Molecular diagnosis of bloodstream infections with a new dual-priming oligonucleotide-based multiplex PCR assay


Por: Carrara, L, Navarro, F, Turbau, M, Seres, M, Moran, I, Quintana, I, Martino, R, Gonzalez, Y, Brell, A, Cordon, O, Diestra, K, Mata, C, Mirelis, B, Coll, P

Publicada: 1 nov 2013
Resumen:
Mortality from bloodstream infections (BSIs) correlates with diagnostic delay and the use of inappropriate empirical treatment. Early PCR-based diagnosis could decrease inappropriate treatment, improving patient outcome. The aim of the present study was to assess the clinical utility of this molecular technology to diagnose BSIs. We assessed a new dual-priming oligonucleotide-based multiplex PCR assay, the Magicplex Sepsis Test (MST) (Seegene), along with blood culture (BC). A total of 267 patients from the intensive care unit and haematology and emergency departments were enrolled. Clinical data were also used by physicians to determine the likelihood of infection. Ninety-eight (37%) specimens were positive: 29 (11%) by both the MST and BC, 29 (11%) by the MST only, and 40 (15%) by BC only. The proportion of agreement between the two methods was 73% (Cohen's kappa: 0.45; 0.28-0.6; indicating fair to moderate agreement). According to clinical assessment, 63 (64%) positive specimens were considered BSIs: 23 (36%) were positive by both the MST and BC, 22 (35%) were positive only by BC, and 18 (29%) were positive only by the MST. Thirty-eight (14%) positive specimens by the MST and/or BC were considered as contaminants. Of 101 specimens collected from patients receiving antibiotics, 20 (20%) were positive by the MST and 32 (32%) by BC. Sensitivity and specificity were 65% and 92%, respectively, for the MST and 71% and 88%, respectively for BC. We concluded that the MST shows a high specificity but changes in design are needed to increase bacteraemia detection. For viability in clinical laboratories, technical improvements are also required to further automate the process.

Filiaciones:
Carrara, L:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Navarro, F:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Turbau, M:
 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

 Hosp Santa Cruz & St Pau, Serv Urgencias Gen, Barcelona 08025, Spain

Seres, M:
 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

 Hosp Santa Cruz & St Pau, Serv Urgencias Gen, Barcelona 08025, Spain

Moran, I:
 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

 Hosp Santa Cruz & St Pau, Serv Med Intens, Barcelona 08025, Spain

Quintana, I:
 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

 Hosp Santa Cruz & St Pau, Serv Med Intens, Barcelona 08025, Spain

Martino, R:
 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

 Hosp Santa Cruz & St Pau, Serv Hematol, Barcelona 08025, Spain

Gonzalez, Y:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Brell, A:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Cordon, O:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Diestra, K:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Mata, C:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Mirelis, B:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain

Coll, P:
 Hosp Santa Cruz & St Pau, Microbiol Serv, Barcelona 08025, Spain

 Biomed Res Inst Sant Pau IIB Sant Pau, Barcelona 08025, Spain
ISSN: 00222615





JOURNAL OF MEDICAL MICROBIOLOGY
Editorial
MICROBIOLOGY SOC, CHARLES DARWIN HOUSE, 12 ROGER ST, LONDON WC1N 2JU, ERKS, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 62 Número:
Páginas: 1673-1679
WOS Id: 000328306300006
ID de PubMed: 23924662

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