Cargando…

Performance of a multiplex polymerase chain reaction panel for identifying bacterial pathogens causing pneumonia in critically ill patients with COVID-19

The FilmArray® Pneumonia Plus (FA-PP) panel can provide rapid identifications and semiquantitative results for many pathogens. We performed a prospective single-center study in 43 critically ill patients with coronavirus disease 2019 (COVID-19) in which we performed 96 FA-PP tests and cultures of bl...

Descripción completa

Detalles Bibliográficos
Autores principales: Caméléna, François, Moy, Anne-Clotilde, Dudoignon, Emmanuel, Poncin, Thibaut, Deniau, Benjamin, Guillemet, Lucie, Le Goff, Jérôme, Budoo, Mélissa, Benyamina, Mourad, Chaussard, Maïté, Coutrot, Maxime, Lafaurie, Matthieu, Plaud, Benoît, Mebazaa, Alexandre, Depret, François, Berçot, Béatrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7441025/
https://www.ncbi.nlm.nih.gov/pubmed/33069002
http://dx.doi.org/10.1016/j.diagmicrobio.2020.115183
Descripción
Sumario:The FilmArray® Pneumonia Plus (FA-PP) panel can provide rapid identifications and semiquantitative results for many pathogens. We performed a prospective single-center study in 43 critically ill patients with coronavirus disease 2019 (COVID-19) in which we performed 96 FA-PP tests and cultures of blind bronchoalveolar lavage (BBAL). FA-PP detected 1 or more pathogens in 32% (31/96 of samples), whereas culture methods detected at least 1 pathogen in 35% (34/96 of samples). The most prevalent bacteria detected were Pseudomonas aeruginosa (n = 14) and Staphylococcus aureus (n = 11) on both FA-PP and culture. The FA-PP results from BBAL in critically ill patients with COVID-19 were consistent with bacterial culture findings for bacteria present in the FA-PP panel, showing sensitivity, specificity, and positive and negative predictive value of 95%, 99%, 82%, and 100%, respectively. Median turnaround time for FA-PP was 5.5 h, which was significantly shorter than for standard culture (26 h) and antimicrobial susceptibility testing results (57 h).