BACKGROUND: Equity in vaccination coverage is a cornerstone for a successful public health response to COVID-19. To deepen understanding of the extent to which vaccination coverage compares with initial strategies for equitable vaccination, we explore primary vaccine series and booster rollout over time and by race/ethnicity, social vulnerability, and geography. METHODS AND FINDINGS: We analyzed data from the Missouri Department of Health and Senior Services on all COVID-19 vaccinations administered across 7 counties in the St. Louis region and 4 counties in the Kansas City region. We compared rates of receiving the primary COVID-19 vaccine series and boosters relative to time, race/ethnicity, zip-code-level Social Vulnerability Index (SVI), vaccine location type, and COVID-19 disease burden. We adapted a well-established tool for measuring inequity-the Lorenz curve-to quantify inequities in COVID-19 vaccination relative to these key metrics. Between 15 December 2020 and 15 February 2022, 1,763,036 individuals completed the primary series and 872,324 received a booster. During early phases of the primary series rollout, Black and Hispanic individuals from high SVI zip codes were vaccinated at less than half the rate of White individuals from low SVI zip codes, but rates increased over time until they were higher than rates in White individuals after June 2021; Asian individuals maintained high levels of vaccination throughout. Increasing vaccination rates in Black and Hispanic communities corresponded with periods when more vaccinations were offered at small community-based sites such as pharmacies rather than larger health systems and mass vaccination sites. Using Lorenz curves, zip codes in the quartile with the lowest rates of primary series completion accounted for 19.3%, 18.1%, 10.8%, and 8.8% of vaccinations while representing 25% of the total population, cases, deaths, or population-level SVI, respectively. When tracking Gini coefficients, these disparities were greatest earlier during rollout, but improvements were slow and modest and vaccine disparities remained across all metrics even after 1 year. Patterns of disparities for boosters were similar but often of much greater magnitude during rollout in fall 2021. Study limitations include inherent limitations in the vaccine registry dataset such as missing and misclassified race/ethnicity and zip code variables and potential changes in zip code population sizes since census enumeration. CONCLUSIONS: Inequities in the initial COVID-19 vaccination and booster rollout in 2 large US metropolitan areas were apparent across racial/ethnic communities, across levels of social vulnerability, over time, and across types of vaccination administration sites. Disparities in receipt of the primary vaccine series attenuated over time during a period in which sites of vaccination administration diversified, but were recapitulated during booster rollout. These findings highlight how public health strategies from the outset must directly target these deeply embedded structural and systemic determinants of disparities and track equity metrics over time to avoid perpetuating inequities in healthcare access.
BACKGROUND: Equity in vaccination coverage is a cornerstone for a successful public health response to COVID-19. To deepen understanding of the extent to which vaccination coverage compares with initial strategies for equitable vaccination, we explore primary vaccine series and booster rollout over time and by race/ethnicity, social vulnerability, and geography. METHODS AND FINDINGS: We analyzed data from the Missouri Department of Health and Senior Services on all COVID-19 vaccinations administered across 7 counties in the St. Louis region and 4 counties in the Kansas City region. We compared rates of receiving the primary COVID-19 vaccine series and boosters relative to time, race/ethnicity, zip-code-level Social Vulnerability Index (SVI), vaccine location type, and COVID-19 disease burden. We adapted a well-established tool for measuring inequity-the Lorenz curve-to quantify inequities in COVID-19 vaccination relative to these key metrics. Between 15 December 2020 and 15 February 2022, 1,763,036 individuals completed the primary series and 872,324 received a booster. During early phases of the primary series rollout, Black and Hispanic individuals from high SVI zip codes were vaccinated at less than half the rate of White individuals from low SVI zip codes, but rates increased over time until they were higher than rates in White individuals after June 2021; Asian individuals maintained high levels of vaccination throughout. Increasing vaccination rates in Black and Hispanic communities corresponded with periods when more vaccinations were offered at small community-based sites such as pharmacies rather than larger health systems and mass vaccination sites. Using Lorenz curves, zip codes in the quartile with the lowest rates of primary series completion accounted for 19.3%, 18.1%, 10.8%, and 8.8% of vaccinations while representing 25% of the total population, cases, deaths, or population-level SVI, respectively. When tracking Gini coefficients, these disparities were greatest earlier during rollout, but improvements were slow and modest and vaccine disparities remained across all metrics even after 1 year. Patterns of disparities for boosters were similar but often of much greater magnitude during rollout in fall 2021. Study limitations include inherent limitations in the vaccine registry dataset such as missing and misclassified race/ethnicity and zip code variables and potential changes in zip code population sizes since census enumeration. CONCLUSIONS: Inequities in the initial COVID-19 vaccination and booster rollout in 2 large US metropolitan areas were apparent across racial/ethnic communities, across levels of social vulnerability, over time, and across types of vaccination administration sites. Disparities in receipt of the primary vaccine series attenuated over time during a period in which sites of vaccination administration diversified, but were recapitulated during booster rollout. These findings highlight how public health strategies from the outset must directly target these deeply embedded structural and systemic determinants of disparities and track equity metrics over time to avoid perpetuating inequities in healthcare access.
The initial wave of coronavirus disease 2019 (COVID-19) redemonstrated and highlighted historical inequities in health by race and ethnicity and other social indicators of vulnerability [1-3], prompting a range of efforts to design public health services that redress inequity in the COVID-19 response. Across a wide range of indicators, disease burden as measured by COVID-19 cases, hospitalizations, and mortality has disproportionately affected minoritized communities [1-3]. Initial responses to COVID-19 through established channels were thus accompanied by additional efforts to address the evolving disparities. Nevertheless, minoritized and vulnerable communities still had reduced access to testing and treatments and experienced disproportionate impacts of social distancing and lockdown policies on employment, education, and housing [4-8]. Against this backdrop, achieving equitable vaccination has been and continues to be one of the most critical public health challenges for mitigating the impact of the COVID-19 pandemic and achieving long-term control.Closer examination of equity in the vaccine response evaluating the extent to which health systems performed in this domain is still necessary, and something that has not clearly been documented in the literature to date. Whereas equality simply refers to provision of equal resources to every individual regardless of need, equitable approaches acknowledge that individuals will have different risks, needs, or opportunities and that access to or distribution of resources needs to take these differences into account. Strategies and frameworks to guide the equitable allocation and distribution of vaccines were developed when vaccines for SARS-CoV-2 became available in December 2020 [9,10], but empirical examination of how actual primary vaccine series and subsequent booster efforts aligned with the initial goals set out for equity is still needed. For example, several strategies proposed formally considering geography, social vulnerability, or race/ethnicity in plans to prioritize and distribute vaccinations in response to the known inequities in exposure risk and disease burden across these metrics [11-13]. Examinations of equity must thus document patterns of vaccination across race/ethnicity, social vulnerability, and geography and over time, and how vaccinations are delivered, to understand the mechanisms that give rise to disparities and to yield key insights into successes, failures, and steps for redress to achieve equitable vaccination strategies.In this paper, we deepen our understanding of COVID-19 vaccine-related disparities by examining inequities in vaccination in the St. Louis and Kansas City regions in Missouri—regions with a history of health disparities—across several key metrics. We characterize rates of receiving the primary vaccine series and boosters over time and by race/ethnicity, social vulnerability, disease burden, geography, and vaccination location type. We use Lorenz curves and Gini coefficients—tools from economics commonly used to measure inequity in a population—to quantify and track inequities in COVID-19 vaccination over time relative to different metrics for conceptualizing equity [14]. The novel application of this methodology—which we previously used to characterize COVID-19 testing disparities [4]—has potential to yield deeper insights into the progress made towards vaccine equity in these regions, which may then better inform health policy solutions to address remaining gaps.
Methods
Ethics statement
The study was approved by the institutional review board at Washington University in St. Louis (IRB ID# 202009021). The research in this paper was not prespecified and consists of secondary analysis of preexisting de-identified data. This paper was prepared according to STROBE guidelines (S1 STROBE Checklist).
Study setting and data
We sought to assess disparities in COVID-19 vaccination across the 7 counties in the St. Louis region (St. Louis City, St. Louis County, St. Charles, Jefferson, Franklin, Lincoln, and Warren; total population 2,095,978: 19.2% Black, 73.1% White, 3.0% Hispanic, 3.2% Asian) and the 4 counties in the Kansas City region (Jackson, Clay, Cass, and Platte; total population 1,121,224: 16.8% Black, 73.2% White, 8.2% Hispanic, 2.0% Asian). These counties make up the broader metropolitan areas located within Missouri for these 2 cities. Vaccines first became available on 15 December 2020, and all individuals became eligible on 29 March 2021. We used data from the Missouri Department of Health and Senior Services on SARS-CoV-2 vaccines administered in Missouri to individuals 12 years old and up between 15 December 2020 and 15 February 2022. Reporting of vaccinations was mandated, so this database is expected to contain near complete data on all vaccinations administered in Missouri. This individual-level dataset contains vaccination date, type, and dose number; administration site; and patient age, sex, race/ethnicity, and zip code, and was de-duplicated and cleaned by the Missouri Department of Health and Senior Services. We used 2020 census data to obtain age-, sex-, and race-stratified zip code population estimates and 2018 American Community Survey (ACS) data to obtain sociodemographic and socioeconomic characteristics of individual zip codes as well as the Centers for Disease Control and Prevention’s Social Vulnerability Index (SVI). The SVI is a composite metric that captures a community’s vulnerability to external stresses on human health and is calculated from 15 ACS variables measuring demographics, socioeconomic status, household composition, and infrastructure [15].
