Published on in Vol 7, No 3 (2021): March

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/24696, first published .
The Relationship Between the Global Burden of Influenza From 2017 to 2019 and COVID-19: Descriptive Epidemiological Assessment

The Relationship Between the Global Burden of Influenza From 2017 to 2019 and COVID-19: Descriptive Epidemiological Assessment

The Relationship Between the Global Burden of Influenza From 2017 to 2019 and COVID-19: Descriptive Epidemiological Assessment

Original Paper

1Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, United States

2ENDA Santé, Dakar, Senegal

3Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia

4Department of Environmental Health, Faculty of Health Sciences, University of Johannesburg, Johannesburg, South Africa

5Department of Medicine, St. Michael’s Hospital, Unity Health Toronto, Toronto, ON, Canada

6Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada

*all authors contributed equally

Corresponding Author:

Stefan David Baral, MPH, MD

Department of Epidemiology

Bloomberg School of Public Health

Johns Hopkins University

615 N. Wolfe Street

Baltimore, MD, 21205

United States

Phone: 1 410 502 8975

Email: sbaral@jhu.edu


Background: SARS-CoV-2 and influenza are lipid-enveloped viruses with differential morbidity and mortality but shared modes of transmission.

Objective: With a descriptive epidemiological framing, we assessed whether recent historical patterns of regional influenza burden are reflected in the observed heterogeneity in COVID-19 cases across regions of the world.

Methods: Weekly surveillance data reported by the World Health Organization from January 2017 to December 2019 for influenza and from January 1, 2020 through October 31, 2020, for COVID-19 were used to assess seasonal and temporal trends for influenza and COVID-19 cases across the seven World Bank regions.

Results: In regions with more pronounced influenza seasonality, COVID-19 epidemics have largely followed trends similar to those seen for influenza from 2017 to 2019. COVID-19 epidemics in countries across Europe, Central Asia, and North America have been marked by a first peak during the spring, followed by significant reductions in COVID-19 cases in the summer months and a second wave in the fall. In Latin America and the Caribbean, COVID-19 epidemics in several countries peaked in the summer, corresponding to months with the highest influenza activity in the region. Countries from regions with less pronounced influenza activity, including South Asia and sub-Saharan Africa, showed more heterogeneity in COVID-19 epidemics seen to date. However, similarities in COVID-19 and influenza trends were evident within select countries irrespective of region.

Conclusions: Ecological consistency in COVID-19 trends seen to date with influenza trends suggests the potential for shared individual, structural, and environmental determinants of transmission. Using a descriptive epidemiological framework to assess shared regional trends for rapidly emerging respiratory pathogens with better studied respiratory infections may provide further insights into the differential impacts of nonpharmacologic interventions and intersections with environmental conditions. Ultimately, forecasting trends and informing interventions for novel respiratory pathogens like COVID-19 should leverage epidemiologic patterns in the relative burden of past respiratory pathogens as prior information.

JMIR Public Health Surveill 2021;7(3):e24696

doi:10.2196/24696

Keywords



The COVID-19 pandemic has affected each region of the world differently. As of December 2020, Europe and the Americas have registered the highest numbers of COVID-19 cases and deaths, while Southeast Asia, sub-Saharan Africa, and the Western Pacific have experienced comparatively milder epidemics [1]. Heterogeneity in COVID-19 burden has also been observed within cities, across cities, and across regions within a country [2,3]. This heterogeneity likely stems from differences in underlying population structure with respect to age distribution, population and housing density, access to health care, burden of comorbidities, socioeconomic and structural barriers to engagement in health, environmental factors, and the breadth and intensity of public health interventions. Furthermore, there remains active investigation into the heterogeneity of the effects of both COVID-19 and the associated response on potential syndemics, including infectious diseases such as HIV and tuberculosis, and noncommunicable conditions including mental health, reproductive health, and malnutrition [4].

Similar to SARS-CoV-2, the virus that causes COVID-19, influenza is a lipid-enveloped respiratory virus but with a more established evidence base for both effective nonpharmacologic intervention strategies and transmission dynamics [5-7]. Importantly, influenza is associated with a shorter incubation period and with lower mortality than the currently estimated SARS-CoV-2 infection case fatality rate [8-10]. The relative risks of indoor versus outdoor transmission and risks for contact, droplet-based, and aerosolization-mediated transmission are better established for influenza [11-13]. Influenza seasonality and spatial distribution are not fully understood but likely reflect individual, population, and environmental determinants [14]. Moreover, the annual burden and associated mortality secondary to pandemic and nonpandemic seasonal influenza strains vary significantly. The 2009 H1N1 pandemic was estimated to cause over 60 million infections in the United States and resulted in higher mortality among youth but fewer deaths overall, as older people were more likely to be immune [15]. In 2017, there were an estimated 45 million cases of mostly H3N2 and Influenza B in the United States associated with higher mortality, particularly among older adults given limited pre-existing immunity and limited vaccine effectiveness [16]. Environmental factors have been shown to explain, in part, the differences in influenza seasonality between temperate regions where cases peak during winter months and tropical regions, which may have multiple peaks or intermittent influenza activity [17,18]. However, even within specific regions, some countries show influenza transmission patterns that appear distinct from regional trends [19,20].

There have been early reports suggesting shared individual and structural determinants of infection between influenza and SARS-CoV-2. In the United States, there is evidence of higher COVID-19 incidence, morbidity, and mortality among African American communities secondary to underlying inequities, including structural racism [21]. These racial disparities were also observed during the 2009 H1N1 influenza pandemic with similar drivers including higher risk of exposure due to inability to social distance, higher burden of comorbidities, and limited access to health care among African American and other racialized communities [22-24]. Similar early trajectories of COVID-19 and 2009 H1N1 have been noted in South Africa, with higher burdens initially among higher-income communities reporting more travel, with rapid epidemiologic transition to lower-income communities [25]. Finally, increases in COVID-19 in late May and June in some areas of the Southern hemisphere including countries across South America, sub-Saharan Africa, East Asia, and the Pacific were consistent with the timing of the traditional influenza season [26]. Specifically, in South Africa, epidemic growth is consistent with the influenza season and with epicenters of COVID-19 appearing to be similar to areas with increased influenza transmission [27,28].

When this novel coronavirus emerged in early 2020, regional and national forecasting exercises drew on emerging data on the trajectory of detected COVID-19 cases in the epicenters of China and Italy to translate their reproductive rates into best- and worst-case scenarios for populations worldwide. However, despite early comparison of the average mortality of influenza and SARS-CoV-2, there has not been a systematic evaluation of whether historical distributions in influenza burden are relevant in understanding the burden and distribution of SARS-CoV-2 infection. Descriptive epidemiological assessment within and across both influenza and COVID-19 may provide early insight into overlapping individual, structural, and environmental determinants of infection that have implications for public health responses. Moreover, documenting consistencies in the burden of disease across both pathogens may facilitate the generation of testable hypotheses, facilitating future analytic comparisons as well as future pandemic preparedness. In this study, we investigated global influenza transmission patterns from 2017 onward to describe shared trends with the epidemiology of COVID-19.


