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1.
Ann Epidemiol ; 80: 62-68.e3, 2023 04.
Article in English | MEDLINE | ID: covidwho-2275874

ABSTRACT

PURPOSE: When studying health risks across a large geographic region such as a state or province, researchers often assume that finer-resolution data on health outcomes and risk factors will improve inferences by avoiding ecological bias and other issues associated with geographic aggregation. However, coarser-resolution data (e.g., at the town or county-level) are more commonly publicly available and packaged for easier access, allowing for rapid analyses. The advantages and limitations of using finer-resolution data, which may improve precision at the cost of time spent gaining access and processing data, have not been considered in detail to date. METHODS: We systematically examine the implications of conducting town-level mixed-effect regression analyses versus census-tract-level analyses to study sociodemographic predictors of COVID-19 in Massachusetts. In a series of negative binomial regressions, we vary the spatial resolution of the outcome, the resolution of variable selection, and the resolution of the random effect to allow for more direct comparison across models. RESULTS: We find stability in some estimates across scenarios, changes in magnitude, direction, and significance in others, and tighter confidence intervals on the census-tract level. Conclusions regarding sociodemographic predictors are robust when regions of high concentration remain consistent across town and census-tract resolutions. CONCLUSIONS: Inferences about high-risk populations may be misleading if derived from town- or county-resolution data, especially for covariates that capture small subgroups (e.g., small racial minority populations) or are geographically concentrated or skewed (e.g., % college students). Our analysis can help inform more rapid and efficient use of public health data by identifying when finer-resolution data are truly most informative, or when coarser-resolution data may be misleading.


Subject(s)
COVID-19 , Humans , COVID-19/epidemiology , Massachusetts/epidemiology , Risk Factors , Students , Regression Analysis
2.
J Racial Ethn Health Disparities ; 2022 Sep 02.
Article in English | MEDLINE | ID: covidwho-2007324

ABSTRACT

Infectious disease surveillance frequently lacks complete information on race and ethnicity, making it difficult to identify health inequities. Greater awareness of this issue has occurred due to the COVID-19 pandemic, during which inequities in cases, hospitalizations, and deaths were reported but with evidence of substantial missing demographic details. Although the problem of missing race and ethnicity data in COVID-19 cases has been well documented, neither its spatiotemporal variation nor its particular drivers have been characterized. Using individual-level data on confirmed COVID-19 cases in Massachusetts from March 2020 to February 2021, we show how missing race and ethnicity data: (1) varied over time, appearing to increase sharply during two different periods of rapid case growth; (2) differed substantially between towns, indicating a nonrandom distribution; and (3) was associated significantly with several individual- and town-level characteristics in a mixed-effects regression model, suggesting a combination of personal and infrastructural drivers of missing data that persisted despite state and federal data-collection mandates. We discuss how a variety of factors may contribute to persistent missing data but could potentially be mitigated in future contexts.

3.
Clin Infect Dis ; 75(1): e105-e113, 2022 08 24.
Article in English | MEDLINE | ID: covidwho-1852991

ABSTRACT

BACKGROUND: Estimating the cumulative incidence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is essential for setting public health policies. We leveraged deidentified Massachusetts newborn screening specimens as an accessible, retrospective source of maternal antibodies for estimating statewide seroprevalence in a nontest-seeking population. METHODS: We analyzed 72 117 newborn specimens collected from November 2019 through December 2020, representing 337 towns and cities across Massachusetts. Seroprevalence was estimated for the Massachusetts population after correcting for imperfect test specificity and nonrepresentative sampling using Bayesian multilevel regression and poststratification. RESULTS: Statewide seroprevalence was estimated to be 0.03% (90% credible interval [CI], 0.00-0.11) in November 2019 and rose to 1.47% (90% CI: 1.00-2.13) by May 2020, following sustained SARS-CoV-2 transmission in the spring. Seroprevalence plateaued from May onward, reaching 2.15% (90% CI: 1.56-2.98) in December 2020. Seroprevalence varied substantially by community and was particularly associated with community percent non-Hispanic Black (ß = .024; 90% CI: 0.004-0.044); i.e., a 10% increase in community percent non-Hispanic Black was associated with 27% higher odds of seropositivity. Seroprevalence estimates had good concordance with reported case counts and wastewater surveillance for most of 2020, prior to the resurgence of transmission in winter. CONCLUSIONS: Cumulative incidence of SARS-CoV-2 protective antibody in Massachusetts was low as of December 2020, indicating that a substantial fraction of the population was still susceptible. Maternal seroprevalence data from newborn screening can inform longitudinal trends and identify cities and towns at highest risk, particularly in settings where widespread diagnostic testing is unavailable.