Analyses
Our analyses seek to characterize patterns of disparities in receiving the primary vaccine series and boosters over time by examining rates of vaccination with respect to race/ethnicity and social vulnerability, changes in the types of locations vaccines were being administered, and the extent to which vaccine administration was equitable between zip codes. We adapted methods that we had previously used to assess disparities related to COVID-19 testing and extended them to COVID-19 vaccination [4].First, we estimated the rates and cumulative incidence of COVID-19 vaccination over time stratifying individuals by race/ethnicity (i.e., Black, White, Hispanic, or Asian) and whether they lived in a zip code with a low, medium, or high SVI (i.e., less than 0.333, 0.333 to 0.666, or greater than or equal to 0.666, respectively). We examined completion rates for the primary vaccine series (defined as 2 doses of either BNT162b2 mRNA [Pfizer] or mRNA-1273 [Moderna] or a single dose of Ad26.COV2.S [Johnson & Johnson]) and boosters (defined as a single dose of any vaccine after completing the primary series).Second, we examined vaccine distribution by the type of site at which individuals received their primary vaccine series and boosters over time and by race/ethnicity and zip-code-level SVI. We categorized vaccine administration sites into health facilities (e.g., clinics, hospitals, and health-system-affiliated sites) that administered a small, medium, or large volume of vaccinations (i.e., less than 1,000, 1,000 to 10,000, or greater than 10,000 unique individuals vaccinated, respectively), public health departments (including mass vaccination sites), pharmacies, employer/school-based sites, and other (e.g., dialysis centers, home health, nursing homes, mental health/psychiatric facilities, and correctional facilities).Third, we generated modified versions of Lorenz curves to assess the relative equity in the distribution of COVID-19 vaccinations across zip codes. Lorenz curves—originally developed by economists to graphically represent income equality—have more recently been leveraged as a tool for public health [14,16,17]. Lorenz curves are generated by plotting the cumulative proportion of the total population against the cumulative proportion of a resource after sorting values in ascending order. The curve follows a straight line at a 45° angle when a resource is equitably distributed across the population and becomes more convex with increasing inequity. In general, equitable vaccination strategies seek to balance the number of vaccines with the overall risk of disease in a community, but the most appropriate metric of equity for so doing will depend on whether one considers the goal to be creating balance between vaccination rates relative to the total population, overall disease burden (i.e., number of COVID-19 cases or deaths), or risk factors (i.e., social vulnerability) in a community. To examine vaccine equity from these different perspectives, we adapted the Lorenz curve method to examine disparities in receiving the primary vaccine series and boosters relative to several relevant metrics: (1) the total population, (2) the number of diagnosed COVID-19 cases, (3) the number of COVID-19 deaths, and (4) population-level social vulnerability, which we defined as the zip-code-level SVI multiplied by zip code population. For each curve, we calculated Gini coefficients—a measure of equality/inequality between 0 and 1, with 0 indicating perfect equality and 1 indicating perfect inequality—and assessed how these changed over time [18]. We also grouped zip codes into quartiles based on their position on Lorenz curves and assessed differences in zip-code-level sociodemographic and socioeconomic characteristics using Kruskal–Wallis tests.Fourth, we generated bubble plots to compare primary vaccine series and booster completion rates for Black, Hispanic, and Asian residents relative to White residents living in the same zip code. For these analyses, we considered only zip codes whose populations had at least 25 individuals from each of the racial/ethnic groups to avoid extreme outliers from small denominators.Lastly, we performed univariate and multivariable mixed-effects Poisson regression to identify individual (e.g., sex, race/ethnicity, age) and zip-code-level (e.g., SVI, racial makeup, health insurance coverage) factors independently associated with receiving the primary vaccine series and boosters; in multivariable models, we excluded zip-code-level variables that would be expected to relate directly to SVI (e.g., poverty and median income). We applied an established method for using Poisson regression with robust variances to estimate risk ratios from binary outcomes [19,20]. We leveraged vaccination and 2020 census data to estimate the number of unvaccinated individuals across strata of age, sex, and race/ethnicity in each zip code. We visually assessed for linearity in the relationship between continuous variables and outcomes and present variables with nonlinear relationships as categorical variables (i.e., age and zip code SVI). The effect of race/ethnicity and racism on health outcomes is mediated by (as opposed to confounded by) ecological structural factors such socioeconomic status; thus, unadjusted analyses assess the overall association with race/ethnicity and racism while adjusted analyses can be thought of as assessing the contribution of systemic racism that still remains after adjusting for the mediating effects of measured ecological factors [21-23].To account for missingness in race/ethnicity and patient zip code variables, we performed multiple imputation using multivariate normal imputation methods (n = 50 imputations) [24-26]. For zip codes, we first transformed them to the latitude and longitude of their centroid, ran the multiple imputation model, and then transformed multiply imputed latitude and longitude values back into zip codes. Missingness was highly dependent on vaccination date and administration site, and thus the missing at random assumption required for unbiased imputation (i.e., that missingness was random conditional on all the variables included in the imputation model [administration site, vaccination date, sex, age, race/ethnicity, zip code latitude and longitude, type of vaccine]) was very plausible in our setting [24-26].All analyses were conducted using Stata/MP 17.0 and R 3.2.4.
Results
Between 15 December 2020 to 15 February 2022, 4,741,806 total COVID-19 vaccines were administered to 2,019,715 unique individuals across the 7 counties in the St. Louis region and the 4 counties in the Kansas City region. Among those receiving at least 1 dose in St. Louis and Kansas City, 1,763,036 (87.3%) completed the primary series, and 872,324 (43.2%) received a booster. Of those who completed the primary series, 81.2% of individuals did so by 15 June 2021 (Tables 1, 2, S1, and S2).
Table 1
Characteristics of individuals completing the primary series.
Characteristic
Overall (n = 1,763,036)
Black (n = 226,520)
White (n = 1,089,138)
Hispanic (n = 60,079)
Asian (n = 47,842)
High SVI (n = 202,822)
Medium SVI (n = 527,677)
Low SVI (n = 1,032,218)
Sex*, n (%)
Male
797,909 (45.3%)
92,565 (40.9%)
503,427 (46.2%)
29,867 (49.7%)
22,418 (46.9%)
86,641 (42.8%)
237,048 (45.0%)
474,051 (46.0%)
Female
963,261 (54.7%)
133,897 (59.1%)
585,515 (53.8%)
30,179 (50.3%)
25,400 (53.1%)
115,946 (57.2%)
289,832 (55.0%)
