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dc.contributor.authorBridge, Sarah
dc.contributor.authorHullsiek, Kathy Huppler
dc.contributor.authorNerima, Carol
dc.contributor.authorEvans, Emily E.
dc.contributor.authorNuwagira, Edwin
dc.contributor.authorStadelmana, Anna M.
dc.contributor.authorTrana, Tu
dc.contributor.authorKim, Grace
dc.contributor.authorTadeo, Kiiza K.
dc.contributor.authorKwizera, Richard
dc.contributor.authorMwesigyea, James
dc.contributor.authorEllis, Jayne
dc.contributor.authorCresswell, Fiona V.
dc.contributor.authorMeya, David B.
dc.contributor.authorMuzooraa, Conrad
dc.contributor.authorBoulware, David R.
dc.contributor.authorRhein, Joshua
dc.date.accessioned2022-05-19T10:04:11Z
dc.date.available2022-05-19T10:04:11Z
dc.date.issued2021
dc.identifier.citationBridge, S., Hullsiek, K. H., Nerima, C., Evans, E. E., Nuwagira, E., Stadelman, A. M., ... & Rhein, J. (2021). Evaluation of the BioFire® FilmArray® Meningitis/Encephalitis panel in an adult and pediatric Ugandan population. Journal of Medical Mycology, 31(3), 101170.en_US
dc.identifier.urihttp://ir.must.ac.ug/xmlui/handle/123456789/1974
dc.description.abstractBackground: Meningitis causes significant mortality in sub-Saharan Africa and limited diagnostics exist. We evaluated the utility of the BioFire_ FilmArray_ Meningitis/Encephalitis multiplex PCR panel (BioFire ME) in HIV-infected adults and HIV-infected and uninfected children presenting with suspected meningitis in Uganda. Methods: We tested cerebrospinal fluid (CSF) using a stepwise meningitis diagnostic algorithm including Bio- Fire ME. We determined the diagnostic performance of BioFire ME for cryptococcal meningitis, using cryptococcal antigen (CrAg) and CSF culture as reference standards, and assessed other central nervous system (CNS) pathogens identified by the panel. Results: We evaluated 328 adult and 42 pediatric CSF specimens using BioFire ME. Of the adult CSF samples tested, 258 were obtained at baseline, and 70 were obtained from repeat lumbar punctures in cryptococcal meningitis. For Cryptococcus, sensitivity was 82%, specificity was 98%, PPV was 98%, and NPV was 79% in baseline pecimens using CSF CrAg as the reference standard. Among follow-up specimens, a negative BioFire ME for Cryptococcus predicted CSF culture sterility with 84% NPV. Overall sensitivity was decreased at low fungal burdens: 29% for 0−99 Cryptococcus CFU/mL compared to 94% for ≥100 CFU/mL in baseline specimens. Other pathogens detected included E. Coli, H. influenzae, S. pneumoniae, CMV, enterovirus, HSV, HHV-6, and VZV. Two specimens tested positive for S. pneumoniae and one for Cryptococcus in the pediatric population. Conclusions: Multiplex PCR is a promising rapid diagnostic test for meningitis in adults and children in resource-limited settings. Cryptococcus at low fungal burdens in CSF may be missed by BioFire MEen_US
dc.description.sponsorshipUnited States Fogarty International Center (K01TW010268, R25TW009345), National Institute of Neurologic Diseases and Stroke (R01NS086312), National Institute of Allergy and Infectious Diseases (T32AI055433).en_US
dc.language.isoen_USen_US
dc.publisherJournal of Medical Mycologyen_US
dc.subjectUgandaen_US
dc.subjectMeningitisen_US
dc.subjectMultiplex PCRen_US
dc.subjectHIVen_US
dc.subjectCryptococcal meningitisen_US
dc.subjectSensitivityen_US
dc.titleEvaluation of the BioFire FilmArray Meningitis/Encephalitis panel in an adult and pediatric Ugandan populationen_US
dc.typeArticleen_US


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