Abstract

The Lesotho guidelines for the management of drug-resistant tuberculosis (TB) recommend initiation of patients diagnosed with rifampicin resistant (RR)-TB on a standardized drug resistant regimen while awaiting confirmation of rifampicin resistant TB (RR-TB) and complete drug susceptibility test results. Review of diagnostic records between 2014 and 2016 identified 518 patients with RR-TB. Only 314 (60.6%) patients could be linked to treatment records at the Lesotho MDR hospital. The median delay in treatment initiation from the availability of Xpert MTB/RIF assay result was 12 days (IQR 7–19). Only 32% (101) of patients had a documented first-line drug resistant test. MDR-TB was detected in 56.4% of patients while 33.7% of patients had rifampicin mono-resistance. Only 7.4% of patients assessed for second-line resistance had a positive result (resistance to fluoroquinolone). Treatment success was 69.8%, death rate was 28.8%, loss to follow up was 1.0%, and 0.4% failed treatment. Death was associated with positive or unavailable sputum smear at the end of first month of treatment (Fisher exact p < 0.001) and older age (p = 0.007). Urgent attention needs to be given to link patients with RR-TB to care worldwide. The association of death rate with positive sputum smear at the end of the first month of treatment should trigger early individualization of treatment.

Highlights

  • In 2018, the World Health Organization (WHO) estimated the number of rifampicin resistant tuberculosis (RR-TB) cases to be 484 000, which is a slight decrease compared to the 558 000 cases estimated globally in 20171

  • The current Lesotho National Guidelines for Tuberculosis recommends initiation of all patients diagnosed with rifampicin resistant TB (RR-TB) using the Xpert MTB/RIF assay on a standard drug resistant TB treatment regimen

  • We aimed to determine the proportion of patients with RR-TB linked to care, the turnaround time for treatment initiation, factors associated with delays, and to assess treatment outcomes for patients diagnosed with RR-TB using the Xpert MTB/RIF assay

Read more

Summary

Introduction

In 2018, the World Health Organization (WHO) estimated the number of rifampicin resistant tuberculosis (RR-TB) cases to be 484 000, which is a slight decrease compared to the 558 000 cases estimated globally in 20171. The implementation of GeneXpert has aimed to improve TB case detection due to the high accuracy of the test, reduce the time to TB diagnosis and treatment initiation due to the rapidity of the test, and improve TB treatment outcomes by earlier identification of patients with RR-TB4,5. The current Lesotho National Guidelines for Tuberculosis recommends initiation of all patients diagnosed with RR-TB using the Xpert MTB/RIF assay on a standard drug resistant TB treatment regimen. This standard regimen may be adjusted with each patient receiving a personal regimen (individualization) based on subsequent drug susceptibility test (DST) results. We aimed to determine the proportion of patients with RR-TB linked to care, the turnaround time for treatment initiation, factors associated with delays, and to assess treatment outcomes for patients diagnosed with RR-TB using the Xpert MTB/RIF assay

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call