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. 2023 Jun;12(6):1445-1463.
doi: 10.1007/s40121-023-00815-z. Epub 2023 Jun 1.

Rapid Diagnostic Test Value and Implementation in Antimicrobial Stewardship Across Low-to-Middle and High-Income Countries: A Mixed-Methods Review

Affiliations

Rapid Diagnostic Test Value and Implementation in Antimicrobial Stewardship Across Low-to-Middle and High-Income Countries: A Mixed-Methods Review

Luke S P Moore et al. Infect Dis Ther. 2023 Jun.

Abstract

Despite technological advancements in infectious disease rapid diagnostic tests (RDTs) and use to direct therapy at the per-patient level, RDT utilisation in antimicrobial stewardship programmes (ASPs) is variable across low-to-middle income and high-income countries. Key insights from a panel of seven infectious disease experts from Colombia, Japan, Nigeria, Thailand, the UK, and the USA, combined with evidence from a literature review, were used to assess the value of RDTs in ASPs. From this, a value framework is proposed which aims to define the benefits of RDT use in ASPs, separate from per-patient benefits. Expert insights highlight that, to realise the value of RDTs within ASPs, effective implementation is key; actionable advice for choosing an RDT is proposed. Experts advocate the inclusion of RDTs in the World Health Organization Model List of essential in vitro diagnostics and in iterative development of national action plans.

Keywords: Antimicrobial resistance; Antimicrobial stewardship; Antimicrobial stewardship programmes; High-, middle-, and low-income countries; Infectious disease RDT; Point-of-care testing; Rapid diagnostic tests.

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Conflict of interest statement

Luke S. P. Moore has consulted for or received speaker fees from bioMerieux (2013–2022), Pfizer (2018–2022), Eumedica (2016–2022), Kent Pharma (2021), Umovis Lab (2020–2021), Shionogi (2021–2022), Pulmocide (2021), Sumitovant (2021–2022), and received research grants from the National Institute for Health Research (2013–2022), CW+ Charity (2018–2022), Infectopharm (2022), and LifeArc (2020–2022). Anucha Apisarnthanarak declares no competing interests. Eric Wenzler reports grants from Qiagen and Shionogi Inc (research grant paid to institution), and personal fees from Abbvie Inc, Ferring Pharmaceuticals, Qiagen, Melinta Therapeutics, Astellas Pharma and Venatorx Pharmaceuticals. Maria Virginia Villegas reports grants from Pfizer and bioMerieux, personal fees from Pfizer, MSD and bioMerieux and support for meetings from Pfizer and bioMerieux. Rita O. Oladele declares no competing interests. Timothy M. Rawson reports personal fees from bioMeriuex, Roche Diagnostics Ltd and Pfizer. Yohei Doi reports personal fees from Gilead Sciences, MSD, GSK, Shionogi, Meiji Seika Pharma, Moderna, bioMerieux, Chugai, FujiFilm, MSD and Eiken Chemical.

Figures

Fig. 1
Fig. 1
Main barriers to use of RDTs, derived from EWG semi-structured interviews. EWG expert working group, RDT rapid diagnostic test
Fig. 2
Fig. 2
The value of RDT use in ASPs to key stakeholders: hospitals, clinicians, patients, and society. AMS antimicrobial stewardship, ASP antimicrobial stewardship programme, RDT rapid diagnostic test
Fig. 3
Fig. 3
EWG perspectives on RDT use across the patient care pathway. EWG expert working group, HCP healthcare professional, RDT rapid diagnostic test

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