Impact of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Vaccination and Pediatric Age on Delta Variant Household Transmission

Author:

Ng Oon Tek123,Koh Vanessa4,Chiew Calvin J5,Marimuthu Kalisvar126,Thevasagayam Natascha May4,Mak Tze Minn7,Chua Joon Kiat8,Ong Shannen Si Hui8,Lim Yong Kai8,Ferdous Zannatul12,Johari Alifa Khairunnisa bte12,Cui Lin7,Lin Raymond Tzer Pin67,Tan Kelvin Bryan8910,Cook Alex R9,Leo Yee Sin236911,Lee Vernon J M59

Affiliation:

1. Department of Infectious Diseases, National Centre for Infectious Diseases , Singapore

2. Department of Infectious Diseases, Tan Tock Seng Hospital , Singapore

3. Lee Kong Chian School of Medicine, Nanyang Technological University , Singapore

4. Infectious Disease Research and Training Office, National Centre for Infectious Diseases , Singapore

5. Communicable Diseases Division, Ministry of Health , Singapore

6. Yong Loo Lin School of Medicine, National University of Singapore and National University Health System , Singapore

7. National Public Health Laboratory, National Centre for Infectious Diseases , Singapore

8. Crisis Strategy and Operations Group, Ministry of Health , Singapore

9. Saw Swee Hock School of Public Health, National University of Singapore and National University Health System , Singapore

10. Centre for Regulatory Excellence, Duke-National University of Singapore Medical School , Singapore

11. Executive Director’s Office, National Centre for Infectious Diseases , Singapore

Abstract

Abstract Background In Singapore, quarantine of all close contacts with entry and exit polymerase chain reaction testing enabled evaluation of the impact of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination and pediatric age on transmission of the Delta variant. Methods This retrospective cohort study included all household close contacts between 1 March 2021 and 31 August 2021. Results Among 8470 Delta variant-exposed contacts linked to 2583 indices, full-vaccination of the index with BNT162b2 or mRNA-1273 was associated with reduction in acquisition by contacts (adjusted odds ratio [aOR], 0.56; 95% robust confidence interval [RCI], .44–.71 and aOR, 0.51; 95% RCI, .27–.96, respectively). Compared with young adults (aged 18–29 years), children (aged 0–11 years) were significantly more likely to transmit (aOR, 2.37; 95% RCI, 1.57–3.60) and acquire (aOR, 1.43; 95% RCI, 1.07–1.93) infection, vaccination considered. Longer duration from vaccination completion among contacts was associated with decline in protection against acquisition (first-month aOR, 0.42; 95% RCI, .33–.55; fifth-month aOR, 0.84; 95% RCI, .55–.98; P < .0001 for trend) and symptomatic disease (first-month aOR, 0.30; 95% RCI, .23–.41; fifth-month aOR, 0.62; 95% RCI, .38–1.02; P < .0001 for trend). Contacts immunized with mRNA-1273 had significant reduction in acquisition (aOR, 0.73; 95% RCI, .58–.91) compared with BNT162b2. Conclusions Among household close contacts, vaccination prevented onward SARS-CoV-2 transmission and there was in­creased risk of SARS-CoV-2 acquisition and transmission among children compared with young adults. Time after completion of vaccination and vaccine type affected SARS-CoV-2 acquisition.

Funder

NMRC COVID-19 Research Fund

NMRC Collaborative Grants: Collaborative Solutions Targeting Antimicrobial Resistance Threats in Health Systems

Singapore Population Health Improvement Centre

NMRC Clinician Scientist Award

NMRC Clinician Scientist Individual Research Grant

German Federal Ministry of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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