NOTE: This dataset has been retired and marked as historical-only. Only Chicago residents are included based on the home ZIP Code as provided by the medical provider. If a ZIP was missing or was not valid, it is displayed as "Unknown". Cases with a positive molecular (PCR) or antigen test are included in this dataset. Cases are counted based on the week the test specimen was collected. For privacy reasons, until a ZIP Code reaches five cumulative cases, both the weekly and cumulative case counts will be blank. Therefore, summing the “Cases - Weekly” column is not a reliable way to determine case totals. Deaths are those that have occurred among cases based on the week of death. For tests, each test is counted once, based on the week the test specimen was collected. Tests performed prior to 3/1/2020 are not included. Test counts include multiple tests for the same person (a change made on 10/29/2020). PCR and antigen tests reported to Chicago Department of Public Health (CDPH) through electronic lab reporting are included. Electronic lab reporting has taken time to onboard and testing availability has shifted over time, so these counts are likely an underestimate of community infection. The “Percent Tested Positive” columns are calculated by dividing the number of positive tests by the number of total tests . Because of the data limitations for the Tests columns, such as persons being tested multiple times as a requirement for employment, these percentages may vary in either direction from the actual disease prevalence in the ZIP Code. All data are provisional and subject to change. Information is updated as additional details are received. To compare ZIP Codes to Chicago Community Areas, please see http://data.cmap.illinois.gov/opendata/uploads/CKAN/NONCENSUS/ADMINISTRATIVE_POLITICAL_BOUNDARIES/CCAzip.pdf. Both ZIP Codes and Community Areas are also geographic datasets on this data portal. Data Source: Illinois National Electronic Disease Surveillance System, Cook County Medical Examiner’s Office, Illinois Vital Records, American Community Survey (2018)
Tazewell County COVID-19 Dashboard
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United States COVID-19: No. of Deaths: To Date: Illinois data was reported at 42,005.000 Person in 10 May 2023. This stayed constant from the previous number of 42,005.000 Person for 09 May 2023. United States COVID-19: No. of Deaths: To Date: Illinois data is updated daily, averaging 27,061.000 Person from Jan 2020 (Median) to 10 May 2023, with 1205 observations. The data reached an all-time high of 42,005.000 Person in 10 May 2023 and a record low of 0.000 Person in 16 Mar 2020. United States COVID-19: No. of Deaths: To Date: Illinois data remains active status in CEIC and is reported by Illinois Department of Public Health. The data is categorized under High Frequency Database’s Disease Outbreaks – Table US.D001: Center for Disease Control and Prevention: Coronavirus Disease 2019 (COVID-2019).
NOTE: This dataset has been retired and marked as historical-only.
This dataset is a companion to the COVID-19 Daily Cases and Deaths dataset (https://data.cityofchicago.org/d/naz8-j4nc). The major difference in this dataset is that the case, death, and hospitalization corresponding rates per 100,000 population are not those for the single date indicated. They are rolling averages for the seven-day period ending on that date. This rolling average is used to account for fluctuations that may occur in the data, such as fewer cases being reported on weekends, and small numbers. The intent is to give a more representative view of the ongoing COVID-19 experience, less affected by what is essentially noise in the data.
All rates are per 100,000 population in the indicated group, or Chicago, as a whole, for “Total” columns.
Only Chicago residents are included based on the home address as provided by the medical provider.
Cases with a positive molecular (PCR) or antigen test are included in this dataset. Cases are counted based on the date the test specimen was collected. Deaths among cases are aggregated by day of death. Hospitalizations are reported by date of first hospital admission. Demographic data are based on what is reported by medical providers or collected by CDPH during follow-up investigation.
Denominators are from the U.S. Census Bureau American Community Survey 1-year estimate for 2018 and can be seen in the Citywide, 2018 row of the Chicago Population Counts dataset (https://data.cityofchicago.org/d/85cm-7uqa).
All data are provisional and subject to change. Information is updated as additional details are received and it is, in fact, very common for recent dates to be incomplete and to be updated as time goes on. At any given time, this dataset reflects cases and deaths currently known to CDPH.
Numbers in this dataset may differ from other public sources due to definitions of COVID-19-related cases and deaths, sources used, how cases and deaths are associated to a specific date, and similar factors.
