Abstract
The COVID-19 pandemic triggered an unprecedented rise in mortality that translated into life expectancy losses around the world, with only a few exceptions. We estimate life expectancy changes in 29 countries since 2020 (including most of Europe, the United States and Chile), attribute them to mortality changes by age group and compare them with historic life expectancy shocks. Our results show divergence in mortality impacts of the pandemic in 2021. While countries in western Europe experienced bounce backs from life expectancy losses of 2020, eastern Europe and the United States witnessed sustained and substantial life expectancy deficits. Life expectancy deficits during fall/winter 2021 among people ages 60+ and <60 were negatively correlated with measures of vaccination uptake across countries (r60+ = −0.86; two-tailed P < 0.001; 95% confidence interval, −0.94 to −0.69; r<60 = −0.74; two-tailed P < 0.001; 95% confidence interval, −0.88 to −0.46). In contrast to 2020, the age profile of excess mortality in 2021 was younger, with those in under-80 age groups contributing more to life expectancy losses. However, even in 2021, registered COVID-19 deaths continued to account for most life expectancy losses.
Subject terms: Infectious diseases, Epidemiology
In 2021, life expectancies returned to pre-pandemic levels in parts of western Europe but further worsened in eastern Europe, the United States and Chile. Life expectancy deficits were negatively correlated with vaccine uptake in later 2021.
Main
Period life expectancy (LE) is a summary measure of current population health. If mortality increases in a population, LE declines. Conversely, if mortality declines, LE increases. The measure is age-standardized and thus commonly employed for international comparisons of population health. In this paper we investigate LE changes since the start of the pandemic, distinguishing countries that saw worsening losses from countries that managed to bounce back from their LE drop in 2020.
Most countries experienced sizable gains in LE during the second half of the twentieth century1. However, at the turn of the twenty-first century, the rate of improvement in LE slowed in many high-income countries prior to the COVID-19 pandemic2, such as the United States3, England and Wales4, and Scotland5, among others3. The COVID-19 crisis triggered a mortality shock resulting in LE declines in 2020 of a magnitude not observed in the recent history of high-income countries6–9. While data limitations have precluded in-depth analyses in low-to-middle-income countries, emerging evidence suggests even larger losses than those observed in high-income countries (such as in India10 and Latin America11–13). Only very few countries did not witness declines in LE in 2020, including Norway, Denmark, Finland (for females only), New Zealand and Australia6,7,14,15.
Fluctuations in LE are not uncommon. Typically, LE declines are quickly followed by bounce backs16,17. In contrast to these short-term fluctuations, however, the COVID-19 pandemic induced global and severe mortality shocks in 2020 and, as of spring 2022, is still ongoing. Throughout 2021, the impact of the pandemic became more heterogeneous across populations with differences in prior infection, non-pharmaceutical interventions and vaccination uptake, all influencing the pandemic’s course. Emerging estimates of LE losses based on excess deaths suggest that most western European countries are expected to partly recover from the losses observed in 2020, while other countries (including the United States and Russia) will suffer further LE declines18.
We examine LE changes since 2019 in 29 countries, including most of Europe, the United States and Chile, using data on all-cause mortality from the Short-Term Mortality Fluctuations Database19 following a previously validated methodology6. We distinguish between annual LE changes and LE deficits, with the former showing the raw year-to-year difference and the latter indicating the difference between observed and expected LE had pre-pandemic trends continued. Using decomposition techniques, we describe which age groups and to what extent registered COVID-19 deaths contributed to recent trends and deficits in LE. We compare the magnitude and length of the current global LE decline with prominent mortality shocks during the twentieth century. All our results are reported for females, males and the total population. We further investigate associations between LE changes and vaccination uptake. Our results quantify the mortality burden of COVID-19 in 2021 and contribute to the debate about recent trends in LE from a cross-national perspective.
Results
Changes in LE since 2019
Among the 29 countries analysed, 8 countries saw significant LE bounce backs from 2020 losses: Belgium (+10.8 months; 95% confidence interval (CI), 9.7 to 11.9; H0: μ ≤ 0; P < 0.001), Switzerland (+7.7; 95% CI, 6.4 to 8.8; P < 0.001), Spain (+7.6; 95% CI, 7.1 to 8.1; P < 0.001), France (+5.0; 95% CI, 4.4 to 5.6; P < 0.001), England and Wales (+2.1; 95% CI, 1.6 to 2.7; P < 0.001), Italy (+5.1; 95% CI, 4.6 to 5.5; P < 0.001), Sweden (+7.5; 95% CI, 6.0 to 8.6; P < 0.001) and Slovenia (+3.1; 95% CI, 0.4 to 5.7; P = 0.010). Compounding the 2020 losses, LE dropped significantly further throughout 2021 in 12 countries: Bulgaria (−25.1 months; 95% CI, −23.4 to −26.6; H0: μ ≥ 0; P < 0.001), Chile (−8.0; 95% CI, −7.0 to −9.0; P < 0.001), the Czech Republic (−10.4; 95% CI, −9.4 to −11.5; P < 0.001), Germany (−3.1; 95% CI, −2.7 to −3.5; P < 0.001), Estonia (−21.5; 95% CI, −17.6 to −25.1; P < 0.001), Greece (−12.4; 95% CI, −11.0 to −13.8; P < 0.001), Croatia (−11.6; 95% CI, −9.7 to −13.3; P < 0.001), Hungary (−16.4; 95% CI, −15.3 to −17.6; P < 0.001), Lithuania (−7.9; 95% CI, −5.4 to −10.5; P < 0.001), Poland (−12.1; 95% CI, −11.3 to −12.7; P < 0.001), Slovakia (−23.9; 95% CI, −22.3 to −25.7; P < 0.001) and the United States (−2.7; 95% CI, −2.2 to −3.1; P < 0.001). LE in Scotland and Northern Ireland remained at approximately the same depressed levels as in 2020, indicating a constant excess mortality. In terms of LE changes since 2019, the extremes are marked by Bulgaria, with record compound LE losses across 2020 and 2021, and France, Belgium, Switzerland and Sweden, all with complete LE bounce backs from substantial prior losses. Of the three countries that experienced no LE loss in 2020 (Denmark, Norway and Finland), only Norway had a significantly higher LE in 2021 than in 2019 (Fig. 1 and Table 1).
Table 1.