Data Abstraction and Assessment of Eligibility

Influenza

We used publicly available data to characterize temporal patterns of influenza across seven regions between 2017 and 2019. Organization of countries into regions was based on World Bank classifications (ie, East Asia and the Pacific, Europe and Central Asia, Latin America and the Caribbean, Middle East and North Africa, North America, South Asia, and sub-Saharan Africa). Within each region, we assessed country-specific weekly reported cases of influenza, including both Influenza A and B, from January 1, 2017, to December 31, 2019. Data were abstracted from FluNet, a global web-based tool developed by the World Health Organization for influenza virologic surveillance, which captures weekly laboratory-confirmed influenza cases. FluNet aggregates data from the National Influenza Centres of the Global Influenza Surveillance and Response System and other national influenza reference laboratories. Since more temperate zones in the Northern and Southern Hemispheres have generally opposing seasonal influenza trends, we report influenza case counts by calendar year from January 1 to December 31, which also facilitates comparisons with COVID-19. Finally, influenza case counts for the calendar year of 2020 were excluded given that public health measures focused on COVID-19 prevention and mitigation likely decreased seasonal influenza cases substantially for this time period [29]. The suspension of FluView, the core influenza reporting system in the United States, further precluded the exclusion of 2020 influenza case counts.

We assessed patterns of missing data for each country and by year to determine eligibility for inclusion in analyses. For each year, countries where ≥90% of available weekly case reports were complete (assessed as the total number of nonmissing records over the total number of all included weeks for that year) were included in the analyses. For countries where data were <90% complete, we made the following determination:

  • Countries where data missingness appeared to follow a seasonal pattern (eg, data were missing only for weeks outside of the known influenza season, likely reflecting country-specific seasonal influenza reporting guidelines) were retained in analyses.
  • Countries where weekly case counts were <90% complete and did not appear to follow a seasonal pattern were denoted as missing.
COVID-19

We abstracted the daily number of COVID-19 cases reported between January 1 and October 31, 2020, for all countries and corresponding World Bank regions using data from the World Health Organization Coronavirus Situation Report. As we are in the first year of COVID-19, it was not possible to assess missingness of data similar to the methods used for influenza.

Regional Influenza and COVID-19 Burden

Influenza

We assessed the overall burden of influenza for all included countries across and within each region. To do so, we summed the absolute number of weekly influenza cases for each region, country, and year (January 1 to December 31 of each year) given the temporal variability in influenza seasons worldwide. Countries were ranked in descending order within each region from the highest to lowest number of absolute cases overall and for 2017, 2018, and 2019.

COVID-19

We assessed, and similarly ranked in descending order, cumulative cases of COVID-19 as reported through October 31, 2020, within each region.

Comparison of Regional Burden of Influenza and COVID-19

We used regional plots for both influenza and COVID-19 cases to visualize cross-pathogen comparisons. For each region, we plotted the mean number of weekly influenza cases for the five highest ranked countries across 2017, 2018, and 2019. Influenza cases were averaged to ensure observed trends were robust to one-off spikes or changes to reporting systems in select years. Daily COVID-19 cases for the five highest ranked countries within each region were plotted using a 7-day moving average. We similarly plotted influenza and COVID-19 cases using per-capita proportions for these countries to facilitate standardized comparisons across countries and regions. Plots were visually inspected to confirm temporal patterns, and we described similarities or differences across and within all regions.

Within-Country Comparison of Influenza and COVID-19

We used plots to visually compare within-country trends for both influenza and COVID-19 over time. We assessed the top 20 countries with the highest burden of COVID-19 for each region, further restricting plots to those countries where influenza data were eligible for inclusion. As with regional comparisons, we plotted the mean number of weekly influenza cases across 2017, 2018, and 2019, and daily COVID-19 cases were plotted using a 7-day moving average.


Influenza cases were assessed for 171 countries. For each year, more than half (ranging from n=95, 55.6% to n=97, 56.7%) of all countries reported ≥90% complete data (Multimedia Appendix 1). The proportion of countries where data were <90% complete but followed a pattern of seasonal missingness were also included in influenza analyses and ranged from 22.8% (n=39) in 2017 to 24.0% (n=41) in 2019. Differences in data completion and patterns of missingness were evident across all regions. The overall influenza burden between 2017 and 2019 varied by region and by countries within all seven identified regions (Table 1). Regions with the highest absolute burden of influenza included North America (903,554 cases), Europe and Central Asia (599,820 cases), and East Asia and the Pacific (389,657 cases). Countries with the highest proportion of regional influenza cases were as follows: East Asia and the Pacific (China: 302,126/389,657, 77.5%); Europe and Central Asia (the United Kingdom: 106,087/599,020, 17.7%), Latin America and the Caribbean (Mexico: 18,976/93,172, 20.2%), Middle East and North Africa (Qatar: 27,363/67,610, 40.5%), North America (the United States: 749,472/903,554, 82.9%), South Asia (India: 14,895/31,992, 46.6%), and sub-Saharan Africa (South Africa: 3534/18,930, 18.7%). Across regions, countries with the highest overall burden of influenza from 2017 to 2019 included the United States (749,472 cases), China (302,126 cases), Canada (154,082 cases), the United Kingdom (106,087 cases), and Norway (71,727 cases).

Regions with the highest absolute burden of COVID-19 included Latin America and the Caribbean (11,045,364 cases), Europe and Central Asia (9,197,241 cases), South Asia (9,107,653 cases), and North America (9,081,471 cases; Table 2). Within each region, countries with the highest proportion of COVID-19 regional cases were as follows: East Asia and the Pacific (Indonesia: 406,945/1,191,632, 34.2%); Europe and Central Asia (Russia: 1,618,116/9,197,241, 17.6%), Latin America and the Caribbean (Brazil: 5,494,376/11,045,364, 49.7%), Middle East and North Africa (Iran: 604,952/2,662,465, 22.7%), North America (the United States: 8,852,730/9,081,471, 97.5%), South Asia (India: 8,137,119/9,107,653, 89.3%), and sub-Saharan Africa (South Africa: 723,682/1,139,329, 63.5%; Table 2). Specific countries with the highest overall burden of COVID-19 cases as of October 31, 2020, included the United States (8,852,730 cases), India (8,137,119 cases), Brazil (5,494,376 cases), Russia (1,618,116 cases), and France (1,299,278 cases; Table 2).

Seasonal variation in influenza cases was observed within all regions. Seasonal trends were most pronounced across countries for North America, Europe and Central Asia, the Middle East and North Africa, East Asia and the Pacific, and Latin America and the Caribbean (Multimedia Appendix 2). Seasonal trends were also evident but largely inconsistent across countries within South Asia and sub-Saharan Africa. These dynamics were mainly present when trends were assessed by per capita proportions instead of case counts (Multimedia Appendix 3).

COVID-19 epidemics generally followed trends similar to those observed for influenza from 2017 to 2019 in the regions with the most pronounced influenza seasonal trends (Multimedia Appendix 3). This was more apparent in Europe and Central Asia with an early wave of COVID-19 epidemics in several countries from March to May 2020 followed by significant drops in transmission in the summer and a second wave in the fall. With the exception of the United States that has seen sustained transmission over the year, North America (Canada and Bermuda) have had COVID-19 epidemics largely similar to those observed in European countries. In Latin America and the Caribbean, COVID-19 epidemics in Brazil, Argentina, Peru, and Colombia peaked during the summer and started decreasing in fall corresponding to influenza trends in the region. Countries in sub-Saharan Africa, South Asia, and the Middle East and North Africa have shown more heterogeneity in their COVID-19 epidemics.

