FMOLHS OLOL Physician Group Zielinski 'lemondropped' Medicaid beneficiary in COVID PHE defying Federal, State, Local Involuntary Disenrollment Moratoria Act for any reason--Blackballed and Dismissed and Denied Treatment by 2 more providers, while never offered Due Process or Appeal - Medical Record Locked - Ignored in Silence Never Contacted by ANY physician, administrator, nor executive (including my cousin) I was Referred for Cancer Biopsy - I thought I MIGHT receive Care: After 1 week No Contact I have Appointment ... in 1 month--FOR CANCER
Continuity
of medication between mental health
providers (MHPs) and primary care providers (PCPs) after a new consultation
bMedication
groups: hypnotic-benzodiazepine, alprazolam, buspirone, clonazepam,
diazepam, lorazepam, triazolam, zaleplon, and zolpidem; dementia
medications, donepezil, rivastigmine, and memantine; antidepressants,
amitriptyline, bupropion, citalopram, doxepin, duloxetine, escitalopram,
fluoxetine, mirtazapine, nortriptyline, paroxetine, sertraline,
trazodone, and venlafaxine; antipsychotic and related, aripiprazole,
benztropine, haloperidol, olanzapine, perphenazine, quetiapine,
risperidone, thiothixene, and ziprasidone Appealing Treatment and
Reimbursement Denials Appeal Strategies The APA recommends the
following: 1.
Request and review a copy of the MCO’s appeals procedures and utilization review (UR) criteria before initiating any appeals.
2.
Ask for the case manager’s credentials.
Denials of psychiatrists services should be made only by psychiatrists.
3.
Request written notification of the reasons for denial and a description of the information required for approval.
This will ensure that subsequent submissions “fit the bill.” 4.
Request
names and addresses of the people who should receive applications for
an appeal and find out the MCO’s deadline for appeals.
5.
Meet all UR and appeal deadlines.
If you do not, the merits of your case may not matter.
Certification denials due to “administrative noncompliance” are rarely overturned.
If
the case is denied on an administrative basis (i e , a request for
continued certification was not made within the specified time,
precertification procedures were not followed, or there were benefit
coverage exclusions), you’ll need to explain any extenuating
circumstances in your appeal.
6.
If your appeal is denied, appeal again.
Many companies offer three or four levels of appeal.
It is advisable to exhaust all levels of appeal before initiating litigation, should you be forced to proceed that way.
7.
Be concise.
Don’t send more information than necessary and be sure to get permission from your patient to release that information.
8.
Request peer review with a psychiatrist trained in the same subspecialty who has experience in the treatment requested.
9.
In an emergency situation, request an “expedited appeal” over the telephone with the consulting psychiatrist.
Most MCOs have such services.
10.
If applicable, ask the patient to enlist the support of his or her Personnel/ Human Resources Department.
MCOs are often more responsive to their paying clientsscomplaints than to complaints from physicians.
11.
In
cases that are slow to respond to standard treatments, ask the company
to “flex benefits” by working with you to find a cost-effective,
alternative treatment approach.
12.
If coverage is
denied after appealing, some companies may allow you to request an
external review of the case with or without some cost-sharing.
13.
In truly egregious cases, copy your appeal to the state insurance commissioner.
Seeing such a “cc” may elicit a more rapid and favorable response.
14.
Contact any professional association you belong to and any consumer advocacy groups that may be helpful.
A complaint lodged by several parties will be stronger.
Letter
of Appeal The following are some suggestions for inclusion in a letter
of appeal: • Include any literature that supports your case, including
references to the APA’s practice guidelines.
This may help convince the reviewer that the proposed treatment will result in the desired outcome.
• Be candid about the patient’s condition.
Describe
any changes in diagnosis, comorbidities, progression, or regression of
the patient’s condition; special treatments such as suicide restraints
and seclusion; neurological testing and other medical tests;
medications; and any self-injury or assaultive behavior.
• Clearly relate the level of care requested to the patient’s condition.
Information should be based on objective reasoning, not just opinion.
• Describe the next step of treatment, providing goals and an approximate time frame for the completion of treatment.
This will promote the idea that you have an action-oriented approach.
• If applicable, recommend alternative treatments for the patient.
• Present evidence of similar cases where the care was approved by the same plan.
• Appeal with a collaborative spirit.
If you need further assistance, call the APA Practice Management HelpLine at (800) 343-4671.