557,335 (54.0%)
Age category*, n (%)
12–19 years
160,216 (9.1%)
23,041 (10.2%)
93,963 (8.6%)
8,365 (13.9%)
5,227 (10.9%)
18,727 (9.2%)
42,966 (8.1%)
98,503 (9.5%)
20–34 years
331,936 (18.8%)
41,758 (18.4%)
199,525 (18.3%)
16,722 (27.8%)
14,901 (31.1%)
39,559 (19.5%)
105,291 (20.0%)
186,960 (18.1%)
35–44 years
257,408 (14.6%)
32,393 (14.3%)
156,842 (14.4%)
11,324 (18.8%)
9,133 (19.1%)
29,400 (14.5%)
74,321 (14.1%)
153,638 (14.9%)
45–54 years
251,004 (14.2%)
36,568 (16.1%)
151,349 (13.9%)
9,403 (15.6%)
7,800 (16.3%)
29,668 (14.6%)
73,131 (13.9%)
148,161 (14.4%)
55–64 years
304,054 (17.2%)
43,336 (19.1%)
192,128 (17.6%)
7,432 (12.4%)
5,185 (10.8%)
37,112 (18.3%)
93,520 (17.7%)
173,368 (16.8%)
65–74 years
263,353 (14.9%)
31,420 (13.9%)
170,469 (15.7%)
4,342 (7.2%)
3,502 (7.3%)
29,352 (14.5%)
80,562 (15.3%)
153,402 (14.9%)
75+ years
195,065 (11.1%)
18,004 (7.9%)
124,862 (11.5%)
2,486 (4.1%)
2,094 (4.4%)
18,964 (9.4%)
57,886 (11.0%)
118,186 (11.4%)
Race/ethnicity*, n (%)
Black
226,520 (13.3%)
—
—
—
—
99,431 (50.7%)
84,173 (16.6%)
42,860 (4.3%)
White
1,089,138 (64.1%)
—
—
—
—
48,758 (24.8%)
310,296 (61.4%)
729,935 (73.2%)
Hispanic
60,079 (3.5%)
—
—
—
—
13,045 (6.7%)
19,738 (3.9%)
27,288 (2.7%)
Asian
47,842 (2.8%)
—
—
—
—
3,319 (1.7%)
13,333 (2.6%)
31,174 (3.1%)
Other
275,054 (16.2%)
—
—
—
—
31,689 (16.2%)
78,010 (15.4%)
165,302 (16.6%)
Median zip code SVI (IQR)
0.29 (0.16, 0.47)
0.57 (0.41, 0.79)
0.25 (0.15, 0.42)
0.37 (0.20, 0.63)
0.24 (0.15, 0.44)
0.79 (0.75, 0.86)
0.47 (0.41, 0.53)
0.18 (0.13, 0.25)
Vaccine location type, n (%)
Small volume health facility
53,828 (3.1%)
9,477 (4.2%)
31,848 (2.9%)
1,632 (2.7%)
983 (2.1%)
7,638 (3.8%)
16,854 (3.2%)
29,315 (2.8%)
Medium volume health facility
246,975 (14.0%)
28,443 (12.6%)
156,876 (14.4%)
8,632 (14.4%)
5,746 (12.0%)
25,482 (12.6%)
72,552 (13.7%)
148,901 (14.4%)
Large volume health facility
423,980 (24.0%)
51,549 (22.8%)
276,770 (25.4%)
7,798 (13.0%)
10,019 (20.9%)
39,691 (19.6%)
115,636 (21.9%)
268,614 (26.0%)
Pharmacy
655,285 (37.2%)
80,441 (35.5%)
390,072 (35.8%)
28,621 (47.6%)
18,317 (38.3%)
81,837 (40.3%)
205,835 (39.0%)
367,514 (35.6%)
Health department
304,999 (17.3%)
40,798 (18.0%)
192,537 (17.7%)
11,171 (18.6%)
10,606 (22.2%)
36,329 (17.9%)
93,509 (17.7%)
175,068 (17.0%)
Employer/school
39,286 (2.2%)
7,960 (3.5%)
21,035 (1.9%)
981 (1.6%)
1,614 (3.4%)
5,701 (2.8%)
12,397 (2.3%)
21,175 (2.1%)
Other
38,683 (2.2%)
7,852 (3.5%)
20,000 (1.8%)
1,244 (2.1%)
557 (1.2%)
6,144 (3.0%)
10,894 (2.1%)
21,631 (2.1%)
Primary series vaccine type, n (%)
J&J
115,409 (6.5%)
18,363 (8.1%)
71,603 (6.6%)
4,658 (7.8%)
2,271 (4.7%)
16,193 (8.0%)
37,860 (7.2%)
61,316 (5.9%)
Moderna
485,296 (27.5%)
59,402 (26.2%)
286,140 (26.3%)
16,355 (27.2%)
10,988 (23.0%)
59,493 (29.3%)
156,016 (29.6%)
269,695 (26.1%)
Pfizer
1,162,331 (65.9%)
148,755 (65.7%)
731,395 (67.2%)
39,066 (65.0%)
34,583 (72.3%)
127,136 (62.7%)
333,801 (63.3%)
701,207 (67.9%)
Booster received, n (%)
872,324 (49.5%)
84,564 (37.3%)
569,411 (52.3%)
20,094 (33.4%)
23,411 (48.9%)
74,292 (36.6%)
245,129 (46.5%)
552,779 (53.6%)
Time period, n (%)
15 Dec 2020–15 Jun 2021
1,431,263 (81.2%)
153,724 (67.9%)
916,653 (84.2%)
43,003 (71.6%)
41,484 (86.7%)
138,841 (68.5%)
415,767 (78.8%)
876,398 (84.9%)
16 Jun 2021–15 Dec 2021
311,744 (17.7%)
67,342 (29.7%)
162,831 (14.9%)
15,699 (26.1%)
5,815 (12.2%)
59,482 (29.3%)
105,018 (19.9%)
147,189 (14.3%)
16 Dec 2021–15 Feb 2022
20,029 (1.1%)
5,454 (2.4%)
9,654 (0.9%)
1,377 (2.3%)
543 (1.1%)
4,499 (2.2%)
6,892 (1.3%)
8,631 (0.8%)
*Overall missing values: sex, 1,866; race, 64,403; zip code, 319.
J&J, Johnson & Johnson; SVI, Social Vulnerability Index.
Table 2
Characteristics of individuals receiving a booster vaccination.
Characteristic
Overall (n = 872,324)
Black (n = 84,564)
White (n = 569,411)
Hispanic (n = 20,094)
Asian (n = 23,411)
High SVI (n = 74,292)
Medium SVI (n = 245,129)
Low SVI (n = 552,779)
Sex*, n (%)
Male
375,780 (43.1%)
32,955 (39.0%)
250,231 (43.9%)
9,324 (46.4%)
10,758 (46.0%)
29,909 (40.3%)
104,287 (42.6%)
241,523 (43.7%)
Female
496,405 (56.9%)
51,605 (61.0%)
319,154 (56.1%)
10,769 (53.6%)
12,647 (54.0%)
44,371 (59.7%)
140,778 (57.4%)
311,193 (56.3%)
Age category*, n (%)
12–19 years
41,139 (4.7%)
3,290 (3.9%)
26,448 (4.6%)
1,589 (7.9%)
1,826 (7.8%)
2,372 (3.2%)
8,904 (3.6%)
29,858 (5.4%)
20–34 years
110,416 (12.7%)
7,706 (9.1%)
71,982 (12.6%)
3,986 (19.8%)
6,181 (26.4%)
7,926 (10.7%)
32,664 (13.3%)
69,803 (12.6%)
35–44 years
111,695 (12.8%)
8,628 (10.2%)
73,872 (13.0%)
3,443 (17.1%)
4,616 (19.7%)
7,855 (10.6%)
28,751 (11.7%)
75,067 (13.6%)
45–54 years
118,579 (13.6%)
13,504 (16.0%)
75,541 (13.3%)
3,542 (17.6%)
4,299 (18.4%)
10,062 (13.5%)
31,484 (12.8%)
77,018 (13.9%)
55–64 years
169,867 (19.5%)
20,789 (24.6%)
110,789 (19.5%)
3,502 (17.4%)
2,927 (12.5%)
16,817 (22.6%)
49,656 (20.3%)
103,369 (18.7%)
65–74 years
181,986 (20.9%)
19,328 (22.9%)
120,069 (21.1%)
2,534 (12.6%)
2,202 (9.4%)
17,545 (23.6%)
53,781 (21.9%)
110,642 (20.0%)
75+ years
138,642 (15.9%)
11,319 (13.4%)
90,710 (15.9%)
1,498 (7.5%)
1,360 (5.8%)
11,715 (15.8%)
39,889 (16.3%)
87,022 (15.7%)
Race/ethnicity*, n (%)
Black
84,564 (9.9%)
—
—
—
—
33,706 (46.2%)
32,536 (13.6%)
18,306 (3.4%)
White
56,9411 (66.5%)
—
—
—
—
21,793 (29.9%)
152,881 (63.8%)
394,667 (72.6%)
Hispanic
20,094 (2.3%)
—
—
—
—
2,739 (3.8%)
6,190 (2.6%)
11,161 (2.1%)
Asian
23,411 (2.7%)
—
—
—
—
1,255 (1.7%)
6,166 (2.6%)
15,986 (2.9%)
Other
159,118 (18.6%)
—
—
—
—
13,505 (18.5%)
41,824 (17.5%)
103,764 (19.1%)
Median zip code SVI (IQR)
0.25 (0.16, 0.47)
0.57 (0.34, 0.77)
0.23 (0.15, 0.38)
0.31 (0.16, 0.48)
0.22 (0.15, 0.42)
0.79 (0.71, 0.86)
0.47 (0.41, 0.53)
0.17 (0.12, 0.24)
Booster location type, n (%)
Small volume health facility
41,300 (4.7%)
7,073 (8.4%)
25,989 (4.6%)
808 (4.0%)
954 (4.1%)
5,210 (7.0%)
11,627 (4.7%)
24,456 (4.4%)
Medium volume health facility
86,703 (9.9%)
12,227 (14.5%)
51,780 (9.1%)
1,815 (9.0%)
2,289 (9.8%)
9,607 (12.9%)
21,987 (9.0%)
55,100 (10.0%)
Large volume health facility
71,385 (8.2%)
9,290 (11.0%)
47,164 (8.3%)
956 (4.8%)
1,856 (7.9%)
6,614 (8.9%)
19,927 (8.1%)
44,839 (8.1%)
Pharmacy
610,285 (70.0%)
46,383 (54.8%)
409,591 (71.9%)
14,519 (72.3%)
17,050 (72.8%)
44,096 (59.4%)
169,980 (69.3%)
396,131 (71.7%)
Health department
37,460 (4.3%)
6,514 (7.7%)
21,900 (3.8%)
1,369 (6.8%)
607 (2.6%)
6,001 (8.1%)
14,181 (5.8%)
17,260 (3.1%)
Employer/school
6,469 (0.7%)
591 (0.7%)
3,767 (0.7%)
177 (0.9%)
473 (2.0%)
383 (0.5%)
2,108 (0.9%)
3,976 (0.7%)
Other
18,722 (2.1%)
2,486 (2.9%)
9,220 (1.6%)
450 (2.2%)
182 (0.8%)
2,381 (3.2%)
5,319 (2.2%)
11,017 (2.0%)
Booster vaccine type, n (%)
J&J
8,801 (1.0%)
1,748 (2.1%)
5,188 (0.9%)
306 (1.5%)
118 (0.5%)
1,365 (1.8%)
2,972 (1.2%)
4,460 (0.8%)
Moderna
293,809 (33.7%)
26,933 (31.8%)
189,263 (33.2%)
7,175 (35.7%)
7,127 (30.4%)
26,406 (35.5%)
86,414 (35.3%)
180,946 (32.7%)
Pfizer
569,714 (65.3%)
55,883 (66.1%)
374,960 (65.9%)
12,613 (62.8%)
16,166 (69.1%)
46,521 (62.6%)
155,743 (63.5%)
367,373 (66.5%)
Booster time period, n (%)
15 Dec 2020–15 Jun 2021
9,722 (1.1%)
1,079 (1.3%)
6,102 (1.1%)
260 (1.3%)
206 (0.9%)
950 (1.3%)
2,749 (1.1%)
6,019 (1.1%)
16 Jun 2021–15 Dec 2021
592,768 (68.0%)
50,098 (59.2%)
390,295 (68.5%)
11,318 (56.3%)
13,512 (57.7%)
45,797 (61.6%)
164,223 (67.0%)
382,674 (69.2%)
16 Dec 2021–15 Feb 2022
269,834 (30.9%)
33,387 (39.5%)
173,014 (30.4%)
8,516 (42.4%)
9,693 (41.4%)
27,545 (37.1%)
78,157 (31.9%)
164,086 (29.7%)
*Overall missing values: sex, 139; race/ethnicity, 15,726; zip code, 124.