Data Source: Illinois National Electronic Disease Surveillance System, Cook County Medical Examiner’s Office, U.S. Census Bureau American Community Survey
NOTE: This dataset is no longer being updated but is being kept for historical reference. For current data on respiratory illness visits and respiratory laboratory testing data please see Influenza, COVID-19, RSV, and Other Respiratory Virus Laboratory Surveillance and Inpatient, Emergency Department, and Outpatient Visits for Respiratory Illnesses.
This is the place to look for important information about how to use this dataset, so please expand this box and read on!
This is the source data for some of the metrics available at https://www.chicago.gov/city/en/sites/covid-19/home/reopening-chicago.html#reopeningmetrics.
For all datasets related to COVID-19, see https://data.cityofchicago.org/browse?limitTo=datasets&sortBy=alpha&tags=covid-19.
The National Syndromic Surveillance Program (NSSP), a collaboration among CDC, federal partners, local and state health departments, and academic and private sector partners, is used to capture information during an Emergency Department (ED) visit. ED data can include information that are collected before cases are diagnosed or laboratory results are confirmed, providing an early warning system for infections, like COVID-19.
This dataset includes reports of COVID-19-Like illness (CLI) and COVID-19 diagnosed during an ED visit. CLI is defined as fever and cough or shortness of breath or difficulty breathing with or without the presence of a coronavirus diagnosis code. Visits meeting the CLI definition that also have mention of flu or influenza are excluded.
This dataset also includes ED visits among persons who have been diagnosed or laboratory confirmed to have COVID-19. During the initial months of the COVID-19 pandemic COVID-19 diagnoses counts are artificially low, due to varying eligibility requirements and availability of testing.
Over the course of the COVID-19 pandemic, public health best practices migrated from focusing on CLI to focusing on diagnosed cases. This dataset originally contained only CLI columns. In June 2021, the diagnosis columns were added, back filled to the start of the pandemic but with the caveat noted above. Roughly simultaneously, updating of the CLI columns was discontinued, although previously existing data were kept. Reflecting the new columns, the name of the dataset was changed from “COVID-Like Illness (CLI) Emergency Department Visits” to “COVID-Like Illness (CLI) and COVID-19 Diagnosis Emergency Department Visits” at the same time.
Data Source: Illinois Hospital Emergency Departments reporting to CDPH through the National Syndromic Surveillance Project (NSSP)
31.5.2023: נוספה טבלה חדשה - נבדקים על פי סטטוס חיסוני. טבלה זו מציגה את הנבדקים על פי תאריכים וקטגוריות גיל וכמו כן, על פי הסטטוס החיסוני של הנבדקים. בנוסף, עודכנה טבלת המאומתים. 17.5.2023: עודכנה טבלת המחלימים עם מספר מנות החיסון טרם המחלה הראשונה 3.5.2023: נעשו עידכונים בטבלאות הבאות: - טבלת נפטרים - התווספה עמודה המציינת את מספר מנות החיסון שהתקבלו טרם הפטירה. - טבלת גילאי המתחסנים - התווספה עמודה המכילה נתונים על מנת חיסון חמישית בקרב בני 18 - טבלת האוכלוסייה הצעירה - התווספה עמודה מנה רביעית אנא קראו היטב את קבצי ה- readme הרלוונטיים המתארים את השינויים בטבלאות. 25.1.2022 - מעתה יפורסמו רק טבלת הישובים וטבלת האזורים הסטטיסטיים לפני השימוש במאגר, יש לקרוא את COVID-19.PDF ו-DISCLAIMER.PDF. יש בקבצי ה-README מידע חיוני, שיעזור בהבנת הנתונים. צוות תמנ"ע במשרד הבריאות ישמח לשמוע על התובנות שלכם בכתובת מייל המחבר שמופיע בתחתית העמוד.
