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Name ___Date of Birth ___You are being referred to Oklahoma Cancer Specialists and Research Institute for Cascade testing. Cascade testing is the performance of genetic risk counseling and testing
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How to fill out cascade genetic risk education
How to fill out cascade genetic risk education
01
Identify individuals with a known genetic mutation that increases cancer risk.
02
Offer genetic testing to family members of the affected individuals.
03
Educate family members about the implications of the genetic mutation and their risk of developing cancer.
04
Provide options for increased surveillance, risk-reducing strategies, or preventive measures.
05
Encourage family members to cascade the information to other at-risk relatives.
Who needs cascade genetic risk education?
01
Individuals with a known genetic mutation that increases cancer risk.
02
Family members of individuals with a known genetic mutation.
03
Healthcare providers involved in cancer risk assessment and management.
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What is cascade genetic risk education?
Cascade genetic risk education is a process of educating individuals and their family members about their genetic risk for a particular disease or condition, and the steps that can be taken to manage that risk.
Who is required to file cascade genetic risk education?
Healthcare providers who have identified a genetic risk in a patient are required to file cascade genetic risk education for the patient and their family members.
How to fill out cascade genetic risk education?
Healthcare providers can fill out cascade genetic risk education by documenting the genetic risk information, recommended actions, and educational materials provided to the patient and their family members.
What is the purpose of cascade genetic risk education?
The purpose of cascade genetic risk education is to empower individuals and their family members to make informed decisions about their health based on their genetic risk information.
What information must be reported on cascade genetic risk education?
Cascade genetic risk education must include the genetic risk information, recommended actions, and educational materials provided to the patient and their family members.
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