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Results Found: 13
  • Atherosclerosis Risk in Community Study

    Alternate Title(s)
    ARIC
    Description

    The Atherosclerosis Risk in Communities Study is a prospective epidemiological study conducted in four U.S. communities. ARIC is designed to investigate the causes of atherosclerosis and its clinical outcomes, and variations in cardiovascular risk factors, medical care, and disease by race, gender, location, and date. ARIC consists of two parts: a Cohort Component and a Community Surveillance Component. Data includes physiological data about participants, health history, dietary history, medication history, ECG data, demographic details, and administrative data.

    Subject
    Delivery of Health Care
    Population Characteristics
    Quality of Health Care
    Risk Factors
    Geographic Coverage
    Multiple States
    Access Rights
    Fee Required
    Application Required
    Local Expert for NYU
    Saul Blecker
  • Women's Health Initiative

    Alternate Title(s)
    WHI
    Description

    The Women's Health Initiative (WHI) is a long-term national health study that focuses on strategies for preventing heart disease, breast cancer, colorectal cancer, and osteoporotic fractures in postmenopausal women. The study includes data from 161,808 women aged 50-79. Datasets include information on demographics, diet, medical and physical measurements, medical history, outcomes (both adjudicated and self-reported), psychological habits, social habits, personal habits, genotypes, and specimen results.

    Subject
    Cancer
    Chronic Disease
    Health Status
    Geographic Coverage
    National
    Access Rights
    Application Required
    Local Expert for NYU
    Caroline Blaum
    Jeffrey Berger
    Lila Nachtigall
  • Framingham Heart Study

    Alternate Title(s)
    FHS
    Authors
    Vasan S. Ramachandran
    Emelia J. Benjamin
    L. Adrienne Cupples
    R. Curtis Ellison
    7 more author(s)...
    Description

    The Framingham Heart Study (FHS) is dedicated to identifying common factors or characteristics that contribute to cardiovascular disease (CVD). In 1948, an original cohort of 5,209 men and women between 30 and 62 years old were recruited from Framingham, MA. An Offspring Cohort began in 1971, an Omni Cohort in 1994, a Third Generation Cohort in 2002, a New Offspring Spouse Cohort in 2004 and a Second Generation Omni Cohort in 2003. Core research in the dataset focuses on cardiovascular and cerebrovascular diseases. The data include biological specimens, molecular genetic data, phenotype data, samples, images, participant vascular functioning data, physiological data, demographic data, and ECG data.It is a collaborative project of the National Heart, Lung and Blood Institute and Boston University.

    Subject
    Population Characteristics
    Risk Factors
    Geographic Coverage
    Other Regions
    Access Rights
    Fee Required
    Free to all with registration
    Application Required
    Local Expert for NYU
    Niyati Parekh
    Yixin Fang
  • American College of Cardiology National Cardiovascular Data Registry ACTION: NYU Langone Submission
    NYU Dataset

    Alternate Title(s)
    ACC - NCDR ACTION
    Description

    This dataset is the NYU Langone submission to the ACC NCDR ACTION registry.The American College of Cardiology National Cardiovascular Data Registry (ACC NCDR) ACTION registry focuses on high risk STEMI/NSTEMI patient demographics. The registry takes in demographics, provider and facility characteristics, adverse event rates, AMI performance measures, quality measures, test measures, dosing errors, risk-adjusted metrics, transfer facility therapies, reperfusion strategies, ACC/AHA guideline adherence, and registry performance award data.

    NYU Langone Health ceased participation in this program in 2017. Legacy data, up to February 2017, is still available.

    Subject
    Delivery of Health Care
    Population Characteristics
    Quality of Health Care
    Geographic Coverage
    New York (City)
    Access Rights
    Application Required
    NYU Langone Health Only
    Local Expert for NYU
    Matthew Farrell
  • Jackson Heart Study

    Alternate Title(s)
    JHS
    Description

    The Jackson Heart Study (JHS) is a population-based longitudinal study based in Jackson, Mississippi that investigates cardiovascular disease among African Americans, including congenital heart disease, strokes, and high blood pressure. The primary objective is to investigate cardiovascular disease in African Americans in order to better address health disparities. The JHS is a community-based observational study of 5306 participants, all of whom are African American adults from urban and rural areas of the Jackson, MS metropolitan statistical area. It is a collaborative research project by the University of Mississippi Medical Center, Jackson State University, and Tougaloo College.

