Evidence map›Paper›PMID 34982766›Full record

ArticlePLoS computational biology2022

Microsimulation based quantitative analysis of COVID-19 management strategies.

István Z Reguly, Dávid Csercsik, János Juhász, Kálmán Tornai, Zsófia Bujtár, Gergely Horváth, Bence Keömley-Horváth, Tamás Kós, György Cserey, Kristóf Iván and 4 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

14 authors.

István Z RegulyFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0002-4385-4204
Dávid CsercsikFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0002-5917-1352
János JuhászFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0002-1307-7387
Kálmán TornaiFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0003-1852-0816
Zsófia BujtárFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.
Gergely HorváthFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0003-3316-1698
Bence Keömley-HorváthFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0002-6404-2598
Tamás KósFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0001-5105-4699
György CsereyFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0002-6836-1502
Kristóf IvánFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0003-3637-3979
Sándor PongorFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.
Gábor SzederkényiFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0003-4199-6089
Gergely RöstBolyai Institute, University of Szeged, Szeged, Hungary.ORCID 0000-0001-9476-3284
Attila Csikász-NagyFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary.ORCID 0000-0002-2919-5601

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pandemic management requires reliable and efficient dynamical simulation to predict and control disease spreading. The COVID-19 (SARS-CoV-2) pandemic is mitigated by several non-pharmaceutical interventions, but it is hard to predict which of these are the most effective for a given population. We developed the computationally effective and scalable, agent-based microsimulation framework PanSim, allowing us to test control measures in multiple infection waves caused by the spread of a new virus variant in a city-sized societal environment using a unified framework fitted to realistic data. We show that vaccination strategies prioritising occupational risk groups minimise the number of infections but allow higher mortality while prioritising vulnerable groups minimises mortality but implies an increased infection rate. We also found that intensive vaccination along with non-pharmaceutical interventions can substantially suppress the spread of the virus, while low levels of vaccination, premature reopening may easily revert the epidemic to an uncontrolled state. Our analysis highlights that while vaccination protects the elderly from COVID-19, a large percentage of children will contract the virus, and we also show the benefits and limitations of various quarantine and testing scenarios. The uniquely detailed spatio-temporal resolution of PanSim allows the design and testing of complex, specifically targeted interventions with a large number of agents under dynamically changing conditions.

Indexed as

Models, TheoreticalAdolescentAdultAgedAlgorithmsChildCOVID-19HumansMiddle AgedPandemicsQuarantineSARS-CoV-2Young Adult

Identifiers

PMID34982766
PMCPMC8759654

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.