HIPAA Privacy: Leveraging Clinical
System Automation and Workflow Design (Parts 1, 2 and 3)
by Rod Walker, FACHE, FHFMA and Pelvia
Woods, RN
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PAGE 1 |
| Health care organizations are facing the arduous task of redesigning
the operational process associated with patient care in order to
increase compliance with the privacy regulations of HIPAA. While HIPAA
requirements may appear daunting, practical operational solutions can be
achieved by combining a robust clinical system’s application tool set
with a creative workflow design. Given the right tools and a workflow
design process, health care organizations can address HIPAA at each
juncture in the patient encounter cycle, ranging from pre-registration
to the bedside encounter.
Clinical systems contain a tool set that can create or alter system
functionality to better support a health care organization’s operational
processes, such as HIPAA privacy compliance. The key to an
organization’s success in using this approach is to ensure that its
clinical systems tool set is robust and can provide the latitude and
flexibility needed for adapting to new workflow designs.
This article identifies potential operational challenges posed by
HIPAA privacy requirements and presents solutions that can be
constructed through automation toolsets of a computerized patient record
(CPR), and through creative workflow design.
Consent and authorization
How do you capture information during the first patient encounter that
will meet the ongoing operational needs of all departments for HIPAA
compliance?
The answer can be extracted from the HIPAA language. Covered entities
must obtain consents and authorizations in order to authorize the
receipt, use and release of patient identifiable information. While
obtaining consents and authorizations is not new, the unilateral
(national) requirement to obtain authorization before receiving or
acting on it includes the re-disclosure of the information under HIPAA.
This challenge requires providers (covered entities) to develop a
process for addressing consents and authorizations when the patient
enters the organization. It's easy to develop a paper process to comply
with this requirement, but in order to actually improve operational
efficiencies and not create another bureaucratic process, providers must
look to automating application changes and workflow process redesign.
Here's an example of a potential solution. If a CPR or financial
system tool set allows for documentation of all the necessary consents
and authorizations, it can be stored online as part of the patient’s
medical record. If this is done, then the status of each required form
can be accessed for review on an as needed basis. This will improve
confirmations for forms and enable better cycle time for decisions based
on properly obtaining authorizations and consents.
Benefits should be realized in the following operational areas:
- Consents for treatment/payment/health care operations (TPO) can be
documented by registrars at the first encounter and displayed for
business office and medical records personnel who need to confirm
completion of forms before releasing information for TPO purposes.
Furthermore, if a patient specifically requests that his/her
information not be shared with other recipients, the request can also
be documented in the CPR and made available online to medical records
or business office staff without the need for someone to manually pull
the paper chart out of storage. This greatly improves operational
efficiency.
- Procedure-specific authorizations can be documented in the CPR by
nurses and clinicians during the patient intake assessment. This
information can then be accessed online by physicians for confirmation
before performing any medical procedures. Online access improves cycle
time by eliminating delays associated with confirming receipt of
authorizations. Also, designing CPR-based workflow as a standard part
of the patient assessment eliminates errors of omission.
- Missing consents and authorizations will always be a challenge in
health care because there are many ways patients can be admitted or
treated without first obtaining signatures on consents (e.g.,
emergencies and childbirth). When this happens, it is important for
the organization to have a process for identifying patients with
missing signatures. If the forms are documented online, then those
without signatures can be identified. Using automated tool sets can
identify missing patient documents and thereby improve HIPAA
compliance and operational efficiency.
Role-based access to information
How can a CPR be leveraged to ensure that access to patient
information is limited to a defined set of data based on the role of the
employee?
Under HIPAA, covered entities must ensure that access to patient
information is limited to "minimally necessary" information rather than
providing full access to everything without regard to what is needed for
someone to perform their job. This speaks to the role-based design of
information access. With an electronic medical record, it is easy to
store and retrieve information; however, if role-based access is not
included, an organization increases its chances of a privacy breach.
That's why it is important to conduct an operational workflow analysis
to confirm the activities associated with specific personnel so that
they can be assigned appropriate information to access on the CPR.
Once workflow is documented and operational enhancements are made
through process redesign, the CPR’s tool set can then be leveraged. By
creating a hierarchical design for "re-disclosure" from least sensitive
to most sensitive, the tool set can assign security levels for each
definition of information. The security levels can then be assigned to
all employee types in order to ensure that each has an appropriate and
minimally necessary access limit for his/her role. Using employee types
to define security levels, rather than having it customized to the
individual employee, is much more manageable and operationally efficient
for both system deployment and ongoing system management.
Protocol-based release of information
How can an organization ensure that re-disclosure or release of
information conforms to a pre-approved protocol and is also at a
role-based access level?
Under HIPAA, organizations are required to exercise reasonable and
appropriate measures for managing access to and release of information.
While this can be done with most CPR systems, the process can be
strengthened if conducted with a workflow analysis and protocol-based
procedure. This determines what can be released and by whom. The CPR
should be leveraged to manage release of information requests by pushing
requests to the appropriate resources automatically. The result will be
strong HIPAA compliance and operational efficiencies.