Net LE difference from 2019 to 2021 | LE changes in 2020 | LE changes in 2021 | LE deficit in 2021 | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AT1 | ES2 | 95% CI | AT | ES | 95% CI | AT | ES | 95% CI | AT | ES | 95% CI | |||||
Austria | ↓60+ | −7.6 | (−8.8, | −6.4) | ↓60+ | −8.1 | (−9.4, | −6.9) | ↑60+ | +0.5 | (−1.1, | +1.7) | ↓60+ | −12.0 | (−10.6, | −13.3) |
Belgium | ↓60+ | −1.2 | (−2.2, | +0.1) | ↓60+ | −12.0 | (−13.0, | −10.8) | ↑60+ | +10.8 | (+9.7, | +11.9) | ↓60+ | −6.8 | (−5.7, | −7.9) |
Bulgaria | ↓60+ | −43.0 | (−44.5, | −41.4) | ↓60+ | −17.8 | (−19.8, | −16.2) | ↓60+ | −25.1 | (−26.6, | −23.4) | ↓60+ | −46.2 | (−44.5, | −48.0) |
Switzerland | ↓<60 | −0.5 | (−1.7, | +0.6) | ↓60+ | −8.2 | (−9.5, | −6.7) | ↑60+ | +7.7 | (+6.4, | +8.8) | ↓60+ | −6.2 | (−4.9, | −7.4) |
Chile | ↓60+ | −21.1 | (−22.3, | −19.9) | ↓60+ | −13.1 | (−14.2, | −11.7) | ↓<60 | −8.0 | (−9.0, | −7.0) | ↓60+ | −24.4 | (−23.3, | −25.6) |
Czech Republic | ↓60+ | −21.9 | (−22.8, | −20.8) | ↓60+ | −11.6 | (−12.6, | −10.5) | ↓60+ | −10.4 | (−11.5, | −9.4) | ↓60+ | −26.0 | (−24.9, | −27.0) |
Germany | ↓60+ | −5.7 | (−6.2, | −5.3) | ↓60+ | −2.6 | (−3.1, | −2.2) | ↓60+ | −3.1 | (−3.5, | −2.7) | ↓60+ | −10.2 | (−9.8, | −10.6) |
Denmark | ↓60+ | −0.4 | (−1.9, | +1.4) | ↑60+ | +1.1 | (−0.3, | +2.8) | ↓60+ | −1.5 | (−3.3, | +0.1) | ↓60+ | −3.9 | (−2.2, | −5.6) |
Estonia | ↓60+ | −23.2 | (−26.9, | −19.3) | ↓60+ | −1.8 | (−6.5, | +3.0) | ↓60+ | −21.5 | (−25.1, | −17.6) | ↓60+ | −29.3 | (−25.6, | −32.7) |
Spain | ↓60+ | −7.4 | (−8.0, | −6.7) | ↓60+ | −15.0 | (−15.5, | −14.4) | ↑60+ | +7.6 | (+7.1, | +8.1) | ↓60+ | −13.3 | (−12.8, | −14.0) |
Finland | ↓60+ | −0.3 | (−2.0, | +1.7) | ↓60+ | −0.4 | (−1.9, | +1.4) | ↑<60 | +0.1 | (−1.5, | +1.8) | ↓60+ | −3.4 | (−1.2, | −5.1) |
France | ↓60+ | −1.2 | (−1.7, | −0.6) | ↓60+ | −6.2 | (−6.7, | −5.6) | ↑60+ | +5.0 | (+4.4, | +5.6) | ↓60+ | −4.5 | (−3.7, | −5.1) |
England and Wales | ↓60+ | −9.3 | (−9.8, | −8.9) | ↓60+ | −11.5 | (−12.1, | −11.0) | ↑60+ | +2.1 | (+1.6, | +2.7) | ↓60+ | −12.7 | (−12.1, | −13.3) |
Northern Ireland | ↓60+ | −9.5 | (−12.9, | −7.0) | ↓60+ | −8.6 | (−11.4, | −5.4) | ↓<60 | −0.9 | (−3.4, | +2.5) | ↓60+ | −13.0 | (−9.4, | −15.8) |
Scotland | ↓60+ | −9.6 | (−11.7, | −7.9) | ↓60+ | −8.9 | (−10.7, | −7.3) | ↓<60 | −0.7 | (−2.6, | +0.8) | ↓<60 | −10.2 | (−8.5, | −11.5) |
Greece | ↓60+ | −15.5 | (−16.8, | −14.2) | ↓60+ | −3.2 | (−4.3, | −1.8) | ↓60+ | −12.4 | (−13.8, | −11.0) | ↓60+ | −18.4 | (−17.2, | −19.7) |
Croatia | ↓60+ | −21.0 | (−23.0, | −19.5) | ↓60+ | −9.4 | (−11.7, | −7.6) | ↓60+ | −11.6 | (−13.3, | −9.7) | ↓60+ | −27.0 | (−25.0, | −28.9) |
Hungary | ↓60+ | −24.6 | (−26.0, | −23.2) | ↓60+ | −8.2 | (−9.3, | −7.0) | ↓60+ | −16.4 | (−17.6, | −15.3) | ↓60+ | −29.5 | (−28.3, | −30.9) |
Iceland | ↓<60 | −2.1 | (−10.5, | +5.6) | ↓<60 | −3.2 | (−10.6, | +4.0) | ↑60+ | +1.0 | (−5.3, | +8.5) | ↓<60 | −4.7 | (+3.1, | −14.3) |
Italy | ↓60+ | −7.4 | (−7.9, | −6.9) | ↓60+ | −12.6 | (−13.0, | −12.1) | ↑60+ | +5.1 | (+4.6, | +5.5) | ↓60+ | −13.5 | (−13.0, | −14.1) |
Lithuania | ↓60+ | −25.7 | (−28.3, | −23.2) | ↓60+ | −17.8 | (−20.4, | −15.2) | ↓60+ | −7.9 | (−10.5, | −5.4) | ↓60+ | −37.5 | (−34.9, | −39.9) |
Netherlands | ↓60+ | −7.4 | (−8.4, | −6.7) | ↓60+ | −7.7 | (−8.5, | −6.8) | ↑60+ | +0.3 | (−0.7, | +1.0) | ↓60+ | −11.0 | (−10.1, | −12.0) |
Norway | ↑<60 | +1.7 | (+0.4, | +3.6) | ↑60+ | +2.0 | (+0.4, | +3.9) | ↓60+ | −0.3 | (−2.0, | +1.5) | ↓60+ | −2.4 | (−0.9, | −4.4) |
Poland | ↓60+ | −26.6 | (−27.4, | −25.8) | ↓60+ | −14.5 | (−15.4, | −13.8) | ↓60+ | −12.1 | (−12.7, | −11.3) | ↓60+ | −30.5 | (−29.8, | −31.1) |
Portugal | ↓60+ | −7.6 | (−9.1, | −6.5) | ↓60+ | −8.3 | (−9.4, | −7.2) | ↑60+ | +0.7 | (−0.8, | +2.0) | ↓60+ | −10.8 | (−9.4, | −12.1) |
Sweden | ↓60+ | −0.1 | (−1.1, | +1.0) | ↓60+ | −7.6 | (−8.6, | −6.4) | ↑60+ | +7.5 | (+6.0, | +8.6) | ↓60+ | −4.9 | (−3.7, | −6.0) |
Slovenia | ↓60+ | −7.3 | (−10.8, | −4.8) | ↓60+ | −10.4 | (−13.6, | −7.7) | ↑60+ | +3.1 | (+0.4, | +5.7) | ↓60+ | −8.5 | (−5.5, | −11.7) |
Slovakia | ↓60+ | −33.1 | (−34.8, | −31.6) | ↓60+ | −9.2 | (−11.2, | −7.6) | ↓60+ | −23.9 | (−25.7, | −22.3) | ↓60+ | −39.1 | (−37.1, | −40.8) |
United States | ↓<60 | −28.2 | (−28.7, | −27.8) | ↓60+ | −25.5 | (−26.0, | −25.1) | ↓<60 | −2.7 | (−3.1, | −2.2) | ↓60+ | −33.0 | (−32.4, | −33.5) |
1Attribution of life expectancy changes to mortality increases among primarily ↓60+, solely ↓60+, primarily ↓<60 or solely ↓<60, or mortality decreases among primarily ↑60+, solely ↑60+, primarily ↑<60 or solely ↑<60.
2Central estimate in months. LE deficit is defined as observed minus expected LE had pre-pandemic mortality trends continued.
