4.7 Article

Xpert Mycobacterium tuberculosis/Rifampicin-Detected Rifampicin Resistance is a Suboptimal Surrogate for Multidrug-resistant Tuberculosis in Eastern Democratic Republic of the Congo: Diagnostic and Clinical Implications

期刊

CLINICAL INFECTIOUS DISEASES
卷 73, 期 2, 页码 E362-E370

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa873

关键词

GenoType MTBDRplus assay; drug resistance; rpoB mutations; inhA mutations; DRC

资金

  1. Vlaamse Interuniversitaire Raad-Universitaire Ontwikkelingssamenwerking (VLIR-UOS) Institutional University Cooperation (IUC) [PRDC 2012MP80]
  2. Ghent University
  3. Katholieke Universiteit Leuven in Belgium
  4. Universite Catholique de Bukavu in the DRC
  5. Global Affairs Canada through STOP TB Partnership, a TB REACH Wave-2 grant

向作者/读者索取更多资源

In a study conducted in eastern Democratic Republic of the Congo, it was found that Xpert had a high sensitivity for detecting RIF resistance but a low positive-predictive value for MDR-TB. Comprehensive resistance testing for both INH and RIF should be performed in this setting.
Background. Rifampicin (RIF) resistance is highly correlated with isoniazid (INH) resistance and used as proxy for multidrug-resistant tuberculosis (MDR-TB). Using MTBDRplus as a comparator, we evaluated the predictive value of Xpert MTB/RIF (Xpert)-detected RIF resistance for MDR-TB in eastern Democratic Republic of the Congo (DRC). Methods. We conducted a cross-sectional study involving data from new or retreatment pulmonary adult TB cases evaluated between July 2013 and December 2016. Separate, paired sputa for smear microscopy and MTBDRpIus were collected. Xpert testing was performed subject to the availability of Xpert cartridges on sample remnants after microscopy. Results. Among 353 patients, 193 (54.7%) were previously treated and 224 (63.5%) were MTBDRplus TB positive. Of the 224,43 (19.2%) were RIF monoresistant, 11 (4.9%) were INH monoresistant, 53 (23.7%) had MDR-TB, and 117 (52.2%) were RIF and INH susceptible. Overall, among the 96 samples detected by MTBDRplus as RIF resistant, 53 (55.2%) had MDR-TB. Xpert testing was performed in 179 (50.7%) specimens; among these, 163 (91.1%) were TB positive and 73 (44.8%) RIF resistant. Only 45/73 (61.6%) Xpert-identified RIF-resistant isolates had concomitant MTBDRplus-detected INH resistance. Xpert had a sensitivity of 100.0% (95% CI, 92.1-100.0) for detecting RIF resistance but a positive-predictive value of only 61.6% (95% CI, 49.5-72.8) for MDR-TB. The most frequent mutations associated with RIF and INH resistance were S531L and 5315T1, respectively. Conclusions. In this high-risk MDR-TB study population, Xpert had low positive-predictive value for the presence of MDR-TB. Comprehensive resistance testing for both INH and RIF should be performed in this setting.

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