Similarities between COVID-19 and influenza trends were more marked within individual countries irrespective of region (Multimedia Appendix 4). Peaks of COVID-19 epidemics in exemplary countries, including Australia, Brazil, India, South Asia, and South Africa, coincided with months of peak influenza activity in those countries from 2017 to 2019 (Multimedia Appendix 5).

Table 1. Influenza cases for top 15 countries by World Bank region, overall and by year from January 1, 2017, to December 31 2019.a
RegionsOverall influenza cases, n (%)2019 influenza cases, n (%)2018 influenza cases, n (%)2017 influenza cases, n (%)
Sub-Saharan Africa18,930 (100.0)7521 (100.0)5785 (100.0)5624 (100.0)

South Africa3534 (18.7)1164 (15.6)1160 (20.1)1210 (21.5)

Ghana2383 (12.6)1172 (15.5)742 (12.8)469 (8.3)

Senegal1783 (9.4)483 (6.4)480 (8.3)820 (14.6)

Madagascar1117 (5.9)451 (6.0)298 (5.2)368 (6.5)

Cameroon1098 (5.8)332 (4.4)319 (5.5)447 (7.9)

Ivory Coast1057 (5.6)458 (6.1)262 (4.5)337 (6.0)

Togo988 (5.2)501 (6.7)254 (4.4)233 (4.1)

Zambia971 (5.1)426 (5.7)391 (6.8)154 (2.7)

Tanzania876 (4.6)242 (3.2)330 (5.7)304 (5.4)

Mauritius767 (4.1)570 (7.6)102 (1.8)95 (1.7)

Uganda621 (3.3)179 (2.4)b404 (7.2)

Mali5441 (2.9)235 (3.1)144 (2.5)165 (2.9)

Ethiopia534 (2.8)214 (2.8)203 (3.5)117 (2.1)

Kenya461 (2.4)220 (2.9)216 (3.7)

Burkina Faso398 (2.1)236 (4.1)


Niger144 (1.9)117 (2.1)

Central African Republic177 (3.1)109 (1.9)
East Asia and Pacific389,657 (100.0)158,173 (100.0)101,937 (100.0)129,547 (100.0)

China302,126 (77.5)122,757 (77.6)80,297 (78.8)99,072 (76.5)

Japan29,449 (7.6)10,029 (6.3)9076 (8.9)10,344 (8.0)

Australia28,775 (7.4)14,002 (8.9)4264 (4.2)10,509 (8.1)

Republic of Korea4958 (1.3)1702 (1.1)1952 (1.9)1304 (1.0)

Thailand3640 (0.9)1568 (1.0)784 (0.8)1288 (1.0)

Singapore3258 (0.8)1154 (0.7)1106 (1.1)998 (0.8)

New Zealand2377 (0.6)957 (0.6)475 (0.5)945 (0.7)

Malaysia2270 (0.6)1115 (0.7)493 (0.5)662 (0.5)

Indonesia2251 (0.6)496 (0.3)710 (0.7)1045 (0.8)

Lao People\'s Democratic Republic2039 (0.5)590 (0.4)661 (0.6)788 (0.6)

Mongolia1746 (0.4)909 (0.6)304 (0.3)533 (0.4)

Vietnam1493 (0.4)355 (0.2)345 (0.3)793 (0.6)

Myanmar1340 (0.3)806 (0.5)431 (0.3)

New Caledonia1036 (0.3)541 (0.3)291 (0.3)

Democratic People\'s Republic of Korea851 (0.2)474 (0.5)

Philippines346 (0.2)268 (0.2)

Cambodia234 (0.2)226 (0.2)
South Asia31,992 (100.0)17,313 (100.0)5401 (100.0)9278 (100.0)

India14,895 (46.6)10,428 (60.2)1880 (34.8)2587 (27.9)

Nepal5678 (17.7)2569 (14.8)957 (17.7)2152 (23.2)

Sri Lanka3794 (11.9)486 (2.8)947 (17.5)2361 (25.4)

Bangladesh3647 (11.4)1783 (10.3)673 (12.5)1191 (12.8)

Bhutan1487 (4.6)679 (3.9)364 (6.7)444 (4.8)

Pakistan1002 (3.1)1002 (5.8)

Maldives916 (2.9)88 (0.5)393 (7.3)435 (4.7)

Afghanistan573 (1.8)278 (1.6)187 (3.5)108 (1.2)
Middle East and North Africa67,610 (100.0)31,348 (100.0)21,224 (100.0)15,038 (100.0)

Qatar27,363 (40.5)8365 (26.7)11,450 (53.9)7548 (50.2)

Iran9445 (14.0)7387 (23.6)1430 (6.7)628 (4.2)

Kuwait6601 (9.8)6601 (21.1)

Oman5788 (8.6)1376 (4.4)1388 (6.5)3024 (20.1)

Egypt4986 (7.4)2339 (7.5)2072 (9.8)575 (3.8)

Israel4543 (6.7)1796 (5.7)1602 (7.5)1145 (7.6)

Saudi Arabia4302 (6.4)2423 (7.7)1179 (5.6)700 (4.7)

Malta1385 (2.0)880 (4.1)505 (3.4)

Jordan891 (1.3)366 (1.2)273 (1.3)252 (1.7)

Tunisia860 (1.3)203 (0.6)315 (1.5)342 (2.3)

Bahrain488 (0.7)197 (0.6)202 (1.0)89 (0.6)

Lebanon481 (0.7)262 (0.8)123 (0.6)96 (0.6)

Algeria477 (0.7)33 (0.1)310 (1.5)134 (0.9)
Latin America and Caribbean93,712 (100.0)33,308 (100.0)31,606 (100.0)28,798 (100.0)

Mexico18,976 (20.2)6963 (20.9)5667 (17.9)6346 (22.0)

Argentina17,658 (18.8)6477 (19.4)4615 (14.6)6566 (22.8)

Brazil16,477 (17.6)3459 (10.4)7012 (22.2)6006 (20.9)

Chile15,783 (16.8)7371 (22.1)4192 (13.3)4220 (14.7)

Colombia3549 (3.8)1316 (4.0)1425 (4.5)808 (2.8)

Nicaragua3501 (3.7)1419 (4.3)1320 (4.2)762 (2.6)

Paraguay3378 (3.6)1498 (4.5)932 (2.9)948 (3.3)

Bolivia3371 (3.6)430 (1.3)2068 (6.5)873 (3.0)

Peru1651 (1.8)349 (1.0)1061 (3.4)241 (0.8)

Ecuador1393 (1.5)615 (1.8)778 (2.5)

Costa Rica1266 (1.4)505 (1.5)591 (2.1)

Guatemala863 (0.9)322 (1.0)228 (0.8)

Cuba846 (0.9)463 (1.4)238 (0.8)145 (0.5)

Panama846 (0.9)382 (1.1)262 (0.9)

Haiti809 (0.9)358 (1.1)340 (1.1)

Jamaica479 (1.4)

Honduras322 (1.0)

Dominican Republic203 (0.6)

Uruguay197 (0.7)

El Salvador288 (1.0)
North America903,554 (100.0)310,724 (100.0)334,093 (100.0)258,737 (100.0)