In all countries, LE in 2021 was lower than expected under the continuation of pre-pandemic trends. Bulgaria, Chile, Croatia, the Czech Republic, Estonia, Germany, Greece, Hungary, Lithuania, Poland and Slovakia suffered substantially higher LE deficits in 2021 than in 2020, indicating a worsening mortality burden over the course of the pandemic (Extended Data Figs. 1–3).
Bulgaria experienced 17.8 months of LE decline in 2020 (95% CI, −16.5 to −19.8; H0: μ ≥ 0; P < 0.001). This substantial decline was compounded by an even larger loss of 25.1 months (95% CI, −23.4 to −26.6; P < 0.001) below the 2020 level in 2021, leaving the country with a net LE loss of 43.0 months (95% CI, −41.4 to −44.5; P < 0.001) since 2019. Bulgaria is the most severe example regarding LE losses among the nine countries from the former Eastern Bloc (Bulgaria, Slovakia, Lithuania, Poland, Estonia, Hungary, the Czech Republic, Croatia and Slovenia). Except Slovenia, all these countries suffered compound LE losses in 2021. Estonia stands out as the country with the third-largest LE losses in 2021 but almost no losses in 2020. Substantial compound losses were also observed in Chile and Greece. In contrast, after an 8-month LE loss in 2020, Switzerland experienced a bounce back of 7.7 months (95% CI, 6.4 to 8.8; H0: μ ≤ 0; P < 0.001). Belgium, Sweden, France, Italy and Spain joined Switzerland as countries that witnessed bounce backs from substantial LE losses in 2020, with the first three countries having regained the LE levels of 2019 (Fig. 1 and Table 1).
Age contributions to LE changes
In 2021, the pandemic death toll shifted towards younger age groups. For example, while US mortality for ages 80+ returned to pre-pandemic levels in 2021, overall LE losses grew due to worsening mortality in ages below 60. Mortality increases among ages below 60 contributed LE losses of −7.2 months (95% CI, −7.0 to −7.4; H0: μ ≥ 0; P < 0.001) in 2021 compared with 2020. These LE losses among the young cancel the LE bounce backs among the older population and yield a net LE drop in 2021 of −2.7 months (95% CI, −2.2 to −3.1; H0: μ ≥ 0; P < 0.001) for the United States (Fig. 2). Excess mortality among under-60s explained more than half of the loss in US LE since the start of the pandemic (58.9%; 95% CI, 57.9 to 59.8; H0: μ ≤ 50%; P < 0.001). LE losses in the under-60s, especially for males, were considerably higher in the United States than in most other countries in 2020 as well6.
The pattern of the shift in excess mortality away from the oldest ages in 2021 compared with 2020 is also evident in Austria, Belgium, the Czech Republic, England and Wales, Germany, the Netherlands, Northern Ireland, Poland, Portugal, Scotland, Slovakia, Slovenia and Spain (Fig. 2). In 11 of the 16 countries with LE losses in 2021, the under-60 age groups contributed significantly more to LE loss in 2021 than in 2020 (one-tailed, P < 0.05). Among the 13 countries that partially or completely bounced back from their LE losses in 2020, 10 (Austria, Belgium, Switzerland, Spain, France, England and Wales, Italy, Netherlands, Sweden and Slovenia) achieved the bounce back primarily or solely due to normalizing mortality among the older population (H0: μ ≤ 50% contribution of ages 60+ to LE change; P < 0.05; Table 1). Croatia, Greece, Hungary, Northern Ireland and Slovakia saw almost no losses in the 40–59 age group in 2020 but substantial excess mortality in the same group in 2021 (Fig. 2).
Despite the shift towards a greater contribution of excess mortality from younger age groups in 2021, increased mortality among those aged 60+ remained the most important contributor to LE losses compared with pre-pandemic levels (Table 1). LE dropped in 28 of the 29 countries analysed from 2019 to 2021, with only Norway exceeding the 2019 levels. Excess mortality in ages 60+ was the main or sole contributor to these losses in 19 of 28 countries (Austria, Bulgaria, Chile, the Czech Republic, Germany, Estonia, Spain, France, England and Wales, Greece, Croatia, Hungary, Italy, Lithuania, the Netherlands, Poland, Portugal, Slovenia and Slovakia, H0: μ ≤ 50% contribution of ages 60+ to LE change; P < 0.05), with the United States being the prominent exception. In 2020, the LE losses of every country witnessing significant losses were explained primarily or solely by mortality increases in ages 60+. The LE changes in 2021 were, however, sometimes driven by mortality dynamics below age 60. France stands out as the only country that suffered significant LE losses since 2019 without increased mortality among those under 60 (Table 1 and Fig. 2).