Discover the latest resources, maps and information about the coronavirus (COVID-19) outbreak in your community
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Introduction: The spread of Coronavirus Disease 2019 (COVID-19) across the United States has highlighted the long-standing nationwide health inequalities with socioeconomically challenged communities experiencing a higher burden of the disease. We assessed the impact of neighborhood socioeconomic characteristics on the COVID-19 prevalence across seven selected states (i.e., Arizona, Florida, Illinois, Maryland, North Carolina, South Carolina, and Virginia).Methods: We obtained cumulative COVID-19 cases reported at the neighborhood aggregation level by Departments of Health in selected states on two dates (May 3rd, 2020, and May 30th, 2020) and assessed the correlation between the COVID-19 prevalence and neighborhood characteristics. We developed Area Deprivation Index (ADI), a composite measure to rank neighborhoods by their socioeconomic characteristics, using the 2018 US Census American Community Survey. The higher ADI rank represented more disadvantaged neighborhoods.Results: After controlling for age, gender, and the square mileage of each community we identified Zip-codes with higher ADI (more disadvantaged neighborhoods) in Illinois and Maryland had higher COVID-19 prevalence comparing to zip-codes across the country and in the same state with lower ADI (less disadvantaged neighborhoods) using data on May 3rd. We detected the same pattern across all states except for Florida and Virginia using data on May 30th, 2020.Conclusion: Our study provides evidence that not all Americans are at equal risk for COVID-19. Socioeconomic characteristics of communities appear to be associated with their COVID-19 susceptibility, at least among those study states with high rates of disease.
Discover the latest resources, maps and information about the coronavirus (COVID-19) outbreak in your community
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Il set di dati contiene gli ultimi dati pubblici disponibili sul COVID-19, tra cui un aggiornamento quotidiano sulla situazione, la curva epidemiologica e la distribuzione geografica globale (UE/SEE e Regno Unito, in tutto il mondo). Il 12 febbraio 2020 il nuovo coronavirus è stato denominato sindrome respiratoria acuta grave da coronavirus 2 (SARS-CoV-2), mentre la malattia ad esso associata è ora denominata COVID-19. L'ECDC sta monitorando da vicino l'epidemia e fornisce valutazioni dei rischi per guidare gli Stati membri dell'UE e la Commissione europea nelle loro attività di risposta.
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Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infects both people and animals and may cause significant respiratory problems, including lung illness: Corona Virus Disease 2019 (COVID-19). Swabs taken from the throat and nose of people who have the illness or are suspected of having it have shown this pathogenic virus. When SARS-CoV-2 infects the upper and lower respiratory tracts, it may induce moderate to severe respiratory symptoms, as well as the release of pro-inflammatory cytokines including interleukin 6 (IL-6). COVID-19-induced reduction of IL-6 in an inflammatory state may have a hitherto undiscovered therapeutic impact. Many inflammatory disorders, including viral infections, has been found to be regulated by IL-6. In individuals with COVID-19, one of the primary inflammatory agents that causes inflammatory storm is IL-6. It promotes the inflammatory response of virus infection, including the virus infection caused by SARS-CoV-2, and provides a new diagnostic and therapeutic strategy. In this review article, we highlighted the functions of IL-6 in the coronavirus, especially in COVID-19, showing that IL-6 activation plays an important function in the progression of coronavirus and is a rational therapeutic goal for inflammation aimed at coronavirus.
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Knowledge graph extracted from 14,229 papers and 6217 abstracts from the CORD-19 Dataset. Data taken from the University of Illinois Urbana-Champaign with permission from the authors: Qingyun Wang (UIUC), Heng Ji (UIUC), Jiawei Han (UIUC), Shih-Fu Chang (Columbia), Kyunghyun Cho (NYU)
The Knowledge Graph follows the ontology introduced in the Comparative Toxicogenomics Database. It's comprised of 50,752 Gene nodes, 10,781 Disease nodes, 5,738 Chemical nodes, and 535 Organism nodes. These nodes are connected by 133 relation types including Gene–Chemical–Interaction Relationships, Chemical–Disease Associations, Gene–Disease Associations, Chemical–GO Enrichment Associations and Chemical–Pathway Enrichment Associations. Entities also play some certain roles in 13 Event types, including Gene expression, Transcription, Localization, Protein catabolism , Binding, Protein modification, Phosphorylation , Ubiquitination, Acetylation, Deacetylation, Regulation, Positive regulation, Negative regulation.
