ATHNdataset Registry

Participants who agree to participate will let their health information be included in the ATHNdataset Registry, and the information will be updated regularly to reflect the participant's current health status. This registry includes collecting, storing and managing health information through a secure database. The following health information will be collected:

• Demographics (e.g., age, gender, income, education/occupation)
• The type of blood disorder you have
• Date you were diagnosed, or symptoms began
• Family history of the disorder
• Testing and assessments
• Physical exams
• Height, weight
• Vital signs, including blood pressure and heart rate
• Laboratory tests (results from blood or urine testing, or biological specimens)
• Genetic test results
• Imaging results (X-rays, CT scans, etc.)
• Pharmacokinetic testing results (how drugs are processed in the body)
• Medications used and any problems with use
• Types of bleeds, pain and clotting problems
• Treatments that stop your bleeding or clotting problems from occurring or getting worse
• Surgeries and/or procedures
• Immunizations (vaccines)
• Devices
• Routine care visits and injuries (trauma)
• Other illnesses and diseases you may have
• Allergies
• Patient-reported outcomes (PROs), questionnaires, and surveys
• Payment details for treatment, including insurance companies and health plans

Inclusion criteria

• Any participant evaluated for or the potential to have a blood disorder who has an encounter with an ATHN Affiliate.
• Participants of any age.
• Participant is able to provide consent or assent; a Legally Authorized Representative (LAR) may provide consent on a participant's behalf if a participant is unable to provide self-consent

Exclusion criteria

• Any participant unable to provide consent or assent to participate in the ATHNdataset