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. 2021 Mar 18;58:69–75. doi: 10.1016/j.annepidem.2021.03.006

COVID-19 mortality in California based on death certificates: disproportionate impacts across racial/ethnic groups and nativity

Erika Garcia a,, Sandrah P Eckel a, Zhanghua Chen a, Kenan Li b, Frank D Gilliland a
PMCID: PMC8005258  NIHMSID: NIHMS1685155  PMID: 33746033

Abstract

Purpose

To examine characteristics of coronavirus disease 2019 (COVID-19) decedents in California (CA) and evaluate for disproportionate mortality across race/ethnicity and ethnicity/nativity.

Methods

COVID-19 deaths were identified from death certificates. Age-adjusted mortality rate ratios (MRR) were compared across race/ethnicity. Proportionate mortality rates (PMR) were compared across race/ethnicity and by ethnicity/nativity.

Results

We identified 10,200 COVID-19 deaths in CA occurring February 1 through July 31, 2020. The most frequently observed characteristics among decedents were age 65 years or above, male, Hispanic, foreign-born, and educational attainment of High School or below. MRR indicated elevated COVID-19 morality rates among Asian/Pacific Islander, Black, and Hispanic groups compared with the White group, with Black and Hispanic groups having the highest MRR at 2.75 (95%CI: 2.54–2.97) and 4.18 (95%CI: 3.99–4.37), respectively. Disparities were larger at younger ages. Similar results were observed with PMR, and patterns of age-racial/ethnic disparities remained in analyses stratified by education. Elevated PMR were observed in all ethnicity/nativity groups, especially foreign-born Hispanic individuals, relative to U.S.-born non-Hispanic individuals. These were generally larger at younger ages and persisted after stratifying by education.

Conclusions

Differential COVID-19 mortality was observed in California across racial/ethnic groups and by ethnicity/nativity groups with evidence of greater disparities among younger age groups. Identifying COVID-19 disparities is an initial step toward mitigating disease impacts in vulnerable communities.

Keywords: COVID-19, Mortality, Disparities, Race, Ethnicity, Nativity

Abbreviations: AI/AN, American Indian/Alaskan Native; A/PI, Asian/Pacific Islander; CA, California; CCDF, California Comprehensive Death Files; CCMDF, California Comprehensive Master Death File; COVID-19, Coronavirus disease 2019; ICD-10, International Statistical Classification of Diseases and Related Health Problems; MR, mortality rates; MRR, mortality rate ratios; PM, proportionate mortality; PMR, proportionate mortality rates; U.S., United States

Introduction

There is a growing body of literature on the differential impacts of the coronavirus disease 2019 (COVID-19) in historically marginalized groups in the United States (U.S.), including disease incidence [1], [2], [3], hospitalization [4], [5], [6], [7], [8], severity [5,9,10], and mortality [[3], [4], [5],[11], [12], [13]]. Identifying COVID-19 disparities is an initial step toward mitigating disease impacts in vulnerable communities. Much of the current evidence, however, has relied on ecologic analyses using aggregate data for both the characteristic under study (e.g., percentage Black in a county) and COVID-19 outcome (e.g., county-level mortality) [1,3,11,[13], [14], [15]]. Studies that have been conducted with individual-level data are primarily derived from hospital/healthcare networks or insurance companies [2,4,6,7,9,16], which may not be representative of COVID-19 impacts in the general population given barriers to healthcare access and insurance among historically marginalized groups. Use of death certificate data allows for investigation into individual-level characteristics, captures all individuals in the catchment area, and does not suffer from substantial under-reporting of key characteristics as was seen for race/ethnicity information for COVID-19 decedents early in the pandemic. It is important to note that any disparities observed for COVID-19 morality are an accumulation of disproportionate impacts along the entire continuum of COVID-19 disease, beginning with exposure to the virus and culminating in death. The mechanisms and magnitudes of disparities likely differ for each step of the disease pathway [17]. Appropriate estimates of disease are needed, not only by single factors, such as racial/ethnic group, but also by intersections with other factors, such as with age, sex, and educational attainment, which considers that groups are not homogenous and indeed reflect diverse experiences and impacts of the pandemic [18], [19], [20]. Intersectional analysis allows for a more nuanced understanding of disparate burden of COVID-19, which is crucially needed to design and implement effective public health interventions to mitigate disease impacts.

The objective of this study was to examine demographic characteristics of COVID-19 decedents in California (CA)—which as of September 2020 is among the hardest hit states in terms of cases and deaths [21]—and evaluate for disproportionate mortality across these characteristics. In addition to descriptive information on decedents, COVID-19 mortality was compared across racial/ethnic groups considering age, sex, and education using mortality rate ratios (MRR) and proportionate mortality ratios (PMR). We also examined COVID-19 mortality by ethnicity and nativity combined, considering age and education, with PMR.

