Cargando…

Using rapid point-of-care tests to inform antibiotic choice to mitigate drug resistance in gonorrhoea

BACKGROUND: The first cases of extensively drug resistant gonorrhoea were recorded in the United Kingdom in 2018. There is a public health need for strategies on how to deploy existing and novel antibiotics to minimise the risk of resistance development. As rapid point-of-care tests (POCTs) to predi...

Descripción completa

Detalles Bibliográficos
Autores principales: Vegvari, Carolin, Grad, Yonatan H, White, Peter J, Didelot, Xavier, Whittles, Lilith K, Scangarella-Oman, Nicole E, Mitrani-Gold, Fanny S, Dumont, Etienne, Perry, Caroline R, Gilchrist, Kim, Hossain, Mohammad, Mortimer, Tatum D, Anderson, Roy M, Gardiner, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Centre for Disease Prevention and Control (ECDC) 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596916/
https://www.ncbi.nlm.nih.gov/pubmed/33124551
http://dx.doi.org/10.2807/1560-7917.ES.2020.25.43.1900210
Descripción
Sumario:BACKGROUND: The first cases of extensively drug resistant gonorrhoea were recorded in the United Kingdom in 2018. There is a public health need for strategies on how to deploy existing and novel antibiotics to minimise the risk of resistance development. As rapid point-of-care tests (POCTs) to predict susceptibility are coming to clinical use, coupling the introduction of an antibiotic with diagnostics that can slow resistance emergence may offer a novel paradigm for maximising antibiotic benefits. Gepotidacin is a novel antibiotic with known resistance and resistance-predisposing mutations. In particular, a mutation that confers resistance to ciprofloxacin acts as the ‘stepping-stone’ mutation to gepotidacin resistance. AIM: To investigate how POCTs detecting Neisseria gonorrhoeae resistance mutations for ciprofloxacin and gepotidacin can be used to minimise the risk of resistance development to gepotidacin. METHODS: We use individual-based stochastic simulations to formally investigate the aim. RESULTS: The level of testing needed to reduce the risk of resistance development depends on the mutation rate under treatment and the prevalence of stepping-stone mutations. A POCT is most effective if the mutation rate under antibiotic treatment is no more than two orders of magnitude above the mutation rate without treatment and the prevalence of stepping-stone mutations is 1–13%. CONCLUSION: Mutation frequencies and rates should be considered when estimating the POCT usage required to reduce the risk of resistance development in a given population. Molecular POCTs for resistance mutations and stepping-stone mutations to resistance are likely to become important tools in antibiotic stewardship.