An Assessment of a New Rapid Multiplex PCR Assay for the Diagnosis of Meningoencephalitis.
Genoveva CuestaPedro Puerta-AlcaldeAndrea VergaraEnric RosesJordi BoschCliment Casals-PascualAlex SorianoMª Ángeles MarcosSergi SanzJordi VilaPublished in: Diagnostics (Basel, Switzerland) (2024)
The rapid and broad microbiological diagnosis of meningoencephalitis (ME) has been possible thanks to the development of multiplex PCR tests applied to cerebrospinal fluid (CSF). We aimed to assess a new multiplex PCR panel (the QIAstat-Dx ME panel), which we compared to conventional diagnostic tools and the Biofire FilmArray ME Panel. The pathogens analyzed using both methods were Escherichia coli K1, Haemophilus influenzae , Listeria monocytogenes , Neisseria meningitidis , Streptococcus agalactiae , Streptococcus pneumoniae , Enterovirus, herpes simplex virus 1-2, human herpesvirus 6, human parechovirus, varicella zoster virus, and Cryptococcus neoformans/gattii . We used sensitivity, specificity, PPV, NPV, and kappa correlation index parameters to achieve our objective. Fifty CSF samples from patients with suspected ME were included. When conventional methods were used, 28 CSF samples (56%) were positive. The sensitivity and specificity for QIAstat-Dx/ME were 96.43% (CI95%, 79.8-99.8) and 95.24% (75.2-99.7), respectively, whereas the PPV and NPV were 96.43% (79.8-99.8) and 95.24% (75.1-99.7), respectively. The kappa value was 91.67%. Conclusions: A high correlation of the QIAstat-Dx ME panel with reference methods was shown. QIAstat-Dx ME is a rapid-PCR technique to be applied in patients with suspected ME with a high accuracy.
Keyphrases
- real time pcr
- cerebrospinal fluid
- high throughput
- endothelial cells
- escherichia coli
- nuclear factor
- listeria monocytogenes
- herpes simplex virus
- loop mediated isothermal amplification
- induced pluripotent stem cells
- pluripotent stem cells
- biofilm formation
- toll like receptor
- multidrug resistant
- single cell
- antimicrobial resistance