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Releasing information in healthcare: Who, what, when, where & why

Releasing information in healthcare: Who, what, when, where & why

The Health Insurance Portability and Accountability Act (HIPAA) imposes stringent confidentiality regulations on medical professionals. However, there are specific situations where they are legally permitted or required to release patient information. Circumstances that allow a medical professional to release information vary depending on who is releasing the information, what information is being released, when it is being released, and where it is being released

 

The release of information

The HHS Enforcement Highlights page reveals that, since the compliance date of the Privacy Rule in April 2003, the agency has received more than 358,975 complaints alleging violations of HIPAA, initiated over 1,188 compliance reviews, and resolved 356,075 (98%) of the cases. Of those 358,975 complaints, more than 246,929 have been rejected because “the complaint did not present an eligible case for enforcement.” The most common reasons for complaints being rejected were:

  • The alleged privacy violation was by an entity not covered by HIPAA.
  • The complaint was withdrawn or submitted after the 180-day limit.
  • The activity described was not a health information privacy violation.

So, what circumstances allow a medical professional to release information?

 

Who can release the information?

Different healthcare professionals may be authorized to release patient information based on their roles and responsibilities within the healthcare system. This can include:

  • Physicians and specialists: They might release information for treatment purposes or when referring patients to other healthcare providers.
  • Nurses and allied health professionals: They may share information necessary for the continuity of care within their scope of practice.
  • Administrative staff: They often handle information for billing, payment, and operational purposes, ensuring compliance with healthcare regulations.

 

What information can be released?

The type of information that can be released varies depending on the circumstances and legal requirements. Here are some common scenarios:

  • Patient consent: When a patient provides explicit written consent, healthcare professionals can release the specified information, which might include medical records, test results, treatment plans, and personal health information (PHI).
  • Treatment, payment, and healthcare operations (TPO):
    • Treatment: Medical history, diagnosis, test results, and medications can be shared for coordination of care.
    • Payment: Information required for billing and payment processes, including insurance details and records of services provided.
    • Healthcare operations: Data used for quality assessment, internal audits, business planning, and fraud detection.
  • Public health activities: Identifiable health information related to disease control, immunization records, and data on adverse reactions to medications or devices can be released to public health authorities.
  • Legal requirements: Specific conditions or events must be reported, such as suspected abuse or neglect, injuries related to criminal activity, and other legally mandated disclosures.
  • Judicial and administrative proceedings: In response to a court order or subpoena, healthcare professionals may need to release medical records, testimonies, or other relevant documentation.
  • Law enforcement purposes: Limited identifying information, details about injuries related to crimes, and compliance with legal orders can be shared with law enforcement officials.
  • Research: With IRB approval or patient consent, de-identified health information or specific data necessary for research can be released.
  • Organ and tissue donation: Medical history and compatibility information can be shared with donation organizations.
  • Coroners, medical examiners, and funeral directors: Information necessary to identify a deceased person or determine the cause of death can be released.
  • Essential government functions: Health information related to military activities, national security, and public officials' protection can be disclosed.
  • Workers’ compensation: Details of work-related injuries or illnesses necessary to process compensation claims can be released.
  • Imminent threats: Information necessary to prevent or mitigate serious and imminent threats to health or safety can be disclosed.

 

The Minimum Necessary Rule

The Minimum Necessary Rule is a fundamental principle under HIPAA that mandates healthcare professionals to make reasonable efforts to disclose only the minimum amount of PHI necessary to achieve the intended purpose of the use, disclosure, or request. This rule applies to all forms of PHI disclosure, whether for treatment, payment, healthcare operations, or other permissible reasons. The goal is to protect patient privacy by ensuring that sensitive information is not unnecessarily exposed or shared. 

See also: A guide to HIPAA's minimum necessary standard

 

When can information be released?

Timing is critical when it comes to releasing patient information. Information should only be released when:

  • Proper authorization is obtained: Ensure that valid patient consent or legal authorization is in place.
  • Immediate need: For treatment purposes, during emergencies, or when public health or safety is at risk.
  • Legal compliance: When required by law, such as mandatory reporting of certain conditions or in response to legal orders.

 

Where can information be released?

The location or entity to which information is released is also a determining factor:

  • To other healthcare providers: For treatment continuity and specialist consultations.
  • To insurance companies: For payment and billing purposes.
  • To public health authorities: For disease control and public health monitoring.
  • To legal entities: In compliance with court orders, subpoenas, or law enforcement requests.
  • To research institutions: For approved research projects with proper safeguards.
  • To donation organizations: For organ and tissue donation processes

 

FAQs

What should be included in a patient’s consent form for releasing information?

A patient’s consent form for releasing information should include:

  • A clear description of the information to be released.
  • The purpose of the disclosure.
  • The entities or individuals to whom the information will be disclosed.
  • The duration for which the consent is valid.
  • The patient’s signature and the date of consent.
  • A statement informing the patient of their right to revoke consent at any time.

 

How can healthcare professionals ensure that only the minimum necessary information is disclosed?

To ensure minimal disclosure, healthcare professionals should meticulously review each specific request for information, providing only the details directly relevant to the request. Implementing role-based access controls is essential to limit access and disclosure of patient information to authorized personnel only. Utilizing checklists and SOPs can also guide staff in adhering to the minimum necessary standards for different types of disclosures. Regularly auditing disclosures helps verify compliance with the minimum necessary rule, ensuring that patient privacy is consistently maintained.