Sex differences in LE changes
Recent trends of a decreasing gap in LE between females and males20 were disrupted by the pandemic. Consistent with previous research, females showed higher LE in the 29 countries in our analysis. The magnitude of the gap in 2021 varied from 3.17 years in Norway (95% CI, 2.95 to 3.37; H0: μ ≤ 0; P < 0.001) to more than 9.65 years in Lithuania (95% CI, 9.20 to 9.90; P < 0.001). However, our results show that the female advantage in LE significantly (H0: μ ≤ 0; P < 0.05) increased in 16 of the 29 countries during the pandemic, thereby widening the sex gap (Fig. 3). This finding indicates that in most countries, males were more affected by excess deaths. The biggest increase in the sex gap was observed in the United States, where the gap increased by almost a year from 5.72 to 6.69 years (+0.97 years; 95% CI, 0.90 to 1.04; H0: μ ≤ 0; P < 0.001). The narrowing sex gaps observed in six countries were not significant. See Extended Data Figs. 4–7 and Supplementary Tables 1 and 2 for further sex-specific results on LE levels and changes.
LE deficit contributions by cause of death and age
Officially registered COVID-19 deaths explained most of the LE deficit in the year 2021 across Europe, the United States and Chile (Fig. 4). The Netherlands is the single exception where causes other than COVID-19 explained more than half (51.7%) of the 2021 LE deficit. Conversely, France, Slovenia, and England and Wales stand out as three countries where mortality due to non-COVID deaths was lower than expected in 2021. In the majority of countries, the age group 60–79 contributed the most to the LE deficit in 2021. The exceptions were Scotland and Germany, the former having the largest contributions among ages 40–59 (0.45 of the 0.86 years of total LE deficit), the latter among ages 80+ (0.43 of the 0.86 years of total LE deficit). Note that COVID-19-related deaths are counted differently across countries and that some cross-country differences are explained by different reporting conventions as outlined in the Discussion. As CIs do not account for these biases, we chose to not report them for this section.
LE deficit by vaccination uptake
Higher vaccination uptake by October 2021 was associated with smaller LE deficits in quarter 4 of 2021 across countries among ages 60+ and <60 (r60+ = −0.86; two-tailed P < 0.001; 95% CI, −0.94 to −0.69; r<60 = −0.74; two-tailed P < 0.001; 95% CI, −0.88 to −0.46; Fig. 5). Eastern Europe, especially Bulgaria, had lower vaccination uptake and showed bigger deficits in LE, while the opposite was true for most central and western European countries.
The direction of this association was the same when comparing the contributions of the age groups <60 and 60+ to the LE deficit in 2021, albeit with variation in the strength of the association. Vaccination uptake for people 60+ showed a stronger association with LE deficits.
Prominent outliers indicate a confounded relationship between vaccination uptake and LE losses. For those under age 60, the United States saw a far higher LE deficit than countries with comparable overall vaccination shares, such as the Netherlands, Austria and Switzerland. For ages 60+, Slovakia, Croatia and Hungary stand out as countries with surprisingly high LE deficits given their vaccination uptake. Finer-grained details of the age prioritization of vaccine roll-out and the types of vaccines used may account for some of these differences, as well as correlations between vaccine uptake and compliance with non-pharmaceutical interventions or the overall health care system capacity.
Comparison with past mortality shocks
To contextualize the severity of the LE losses during the COVID-19 pandemic, we examined historical mortality crises over the past 120 years and qualitatively compared them with LE declines since 2019. As shown in Fig. 6, the first half of the twentieth century witnessed several mortality shocks leading to LE declines across consecutive years, but in most cases these were followed by immediate bounce backs. In the past 40 years, the frequency of mortality crises fell markedly. Supplementary Table 3 shows the total negative or overall change in LE during the period of a mortality crisis and the year at which recovery to pre-crisis LE was reached.
During World War I and the Spanish flu epidemic, all countries for which historical data are available experienced substantial losses in LE—the largest annual declines in LE in the past 120 years. In most countries, LE declined continuously throughout the four-year period of the crises, but the losses were the largest in 1918. The steepest declines in LE during 1914–1918 were seen in Italy (−22.7 years) and France (−16.5 years). Denmark, similarly to patterns during COVID-19, experienced the lowest decline in LE during Spanish flu—only one year. Notably, even after all these substantial losses in LE, the recovery to pre-crisis levels was achieved in one or two years (Supplementary Table 3).
Mortality patterns during World War II were somewhat different. While most countries suffered some years with substantial LE declines during 1939–1945, the bounce backs occurred during the war or just after it. In the Netherlands, the famine known as Hunger Winter caused LE declines in 1945 of 5.7 years, but LE had already recovered to pre-war (1938) levels by 194621.
Numerous flu epidemics occurred over the second half of the twentieth century, but LE during these flu seasons usually declined only very slightly, if at all. Moreover, bounce backs were always immediate, except in cases of wider health crises, such as the recovery from the 2015 influenza season in Scotland and United States, where LE was already stagnating before the epidemic5. Overall, the losses during these flu epidemics were substantially smaller than the declines in LE during the COVID-19 pandemic.
The most prominent example of a protracted mortality crisis in the past 50 years is provided by Russia and Eastern Bloc countries. From 1960s onwards, these countries experienced an extended period of continuous stagnation in LE, in which bounce backs to pre-decline levels were attained only in the twenty-first century22. These patterns reflect the deep-rooted structural nature of the mortality crisis in the populations that failed to proceed with the health transition23. The most pronounced drop in LE happened in these countries in late 1980s and early 1990s (Fig. 6), which mirrored the previous brief period of success in lowering mortality24 as a direct result of Gorbachev’s anti-alcohol campaign25. In contrast to epidemic or war-related shocks, the mortality crisis in the formerly Eastern Bloc countries was structural, and the bounce backs of LE were very slow. The magnitude of LE losses witnessed during COVID-19 in the formerly Eastern Bloc countries are comparable to those observed during the Soviet mortality crisis.