Methods

Study setting and population

Data on causes of death, race/ethnicity, sex, age, educational attainment, country of birth, and county of residence were obtained using the California Comprehensive Death Files (CCDF) and California Comprehensive Master Death File (CCMDF) from the California Department of Public Health, Center for Health Statistics and Informatics for 2016 to 2020 (CCMDF for 2016–2018 and CCDF for 2019–2020). Data for 2020 were updated weekly and last date of data export used in this analysis was September 9, 2020. Race/ethnicity were grouped into non-Hispanic White, non-Hispanic Black, Asian/Pacific Islander (regardless of Hispanicity; Asian/PI), American Indian/Alaskan Native (regardless of Hispanicity; AI/AN), Hispanic (excludes A/PI, AI/AN), and Multiracial/Other/Unknown. County of birth was used to define decedents’ nativity status, categorized as U.S.-born or foreign-born. Categories of ethnicity and nativity combined were U.S.-born non-Hispanic, U.S.-born Hispanic, Foreign-born non-Hispanic, and Foreign-born Hispanic, using Hispanicity as defined for race/ethnicity. This study was approved by the Committee for the Protection of Human Subjects of the state of CA.

COVID-19-related deaths

Mortality data included the 10th revision of the International Statistical Classification of Diseases and Related Health Problems (ICD-10) codes for underlying cause of death and up to 20 relevant conditions. Effective April 1, 2020, there was a new ICD-10 code for COVID-19, U07.1; however, because we used the dynamic CCDF file with weekly updates for recent mortality, final coded data on underlying cause of death and relevant conditions were not available for all 2020 deaths. Thus, we developed an algorithm using the code U07.1 and a keyword search to identify COVID-19-related deaths and applied it to all deaths occurring after February 1, 2020 (eFig. 1 ). Among deaths with coded data on underlying cause of death and relevant conditions, our algorithm correctly identified 99.95% of deaths coded with U07.1. Analyses were restricted to COVID-19-related deaths occurring February 1-July 31, 2020.

Fig. 1.

Fig 1

Age-standardized COVID-19 mortality rates for all ages and select ages by race/ethnicity. Mortality rates are per 100,000 person-years. Bars represent 95% confidence intervals.

Statistical analysis

Temporal trends in COVID-19 mortality in CA during the study period are presented. Descriptive statistics among decedents identified as having COVID-19 mortality were presented for the entire study period as well as for subperiods with distinct patterns in mortality (i.e., distinct “epidemic periods”).

COVID-19 age-adjusted mortality rates (MR) per 100,000 person-years were calculated using direct standardization to the 2019 CA population using 5-year age intervals and were compared across racial/ethnic groups using mortality rate ratios (MRR) by sex and epidemic period, accounting for variation in observation time. Non-Hispanic White was used as the referent group. Population estimates were obtained from the CDC WONDER Online Database using the Bridged-Race Population Estimates for CA [22] and racial/ethnic groups were combined to align with the categories described above (does not include “Multiracial/Other/Unknown” group). Age-adjusted MR were also calculated and compared across racial/ethnic groups using MRR for selected counties with greater than 500 COVID-19 deaths using 2019 county-specific population estimates for both population and direct standardization. COVID-19 age-specific MR were calculated and compared across racial/ethnic groups using MRR by age groups (excluding 0–19 years category, which had only 5 deaths) and sex.

Analyses using proportionate mortality (PM) were restricted to deaths among decedents aged 20 years and older and occurring March 1-July 31 (only 2 COVID-19 deaths occurred before March 1, 2020). PM was defined as number of COVID-19 deaths in a specified subpopulation (e.g., a certain racial/ethnic group) divided by average all-cause mortality in the same subpopulation occurring March 1-July 31 in 2016–2019 among decedents aged 20 years and older (multiplied by 100 to be akin to a percentage). The PM metric allows for COVID-19 mortality to be interpreted as a percentage of “typical” mortality in a group. Mortality for past years was restricted to match the time frame for 2020 COVID-19 deaths to account for annual trends in mortality. All-cause mortality in 2020 was not used as the reference, which would have been common for PM. This is because evidence suggests all-cause mortality has been affected by the pandemic not only through COVID-19 mortality [23]. PM ratios (PMR) were used to compare across decedent characteristics, including racial/ethnic group, sex, educational attainment, and ethnicity and nativity combined, as well as combinations of these. Educational attainment may serve as a proxy for socioeconomic status which is linked with healthcare access, co-morbidities, and other factors such as employment type that may impact COVID-19 infection and mortality [24], [25], [26], [27]. Because the PMR metric relies on all-cause mortality, we additionally examined differences in all-cause mortality rates for 2019 by age among racial/ethnic groups using 2019 death data and population estimates.

All analyses were performed using SAS statistical software version 9.4 (SAS Institute Inc., Cary, NC) and statistical tests were based on 2-sided tests with α = 0.05. Standard errors and 95% confidence intervals (95%CI) were computed using standard methods (see eMethods) [28].

Results

We identified 10,200 COVID-19 deaths occurring in CA between February 1 and July 31, 2020. Distinct temporal patterns in weekly mortality identified three periods in the COVID-19 epidemic in CA (eFig. 2 ): the first period, through April 19, had an upward trend; the second period, April 20–June 16, demonstrated a steady slight decline; the third period, June 17-July 31, had an upward trend similar to the first period. Distribution of characteristics among decedents with COVID-19 mortality are shown for the entire study period (Table 1 ) and by the three epidemic periods (eTable 1). Decedents were consistently older, more likely to be male, had lower educational attainment, and most were foreign-born. Hispanic was the predominant race/ethnicity among decedents, which increased proportionately during the epidemic.

Fig. 2.

Fig 2

Age-standardized COVID-19 mortality rate ratios for all ages and select ages by race/ethnicity. Bars represent 95% confidence intervals. Referent group is non-Hispanic Whites.

Table 1.

Distribution of selected characteristics among decedents identified as having COVID-19 mortality, California, February 1–July 31, 2020

N (%)
Deaths 10,200
Age
0–19 5 (0.1)
20–44 421 (4.1)
45–54 710 (7.0)
55–64 1467 (14.4)
65–74 2222 (21.8)
75–84 2450 (24.0)
85 or older 2925 (28.7)
Sex
Male 5914 (58.0)
Female 4286 (42.0)
Race/ethnicity
Hispanic (excludes A/PI, AI/AN) 4914 (48.2)
Mexican 3333 (67.8)
Other Hispanic 1581 (32.2)
NH White 3025 (29.7)
Asian/Pacific Islander 1290 (12.7)
Filipino 441 (34.2)
Chinese 251 (19.5)
Korean 207 (16.1)
Vietnamese 97 (7.5)
Japanese 82 (6.4)
Other Asian 212 (16.4)
Black 804 (7.9)
Multiracial/other/unknown 124 (1.2)
American Indian/Alaskan Native 43 (0.4)
Educational Attainment
Less than high school 3637 (35.7)
High school 3027 (29.7)
Some college 1040 (10.2)
Associate degree 478 (4.7)
Bachelor's degree 966 (9.5)
Graduate degree 499 (4.9)
Unknown 553 (5.4)
Country of birth
United States 4413 (43.3)
Mexico 2942 (28.8)
Philippines 442 (4.3)
El Salvador 364 (3.6)
Guatemala 219 (2.2)
South Korea 195 (1.9)
Other country 1302 (12.8)
Unknown 323 (3.2)

Mortality rate ratios

Morality rates were considerably higher among older individuals, but with differences observed across racial/ethnic groups (Fig. 1). Compared with the White group, MRR were elevated among Asian/PI, Black, and Hispanic groups, with Black and Hispanic groups having the highest MRR at 2.75 (95%CI: 2.54–2.97) and 4.18 (95%CI: 3.99–4.37), respectively (Fig. 2 and eFig. 3 ; eTable 2 ). This pattern persisted within each epidemic period (eFig. 3). Analyses by county of residence for counties with greater than 500 COVID-19 deaths (Los Angeles, Orange, Riverside, San Bernardino, and San Diego Counties) showed that while there were some differences in specific MRRs estimated by racial/ethnic group, the overall pattern of COVID-19 mortality disparity persisted (eFig. 4).

Fig. 3.

Fig 3

Proportionate mortality ratios for COVID-19 by race/ethnicity, age, and educational attainment. Proportionate mortality ratios are based on COVID-19 deaths occurring between March 1-July 31, 2020 among decedents aged 20 years and older. Subpopulation proportionate mortalities were calculated using all-cause mortality in the same subpopulation occurring March 1–July 31 in 2016–2019 among decedents aged 20 years and older. Bars represent 95% confidence intervals. Referent group for PMR is non-Hispanic White.

Table 2.

Proportionate mortality (PM) and proportionate mortality ratio (PMR) by ethnicity and nativity combined, age, and educational attainment for COVID-19 deaths among decedents aged 20 years and older, California, March 1–July 31, 2020

High school or less Some college or more
Ethnicity and nativity combined Age COVID-19 Deaths PM (95% CI)a PMR (95% CI) COVID-19 Deaths PM (95% CI)a PMR (95% CI)
U.S.-born non-Hispanic 20 to 64 295 3.6 (3.2–4.0) Referent 223 3.1 (2.7–3.5) Referent
65 to 74 309 5.7 (5.1–6.3) Referent 315 4.3 (3.8–4.8) Referent
75 to 84 441 6.1 (5.6–6.7) Referent 468 5.4 (4.9–5.9) Referent
85<= 602 4.9 (4.6–5.3) Referent 532 4.4 (4.0–4.8) Referent
U.S.-born Hispanic 20 to 64 272 10.1 (9.0–11.4) 2.81 (2.40–3.29) 130 10.4 (8.8–12.4) 3.40 (2.76–4.18)
65 to 74 170 18.1 (15.6–21.1) 3.20 (2.69–3.80) 67 13.0 (10.2–16.5) 3.06 (2.39–3.92)
75 to 84 166 14.0 (12.0–16.3) 2.29 (1.94–2.71) 40 9.2 (6.8–12.6) 1.71 (1.26–2.33)
85<= 236 12.1 (10.7–13.8) 2.46 (2.13–2.84) 33 8.6 (6.1–12.1) 1.96 (1.40–2.74)
Foreign-born non-Hispanic 20 to 64 84 6.7 (5.4–8.4) 1.87 (1.48–2.37) 138 7.9 (6.7–9.3) 2.57 (2.09–3.16)
65 to 74 109 9.3 (7.7–11.2) 1.63 (1.32–2.01) 180 11.5 (10.0–13.4) 2.71 (2.27–3.23)
75 to 84 224 10.0 (8.8–11.4) 1.63 (1.40–1.90) 207 9.5 (8.3–10.9) 1.77 (1.51–2.07)
85<= 506 12.1 (11.1–13.2) 2.46 (2.20–2.75) 265 10.1 (8.9–11.4) 2.30 (1.99–2.64)
Foreign-born Hispanic 20 to 64 1177 38.7 (36.6–41.0) 10.73 (9.51–12.11) 161 25.6 (21.9–29.9) 8.35 (6.93–10.05)
65 to 74 792 45.2 (42.1–48.4) 7.96 (7.06–8.98) 94 31.5 (25.7–38.5) 7.39 (6.06–9.02)
75 to 84 691 32.4 (30.1–35.0) 5.31 (4.76–5.92) 59 19.2 (14.9–24.7) 3.55 (2.78–4.54)
85<= 547 23.7 (21.8–25.8) 4.80 (4.31–5.34) 50 15.2 (11.5–20.0) 3.46 (2.64–4.52)
a