Independent
Review Organizations (IROs) Most states have enacted independent review
laws that require disagreements over what constitutes a health plan
coverage to be decided by a review done by a medical expert or panel of
medical experts who have no affiliation with the health plan.
Laws vary from state to state as to whether the review decisions are binding, but they are in most states.
Currently, approximately 50 percent of the disputes taken to independent review result in the reversal of a coverage denial.
An
independent, external review, however, can only be accessed after the
internal appeals process established by individual MCOs has been
completely exhausted.
Although independent reviews have been
around for years, there is still a lack of public awareness about the
process, and patients generally do not take advantage of the reviews
despite claims denial letters that inform them about their availability.
In
2005 the Kaiser Family Foundation published a guide to handling health
plan disputes that provides specific information about how to access the
independent review organizations in each state that has mandated the
independent review process.
This document still has valuable information.
It can be downloaded at handling-disputes-with-your-employer-or-private-health-plan/ .
The
APA encourages patients, and their physicians, to take advantage of
this vehicle for resolving disputes that arise in obtaining appropriate
mental health care.
Mental Health and Substance Use Disorder
Insurance Coverage and Model Legislation APA has created
parity-implementation legislation for all 50 states and the District of
Columbia.
The legislation is designed to require transparency and accountability from insurers and state regulators.
Each state has legislation that is tailored specifically for that state's terminology and formatting.
Overview
of Mental Health and Substance Use Disorder Parity State Model Parity
Legislation Adapted to All 50 States and the District of Columbia
Comprehensive State Model Parity Legislation for Each State Model Parity
Legislation Addressing Insurer Reporting Requirements Model Parity
Legislation Addressing Commissioner Implementation Requirements Model
Parity Legislation Addressing MAT Coverage Provisions Contact APA's
Department of Government Relations Team Overview of Mental Health and
Substance Use Disorder Parity President George W Bush signed the Mental
Health Parity and Addiction Equity Act into law on October 3, 2008.
The Act was sponsored by Congressman Patrick J Kennedy (D RI).
Parity
as a concept is very simple: insurance coverage for mental health and
substance use disorder care should be no more restrictive than insurance
coverage for any other medical condition.
However, the Federal Parity Law is very complex, and implementation of the law can be challenging.
Insurers
have done a very good job of coming into compliance with some of the
more straightforward components of the law, such as making sure copays
and visit limits for mental health and addiction care are no more
restrictive than they are for other medical care.
how long is too long for a cancer biopsy
However, insurers are likely not complying with some of the more complicated components of the law, albeit unintentionally.
Many
of these trouble spots relate to how insurers design and apply their
managed care practices, such as prior authorization requirements, step
therapy, and requirements for providers to join an insurer's network.
Often,
insurers design and apply these managed care techniques in ways that
are more restrictive for mental health and substance use disorder
treatment than for other medical treatment, which violates the Federal
Parity Law and can lead to deaths from suicides, overdoses and other
forms of preventable death.
States have primary enforcement authority over insurers that sell health insurance policies in their states.
While
there is growing interest by state insurance departments to implement
the law and increasing willingness by insurers to submit data to
regulators demonstrating compliance, there is much uncertainty about how
to do so in an efficient manner that meets the tests of the law.
This legislation provides a roadmap for how insurers and regulators can secure compliance without undue administrative burden.
First,
the legislation establishes reporting requirements for insurers to
demonstrate how they design and apply their managed care tactics, so
regulators can determine if there is compliance with the law.
Second, the legislation specifies how state insurance departments can implement parity and then report on their activities.
And third, the legislation eliminates some managed care barriers to medication-assisted treatment for substance use disorders.
While those provisions are not purely parity requirements, they can be a vital tool in combating the opioid epidemic.
Top
State Model Parity Legislation Adapted to All 50 States and the
District of Columbia One of the American Psychiatric Association's major
legislative goals is to achieve mental health parity and parity
enforcement across the country.
To that end, model parity
legislation has been specifically adapted for each state, amending the
appropriate sections of state code or creating new sections in the right
titles or chapters.
This model legislation also uses the
correct terminology for MH/SUD used in each state, the correct
terminology for health insurers, and the right terminology for the
insurance commissioner.
Additionally, each bill is formatted exactly as bills are drafted in that state.
There
are four versions for each state: one comprehensive bill and then three
smaller bills that are each of the components of the comprehensive bill
(addressing insurer reporting requirements, addressing commissioner
implementation requirements, or addressing MAT coverage provisions).
This
allows each state to address the needs within that state, such as
pursuing an incremental strategy or the comprehensive model legislation.
Please find the different versions for each state below.
Top
Comprehensive State Model Parity Legislation for Each State This is the
comprehensive version of the state model parity legislation, which
includes provisions for insurer reporting requirements, commissioner
implementation requirements, and addressing MAT coverage provisions.
Find
your state's comprehensive model parity legislation Alabama Alaska
Arizona Arkansas California Colorado Connecticut Delaware District of
Columbia Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas
Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota
Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey
New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon
Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas
Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming Top
Model Parity Legislation Addressing Insurer Reporting Requirements This
version of the model parity legislation is the section that only
addresses insurer reporting requirements.
Contact APA's Department of Government Relations Team For more
information on how your state can get involved in advancing mental
health parity, please contact APA Director of Government Relations Erin
Berry Philp at ephilp@psych.org
[Date] [Name and mailing address of
payer] To Whom It May Concern: I have been seeing [patient name] since
[provide date care began] to treat his/her [provide diagnoses, and any
problems this may cause in patient’s life if applicable.
For example: Anxiety that has limited her ability to fulfill her duties at work].
[Provide a chronology of the patient’s treatment and explain why you need to either continue or initiate the denied care.
If
the company is denying the frequency of care, the chronology will
provide an example of how patient decompensated when care was provided
with less frequency.
If the denial is for a medication, provide a
history of prescribing and explain why you have come to the decision
that it’s necessary to either continue or initiate treatment with the
denied drug.
Explain any of the patient’s stated concerns/preferences that influenced your decision.
Be
sure to provide examples of what might occur if care continues to be
denied and how this would be detrimental to the patient’s health.
Always be as specific as you can.] I have attached articles that support provision of this care to [patient name].
[if you can find literature to support the care that is being denied, this can be a very valuable asset.
The
APA’s Practice Guidelines can be a good source for support since most
insurers say they use them in developing their treatment guidelines.]
Sincerely, [Name and contact information]
A Key Acronyms The following
abbreviations are used in this Guide, and are defined in the glossary or
within the text: ACA—The Patient Protection and Affordable Care Act
(see also PPACA) AHP—Association Health Plan CMS—U S Centers for
Medicare and Medicaid Services COC—Certificate of Coverage DOL—U S
Department of Labor EAP—Employee Assistance Program EHBs—Essential
Health Benefits EOB—Explanation of Benefits EOC—Evidence of Coverage
EPO—Exclusive Provider Organization ERISA—Employee Retirement Income
Security Act of 1974 FDA—U S Food and Drug Administration FEHB
Program—Federal Employees Health Benefits Program FFS—Fee-for-Service
FR—Financial Requirement HDHP—High Deductible Health Plans HHS—U S
Department of Health and Human Services HIPAA—Health Insurance
Portability and Accountability Act HMO—Health Maintenance Organization
HSA—Health Savings Account IOP—Intensive Outpatient Program
IRO—Independent Review Organization MBHO—Managed Behavioral Health
Organization MEWA—Multiple Employer Welfare Arrangement Plans
MH/SUD—Mental Health and Substance Use Disorders MHPAEA—The Mental
Health Parity and Addiction Equity Act of 2008, also known as the
Federal Parity Law NQTL—Non-Quantitative Treatment Limitation
PCP—Primary Care Provider PHP—Partial Hospitalization Program PPACA—The
Patient Protection and Affordable Care Act (see also ACA) POS—Point of
Service PPO—Preferred Provider Organization QTL—Quantitative Treatment
Limitation SBC—Summary Benefits and Coverage SPD—Summary Plan
Description TPA —Third Party Administrator UCR—Usual, Customary and
Reasonable UM—Utilization Management Call to Action: Ten Steps A lthough
many success stories exist where a patient or ordering provider’s
appeal was handled in a timely and efficient manner by a health plan,
those cases are the exception and not the norm.
The good news is that the building blocks to achieve true parity implementation are now in place, but more remains to be done.
The following ten steps will advance mental health parity by improving the appeals process for all: 1.
Increase Awareness of the Appeal Process.
The appeals process is enormously complex.
Many individuals do not know they have the right to file an appeal upon receiving an adverse benefit determination.
Health
plans and regulators should work together to ensure that all enrollees
are aware of their rights through targeted public education campaigns.
