• In circumstances where there is no information available to populate one or more of the
fields previously listed, either because the MIPS eligible clinicians can be excluded from
recording such information or because there is no information to record (for example, no
medication allergies or laboratory tests), the MIPS eligible clinician may have an indication
that the information is not available and still meet the objective and its associated measure.
• The patient must be able to access this information on demand, such as through a patient
portal or personal health record (PHR) or by other online electronic means. We note that
while a covered entity may be able to fully satisfy a patient's request for information through
VDT, the measure does not replace the covered entity's responsibilities to meet the broader
requirements under HIPAA to provide an individual, upon request, with access to PHI in a
designated record set.
• MIPS eligible clinicians should also be aware that while the measure is limited to the
capabilities of CEHRT to provide online access, there may be patients who cannot access
their EHRs electronically because of a disability. MIPS eligible clinicians who are covered by
civil rights laws must provide individuals with disabilities equal access to information and
appropriate auxiliary aids and services as provided in the applicable statutes and
regulations.
• For the measure, MIPS eligible clinicians must offer all four functionalities (view, download,
transmit, and access through API) to their patients. Patient health information needs to be
made available to each patient for view, download, and transmit within 4 business days of
the information being available to the clinician for each and every time that information is
generated whether the patient has been "enrolled" for three months or for three years.
• A patient who has multiple encounters during the performance period, or even in
subsequent performance periods in future years, needs to be provided access for each
encounter where they are seen by the MIPS eligible clinician.
• If a patient elects to "opt out" of participation, that patient must still be included in the
denominator.
• If a patient elects to “opt out” of participation, the MIPS eligible clinician may count that
patient in the numerator if the patient is provided all of the necessary information to
subsequently access their information, obtain access through a patient-authorized
representative, or otherwise opt-back-in without further follow up action required by the
clinician.
• The MIPS eligible clinician must continue to update the information accessible to the patient
each time new information is available.
• For view, download, and transmit functionality, the required content is:
o United States Core Data for Interoperability (USCDI)
(https://www.healthit.gov/isa/united-states-core-data-interoperability-uscdi)
o Provider's name and office contact information.
o Laboratory test report(s).
o Diagnostic image report(s).
• For API functionality the required data set is the USCDI (https://www.healthit.gov/isa/united-
states-core-data-interoperability-uscdi)