Impact of COVID-19-related disruptions to measles, meningococcal A, and yellow fever vaccination in 10 countries
- Imperial College London, Switzerland
- London School of Hygiene & Tropical Medicine, United Kingdom
- University of Notre Dame, France
- University of Cambridge, United Kingdom
- Institute for Disease Modelling, United States
- Imperial College London, United Kingdom
- Pennsylvania State University, United States
- Kaiser Permanente Washington,, United States
- University of Notre Dame, United States
Abstract
Background: Childhood immunisation services have been disrupted by COVID-19. WHO recommends considering outbreak risk using epidemiological criteria when deciding whether to conduct preventive vaccination campaigns during the pandemic.
Methods: We used 2-3 models per infection to estimate the health impact of 50% reduced routine vaccination coverage and delaying campaign vaccination for measles, meningococcal A and yellow fever vaccination in 3-6 high burden countries per infection.
Results: Reduced routine coverage in 2020 without catch-up vaccination may increase measles and yellow fever disease burden in the modelled countries. Delaying planned campaigns may lead to measles outbreaks and increases in yellow fever burden in some countries. For meningococcal A vaccination, short term disruptions in 2020 are unlikely to have a significant impact.
Conclusion: The impact of COVID-19-related disruption to vaccination programs varies between infections and countries.
Funding: Bill and Melinda Gates Foundation and Gavi, the Vaccine Alliance.
Data availability
All code, data inputs and outputs used to generate the results in the manuscript (apart from projections about vaccine coverage beyond 2020 which are commercially confidential property of Gavi) are available at: https://github.com/vimc/vpd-covid-phase-I.
Article and author information
Author details
Katy A M Gaythorpe
Funding
Gavi, the Vaccine Alliance and the Bill & Melinda Gates Foundation (OPP1157270 and INV-016832)
- Katy A M Gaythorpe
- Kaja Abbas
- John Huber
- Andromachi Karachaliou
- Niket Thakkar
- Kim Woodruff
- Xiang Li
- Susy Echeverria-Londono
- Matthew Ferrari
- Michael Jackson
- Kevin McCarthy
- Alex T Perkins
- Caroline Trotter
- Mark Jit
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Reviewing Editor
- Talía Malagón, McGill University, Canada
Version history
- Received: January 29, 2021
- Accepted: June 23, 2021
- Accepted Manuscript published: June 24, 2021 (version 1)
- Accepted Manuscript updated: June 25, 2021 (version 2)
- Version of Record published: July 7, 2021 (version 3)
- Version of Record updated: July 20, 2021 (version 4)
Copyright
© 2021, Gaythorpe et al.
This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.
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Impact of COVID-19-related disruptions to measles, meningococcal A, and yellow fever vaccination in 10 countries
eLife 10:e67023.
https://doi.org/10.7554/eLife.67023
Further reading
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- Epidemiology and Global Health
Paxlovid, a SARS-CoV-2 antiviral, not only prevents severe illness but also curtails viral shedding, lowering transmission risks from treated patients. By fitting a mathematical model of within-host Omicron viral dynamics to electronic health records data from 208 hospitalized patients in Hong Kong, we estimate that Paxlovid can inhibit over 90% of viral replication. However, its effectiveness critically depends on the timing of treatment. If treatment is initiated three days after symptoms first appear, we estimate a 17% chance of a post-treatment viral rebound and a 12% (95% CI: 0%-16%) reduction in overall infectiousness for non-rebound cases. Earlier treatment significantly elevates the risk of rebound without further reducing infectiousness, whereas starting beyond five days reduces its efficacy in curbing peak viral shedding. Among the 104 patients who received Paxlovid, 62% began treatment within an optimal three-to-five-day day window after symptoms appeared. Our findings indicate that broader global access to Paxlovid, coupled with appropriately timed treatment, can mitigate the severity and transmission of SARS-Cov-2.
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- Epidemiology and Global Health
Background:
Circulating omega-3 and omega-6 polyunsaturated fatty acids (PUFAs) have been associated with various chronic diseases and mortality, but results are conflicting. Few studies examined the role of omega-6/omega-3 ratio in mortality.
Methods:
We investigated plasma omega-3 and omega-6 PUFAs and their ratio in relation to all-cause and cause-specific mortality in a large prospective cohort, the UK Biobank. Of 85,425 participants who had complete information on circulating PUFAs, 6461 died during follow-up, including 2794 from cancer and 1668 from cardiovascular disease (CVD). Associations were estimated by multivariable Cox proportional hazards regression with adjustment for relevant risk factors.
Results:
Risk for all three mortality outcomes increased as the ratio of omega-6/omega-3 PUFAs increased (all Ptrend <0.05). Comparing the highest to the lowest quintiles, individuals had 26% (95% CI, 15–38%) higher total mortality, 14% (95% CI, 0–31%) higher cancer mortality, and 31% (95% CI, 10–55%) higher CVD mortality. Moreover, omega-3 and omega-6 PUFAs in plasma were all inversely associated with all-cause, cancer, and CVD mortality, with omega-3 showing stronger effects.
Conclusions:
Using a population-based cohort in UK Biobank, our study revealed a strong association between the ratio of circulating omega-6/omega-3 PUFAs and the risk of all-cause, cancer, and CVD mortality.
Funding:
Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institute of Health under the award number R35GM143060 (KY). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
