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Spatial heterogeneity of extensively drug resistant-tuberculosis in Western Cape Province, South Africa.
Sy, Karla Therese L; Leavitt, Sarah V; de Vos, Margaretha; Dolby, Tania; Bor, Jacob; Horsburgh, C Robert; Warren, Robin M; Streicher, Elizabeth M; Jenkins, Helen E; Jacobson, Karen R.
Afiliación
  • Sy KTL; Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA.
  • Leavitt SV; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • de Vos M; DSI-NRF Centre of Excellence for Biomedical Tuberculosis Research/South African Medical Research Council Centre for Tuberculosis Research, Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
  • Dolby T; National Health Laboratory Service, Cape Town, South Africa.
  • Bor J; Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA.
  • Horsburgh CR; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • Warren RM; Department of Epidemiology, Boston University School of Public Health, Boston, MA, USA.
  • Streicher EM; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • Jenkins HE; Department of Global Health, Boston University School of Public Health, Boston, MA, USA.
  • Jacobson KR; Section of Infectious Diseases, School of Medicine and Boston Medical Center, Boston University, Boston, MA, USA.
Sci Rep ; 12(1): 10844, 2022 06 27.
Article en En | MEDLINE | ID: mdl-35760977
Tuberculosis (TB) remains a leading infectious disease killer globally. Treatment outcomes are especially poor among people with extensively drug-resistant (XDR) TB, until recently defined as rifampicin-resistant (RR) TB with resistance to an aminoglycoside (amikacin) and a fluoroquinolone (ofloxacin). We used laboratory TB test results from Western Cape province, South Africa between 2012 and 2015 to identify XDR-TB and pre-XDR-TB (RR-TB with resistance to one second-line drug) spatial hotspots. We mapped the percentage and count of individuals with RR-TB that had XDR-TB and pre-XDR-TB across the province and in Cape Town, as well as amikacin-resistant and ofloxacin-resistant TB. We found the percentage of pre-XDR-TB and the count of XDR-TB/pre-XDR-TB highly heterogeneous with geographic hotspots within RR-TB high burden areas, and found hotspots in both percentage and count of amikacin-resistant and ofloxacin-resistant TB. The spatial distribution of percentage ofloxacin-resistant TB hotspots was similar to XDR-TB hotspots, suggesting that fluoroquinolone-resistace is often the first step to additional resistance. Our work shows that interventions used to reduce XDR-TB incidence may need to be targeted within spatial locations of RR-TB, and further research is required to understand underlying drivers of XDR-TB transmission in these locations.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tuberculosis Resistente a Múltiples Medicamentos / Tuberculosis Extensivamente Resistente a Drogas / Mycobacterium tuberculosis Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tuberculosis Resistente a Múltiples Medicamentos / Tuberculosis Extensivamente Resistente a Drogas / Mycobacterium tuberculosis Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos