COVID-19 Surveillance in the Biobank at the Colorado Center for Personalized Medicine: Observational Study
Open Access
- 13 June 2022
- journal article
- research article
- Published by JMIR Publications Inc. in JMIR Public Health and Surveillance
- Vol. 8 (6) , e37327
Abstract
Background: Characterizing the experience and impact of the COVID-19 pandemic among various populations remains challenging due to the limitations inherent in common data sources, such as electronic health records (EHRs) or cross-sectional surveys. Objective: This study aims to describe testing behaviors, symptoms, impact, vaccination status, and case ascertainment during the COVID-19 pandemic using integrated data sources. Methods: In summer 2020 and 2021, we surveyed participants enrolled in the Biobank at the Colorado Center for Personalized Medicine (CCPM; N=180,599) about their experience with COVID-19. The prevalence of testing, symptoms, and impacts of COVID-19 on employment, family life, and physical and mental health were calculated overall and by demographic categories. Survey respondents who reported receiving a positive COVID-19 test result were considered a “confirmed case” of COVID-19. Using EHRs, we compared COVID-19 case ascertainment and characteristics in EHRs versus the survey. Positive cases were identified in EHRs using the International Statistical Classification of Diseases, 10th revision (ICD-10) diagnosis codes, health care encounter types, and encounter primary diagnoses. Results: Of the 25,063 (13.9%) survey respondents, 10,661 (42.5%) had been tested for COVID-19, and of those, 1366 (12.8%) tested positive. Nearly half of those tested had symptoms or had been exposed to someone who was infected. Young adults (18-29 years) and Hispanics were more likely to have positive tests compared to older adults and persons of other racial/ethnic groups. Mental health (n=13,688, 54.6%) and family life (n=12,233, 48.8%) were most negatively affected by the pandemic and more so among younger groups and women; negative impacts on employment were more commonly reported among Black respondents. Of the 10,249 individuals who responded to vaccination questions from version 2 of the survey (summer 2021), 9770 (95.3%) had received the vaccine. After integration with EHR data up to the time of the survey completion, 1006 (4%) of the survey respondents had a discordant COVID-19 case status between EHRs and the survey. Using all longitudinal EHR and survey data, we identified 11,472 (6.4%) COVID-19-positive cases among Biobank participants. In comparison to COVID-19 cases identified through the survey, EHR-identified cases were younger and more likely to be Hispanic. Conclusions: We found that the COVID-19 pandemic has had far-reaching and varying effects among our Biobank participants. Integrated data assets, such as the Biobank at the CCPM, are key resources for population health monitoring in response to public health emergencies, such as the COVID-19 pandemic.Keywords
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This publication has 23 references indexed in Scilit:
- Characteristics of Adult Outpatients and Inpatients with COVID-19 — 11 Academic Medical Centers, United States, March–May 2020MMWR. Morbidity and Mortality Weekly Report, 2020
- Overcoming the ‘tyranny of the urgent’: integrating gender into disease outbreak preparedness and responseGender & Development, 2019
- Socioeconomic Status and Racial or Ethnic Differences in Participation: Web-Based SurveyJMIR Research Protocols, 2019
- Selfish-rational non-vaccination: Experimental evidence from an interactive vaccination gameJournal of Economic Behavior & Organization, 2016
- A gendered human rights analysis of Ebola and Zika: locating gender in global health emergenciesInternational Affairs, 2016
- Exploring and Promoting Prosocial Vaccination: A Cross-Cultural Experiment on Vaccination of Health Care PersonnelBioMed Research International, 2016
- Comparison of the information provided by electronic health records data and a population health survey to estimate prevalence of selected health conditions and multimorbidityBMC Public Health, 2013
- Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group studyJournal of Community Genetics, 2011
- Addressing the Challenges of Latino Health Research: Participatory Approaches in an Emergent Urban CommunityJournal of the National Medical Association, 2009
- Research electronic data capture (REDCap)—A metadata-driven methodology and workflow process for providing translational research informatics supportJournal of Biomedical Informatics, 2009