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Health Information Exchange is the process of electronic sharing of health-related information among organizations. Ethical importance: promotes efficiency and safety in patient care, requires secure data transfer, and respects patient consent.

Predictive Analytics in Healthcare uses historical and real-time data to forecast potential future outcomes for patients. Ethical importance: improves preventive care, but raises fair use concerns about data and necessitates transparency.

Telemedicine is the delivery of health care services through telecommunications technologies. Ethical importance: provides access to care for remote patients, necessitates secure communication channels, and ensures informed consent.

De-identification of Data refers to the process of removing or modifying personal information from health records to protect patient privacy. Ethical importance: essential for patient anonymity in data sharing and research, prevents unauthorized use of data.

An Electronic Health Record is a digital version of a patient's paper chart, containing a more comprehensive patient history. Ethical importance: ensures accuracy and integrity of patient information, protects confidentiality, and improves care quality.

Informed Consent in E-Health is the process of educating and obtaining permission from patients before using digital tools in their care. Ethical importance: empowers patients to make educated decisions, respects patient autonomy, and prevents coercion.