TY - JOUR
T1 - Modelling multiplex testing for outbreak control
AU - Fyles, Martyn
AU - Overton, Christopher E.
AU - Ward, Thomas
AU - Bennett, Emma
AU - Fowler, Tom
AU - Hall, Ian
N1 - Publisher Copyright:
© 2024
PY - 2024/12
Y1 - 2024/12
N2 - During the SARS-CoV-2 pandemic, polymerase chain reaction (PCR) and lateral flow device (LFD) tests were frequently deployed to detect the presence of SARS-CoV-2. Many of these tests were singleplex, and only tested for the presence of a single pathogen. Multiplex tests can test for the presence of several pathogens using only a single swab, which can allow for: surveillance of more pathogens, targeting of antiviral interventions, a reduced burden of testing, and lower costs. Test sensitivity, however, particularly in LFD tests, is highly conditional on the viral concentration dynamics of individuals. To inform the use of multiplex testing in outbreak detection it is therefore necessary to investigate the interactions between outbreak detection strategies and the differing viral concentration trajectories of key pathogens. Viral concentration trajectories are estimated for SARS-CoV-2 and Influenza A/B. Testing strategies for the first five symptomatic cases in an outbreak are then simulated and used to evaluate key performance indicators. Strategies that use a combination of multiplex LFD and PCR tests achieve; high levels of detection, detect outbreaks rapidly, and have the lowest burden of testing across multiple pathogens. Influenza B was estimated to have lower rates of detection due to its modelled viral concentration dynamics.
AB - During the SARS-CoV-2 pandemic, polymerase chain reaction (PCR) and lateral flow device (LFD) tests were frequently deployed to detect the presence of SARS-CoV-2. Many of these tests were singleplex, and only tested for the presence of a single pathogen. Multiplex tests can test for the presence of several pathogens using only a single swab, which can allow for: surveillance of more pathogens, targeting of antiviral interventions, a reduced burden of testing, and lower costs. Test sensitivity, however, particularly in LFD tests, is highly conditional on the viral concentration dynamics of individuals. To inform the use of multiplex testing in outbreak detection it is therefore necessary to investigate the interactions between outbreak detection strategies and the differing viral concentration trajectories of key pathogens. Viral concentration trajectories are estimated for SARS-CoV-2 and Influenza A/B. Testing strategies for the first five symptomatic cases in an outbreak are then simulated and used to evaluate key performance indicators. Strategies that use a combination of multiplex LFD and PCR tests achieve; high levels of detection, detect outbreaks rapidly, and have the lowest burden of testing across multiple pathogens. Influenza B was estimated to have lower rates of detection due to its modelled viral concentration dynamics.
KW - Detection
KW - Influenza
KW - Lateral flow device
KW - Multiplex
KW - Outbreak
KW - Polymerase Chain Reaction
KW - SARS-CoV-2
KW - Test sensitivity
KW - Testing
KW - Viral concentration
UR - http://www.scopus.com/inward/record.url?scp=85206075342&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/c528080e-40d2-3e40-b298-f4ac79eac466/
U2 - 10.1016/j.jinf.2024.106303
DO - 10.1016/j.jinf.2024.106303
M3 - Article
C2 - 39362473
AN - SCOPUS:85206075342
SN - 0163-4453
VL - 89
JO - Journal of Infection
JF - Journal of Infection
IS - 6
M1 - 106303
ER -