Subpopulation PM were calculated using all-cause mortality in the same subpopulation occurring March 1–July 31 in 2016–2019 among decedents aged 20 years and older.

Age-specific MRR revealed greater differences among racial/ethnic groups, with greater disproportionate mortality among younger Black and Hispanic individuals (Fig. 2; eTable 3). Compared with White individuals aged 20–54 years, the MR was 4.7-fold (95%CI: 3.5–6.3) higher among Black individuals and 8.5-fold (95%CI: 6.9–10.4) higher among Hispanic individuals of the same age. When examined by sex, disparities observed among decedents aged less than 84 years were higher among females in the Black group and among males in the Hispanic group. In the Asian/PI group, mortality disparity was greatest among those aged 85 year or more, with the largest MRR observed for females, 1.70 (95%CI: 1.50–1.93).

Proportionate mortality

Univariate analyses using PMR found elevated PM in males compared with females, in all non-White racial/ethnic groups, in decedents with lower educational attainment, and in all ethnicity/nativity groups relative to U.S.-born non-Hispanic (eTable 4).

Analyses comparing across racial/ethnic groups by age demonstrated greater disparities among younger decedents, similar to those observed with MRR (eTable 5). Elevated PMR persisted in analyses stratified by education (Fig. 3; eTable 6). For example, among decedents aged 20–64 years with high school education or less, the PM in the Hispanic group was 8.5-fold (95%CI: 7.4–9.9) higher compared with the White group. For the same age group, but among those with some college or more, the PMR for Hispanics remained highly elevated at 7.0 (95%CI: 5.8–8.6). All-cause mortality rates for 2019 were lower compared with the White group for all racial/ethnic group, except the Black group which were higher. This may lead PMR to over or underestimate true COVID-19 mortality disparities which should be considered when interpreting these results These differences, however, were not sufficiently large to explain away all disparities observed (eFig. 5). Adjusting PMR for differences in all-cause mortality produces estimates similar to MRR reported above (eTable 7).

When examining ethnicity and nativity combined by age, elevated PMR were observed for all groups, especially for the foreign-born Hispanic group, relative to the U.S.-born non-Hispanic group (eTable 8). PMR were generally larger among younger age groups. After accounting for educational attainment by stratification, elevated PMR remained (Table 2). Among decedents aged 20–64 years, PMR for foreign-born Hispanic compared with U.S.-born non-Hispanic among those with a high school education or less was PMR = 10.7 (95%CI: 9.5–12.1), while among those with some college or more was PMR = 8.4 (95%CI: 6.9–10.1).

Discussion

This study used death certificate data to identify decedents with COVID-19 mortality in CA and to investigate demographic characteristics associated with mortality using two different metrics of association, MRR and PMR. Disproportionate COVID-19 mortality was observed among Black, Hispanic, and Asian/PI groups in CA. Larger relative disparities were observed at younger ages for Black and Hispanic individuals. Disparities persisted after accounting for educational attainment, serving here as a proxy for socioeconomic status. Disproportionate mortality was also observed by combinations of ethnicity and nativity, with all groups (especially foreign-born Hispanic individuals) having greater COVID-19 mortality compared with U.S.-born non-Hispanic individuals, particularly at younger ages. Disparities by nativity remained in analyses controlling for educational attainment. The larger disparities in younger age groups are particularly important given younger populations may be overlooked in public health campaigns due to their overall lower risk of severe disease. Here, however, we observed the mortality rate for Black individuals aged 55–64 to be higher than mortality rate for White individuals 10 years older, and the mortality rate for Hispanic individuals aged 55–64 years to be approaching mortality rate for White individuals 20 years older. The much larger disparities observed in MRR for Hispanic individuals compared with Black individuals, for all ages but particularly for younger ages, are likely driven in part by the high COVID-19 mortality observed for foreign-born Hispanic individuals. Younger populations should be included among targets in public health interventions. Disparities in COVID-19 mortality may be driven by a variety of factors, including complex interaction between social and structural determinates of health, barriers to accessing care, higher prevalence of underlying co-morbidities associated with more severe COVID-19 disease and adverse outcomes, and differential exposure to virus due to working and living conditions [24,[29], [30], [31], [32], [33], [34]]—which maybe different and interact differently among the different groups (race/ethnicity and ethnicity/nativity) and subgroups (age-race/ethnicity and age-ethnicity/nativity groups) examined here.