For example, if you build a system with defined security levels and
role-based assignments, then you can also use online work queues to
forward information release requests to those with appropriate security
levels. For example, a request for a copy of a discharge summary may be
considered routine or a mid-level sensitivity release may be handled by
the regular record release personnel in the HIM department. By
documenting the request online, it can be labeled with the type of
request for information. It can also be placed in the online work queues
for the HIM staff based on pre-approved protocols. However, if a more
sensitive request is received via court order (e.g., for psychotherapy
notes, which are typically assigned the highest levels of sensitivity
for re-disclosure), that request must be documented. The CPR could
recognize it as a non-routine request and subsequently route it to a
medical records supervisor. The result would require a higher level of
scrutiny and decision-making in responding to the request.
Another consideration comes into play when printing records from a
CPR. If role-based access is tied to security levels and correlates to a
specific printing function, reprinting a medical record can be limited
to a protocol defined by a person's role. This ensures that if a request
for information is erroneously channeled to an inappropriate resource,
then the risk of having that information re-disclosed outside of the
approved protocol is minimized.
Mr. Walker is partner and COO of Negley, Ott & Associates, Inc. of
Savannah, Ga. Previously, he was vice president and CIO at Forrest
General Hospital in Hattiesburg, Miss. Prior to that he was the CIO at
The Emory Clinic in Atlanta.
Ms. Woods is clinical systems consultant at Negley, Ott &
Associates, Inc. of Savannah, Ga. |
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Page 2 |
| In the first installment of this series, we explained the importance
of capturing all patient encounter information to meet the ongoing
operational needs of all departments and to meet the HIPAA requirements.
In this installment, we'll explain how covered entities (health care
providers) can automate the process of obtaining patient signatures for
acknowledging the information management practices of the organization.
Under HIPAA, covered entities must inform patients about the
organization’s information management practices, how they use and
disclose patient information, and how they obtain signatures on consents
or authorizations. While this can be done manually, the use of a
computerized patient record’s (CPR) automation tool set can accurately
and efficiently improve the process. For example, printing an
acknowledgement statement requires consents and/or authorizations at the
end of the registration process to ensure production of the required
forms by the registration staff.
Furthermore, if the patient account (outpatient, inpatient,
psychiatric, lab specimen, etc.) has any bearing on which forms should
be signed, then those specific forms (reports) can be generated based
upon the type of account created during the registration process. Due to
the frequent turnover of registration personnel, it is difficult to
ensure all staff has an accurate understanding of the different types of
forms that need signatures. This process can be automated to minimize
errors. The same concept can also be applied in responding to requests
for information re-disclosures within the medical records department. If
the information being requested is associated with an authorization or
consent, then staff can easily determine if the appropriate forms are
already in the record.
Amendments to patient records
How can an organization ensure a proper response to patient requests for
record amendments within a timely manner?
Under HIPAA, health care providers must process requests and respond
within a specific time frame when patients want to update their records.
While providers do not have to comply with the amendment request, they
must manage the process in a timely manner. Some providers refuse record
amendments for legitimate reasons but must still go through the process
of responding and documenting the response. They must also explain the
reason for not making the record amendment. Using the automation tool
set in a CPR, the provider can document all requests online and route
each to a supervisor for review in the work queue. The supervisor will
determine whether or not to update the chart since this is frequently
considered a non-routine request. By entering the request online with
the date and time it was received, the provider can generate reports to
management personnel.
Accounting for disclosures
How can an organization use the CPR to automate the reporting of
disclosures and comply with HIPAA’s accounting of information release?
Providers must provide an accounting of disclosures for treatment,
payment or health care operations. This means that requests for
information of a patient’s record must be in a format that allows for
subsequent reporting. By using the CPR’s tool set, organizations can
document all requests and disclosures online by type of disclosure. A
demand report can show such releases for a patient's accounting.
An automated accounting approach is more accurate and efficient
because it does not require records to be pulled from storage. All
information access is accomplished via the nearest keyboard.
Restrictions on disclosures
How can an organization use the CPR to help manage restrictions on
release of information to specific individuals or entities?
Providers must also respond to requests from patients to restrict
disclosure of information to specific individuals or entities. While
they do not have to comply with the restriction, if they say they will
comply, then they are legally bound to do so. By using the CPR tool set
to document these restrictions, registration and medical records clerks
can create a record of requests for restrictions.
These requests can automatically be sent to a supervisor in the
medical records department who can determine whether the restrictions
are appropriate. If a patient later removes a restriction, the same
documentation process and online queue can be used for managing the
operational aspects. This process enables the organization to retain an
audit trail of restrictions. Once the restriction is documented, it can
be referenced from any PC or access device without the need to pull a
paper chart.
Mr. Walker is partner and COO of Negley, Ott & Associates, Inc. of
Savannah, Ga. Previously, he was vice president and CIO at Forrest
General Hospital in Hattiesburg, Miss. Prior to that he was the CIO at
The Emory Clinic in Atlanta.