J&J, Johnson & Johnson; SVI, Social Vulnerability Index.
*Overall missing values: sex, 1,866; race, 64,403; zip code, 319.J&J, Johnson & Johnson; SVI, Social Vulnerability Index.*Overall missing values: sex, 139; race/ethnicity, 15,726; zip code, 124.J&J, Johnson & Johnson; SVI, Social Vulnerability Index.
Rates of COVID-19 primary and booster vaccination by race/ethnicity and SVI over time
The rate of primary COVID-19 vaccination steadily increased until peaking in mid-April 2021. This was followed by rapid decline, with smaller upticks at the end of May 2021 and then during the Delta wave beginning in July 2021; there was no corresponding uptick in vaccination rates during the Omicron wave beginning in mid-December 2021 (Figs 1 and S1–S4; S3 Table). Up through April 2021, White individuals from zip codes with low SVI were vaccinated at a rate greater than 2 times that of Black and Hispanic individuals from high SVI zip codes, but the rate ratio declined over time. Asian individuals from all zip codes were vaccinated at the highest rates. During the same early period, Black and Hispanic individuals from low SVI zip codes were vaccinated at rates somewhat similar to or higher than those of White individuals from medium and high SVI zip codes. After June 2021, Black and Hispanic individuals from high, medium, and low SVI zip codes were vaccinated at higher rates than White individuals, although this was also during periods with lower absolute numbers of vaccinations (Figs 1 and S1–S4; S3 Table). Patterns were largely similar across St. Louis and Kansas City (S2 and S3 Figs).
Fig 1
Rates and cumulative incidence of receiving the primary COVID-19 vaccination series and boosters by race/ethnicity and SVI over time.
Initial series and booster vaccinations for Black (A and B), White (C and D), Hispanic (E and F), and Asian (G and H) individuals. Estimates represent 7-day moving averages derived from multiply imputed datasets. Denominators represent the total population aged 12 years and older. Low SVI indicates zip codes with SVI less than 0.333, medium SVI indicates zip codes with SVI between 0.333 and 0.666, and high SVI indicates zip codes with SVI greater than 0.666. SVI, Social Vulnerability Index.
Rates and cumulative incidence of receiving the primary COVID-19 vaccination series and boosters by race/ethnicity and SVI over time.
Initial series and booster vaccinations for Black (A and B), White (C and D), Hispanic (E and F), and Asian (G and H) individuals. Estimates represent 7-day moving averages derived from multiply imputed datasets. Denominators represent the total population aged 12 years and older. Low SVI indicates zip codes with SVI less than 0.333, medium SVI indicates zip codes with SVI between 0.333 and 0.666, and high SVI indicates zip codes with SVI greater than 0.666. SVI, Social Vulnerability Index.Booster rates increased starting in October 2021 and peaked in early December 2021 at the beginning of the Omicron wave, albeit at much lower levels than for the primary vaccine series, and started to decline in January 2022. Patterns of disparities across race/ethnicity were similar for boosters and completion of the primary series (Figs 1 and S1–S4; S3 Table).
Locations of COVID-19 vaccination over time
Early during the vaccination campaign, the vast majority of vaccines were delivered through medium and large volume health facilities (Fig 2). From February through April 2021, a substantial proportion were also delivered through public health departments (including mass vaccination sites). After April 2021, the proportion of vaccines administered through pharmacies steadily increased, accounting for about 70% of vaccines administered after July 2021. Black individuals received comparatively more vaccines through employer/school-sponsored sites, small volume health facilities, or other facilities such as dialysis centers, home health, and nursing homes, and fewer from pharmacies and health departments. Hispanic and Asian individuals received comparatively more vaccines through pharmacies and health departments; Hispanic individuals also received relatively few vaccines from large volume health facilities. Again, patterns were qualitatively similar for boosters (Fig 2).
Fig 2
Distribution of primary COVID-19 vaccine series and boosters by location type over time and by SVI and race/ethnicity.
Primary series and booster vaccination over time (A and C) and by SVI and race/ethnicity (B and D). Low SVI indicates zip codes with SVI less than 0.333, medium SVI indicates zip codes with SVI between 0.333 and 0.666, and high SVI indicates zip codes with SVI greater than 0.666. Health facilities were categorized as small, medium, or large volume based on whether they vaccinated less than 1,000, 1,000 to 10,000, or greater than 10,000 unique individuals. Other facilities included dialysis centers, home health, nursing homes, mental health/psychiatric facilities, and correctional facilities. Primary series vaccines were allocated to the location where the series was completed. SVI, Social Vulnerability Index.
Distribution of primary COVID-19 vaccine series and boosters by location type over time and by SVI and race/ethnicity.
Primary series and booster vaccination over time (A and C) and by SVI and race/ethnicity (B and D). Low SVI indicates zip codes with SVI less than 0.333, medium SVI indicates zip codes with SVI between 0.333 and 0.666, and high SVI indicates zip codes with SVI greater than 0.666. Health facilities were categorized as small, medium, or large volume based on whether they vaccinated less than 1,000, 1,000 to 10,000, or greater than 10,000 unique individuals. Other facilities included dialysis centers, home health, nursing homes, mental health/psychiatric facilities, and correctional facilities. Primary series vaccines were allocated to the location where the series was completed. SVI, Social Vulnerability Index.
COVID-19 vaccine disparities across zip codes using Lorenz curves
Modified Lorenz curves depict the distribution of COVID-19 vaccinations with respect to the total population, diagnosed COVID-19 cases, COVID-19 deaths, and population-level SVI across zip codes (Fig 3). For the primary vaccine series, zip codes in the quartile with the lowest rates of vaccinations accounted for 19.3%, 18.1%, 10.8%, and 8.8% of vaccines while representing 25% of the total population, cases, deaths, or population-level SVI, respectively. These zip codes, in general, had higher proportions of Black residents, lower median incomes, higher rates of poverty, lower rates of health insurance coverage, a higher proportion of residents employed in the service sector, and a higher rate of COVID-19 deaths (Fig 3; S4–S7 Tables). In contrast, zip codes with the highest rates of vaccination accounted for 30.7%, 35.0%, 44.2%, and 56.1% of vaccinations while representing 25% of the total population, cases, deaths, or population-level SVI, respectively. These zip codes tended to have a lower percentage of Black residents and to be more socioeconomically advantaged (Fig 3; S4–S7 Tables). These patterns were similar, but demonstrated a greater magnitude of disparities, for boosters (Fig 3; S4–S7 Tables).
Fig 3
Lorenz curves of disparities in COVID-19 vaccinations.
This figure depicts modified Lorenz curves examining disparities in COVID-19 vaccinations as of 15 February 2022. The units of analysis are zip codes, and they are color-coded by their SVI. The dashed line represents equitable distribution, where 50% of vaccinations are distributed in zip codes accounting for 50% of the population, cases, deaths, or total social vulnerability. The Lorenz curves measure disparities in the distribution of receiving the primary vaccine series or a booster relative to the total population aged 12 years or older (A and B), diagnosed COVID-19 cases (C and D), COVID-19 deaths (E and F), and total social vulnerability (G and H). SVI, Social Vulnerability Index.
Lorenz curves of disparities in COVID-19 vaccinations.
This figure depicts modified Lorenz curves examining disparities in COVID-19 vaccinations as of 15 February 2022. The units of analysis are zip codes, and they are color-coded by their SVI. The dashed line represents equitable distribution, where 50% of vaccinations are distributed in zip codes accounting for 50% of the population, cases, deaths, or total social vulnerability. The Lorenz curves measure disparities in the distribution of receiving the primary vaccine series or a booster relative to the total population aged 12 years or older (A and B), diagnosed COVID-19 cases (C and D), COVID-19 deaths (E and F), and total social vulnerability (G and H). SVI, Social Vulnerability Index.When examining changes in Gini coefficients and vaccine inequities between zip codes over time, inequities were extremely high during the initial periods of the primary series rollout, but began to slowly decrease after February 2021 relative to population, deaths, and total social vulnerability, but improvements relative to diagnosed cases plateaued around May 2021. Nevertheless, these improvements were slow and modest, and vaccine inequities between zip codes remained substantial for all metrics through January 2022 (Figs 4 and S5). With respect to boosters, Gini coefficients once again were very high in the beginning of rollout, followed by slow improvement relative to population, cases, and deaths; Gini coefficients did not improve (and even worsened initially) relative to total social vulnerability (Figs 4 and S6). There were limited improvements after December 2021 during the Omicron wave.
Fig 4
Temporal patterns in COVID-19 vaccine inequities.
This figure depicts patterns in the Gini coefficients over time for inequities in receiving the primary vaccine series (A) and a booster (B) relative to population, diagnosed COVID-19 cases, COVID-19 deaths, and population-level social vulnerability. Gini coefficients were calculated on a weekly basis from Lorenz curves generated up through that time interval. SVI, Social Vulnerability Index.
Temporal patterns in COVID-19 vaccine inequities.