United States749,472 (82.9)267,528 (86.1)267,611 (80.1)214,333 (82.8)

Canada154,082 (17.1)43,196 (13.9)66,482 (19.9)44,404 (17.2)
Europe and Central Asia599,020 (100.0)224,554 (100.0)235,606 (100.0)138,870 (100.0)

United Kingdom106,087 (17.7)42,448 (18.9)44,120 (18.7)19,519 (14.1)

Norway71,727 (12.0)22,282 (9.9)32,966 (14.0)16,479 (11.9)

France62,672 (10.5)25,405 (11.3)21,610 (9.2)15,657 (11.3)

Spain49,971 (8.3)17,232 (7.7)19,973 (8.5)12,766 (9.2)

Russian Federation49,289 (8.2)19,340 (8.6)15,314 (6.5)14,635 (10.5)

Sweden46,472 (7.8)13,823 (6.2)21,407 (9.1)11,242 (8.1)

Switzerland35,856 (6.0)14,096 (6.3)11,918 (5.1)9842 (7.1)

Denmark33,599 (5.6)11,835 (5.3)17,120 (7.3)4644 (3.3)

Italy13,539 (2.3)6361 (2.8)4382 (1.9)2796 (2.0)

Portugal11,904 (2.0)6634 (3.0)3984 (1.7)

Netherlands11,430 (1.9)5166 (2.3)2836 (1.2)3428 (2.5)

Austria11,311 (1.9)4097 (1.8)5143 (2.2)2071 (1.5)

Ireland10,964 (1.8)4201 (1.9)4984 (2.1)1779 (1.3)

Slovenia10,502 (1.8)3576 (1.6)3020 (1.3)3906 (2.8)

Croatia9216 (1.5)4823 (2.1)1796 (1.3)

Latvia2785 (1.2)3121 (2.2)

aExcludes countries with missing influenza data.

bCountry was not in top 15 for this year.

Table 2. COVID-19 cases for top 15 countries by World Bank region, from January 1 to October 31, 2020.
RegionCOVID-19 cases, n (%)
Sub-Saharan Africa1,139,329 (100.0)

South Africa723,682 (63.5)

Ethiopia95,789 (8.4)

Nigeria62,691 (5.5)

Kenya53,797 (4.7)

Ghana48,055 (4.2)

Cameroon21,793 (1.9)

Cote d\'Ivoire20,628 (1.8)

Madagascar16,968 (1.5)

Zambia16,415 (1.4)

Senegal15,593 (1.4)

Sudan13,804 (1.2)

Namibia12,907 (1.1)

Mozambique12,777 (1.1)

Uganda12,410 (1.1)

Guinea12,020 (1.1)
East Asia and Pacific1,191,632 (100.0)

Indonesia406,945 (34.2)

Philippines378,933 (31.8)

Japan100,392 (8.4)

China91,893 (7.7)

Singapore58,003 (4.9)

Myanmar51,496 (4.3)

Malaysia30,889 (2.6)

Australia27,582 (2.3)

Republic of Korea26,511 (2.2)

French Polynesia7262 (0.6)

Guam4579 (0.4)

Thailand3780 (0.3)

New Zealand1601 (0.1)

Vietnam1177 (0.1)

Papua New Guinea589 (0.0)
South Asia9,107,653 (100.0)

India8,137,119 (89.3)

Bangladesh406,364 (4.5)

Pakistan332,186 (3.6)

Nepal168,235 (1.8)

Afghanistan41,334 (0.5)

Maldives11,643 (0.1)

Sri Lanka10,424 (0.1)

Bhutan348 (0.0)
Middle East and North Africa2,662,465 (100.0)

Iran604,952 (22.7)

Iraq470,633 (17.7)

Saudi Arabia346,880 (13.0)

Morocco215,294 (8.1)

Qatar132,343 (5.0)

United Arab Emirates131,508 (4.9)

Kuwait125,337 (4.7)

Oman114,434 (4.3

Egypt107,385 (4.0)

Bahrain81,466 (3.1)

Lebanon79,529 (3.0)

Jordan69,306 (2.6)

West Bank and Gaza64,741 (2.4)

Libya60,628 (2.3)

Tunisia58,029 (2.2)
Latin America and the Caribbean11,045,364 (100.0)

Brazil5,494,376 (49.7)

Argentina1,143,800 (10.4)

Colombia1,053,122 (9.5)

Mexico912,811 (8.3)

Peru897,594 (8.1)

Chile508,571 (4.6)

Ecuador167,147 (1.5)

Bolivia141,484 (1.3)

Panama132,045 (1.2)

Dominican Republic126,332 (1.1)

Costa Rica107,570 (1.0)

Guatemala107,339 (1.0)

Honduras96,150 (0.9)

Venezuela91,280 (0.8)

Puerto Rico65,743 (0.2)
North America9,081,471 (100.0)

United States8,852,730 (97.5)

Canada228,542 (2.5)

Bermuda199 (0.0)
Europe and Central Asia9,197,241 (100.0)

Russian Federation1,618,116 (17.6)

France1,299,278 (14.1)

Spain1,212,190 (13.2)

United Kingdom989,749 (10.8)

Italy647,674 (7.0)

Germany518,753 (5.6)

Belgium441,807 (4.8)

Ukraine387,481 (4.2)

Turkey373,154 (4.1)

Netherlands340,974 (3.7)

Poland340,834 (3.7)

Czech Republic323,673 (3.5)

Israel314,244 (3.4)

Romania235,586 (2.6)

Switzerland153,728 (1.7)

In this descriptive epidemiological study, we found ecological consistency between the seasonal influenza trends from 2017 to 2019 and the COVID-19 trends seen to date. Specifically, this similarity was highest in regions with more pronounced influenza seasonality, including North America, Europe and Central Asia, and Latin America and the Caribbean, where peaks of COVID-19 cases coincided with periods of high influenza activity. In East Asia and the Pacific and sub-Saharan Africa, there was more marked heterogeneity in COVID-19 pandemics in countries of these regions. However, within-country comparisons of 2017-2019 influenza epidemics and COVID-19 cases were evident irrespective of region. The ecological consistency in the seasonal trends of COVID-19 and the recent burden of influenza is suggestive of likely shared individual, structural, and environmental determinants of infection, which has implications for public health.

Outside of public health interventions, there is generally less consensus on the determinants that potentiate or inhibit COVID-19 transmission. However, given decades of study, there is more information available on the individual, population, and environmental determinants of influenza. At the individual level, underlying immunity is related to previous exposure to similar strains and vaccine uptake and effectiveness. Effectiveness of vaccines depends on circulating influenza strains (ie, pandemic and nonpandemic or seasonal) secondary to antigenic drift and shift of influenza viruses. Population-level characteristics include vaccine coverage and shield immunity, indoor air quality, population density, social norms, and health care infrastructure [30-32]. Environmental factors affecting influenza include temperature, air pollution, and humidity [30,33]. Given how rapidly COVID-19 has emerged, conclusions of different studies exploring the role of environmental conditions have differed significantly. One study found no associations between latitude and temperature with COVID-19 epidemic growth using a 2-week exposure period in March 2020 across 144 geopolitical areas [34]. However, a “living” review leveraging data from December 2019 onward from nearly 4000 locations worldwide showed significant differences in COVID-19 burden associated with temperature, humidity, pollution, and other environmental factors [35]. Collectively, these studies suggest the potential for at least some seasonal variation secondary to changes in environmental conditions in the transmission of SARS-CoV-2 similar to other respiratory pathogens, including influenza and other seasonal coronaviruses [36-39].

