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Optimising treatments for sexually transmitted infections: surveillance, pharmacokinetics and pharmacodynamics, therapeutic strategies, and molecular resistance prediction
Department of Medicine, University of North Carolina, Chapel Hill, NC, USA.
Department of Medicine, Wake Forest University, Winston Salem, NC, USA; Division of Sexually Transmitted Diseases Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Department of Medicine, University of Washington, Seattle, WA, USA.
Global HIV, Hepatitis and Sexually Transmitted Infections Programme, WHO, Geneva, Switzerland.
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2020 (engelsk)Inngår i: The Lancet - Infectious diseases, ISSN 1473-3099, E-ISSN 1474-4457, Vol. 20, nr 8, s. e181-e191Artikkel, forskningsoversikt (Fagfellevurdert) Published
Abstract [en]

Progressive antimicrobial resistance in Neisseria gonorrhoeae, Mycoplasma genitalium, and Trichomonas vaginalis has created a pressing need for treatment optimisations for sexually transmitted infections (STIs). In this Review, we aim to highlight urgent needs in global STI management, including: (1) improved surveillance to monitor antimicrobial resistance and clinical outcomes; (2) systematic pharmacokinetic and pharmacodynamic evaluations to ensure resistance suppression and bacterial eradication at all sites of infection; (3) development of novel, affordable antimicrobials; and (4) advancements in new molecular and point-of-care tests to detect antimicrobial resistance determinants. Antimicrobial resistance among STIs is a global public health crisis. Continuous efforts to develop novel antimicrobials will be essential, in addition to other public health interventions to reduce the global STI burden. Apart from prevention through safer sexual practices, the development of STI vaccines to prevent transmission is a crucial research priority.

sted, utgiver, år, opplag, sider
Elsevier, 2020. Vol. 20, nr 8, s. e181-e191
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-84242DOI: 10.1016/S1473-3099(20)30171-7ISI: 000559753300007PubMedID: 32569625Scopus ID: 2-s2.0-85089028165OAI: oai:DiVA.org:oru-84242DiVA, id: diva2:1460910
Merknad

Funding Agency:

US National Institute of Health's (NIH's) Division of Microbiology and Infectious Diseases of the National Institute of Allergy and Infectious Diseases  HHSN272201300012

Tilgjengelig fra: 2020-08-25 Laget: 2020-08-25 Sist oppdatert: 2024-01-17bibliografisk kontrollert

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