This figure depicts patterns in the Gini coefficients over time for inequities in receiving the primary vaccine series (A) and a booster (B) relative to population, diagnosed COVID-19 cases, COVID-19 deaths, and population-level social vulnerability. Gini coefficients were calculated on a weekly basis from Lorenz curves generated up through that time interval. SVI, Social Vulnerability Index.
COVID-19 vaccine disparities within zip codes
In zip codes with lower vaccination coverage (which also tended to have higher SVI), Black, Hispanic, and Asian individuals generally had lower rates of primary series completion than White individuals residing in the same zip code (Figs 5 and S7). However, in zip codes with high vaccine coverage (which also tended to have low SVI), Black, Hispanic, and Asian individuals often had higher primary series completion than White individuals in the same zip code. For boosters, Black and Hispanic individuals had lower vaccination rates than White individuals across most zip codes, although Asian individuals tended slightly to have higher booster rates (Figs 5 and S7).
Fig 5
Disparities in COVID-19 primary vaccine series and boosters among Black, Hispanic, and Asian versus White residents of the same zip code.
This figure depicts vaccination rates for the primary series and boosters for Black (A and B), Hispanic (C and D), and Asian (E and F) residents compared to the White residents of the same zip code. Each marker represents a single zip code. Markers are color-coded by the zip code SVI and sized by the total number of vaccines administered in the zip code. The dashed line represents equitable vaccine distribution between the racial/ethnic groups being compared. Points above the dashed line indicate that there was decreased vaccination in Black, Hispanic, or Asian residents compared to White residents (and vice versa). SVI, Social Vulnerability Index.
Disparities in COVID-19 primary vaccine series and boosters among Black, Hispanic, and Asian versus White residents of the same zip code.
This figure depicts vaccination rates for the primary series and boosters for Black (A and B), Hispanic (C and D), and Asian (E and F) residents compared to the White residents of the same zip code. Each marker represents a single zip code. Markers are color-coded by the zip code SVI and sized by the total number of vaccines administered in the zip code. The dashed line represents equitable vaccine distribution between the racial/ethnic groups being compared. Points above the dashed line indicate that there was decreased vaccination in Black, Hispanic, or Asian residents compared to White residents (and vice versa). SVI, Social Vulnerability Index.
Factors associated with receiving the primary vaccine series and boosters
In multivariable mixed-effects Poisson regression, Black and Hispanic individuals had slightly lower rates of completing the primary vaccine series compared to White individuals (adjusted rate ratio [aRR] 0.94 [95% CI 0.93–0.94] and 0.96 [95% CI 0.95–0.97], respectively), while Asian individuals had slightly higher rates (aRR 1.03 [95% CI 1.02–1.03]). Living in a medium or high SVI zip code was also associated with a lower vaccination rate compared to living in a low SVI zip code (aRR 0.92 [95% CI 0.91–0.92] and 0.88 [95% CI 0.88–0.89], respectively) (Table 3). Additional factors associated with increased vaccination were being female and being 12 to 19 years old or 55 years old or older (as compared to 45 to 54 years old); individuals 20 to 34 years old had decreased vaccination rates. Differences in receipt of a booster vaccine were substantially higher across race, age, sex, and zip code SVI compared to the differences in completion of the primary vaccine series, except that 12- to 19-year-olds were less likely to receive a booster (Table 3).
Table 3
Poisson model of individual- and zip code-level factors associated with receipt of primary COVID-19 vaccination series and booster.
Factor
Primary series
Booster
Unadjusted risk ratio (95% CI)
p-Value
Adjusted risk ratio (95% CI)
p-Value
Unadjusted risk ratio (95% CI)
p-Value
Adjusted risk ratio (95% CI)
p-Value
Race/ethnicity
Black
0.86 (0.86–0.86)
<0.001
0.94 (0.93–0.94)
<0.001
0.65 (0.66–0.66)
<0.001
0.83 (0.82–0.83)
<0.001
White
1 (REF)
1 (REF)
1 (REF)
1 (REF)
Hispanic
0.89 (0.88–0.89)
0.96 (0.95–0.97)
0.60 (0.59–0.60)
0.76 (0.75–0.77)
Asian
1.00 (0.99–1.00)
1.03 (1.02–1.03)
0.96 (0.95–0.97)
1.08 (1.07–1.09)
Other
1.72 (1.71–1.72)
1.65 (1.65–1.66)
1.88 (1.88–1.89)
1.76 (1.76–1.77)
Age category
12–19 years
1.28 (1.28–1.29)
<0.001
1.27 (1.26–1.27)
<0.001
0.77 (0.77–0.78)
<0.001
0.76 (0.75–0.76)
<0.001
20–34 years
0.83 (0.83–0.83)
0.84 (0.84–0.84)
0.59 (0.59–0.60)
0.61 (0.60–0.61)
35–44 years
1.01 (1.01–1.02)
1.01 (1.01–1.01)
0.92 (0.92–0.93)
0.92 (0.92–0.93)
45–54 years
1 (REF)
1 (REF)
1 (REF)
1 (REF)
55–64 years
1.11 (1.11–1.12)
1.11 (1.10–1.11)
1.31 (1.30–1.32)
1.29 (1.28–1.30)
65–74 years
1.34 (1.33–1.34)
1.30 (1.30–1.30)
1.93 (1.92–1.94)
1.83 (1.82–1.84)
≥75 years
1.31 (1.31–1.31)
1.24 (1.24–1.25)
1.93 (1.92–1.94)
1.77 (1.76–1.78)
Sex
Male
1 (REF)
<0.001
1 (REF)
<0.001
1 (REF)
<0.001
1 (REF)
<0.001
Female
1.09 (1.08–1.09)
1.07 (1.07–1.07)
1.19 (1.18–1.19)
1.13 (1.13–1.14)
Zip-code-level characteristics
Social Vulnerability Index
Low
1 (REF)
<0.001
1 (REF)
<0.001
1 (REF)
<0.001
1 (REF)
<0.001
Medium
0.87 (0.87–0.87)
0.92 (0.91–0.92)
0.77 (0.77–0.77)
0.83 (0.82–0.83)
High
0.80 (0.80–0.81)
0.88 (0.88–0.89)
0.59 (0.58–0.59)
0.69 (0.68–0.69)
Total population, per 10,000 increase
1.04 (1.04–1.04)
<0.001
1.02 (1.02–1.02)
<0.001
1.06 (1.05–1.06)
<0.001
1.02 (1.02–1.02)
<0.001
Percent Black, per 10% increase
0.98 (0.98–0.98)
<0.001
—*
—*
0.95 (0.95–0.95)
<0.001
—*
—*
Median income, per $15,000 increase
1.05 (1.05–1.05)
<0.001
—*
—*
1.11 (1.11–1.11)
<0.001
—*
—*
Percent below poverty line, per 2.5% increase
0.97 (0.97–0.97)
<0.001
—*
—*
0.93 (0.93–0.93)
<0.001
—*
—*
Percent without health insurance, per 2.5% increase
0.96 (0.96–0.96)
<0.001
—*
—*
0.90 (0.90–0.90)
<0.001
—*
—*
Percent in healthcare industry, per 2.5% increase
1.02 (1.01–1.02)
<0.001
—*
—*
1.04 (1.04–1.04)
<0.001
—*
—*
Percent in service industry, per 2.5% increase
0.97 (0.97–0.97)
<0.001
—*
—*
0.92 (0.92–0.92)
<0.001
—*
—*
Vaccine sites per 10,000, per 1 site increase
1.01 (1.01–1.01)
<0.001
1.01 (1.01–1.01)
<0.001
1.01 (1.01–1.01)
<0.001
1.01 (1.01–1.01)
<0.001
Cases per 100,000, per 1,500 increase
1.01 (1.01–1.01)
<0.001
1.00 (1.00–1.00)
<0.001
1.01 (1.01–1.01)
0.99 (0.99–0.99)
<0.001
Deaths per 100,000, per 50 increase
1.00 (1.00–1.00)
<0.001
1.00 (1.00–1.00)
<0.001
1.00 (1.00–1.01)
1.00 (1.00–1.00)
0.14
Region
St. Louis
1 (REF)
<0.001
1 (REF)
<0.001
1 (REF)
<0.001
1 (REF)
<0.001
Kansas City
0.92 (0.92–0.93)
0.95 (0.95–0.96)
0.87 (0.87–0.87)
0.93 (0.93–0.94)
Continuous variables are scaled so that a 1-unit increase represents approximately half of the interquartile range for that variable.
*Excluded from multivariable model due to collinearity with Social Vulnerability Index.
CI, confidence interval; REF, reference value.
Continuous variables are scaled so that a 1-unit increase represents approximately half of the interquartile range for that variable.*Excluded from multivariable model due to collinearity with Social Vulnerability Index.CI, confidence interval; REF, reference value.
