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Treatment of Multidrug-resistant or Rifampicin-resistant Tuberculosis With an All-oral 9-month Regimen Containing Linezolid or Ethionamide in South Africa: A Retrospective Cohort Study.
Morgan, Hannah; Ndjeka, Norbert; Hasan, Tasnim; Gegia, Medea; Mirzayev, Fuad; Nguyen, Linh N; Schumacher, Samuel; Schlub, Timothy E; Naidoo, Kogieleum; Fox, Greg J.
Afiliación
  • Morgan H; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
  • Ndjeka N; National Department of Health, Tuberculosis Control and Management Cluster, Pretoria, South Africa.
  • Hasan T; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
  • Gegia M; Global Tuberculosis Program, World Health Organisation, Geneva, Switzerland.
  • Mirzayev F; Global Tuberculosis Program, World Health Organisation, Geneva, Switzerland.
  • Nguyen LN; Global Tuberculosis Program, World Health Organisation, Geneva, Switzerland.
  • Schumacher S; Global Tuberculosis Program, World Health Organisation, Geneva, Switzerland.
  • Schlub TE; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
  • Naidoo K; Nelson R Mandela School of Medicine, University of KwaZulu Natal, Durban, South Africa.
  • Fox GJ; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Clin Infect Dis ; 78(6): 1698-1706, 2024 Jun 14.
Article en En | MEDLINE | ID: mdl-38525535
ABSTRACT

BACKGROUND:

In 2019, the South African tuberculosis program replaced ethionamide with linezolid as part of an all-oral 9-month regimen. We evaluated treatment outcomes for patients assigned to regimens including linezolid in 2019 and ethionamide in 2017.

METHODS:

This retrospective cohort study included patients treated for multidrug-resistant/rifampicin-resistant tuberculosis throughout South Africa between 1 January and 31 December 2017 and 1 January to 31 December 2019. The cohort treated with a 9-month regimen containing ethionamide for four months, was compared with a cohort treated with a 9-month regimen containing linezolid for 2 months. The regimens were otherwise identical. Inverse probability weighting of propensity scores was used to adjust for potential confounding. A log-binomial regression model was used to estimate adjusted relative risk (aRR) comparing 24-month outcomes between cohorts including treatment success, death, loss to follow up, and treatment failure. Adverse event data were available for the linezolid cohort.

FINDINGS:

In total, 817 patients were included in the cohort receiving ethionamide and 4244 in the cohort receiving linezolid. No evidence for a difference was observed between linezolid and ethionamide regimens for treatment success (aRR = 0.96, 95% confidence interval [CI] .91-1.01), death (aRR = 1.01, 95% CI .87-1.17) or treatment failure (aRR = 0.87, 95% CI .44-1.75). Loss to follow-up was more common in the linezolid group, although estimates were imprecise (aRR = 1.22, 95% CI .99-1.50).

CONCLUSIONS:

No significant differences in treatment success and survival were observed with substitution of linezolid for ethionamide as a part of an all-oral 9-month regimen. Linezolid is an acceptable alternative to ethionamide in this shorter regimen for treatment of multidrug-resistant/rifampicin-resistant tuberculosis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Rifampin / Tuberculosis Resistente a Múltiples Medicamentos / Etionamida / Linezolid / Antituberculosos Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Africa Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2024 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Rifampin / Tuberculosis Resistente a Múltiples Medicamentos / Etionamida / Linezolid / Antituberculosos Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Africa Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2024 Tipo del documento: Article País de afiliación: Australia