What types of information are typically collected during patient registration?

During patient registration, the focus is primarily on gathering essential information that forms the foundation for a patient's record and facilitates their care. Patient demographics, which include details such as name, address, date of birth, and contact information, are crucial for identifying and communicating with the patient.

Insurance details are equally important because they determine the coverage for medical services, help in the billing process, and ensure that the provider can accurately file claims with the insurance company. This includes information about the insurance provider, policy number, and any necessary identification details.

Additionally, collecting medical history is critical as it provides healthcare providers with insight into the patient's past health issues, allergies, medications, and treatments. This information greatly aids in ensuring appropriate and effective care is administered, as it allows for informed clinical decisions and a tailored treatment plan for the patient.

While the other options mention aspects of patient interaction or specific types of insurance, they do not encompass the fundamental elements that are universally captured during the registration process. Patient preferences and lifestyle choices, although relevant, do not form the core dataset required for initial registration, hence making them less standard in this context.