Discussion
Our analyses characterized disparities in the COVID-19 vaccination campaign in the St. Louis and Kansas City regions across racial/ethnic communities, across levels of social vulnerability, over time, and across types of vaccine administration sites. We describe changes in the rates of receiving the primary COVID-19 vaccination series and boosters across race/ethnicity and social vulnerability and highlight how these changes corresponded with shifts in the types of locations where individuals were vaccinated. We also use Lorenz curves and Gini coefficients to quantify disparities in vaccinations with respect to population, COVID-19-related disease burden, and social vulnerability. Overall, these results provide a deeper characterization the systemic inequities in distribution of one of the most critical (and initially scarce) resources for controlling the COVID-19 pandemic but one that is immediately actionable: COVID-19 vaccinations.These analyses provide a deeper understanding of the patterns of vaccine inequities over time, and we note that disparities were greatest earlier on but have also largely persisted over time, with minimal improvement since April 2020. Furthermore, they emerged anew with the booster rollout in fall 2021. Early during vaccination, rates of completing the primary vaccine series were highest among White and Asian individuals in zip codes with low SVI. During this early period, a vast majority of vaccines were administered through health systems and also mass vaccination sites coordinated by public health departments. The relationship between race/ethnicity and zip code SVI is salient during this period: Black and Hispanic individuals living in high SVI zip codes had strikingly lower rates of vaccination compared to other groups, whereas Black and Hispanic individuals in low SVI zip codes had similar to somewhat higher rates of vaccination compared to White individuals in medium and high SVI zip codes. Over time, and particularly after all adults became eligible for vaccination, rates of vaccination among Black and Hispanic individuals across all SVI zip codes started to exceed those among White individuals. During these periods, sites of vaccine administration also diversified and shifted more towards pharmacies and other small community-based sites (and were much less likely to be at very large facilities). When quantifying these disparities using Lorenz curves, we note that disparities in vaccinations were highest relative to population-level social vulnerability and deaths, but still evident—albeit reduced—even when considering vaccinations relative to the overall population and diagnosed COVID-19 cases. Lastly, when examining disparities within zip codes, we see consistently higher rates of vaccination among White individuals compared to Black individuals, with the starkest difference in high SVI zip codes. Unfortunately, despite the slow progress from the early periods in improving equity in completion of the primary vaccine series, the same patterns of disparities were repeated again during the booster rollout, and were often of greater magnitude.It is critical to understand these trends in the context of the underlying structural driving forces and decisions leading to these vaccination patterns, both of which are relevant nationally and not specific to Missouri. First, the high levels of disparities seen in the earlier stages of the primary vaccine series and booster rollouts likely reflect the fact that healthcare workers and older individuals were eligible for vaccination first, factors that are also associated with higher socioeconomic status and lower SVI [9,10]. Second, the early phases of the primary vaccine series rollout occurred primarily at sites associated with large health systems. However, these are also the sites at which Black and Hispanic individuals—and particularly those from high SVI zip codes—were comparatively less likely to ultimately receive vaccinations, highlighting a critical issue related to vaccine access among racially and ethnically marginalized and socially vulnerable communities [27-32]. Although large health systems may have been more readily able to overcome logistic issues and provide the robust cold chain needed for mRNA vaccines, they have limited mandates and expertise for implementing large-scale public health initiatives. Even prior to the pandemic, the significant disparities in who accesses care at these health systems and who is outside of them were well-known [30,33]. Physical access, challenges with scheduling (particularly online), disparities in insurance, lack of community partnerships, and mistrust of large institutions that have largely neglected underserved communities often serve as salient barriers to care-seeking in large health systems for individuals from high SVI communities [27,30,34,35]. Vaccination campaigns are a public health strategy that requires broad reach into communities that large health systems do not have and were not designed for; thus, the strategies relying on these systems did not reach the most vulnerable populations essentially by design, even though the vaccines themselves were freely available. These patterns seen in both the primary vaccine series and booster rollout were also mirrored in prior research from our group examining disparities in COVID-19 testing, and their origins can be traced back to many of the same root causes [4]. Ultimately, the repeated reliance on systems with a history of providing lower access to certain segments of the population is representative of how structural inequities also became embedded in COVID-19 vaccine rollout from its onset and serves as a cautionary tale, albeit one that has been told too many times before.Overall vaccination rates and patterns over time in Black and Hispanic populations and high SVI zip codes further underscore the deeply embedded systemic nature of racialized disparities and the highly intersectional nature of systemic racism and social vulnerability [1,27-30,33-35]. Even though several vaccination strategies sought to prioritize Black and Hispanic individuals living in high SVI zip codes, given their high burden of disease earlier on [11,12,36-38], these groups still had dramatically lower vaccination rates compared to White and Asian individuals in the same high SVI zip codes and those from zip codes with low SVI. As the initial vaccine rollout progressed, though, vaccination rates in Black and Hispanic populations did eventually exceed those in White (though not Asian) populations. This coincided with wider vaccine availability and a shift toward vaccine administration at smaller centers such as pharmacies. Again, these changes in vaccination rates over time may be indicative of increased access to vaccinations in Black, Hispanic, and other socially vulnerable communities through community-based settings as opposed to large health systems [30,34,37,39]. These patterns must also be contextualized within the growing literature on vaccine confidence and hesitancy. Vaccine hesitancy is not monolithic and ranges from beliefs in conspiracy theories and skepticism about COVID-19 to more nuanced concerns regarding safety, side effects, inability to take time off work, observing others safely vaccinated (i.e., social proof), and lack of trusted messaging [29,33-35,40-42]; its patterns and trends across communities also vary [43,44]. Qualitative studies have shown that lack of vaccine confidence in Black communities in particular stems largely from histories of systematic mistreatment and racism—which include failed contemporary responses to COVID-19—leading to mistrust of larger institutions and concerns over bearing the burden of unfavorable safety and side effect profiles (particularly given the rapid timeline of vaccine development and shifting messaging over the need for additional doses) [29,35]. However, rates of primary series completion in the Black population also likely increased as confidence in vaccinations improved over time, more of the population was safely vaccinated (i.e., social proof), purposeful and targeted messaging was delivered from trusted sources, and there were more opportunities to discuss specific questions and concerns with trusted healthcare providers [43,44]. Although a common pattern with the diffusion of many innovations, it is critical to contextualize the structural disparities leading to this late adoption.Although multiple strategies were put forth early in order prioritize equitable vaccination, our analysis shows that we were far from achieving such goals when examined from several metrics. Early vaccine allocation strategies designed to maximize benefits when supply was limited included considerations for prioritizing groups with higher risk for COVID-19 exposure or who had experienced higher burden of COVID-19 disease using metrics such as geography, SVI, and race/ethnicity (in addition to using age, comorbidities, and high-risk occupations) [11-13,36-38]. Still, these strategies mostly focused on determining vaccine eligibility, but eligibility for or availability of vaccines doesn’t equate to adequate access. Indeed, achieving equity would have also required early concomitant prioritization and efforts to target structural barriers to vaccine uptake and reasons for later adoption [45]. Several programs demonstrated success using early, low barrier, and widely available access to vaccines at community-based sites (as opposed to mass vaccination sites and large health systems, often requiring online registration) in areas with high social vulnerability, coupled with abundant opportunities to connect with and discuss concerns with trusted sources of information [30,34,41,46-50]. A program in San Francisco leveraged a community-based vaccination site near a transportation hub to target both access and trust-related barriers, and leveraged both high-touch (e.g., going door-to-door to provide information and register individuals) and low-touch methods (e.g., flyers and advertisements) [50]. Approaches like these are even more important during the later stages of vaccination rollout, when large or mass vaccination sites—which allow for high volume for those already eager to be vaccinated—are likely at the limits of their reach.There are several limitations to our analysis. First, reporting of all vaccinations was mandated by the state, but race/ethnicity and zip code were not reported consistently, particularly at smaller sites. Still, as this missingness was highly dependent on vaccination date and site, multiple imputation would still yield unbiased results even with higher levels of missingness [24-26]. Second, there may also have been misclassification of zip codes of individuals if permanent addresses did not match where people were actually living at the time of vaccination, or in our categorization of vaccine location types. However, any misclassification was likely small, and there is no reason to believe that there was systemic error that would substantially bias our results. Third, we used zip code population estimates from the 2020 census data, but true population sizes—and thus the appropriate denominators for some analyses—may have changed since then, particularly due to the well-documented migrations that occurred during the early phases of the pandemic. Fourth, we lacked complementary data that could help contextualize our findings (e.g., association between race/ethnicity and time or location of vaccination) and help characterize the relationship with potential drivers of these disparities, such as data on occupation, health insurance status, linkage to primary care, and vaccination awareness, knowledge, beliefs, and intentions. Fourth, in this analysis we were unable to provide more granular details or include separate categories for other racial/ethnic minorities such as indigenous or multi-racial individuals, due to either small populations in the regions that would lead to unstable statistical estimates or the inability to link these population across data sources. Still, although we do include Black, White, Hispanic, and Asian communities, it remains critical to also assess disparities across other minoritized communities, acknowledging that the multidimensional nature of health disparities and unique drivers across these different communities warrant dedicated attention and public health action.In conclusion, we provide nuanced characterizations of the disparities in COVID-19 vaccination across racial/ethnic communities, across levels of social vulnerability, over time, and across types of vaccine administration sites after 1 year of vaccination. Equitable COVID-19 vaccination is one of the most critical targets for successfully ending the pandemic, but, despite substantial discussion on how to effectively do so, it is clear that our strategies—both nationally and in Missouri—have yet to overcome the deeply entrenched systemic inequities in healthcare and society. Future planning for proactive and considered public health strategies in the face of pandemic emergencies—as opposed to reactive approaches—is needed to ensure that our responses are equitable from the outset and do not disproportionately affect minority communities both in the United States and globally.
Cumulative incidence of primary COVID-19 vaccination series and booster completion by race/ethnicity and SVI.
(DOCX)Click here for additional data file.
St. Louis: Rates and cumulative incidence of receiving the primary COVID-19 vaccination series and boosters by race/ethnicity and SVI over time.
(DOCX)Click here for additional data file.
