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HIPAA and RESEARCH 101

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Photos. 04/06/03. HIPAA & Research 101. 3. HIPAA Research Requirements. for ... When annual Continuing Review is due a revised informed consent incorporating ... – PowerPoint PPT presentation

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Title: HIPAA and RESEARCH 101


1
HIPAA and RESEARCH101
2
What is Protected Health Information (PHI)?
  • Name
  • Address
  • Telephone Number
  • Fax Number
  • Email Address
  • Date of Birth
  • Social Security Number
  • Medical Record Number
  • Account numbers
  • Diagnosis
  • Test results
  • Dates of Treatment
  • Vehicle ID numbers
  • Device ID numbers
  • Biometrics
  • Photos

3
HIPAA Research Requirements for Using/Disclosing
PHI
  • Specific Authorization
  • Signed by patient/patient representative.
  • Projects approved after 4/13/03 Authorization to
    be incorporated into the research informed
    consent.
  • See Informed Consent Guidelines with HIPAA
    Language.
  • Projects approved before 4/13/03 use stand alone
    Authorization.
  • See Authorization to Release PHI for Research
    Purposes.
  • At Continuing Review revise consent to include
    HIPAA language.
  • Researcher must save for 6 years.
  • Waiver of Authorization
  • PI must submit a Request for Waiver of
    Authorization.
  • Waiver must be approved and signed by the IRB.
  • PI must save for 6 years.

4
Exceptions to HIPAA Authorization or WaiverIf
the Research falls into one of the following 4
categories, it does not require HIPAAA review by
the IRB, however, it still requires IRB review
and approval
  • De-Indentified PHI
  • PHI used to develop a research proposal
  • PHI of Deceased Individuals
  • Limited Data Set

5
1. DE-IDENTIFIED PHI
  • Limited identifiers may remain if, even in
    combination, the identifiers could not
    realistically be traced to an individual patient.
  • Example zip code and date of admission/service
  • Submit proposal for IRB review and approval.

6
2. PHI Used Preparatory to Research
  • PHI can not be removed from covered entity
    (Childrens).
  • PI must submit a Data Collection for Review
    Preparatory to Research form to the IRB with
    proposal for review and approval.

7
3. PHI of Deceased Individuals
  • PI must submit a Research on Decedents
    Information form to the IRB with proposal for
    review and approval.

8
4. Limited Data Set There must be a Data Use
Agreement between Childrens and the recipient
of the Limited Data Set
  • A Limited Data Set may include
  • Town, city, state and zip code.
  • Elements of dates directly related to an
    individual including
  • Birth Date
  • Admission Date
  • Discharge Date
  • Date of Death
  • A Limited Data Set must exclude
  • Direct identifiers of the individual or their
    relatives, employers, or household members.
  • Name
  • Address (other than town, city, state,zip code)
  • Telephone and/or Fax numbers
  • Email address
  • Social Security Number
  • Medical Record Number
  • Health Plan numbers
  • Account Numbers
  • Certificate/Licenses numbers
  • Vehicle Identifiers
  • Device Identifers
  • Biometric Identifiers
  • Full face photos
  • Any other number, characteristic or code that
    could be used to identify the individual

9
How can you be HIPAA Compliant?
  • IRB approval before 4/13/03
  • Patients enrolled after 4/13/03 must sign an
    Authorization to Release PHI for Research
    Purposes.
  • See Authorization to Release Protected Health
    Information for Research Purposes.
  • When annual Continuing Review is due a revised
    informed consent incorporating HIPAA language
    must be reviewed and approved by the IRB.
  • IRB approval after 4/13/03
  • Informed Consent with HIPAA language must be
    reviewed and approved by the IRB.
  • IRB approval after 10/31/03
  • Informed Consent and Stand Alone Authorization
    must be reviewed and approved by the IRB.

10
DATA BASES CONTAINING PHI
  • For Clinical Purposes only
  • No IRB Requirement
  • For Research Purposes
  • Submit proposal to IRB for review and approval
    with Informed Consent containing HIPAA language
  • OR
  • Submit proposal to IRB for review and approval
    with Request for Waiver of Authorization and
    waiver of informed consent.
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