Imperial College London

ProfessorPaulFreemont

Faculty of MedicineDepartment of Infectious Disease

Chair in Protein Crystallography
 
 
 
//

Contact

 

+44 (0)20 7594 5327p.freemont

 
 
//

Location

 

259Sir Alexander Fleming BuildingSouth Kensington Campus

//

Summary

 

Publications

Citation

BibTex format

@article{Crone:2021:10.12688/wellcomeopenres.17226.1,
author = {Crone, M and Randell, P and Herm, Z and Anand, A and Missaghian-Cully, S and Perelman, L and Pantelidis, P and Freemont, P},
doi = {10.12688/wellcomeopenres.17226.1},
journal = {Wellcome Open Research},
pages = {1--13},
title = {Rapid design and implementation of an adaptive pooling workflow for SARS-CoV-2 testing in an NHS diagnostic laboratory: a proof-of-concept study},
url = {http://dx.doi.org/10.12688/wellcomeopenres.17226.1},
volume = {6},
year = {2021}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Background: Diagnostic laboratories are currently required to provide routine testing of asymptomatic staff and patients as a part of their clinical screening for SARS-CoV-2 infection. However, these cohorts display very different disease prevalence from symptomatic individuals and testing capacity for asymptomatic screening is often limited. Group testing is frequently proposed as a possible solution to address this; however, proposals neglect the technical and operational feasibility of implementation in a front-line diagnostic laboratory.Methods: Between October and December 2020, as a seven-week proof of concept, we took into account scientific, technical and operational feasibility to design and implement an adaptive pooling strategy in an NHS diagnostic laboratory in London (UK). We assessed the impact of pooling on analytical sensitivity and modelled the impact of prevalence on pooling strategy. We then considered the operational constraints to model the potential gains in capacity and the requirements for additional staff and infrastructure. Finally, we developed a LIMS-agnostic laboratory automation workflow and software solution and tested the technical feasibility of our adaptive pooling workflow.Results: First, we determined the analytical sensitivity of the implemented SARS-CoV-2 assay to be 250 copies/mL. We then determined that, in a setting with limited analyser capacity, the testing capacity could be increased by two-fold with pooling, however, in a setting with limited reagents, this could rise to a five-fold increase. These capacity increases could be realized with modest additional resource and staffing requirements whilst utilizing up to 76% fewer plastic consumables and 90% fewer reagents. Finally, we successfully implemented a plate-based pooling workflow and tested 920 patient samples using the reagents that would usually be required to process just 222 samples.Conclusions: Adaptive pooled testing is a scientifically, technically and operatio
AU - Crone,M
AU - Randell,P
AU - Herm,Z
AU - Anand,A
AU - Missaghian-Cully,S
AU - Perelman,L
AU - Pantelidis,P
AU - Freemont,P
DO - 10.12688/wellcomeopenres.17226.1
EP - 13
PY - 2021///
SN - 2398-502X
SP - 1
TI - Rapid design and implementation of an adaptive pooling workflow for SARS-CoV-2 testing in an NHS diagnostic laboratory: a proof-of-concept study
T2 - Wellcome Open Research
UR - http://dx.doi.org/10.12688/wellcomeopenres.17226.1
UR - https://wellcomeopenresearch.org/articles/6-268/v1
UR - http://hdl.handle.net/10044/1/92067
VL - 6
ER -