Dynamic Network Strategies for SARS-CoV-2 Control on a Cruise Ship.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
06 Oct 2020
Historique:
pubmed: 11 9 2020
medline: 11 9 2020
entrez: 10 9 2020
Statut: epublish

Résumé

SARS-CoV-2 outbreaks have occurred on several nautical vessels, driven by the high-density contact networks on these ships. Optimal strategies for prevention and control that account for realistic contact networks are needed. We developed a network-based transmission model for SARS-CoV-2 on the Diamond Princess outbreak to characterize transmission dynamics and to estimate the epidemiological impact of outbreak control and prevention measures. This model represented the dynamic multi-layer network structure of passenger-passenger, passenger-crew, and crew-crew contacts, both before and after the large-scale network lockdown imposed on the ship in response to the disease outbreak. Model scenarios evaluated variations in the timing of the network lockdown, reduction in contact intensity within the sub-networks, and diagnosis-based case isolation on outbreak prevention. We found that only extreme restrictions in contact patterns during network lockdown and idealistic clinical response scenarios could avert a major COVID-19 outbreak. Contact network changes associated with adequate outbreak prevention were the restriction of passengers to their cabins, with limited passenger-crew contacts. Clinical response strategies required for outbreak prevention included early mass screening with an ideal PCR test (100% sensitivity) and immediate case isolation upon diagnosis. Public health restrictions on optional leisure activities like these should be considered until longer-term effective solutions such as a COVID-19 vaccine become widely available.

Identifiants

pubmed: 32909009
doi: 10.1101/2020.08.26.20182766
pmc: PMC7480061
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI138783
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Commentaires et corrections

Type : UpdateIn

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Auteurs

Samuel M Jenness (SM)

Emory University Rollins School of Public Health, Atlanta, GA 30322, USA.

Kathryn S Willebrand (KS)

Yale Institute of Global Health, New Haven, CT 06510, USA.
Yale School of Public Health, New Haven, CT 06510, USA.

Amyn A Malik (AA)

Yale Institute of Global Health, New Haven, CT 06510, USA.
Yale School of Medicine, New Haven, CT 06510, USA.

Benjamin A Lopman (BA)

Emory University Rollins School of Public Health, Atlanta, GA 30322, USA.

Saad B Omer (SB)

Yale Institute of Global Health, New Haven, CT 06510, USA.
Yale School of Public Health, New Haven, CT 06510, USA.
Yale School of Medicine, New Haven, CT 06510, USA.
Yale School of Nursing, Orange, CT 06477, USA.

Classifications MeSH