Discussion
The COVID-19 pandemic led to global increases in mortality and declines in period LE that are without precedent over the past 70 years. The scale of these losses was clear by the end of 2020. By the end of 2021, it was clear that the pandemic had induced a protracted mortality shock in the United States and many European countries, measured as either compounded LE losses or persistent LE below pre-pandemic levels. Even the best-performing countries were lagging behind their LE projections for 2021 given a continuation of pre-pandemic trends. Nevertheless, in 2021, Sweden, Switzerland, Belgium and France managed to bounce back from substantial LE losses in 2020 to pre-pandemic levels. Demographically, they achieved this by reducing mortality among ages 60+ back to 2019 levels while avoiding the mortality burden shift to younger ages as seen in other countries during 2021.
Denmark, Finland and Norway, while lagging behind their projected LE for 2021, managed to remain at pre-pandemic LE levels throughout 2020 and 2021. Here we may see the combination of campaigns delivering vaccines faster to more people than the European Union average, effective non-pharmaceutical public health interventions and high baseline capacities of the health care systems.
It is important to note that even for those countries that approached pre-pandemic levels of LE in 2021, substantial damage was already done. This is especially relevant for Sweden, which experienced pre-pandemic levels of LE in 2021 but, unlike its Scandinavian neighbours, suffered a substantial LE loss in 2020. While period mortality and consequentially LE can revert back to normal levels, the years of life lost during the period of elevated mortality and declining LE cannot be regained. As a measure of the current mortality conditions in a population, a return to pre-pandemic LE levels simply indicates a normalization of the mortality risk.
We observed stark cross-country differences in 2021 LE deficits, with bigger losses in countries with lower pre-pandemic LE. Geographically, this presents as an East–West division in Europe, which is also aligned with differences in vaccination uptake during 2021, with generally lower vaccination rates in eastern Europe than in the West. This pattern raises questions regarding the future of European mortality convergence, a stated goal of the European Union26.
Eastern European countries had a distinctive pattern of mortality development in the twentieth century. Early on, highly centralized governance and directive economies contributed to mortality reductions through the implementation of public health measures, and these countries were very successful in the early stages of their epidemiological transition27. Yet, in the second part of the century, these countries witnessed mortality stagnation as these centralized channels were less effective at curbing mortality linked to behavioural factors such as smoking and alcohol28,29. Recent years have seen rapid catch-up LE convergence between eastern and western Europe, after the periods of LE declines seen in the 1980s and 1990s23,30. It remains to be seen whether persistent COVID-19 losses in eastern Europe and diminishing losses in western Europe will create a new East/West divide and divergence in LE in the years to come.
In the United States, the pandemic has accentuated the pre-existing mid-life mortality crisis. This is clear from the strong contribution of increasing mortality below age 60 to LE losses in 2020 and 2021. Because non-COVID mortality also increased in these ages, this may be interpreted as the continuation and worsening of a pre-existing mortality crisis among working-age adults31. In 2020, the largest share of non-COVID excess deaths in US males was from external causes (primarily due to drug overdoses and homicides), nearly 80% of which occurred at working ages32. Preliminary data show continued increases in deaths due to drug overdoses in 202133. However, part of the effect may be due to the under-registration of COVID-19 deaths among the working-age population. Differences in vaccine uptake by age may also have contributed to the shift to younger mortality in the United States. By 1 July, when vaccines were already available in the United States, only 66.9% of 50- to 64-year-olds were fully vaccinated compared with 82.3% of 65- to 74-year-olds (as per the COVID Data Tracker of the Centers for Disease Control and Prevention). This means that older age groups were better protected during the large Delta wave in the United States in the summer/autumn of 2021 than during previous waves. Pre-pandemic differences in underlying conditions such as obesity and diabetes may also have contributed to an increased mortality burden in working-age US adults compared with their European counterparts34. Regarding global comparisons, the evidence for co-morbidity prevalence as an important predictor of cross-country COVID-19 mortality differences is still weak35.
In 2021, the pandemic’s death toll shifted to younger ages. While most countries reduced mortality at older ages, countries that bounced back were able to avoid the mortality increases in those under 60 that accounted for a higher share of losses in 2021. Whether this shift towards the young reflects differences in vaccine protection, behavioural responses or deaths from indirect causes remains to be understood. The inconsistent registration of deaths due to COVID-19 across countries36 complicates any cause-of-death attribution analysis, including ours. We found lower-than-expected mortality due to non-COVID-19 causes in 2021 in Belgium, England and Wales, France, and Slovenia (Fig. 4). Whether these results are an artefact of an overly broad definition of COVID-19-related deaths or point towards a genuine decline in non-COVID mortality (due to, for example, mortality displacement or the lack of flu deaths) is unclear at this point. For France, overcounting COVID-19 deaths seems unlikely, as the underlying data on COVID-19 death counts used here originate from Santé Publique France, which uses a very strict definition of “death due to COVID-19”36.
COVID-19 was the largest contributor to the 2021 LE deficit in all analysed countries except the Netherlands. This is despite different reporting standards and thus provides additional strong evidence for the direct effect of COVID-19 on increases in mortality. The result for the Netherlands may be spurious, as Karlinsky and Kobak37 found indirect evidence of substantial under-reporting of deaths due to COVID-19 in the Netherlands during the fall/winter wave in 2021 when comparing excess deaths with COVID-19 deaths (we retrieved updated results for 2021 from the authors’ GitHub repository at github.com/dkobak/excess-mortality on 15 February 2021). However, because factors other than undercounting can influence the relationship between COVID-19 deaths and excess deaths, more detailed cause-of-death information is needed to assess the impact of non-COVID-19-related mortality on 2021 LE deficits.
As the calculation of LE losses requires timely data on population and death counts by age, we are limited in our analysis to those countries with a reliable vital statistics registration system. Consequently, our international analysis based on 29 high- and middle-income countries may give a skewed impression of the global impact of COVID-19 on LE. Indirect LE estimates for 2020–2021 based on excess deaths18 indicate substantial losses across South America, which match or exceed the losses we estimated for eastern Europe. India and select countries in the Middle East probably had losses on par with the United States, whereas Russia and Mexico suffered LE losses in excess of the 42 months we estimated for Bulgaria. Little is known about the African continent, due to a lack of reliable death registration, and China, due to restricted access to the data. Putting our results in context with these indirect estimates, while the LE losses in central, western and northern Europe over the first two years of the pandemic were drastic given the long trend of declining mortality, they were probably low when compared across the globe.