Influenza seasonality is more pronounced in more temperate areas of the Northern and Southern Hemispheres, consistent with opposing fall and winter seasons. A recent assessment of the seasonality of infectious pathogens included individual-level determinants such as growing immunity throughout an influenza season secondary to vaccination or exposure that results in achieving effective levels of shield immunity, limiting transmission [40]. There has been some study of existing immunity to COVID-19 mediated via cross-reactivity with other coronaviruses [40,41]. However, decreased populationwide immunity could result in sustained transmission even during times with less transmission of other respiratory pathogens. Influenza seasonality may also be secondary to population-level changes, including potentially higher crowding in colder weather, increased use of respite care and housing, people returning to work and school, and increased use of transit services that may collectively facilitate transmission. Environmental conditions may further affect individual susceptibility to infection as well as contact or respiratory droplet transmission patterns. Although there is likely a relationship between testing infrastructure and influenza reporting, the consistency in the COVID-19 and influenza trends among countries within each region was notable. COVID-19 emerged in East Asia and the Pacific though there was relatively limited COVID-19 spread in several settings in March and April 2020, potentially secondary to widely implemented nonpharmacologic interventions [29]. Notably, and consistent with influenza season, there was a resurgence of COVID-19 in Australia starting in July and ending in September 2020 [42-44].

A hallmark of COVID-19 has been the role of social determinants of health with socioeconomic status, living conditions, access to health care, and underlying comorbidities being consistent predictors of COVID-19 incidence and mortality worldwide [45,46]. Moreover, structural factors including racism have been documented in several settings including the United States, the United Kingdom, Sweden, and Canada but are likely relevant in more settings not reporting on the racial identity of those affected [21,47,48]. Notably, similar disparities were observed in the 2009 H1N1 pandemic in the United States, though there has been limited documentation of socioeconomic disparities of influenza in most settings [22,49]. Although disparities are well documented for other infectious diseases such as HIV, these disparities evolve across cycles of transmission spanning years. Given how rapidly disparities emerged with COVID-19, interventions to address disparities may be observable over shorter time horizons and provide insight into effective interventions to address pervasive social health inequities. Secondary to intersections of differential access to health care and medical mistrust, the development of a generally effective vaccine has not mitigated disparities [50-52]. Leveraging frameworks focused on optimizing implementation of influenza vaccination strategies including increased equity will be critical in informing SARS-CoV-2 vaccines when available [53,54]. Moreover, there has been substantial research into studying correlates of protection for influenza vaccine development as well as the role of cellular immunity in complementing the humoral response, which are both actively being studied for COVID-19 [55-58]. Finally, COVID-19 is rapidly increasing our understanding of postviral morbidities including chronic fatigue syndrome and chronic myofascial pain syndromes as well as potential cardiovascular complications [59]. Although postviral complications have been described for other viruses, the known exposure to COVID-19 as an etiological agent may provide further insight into the mechanisms and potential interventions [60-65].

This study has several limitations. The risk of ecological fallacy is relevant where individuals in generally lower burden regions or countries may have high risks of acquisition and transmission secondary to microepidemics, including in those in congregate living settings, refugee and migrant work camps, long-term care facilities, homeless shelters, and prisons. The missingness in data aggregated by FluNet is another limitation. We assumed that countries where influenza data was missing in a seasonal pattern was a reflection of few case counts or reduced reporting outside of the typical influenza season, and indeed, seasonal “missingness” was most apparent for countries in the European region, where the influenza season has been well documented. However, by excluding countries with >10% data missingness that did not follow a seasonal influenza pattern, several countries in the Pacific and in sub-Saharan Africa (eg, Sudan) were not included in the comparison of rankings despite high COVID-19 and influenza burden. There have been examples of COVID-19 resurgence outside of traditional influenza season, such as in South Africa, potentially due to the emergence of new variants of COVID-19, highlighting the complex intersection of transmission drivers in specific subnational areas [66]. Finally, there have been dramatic decreases in the burden of influenza in the 2020 season likely due to an intersection of nonpharmacological interventions’ effects combined with decreases in international travel. It is unclear how this will affect vulnerability to future seasons of influenza [67].

In addition, absolute influenza and COVID-19 case counts were reported rather than positivity rates; assuming that biases are present in interpreting positivity rates (eg, laboratory infrastructure implementing broad testing strategies), these biases are likely reflected in the total number of cases across both influenza and COVID-19. Heterogeneity in testing capacity, test kit availability, and guidelines for prioritizing testing eligibility for COVID-19 may additionally challenge direct comparisons between COVID-19 and influenza case counts across countries. Testing capacity for COVID-19 has been highly dynamic, with continued limited capacity to meet screening and testing demands still evident in some countries [68]. In the case of influenza, countrywide variations in diagnostic testing strategies may belie differences in case detection. For instance, rapid influenza diagnostic tests are commonly used in clinical settings in many countries yet have documented lower sensitivity relative to other diagnostic methods [69].

Relatedly, contact tracing strategies for COVID-19 may vary across and within countries. As the pandemic has progressed, strategies have adapted to testing individuals with exposure to confirmed cases, irrespective of their symptomology [70]. This approach is not typically used for influenza. Finally, evidence suggests that nonpharmaceutical interventions for COVID-19 may concurrently limit influenza spread, due to their shared modes of transmission [29,71]. Although COVID-19 transmission has likely persisted due to unknown baseline population immunity, limited influenza detection may reflect decreased propensity for testing outside of the influenza season in some countries, as previously highlighted. Nonetheless, these data further underscore the potential utility to leverage our understanding and mitigation strategies for other respiratory pathogens to understand and combat COVID-19 and future pandemics due to respiratory pathogens.

The results presented here suggest shared regional differential distribution in the global burden of COVID-19 with that of influenza. This ecological overlap suggests that the underlying dynamics of influenza and COVID-19 transmission are similar, as they relate to spatial, seasonal, and population structure, and the disparities that lead to disproportionate vulnerabilities in various population groups. In considering the host–pathogen–environment framework commonly used for infectious diseases, emerging infections represent novel pathogens, but the populations and environment under which they emerge and spread are the same. Likewise, the similarities observed here suggest the potential utility of informing COVID-19 prevention and mitigation interventions, with the vast data available characterizing critical issues including the relative risks of indoor versus outdoor transmission; risks of aerosolization for influenza; and even optimal delivery of vaccines, chemoprophylaxis, and treatment strategies. Ultimately, regional and national public health systems preparing and responding to the current and future waves of COVID-19 may benefit from evaluating the relative burden of past respiratory pathogens and the impact of nonpharmacologic, pharmacologic, and prophylactic intervention strategies as prior information when forecasting and implementing interventions, and when evaluating the transmission impact of interventions applied to date in the context of potential seasonal effects on transmission.

Conflicts of Interest

None declared.

Multimedia Appendix 1

Categories of missingness for 171 countries reporting influenza cases between January 2017 and December 2019 extracted from FluNet, overall and by region.