Kansas City: Rates and cumulative incidence of receiving the primary COVID-19 vaccination series and boosters by race/ethnicity and SVI over time.
(DOCX)Click here for additional data file.
Rates of diagnosed cases and deaths from COVID-19.
(DOCX)Click here for additional data file.
Lorenz curves of disparities in COVID-19 vaccinations over time—primary series.
(DOCX)Click here for additional data file.
Lorenz curves of disparities in COVID-19 vaccinations over time—booster.
(DOCX)Click here for additional data file.
Disparities in COVID-19 primary vaccine series and boosters among Black, Hispanic, and Asian versus White residents in the same zip code over time.
(DOCX)Click here for additional data file.
STROBE checklist.
(DOCX)Click here for additional data file.
Characteristics of individuals completing the primary vaccine series.
(DOCX)Click here for additional data file.
Characteristics of individuals receiving a booster vaccination.
(DOCX)Click here for additional data file.
Rates of initiating/completing primary vaccine series and boosters by race/ethnicity and SVI.
(DOCX)Click here for additional data file.
Characteristics of zip codes by quartile of Lorenz curve—number of COVID-19 vaccinations relative to total population.
(DOCX)Click here for additional data file.
Characteristics of zip codes by quartile of Lorenz curve—number of COVID-19 vaccinations relative to diagnosed COVID-19 cases.
(DOCX)Click here for additional data file.
Characteristics of zip codes by quartile of Lorenz curve—number of COVID-19 vaccinations relative to deaths due to COVID-19.
(DOCX)Click here for additional data file.
Characteristics of zip codes by quartile of Lorenz curve—number of COVID-19 vaccinations relative to total SVI.
(DOCX)Click here for additional data file.8 Apr 2022Dear Dr Mody,Thank you for submitting your manuscript entitled "Characterizing Equity in COVID-19 Vaccine Distribution: A Population-Level Analysis quantifying disparities across social vulnerability, race, location, and time." for consideration by PLOS Medicine.Your manuscript has now been evaluated by the PLOS Medicine editorial staff and I am writing to let you know that we would like to send your submission out for external assessment.However, we first need you to complete your submission by providing the metadata that is required for full assessment. To this end, please login to Editorial Manager where you will find the paper in the 'Submissions Needing Revisions' folder on your homepage. Please click 'Revise Submission' from the Action Links and complete all additional questions in the submission questionnaire.Please re-submit your manuscript within two working days, i.e. by Apr 12 2022 11:59PM.Login to Editorial Manager here: https://www.editorialmanager.com/pmedicineOnce your full submission is complete, your paper will undergo a series of checks in preparation for assessment.Feel free to email us at plosmedicine@plos.org if you have any queries relating to your submission.Kind regards,Richard Turner, PhDSenior Editor, PLOS Medicinerturner@plos.org18 May 2022Dear Dr. Mody,Thank you very much for submitting your manuscript "Characterizing Equity in COVID-19 Vaccine Distribution: A Population-Level Analysis quantifying disparities across social vulnerability, race, location, and time." (PMEDICINE-D-22-01093R1) for consideration at PLOS Medicine.Your paper was discussed with an academic editor with relevant expertise and sent to independent reviewers, including a statistical reviewer. The reviews are appended at the bottom of this email and any accompanying reviewer attachments can be seen via the link below:[LINK]In light of these reviews, we will not be able to accept the manuscript for publication in the journal in its current form, but we would like to invite you to submit a revised version that addresses the reviewers' and editors' comments fully. You will recognize that we cannot make a decision about publication until we have seen the revised manuscript and your response, and we expect to seek re-review by one or more of the reviewers.In revising the manuscript for further consideration, your revisions should address the specific points made by each reviewer and the editors. 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You can see our competing interests policy here: http://journals.plos.org/plosmedicine/s/competing-interests.Please use the following link to submit the revised manuscript:https://www.editorialmanager.com/pmedicine/Your article can be found in the "Submissions Needing Revision" folder.To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocolsPlease ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.Please let me know if you have any questions, and we look forward to receiving your revised manuscript.Sincerely,Richard Turner, PhDSenior editor, PLOS Medicinerturner@plos.org-----------------------------------------------------------Requests from the editors:Please adapt the competing interest statement (submission form) to include "EHG is a member of PLOS Medicine's Editorial Board" or similar.We ask you to restructure the title to better match journal style and suggest: "Quantifying disparities in COVID-19 vaccine distribution by social vulnerability, ethnicity, location, and time: A population-level analysis".Please also state where the study was done in the title.Please add a new final sentence to the "Methods and findings" subsection of your abstract, which should begin "Study limitations include ..." or similar and should quote 2-3 of the study's main limitations.After the abstract, please add a new and accessible "Author summary" section in non-identical prose. You may find it helpful to consult one or two recent research papers published in PLOS Medicine to get a sense of the preferred style.The sentence at line 99 beginning "The novel application ..." is really an item of discussion, and so should be removed or relocated to the Discussion.Early in the Methods section (main text), please state whether the study had a protocol or prespecified analysis plan, and if so attach the relevant document as a supplementary file, referred to in the text.Please highlight any non-prespecified analyses.We suggest substituting "ethnicity" for "race" throughout.Please remove the information on funding and competing interests from the end of the main text. In the event of publication, this information will appear in the article metadata via entries in the submission form, and does not need to be duplicated.In the reference list, please use the journal name abbreviation "PLoS ONE".Noting reference 4 and others, please ensure that all references have full access details.Please add a completed checklist for the most appropriate reporting guideline, e.g., STROBE, as an attachment, labelled "S1_STROBE_Checklist" or similar and referred to as such in the Methods section (main text).In the checklist, please ensure that individual items are referred to by section (e.g., "Methods") and paragraph number, not by line or page numbers as these generally change in the event of publication.Comments from the reviewers:*** Reviewer #1:This is an excellent, well-written article that brings a health equity lens to the rollout of SARS-CoV-2 vaccination in two large cities in Missouri. The data are population-based and the study produced collaboratively by academic researchers and health department staff. Despite COVID-19 vaccines being freely available, how they are made available will affect who gets them quickly enough to derive the most reduced risk in the burden of infection (hospitalizations, long COVID, deaths). The authors contextualize their findings in terms of both historical systemic racism in medicine and public health, as well as how implementation intended to counter inequities did not prevent what ended up being substantial racial/ethnic and social inequity in the uptake of vaccines. I have a few comments and suggestions intended to help improve the quality and impact of their manuscript:1. Is there a way to examine, or at least discuss, vaccine uptake as it relates to timing of major surges. That is, in addition to having lower cumulative vaccination rates, were minoritized and vulnerable communities also less likely to be vaccinated in advance of the delta and omicron surges? This speaks to the timing of vaccination, which is an important dimension. Some of it is alluded to in Figure 1.2. Outcome of vaccine uptake. There has been some concern about the quality of vaccine coverage data as derived from registries (e.g., double counting, denominator issues). For example, vaccine coverage rates well above 100% for some racial/ethnic groups. Related, 2018 census data may not reflect differential in and out migration that occurred in many jurisdictions during the early phase of the pandemic especially. The authors should at least acknowledged this as a potential limitation. But if they did any investigative work around this with their own data, it would be worth highlighting so that other jurisdictions factor these issues in as well.3. The authors describe how much of the initial vaccine rollout was through large medical centers and health care providers. They note that pre-existing disparities in health care access barriers would be perpetuated under this model, which is true. But I think it is worth pulling back the lens even more. Getting vaccinated is not health care. It is a preventive action that requires broad reach in communities to achieve the requisite coverage. By definition, focusing on medical centers and the health care system as points of distribution for an intervention that requires broad community reach outside the health care system is in my view one key example of how and why disparities were created early on. The health care system, hospitals, and medical providers have no public health mandate and no management/implementation expertise in this areas. Thus, they are always going to be the wrong choice for the major node of implementation of a large scale public health initiative that by definition must reach those outside the health care system. Suggest a re-framing.4. I am having a heard time wrapping my head around how a sample sizes of 32K Hispanic, 38K Asian, and 187K multiracial are too small to produce useful estimates (Discussion, Line 361), especially since they are not samples, but near full enumerations of those populations in each city. Please consider presenting more nuanced groupings than Black-White-Other.5. For the SVI variable in Table 1, consider presenting low, medium, and high so readers can appreciate any gradient that may be there. Related, did the authors check that relationships were in fact linear in models where continuous exposures were examined (i.e., in models presented in Table 2)? If so, this should be stated in the methods. If not, the authors should examine these variables with fewer smoothing assumptions (e.g., as 3+ level categorical variables).