This work was created by Qingyun Wang (UIUC), Heng Ji (UIUC), Jiawei Han (UIUC), Shih-Fu Chang (Columbia), Kyunghyun Cho (NYU)
Their research is based upon work supported in part by U.S. DARPA KAIROS Program No. FA8750-19-2-1004, U.S. DARPA AIDA Program # FA8750-18-2-0014 and U.S. NSF No. 1741634. The views and conclusions contained herein are those of the authors and should not be interpreted as necessarily representing the official policies, either expressed or implied, of DARPA, or the U.S. Government. The U.S. Government is authorized to reproduce and distribute reprints for governmental purposes notwithstanding any copyright annotation therein.
As of March 10, 2023, the state with the highest number of COVID-19 cases was California. Almost 104 million cases have been reported across the United States, with the states of California, Texas, and Florida reporting the highest numbers.
From an epidemic to a pandemic The World Health Organization declared the COVID-19 outbreak a pandemic on March 11, 2020. The term pandemic refers to multiple outbreaks of an infectious illness threatening multiple parts of the world at the same time. When the transmission is this widespread, it can no longer be traced back to the country where it originated. The number of COVID-19 cases worldwide has now reached over 669 million.
The symptoms and those who are most at risk Most people who contract the virus will suffer only mild symptoms, such as a cough, a cold, or a high temperature. However, in more severe cases, the infection can cause breathing difficulties and even pneumonia. Those at higher risk include older persons and people with pre-existing medical conditions, including diabetes, heart disease, and lung disease. People aged 85 years and older have accounted for around 27 percent of all COVID-19 deaths in the United States, although this age group makes up just two percent of the U.S. population
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BackgroundMany COVID-19 patients reveal a marked decrease in their lymphocyte counts, a condition that translates clinically into immunodepression and is common among these patients. Outcomes for infected patients vary depending on their lymphocytopenia status, especially their T-cell counts. Patients are more likely to recover when lymphocytopenia is resolved. When lymphocytopenia persists, severe complications can develop and often lead to death. Similarly, IL-10 concentration is elevated in severe COVID-19 cases and may be associated with the depression observed in T-cell counts. Accordingly, this systematic review and meta-analysis aims to analyze T-cell subsets and IL-10 levels among COVID-19 patients. Understanding the underlying mechanisms of the immunodepression observed in COVID-19, and its consequences, may enable early identification of disease severity and reduction of overall morbidity and mortality.MethodsA systematic search was conducted covering PubMed MEDLINE, Scopus, Web of Science, and EBSCO databases for journal articles published from December 1, 2019 to March 14, 2021. In addition, we reviewed bibliographies of relevant reviews and the medRxiv preprint server for eligible studies. Our search covered published studies reporting laboratory parameters for T-cell subsets (CD4/CD8) and IL-10 among confirmed COVID-19 patients. Six authors carried out the process of data screening, extraction, and quality assessment independently. The DerSimonian-Laird random-effect model was performed for this meta-analysis, and the standardized mean difference (SMD) and 95% confidence interval (CI) were calculated for each parameter.ResultsA total of 52 studies from 11 countries across 3 continents were included in this study. Compared with mild and survivor COVID-19 cases, severe and non-survivor cases had lower counts of CD4/CD8 T-cells and higher levels of IL-10.ConclusionOur findings reveal that the level of CD4/CD8 T-cells and IL-10 are reliable predictors of severity and mortality in COVID-19 patients. The study protocol is registered with the International Prospective Register of Systematic Reviews (PROSPERO); registration number CRD42020218918.Systematic Review Registrationhttps://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42020218918, identifier: CRD42020218918.
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This dataset is used in the analyses reported in the review entitled "Interleukin (IL)-1 blocking agents for the treatment of COVID-19 A living systematic review"
IL-1 blockers are beneficial in inflammation-associated pathologies, such as rheumatoid arthritis (Mertens 2009) and possibly also in the subgroup of patients with severe sepsis where the inflammasome pathway is involved (Shakoory 2016). Similar benefits were reported in children with secondary macrophage activation syndrome, including cases triggered by viral infections (Mehta 2020b).
In this review we aimed to assess the effectiveness of IL-1 blocking agents compared to placebo, standard of care or no treatment on outcomes in patients with COVID-19.
This review is part of a larger project: the COVID-NMA project. We set-up a platform (https://covid-nma.com) where all our results are made available and updated bi-weekly.
The dataset analyses the impact of the COVID-19 pandemic in Romania.