Differences in COVID-19 mortality can develop anywhere along the disease continuum from exposure, to incidence, severity, and then ultimately death. The mechanisms and magnitude of these difference are likely different for different groups (e.g., younger Black group, older Asian/PI, etc.) at different points along the pathway. Several studies have reported differential COVID-19 impacts across racial/ethnic groups including for incidence [1,35], severity [[4], [5], [6],[8], [9], [10]], death [12,13,27], however few studies have examined outcomes by nativity [36]. Ecologic studies have reported COVID-19 incidence rates to be positively associated with higher population percentage Black [14,26,37], Hispanic/Latino [15,26,34,37], or foreign-born [26,37]. In a Massachusetts study the association for Latino population percentage was attenuated after accounting for percent foreign-born noncitizens living in a community, mean household size, and share of food service workers (all which were also positively associated with incidence) [37]. In contrast, the association for Black population percentage was not attenuated [37]. In a study across 22 states, a disproportionate number of incident COVID-19 cases relative to population demographics was reported for Hispanic, Black, AI/AN, Asian, and Native Hawaiian/Pacific Islander individuals in counties considered hotspots for COVID-19 incidence [1]. Healthcare system-based studies have reported greater severe acute respiratory syndrome coronavirus 2 testing and test positivity rate for non-English speakers compared with English-speakers [36] and higher odds of infection for non-Hispanic Black and Hispanic individuals adjusting for demographic and socioeconomic characteristics [35]. Higher hospitalization has been reported for Black and Hispanic patients, even after adjusting for co-morbidities and demographic and socioeconomic factors [4,6,8]. Among patients hospitalized with COVID-19 infection, non-White patients were more likely to present with higher disease severity, which was associated with worse outcomes [10].

These disproportionate effects in disease incidence and severity contribute to COVID-19 mortality disparities, which have been reported based on aggregate data or healthcare system-based studies for Black and Hispanic individuals. A study using aggregate data on COVID-19 from regions across the U.S. report disproportionately higher COVID-19 mortality relative to population size for Black individuals and higher estimated case-fatality [12]. Among rural counties, average daily increase in COVID-19 mortality rates were significantly higher in counties with the largest shares of Black and Hispanic residents [13]. A study using electronic medical record data from 24 healthcare organization reported Black individuals having a greater odds of COVID-19 mortality, even after controlling for age, sex, and several co-morbidities [27]. Differences between Black and White individuals were larger in those less than 50 years of age, similar to larger MRR and PMR observed in younger age groups in the present study. Not all studies examining race/ethnicity have observed difference in COVID-19 mortality. A large study using data from 92 U.S. hospitals found that after adjusting for a variety of factors including comorbidities, insurance, and neighborhood deprivation there was no difference in mortality between Black and White patients with COVID-19 [7]. Similarly, a study in Louisiana found that after adjusting for sociodemographic and clinical factors, in-hospital mortality was not different between Black and White patients [4]. It may be that once COVID-19 patients are ill to the point of hospitalization, differences in mortality are less appreciable. Overall, this evidence taken together supports the notion that mortality differences across racial/ethnic groups and by ethnicity/nativity reported in the present study are likely the cumulative effects across the entire pathway of disease.

Quantification of COVID-19 mortality disparities is needed so effective public health interventions can be developed to mitigate disproportionate burden of the pandemic on vulnerable populations [38]. Factors that may contribute to mortality disparities and could be targets for interventions include barriers to healthcare access including medical mistrust and insurance, living and working conditions, being essential/frontline workers, underlying health conditions including suboptimal disease management, and social and structural determinants of health [24,[29], [30], [31], [32], [33],39]. Interactions between structural, social, and individual factors that contribute to differential COVID-19 mortality are complex and vary not only across these different historically marginalized groups (e.g., Black, Hispanic, Asian/PI, foreign-born Hispanic), but also within these groups (e.g., younger and older Hispanic individuals). Public health interventions and policies should consider the differing and complex risk structure across and within these groups. For example, differential workplace exposure may contribute to increased mortality among younger Black and Hispanic, including foreign-born Hispanic, individuals. People of color are more likely to be employed in essential industries and in occupations with more exposure to infections and close proximity to others [30]. Black workers in particular face an elevated risk for these factors [30]. A study of workplace COVID-19 outbreaks in Utah found 73% of cases were in Hispanic or non-White workers, whereas Hispanic and non-White workers represent only 24% of the workforce in affected industries [33]. Immigrant families faced additional complicating factors (e.g., employment in jobs with higher potential exposure, no/inadequate health insurance and paid leave, multigenerational housing, etc. [40,41]) which must be considered for public health planning. For example public charge regulations may have disincentivized immigrant families from accessing healthcare if they become symptomatic [40,41]. This delays testing and treatment and may increase disease transmission risk within their home and communities [40,41].

