Data, US Health Census, Stats, and more
This area provides data regarding health and healthcare in the United States.
This area provides data regarding health and healthcare in the United States.
Agency for Healthcare Research and Quality (AHRQ) and CDC Health Disparities Report.
This public report of ambulatory surgical center (ASC) quality data has been made possible through the voluntary efforts of participants in the ASC Quality Collaboration. The following organizations agreed to collect and submit clinical quality data reflecting patient admissions* from January 1, 2016 through March 31, 2016: Ambulatory Surgery Center Association; Ambulatory Surgical Centers of America (ASCOA); AmSurg; ASD Management; Covenant Surgical Partners; HCA Ambulatory Surgery Division; Practice Partners in Healthcare, Inc; Regent Surgical Health, Surgical Care Affiliates (SCA); Surgery Partners-Symbion; United Surgical Partners International (USPI) and Visionary Enterprises, Inc. This quarter's data has been collected from 1,527 ASCs -- including 999 multispecialty ASCs and 528 single specialty ASCs -- representing every state.
This report presents aggregated performance data for ASC facility-level quality measures developed by the ASC Quality Collaboration
For more than 20 years, the Dartmouth Atlas Project has documented glaring variations in how medical resources are distributed and used in the United States. The project uses Medicare data to provide information and analysis about national, regional, and local markets, as well as hospitals and their affiliated physicians. This research has helped policymakers, the media, health care analysts and others improve their understanding of our health care system and forms the foundation for many of the ongoing efforts to improve health and health systems across America.
The FastStats site provides quick access to statistics on topics of public health importance and is organized alphabetically. Links are provided to publications that include the statistics presented, to sources of more data, and to related web pages.
Per HCUP - The Healthcare Cost and Utilization Project (HCUP) is a family of healthcare databases and related software tools and products developed through a Federal-State-Industry partnership and sponsored by the Agency for Healthcare Research and Quality (AHRQ). HCUP databases bring together the data collection efforts of State data organizations, hospital associations, private data organizations, and the Federal government to create a national information resource of encounter-level health care data (HCUP Partners). HCUP includes the largest collection of longitudinal hospital care data in the United States, with all-payer, encounter-level information beginning in 1988. These databases enable research on a broad range of health policy issues, including cost and quality of health services, medical practice patterns, access to health care programs, and outcomes of treatments at the national, State, and local market levels.
Per HealthyPeople.gov - DATA2020, the Healthy People 2020 interactive data tool, allows users to explore the data and technical information related to the Healthy People 2020 objectives.
Consumer Assessment of Healthcare Providers and Systems (CAHPS) surveys ask consumers and patients to report on and evaluate their experiences with health care. These surveys cover topics that are important to consumers and focus on aspects of quality that consumers are best qualified to assess, such as the communication skills of providers and ease of access to health care services.
Per Hospital Consumer Assessment of Healthcare Providers and Systems (HCAHPS) - HCAHPS On-Line, the official HCAHPS Web site, houses a series of tables that summarize current and historic HCAHPS results. These HCAHPS Tables, available exclusively on HCAHPS On-Line, are based on the HCAHPS data participating hospitals submit to CMS.
Below is a link to the Summary Analysis and Tables of State scores.
Per National Amyotrophic Lateral Sclerosis (ALS) Registry - ATSDR - Amyotrophic lateral sclerosis (ALS), sometimes called Lou Gehrig's disease, is a progressive disease that attacks the nerve cells that control voluntary movement. The National ALS Registry is a congressionally mandated registry for persons in the U.S. with ALS. It is the only population-based registry in the U.S. that collects information to help scientists learn more about who gets ALS and its causes.
Choose category or choose location. Select a State
Substance Abuse and Mental Health Services Administration SAMHSA - Data - A-Z Index
Trip is a clinical search engine designed to allow users to quickly and easily find and use high-quality research evidence to support their practice and/or care.
US Health stats - 2015 - publications and trends in health statistics.
This is an online data of the Division of Vital Statistics, including both interactive online data access tools and downloadable public use data files