In 2021, we saw divergence in the impact of the pandemic on population health. While some countries saw bounce backs from stark LE losses thanks to pharmaceutical and non-pharmaceutical public health interventions, others saw sustained and substantial LE deficits. Human populations faced multiple mortality crises during the twentieth century, yet LE kept increasing globally in the medium and long term, especially in the second half of the twentieth century. While COVID-19 has been the most severe global mortality shock since World War II, we will have to wait to know whether and how longer-term LE trends are altered by the pandemic. Extrapolating our findings from 2021, it is plausible that countries with ineffective public health responses will see a protracted health crisis induced by the pandemic, with medium-term stalls in LE improvements, while other regions manage a smoother recovery to return to pre-pandemic trends.
Methods
LE estimation and decomposition
The calculation of period LE requires data on death counts and population exposures by single years of age. Timely information on death counts across all causes from 2015 through 2021 was sourced from the Short Term Mortality Fluctuations Input Database19,38, which continuously collects weekly death counts by age and sex from statistical offices. The 38 countries represented in the database have been selected on the basis of the completeness of their death registration and census data. To allow for a reliable estimation of LE changes and their age contributions, we further selected the 29 countries for which death counts for 2020 and 2021 were reported across at least ten distinct age groups. These weekly counts were aggregated into annual counts and, due to various age groupings used in the source data, harmonized into single age groups from 0 to 85+ using the penalized composite link model39,40, a non-parametric disaggregation technique for histograms of count data. Separate tables of harmonized counts were created for males, females and the total population in each country. Our methodology for age disaggregation follows that of Aburto et al.6 and has been thoroughly validated for accurate LE estimates consistent with those based on unabridged data. Mid-year population estimates by age and sex for the years 2015–2021 were sourced from the United Nations World Population Prospects (WPP)41 and converted into person-years of exposures, taking into account the varying number of weeks in an ISO year42 to be consistent with death-count reporting in our raw data. For Scotland and England and Wales, we projected mid-year population for 2020 and 2021 on the basis of data from the respective national statistical offices (NSOs). A sensitivity analysis with alternative population estimates taken from NSOs is provided in the Supplementary Information. To attribute changes in LE to changes in mortality from deaths registered as due to COVID-19, we sourced age- and sex-specific COVID-19 death counts from the COVerAGE-DB database43. All data were downloaded on 26 April 2022.
Annual period life tables calculated via standard demographic techniques44 were used to estimate LE from 2015 to 2021. To quantify the LE loss directly attributable to COVID-19, we further assembled cause-deleted life tables with ‘deaths registered as due to COVID-19’ and ‘other deaths’ as possible decrements45. Using the Arriaga decomposition technique46, we attributed annual changes in LE to changes in age-specific all-cause mortality. Additionally, we calculated LE deficits for 2020 and 2021 defined as observed LE minus expected LE based on a continuation of pre-pandemic trends. These expected LEs were derived from Lee–Carter forecasts47 of age-specific death rates over the years 2015 through 2019. We performed an Arriaga decomposition of the LE deficits in 2021 into age-specific contributions from COVID-19 and non-COVID-19 mortality. CIs around our LE estimates, LE differences, LE deficits, LE decompositions and LE sex differences were derived from 100 Poisson simulations of the harmonized death counts. Where applicable, we calculated the associated P values from a shifted empirical distribution function of the Poisson-bootstrapped estimates under the null.
To analyse the cross-country relationship between LE deficits and vaccination uptake during fall and winter 2021, we calculated life tables and LE deficits for the fourth quarter of the year. To do so, we used the weekly death counts over weeks 40 through 52 and adjusted population exposures.
The analyses are fully reproducible with source code and data archived with Zenodo (10.5281/zenodo.6861804). We also archived CSV files of the table and figure data (10.5281/zenodo.6861843) and the harmonized life table data informing all analyses in this paper (10.5281/zenodo.6861866).
Estimation of age-specific vaccination uptake
Data on age-specific vaccinations were collected from the COVerAGE-DB43. Vaccination uptake was calculated with mid-year population data for 2020 from the WPP41 and the Human Mortality Database. The vaccination measures were age harmonized using the penalized composite link model. Vaccination counts with missing age information were redistributed according to the observed age distribution of vaccinations in a given country. From the available data, for each country we calculated the share of the population that was fully vaccinated as of 1 October 2021 separately for people below age 60 and above 60. A full vaccination was defined as either two vaccinations or a single vaccination of the vaccine from Johnson & Johnson.
Population exposure sensitivity analysis
The results presented in the main text rely on population exposures from the WPP, which were issued prior to the COVID-19 pandemic. The COVID-19 pandemic has altered population age structure in some countries, reducing the number of people ages 60 and older. The WPP population projections used in this paper do not account for this effect and thus may overestimate the population in the oldest age groups in 2020 and 2021, resulting in negatively biased death rates and positively biased bounce backs. To test how sensitive our results are to the WPP-based denominators, we performed a sensitivity analysis to compare WPP-based denominators used in the analysis with population estimates (or projections in most cases for 2021) reported by the NSOs of the countries analysed. We then assessed the effects of using these two different sources of population exposures on LE estimates.
As shown in Supplementary Table 4, the overall differences between WPP and NSO mid-year population estimates for 2019, 2020 and 2021 (when available) are generally small and are not consistently positive or negative. Countries that show the largest deviations (such as France) in fact show positive deviations; that is, WPP-based population estimates are smaller than those reported for NSOs for 2020. In age-specific comparisons, we find a high correlation between the WPP- and NSO-based population estimates.
Supplementary Fig. 1 shows estimates of LE using NSO-based denominators compared to WPP-based denominators for 2019, 2020 and 2021 when available. LE estimates using the two different sources for denominators are concordant and largely lie on or close to the x = y line. When the two diverge, the divergence shows NSO-based estimates slightly overestimating LE relative to WPP estimates in 2019. While the direction of the LE changes across both sources is thus the same, the more optimistic LE levels in 2019 imply that NSO-based denominators indicate slightly larger losses in LE between 2019 and 2020, and for the few countries for which 2021 estimates are available, more positive bounce backs in 2021.