DOCX File , 22 KB

Multimedia Appendix 2

Weekly trends in new COVID-19 cases (left panel, solid lines) and influenza cases (right panel, dashed lines) presented by World Bank region. Daily COVID-19 cases were extracted from the World Health Organization and are presented as a 7-day moving average between January 1 and October 31, 2020. Weekly influenza cases were extracted from FluNet and averaged by week across all reporting years (2017-2019).

PDF File (Adobe PDF File), 2469 KB

Multimedia Appendix 3

Weekly trends in new COVID-19 cases per capita (left panel, solid lines) and influenza cases per capita (right panel, dashed lines) presented by World Bank region. Daily COVID-19 cases were extracted from the World Health Organization and are presented as a 7-day moving average, per 100,000 persons, between January 1 and October 31, 2020. Weekly influenza cases were extracted from FluNet and averaged by week, per 100,000 persons, across all reporting years (2017-2019).

PDF File (Adobe PDF File), 2429 KB

Multimedia Appendix 4

Weekly trends in new COVID-19 cases (solid lines) and influenza cases (dashed lines) presented by country. Daily COVID-19 cases were extracted from the World Health Organization and are presented as a 7-day moving average between January 1 and October 31, 2020. Weekly influenza cases were extracted from FluNet and averaged by week across all reporting years (2017-2019).

ZIP File (Zip Archive), 6293 KB

Multimedia Appendix 5

Weekly trends in new COVID-19 cases (solid lines) and influenza cases (dashed lines) presented for exemplary countries. Daily COVID-19 cases were extracted from the World Health Organization and are presented as a 7-day moving average between January 1 and October 31, 2020. Weekly influenza cases were extracted from FluNet and averaged by week across all reporting years (2017-2019).