Ms. Woods is clinical systems consultant at Negley, Ott &
Associates. |
|
Page 3 |
| In the first installment of this series, we explained the importance
of capturing all patient encounter information to meet the ongoing
operational needs of all departments and to meet the HIPAA requirements.
In the second installment, we explained how covered entities can
automate the process of obtaining patient signatures for acknowledging
the information management practices of the organization. In this
installment, we'll discuss how a computerized patient record (CPR) can
be used to augment the role of your organization's chief privacy
officer.
Under HIPAA, an organizational privacy officer is the cornerstone to
compliance. In order for the privacy officer to be effective in a CPR
environment, he or she must be able to identify actual or potential
breaches of patient information. This can be achieved if the CPR
provides three basic capabilities:
Chart access audit -- Auditing access to a patient’s record
should be fundamental to a CPR system. You should be able to run a
demand report of all who have accessed the patient’s record.
Furthermore, if this audit report is refined for a specific employee or
patient, then it greatly improves the privacy officer's effectiveness.
Staff assignments -- CPR systems typically have functions that
allow staff to be assigned to a specific patient. When a provider uses
this function, he or she greatly improves the reporting accuracy of
chart access audits. Assigning staff to a specific patient can help
generate audit reports for circumstances where the access was by staff
not assigned to the patient’s care. This refined reporting results in a
more focused audit and improves the operational effectiveness and
efficiency of the privacy officer.
Terminal address access -- The previous two references are
helpful to the privacy officer in identifying unauthorized access to
charts. However, if the CPR does not have this capability or if the
organization does not use its function, then another level of
unauthorized access can occur. Each computer used to access a network
has a logical address. These addresses can be associated with certain
locations such as a nursing unit or a department. The address within a
location can be used in conjunction with the chart access audit to
identify when a device was used to access a patient’s record and was in
a suspicious location (i.e., a location not in the patient care area).
For example, if a computer in the maintenance department is used to
access a patient’s record, then it would be considered suspicious and
the privacy officer should investigate.
Reprinting records
How can an organization identify when a chart has been reprinted in
order to determine if the reprint was for an authorized purpose?
Most CPR systems allow for audit reporting, but this is only
partially helpful in managing the release or re-disclosure process. If a
CPR can print all or part of the record, then an organization should
decide where that function can be used and by which personnel. Most
clinicians using a CPR will want to print a chart on occasion, so it is
necessary to develop a way to audit who has printed from a patient’s
chart. As indicated in the previous section, the CPR can be refined by
using a demand reporting function to recreate the chart or parts of it
in hard-copy format. The reporting function can be built with defined
databases to designate which users or roles can use the function. It can
also limit what can be printed based on the security levels assigned to
the user.
By using data element dependency logic within the reprint function,
notices to the privacy officer can be sent directly for each reprinted
record. This enables the privacy officer to know as soon as a record is
printed. If the reprint function is designed to prompt the user to
document the reason for the printing, then this will enhance the privacy
officer's ability to discern routine (appropriate) reprints from those
who are unauthorized.
Dealing with business associates
How can an organization use the CPR to manage the information release
process when dealing with business associates?
Under HIPAA, providers must secure signed agreements with business
associates that govern the use and disposition of information they share
with their business associates. Because many business associates are
typically added and deleted every day in a health care setting, it's
difficult for admissions staff, business office staff or medical records
staff to keep up with whether they are authorized to re-disclose
information to a business associate. By using the CPR tool set,
organizations can simplify the process. If the list of approved business
associates is maintained in a user-defined database, it can be linked
into the record-reprinting function. By doing this, the approved list of
recipients can be displayed each time a provider responds to a request
for information. That way, no matter how often the list changes, the
clerical staff processing the request need only pull up the list to know
if the recipient is authorized. This eliminates having to type listings
and send them through interoffice mail and prevents the headaches of
wondering whether the staff has the most recent listing.
Improving compliance
Is it really better to use a CPR tool set and workflow re-design
approach to improve means of compliance with HIPAA?
While many health care organizations have already started deploying a
CPR, many still rely on the paper record. HIPAA is coming, but it does
not require a CPR. However, it does stipulate that providers begin to
migrate toward more electronic platforms in order to support EDI, which
is the foundation of anticipated cost savings and one of the primary
reasons for HIPAA.
If an organization has embarked on the CPR journey or plans to do so
soon, IT executives and administrators should evaluate how the CPR can
be leveraged to not only improve operational efficiencies, but also to
demonstrate greater compliance with the regulations. Otherwise, the
organization is likely to maintain two separate and duplicate operating
environments and end up being less efficient operationally once a CPR
system is deployed.
Mr. Walker is partner and COO of Negley, Ott & Associates, Inc. of
Savannah, Ga. Previously, he was vice president and CIO at Forrest
General Hospital in Hattiesburg, Miss. Prior to that he was the CIO at
The Emory Clinic in Atlanta.
Ms. Woods is clinical systems consultant at Negley, Ott &
Associates, Inc. of Savannah, Ga. |
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