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Confidentiality
Genetic and other shared information
Confidentiality guidance: Genetic and other shared information
67. Genetic and some other information about your patient might at the same time also be information about others the patient shares genetic or other links with. The diagnosis of an illness in the patient might, for example, point to the certainty or likelihood of the same illness in a blood relative.
68. Most patients will readily share information about their own health with their children and other relatives, particularly if they are advised that it might help those relatives to:
(a) get prophylaxis or other preventative treatments or interventions
(b) make use of increased surveillance or other investigations, or
(c) prepare for potential health problems.
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69. However, a patient might refuse to consent to the disclosure of information that would benefit others, for example where family relationships have broken down, or if their natural children have been adopted. In these circumstances, disclosure might still be justified in the public interest (
see paragraphs 36 to 56
). If a patient refuses consent to disclosure, you will need to balance your duty to make the care of your patient your first concern against your duty to help protect the other person from serious harm. If practicable, you should not disclose the patient’s identity in contacting and advising others of the risks they face.
Sharing information with a patient's partner, carers, relatives or friends
Disclosure after a patient's death
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Supplementary guidance
The Review of Good Medical Practice
Good Medical Practice
List of ethical guidance
Protecting children and young people
0-18 years
Accountability in Multi-disciplinary and Multi-Agency Mental Health Teams
Taking up and ending appointments
Making and using visual and audio recordings of patients
Confidentiality
Contents
About this guidance
Principles
Protecting information
Disclosures required by law
Disclosing information with consent
The public interest
Disclosures about patients who lack capacity to consent
Sharing information with a patient's partner, carers, relatives or friends
Genetic and other shared information
Disclosure after a patient's death
Supplementary information
Learning materials
Conflicts of interest
Consent guidance
End of life care
Maintaining boundaries
Research guidance
Leadership and management for all doctors (2012)
Personal beliefs and medical practice
Good practice in prescribing medicines (2008)
Good practice in prescribing and managing medicines and devices (2013)
Raising and acting on concerns about patient safety (2012)
Writing references (2012)
Reporting criminal and regulatory proceedings within and outside the UK
Duties of a doctor
Remote prescribing via telephone, fax, video-link or online
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