PDF File (Adobe PDF File), 1074 KB

References

  1. Weekly epidemiological update - 29 December 2020. World Health Organization. 2020.   URL: https://www.who.int/publications/m/item/weekly-epidemiological-update---29-december-2020 [accessed 2021-01-01]
  2. Devlin H. Regional differences in Covid-19 transmission rate emerge in England. The Guardian. 2020 May 15.   URL: https:/​/www.​theguardian.com/​world/​2020/​may/​15/​regional-differences-in-covid-19-transmission-rate-emerge-in-england [accessed 2021-01-01]
  3. CDC COVID-19 Response Team. Geographic differences in COVID-19 cases, deaths, and incidence - United States, February 12-April 7, 2020. MMWR Morb Mortal Wkly Rep 2020 Apr 17;69(15):465-471. [CrossRef] [Medline]
  4. Baral S, Rao A, Twahirwa Rwema JO, Lyons C, Cevik M, Kågesten AE, et al. Competing health risks associated with the COVID-19 pandemic and response: a scoping review. medRxiv. Preprint posted online January 8, 2021. [CrossRef] [Medline]
  5. Ahmed F, Zviedrite N, Uzicanin A. Effectiveness of workplace social distancing measures in reducing influenza transmission: a systematic review. BMC Public Health 2018 Apr 18;18(1):518 [FREE Full text] [CrossRef] [Medline]
  6. Long Y, Hu T, Liu L, Chen R, Guo Q, Yang L, et al. Effectiveness of N95 respirators versus surgical masks against influenza: a systematic review and meta-analysis. J Evid Based Med 2020 May;13(2):93-101 [FREE Full text] [CrossRef] [Medline]
  7. Feng S, Shen C, Xia N, Song W, Fan M, Cowling BJ. Rational use of face masks in the COVID-19 pandemic. Lancet Respir Med 2020 May;8(5):434-436 [FREE Full text] [CrossRef] [Medline]
  8. Lessler J, Reich NG, Brookmeyer R, Perl TM, Nelson KE, Cummings DA. Incubation periods of acute respiratory viral infections: a systematic review. Lancet Infect Dis 2009 May;9(5):291-300 [FREE Full text] [CrossRef] [Medline]
  9. Baud D, Qi X, Nielsen-Saines K, Musso D, Pomar L, Favre G. Real estimates of mortality following COVID-19 infection. Lancet Infect Dis 2020 Jul;20(7):773 [FREE Full text] [CrossRef] [Medline]
  10. Faust JS, Del Rio C. Assessment of deaths from COVID-19 and from seasonal influenza. JAMA Intern Med 2020 Aug 01;180(8):1045-1046. [CrossRef] [Medline]
  11. Yang W, Elankumaran S, Marr LC. Concentrations and size distributions of airborne influenza A viruses measured indoors at a health centre, a day-care centre and on aeroplanes. J R Soc Interface 2011 Aug 07;8(61):1176-1184 [FREE Full text] [CrossRef] [Medline]
  12. Marr LC, Tang JW, Van Mullekom J, Lakdawala SS. Mechanistic insights into the effect of humidity on airborne influenza virus survival, transmission and incidence. J R Soc Interface 2019 Jan 31;16(150):20180298 [FREE Full text] [CrossRef] [Medline]
  13. Yang W, Marr LC. Dynamics of airborne influenza A viruses indoors and dependence on humidity. PLoS One 2011;6(6):e21481 [FREE Full text] [CrossRef] [Medline]
  14. Moriyama M, Hugentobler WJ, Iwasaki A. Seasonality of respiratory viral infections. Annu Rev Virol 2020 Sep 29;7(1):83-101. [CrossRef] [Medline]
  15. Hancock K, Veguilla V, Lu X, Zhong W, Butler EN, Sun H, et al. Cross-reactive antibody responses to the 2009 pandemic H1N1 influenza virus. N Engl J Med 2009 Nov 12;361(20):1945-1952. [CrossRef] [Medline]
  16. Allen JD, Ross TM. H3N2 influenza viruses in humans: viral mechanisms, evolution, and evaluation. Hum Vaccin Immunother 2018;14(8):1840-1847 [FREE Full text] [CrossRef] [Medline]
  17. Tamerius JD, Shaman J, Alonso WJ, Alonso WJ, Bloom-Feshbach K, Uejio CK, et al. Environmental predictors of seasonal influenza epidemics across temperate and tropical climates. PLoS Pathog 2013 Mar;9(3):e1003194 [FREE Full text] [CrossRef] [Medline]
  18. Hirve S, Newman LP, Paget J, Azziz-Baumgartner E, Fitzner J, Bhat N, et al. Influenza seasonality in the tropics and subtropics - when to vaccinate? PLoS One 2016;11(4):e0153003 [FREE Full text] [CrossRef] [Medline]
  19. Saha S, Chadha M, Shu Y, Group of Asian Researchers on Influenza (GARI). Divergent seasonal patterns of influenza types A and B across latitude gradient in Tropical Asia. Influenza Other Respir Viruses 2016 May;10(3):176-184. [CrossRef] [Medline]
  20. Xu Z, Li Z, Hu W. Global dynamic spatiotemporal pattern of seasonal influenza since 2009 influenza pandemic. Infect Dis Poverty 2020 Jan 03;9(1):2 [FREE Full text] [CrossRef] [Medline]
  21. Millett GA, Jones AT, Benkeser D, Baral S, Mercer L, Beyrer C, et al. Assessing differential impacts of COVID-19 on black communities. Ann Epidemiol 2020 Jul;47:37-44 [FREE Full text] [CrossRef] [Medline]
  22. Quinn SC, Kumar S, Freimuth VS, Musa D, Casteneda-Angarita N, Kidwell K. Racial disparities in exposure, susceptibility, and access to health care in the US H1N1 influenza pandemic. Am J Public Health 2011 Feb;101(2):285-293 [FREE Full text] [CrossRef] [Medline]
  23. Bibbins-Domingo K. This time must be different: disparities during the COVID-19 pandemic. Ann Intern Med 2020 Aug 04;173(3):233-234 [FREE Full text] [CrossRef] [Medline]
  24. Kirby T. Evidence mounts on the disproportionate effect of COVID-19 on ethnic minorities. Lancet Respir Med 2020 Jun;8(6):547-548 [FREE Full text] [CrossRef] [Medline]
  25. Phaswana-Mafuya N, Shisana O, Gray G, Zungu N, Bekker L, Kuonza L, et al. The utility of 2009 H1N1 pandemic data in understanding the transmission potential and estimating the burden of COVID-19 in South Africa to guide mitigation strategies. S Afr Med J 2020 May 25;110(7):576-577. [CrossRef] [Medline]
  26. Collyns D. Peru’s coronavirus response was ‘right on time’ – so why isn't it working? The Guardian. 2020 May 20.   URL: https://www.theguardian.com/global-development/2020/may/20/peru-coronavirus-lockdown-new-cases [accessed 2021-01-01]
  27. Weekly respiratory pathogens surveillance report - week 23. National Institute for Communicable Diseases. 2020.   URL: https://www.nicd.ac.za/wp-content/uploads/2020/06/Weekly-Pathogens-surveillance-report-week-23.pdf [accessed 2021-01-01]
  28. National COVID-19 daily report. National Institute for Communicable Diseases. 2020 Jun 15.   URL: https:/​/www.​nicd.ac.za/​wp-content/​uploads/​2020/​06/​COVID19-Daily-Report-National-Public-15June2020.​pdf [accessed 2021-01-01]
  29. Cowling BJ, Ali ST, Ng TWY, Tsang TK, Li JCM, Fong MW, et al. Impact assessment of non-pharmaceutical interventions against coronavirus disease 2019 and influenza in Hong Kong: an observational study. Lancet Public Health 2020 May;5(5):e279-e288 [FREE Full text] [CrossRef] [Medline]
  30. Lofgren E, Fefferman NH, Naumov YN, Gorski J, Naumova EN. Influenza seasonality: underlying causes and modeling theories. J Virol 2007 Jun;81(11):5429-5436 [FREE Full text] [CrossRef] [Medline]
  31. Luongo JC, Fennelly KP, Keen JA, Zhai ZJ, Jones BW, Miller SL. Role of mechanical ventilation in the airborne transmission of infectious agents in buildings. Indoor Air 2016 Oct;26(5):666-678 [FREE Full text] [CrossRef] [Medline]
  32. Fuhrmann C. The effects of weather and climate on the seasonality of influenza: what we know and what we need to know. Geography Compass 2010 Jul;4(7):718-730. [CrossRef]
  33. Lowen AC, Steel J. Roles of humidity and temperature in shaping influenza seasonality. J Virol 2014 Jul;88(14):7692-7695 [FREE Full text] [CrossRef] [Medline]
  34. Jüni P, Rothenbühler M, Bobos P, Thorpe KE, da Costa BR, Fisman DN, et al. Impact of climate and public health interventions on the COVID-19 pandemic: a prospective cohort study. CMAJ 2020 May 25;192(21):E566-E573 [FREE Full text] [CrossRef] [Medline]
  35. Xu R, Rahmandad H, Gupta M, DiGennaro C, Ghaffarzadegan N, Amini H, et al. The modest impact of weather and air pollution on COVID-19 transmission. medRxiv. Preprint posted online May 24, 2020.
  36. Sajadi MM, Habibzadeh P, Vintzileos A, Shokouhi S, Miralles-Wilhelm F, Amoroso A. Temperature, humidity, and latitude analysis to estimate potential spread and seasonality of coronavirus disease 2019 (COVID-19). JAMA Netw Open 2020 Jun 01;3(6):e2011834 [FREE Full text] [CrossRef] [Medline]
  37. Carleton T, Meng KC. Causal empirical estimates suggest COVID-19 transmission rates are highly seasonal. medRxiv. Preprint posted online March 30, 2020. [CrossRef]
  38. Ficetola GF, Rubolini D. Climate affects global patterns of Covid-19 early outbreak dynamics. medRxiv. Preprint posted online April 20, 2020.
