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AAMC/UHC - Convergent Validity: A forum for AMC’s to Discuss HIPAA
Implementation
The Convergent Validity HIPAA Forum was a great success. Thanks
to all of the members that participated and contributed to the process.
Your assistance in identifying issues, providing solutions and willingness
to share your experience has started the collaborative process off
in the best possible way.
Materials from the meeting are available at http://www.aamc.org/members/gir/hipaa/forum/start.htm
After a great deal of discussion and sharing, the result of the
meeting was that we identified five work groups to address questions
in specific areas. We are working on a very short turnaround- the
work groups need to respond to the questions by December 15 so that
we can then circulate the results to the members for comment. The
final summary will be completed by January 30th.
To move us to this next phase we are now seeking volunteers to
participate in these work groups.
The following are the work groups, their co-chairs, and date of
the first conference call.
** If you are interested in participating in one of the work
groups please send me an email and I will forward the call information
to you. (limited space, first-come basis)**
Workgroup 1: Operations And Implementation Risk
[Conference Call: Dec 2, 12:30 - 1:30 Pm Est]
Co-Chairs:
Maria J. Pekar, M.B.A.
Director, Corporate Compliance
Loyola University Health System |
Joe Schlesinger, Sr.
Manager, HIMS
Stanford Hospital & Clinics |
- Operations:
- Identifying/Operationalizing Restrictions & confidential
communications Restrictions-policy that gives pt rights
to restrictions; Stanford has a form that explains rights
to restriction, including facility opt out and clergy, explains
process and what we will not allow as restriction. Fundraising;
alias allowed; restriction on phone calls; VIP, social stigma,
victims of crime/abuse;
- Determining the Scope of the DRS - DRS-attorneys view
DRS as all information needed to make decision about care
vs. operational view that this is what patient should be
allowed to access, copy, amend. Need solution for the tension.
Policy: anything outside of medical record is duplicative.
- Determining what constitutions the Mental Health DRS -
Psychotherapy notes-what is sufficient protection to provide
for "separately held": In maintenance of notes
in confidential documents with restricted access and restricted
access policy sufficient to satisfy the "separately
held" requirement-in the electronic environment? Separately
held would allow psych note to be eligible for special protections.
- Operationalizing the Family Members "Safe-Harbor"
-Individuals involved in care-professional judgment. Notice
advises that if there are individuals you don't want us
to give information to, you must specifically tell us, otherwise
we assume part of family.
- OHCA-what is clinically integrated enough or not for purposes
of using a joint Notice-e.g. faculty private practices?
- Implementation Risks
- Operationalizing Patient Rights - Patient Rights-once
HIPAA implemented that will be source of complaints; plaintiff
lawyers will see this as litigation opportunity
- Identifying Disclosures That Need to Be Accounted/Operationalizing
the Accounting Process -Accounting of disclosures-employees
must account for those in central data base; developing
a web-based tool where the division is responsible for accounting
for disclosure and a designee may do so (i.e., does not
have to be the direct treatment provider)
- Generating Buy-In Tactics -Privacy at the institutional
level-risk if the departments and faculty and workforce
don't take these to heart and comply
- Identifying BAs for reasons other than TPO; decedents;
- Discuss Shadow records-1) must have inventory of and
track shadow records; or 2) audited and if don't meet audit
requirements, no longer use shadow records; and 3) no disclosures
from shadow records
- Identifying Best-Training Practices - Training-link the
regulation to policy and procedures to training to performance;
continual cycle; is there an IT solution (Tier Track); everyone
has Basic Training and specialized tiers; web-based augmented
by stand-up training
- Combine w/f - Breadth and depth of HIPAA Training--what
is reasonable? How much can you demand of people? Is there
a web-based AHC solution? New staff will be trained during
new employee orientation? Temporary and registry staff?
- Combine w/b - Accounting for: BA for reasons other than
TPO; decedents; public health; victim of abuse, neglect;
health oversight unless law enforcement unless judicial
and administrative proceed; victim of crime; crime on premises;
crime in emergency; research not authorized; avert serious
threat to h & S; military/vets; president; admin of
pub benefit program; worker's comp; any identified non-routine
disclosure
Workgroup 2: Education of the Workforce
[Conference Call: Nov 27, 1:00 -2:00 Pm Est]
Co-Chairs:
Regina Kilkenny, Ph.D.
