| Literature DB >> 30487303 |
Eliseo Albert1, Juan Alberola2, Monserrat Bosque3, Juan José Camarena2, María Ángeles Clari4, María Victoria Domínguez Márquez3, María Gil-Fortuño5, Adelina Gimeno6, José Miguel Nogueira2, María Dolores Ocete7, Nieves Orta4, Josep Prat8, Juan Carlos Rodríguez6, Isabel Valero7, Concepción Gimeno Cardona7, David Navarro9.
Abstract
Previous studies suggested that herpes simplex virus (HSV) PCR testing can be safely deferred in patients with normal cerebrospinal fluid (CSF) white blood cell (WBC) counts and protein levels as long as they are older than 2 years of age and are not immunocompromised, the so-called Reller criteria. In this multicenter study, we retrospectively assessed the validity of these screening criteria in our setting. A total of 4,404 CSF specimens submitted for HSV PCR testing to the respective microbiology laboratories at the participating hospitals between 2012 and 2018 were included. Six commercially available HSV PCR assays were used across the participating centers. Ninety-one of the 4,404 CSF specimens (2.1%) tested were positive for HSV DNA (75 samples for HSV-1 and 16 for HSV-2). Nine patients failed to meet the Reller criteria, of whom seven were deemed to truly have HSV encephalitis. Overall, no significant correlation between HSV PCR cycle threshold (CT ) values and WBC counts or total protein levels was found. In addition, median HSV PCR CT s were comparable between patients who met the Reller criteria and those who did not (P = 0.531). In summary, we show that HSV DNA may be detected in CSF specimens with normal WBC and protein levels collected from immunocompetent individuals older than 2 years with HSV encephalitis. Nevertheless, the data also indicate that the number of cases detected could be lowered at least by half if CSF specimens with borderline WBC counts (4 cells/mm3) as well as children of any age are systematically tested.Entities:
Keywords: central nervous system infections; cerebrospinal fluid; herpes simplex virus
Year: 2019 PMID: 30487303 PMCID: PMC6355537 DOI: 10.1128/JCM.01719-18
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948