This study has limitations. First, while use of death certificate data has many advantages, there were a limited number of available demographic and socioeconomic variables. Augmentation of these data with neighborhood characteristics based on decedent residential address is an area of future work. Second, the variable related to socioeconomic position used in this analysis—educational attainment—is only one dimension of person's socioeconomic status and does not fully capture this complex determinant of health. Further, there may be misreporting of educational attainment on death certificates, with prior studies finding higher underreporting of educational attainment for Black and Hispanic decedents compared with White decedents [42]. This is also likely for foreign-born individuals. Any differential misreporting, however, would be expected to lead to less misclassification among Black and Hispanic (and possibly also foreign-born) decedents categorized as “Some college or more” yet large mortality disparities persisted in stratified analyses. Third, PM, and thus PMR, uses as a comparison all-cause mortality, which if different between groups may over or underestimate differences in mortality between groups. When all-cause mortality rates are lower compared with the referent group, PMR will overestimate differences in COVID-19 mortality, but as discussed differences in all-cause mortality rates were not sufficient to explain all observed COVID-19 disparities. When all-cause mortality rates are higher, such as was observed for Black individuals, the PMR will underestimate differences COVID-19 mortality. This study has several strengths. First, to identify COVID-19 mortality we used death certificate data which captures all mortality in the state and does not restrict to individuals in a healthcare/insurance network. Second, we had information on individual-level demographic characteristics on decedents, which was advantageous in two regards: (i) there was substantial under-reporting of race/ethnicity for COVID-19 decedents early in the pandemic and there is still a lack of reporting by nativity, which precludes analyses by these factors, and (ii) we did not have to rely on aggregate demographic data which could be subject to the ecologic fallacy. Third, because of this individual-level data we were able to examine mortality by several demographic factors in combination to better understand intersectional impacts of COVID-19.

Conclusions

Differential COVID-19 mortality was observed in California across racial/ethnic groups and by ethnicity and nativity combined, with evidence of greater disparities among younger age groups. Patterns of disparities persisted after accounting for educational attainment. Drivers of these disparate COVID-19 impacts are likely multifactorial and involve the interplay of structural, social, and individual factors that must be considered in the design and implementation for public health interventions to effectively mitigate the impacts of this disease.

Acknowledgments

This research was supported by the National Institute of Environmental Health Sciences (P30ES007048), the Hastings Foundation, and by the Keck School of Medicine of USC COVID-19 Research Fund through a generous gift from the W. M. Keck Foundation.

Footnotes

Disclosures: Dr. Garcia reports grants from Keck School of Medicine of USC COVID-19 Research Fund, grants from National Institute of Environmental Health Sciences, during the conduct of the study. Dr. Gilliland has nothing to disclose. Dr. Li has nothing to disclose. Dr. Eckel reports grants from Keck School of Medicine of USC COVID-19 Research Fund, during the conduct of the study; grants from NIH, outside the submitted work. Dr. Chen has nothing to disclose.

Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.annepidem.2021.03.006.

Appendix. Supplementary materials

mmc1.pdf (642.1KB, pdf)

