The microbiological diagnosis of tuberculous meningitis: Results of Haydarpasa-1 study
dc.contributor.author | Erdem, H. | |
dc.contributor.author | Ozturk-Engin, D. | |
dc.contributor.author | Elaldi, N. | |
dc.contributor.author | Gulsun, S. | |
dc.contributor.author | Sengoz, G. | |
dc.contributor.author | Crisan, A. | |
dc.contributor.author | Johansen, I.S. | |
dc.date.accessioned | 2025-01-27T18:56:04Z | |
dc.date.available | 2025-01-27T18:56:04Z | |
dc.date.issued | 2014 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | We aimed to provide data on the diagnosis of tuberculous meningitis (TBM) in this largest case series ever reported. The Haydarpasa-1 study involved patients with microbiologically confirmed TBM in Albania, Croatia, Denmark, Egypt, France, Hungary, Iraq, Italy, Macedonia, Romania, Serbia, Slovenia, Syria and Turkey between 2000 and 2012. A positive culture, PCR or Ehrlich-Ziehl-Neelsen staining (EZNs) from the cerebrospinal fluid (CSF) was mandatory for inclusion of meningitis patients. A total of 506 TBM patients were included. The sensitivities of the tests were as follows: interferon-? release assay (Quantiferon TB gold in tube) 90.2%, automated culture systems (ACS) 81.8%, Löwenstein Jensen medium (L-J) 72.7%, adenosine deaminase (ADA) 29.9% and EZNs 27.3%. CSF-ACS was superior to CSF L-J culture and CSF-PCR (p <0.05 for both). Accordingly, CSF L-J culture was superior to CSF-PCR (p <0.05). Combination of L-J and ACS was superior to using these tests alone (p <0.05). There were poor and inverse agreements between EZNs and L-J culture (? = -0.189); ACS and L-J culture (? = -0.172) (p <0.05 for both). Fair and inverse agreement was detected for CSF-ADA and CSF-PCR (? = -0.299, p <0.05). Diagnostic accuracy of TBM was increased when both ACS and L-J cultures were used together. Non-culture tests contributed to TBM diagnosis to a degree. However, due to the delays in the diagnosis with any of the cultures, combined use of non-culture tests appears to contribute early diagnosis. Hence, the diagnostic approach to TBM should be individualized according to the technical capacities of medical institutions particularly in those with poor resources. © 2013 European Society of Clinical Microbiology and Infectious Diseases. | |
dc.identifier.doi | 10.1111/1469-0691.12478 | |
dc.identifier.endpage | O608 | |
dc.identifier.issn | 1198-743X | |
dc.identifier.issue | 10 | |
dc.identifier.pmid | 24849547 | |
dc.identifier.scopus | 2-s2.0-84913605718 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | O600 | |
dc.identifier.uri | https://doi.org/10.1111/1469-0691.12478 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/12844 | |
dc.identifier.volume | 20 | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | Blackwell Publishing Ltd | |
dc.relation.ispartof | Clinical Microbiology and Infection | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.snmz | KA_Scopus_20250125 | |
dc.subject | PCR; Culture; Diagnosis; Meningitis; Tuberculosis | |
dc.title | The microbiological diagnosis of tuberculous meningitis: Results of Haydarpasa-1 study | |
dc.type | Article |