Evidence map›Paper›PMID 41618184›Full record

ArticleBMC infectious diseases2026

Sample pooling approaches simulated under resource scarcity, lapses in testing capacity, and rapid processing demands for surveillance testing: a data-driven performance comparison.

Catharine Burgess, Alan Curran, Alessandro Ceci, Carla V Finkielstein, Kevin Lahmers

Abstract readComparative Study
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Catharine BurgessDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Tech, Blacksburg, VA, USA.
Alan CurranIndependent Researcher, Perrysburg, OH, USA.
Alessandro CeciFralin Biomedical Research Institute at VTC, Virginia Tech, Roanoke, VA, USA.
Carla V FinkielsteinFralin Biomedical Research Institute at VTC, Virginia Tech, Roanoke, VA, USA. finkielc@vt.edu.
Kevin LahmersDepartment of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Tech, Blacksburg, VA, USA. klahmers@vt.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSample pooling is a critical strategy to meet increased testing demand and conserve resources in surveillance testing. Much of its effectiveness depends on how well optimized the pool size is to the prevalence of infection in the sampled population, which can be difficult to anticipate in many circumstances. Multiple methods exist to better optimize pooling, with unique trade-offs.

methodsPooling optimization methods were simulated to examine trade-offs between surveillance priorities and operational characteristics using SARS-CoV-2 surveillance data and workflows generated by the Virginia Tech Molecular Diagnostics Laboratory under varying capacity conditions. All in-house validation procedures were designed and established exclusively under CLIA to ensure full control of the analytical framework and to accurately reflect true capacity constraints. We used binary surveillance data to run Monte Carlo simulations (MCS) comparing conservative and large fixed pools, historical prevalence optimization (HPO), prevalence estimation testing (PET), truly optimized pooling, and individual testing. Median test counts from the MCS fed a discrete-event simulation (DES) that assessed processing time at different lab capacities under surveillance and outbreak conditions. We then used the combined performance results to build a classification tree to guide method selection under different testing priorities and constraints.

resultsMCS results indicated that small pools (4 samples), HPO, and PET resulted in test counts that were not statistically different from truly optimized pooling (p > 0.05). The DES showed that pooling methods generally performed comparably to individual testing in processing time at low laboratory capacity, but individual testing became faster as capacity increased. Across capacity conditions, individual testing processed fewer than 500 daily samples more quickly, yet it demanded more hands-on time than pooling. Large-scale surveillance favored pooled methods, which were quicker under most conditions, while outbreak scenarios often favored individual testing when capacity wasn’t highly limited. Machine learning analysis highlighted surveillance priorities and sample intake as key determinants in selecting the best pooling optimization method for the given circumstance.

conclusionThis study demonstrates the importance of maintaining multiple pooling optimization approaches and adapting strategies to match evolving demands and potential constraints in surveillance testing. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

COVID-19Pooled TestingComputer SimulationHumansMonte Carlo MethodPrevalenceSARS-CoV-2Specimen HandlingCOVID-19Pooling optimizationProcessing timeResource conservationSARS-CoV-2Surveillance testingTesting capacity

Identifiers

PMID41618184
PMCPMC12930655

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.