Evidence map›Paper›PMID 36435792›Full record

ArticleInfectious diseases of poverty2022

Optimal control strategies of SARS-CoV-2 Omicron supported by invasive and dynamic models.

Jia Rui, Jin-Xin Zheng, Jin Chen, Hongjie Wei, Shanshan Yu, Zeyu Zhao, Xin-Yi Wang, Mu-Xin Chen, Shang Xia, Ying Zhou and 2 more

Abstract read
In one paragraph

Article in Infectious diseases of poverty, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 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

12 authors.

Jia Rui *State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health, Xiamen University, Xiamen, People's Republic of China.
Jin-Xin Zheng *Department of Nephrology, Institute of Nephrology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, People's Republic of China.
Jin Chen *National Institute of Parasitic Diseases at Chinese Center for Disease Control and Prevention, WHO Collaborating Centre for Tropical Diseases, NHC Key Laboratory of Parasites and Vectors Biology of China, Shanghai, 200025, People's Republic of China.
Hongjie Wei *State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health, Xiamen University, Xiamen, People's Republic of China.
Shanshan YuState Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health, Xiamen University, Xiamen, People's Republic of China.
Zeyu ZhaoState Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health, Xiamen University, Xiamen, People's Republic of China.
Xin-Yi WangNational Institute of Parasitic Diseases at Chinese Center for Disease Control and Prevention, WHO Collaborating Centre for Tropical Diseases, NHC Key Laboratory of Parasites and Vectors Biology of China, Shanghai, 200025, People's Republic of China.
Mu-Xin ChenNational Institute of Parasitic Diseases at Chinese Center for Disease Control and Prevention, WHO Collaborating Centre for Tropical Diseases, NHC Key Laboratory of Parasites and Vectors Biology of China, Shanghai, 200025, People's Republic of China.
Shang XiaNational Institute of Parasitic Diseases at Chinese Center for Disease Control and Prevention, WHO Collaborating Centre for Tropical Diseases, NHC Key Laboratory of Parasites and Vectors Biology of China, Shanghai, 200025, People's Republic of China.
Ying ZhouSchool of Global Health, Chinese Center for Tropical Diseases Research, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, People's Republic of China. 14966898@qq.com.
Tianmu ChenState Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health, Xiamen University, Xiamen, People's Republic of China. 13698665@qq.com.
Xiao-Nong ZhouNational Institute of Parasitic Diseases at Chinese Center for Disease Control and Prevention, WHO Collaborating Centre for Tropical Diseases, NHC Key Laboratory of Parasites and Vectors Biology of China, Shanghai, 200025, People's Republic of China. zhouxn1@chinacdc.cn.ORCID http://orcid.org/0000-0003-1417-8427

Funding

China Medical Board No. 20-365National Key Research and Development Program of China 2021YFC2300804National Key Research and Development Program of China 2021YFC2301604Shanghai Jiao Tong University Integrated Innovation Fund No. 2020-01
6 · The paper itself

Abstract

backgroundThere is a raising concern of a higher infectious Omicron BA.2 variant and the latest BA.4, BA.5 variant, made it more difficult in the mitigation process against COVID-19 pandemic. Our study aimed to find optimal control strategies by transmission of dynamic model from novel invasion theory.

methodsBased on the public data sources from January 31 to May 31, 2022, in four cities (Nanjing, Shanghai, Shenzhen and Suzhou) of China. We segmented the theoretical curves into five phases based on the concept of biological invasion. Then, a spatial autocorrelation analysis was carried out by detecting the clustering of the studied areas. After that, we choose a mathematical model of COVID-19 based on system dynamics methodology to simulate numerous intervention measures scenarios. Finally, we have used publicly available migration data to calculate spillover risk.

resultsEpidemics in Shanghai and Shenzhen has gone through the entire invasion phases, whereas Nanjing and Suzhou were all ended in the establishment phase. The results indicated that Rt value and public health and social measures (PHSM)-index of the epidemics were a negative correlation in all cities, except Shenzhen. The intervention has come into effect in different phases of invasion in all studied cities. Until the May 31, most of the spillover risk in Shanghai remained above the spillover risk threshold (18.81-303.84) and the actual number of the spillovers (0.94-74.98) was also increasing along with the time. Shenzhen reported Omicron cases that was only above the spillover risk threshold (17.92) at the phase of outbreak, consistent with an actual partial spillover. In Nanjing and Suzhou, the actual number of reported cases did not exceed the spillover alert value.

conclusionsBiological invasion is positioned to contribute substantively to understanding the drivers and mechanisms of the COVID-19 spread and outbreaks. After evaluating the spillover risk of cities at each invasion phase, we found the dynamic zero-COVID strategy implemented in four cities successfully curb the disease epidemic peak of the Omicron variant, which was highly correlated to the way to perform public health and social measures in the early phases right after the invasion of the virus.

Indexed as

COVID-19SARS-CoV-2ChinaHumansPandemicsBiological invasive theoryDynamic modelsOmicron variantOptimal combination of interventionsSARS-CoV-2Spatial spillover risk

Identifiers

PMID36435792
PMCPMC9701379

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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.