Decentralized Diagnosis and Treatment of Drug-Resistant Tuberculosis in Machakos County, Kenya

Authors

  • Johannes Ndambuki Department of Health and Emergency services, Machakos county, Kenya. Author
  • Tom Decroo Unit of HIV&TB, Department of Clinical Sciences, Institute of Tropical Medicine Antwerp, Kenya Author
  • Lucy Muregi Department of Health and Emergency services, Machakos county, Kenya Author
  • Joseph Nzomo Department of Health and Emergency services, Machakos county, Kenya Author
  • Francis Makokha Directorate of Research and Innovation, Mount Kenya University, Kenya Author
  • Jonathan Nthusi Department of Family Medicine and Community Care, Kabarak University, Kenya Author

DOI:

https://doi.org/10.47363/JPRR/2024(6)166

Keywords:

Drug-Resistant Tuberculosis, Rifampicin-Resistant Tuberculosis, Drug Susceptibility Testing

Abstract

Background: Access to drug susceptibility testing (DST) for drug-resistant tuberculosis (DR-TB) diagnosis is challenging. Between 2016-2019, in Machakos county, Kenya, Xpert MTB/RIF was available in 5 sites. Additional DST was done in the national lab. DR-TB treatment was available in 32 clinics.

Methods: This is a cohort study on DR-TB diagnosis, treatment outcomes, and their predictors in Machakos county, between 2016-2019. Rifampicinresistant TB (RR-TB) was treated with a short treatment regimen (STR). A long regimen was used for patients not eligible for the STR.

Results: Of 85 DR-TB patients, 84 (99%) and 72 (73%) had Xpert MTB/RIF and phenotypic rifampicin DST results, respectively. Of 85, 36 (42%) had rifampicin-susceptible drug-resistant TB (RS/DR-TB); resistance to other first-line drugs than rifampicin) and 49 (58%) had RR-TB. Xpert MTB/RIF and phenotypic DST showed discordant results for rifampicin in 8 patients (7 with RR missed on Xpert MTB/RIF). Of 49 with RR-TB, 45 had second-line DST results. One patient had TB resistant to fluoroquinolone and second-line injectables. Of 36 RS/DR-TB patients, 33 (92%) were treated successfully. Six RRTB patients died before starting treatment. One RR-TB patient was transferred out. Among the remaining 42 RR-TB patients, treatment success was 50% (11/22) for the STR and 80% (16/20) for the long regimen (p=0.04), with more PLHIV among patients on the STR (70% (14/22) vs 30% (6/20), p=0.03). HIV co-infection (aOR 8.5, 95%CI:1.2-59.2) but not STR use (aOR 1.5, 95%CI:0.3-8.1) predicted having a clinically unfavorable outcome (mortality or treatment failure). Seven patients (all RR-TB and HIV-positive) had severe or life-threatening adverse events, of whom 4 died.

Conclusion: RR-TB treatment success was lower than the 75% World Health Organization target. HIV co-infection and adverse events contributed to unsuccessful treatment outcomes. Decentralization of rapid DST, adverse event monitoring and management, and less toxic RR-TB regimens will be key towards improving outcomes.

Author Biographies

  • Johannes Ndambuki, Department of Health and Emergency services, Machakos county, Kenya.

    Johannes Ndambuki, Department of Health and Emergency services, Machakos county, Kenya.

  • Tom Decroo, Unit of HIV&TB, Department of Clinical Sciences, Institute of Tropical Medicine Antwerp, Kenya

    Unit of HIV&TB, Department of Clinical Sciences, Institute of Tropical Medicine Antwerp, Kenya

  • Lucy Muregi, Department of Health and Emergency services, Machakos county, Kenya


    Department of Health and Emergency services, Machakos county, Kenya

  • Joseph Nzomo, Department of Health and Emergency services, Machakos county, Kenya

    Department of Health and Emergency services, Machakos county, Kenya

  • Francis Makokha, Directorate of Research and Innovation, Mount Kenya University, Kenya

    Directorate of Research and Innovation, Mount Kenya University, Kenya

  • Jonathan Nthusi, Department of Family Medicine and Community Care, Kabarak University, Kenya

    Department of Family Medicine and Community Care, Kabarak University, Kenya

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Published

2024-02-09