Reporting summary
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
Supplementary information
Acknowledgements
We thank A. Karlinsky for his help in determining the death count late registration quotas via his invaluable work on the World Mortality Database. We acknowledge the following funding: European Union Horizon 2020 research and innovation programme under Marie Sklodowska-Curie grant agreement no. 896821 (J.M.A. and R.K.), ROCKWOOL Foundation’s Excess Deaths grant (J.M.A. and I.K.), the Leverhulme Trust Large Centre Grant (J.M.A., L.Z., R.K. and J.B.D.), European Research Council grant no. ERC-2021-CoG-101002587 (MORTAL) (J.B.D.), the University of Oxford John Fell Fund (J.M.A., L.Z., R.K. and J.B.D.) and Estonian Research Council grant no. PSG 669 (H.J.). The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
Extended data
Author contributions
Conceptualization: J.S., J.M.A., I.K., M.S.K., H.J. and R.K. Data curation: J.S., M.S.K., I.K., L.Z., H.J. and R.K. Formal analysis: J.S., I.K., M.S.K., L.Z., H.J. and R.K. Investigation: J.S., J.M.A., I.K., M.S.K., L.Z., H.J, J.B.D. and R.K. Methodology: J.S., J.M.A., M.S.K., L.Z. and R.K. Project administration: J.S. Software: J.S., M.S.K., I.K. and H.J. Supervision: J.S., J.M.A. and R.K. Validation: J.S., J.M.A., I.K., M.S.K., L.Z., H.J., J.B.D. and R.K. Visualization: J.S., I.K. and H.J. Writing—original draft: J.S., J.M.A., I.K., M.S.K., L.Z., H.J., J.B.D. and R.K. Writing—review and editing: J.S., J.M.A., I.K., M.S.K., L.Z., H.J., J.B.D. and R.K.
Peer review
Peer review information
Nature Human Behaviour thanks Guillaume Marois and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.
Funding
Open access funding provided by Max Planck Society.
Data availability
We archived CSV files of the table and figure data (10.5281/zenodo.6861843) and the harmonized life table data informing all analyses in this paper (10.5281/zenodo.6861866).
Code availability
Scripts for the R programming language to download the source data for our analysis and to reproduce the results in this paper were archived with Zenodo (10.5281/zenodo.6861804).
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Contributor Information
Jonas Schöley, Email: schoeley@demogr.mpg.de.
José Manuel Aburto, Email: jose.aburto@lshtm.ac.uk.
Ridhi Kashyap, Email: ridhi.kashyap@nuffield.ox.ac.uk.
Extended data
is available for this paper at 10.1038/s41562-022-01450-3.
Supplementary information
The online version contains supplementary material available at 10.1038/s41562-022-01450-3.
References
- 1.Riley JC. Estimates of regional and global life expectancy, 1800–2001. Popul. Dev. Rev. 2005;31:537–543. doi: 10.1111/j.1728-4457.2005.00083.x. [DOI] [Google Scholar]
- 2.Raleigh, V. S. Trends in Life Expectancy in EU and Other OECD Countries: Why Are Improvements Slowing? OECD Health Working Papers (OECD, 2019); 10.1787/223159ab-en
- 3.Ho JY, Hendi AS. Recent trends in life expectancy across high income countries: retrospective observational study. BMJ. 2018;362:k2562. doi: 10.1136/bmj.k2562. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Hiam L, Harrison D, McKee M, Dorling D. Why is life expectancy in England and Wales ‘stalling’? J. Epidemiol. Community Health. 2018;72:404–408. doi: 10.1136/jech-2017-210401. [DOI] [PubMed] [Google Scholar]
- 5.Fenton L, et al. Recent adverse mortality trends in Scotland: comparison with other high-income countries. BMJ Open. 2019;9:e029936. doi: 10.1136/bmjopen-2019-029936. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Aburto, J. M. et al. Quantifying impacts of the COVID-19 pandemic through life-expectancy losses: a population-level study of 29 countries. Int. J. Epidemiol.10.1093/ije/dyab207 (2021). [DOI] [PMC free article] [PubMed]
- 7.Islam N, et al. Effects of COVID-19 pandemic on life expectancy and premature mortality in 2020: time series analysis in 37 countries. BMJ. 2021;375:e066768. doi: 10.1136/bmj-2021-066768. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Andrasfay T, Goldman N. Reductions in 2020 US life expectancy due to COVID-19 and the disproportionate impact on the Black and Latino populations. Proc. Natl Acad. Sci. USA. 2021;118:e2014746118. doi: 10.1073/pnas.2014746118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Mazzuco S, Campostrini S. Life expectancy drop in 2020: estimates based on Human Mortality Database. PLoS ONE. 2022;17:e0262846. doi: 10.1371/journal.pone.0262846. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Yadav, S., Yadav, P. K. & Yadav, N. Impact of COVID-19 on life expectancy at birth in India: a decomposition analysis. BMC Public Health10.1186/s12889-021-11690-z (2021). [DOI] [PMC free article] [PubMed]
- 11.Castro MC, et al. Reduction in life expectancy in Brazil after COVID-19. Nat. Med. 2021;27:1629–1635. doi: 10.1038/s41591-021-01437-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.García-Guerrero VM, Beltrán-Sánchez H. Heterogeneity in excess mortality and its impact on loss of life expectancy due to COVID-19: evidence from Mexico. Can. Stud. Popul. 2021;48:165–200. doi: 10.1007/s42650-021-00051-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Lima EEC, et al. Investigating regional excess mortality during 2020 COVID-19 pandemic in selected Latin American countries. Genus. 2021;77:30. doi: 10.1186/s41118-021-00139-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Canudas-Romo, V., Houle, B. & Adair, T. Quantifying impacts of the COVID-19 pandemic on Australian life expectancy. Int. J. Epidemiol.10.1093/ije/dyab273 (2022). [DOI] [PMC free article] [PubMed]
- 15.Rizzi S, Søgaard J, Vaupel JW. High excess deaths in Sweden during the first wave of COVID-19: policy deficiencies or ‘dry tinder’? Scand. J. Public Health. 2021;50:33–37. doi: 10.1177/14034948211027818. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Saha MV, Davis RE, Hondula DM. Mortality displacement as a function of heat event strength in 7 US cities. Am. J. Epidemiol. 2013;179:467–474. doi: 10.1093/aje/kwt264. [DOI] [PubMed] [Google Scholar]
- 17.Kissler SM, Grad YH. Anticipating racial/ethnic mortality displacement from COVID-19. Am. J. Epidemiol. 2022;191:1519–1152. doi: 10.1093/aje/kwac079. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Heuveline P. Global and national declines in life expectancy: an end-of-2021 assessment. Popul. Dev. Rev. 2022;48:31–50. doi: 10.1111/padr.12477. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Németh L, Jdanov DA, Shkolnikov VM. An open-sourced, web-based application to analyze weekly excess mortality based on the Short-Term Mortality Fluctuations data series. PLoS ONE. 2021;16:e0246663. doi: 10.1371/journal.pone.0246663. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Zarulli V, Kashnitsky I, Vaupel JW. Death rates at specific life stages mold the sex gap in life expectancy. Proc. Natl Acad. Sci. USA. 2021;118:e2010588118. doi: 10.1073/pnas.2010588118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Lumey LH, van Poppel FWA. The Dutch famine of 1944–45: mortality and morbidity in past and present generations. Soc. Hist. Med. 1994;7:229–246. doi: 10.1093/shm/7.2.229. [DOI] [PubMed] [Google Scholar]
- 22.Shkolnikov VM, Andreev EM, McKee M, Leon DA. Components and possible determinants of decrease in Russian mortality in 2004–2010. Demogr. Res. 2013;28:917–950. doi: 10.4054/DemRes.2013.28.32. [DOI] [Google Scholar]
- 23.Timonin, S. et al. Disparities in length of life across developed countries: measuring and decomposing changes over time within and between country groups. Popul. Health Metr.10.1186/s12963-016-0094-0 (2016). [DOI] [PMC free article] [PubMed]
- 24.Zakharov S. Cohort analysis of the Russia’s population mortality: long- and short-term effects of generations’ inequality in the face of death. Stud. Russ. Econ. Dev. 1999;10:199–211. [Google Scholar]
- 25.Leon DA, Shkolnikov VM, McKee M. Alcohol and Russian mortality: a continuing crisis. Addiction. 2009;104:1630–1636. doi: 10.1111/j.1360-0443.2009.02655.x. [DOI] [PubMed] [Google Scholar]
- 26.Solidarity in Health: Reducing Health Inequalities in the EU (European Commission, 2009).