*** Reviewer #2:I mostly confine my remarks to statistical aspects of this paper. The overall method is sound, but I have a few issues to resolve before I can recommend publicationI will note that it could use some more editing for English usage. There are doubled words (had had), misplaced articles ("endured the disproportionate" should not have a "the"), wrong words ("empiric" should be "empirical") and so on. I don't usually comment on grammar, but here, it affects readability and may affect credibility.One non-statistical comment: I think the title should reflect that this study was only in two cities in one state in the USA. As is, it sounds universal.Still on the title, but now statistical: I think it should be "over time" not "and time" -- disparities across social vulnerability, race, and location, over time. After all, while it is true that you can be inequitable regarding place, race, etc, it's hard to be inequitable about time -- July isn't going to complain that it got fewer vaccines than April. Another possibility to end with "controlling for time".p. 5 line 134 What are "health facilities"? Are these hospitals? And you aren't really looking at the size of the facility, but at its vaccination rate. This will surely be related to size, but also to other factors, such as the existence of other facilities nearby. (If a big hospital is near a mass vaccination site, people may go to the latter).p. 6 line 154-156 I wouldn't do this, but, since you also treated this as a continuous variable, it's not so bad.line 160 Rather than % of the population, this should be based on a number of people. ZIP codes are very disparate in population. I know that, in New York City, some ZIP codes have no residents at all (these are large office buildings that have their own ZIP). In Missouri, ZIP codes can have as few as 6 people (63464) and as many as 75,000 (63376) (See https://www.missouri-demographics.com/zip_codes_by_population). The latter one is actually in your data. Just checking St Louis (because I got interested) 63140 has only 347 people).Despite all the above, I think this is a good paper that uses somewhat unusual statistical methods in a good way.Peter Flom*** Reviewer #3:SummaryDifferences in vaccine coverage between populations may result in large disparities in COVID-19 morbidity and mortality. In this paper, the authors assess inequities in COVID-19 vaccine coverage in 7 counties in St. Louis and 4 counties in Kansas City throughout the first year of vaccine availability. The authors specifically look at Black and White populations in these counties and compare vaccination rates relative to the following measures: time, race, zip-code level social vulnerability index (SVI), vaccine location type, and COVID-19 disease burden. The authors summarize inequality using Lorenz curves and Gini coefficients, tools/methods from economics. The key findings from this study are that large inequities in vaccination between Black and White communities were seen early on during vaccine distribution and that inequities only decreased once methods of distribution broadened, and that inequities persist. This is significant because it highlights the importance of public health strategies taking into account structural drivers of inequities.StrengthsThe paper is very well written. The authors do a great job outlining why research on inequities in vaccination rates should look at multiple structural and social determinants to gain a better understanding of how such inequities may be addressed. The methods are well justified and the use of traditional economics methods to describe health inequities is creative. The methods are described clearly in an accessible way that made it so even readers who are not well versed in statistics could understand at a basic level what was done. The graphs and figures are good, but could be made even more clear (details below).Critiques1. The paper is an excellent retrospective look at vaccine rollout. However, I expected a little bit more about what cities or counties can do moving forward in the Omicron era. E.g., Figure 1 looks like cumulative proportion of 1 vaccine dose, would it be fairly easy for authors to look at 2 doses and booster? Given where discussion is now with fully vaccinated meaning at least 2 doses and booster availability, do these results hold up? A full look at booster coverage may be out of scope of the paper. However, there is concern about people not getting boosters and people (disproportionately Black, high SVI) who got their vaccine later were not eligible for boosters during the early Omicron wave. Some additional analysis - or discussion - of this point would be helpful to guide policy makers in applying the findings to the current moment.2. I have several suggestions to make the tables and figures even clearer:- Across all tables and figures, there should be more clarity around what receipt of the COVID-19 vaccination is. Is it 1 dose or 2? Does it include boosters? Does it mean something different at different age groups? This should be clear in the title or note to each table/figure.- Table 2. The regression coefficients for zip-code characteristics are difficult to compare with each other. I'd suggest standardizing the regression coefficients (dividing by the standard deviation of the predictor) to enable comparisons.- Fig 1C and 1D yscale should go 0 to 100% if everyone in the denominator is eligible.- Figure 1, the lines all have colors in a similar tone (making it difficult for the colorblind) and making high/low SVI and White/Black comparisons difficult. I recommend changing the colors/patterns to make the graph easier to read. E.g., change lines to two colors, one color for low SVI and another for high SVI, and then solid lines for Black and dashed lines for White. (or something similar) That change would make it much easier to read this graph.- Figure 2. Font is too small. Consider month abbreviations, consider removing the decimals on the percentages… should be easier to read- Figure 3 - Color coding is interesting and could help people understand intuitively what the Lorenz curves are doing. Where blues and reds are more mixed, the line is closer to diagonal (less inequality) where blues are together and reds are together is where curves are far away from diagonal (more inequality). However, it is rather hard to see colors. Is there a way to make the colors (dots) bigger?- Both of the last two graphs are titled "Figure 4".- The first "Figure 4". Gini coef is a measure of inequality (not disparity), hence the title should refer to trends in inequality, as measured by Gini coef.- The first "Figure 4". I find the 4 lines to be distracting. My eye wanted to compare the lines with each other and understand the difference. But the MAIN point of the figure is that the lines fall over time (as indicated in the title of the figure) and that inequity remains high at the end. If the focus is on temporal trends, I think the figure could be improved by showing just the SVI line - and perhaps showing STL and KC on the same plot.- The second "Figure 4" (i.e. Figure 5 - with 8 panels). I think there's too much going on here. I'd encourage the authors to simplify the figure so the main point is clearer. E.g., panels A-D are enough. Panel A/B show that SVI was correlated with vaccine uptake in blacks, but not in whites (HUGELY IMPORTANT FINDING); panel C/D show that blacks are substantially undervaccinated relative to whites when accounting for case rates. Panels E/F - the data are a bit all over the place, maybe a small numbrs issue with zip-level death rates. Panels G/H - I don't understand what "total SVI in black/white population" means. If the point is that vaccine coverage in inversely associated with social vulnerability, then that point has already been made earlier in the paper.3. STL vs. KC. There were some notable differences between St Louis and Kansas City counties, but little discussion of these differences. Did the cities take any different approaches that affected vaccine coverage?In all, the authors have conducted a timely and important analysis of small area vaccination inequities. Their emphasis on the role of concrete interventions (decentralized vaccine delivery) to mitigate vaccine inequities is a major strength of the paper. The findings will be valuable for policy makers, in addition to pushing the literature forward.Jacob Bor***Any attachments provided with reviews can be seen via the following link:[LINK]13 Jun 2022Submitted filename: PLOS Med Response to Reviewers.docxClick here for additional data file.26 Jul 2022Dear Dr. Mody,Thank you very much for re-submitting your manuscript "Quantifying Inequities in COVID-19 Vaccine Distribution Over Time by social vulnerability, race and ethnicity, and location: A Population-Level Analysis in St. Louis and Kansas City, Missouri" (PMEDICINE-D-22-01093R2) for review by PLOS Medicine.I have discussed the paper with my colleagues and it was also seen again by three reviewers. I am pleased to say that provided the remaining editorial and production issues are dealt with we are planning to accept the paper for publication in the journal.The remaining issues that need to be addressed are listed at the end of this email. Any accompanying reviewer attachments can be seen via the link below. Please take these into account before resubmitting your manuscript:[LINK]***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***In revising the manuscript for further consideration here, please ensure you address the specific points made by each reviewer and the editors. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments and the changes you have made in the manuscript. Please submit a clean version of the paper as the main article file. A version with changes marked must also be uploaded as a marked up manuscript file.Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. If you haven't already, we ask that you provide a short, non-technical Author Summary of your research to make findings accessible to a wide audience that includes both scientists and non-scientists. The Author Summary should immediately follow the Abstract in your revised manuscript. This text is subject to editorial change and should be distinct from the scientific abstract.We expect to receive your revised manuscript within 1 week. Please email us (plosmedicine@plos.org) if you have any questions or concerns.We ask every co-author listed on the manuscript to fill in a contributing author statement. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT.Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocolsPlease review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript.Please note, when your manuscript is accepted, an uncorrected proof of your manuscript will be published online ahead of the final version, unless you've already opted out via the online submission form. If, for any reason, you do not want an earlier version of your manuscript published online or are unsure if you have already indicated as such, please let the journal staff know immediately at plosmedicine@plos.org.If you have any questions in the meantime, please contact me or the journal staff on plosmedicine@plos.org.We look forward to receiving the revised manuscript by Aug 02 2022 11:59PM.Sincerely,Beryne Odeny, PhDPLOS Medicineplosmedicine.org------------------------------------------------------------Requests from Editors:Comments from Reviewers:Reviewer #1: The authors have been very responsive to reviewer and editorial comments.Reviewer #2: The authors have addressed my concerns and I now recommend publicationReviewer #3: The authors have responded to all of my prior concerns in this revision. The manuscript has been strengthened in particular by the full data update (no small amount of work) to include analyses of the full vaccination series and booster coverage. The expanded focus to look at other racial/ethnic groups is welcome, and the decision to de-emphasize the KC vs. STL distinction is reasonable based on the large amount of content presented. The exposition and exhibits are clearer as a result of the suggestions of other reviewers and Editors. The definitions of equity, race/ethnicity, and minoritized are careful and accurate to the U.S. context. The authors should mention explicitly that there were not enough American Indian / Alaska Native persons in the population to be included as a separate category with statistically stable estimates. (There is some understandable consternation in the AIAN research community about being lumped into "Other" without justification.) I have no further critiques of this fine paper.Any attachments provided with reviews can be seen via the following link:[LINK]28 Jul 2022Submitted filename: PLOS Med Response to Reviewers2.docxClick here for additional data file.2 Aug 2022Dear Dr Mody,On behalf of my colleagues and the Academic Editor, Dr. Nicola Low, I am pleased to inform you that we have agreed to publish your manuscript "Quantifying Inequities in COVID-19 Vaccine Distribution Over Time by social vulnerability, race and ethnicity, and location: A Population-Level Analysis in St. Louis and Kansas City, Missouri" (PMEDICINE-D-22-01093R3) in PLOS Medicine.Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. Please be aware that it may take several days for you to receive this email; during this time no action is required by you. 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Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocolsThank you again for submitting to PLOS Medicine. We look forward to publishing your paper.Sincerely,Beryne OdenyPLOS Medicine