References

  • 1.Moore J.T., Ricaldi J.N., Rose C.E., Fuld J., Parise M., Kang G.J., et al. Disparities in incidence of COVID-19 among underrepresented racial/ethnic groups in counties identified as hotspots during June 5-18, 2020 - 22 States, February-June 2020. MMWR Morb Mortal Wkly Rep. 2020;69(33):1122–1126. doi: 10.15585/mmwr.mm6933e1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Rozenfeld Y., Beam J., Maier H., Haggerson W., Boudreau K., Carlson J., et al. A model of disparities: risk factors associated with COVID-19 infection. Int J Equity Health. 2020;19(1):126. doi: 10.1186/s12939-020-01242-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Adhikari S., Pantaleo N.P., Feldman J.M., Ogedegbe O., Thorpe L., Troxel A.B. Assessment of community-level disparities in coronavirus disease 2019 (COVID-19) infections and deaths in large US metropolitan areas. JAMA Network Open. 2020;3(7) doi: 10.1001/jamanetworkopen.2020.16938. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Price-Haywood E.G., Burton J., Fort D., Seoane L. Hospitalization and mortality among Black patients and White patients with Covid-19. N Engl J Med. 2020;382(26):2534–2543. doi: 10.1056/NEJMsa2011686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Poulson M., Geary A., Annesi C., Allee L., Kenzik K., Sanchez S., et al. National disparities in COVID-19 outcomes between Black and White Americans. J Natl Med Assoc. 2020 doi: 10.1016/j.jnma.2020.07.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Azar K.M.J., Shen Z., Romanelli R.J., Lockhart S.H., Smits K., Robinson S., et al. Disparities in outcomes among COVID-19 patients in a large health care system in California. Health Aff (Millwood) 2020;39(7):1253–1262. doi: 10.1377/hlthaff.2020.00598. [DOI] [PubMed] [Google Scholar]
  • 7.Yehia B.R., Winegar A., Fogel R., Fakih M., Ottenbacher A., Jesser C., et al. Association of race with mortality among patients hospitalized with coronavirus disease 2019 (COVID-19) at 92 US hospitals. JAMA Network Open. 2020;3(8) doi: 10.1001/jamanetworkopen.2020.18039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Karaca-Mandic P., Georgiou A., Sen S. Assessment of COVID-19 hospitalizations by race/ethnicity in 12 states. JAMA Intern Med. 2021;181(1):131–134. doi: 10.1001/jamainternmed.2020.3857. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Ebinger J.E., Achamallah N., Ji H., Claggett B.L., Sun N., Botting P., et al. Pre-existing traits associated with Covid-19 illness severity. PLoS ONE. 2020;15(7) doi: 10.1371/journal.pone.0236240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Joseph N.P., Reid N.J., Som A., Li M.D., Hyle E.P., Dugdale C.M., et al. Racial and ethnic disparities in disease severity on admission chest radiographs among patients admitted with confirmed coronavirus disease 2019: a retrospective cohort study. Radiology. 2020;297(3):E303–E312. doi: 10.1148/radiol.2020202602. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Mahajan U.V., Larkins-Pettigrew M. Racial demographics and COVID-19 confirmed cases and deaths: a correlational analysis of 2886 US counties. J Public Health (Oxford, England) 2020;42(3):445–447. doi: 10.1093/pubmed/fdaa070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Holmes L., Jr, Enwere M., Williams J., Ogundele B., Chavan P., Piccoli T., et al. Black-White risk differentials in COVID-19 (SARS-COV2) transmission, mortality and case fatality in the United States: translational epidemiologic perspective and challenges. Int J Environ Res Public Health. 2020;17(12):4322. doi: 10.3390/ijerph17124322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Cheng K.J.G., Sun Y., Monnat S.M. COVID-19 death rates are higher in rural counties with larger shares of Blacks and Hispanics. J Rural Health: official journal of the American Rural Health Association and the National Rural Health Care Association. 2020;36(4):602–608. doi: 10.1111/jrh.12511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Millett G.A., Jones A.T., Benkeser D., Baral S., Mercer L., Beyrer C., et al. Assessing differential impacts of COVID-19 on black communities. Ann Epidemiol. 2020;47:37–44. doi: 10.1016/j.annepidem.2020.05.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Rodriguez-Diaz C.E., Guilamo-Ramos V., Mena L., Hall E., Honermann B., Crowley J.S., et al. Risk for COVID-19 infection and death among Latinos in the United States: examining heterogeneity in transmission dynamics. Ann Epidemiol. 2020;52:46-53 e42. doi: 10.1016/j.annepidem.2020.07.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Alobuia W.M., Dalva-Baird N.P., Forrester J.D., Bendavid E., Bhattacharya J., Kebebew E. Racial disparities in knowledge, attitudes and practices related to COVID-19 in the USA. J Public Health (Oxford, England) 2020;42(3):470–478. doi: 10.1093/pubmed/fdaa069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Holtgrave D.R., Barranco M.A., Tesoriero J.M., Blog D.S., Rosenberg E.S. Assessing racial and ethnic disparities using a COVID-19 outcomes continuum for New York State. Ann Epidemiol. 2020;48:9–14. doi: 10.1016/j.annepidem.2020.06.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Hankivsky O., Kapilashrami A. Global Policy Institute, Queen Mary University of London; London, UK: 2020. Beyond sex and gender analysis: an intersectional view of the COVID-19 pandemic outbreak and response. [Google Scholar]
  • 19.Crenshaw K. Mapping the margins: Intersectionality, identity politics, and violence against women of color. Stan L Rev. 1990;43:1241. [Google Scholar]
  • 20.Collins P.H. Intersectionality's definitional dilemmas. Annu Rev Sociol. 2015;41:1–20. [Google Scholar]
