Continuous surveillance of drug-resistant TB burden in Rwanda: a retrospective cross-sectional study

Author:

Habimana-Mucyo Yves1,Dushime Augustin1,Migambi Patrick1,Habiyambere Innocent1,Semuto Ngabonziza Jean Claude23,Decroo Tom4ORCID

Affiliation:

1. Tuberculosis and Other Respiratory Communicable Diseases Division; HIV/AIDS, Disease Prevention and Control Department ; Rwanda Biomedical Centre, Kigali, Rwanda

2. National Reference Laboratory, Department of Biomedical Services , Rwanda Biomedical Centre, Kigali, Rwanda

3. School of Medicine and Pharmacy, Department of Clinical Biology, College of Medicine and Health Sciences, University of Rwanda , Kigali, Rwanda

4. Unit of HIV and TB, Department of Clinical Sciences, Institute of Tropical Medicine Antwerp, Antwerp , Belgium

Abstract

Abstract Background Since the roll-out of the Xpert MTB/RIF assay, continuous surveillance can provide an estimate of rifampicin-resistant TB (RR-TB) prevalence, provided high drug susceptibility testing (DST) coverage is achieved. We use national data from Rwanda to describe rifampicin DST coverage, estimate the prevalence of RR-TB and assess its predictors. Methods Routinely collected DST data were entered into an electronic TB case-based surveillance system. DST coverage was calculated among all bacteriologically confirmed pulmonary TB patients notified from 1 July 2019 to 30 June 2020 in Rwanda. The prevalence of RR-TB was estimated among those with DST results. Univariable and multivariable analysis was performed to explore predictors for RR TB. Results Among 4066 patients with bacteriologically confirmed pulmonary TB, rifampicin DST coverage was 95.6% (4066/4251). RR-TB was diagnosed in 73 patients. The prevalence of RR-TB was 1.4% (53/3659; 95% CI 1.09 to 1.89%) and 4.9% (20/406; 95% CI 3.03 to 7.51%) in new and previously treated TB cases, respectively. Predictors of RR-TB were: (1) living in Kigali City (adjusted OR [aOR] 1.65, 95% CI 1.03 to 2.65); (2) previous TB treatment (aOR 3.64, 95% CI 2.14 to 6.19); and (3) close contact with a known RR-TB patient (aOR 11.37, 95% CI 4.19 to 30.82). Conclusions High rifampicin DST coverage for routine reporting allowed Rwanda to estimate the RR-TB prevalence among new and previously treated patients.

Publisher

Oxford University Press (OUP)

Subject

Public Health, Environmental and Occupational Health,General Medicine,Health (social science)

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