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Data Protection: Health

Data Protection: Health . Data Protection & Health Data. Data on physical or mental health or condition or sexual life are ‘sensitive personal data’ with special protection but some leeway for: Processing of Data “kept for statistical or research or other scientific purposes”

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Data Protection: Health

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  1. Data Protection: Health

  2. Data Protection & Health Data • Data on physical or mental health or condition or sexual life are ‘sensitive personal data’ with special protection but some leeway for: • Processing of Data “kept for statistical or research or other scientific purposes” • Processing “necessary for medical purposes”(including medical research) and carried out by a “health professional” or someone who owes an equivalent duty of confidentiality • DP and Medical Ethics mutually reinforcing

  3. What are sensitive data? • Physical or mental health (special work needs?) • Racial origin • Political opinions • Religious or other beliefs • Sexual life • Criminal convictions • Alleged commission of offence • Trade Union membership

  4. Genetic Testing • Disability Act 2005 (Part 4): • Informed consent of data subject required • Prohibited in relation to insurance policies, pensions, and mortgages • Subject to DPC prior approval in relation to employment

  5. Best Practice • Anticipate how you intend to use patient data, fully inform patient and get written consentor • Anonymise the data effectively (DP legislation only applies to data attributable to an identifiable person) before using for research – still best to tell the patient • Specific guidance on www.dataprotection.ie

  6. Health-related Scenarios

  7. Scenario 1 • I am a general practitioner or a hospital consultant: can my locum access my patient records? • Yes. The Data Protection Commissioner’s view is that making clinical patient records available to a locum doctor, so that the locum may provide medical care to patients, is compatible with the purpose for which the GP keeps the patient record.

  8. Scenario 2 • Should my secretary or office manager be allowed access to my patient records? • Yes, although only to the extent necessary to enable the secretary or manager to perform their functions. Non-medical professionals should have no need to access clinical material or medical notes, as distinct from administrative details (such as patients' names and addresses). The patient is entitled to an assurance that their medical information will be treated on a need-to-know basis.

  9. Scenario 3 • What about hospital staff having unrestricted access to all patient data? • Cannot be the position in general. Only appropriate to the extent necessary to enable each discipline to perform their functions. Need to know is the key factor here.

  10. Scenario 4 • Do I need to obtain patients’ explicit permission before storing their medical details on computer? • As a general rule, no. The Commissioner’s view is that the patient’s consent for the storage and use of their personal data is implicit in the fact that they come to you, as a medical professional, for help. However, it is good practice to inform patients that you will keep their details on computer and of what use will be made of their data. You will need to obtain clear consent for uses which might not be obvious to the patient.

  11. Scenario 5 • Can I pass patient details on to another health professional for clinical purposes? • If you are passing patient data on to a person or body acting in an agency capacity for you - such as a clinical laboratory - then this is not a "disclosure" under the Data Protection Act, and the Commissioner does not insist on specific patient consent in such cases. However, you should inform the patient in advance that their data will be used in this way.

  12. Scenario 6 • Can I pass patient details on to another health professional for clinical purposes? • If you are passing the patient data to another health professional for guidance and advice on clinical issues, the patient data should be kept anonymous. If you wish to pass on the full patient data, including identifying details, you should obtain the consent of the patient in advance, except in cases of urgent need.

  13. Scenario 7 • Can I pass patient data to the HSE or other bodies for administrative purposes? • You can pass on anonymised or aggregate data, from which individual patients cannot be identified. Ideally, you should inform patients in advance of such uses of their personal data.

  14. Scenario 8 • What if I need to disclose patient data, and I don't have the time to obtain consent? • If patient details are urgently needed to prevent injury or other damage to the health of a person, then you may disclose the details. Section 8(d) of the Act makes special provision for such disclosures. However, if the reason for the disclosure is not urgent, then you will need to obtain consent in advance.

  15. Scenario 9 • Can I as a consultant or hospital doctor use patient data for research or statistical purposes? • Ideally you should make patients aware in advance if you intend to use their data for your own research purposes. However, the Act provides that such uses of personal data are permitted, even where the patient was not informed in advance, provided that no damage or distress is likely to be caused to the individual.

  16. Scenario 10 • Can I disclose patient data to others for research or statistical purposes? • You may pass on anonymised or aggregate data, from which individual patients cannot be identified. Ideally, you should inform patients in advance of such uses of their personal data. If you wish to pass on personal data, including identifying details, you will need to obtain patient consent in advance.

  17. Scenario 11 • Can I allow external researchers access to patient data for medical research purposes? • You remain responsible for protecting the data and ensuring it is not further disclosed. For your protection, the researchers should be tightly bound by duties of confidentiality. Any data extracted must be anonymised. Patients should be informed.

  18. Scenario 12 • Any exemption for cancer research? • Cancer research and screening is an exception to this rule. Under the Health (Provision of Information) Act, 1997, any person may provide any personal information to the National Cancer Registry Board for the purpose of any of its functions; or to the Minister or any body or agency for the purpose of compiling a list of people who may be invited to participate in an approved cancer screening programme.

  19. Scenario 13 • How can researchers avoid duplication of data in respect of the same individual? • Researchers who obtain anonymised data are sometimes faced with the problem that they may be dealing with two or more data-sets from the same individual. To address this problem, it may be permissible for a data controller to make available anonymous data together with a unique coding, which falls short of actually identifying the individual to the researcher (I.e.a data controller might "code" a unique data-set using a patient’s initials and date-of-birth). The researcher should not be in a position to associate the data-set with an identifiable individual.

  20. Scenario 14 • What about clinical audit, quality improvement, risk management?? • Clinical audit, quality improvement, risk management and governance purposes should be covered by the consent obtained from the patient e.g. Patient Information Leaflet. Personal data should only be processed where necessary for the purpose and if the purpose can be achieved without personal data, for example by anonymisation, then the data should be anonymised. This should generally be possible in respect of purposes such as these.

  21. Scenario 15 • What about patient registers? • Essential for patient treatment, follow -up and service-management? If yes, consent to treatment should incorporate consent to going on the database. On the other hand, if optional – obtain a separate consent. Either way, full information should be given to the patient about the processing. • Privacy Enhancing Technologies and the use of anonymisation/pseudonymisation should be used where possible.

  22. Scenario 16 • What about Insurance companies? Explicit consent needed. GP’s should inform patients of the type of information and possible consequences of data to be disclosed. Patients should be given time to view contents. Should not send notes-only give nature of complaint, treatment offered and outcome. Consultants reports should not be given – can be obtained direct.

  23. Scenario 17 • Do my patients have a right to see their medical data? • Yes they do. An individual is entitled to see a copy of any data which you keep relating to him or her on computer. This right of access is subject to a limited exemption in the case of health and medical records, and in the case of social worker records, where allowing access would be likely to damage the physical, mental or emotional well-being of the individual.

  24. Further Guidance • See www.dataprotection.ie for specific guidance on health-related topics

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