  • 21.Dong E., Du H., Gardner L. An interactive web-based dashboard to track COVID-19 in real time. Lancet Infect Dis. 2020;20(5):533–534. doi: 10.1016/S1473-3099(20)30120-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.United States Department of Health and Human Services (US DHHS), Centers for Disease Control and Prevention (CDC), National Center for Health Statistics (NCHS), Bridged-Race Population Estimates, United States July 1st resident population by state, county, age, sex, bridged-race, and Hispanic origin. Compiled from 1990-1999 bridged-race intercensal population estimates (released by NCHS on 7/26/2004); revised bridged-race 2000-2009 intercensal population estimates (released by NCHS on 10/26/2012); and bridged-race Vintage 2019 (2010-2019) postcensal population estimates (released by NCHS on 7/9/2020). CDC WONDER Online Database. http://wonder.cdc.gov/bridged-race-v2019.html. Accessed Sep 2, 2020.
  • 23.Weinberger D.M., Chen J., Cohen T., Crawford F.W., Mostashari F., Olson D., et al. Estimation of excess deaths associated with the COVID-19 pandemic in the United States, March to May 2020. JAMA Intern Med. 2020;180(10):1336–1344. doi: 10.1001/jamainternmed.2020.3391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Dorn A.V., Cooney R.E., Sabin M.L. COVID-19 exacerbating inequalities in the US. Lancet. 2020;395(10232):1243–1244. doi: 10.1016/S0140-6736(20)30893-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Abedi V., Olulana O., Avula V., Chaudhary D., Khan A., Shahjouei S., et al. Racial, economic, and health inequality and COVID-19 infection in the United States. J Racial Ethn Health Disparities. 2020:1–11. doi: 10.1007/s40615-020-00833-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Maroko A.R., Nash D., Pavilonis B.T. COVID-19 and inequity: a comparative spatial analysis of New York city and chicago hot spots. J Urban Health: Bull New York Acad Med. 2020;97(4):461–470. doi: 10.1007/s11524-020-00468-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Harrison S.L., Fazio-Eynullayeva E., Lane D.A., Underhill P., Lip G.Y.H. Comorbidities associated with mortality in 31,461 adults with COVID-19 in the United States: A federated electronic medical record analysis. PLoS Med. 2020;17(9) doi: 10.1371/journal.pmed.1003321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Greenland S., Rothman K.J. In: Modern Epidemiology. 3rd ed. Rothman KJ, Greenland S, Lash TL, editors. Lippincott Williams & Wilkins (LWW); Philadelphia, PA: 2008. Ch. 14: Introduction to Categorical Statistics; pp. 238–257. [Google Scholar]
  • 29.Chamie G., Marquez C., Crawford E., Peng J., Petersen M., Schwab D., et al. SARS-CoV-2 community transmission disproportionately affects Latinx population during Shelter-in-Place in San Francisco. Clin Infect Dis. 2020 doi: 10.1093/cid/ciaa1234. Epub ahead of print. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Hawkins D. Differential occupational risk for COVID-19 and other infection exposure according to race and ethnicity. Am J Ind Med. 2020;63(9):817–820. doi: 10.1002/ajim.23145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Tai D.B.G., Shah A., Doubeni C.A., Sia I.G., Wieland M.L. The Disproportionate Impact of COVID-19 on Racial and Ethnic Minorities in the United States. Clin Infect Dis. 2021;72(4):703–706. doi: 10.1093/cid/ciaa815. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Evans M.K. Covid's Color Line - Infectious Disease, Inequity, and Racial Justice. N Engl J Med. 2020;383(5):408–410. doi: 10.1056/NEJMp2019445. [DOI] [PubMed] [Google Scholar]
  • 33.Bui D.P., McCaffrey K., Friedrichs M., LaCross N., Lewis N.M., Sage K., et al. Racial and Ethnic Disparities Among COVID-19 Cases in Workplace Outbreaks by Industry Sector - Utah, March 6-June 5, 2020. MMWR Morb Mortal Wkly Rep. 2020;69(33):1133–1138. doi: 10.15585/mmwr.mm6933e3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Vijayan T., Shin M., Adamson P.C., Harris C., Seeman T., Norris K.C., et al. Beyond the 405 and the 5: geographic variations and factors associated with SARS-CoV-2 positivity rates in Los Angeles County. Clin Infect Dis. 2020 doi: 10.1093/cid/ciaa1692. Epub ahead of print. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Vahidy F.S., Nicolas J.C., Meeks J.R., Khan O., Pan A., Jones S.L., et al. Racial and ethnic disparities in SARS-CoV-2 pandemic: analysis of a COVID-19 observational registry for a diverse US metropolitan population. BMJ Open. 2020;10(8) doi: 10.1136/bmjopen-2020-039849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Kim H.N., Lan K.F., Nkyekyer E., Neme S., Pierre-Louis M., Chew L., et al. Assessment of disparities in COVID-19 testing and infection across language groups in seattle, Washington. JAMA Network Open. 2020;3(9) doi: 10.1001/jamanetworkopen.2020.21213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Figueroa J.F., Wadhera R.K., Lee D., Yeh R.W., Sommers B.D. Community-level factors associated with racial and ethnic disparities in COVID-19 rates in Massachusetts. Health Aff (Millwood) 2020;39(11):1984–1992. doi: 10.1377/hlthaff.2020.01040. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Webb Hooper M., Napoles A.M., Perez-Stable E.J. COVID-19 and racial/ethnic disparities. JAMA. 2020;323(24):2466–2467. doi: 10.1001/jama.2020.8598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Kopel J., Perisetti A., Roghani A., Aziz M., Gajendran M., Goyal H. Racial and gender-based differences in COVID-19. Front Public Health. 2020;8:418. doi: 10.3389/fpubh.2020.00418. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Cholera R., Falusi O.O., Linton J.M. Sheltering in place in a xenophobic climate: COVID-19 and children in immigrant families. Pediatrics. 2020;146(1) doi: 10.1542/peds.2020-1094. [DOI] [PubMed] [Google Scholar]
  • 41.Wilson F.A., Stimpson J.P. US policies increase vulnerability of immigrant communities to the COVID-19 pandemic. Ann Glob Health. 2020;86(1):57. doi: 10.5334/aogh.2897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Rostron B.L., Boies J.L., Arias E. Education reporting and classification on death certificates in the United States. Vital and health statistics Series 2. Data Eval Methods Res. 2010;(151):1–21. [PubMed] [Google Scholar]

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