Implications of Failure to Routinely Diagnose Resistance to Second-Line Drugs in Patients With Rifampicin-Resistant Tuberculosis on Xpert MTB/RIF: A Multisite Observational Study.

Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

Volume: 64

Issue: 11

Year of Publication: 2018

Affiliated Institutions:  Section of Infectious Diseases, Boston University School of Medicine, Massachusetts. National Health Laboratory Service, Cape Town, South Africa. Infectious Disease Prevention and Health Services Bureau, Prevention and Health Promotion Administration, Maryland Department of Health and Mental Hygiene, Baltimore. Department of Science and Technology/National Research Foundation Centre of Excellence in Biomedical Tuberculosis Research/South Africa Medical Research Council for Molecular Biology and Human Genetics, Stellenbosch University, Tyberberg. Department of Biostatistics, Boston University School of Public Health. Department of Cancer Biology, Dana-Farber Cancer Institute, Cambridge, Massachusetts. Department of Molecular Medicine and Haematology, School of Pathology, University of the Witwatersrand and National Health Laboratory Service, National Priority Program, Johannesburg, South Africa. Department of Epidemiology, University of North Carolina, Chapel Hill.

Abstract summary 

Xpert MTB/RIF (Xpert) detects rifampicin-resistant tuberculosis (RR-tuberculosis), enabling physicians to rapidly initiate a World Health Organization-recommended 5-drug regimen while awaiting second-line drug-susceptibility test (DST) results. We quantified the second-line DST results time and proportion of patients potentially placed on suboptimal therapy.We included RR-tuberculosis patients detected using Xpert at the South African National Health Laboratory Services (NHLS) of the Western Cape between November 2011 and June 2013 and at Eastern Cape, Free State, and Gauteng NHLS between November 2012 and December 2013. We calculated time from specimen collection to phenotypic second-line DST results. We identified isoniazid and ethionamide resistance mutations on line probe assay and performed pyrazinamide sequencing.Among 1332 RR-tuberculosis patients, only 44.7% (596) had second-line DST for both fluoroquinolones and second-line injectable: 55.8% (466 of 835) in the Western Cape and 26.2% (130 of 497) in the other provinces. Patients with smear negative disease and age ≤10 years were less likely to have a result (risk ratio [RR] = 0.72; 95% CI, 0.64-0.81 and RR = 0.49; 95% CI, 0.26-0.79). Median time to second-line DST was 53 days (range, 8-259). Of the 252 patients with complete second-line DST, 101 (40.1%) potentially initiated a suboptimal regimen: 46.8% in the Western Cape and 25.3% in the other provinces.Many South Africans diagnosed with RR-tuberculosis by Xpert initiate a suboptimal regimen, with information to adjust therapy available in half of all patients after a median 7 weeks. Algorithm completion and time delays remain challenging.

Authors & Co-authors:  Jacobson Karen R KR Barnard Marinus M Kleinman Mary B MB Streicher Elizabeth M EM Ragan Elizabeth J EJ White Laura F LF Shapira Ofer O Dolby Tania T Simpson John J Scott Lesley L Stevens Wendy W van Helden Paul D PD Van Rie Annelies A Warren Robin M RM

Study Outcome 

Source Link: Visit source

Statistics
Citations :  World Health Organization. Tuberculosis Diagnostics: Xpert MTB/RIF Test 2014. Available at: http://apps.who.int/iris/bitstream/10665/112469/1/9789241506700_eng.pdf. Accessed on 14 July 2016.
Authors :  14
Identifiers
Doi : 10.1093/cid/cix128
SSN : 1537-6591
Study Population
Male,Female
Mesh Terms
Adult
Other Terms
South Africa;drug resistance.;drug susceptibility;multidrug-resistant tuberculosis;tuberculosis
Study Design
Cross Sectional Study
Study Approach
Country of Study
South Africa
Publication Country
United States