{"title":"Defining drug resistance beyond rifampicin: use of Xpert® MTB/XDR assay in tuberculous meningitis","authors":"Kusum Sharma , Megha Sharma , Ritu Shree , Himanshu Joshi , Neeraj Singla , Ashish Kumar Kakkar , Vijeta Patial , Chamanjot Kaur , Supriya Sharma , Manoj Goyal , Aman Sharma , Navneet Sharma , Manish Modi","doi":"10.1016/j.ijmmb.2025.100912","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><div>– The emerging drug resistance in Tuberculous meningitis (TBM) worsens the prognosis and hamper elimination efforts. The need of the hour is a relatively simple, rapid, near point-of-care test that could allow universal drug susceptibility testing, beyond rifampicin (RIF). The current study evaluated performance of Xpert MTB/XDR in defining drug resistant TBM.</div></div><div><h3>Methods</h3><div>– A total of 45 cerebrospinal fluid samples (29 culture-positive, 16 culture-negative) reported TBM by Xpert MTB/Ultra were subjected to Xpert MTB/XDR to determine susceptibility towards isoniazid (INH), fluoroquinolones (FLQ), second-line injectables (SLID) and ethambutol (ETM). The performance of Xpert MTB/XDR was evaluated against genotypic drug susceptibility testing (line probe assay (LPA) and phenotypic drug susceptibility testing (culture)).</div></div><div><h3>Results</h3><div>– There was 100 % concordance between Xpert MTB/XDR and drug susceptibility using both culture and LPA for INH and SLIDs. For FLQ, the sensitivity and specificity of Xpert MTB/XDR was 93 % and 100 %, respectively against both culture and LPA, as there was one case each reported false-susceptible by Xpert MTB/XDR. The sensitivity and specificity of Xpert MTB/XDR for ETM was 93 % and 100 %, respectively against culture and one case of false-resistance was reported.</div></div><div><h3>Conclusion</h3><div>– Xpert MTB/XDR can serve as a useful tool to rapidly identify resistance to INH, FLQ, SLID and ETM, thus offering targeted therapy to the patients of TBM.</div></div>","PeriodicalId":13284,"journal":{"name":"Indian Journal of Medical Microbiology","volume":"56 ","pages":"Article 100912"},"PeriodicalIF":1.4000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Medical Microbiology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0255085725001252","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose
– The emerging drug resistance in Tuberculous meningitis (TBM) worsens the prognosis and hamper elimination efforts. The need of the hour is a relatively simple, rapid, near point-of-care test that could allow universal drug susceptibility testing, beyond rifampicin (RIF). The current study evaluated performance of Xpert MTB/XDR in defining drug resistant TBM.
Methods
– A total of 45 cerebrospinal fluid samples (29 culture-positive, 16 culture-negative) reported TBM by Xpert MTB/Ultra were subjected to Xpert MTB/XDR to determine susceptibility towards isoniazid (INH), fluoroquinolones (FLQ), second-line injectables (SLID) and ethambutol (ETM). The performance of Xpert MTB/XDR was evaluated against genotypic drug susceptibility testing (line probe assay (LPA) and phenotypic drug susceptibility testing (culture)).
Results
– There was 100 % concordance between Xpert MTB/XDR and drug susceptibility using both culture and LPA for INH and SLIDs. For FLQ, the sensitivity and specificity of Xpert MTB/XDR was 93 % and 100 %, respectively against both culture and LPA, as there was one case each reported false-susceptible by Xpert MTB/XDR. The sensitivity and specificity of Xpert MTB/XDR for ETM was 93 % and 100 %, respectively against culture and one case of false-resistance was reported.
Conclusion
– Xpert MTB/XDR can serve as a useful tool to rapidly identify resistance to INH, FLQ, SLID and ETM, thus offering targeted therapy to the patients of TBM.
期刊介绍:
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