The dataset contains 4 columns: * date - the date of each record, starting from 26 February 2020 * cases - the cumulative number of cases reported each day, in the first days of the pandemic there were multiple press releases about the number of cases, but the sum per day is already aggregated * recovered - the cumulative number of recovered cases * deaths - the cumulative number of deaths * tests - number of tests performed by the date, for the dates with no information, the difference split equally in that interval
This data was collected from: * https://en.wikipedia.org/wiki/2020_coronavirus_pandemic_in_Romania * https://www.digi24.ro/stiri/actualitate/informatii-oficiale-despre-coronavirus-in-romania-1266261 * https://stirioficiale.ro/informatii
Other great data souces: * http://www.ms.ro/comunicate/ * http://www.cnscbt.ro/ * https://instnsp.maps.arcgis.com/apps/opsdashboard/index.html#/5eced796595b4ee585bcdba03e30c127
Thank you for the photo: * https://playtech.ro/stiri/o-minciuna-despre-coronavirus-il-va-costa-ani-grei-de-inchisoare-ce-a-facut-un-barbat-din-campia-turzii-95782
Thanks, https://www.kaggle.com/bjoernjostein/corona-virus-in-norway!
Ce tableau de bord fournit une mise à jour quotidienne de la progression du Coronavirus COVID-19 en France (Métropole et DOM).Il se base sur les données publiées quotidiennement par Santé Publique France.Il comptabilise et représente :Le nombre de cas confirmés au niveau nationalLe nombre de décès au niveau nationalLe nombre de cas confirmés par région (sous forme de graphique et de carte par symboles proportionnels)La part des cas confirmés par rapport à la population, par région (sous forme de carte par dégradé de couleurs)L'évolution dans le temps du nombre de cas confirmés (sous forme de graphique) Il est optimisé pour être affiché sur un navigateur web (ordinateur ou tablette).Il fournit également un lien vers le tableau de bord national en version optimisée pour mobile.Visiter le site Esri France
As of March 10, 2023, the death rate from COVID-19 in the state of New York was 397 per 100,000 people. New York is one of the states with the highest number of COVID-19 cases.
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"SARS-CoV-2 general corpus" includes Italian newspaper articles published in the timespan between January 1, 2020 and June 15, 2020, containing at least one of the following terms: [covid, corona virus, OR coronavirus]. Sources: Corriere della Sera, La Repubblica, Il Sole – 24 Ore, La Stampa, Avvenire, Il Giornale, Il Mattino di Napoli, Il Messaggero.
NOTE: This dataset has been retired and marked as historical-only. Only Chicago residents are included based on the home ZIP Code as provided by the medical provider. If a ZIP was missing or was not valid, it is displayed as "Unknown". Cases with a positive molecular (PCR) or antigen test are included in this dataset. Cases are counted based on the week the test specimen was collected. For privacy reasons, until a ZIP Code reaches five cumulative cases, both the weekly and cumulative case counts will be blank. Therefore, summing the “Cases - Weekly” column is not a reliable way to determine case totals. Deaths are those that have occurred among cases based on the week of death. For tests, each test is counted once, based on the week the test specimen was collected. Tests performed prior to 3/1/2020 are not included. Test counts include multiple tests for the same person (a change made on 10/29/2020). PCR and antigen tests reported to Chicago Department of Public Health (CDPH) through electronic lab reporting are included. Electronic lab reporting has taken time to onboard and testing availability has shifted over time, so these counts are likely an underestimate of community infection. The “Percent Tested Positive” columns are calculated by dividing the number of positive tests by the number of total tests . Because of the data limitations for the Tests columns, such as persons being tested multiple times as a requirement for employment, these percentages may vary in either direction from the actual disease prevalence in the ZIP Code. All data are provisional and subject to change. Information is updated as additional details are received. To compare ZIP Codes to Chicago Community Areas, please see http://data.cmap.illinois.gov/opendata/uploads/CKAN/NONCENSUS/ADMINISTRATIVE_POLITICAL_BOUNDARIES/CCAzip.pdf. Both ZIP Codes and Community Areas are also geographic datasets on this data portal. Data Source: Illinois National Electronic Disease Surveillance System, Cook County Medical Examiner’s Office, Illinois Vital Records, American Community Survey (2018)