed:author | pubmed-author:InderliedClar... | lld:pubmed |
| pubmed-article:21430102 | pubmed:author | pubmed-author:IwakiYuichiY | lld:pubmed |
| pubmed-article:21430102 | pubmed:author | pubmed-author:HoffmanJillJ | lld:pubmed |
| pubmed-article:21430102 | pubmed:author | pubmed-author:IwakiKosuke... | lld:pubmed |
| pubmed-article:21430102 | pubmed:author | pubmed-author:Garcia-GomezJ... | lld:pubmed |
| pubmed-article:21430102 | pubmed:author | pubmed-author:MatsudaKazuko... | lld:pubmed |
| pubmed-article:21430102 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21430102 | pubmed:volume | 49 | lld:pubmed |
| pubmed-article:21430102 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21430102 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21430102 | pubmed:pagination | 2031-4 | lld:pubmed |
| pubmed-article:21430102 | pubmed:dateRevised | 2011-11-1 | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:meshHeading | pubmed-meshheading:21430102... | lld:pubmed |
| pubmed-article:21430102 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21430102 | pubmed:articleTitle | Bacterial identification by 16S rRNA gene PCR-hybridization as a supplement to negative culture results. | lld:pubmed |
| pubmed-article:21430102 | pubmed:affiliation | Division of Infectious Disease, Children's Hospital Los Angeles, and Metic Transplantation Laboratory,Keck School of Medicine, University of Southern California, Los Angeles, California, USA. kmatsuda@usc.edu. | lld:pubmed |
| pubmed-article:21430102 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21430102 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
