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This informed consent form outlines the participation requirements, risks, and benefits associated with the COLLATERAL Study, which investigates transit time flow measurement in coronary surgery and the relationship of collateral flow among different coronary territories.
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How to fill out collateral - informed consent

01
Begin with a clear title stating 'Collateral Informed Consent'.
02
Provide a brief introduction explaining the purpose of collateral consent.
03
Include a section to identify the participant and their relationship to the client.
04
Describe the nature of the overlap and the information to be shared.
05
Outline the potential risks and benefits of sharing this information.
06
Get clear consent from the participant by providing a statement for them to agree to.
07
Include a section for the date, signature of the participant, and signature of the professional.
08
Ensure that the individual knows they can withdraw consent at any time.

Who needs collateral - informed consent?

01
Individuals who are involved in a client's treatment but are not the primary client need collateral-informed consent.
02
Mental health professionals sharing information with family members for care coordination.
03
Clinicians working in multidisciplinary teams where communication about the client is necessary.
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Collateral - informed consent refers to the permission obtained from a patient to share their health information with third parties, ensuring that the patient is aware of and agrees to the disclosure.
Typically, healthcare providers or professionals who are involved in the patient's care and need to share the patient's information with other entities such as family members, insurers, or other healthcare providers are required to file collateral - informed consent.
To fill out collateral - informed consent, one should provide clear and accurate information about the patient, specify the entities with whom information will be shared, describe the purpose of the disclosure, and obtain the patient's signature to confirm their agreement.
The purpose of collateral - informed consent is to protect patient privacy while allowing necessary information sharing, ensuring that patients are aware of who will have access to their medical information and for what purpose.
Information that must be reported on collateral - informed consent includes the patient's name and details, the specific information to be shared, the names of the individuals or organizations receiving the information, the purpose of the disclosure, and the time frame for which consent is granted.
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