Your browser doesn't support javascript.
Two-test algorithms for infectious disease diagnosis: Implications for COVID-19.
Pokharel, Sunil; White, Lisa J; Sacks, Jilian A; Escadafal, Camille; Toporowski, Amy; Mohammed, Sahra Isse; Abera, Solomon Chane; Kao, Kekeletso; Melo Freitas, Marcela De; Dittrich, Sabine.
  • Pokharel S; Nuffield Department of Medicine, Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom.
  • White LJ; Foundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.
  • Sacks JA; Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Escadafal C; Foundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.
  • Toporowski A; Foundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.
  • Mohammed SI; Foundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.
  • Abera SC; National Reference Laboratory, Ministry of Health, Mogadishu, Somalia.
  • Kao K; World Health Organization Country Office in Somalia, Mogadishu, Somalia.
  • Melo Freitas M; Foundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.
  • Dittrich S; Foundation for Innovative New Diagnostics (FIND), Geneva, Switzerland.
PLOS Glob Public Health ; 2(3): e0000293, 2022.
Article in English | MEDLINE | ID: covidwho-1854963
ABSTRACT
Diagnostic assays for various infectious diseases, including COVID-19, have been challenged for their utility as standalone point-of-care diagnostic tests due to suboptimal accuracy, complexity, high cost or long turnaround times for results. It is therefore critical to optimise their use to meet the needs of users. We used a simulation approach to estimate diagnostic outcomes, number of tests required and average turnaround time of using two-test algorithms compared with singular testing; the two tests were reverse transcription polymerase chain reaction (RT-PCR) and an antigen-based rapid diagnostic test (Ag-RDT). A web-based application of the model was developed to visualise and compare diagnostic outcomes for different disease prevalence and test performance characteristics (sensitivity and specificity). We tested the model using hypothetical prevalence data for COVID-19, representing low- and high-prevalence contexts and performance characteristics of RT-PCR and Ag-RDTs. The two-test algorithm when RT-PCR was applied to samples negative by Ag-RDT predicted gains in sensitivity of 27% and 7%, respectively, compared with Ag-RDT and RT-PCR alone. Similarly, when RT-PCR was applied to samples positive by Ag-RDT, specificity gains of 2.9% and 1.9%, respectively, were predicted. The algorithm using Ag-RDT followed by RT-PCR as a confirmatory test for positive patients limited the requirement of RT-PCR testing resources to 16,400 and 3,034 tests when testing a population of 100,000 with an infection prevalence of 20% and 0.05%, respectively. A two-test algorithm comprising a rapid screening test followed by confirmatory laboratory testing can reduce false positive rate, produce rapid results and conserve laboratory resources, but can lead to large number of missed cases in high prevalence setting. The web application of the model can identify the best testing strategies, tailored to specific use cases and we also present some examples how it was used as part of the Access to Covid-19 Tools (ACT) Accelerator Diagnostics Pillar.

Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Observational study / Prognostic study Language: English Journal: PLOS Glob Public Health Year: 2022 Document Type: Article Affiliation country: Journal.pgph.0000293

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Type of study: Diagnostic study / Observational study / Prognostic study Language: English Journal: PLOS Glob Public Health Year: 2022 Document Type: Article Affiliation country: Journal.pgph.0000293