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Community Counts Data Reports

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Data Reports: Available to the Public

The purpose of the data reports listed below is to make available the information collected through the Community Counts project to care providers, public health workers, community advocates, health educators and planners, patients in the bleeding disorders community, and others.

The reports will summarize the following information about Community Counts participants:

  • Demographics (for example race, age, sex, insurance status)
  • Blood and factor product use
  • Bleeding events and complications
  • Inhibitor development
  • Occurrence and treatment of joint and infectious diseases
  • Diseases that occur as a result of aging, and conditions that often occur along with bleeding disorders
  • Use of health services
  • Treatment practices and patterns
  • Treatment-related complications
  • Mortality

Data reports are currently under development. Available reports are listed below.

Community Counts: The HTC Population Profile Data through March 31, 2017 »
The HTC Population Profile is a set of twelve data items collected on patients with bleeding disorders or venous thromboembolism. Updated data tables describing patient characteristics from the HTC Population Profile through March 31st, 2017 are available in this report. Data tables are categorized by annual patient characteristics, factor VIII & factor IX, von Willebrand disease, rare factor deficiencies, platelet disorders and other disorders.

Community Counts: The HTC Population Profile Data through December 31, 2016 »
The HTC Population Profile is a set of twelve data items collected on patients with bleeding disorders or venous thromboembolism. Updated data tables describing patient characteristics from the HTC Population Profile through December 31st, 2016 are available in this report. Data tables are categorized by annual patient characteristics, factor VIII & factor IX, von Willebrand disease and rare factor deficiencies.

Community Counts: The HTC Population Profile Data through September 30, 2016 »
The HTC Population Profile is a set of twelve data items collected on patients with bleeding disorders or venous thromboembolism. Updated data tables describing patient characteristics from the HTC Population Profile through September 30th, 2016 are available in this report. Data tables are categorized by annual patient characteristics, factor VIII & factor IX, von Willebrand disease and rare factor deficiencies.

Community Counts: The HTC Population Profile Data through June 30, 2016 »

Community Counts: The HTC Population Profile Data through March 31, 2016 »

Community Counts: The HTC Population Profile Data through September 30, 2014 »

Learn more about Community Counts »

Browse data reports from Universal Data Collection System »

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