  39. Neher RA, Dyrdak R, Druelle V, Hodcroft EB, Albert J. Potential impact of seasonal forcing on a SARS-CoV-2 pandemic. Swiss Med Wkly 2020 Mar 09;150:w20224. [CrossRef] [Medline]
  40. Cohen J. Why do dozens of diseases wax and wane with the seasons—and will COVID-19? Science. 2020 Mar 13.   URL: https:/​/www.​sciencemag.org/​news/​2020/​03/​why-do-dozens-diseases-wax-and-wane-seasons-and-will-covid-19 [accessed 2021-01-01]
  41. Grifoni A, Weiskopf D, Ramirez SI, Mateus J, Dan JM, Moderbacher CR, et al. Targets of T cell responses to SARS-CoV-2 coronavirus in humans with COVID-19 disease and unexposed individuals. Cell 2020 Jun 25;181(7):1489-1501.e15 [FREE Full text] [CrossRef] [Medline]
  42. Rourke A, Davidson H. Hong Kong imposes restrictions as Covid-19 cases rise across Asia. The Guardian. 2020 Jul 27.   URL: https:/​/www.​theguardian.com/​world/​2020/​jul/​27/​global-report-china-reports-biggest-covid-19-surge-in-months-as-australia-sets-new-infections-record [accessed 2021-01-01]
  43. Packham C. Australia suffers 'disturbing' COVID-19 surge, state curbs wedding parties. Reuters. 2020 Jul 16.   URL: https://www.reuters.com/article/us-health-coronavirus-australia-idUSKCN24I08U [accessed 2021-01-01]
  44. Packham C. Australia tightens restrictions as COVID-19 cases top 10,000. Reuters. 2020.   URL: https://www.reuters.com/article/us-health-coronavirus-australia-idUSKCN24F0AD [accessed 2021-01-01]
  45. Mishra S, Kwong JC, Chan AK, Baral SD. Understanding heterogeneity to inform the public health response to COVID-19 in Canada. CMAJ 2020 Jun 22;192(25):E684-E685. [CrossRef] [Medline]
  46. Okonkwo NE, Aguwa UT, Jang M, Barré IA, Page KR, Sullivan PS, et al. COVID-19 and the US response: accelerating health inequities. BMJ Evid Based Med 2020 Jun 03 [FREE Full text] [CrossRef] [Medline]
  47. Yaya S, Yeboah H, Charles CH, Otu A, Labonte R. Ethnic and racial disparities in COVID-19-related deaths: counting the trees, hiding the forest. BMJ Glob Health 2020 Jun;5(6) [FREE Full text] [CrossRef] [Medline]
  48. Hansson E, Albin M, Rasmussen M, Jakobsson K. Stora skillnader i överdödlighet våren 2020 utifrån födelseland. Läkartidningen 2020:117.
  49. Weinman AL, Sullivan SG, Vijaykrishna D, Markey P, Levy A, Miller A, et al. Epidemiological trends in notified influenza cases in Australia's Northern Territory, 2007-2016. Influenza Other Respir Viruses 2020 Sep;14(5):541-550. [CrossRef] [Medline]
  50. Hall LL, Xu L, Mahmud SM, Puckrein GA, Thommes EW, Chit A. A map of racial and ethnic disparities in influenza vaccine uptake in the Medicare Fee-for-Service Program. Adv Ther 2020 May;37(5):2224-2235 [FREE Full text] [CrossRef] [Medline]
  51. Loiacono MM, Mahmud SM, Chit A, van Aalst R, Kwong JC, Mitsakakis N, et al. Patient and practice level factors associated with seasonal influenza vaccine uptake among at-risk adults in England, 2011 to 2016: an age-stratified retrospective cohort study. Vaccine X 2020 Apr 09;4:100054 [FREE Full text] [CrossRef] [Medline]
  52. Akpalu Y, Sullivan SJ, Regan AK. Association between health insurance coverage and uptake of seasonal influenza vaccine in Brazos County, Texas. Vaccine 2020 Feb 24;38(9):2132-2135. [CrossRef] [Medline]
  53. Wang L, Chen J, Marathe A. A framework for discovering health disparities among cohorts in an influenza epidemic. World Wide Web 2019 Nov;22(6):2997-3020 [FREE Full text] [CrossRef] [Medline]
  54. Webster F, Gidding H, Matthews V, Taylor R, Menzies R. What isn't measured isn't done - eight years with no progress in Aboriginal and Torres Strait Islander adult influenza and pneumococcal vaccination. Aust N Z J Public Health 2019 Dec;43(6):558-562. [CrossRef] [Medline]
  55. Ward BJ, Pillet S, Charland N, Trepanier S, Couillard J, Landry N. The establishment of surrogates and correlates of protection: useful tools for the licensure of effective influenza vaccines? Hum Vaccin Immunother 2018 Mar 04;14(3):647-656 [FREE Full text] [CrossRef] [Medline]
  56. Sekine T, Perez-Potti A, Rivera-Ballesteros O, Strålin K, Gorin JB, Olsson A, Karolinska COVID-19 Study Group. Robust T cell immunity in convalescent individuals with asymptomatic or mild COVID-19. bioRxiv. Preprint posted online June 29, 2020. [CrossRef]
  57. Trombetta CM, Montomoli E. Influenza immunology evaluation and correlates of protection: a focus on vaccines. Expert Rev Vaccines 2016 Aug;15(8):967-976. [CrossRef] [Medline]
  58. Gallais F, Velay A, Wendling MJ, Nazon C, Partisani M, Sibilia J, et al. Intrafamilial exposure to SARS-CoV-2 induces cellular immune response without seroconversion. medRxiv. Preprint posted online June 22, 2020. [CrossRef]
  59. Long B, Brady WJ, Koyfman A, Gottlieb M. Cardiovascular complications in COVID-19. Am J Emerg Med 2020 Jul;38(7):1504-1507 [FREE Full text] [CrossRef] [Medline]
  60. Maggio MC, Cimaz R, Alaimo A, Comparato C, Di Lisi D, Corsello G. Kawasaki disease triggered by parvovirus infection: an atypical case report of two siblings. J Med Case Rep 2019 Apr 24;13(1):104 [FREE Full text] [CrossRef] [Medline]
  61. Puttaraksa K, Pirttinen H, Karvonen K, Nykky J, Naides S, Gilbert L. Parvovirus B19V nonstructural protein NS1 induces double-stranded deoxyribonucleic acid autoantibodies and end-organ damage in nonautoimmune mice. J Infect Dis 2019 Apr 16;219(9):1418-1429 [FREE Full text] [CrossRef] [Medline]
  62. Iglesias-Gamarra A, Restrepo JF, Matteson EL. Small-vessel vasculitis. Curr Rheumatol Rep 2007 Aug;9(4):304-311. [CrossRef] [Medline]
  63. Crudele GDL, Amadasi A, Marasciuolo L, Rancati A, Gentile G, Zoja R. A case report of lethal post-viral lymphocytic myocarditis with exclusive location in the right ventricle. Leg Med (Tokyo) 2016 Mar;19:1-4. [CrossRef] [Medline]
  64. Smatti MK, Cyprian FS, Nasrallah GK, Al Thani AA, Almishal RO, Yassine HM. Viruses and autoimmunity: a review on the potential interaction and molecular mechanisms. Viruses 2019 Aug 19;11(8) [FREE Full text] [CrossRef] [Medline]
  65. Klok FA, Boon GJAM, Barco S, Endres M, Geelhoed JJM, Knauss S, et al. The Post-COVID-19 Functional Status scale: a tool to measure functional status over time after COVID-19. Eur Respir J 2020 Jul;56(1). [CrossRef] [Medline]
  66. Tegally H, Wilkinson E, Giovanetti M, Iranzadeh A, Fonseca V, Giandhari J, et al. Emergence and rapid spread of a new severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) lineage with multiple spike mutations in South Africa. medRxiv. Preprint posted online December 22, 2020. [CrossRef]
  67. Olsen SJ, Azziz-Baumgartner E, Budd AP, Brammer L, Sullivan S, Pineda RF, et al. Decreased influenza activity during the COVID-19 pandemic - United States, Australia, Chile, and South Africa, 2020. MMWR Morb Mortal Wkly Rep 2020 Sep 18;69(37):1305-1309. [CrossRef] [Medline]
  68. Omori R, Mizumoto K, Chowell G. Changes in testing rates could mask the novel coronavirus disease (COVID-19) growth rate. Int J Infect Dis 2020 May;94:116-118 [FREE Full text] [CrossRef] [Medline]
  69. Chartrand C, Pai M. How accurate are rapid influenza diagnostic tests? Expert Rev Anti Infect Ther 2012 Jun;10(6):615-617. [CrossRef] [Medline]
  70. Centers for Disease Control and Prevention. 2020.   URL: https://www.cdc.gov/coronavirus/2019-ncov/php/contact-tracing/contact-tracing-plan/overview.html [accessed 2021-01-01]
  71. Wiemken TL, Shacham E. Identifying potential undocumented COVID-19 using publicly reported influenza-like-illness and laboratory-confirmed influenza disease in the United States: an approach to syndromic surveillance? Am J Infect Control 2020 Aug;48(8):961-963 [FREE Full text] [CrossRef] [Medline]

Edited by G Eysenbach; submitted 01.10.20; peer-reviewed by A Safarnejad, P Nguyen; comments to author 20.10.20; revised version received 18.01.21; accepted 21.01.21; published 02.03.21

Copyright

©Stefan David Baral, Katherine Blair Rucinski, Jean Olivier Twahirwa Rwema, Amrita Rao, Neia Prata Menezes, Daouda Diouf, Adeeba Kamarulzaman, Nancy Phaswana-Mafuya, Sharmistha Mishra. Originally published in JMIR Public Health and Surveillance (http://publichealth.jmir.org), 02.03.2021.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Public Health and Surveillance, is properly cited. The complete bibliographic information, a link to the original publication on http://publichealth.jmir.org, as well as this copyright and license information must be included.