    Subject
    Chronic Disease
    Population Characteristics
    Geographic Coverage
    Other Regions
    Access Rights
    Free to All
    Application Required
    Local Expert for NYU
    Tanya Spruill
  • Effects of recombinant human erythropoietin on platelet activation in acute myocardial infarction
    NYU Dataset

    Authors
    Yi-Da Tang
    Faisal Hasan
    Frank J. Giordano
    Stephen Pfau
    2 more author(s)...
    Description

    This dataset was collected as part of a double-blind, placebo-controlled, randomized clinical trial to determine the effects of intravenous rHuEpo (200U/kg daily for three consecutive days) on measures of platelet and endothelial cell activation, soluble Fas ligand, and peripheral blood mononuclear cell (PBMC) expression of angiogenesis signaling proteins. The study included 44 adults over 21 years of age with ST-segment elevation myocardial infarction (electrocardiographic changes with elevated cardiac enzymes and/or compatible history), treated with successful percutaneous coronary intervention of the culprit lesion (postprocedure Thrombolysis in Myocardial Infarction grade 3 flow), and clinically indicated aspirin (325 mg daily) and clopidogrel therapy (300- to 600- loading dose determined by the attending cardiologist). The subjects were randomized to received intravenous rHuEpo (200U/kg daily for three consecutive days) or matching placebo. The primary safety outcome variables were bleeding time and platelet function assay (PFA) closure time and were determined before the first dose of the study drug, immediately after the dose of the study drug, and 7 days after the last dose. Additional variables collected include soluble P-selectin, von Willebrand factor, complete blood count, and vital signs.

    Subject
    Chronic Disease
    Health Status
    Access Rights
    Application Required
    Author approval required
  • Stroke Warning Information and Faster Treatment Study
    NYU Dataset

    Alternate Title(s)
    SWIFT
    Authors
    Bernadette Boden-Albala
    Joshua Stillman
    Thania Perez
    Laura Evensen
    5 more author(s)...
    Description

    This dataset was generated during the Stroke Warning Information and Faster Treatment (SWIFT) Study. The study aimed to determine the efficacy of a culturally tailed interactive stroke preparedness strategy for acute ischemic stroke (IS) and transient ischemic attack (TIA) patients.

    Patients were included in the study if they had a diagnosis of IS or TIA, were over 19 years old and lived in a household with a telephone. Patients were excluded if they were unable to give informed consent, were discharged to a long term nursing home or requiring 24-hour care, or had a modified Rankin score over 4 at baseline, have severe aphasia limiting comprehension, have a pre-stroke dementia history, or have end-stage disease.

    Variables collected include demographic information, the time between symptom onset and ED arrival, knowledge and attitudes about strokes, and risk factors.

    Subject
    Chronic Disease
    Delivery of Health Care
    Risk Factors
    Geographic Coverage
    New York (City)
    Access Rights
    Application Required
    Author approval required
  • Society of Thoracic Surgeons Adult Cardiac Surgery Registry: NYU Langone Submission
    NYU Dataset

    Alternate Title(s)
    STS Adult Cardiac Surgery
    Description

    This dataset is the NYU Langone submission to the STS Adult Cardiac Surgery registry.The Society of Thoracic Surgeons (STS) Adult Cardiac Surgery Database is a registry of over five million cardiac surgery procedure records and takes in data from over 3,000 surgeons. Collected data includes assessments of patient care, quarterly performance outcomes, anesthesiology quality data, atrial fibrillation data, outcomes analysis, composite measures and risk profiles.

    Subject
    Delivery of Health Care
    Quality of Health Care
    Geographic Coverage
    New York (City)
    Access Rights
    Application Required
    NYU Langone Health Only
    Local Expert for NYU
    Matthew Farrell
  • New York State Department of Health Adult Cardiac Surgery: NYU Langone Submission
    NYU Dataset

    Alternate Title(s)
    NYS DOH Adult Cardiac Surgery
    Description

    This dataset is the NYU Langone submission to the NYS DOH Adult Cardiac Surgery registry.The New York State Department of Health Adult Cardiac Surgery (NYS DOH Adult Cardiac Surgery) registry collects data on risk factors associated with death following coronary artery bypass graft surgery (CABG) and heart valve surgery. The registry also includes data on hospital and physician-specific mortality rates. Data on demographics, clinical characteristics and risk factors are collected.

    Subject
    Delivery of Health Care
    Quality of Health Care
    Risk Factors
    Geographic Coverage
    New York (City)
    Access Rights
    Application Required
    NYU Langone Health Only
  • FAMiLI Study (Food And Microbiome Longitudinal Investigation): NYU Langone Health EHR
    NYU Dataset

    Description

    This dataset was compiled as part of the FAMiLI Study, a study to improve the understanding how the roles of the human microbiome, specifical bacteria in the mouth and gut, and diet are related to various diseases, including cancer, heart disease, and diabetes. The FAMiLI study aims to build a diverse cohort of 15,000 individuals over 5 years. The dataset includes information used to identify individuals who meet the study eligibility requirements, including name, date of birth, address, gender, race, ethnicity, contact information, and preferred language.

    Subject
    Electronic Health Records
    Geographic Coverage
    New York (City)
    Access Rights
    Application Required
    NYU Langone Health Only
    Local Expert for NYU
    Jiyoung Ahn