Assistant Dean
University of Colorado School of Medicine |
Elizabeth D. Winter
Associate General Counsel
University of Utah Health Sciences Center |
- Workforce scope-non-CE students; visiting professors; VIPs;
guests; vendor reps.
- Volunteer Faculty-those who come to the CE and involved in
teaching: they would be HIPAA trained and a part of the workforce;
no BA
- Volunteer Faculty-when our students go into small community
offices with the 1-year delay; we would have to accept the delay;
volunteer faculty may object to student placement if they have
to go through HIPAA training-solution: provide the community
volunteer faculty with the CE's training modules and other HIPAA
materials
- Business associate agreements with those who come into the
CE for teaching: amend current teaching affiliation or clinical
teaching agreements to recognize the function-no BA
- Consequences/sanctions/penalties for those who do not complete
training on time
Workgroup 3: Teaching/Operations
[Conference Call: Dec. 6, 2:00 -3:00 Pm Est]
Co-Chairs:
Maria Faer, M.P.H.
Director of HIPAA and Corporate Compliance
University of California
Office of the President |
Joanne Koterwas
HIPAA Project Manager
Stony Brook University Hospital and Medical Center |
- Resident eligibility to sit for specialty boards and certification-solutions:
a) make this a part of operations; b) ACGME make part of board
requirements to accept certification from privacy officer or
other institutional official so PHI not given to board; : work
with the Boards to change their requirements to allow for Dean
or other official certifying that student has provided records
to CE; work with the AAMC to take the lead for us; look at what
the regs say under operations/#2-can we interpret the language
stating "credentialing" as operations
- Students who are from non-covered entities: can we use Data
Use Agreement or BAA?
Workgroup 4: Institutional Advancement (development,
fundraising, media, marketing, and communications)
[Conference Call: Dec 3, 3:00 -4:00 Pm Est]
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Co-Chairs:
Nancy Dent
Director of Development
University of Texas Health Science Center at San Antonio
Khawar Ali Khan
Acting Director
Annual Giving
University of Pennsylvania
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Craig K. Matthews
Director, Development Marketing
University of California, San Francisco
Martha M. Chase
University Counsel
University of California
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- Authorization-how and at what point
- Physician/provider team can sign on chart that he had spoken
with the patient, then DO can go to patient and get authorization
- Can individuals or groups of individuals be identified for
fundraising lists by department, division, provider without
authorization
- Existing data bases-scrub PHI if can't get authorization;
future data bases get authorization
Workgroup #5: Research
[Conference Call: Dec 3, 4:00 - 5:00 Pm Est]
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Co-Chairs:
Lawrence H. Muhlbaier
specialized tiers; web-based augment
Assistant Research Professor
Duke University Medical Center
Karen Blackwell, M.S.
Director, HIPAA Compliance
University of Kansas Medical Center
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James A. Moran
Executive Director
Research Integrity & Compliance
University of Pennsylvania |
- Is research a part of the covered entity?
- If yes, how have you defined "research"-by
function, individual, site?
- What are advantages and disadvantages?
- Can we reach consensus that AHCs will require research sponsors
to include confidentiality language in contracts so that we
can provide individuals with some level of assurance that PHI
will not be redisclosed?
- Research data bases: Post April 2003
- Who "holds" the data bases-the CE, the faculty
provider, the researcher? How do you locate all data bases
in a CE?
- What are the risks of faculty data bases? What is best
legal protection?
- How do you create
- What are the permissible uses for the data bases
- How does the researcher access data base
- When does researcher need IRB or Privacy Board? When
not
- Recruitment-when a researcher/provider does not have a treatment
relationship to the individual, you can not approach the individual
to participate in the study without individual's authorization.
Time sensitive research studies-e.g., neonates-how can we implement
the contact with the individual in a timely manner? Solution:
Treatment team or someone expected to know the situation may
contact the patient representative
- Common criterion for IRBs to use to access privacy risks;
develop list for routine uses and disclosures and MNS for non-routine
uses and disclosures; define Teaching; define Research
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