Subject(s)
COVID-19 , SARS-CoV-2 , Antibodies, Viral , Bayes Theorem , COVID-19/diagnosis , COVID-19/epidemiology , Humans , Infant, Newborn , Neonatal Screening , Retrospective Studies , Seroepidemiologic Studies , Wastewater , Wastewater-Based Epidemiological Monitoring
4.
Influenza Other Respir Viruses ; 16(2): 213-221, 2022 03.
Article in English | MEDLINE | ID: covidwho-1511324

ABSTRACT

BACKGROUND: The COVID-19 pandemic has highlighted the need for targeted local interventions given substantial heterogeneity within cities and counties. Publicly available case data are typically aggregated to the city or county level to protect patient privacy, but more granular data are necessary to identify and act upon community-level risk factors that can change over time. METHODS: Individual COVID-19 case and mortality data from Massachusetts were geocoded to residential addresses and aggregated into two time periods: "Phase 1" (March-June 2020) and "Phase 2" (September 2020 to February 2021). Institutional cases associated with long-term care facilities, prisons, or homeless shelters were identified using address data and modeled separately. Census tract sociodemographic and occupational predictors were drawn from the 2015-2019 American Community Survey. We used mixed-effects negative binomial regression to estimate incidence rate ratios (IRRs), accounting for town-level spatial autocorrelation. RESULTS: Case incidence was elevated in census tracts with higher proportions of Black and Latinx residents, with larger associations in Phase 1 than Phase 2. Case incidence associated with proportion of essential workers was similarly elevated in both Phases. Mortality IRRs had differing patterns from case IRRs, decreasing less substantially between Phases for Black and Latinx populations and increasing between Phases for proportion of essential workers. Mortality models excluding institutional cases yielded stronger associations for age, race/ethnicity, and essential worker status. CONCLUSIONS: Geocoded home address data can allow for nuanced analyses of community disease patterns, identification of high-risk subgroups, and exclusion of institutional cases to comprehensively reflect community risk.


Subject(s)
COVID-19 , Health Status Disparities , Humans , Massachusetts/epidemiology , Pandemics , SARS-CoV-2
6.
Public Health Rep ; 136(6): 765-773, 2021.
Article in English | MEDLINE | ID: covidwho-1354647

ABSTRACT

OBJECTIVES: Widespread SARS-CoV-2 testing is critical to identify infected people and implement public health action to interrupt transmission. With SARS-CoV-2 testing supplies and laboratory capacity now widely available in the United States, understanding the spatial heterogeneity of associations between social determinants and the use of SARS-CoV-2 testing is essential to improve testing availability in populations disproportionately affected by SARS-CoV-2. METHODS: We assessed positive and negative results of SARS-CoV-2 molecular tests conducted from February 1 through June 17, 2020, from the Massachusetts Virtual Epidemiologic Network, an integrated web-based surveillance and case management system in Massachusetts. Using geographically weighted regression and Moran's I spatial autocorrelation tests, we quantified the associations between SARS-CoV-2 testing rates and 11 metrics of the Social Vulnerability Index in all 351 towns in Massachusetts. RESULTS: Median SARS-CoV-2 testing rates decreased with increasing percentages of residents with limited English proficiency (median relative risk [interquartile range] = 0.96 [0.95-0.99]), residents aged ≥65 (0.97 [0.87-0.98]), residents without health insurance (0.96 [0.95-1.04], and people residing in crowded housing conditions (0.89 [0.80-0.94]). These associations differed spatially across Massachusetts, and localized models improved the explainable variation in SARS-CoV-2 testing rates by 8% to 12%. CONCLUSION: Indicators of social vulnerability are associated with variations in SARS-CoV-2 testing rates. Accounting for the spatial heterogeneity in these associations may improve the ability to explain and address the SARS-CoV-2 pandemic at substate levels.


Subject(s)
COVID-19/diagnosis , COVID-19/epidemiology , Vulnerable Populations/statistics & numerical data , Age Factors , COVID-19 Testing , Housing , Humans , Language , Massachusetts/epidemiology , Pandemics , Public Health , SARS-CoV-2 , Socioeconomic Factors , Spatial Analysis
10.
Oncologist ; 26(5): e898-e901, 2021 05.
Article in English | MEDLINE | ID: covidwho-1156887

ABSTRACT

OBJECTIVE: The aim of this study was to determine the rate of coronavirus disease-19 (COVID-19) among patients with cancer treated with immune checkpoint inhibitors (ICIs). MATERIALS AND METHODS: This was a retrospective study of 1,545 patients with cancer treated with ICIs between July 1, 2019, and February 29, 2020, and 20,418 age-, sex-, and cancer category-matched controls in a large referral hospital system. Confirmed COVID-19 case and mortality data were obtained with Massachusetts Department of Public Health from March 1 through June 19, 2020. RESULTS: The mean age was 66.6 years, and 41.9% were female. There were 22 (1.4%) and 213 (1.0%) COVID-19 cases in the ICI and control groups, respectively. When adjusting for demographics, medical comorbidities, and local infection rates, ICIs did not increase COVID-19 susceptibility. CONCLUSION: ICIs did not increase the rate of COVID-19. This information may assist patients and their oncologists in decision-making surrounding cancer treatment during this pandemic.


Subject(s)
COVID-19 , Neoplasms , Aged , Female , Humans , Immune Checkpoint Inhibitors , Male , Massachusetts , Neoplasms/drug therapy , Retrospective Studies , SARS-CoV-2
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