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1.
International Journal of Prisoner Health ; 19(2):143-156, 2023.
Article in English | ProQuest Central | ID: covidwho-2314964

ABSTRACT

PurposeThis study aims to estimate the overall SARS-CoV-2 seroprevalence and evaluate the accuracy of an antibody rapid test compared to a reference serological assay during a COVID-19 outbreak in a prison complex housing over 13,000 prisoners in Brasília.Design/methodology/approachThe authors obtained a randomized, stratified representative sample of each prison unit and conducted a repeated serosurvey among prisoners between June and July 2020, using a lateral-flow immunochromatographic assay (LFIA). Samples were also retested using a chemiluminescence enzyme immunoassay (CLIA) to compare SARS-CoV-2 seroprevalence and 21-days incidence, as well as to estimate the overall infection fatality rate (IFR) and determine the diagnostic accuracy of the LFIA test.FindingsThis study identified 485 eligible individuals and enrolled 460 participants. Baseline and 21-days follow-up seroprevalence were estimated at 52.0% (95% CI 44.9–59.0) and 56.7% (95% CI 48.2–65.3) with LFIA;and 80.7% (95% CI 74.1–87.3) and 81.1% (95% CI 74.4–87.8) with CLIA, with an overall IFR of 0.02%. There were 78.2% (95% CI 66.7–89.7) symptomatic individuals among the positive cases. Sensitivity and specificity of LFIA were estimated at 43.4% and 83.3% for IgM;46.5% and 91.5% for IgG;and 59.1% and 77.3% for combined tests.Originality/valueThe authors found high seroprevalence of anti-SARS-CoV-2 antibodies within the prison complex. The occurrence of asymptomatic infection highlights the importance of periodic mass testing in addition to case-finding of symptomatic individuals;however, the field performance of LFIA tests should be validated. This study recommends that vaccination strategies consider the inclusion of prisoners and prison staff in priority groups.

2.
researchsquare; 2022.
Preprint in English | PREPRINT-RESEARCHSQUARE | ID: ppzbmed-10.21203.rs.3.rs-1499014.v1

ABSTRACT

Purpose There is evidence that humans can transmit SARS-CoV-2 to cats and dogs. However, there is no evidence that they can transmit it back to humans or play any role in SARS-CoV-2 transmission. Here, we present an exploratory analysis on that matter.Methods We conducted a case control study with participants with flu-like symptoms seeking care at a primary healthcare unit to be tested for COVID-19. They were asked if they owned pet cats and/or dogs in their residences, and this variable was evaluated as exposure.Results The odds ratio of “having dogs and/or cats in the residence” was 1.29 (95%CI 1.08–1.54) of “having only dogs and no cats” was 1.26 (1.05–1.52), and “no dogs and only cats” was 1.29 (0.95–1.75).Conclusion Having a cat/dog in the house can affect the risk of infection by SARS-CoV-2.


Subject(s)
COVID-19
3.
ssrn; 2021.
Preprint in English | PREPRINT-SSRN | ID: ppzbmed-10.2139.ssrn.3898505

ABSTRACT

Summary: The pandemic of COVID-19 has presented as a threat to prison systems worldwide, as overcrowding, limited possibility of social distancing and sanitary restrictions favouring viral spread. SARS-CoV-2 seroprevalence studies in prison settings are important tools to understand transmission and to develop control measures. We aimed to estimate the overall SARS-CoV-2 seroprevalence and evaluated the accuracy of an antibody rapid test compared to a reference serological assay during a COVID-19 outbreak in a prison complex housing over 13,000 inmates in Brasília. Methods: We conducted a repeated serosurvey of IgM/IgG SARS-CoV-2 antibodies among inmates between June 17-July 1 (baseline) and July 8-22, 2020 (21-days follow-up). We obtained a randomized, stratified representative sample of each prison unit. Inmates who accepted to be part of the study were interviewed through a standardised questionnaire covering sociodemographic and clinical characteristics. Blood samples were collected from each participant for the evaluation of SARS-CoV-2 antibodies with a lateral-flow immunochromatographic assay (LFIA). Inmates with negative results in the first serosurvey were interviewed and tested for a second time to evaluate recent symptoms history and serological status 21 days later. Samples were also retested using a chemiluminescence enzyme immunoassay (CLIA) to compare SARS-CoV-2 seroprevalence and 21-days incidence, as well as to estimate the overall infection fatality rate (IFR) and determine the diagnostic accuracy of the LFIA test.Findings: We identified 485 eligible individuals and enrolled 460 participants (94.8%), distributed across four prison units. Baseline and 21-days follow-up seroprevalence were estimated at 52.0% (95%CI 44.9-59.0) and 56.7% (95%CI 48.2-65.3) with the LFIA test; and 80.7% (95%CI 74.1-87.3) and 81.1% (95%CI 74.4-87.8) with the CLIA test, with an overall IFR of 0.02%. There were 78.2% (95%CI 66.7-89.7) symptomatic inmates among the positive cases, and the main symptoms included changes in taste or smell, headache, and fever. Sensitivity and specificity of LFIA test were estimated at 43.4% and 83.3% for IgM; 46.5% and 91.5% for IgG; and 59.1% and 77.3% for combined tests. There was a fair agreement between LFIA and CLIA results (Kappa score 0.23).Interpretation: We found rapid viral spread and high seroprevalence of anti-SARS-CoV-2 antibodies within the prison complex. The occurrence of asymptomatic infection highlights the importance of periodic mass testing in addition to case-finding of symptomatic inmates, however the field performance of LFIA tests should be validated. We recommend that vaccination strategies consider the inclusion of persons deprived of liberty and prison staff in priority groups.Funding: EN, GASR, RH, WNA acknowledge the Brazilian Ministry of Education (MEC) for support the COVID-19 response by University of Brasília (#23106.028855/2020-74). RH, WMR and WNA acknowledge the Federal District Research Foundation (FAP-DF) for grants that supported this research (# 00193-00000495/2020-72). GASR, JHC, WMR, WNA acknowledge the National Research Council (CNPq) for grants that supported this research (# 402957/2020-2)Declaration of Interest: None to declare. Ethical Approval: The study was part of an epidemiological investigation conducted by the Brazilian Field Epidemiology Training Program/Ministry of Health as a response to a public health emergency, and it is supported by the national law 8.080/1990. Moreover, all participants provided informed consent and ethics approval was obtained under the CONEP protocol number 37007220.1.0000.0008.


Subject(s)
COVID-19 , Fever
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