Evidence map›Paper›PMID 35027019›Full record

ArticleBMC public health2022

Quantitative comparison of SARS-CoV-2 nucleic acid amplification test and antigen testing algorithms: a decision analysis simulation model.

Phillip P Salvatore, Melisa M Shah, Laura Ford, Augustina Delaney, Christopher H Hsu, Jacqueline E Tate, Hannah L Kirking

Open access · goldAbstract read
In one paragraph

Article in BMC public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Managing the risks of making the wrong diagnosis: First, do no harm.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2021
    Article
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

7 authors at 2 institutions in 1 country.

Phillip P SalvatoreCOVID-19 Response Team, Centers for Disease Control and Prevention (CDC), 1600 Clifton Road NE, Atlanta, USA. pgx5@cdc.gov.
Melisa M ShahCOVID-19 Response Team, Centers for Disease Control and Prevention (CDC), 1600 Clifton Road NE, Atlanta, USA.
Laura FordCOVID-19 Response Team, Centers for Disease Control and Prevention (CDC), 1600 Clifton Road NE, Atlanta, USA.
Augustina DelaneyCOVID-19 Response Team, Centers for Disease Control and Prevention (CDC), 1600 Clifton Road NE, Atlanta, USA.
Christopher H HsuCOVID-19 Response Team, Centers for Disease Control and Prevention (CDC), 1600 Clifton Road NE, Atlanta, USA.
Jacqueline E TateCOVID-19 Response Team, Centers for Disease Control and Prevention (CDC), 1600 Clifton Road NE, Atlanta, USA.
Hannah L KirkingCOVID-19 Response Team, Centers for Disease Control and Prevention (CDC), 1600 Clifton Road NE, Atlanta, USA.
Centers for Disease Control and Prevention · USEpidemic Intelligence Service · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntigen tests for SARS-CoV-2 offer advantages over nucleic acid amplification tests (NAATs, such as RT-PCR), including lower cost and rapid return of results, but show reduced sensitivity. Public health organizations recommend different strategies for utilizing NAATs and antigen tests. We sought to create a framework for the quantitative comparison of these recommended strategies based on their expected performance.

methodsWe utilized a decision analysis approach to simulate the expected outcomes of six testing algorithms analogous to strategies recommended by public health organizations. Each algorithm was simulated 50,000 times in a population of 100,000 persons seeking testing. Primary outcomes were number of missed cases, number of false-positive diagnoses, and total test volumes. Outcome medians and 95% uncertainty ranges (URs) were reported.

resultsAlgorithms that use NAATs to confirm all negative antigen results minimized missed cases but required high NAAT capacity: 92,200 (95% UR: 91,200-93,200) tests (in addition to 100,000 antigen tests) at 10% prevalence. Selective use of NAATs to confirm antigen results when discordant with symptom status (e.g., symptomatic persons with negative antigen results) resulted in the most efficient use of NAATs, with 25 NAATs (95% UR: 13-57) needed to detect one additional case compared to exclusive use of antigen tests.

conclusionsNo single SARS-CoV-2 testing algorithm is likely to be optimal across settings with different levels of prevalence and for all programmatic priorities. This analysis provides a framework for selecting setting-specific strategies to achieve acceptable balances and trade-offs between programmatic priorities and resource constraints.

Indexed as

COVID-19SARS-CoV-2AlgorithmsCOVID-19 TestingDecision Support TechniquesHumansNucleic Acid Amplification TechniquesSensitivity and SpecificityAntigen testCOVID-19Decision analysisMathematical modelSARS-CoV-2

Identifiers

PMID35027019
PMCPMC8756411
OpenAlexW4226044354

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.