- 27.Vishnevsky A. Mortality in Russia: the second epidemiological revolution that never was. Demogr. Rev. 2015;2:4–33. [Google Scholar]
- 28.Omran AR. The epidemiologic transition: a theory of the epidemiology of population change. Milbank Mem. Fund Q. 1971;49:509–538. doi: 10.2307/3349375. [DOI] [PubMed] [Google Scholar]
- 29.Vallin J, Meslé F. Convergences and divergences: an analytical framework of national and sub-national trends in life expectancy. Genus. 2005;61:83–124. [Google Scholar]
- 30.Aburto JM, van Raalte A. Lifespan dispersion in times of life expectancy fluctuation: the case of central and eastern Europe. Demography. 2018;55:2071–2096. doi: 10.1007/s13524-018-0729-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Woolf SH, Schoomaker H. Life expectancy and mortality rates in the United States, 1959–2017. JAMA. 2019;322:1996–2016. doi: 10.1001/jama.2019.16932. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Glei, D. A. The US midlife mortality crisis continues: excess cause–specific mortality during 2020. Am. J. Epidemiol.10.1093/aje/kwac055 (2022). [DOI] [PMC free article] [PubMed]
- 33.Dyer, O. A record 100000 people in the US died from overdoses in 12 months of the pandemic, says CDC. BMJ10.1136/bmj.n2865 (2021). [DOI] [PubMed]
- 34.Pongiglione, B., Ploubidis, G. & Dowd, J. B. Older adults in the US have worse cardiometabolic health compared to England. J. Gerontol. B10.1093/geronb/gbac023 (2022). [DOI] [PMC free article] [PubMed]
- 35.Thakur, B. et al. A systematic review and meta-analysis of geographic differences in comorbidities and associated severity and mortality among individuals with COVID-19. Sci. Rep.10.1038/s41598-021-88130-w (2021). [DOI] [PMC free article] [PubMed]
- 36.Garcia J, et al. Différences de mortalité par Covid-19: conséquence des imperfections et de la diversité des systèmes de collecte des données. Population. 2021;76:37–76. doi: 10.3917/popu.2101.0037. [DOI] [Google Scholar]
- 37.Karlinsky A, Kobak D. Tracking excess mortality across countries during the COVID-19 pandemic with the World Mortality Dataset. eLife. 2021;10:e69336. doi: 10.7554/eLife.69336. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Jdanov, D., Shkolnikov, V. M., Galarza, A. A., Boe, C. & Barbieri, M. Short-Term Mortality Fluctuations Dataseries Methods Protocol (Max Planck Institute for Demographic Research, 2021); https://mortality.org/Public/STMF_DOC/STMFNote.pdf
- 39.Rizzi S, Gampe J, Eilers PHC. Efficient estimation of smooth distributions from coarsely grouped data. Am. J. Epidemiol. 2015;182:138–147. doi: 10.1093/aje/kwv020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Pascariu, M. D., Dańko, M. J., Schöley, J. & Rizzi, S. ungroup: an R package for efficient estimation of smooth distributions from coarsely binned data. J. Open Source Softw.10.21105/joss.00937 (2018).
- 41.World Population Prospects (Population Division, United Nations, 2021); https://population.un.org/wpp/Download/Standard/Population/
- 42.ISO week date. Wikipediahttps://en.wikipedia.org/w/index.php?title=ISO_week_date&oldid=1007765520 (2021).
- 43.Riffe T, Acosta E, COVerAGE-DB team Data resource profile: COVerAGE-DB: a global demographic database of COVID-19 cases and deaths. Int. J. Epidemiol. 2021;50:390–390f. doi: 10.1093/ije/dyab027. [DOI] [Google Scholar]
- 44.Chiang, C. L. Life Table and Mortality Analysis (World Health Organisation, 1979); http://www.who.int/iris/handle/10665/62916
- 45.Preston, S. H., Heuveline, P. & Guillot, M. Demography (Blackwell, 2001).
- 46.Arriaga EE. Measuring and explaining the change in life expectancies. Demography. 1984;21:83–96. doi: 10.2307/2061029. [DOI] [PubMed] [Google Scholar]
- 47.Lee RD, Carter LR. Modeling and forecasting U.S. mortality. J. Am. Stat. Assoc. 1992;87:659–671. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
We archived CSV files of the table and figure data (10.5281/zenodo.6861843) and the harmonized life table data informing all analyses in this paper (10.5281/zenodo.6861866).
Scripts for the R programming language to download the source data for our analysis and to reproduce the results in this paper were archived with Zenodo (10.5281/zenodo.6861804).