Abstract

BackgroundXpert MTB/RIF (Xpert) is an automated molecular test recommended by World Health Organization (WHO) for diagnosis of tuberculosis (TB). This study evaluated the effect of Xpert implementation on the detection of pulmonary TB (PTB) and rifampicin-resistant TB (RR-TB) cases in Shanghai, China.MethodsXpert was routinely implemented in 2018 for all presumptive PTB patients. All PTB patients above 15 years-old identified within the Provincial TB Control Program during the first half of each of 2017 and 2018, were enrolled to compare the difference in proportions of bacteriological confirmation, patients with drug susceptibility test (DST) results for rifampicin (ie, DST coverage) and RR-TB detection before and after Xpert’s implementation.ResultsA total of 6047 PTB patients were included in the analysis with 1691 tested by Xpert in 2018. Percentages of bacteriological confirmation, DST coverage and RR-TB detection in 2017 and 2018 were 50% vs. 59%, 36% vs. 49% and 2% vs. 3%, respectively (all p-values < 0.05). Among 1103 PTB patients who completed sputum smear, culture and Xpert testing in 2018, Xpert detected an additional 121 (11%) PTB patients who were negative by smear and culture, but missed 248 (23%) smear and/or culture positive patients. Besides, it accounted for an increase of 9% in DST coverage and 1% in RR-TB detection. The median time from first visit to a TB hospital to RR-TB detection was 62 days (interquartile range -IQR 48–84.2) in 2017 vs. 9 days (IQR 2–45.7) in 2018 (p-value < 0.001). In the multivariate model, using Xpert was associated with decreased time to RR-TB detection (adjusted hazard ratio = 4.62, 95% confidence interval: 3.18–6.71).ConclusionsIntegrating Xpert with smear, culture and culture-based DST in a routine setting significantly increased bacteriological confirmation, DST coverage and RR-TB detection with a dramatic reduction in the time to RR-TB diagnosis in Shanghai, China. Our findings can be useful for other regions that attempt to integrate Xpert into routine PTB and RR-TB case-finding cascade. Further study should focus on the identification and elimination of operational level challenges to fully utilize the benefit of rapid diagnosis by Xpert.

Highlights

  • Xpert MTB/RIF (Xpert) Mycobacterium tuberculosis (MTB)/RIF (Xpert) is an automated molecular test recommended by World Health Organization (WHO) for diagnosis of tuberculosis (TB)

  • Xpert® MTB/RIF assay (Cepheid, USA) (Xpert) is a rapid test for TB diagnosis currently endorsed by the WHO [4], which simultaneously tests for Mycobacterium tuberculosis (MTB) and resistance to rifampicin (RIF), providing results within 2 h

  • After excluding patients under 15 years old (31 cases) and those diagnosed as nontuberculous mycobacteria (NTM, 279 cases), 6047 pulmonary TB (PTB) patients were included in the analysis (2017: 2938; 2018: 3109), with a median age of 44 years (IQR 27–62)

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Summary

Introduction

Xpert MTB/RIF (Xpert) is an automated molecular test recommended by World Health Organization (WHO) for diagnosis of tuberculosis (TB). This study evaluated the effect of Xpert implementation on the detection of pulmonary TB (PTB) and rifampicin-resistant TB (RR-TB) cases in Shanghai, China. Sputum smear microscopy, culture and culture-based drug susceptibility test (DST) are used to diagnose TB and MDR/RR-TB. Clinical validation trials have demonstrated high sensitivity and specificity of the test for both MTB and RIF-resistance detection in different settings [4,5,6,7]. Several studies have even suggested that Xpert outperforms culture in salivary sputum [8, 9] and can detect low-levels of RIF-resistance, which might be missed by culture-based DST [10, 11]. The use of Xpert in decentralized settings has significantly increased proportions of bacteriologically confirmed TB and RR-TB and reduced the time to treatment initiation [12,13,14,15]

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