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   <dc:title>Assessment of a Loop-Mediated Isothermal Amplification (LAMP) Assay for the Rapid Detection of Pathogenic Bacteria from Respiratory Samples in Patients with Hospital-Acquired Pneumonia</dc:title>
   <dc:creator>Vergara, Andrea</dc:creator>
   <dc:creator>Boutal, Hervé</dc:creator>
   <dc:creator>Ceccato, Adrian</dc:creator>
   <dc:creator>López, Miriam</dc:creator>
   <dc:creator>Cruells, Adrián</dc:creator>
   <dc:creator>Bueno, Leticia</dc:creator>
   <dc:creator>Moreno-Morales, Javier</dc:creator>
   <dc:creator>Puig de la Bellacasa, Jordi</dc:creator>
   <dc:creator>Castro, Pedro</dc:creator>
   <dc:creator>Torres Martí, Antoni</dc:creator>
   <dc:creator>Marco Reverté, Francesc</dc:creator>
   <dc:creator>Casals Pascual, Climent</dc:creator>
   <dc:creator>Vila Estapé, Jordi</dc:creator>
   <dc:subject>Diagnòstic</dc:subject>
   <dc:subject>Medicina intensiva</dc:subject>
   <dc:subject>Aparell respiratori</dc:subject>
   <dc:subject>Pneumònia adquirida a la comunitat</dc:subject>
   <dc:subject>Diagnosis</dc:subject>
   <dc:subject>Critical care medicine</dc:subject>
   <dc:subject>Respiratory organs</dc:subject>
   <dc:subject>Community-acquired pneumonia</dc:subject>
   <dc:description>Rapid identification of the causative agent of hospital-acquired pneumonia (HAP) will allowan earlier administration of a more appropriate antibiotic and could improve the outcome of thesepatients. The aim of this study was to develop a rapid protocol to identify the main microorganismsinvolved in HAP by loop-mediated isothermal amplification (LAMP) directly from respiratory samples.First of all, a rapid procedure (&lt;30 min) to extract the DNA from bronchoalveolar lavage (BAL),endotracheal aspirate (EA) or bronchoaspirate (BAS) was set up. A specific LAMP forStaphylococcusaureus,Escherichia coli,Klebsiella pneumoniae, Pseudomonas aeruginosa,Stenotrophomonas maltophiliaandAcinetobacter baumanniiwas performed with the extracted solution at 65◦C for 30-40 min. Overall,58 positive BAL and 83 EA/BAS samples were tested. The limits of detection varied according to themicroorganism detected. Validation of the LAMP assay with BAL samples showed that the assay was 100% specific and 86.3% sensitive (positive predictive value of 100% and a negative predictive valueof 50%) compared with culture. Meanwhile for BAS/EA samples, the assay rendered the followingstatistical parameters: 100% specificity, 94.6% sensitivity, 100% positive predictive value and 69.2%negative predictive value. The turnaround time including sample preparation and LAMP was circa1 h. LAMP method may be used to detect the most frequent bacteria causing HAP. It is a simple,cheap, sensitive, specific and rapid assay.</dc:description>
   <dc:date>2020-02-21T12:16:25Z</dc:date>
   <dc:date>2020-02-21T12:16:25Z</dc:date>
   <dc:date>2020-01-11</dc:date>
   <dc:date>2020-02-21T12:16:25Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>2076-2607</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/150965</dc:identifier>
   <dc:identifier>695192</dc:identifier>
   <dc:identifier>31940771</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.3390/microorganisms8010103</dc:relation>
   <dc:relation>Microorganisms, 2020, vol. 8, num. 1, p. 103</dc:relation>
   <dc:relation>https://doi.org/10.3390/microorganisms8010103</dc:relation>
   <dc:rights>cc-by (c) Vergara, Andrea et al., 2020</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/3.0/es</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>10 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>MDPI</dc:publisher>
   <dc:source>Articles publicats en revistes (Fonaments Clínics)</dc:source>
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