Regulators
should also reinforce health plans parity disclosure requirements and
make clear that in both internal and external appeals, a parity
violation is grounds for reversal of a coverage denial.
2.
Promote More Due Process and Transparency.
When
an adverse benefit determination or denial takes place, more
transparency must be provided surrounding how the decision was made and
documented.
At a minimum, health plans must disclose the
clinical and/or coverage criteria used in the decision and clearly
explain the specific steps required to file an appeal.
Regulators
should also enforce requirements that denial letters include a detailed
explanation of why the patient does not meet the plan’s clinical
criteria, a description of the evidence reviewed by the plan, and
address evidence submitted by the patient or their provider.
Otherwise, consumers cannot avail themselves of their appeal rights.
Filing An Appeal Based On a Parity Violation The Kennedy Forum • 3.
Allow Attending Providers and other Advocates to File Appeals.
In some instances, ordering or attending providers are not allowed to file an appeal on behalf of their patients.
This
is counterintuitive and inefficient as the provider is often in the
best position to understand the denial decision and then explain why the
service or treatment is still recommended or why the care was already
delivered.
Providers also have a “leg-up” as they are familiar
with the medical jargon used in the denial letter or throughout the
appeals process.
4.
Simplify the Appeals Process.
Many
patients and ordering providers complain that too many bureaucratic
hurdles and inconsistent requirements exist within the appeals process.
These obstacles have a chilling effect that discourages patients or their representatives from filing an appeal.
Originally,
the appeals process made clear that utilization management (UM) appeals
handled medical necessity or clinical denials, and grievance procedure
appeals handled administrative denials.
Today, model laws from
the National Association of Insurance Commissions (NAIC) and many
jurisdictions have issued regulations that have eroded this formerly
clear bifurcation.
We recommend that one integrated and streamlined appeals process apply no matter the basis of the initial denial.
5.
Standardize the Appeal System Across Market Segments and State Lines.
A national and consistent standard must be implemented to make the appeals process effective.
At present, many different appeal pathways exist.
These
pathways vary based on how the health plan is regulated, the type of
coverage provided, the type of plan sponsor, the jurisdiction,
the type
of denial (e g , based upon a medical necessity or benefit
determination), the timing of the denial (e g , prospective, concurrent
and retrospective), the urgency of the care being requested (i e
standard care versus urgent care), and where the patient is in the
appeals process.
Our goal should be to establish one national
appeals standard that promotes transparency, fairness and due process to
all parties involved.
We can accomplish this unified system
through new model legislation, accreditation standards and Requests for
Proposal (RFP) requirements.
6.
Upgrade the External Review Appeals Process.
Currently, the patient or their authorized representative must specifically request an external review of their claim.
In
most cases, the external review appeal only can be pursued after a
patient first successfully completes an appeal through the health plan.
In some instances, the aggrieved party may not even know they have the right to appeal to an external party.
One
simple way to address this confusion is to automatically refer the
appeal to an independent review organization after the internal appeal
is completed.
For example, Medicare beneficiary appeals are
automatically referred to the external review level, resulting in more
due process.
Filing An Appeal Based On a Parity Violation
The
Kennedy Forum • In addition, the external review process as currently
regulated should be re-examined and potentially upgraded to better
protect consumers.
Ideas include: n Reviewer Identification.
In many cases, the patient does not know who made the final ruling during the external review.
Should
the identity of the external reviewer be revealed or remain anonymous?
Does due process require the person making the judgment to be disclosed
like a judge in court? The Kennedy Forum recommends that the identity of
the reviewer be routinely disclosed.
n Public Disclosure of Decisions.
In
some states, regulators post de-identified external appeal decisions on
their websites, a practice that allows consumers and providers to
understand the types of issues being sent to external appeals, how
external decisions are made, and to identify trends (such as frequent
overturns of denials of coverage for specific treatments).
Greater
disclosure of external appeal decisions would benefit individual
consumers and help frame dialogue with health plans regarding practices
that should be reformed.
n Payment.
In most cases,
health plans contract with two or more external review organizations to
handle the external reviews of their insured population.
Does
the external review organization have an incentive to rule in favor of
the health plan if the health plan also is paying for the cost of the
external review? Should the patient’s health plan pay for the external
review? Or should it be funded by a government agency or through some
sort of fund supported by all health plans in a particular jurisdiction?
The Kennedy Forum recommends that some sort of payment system be set up
through the local jurisdiction rather than through the health plan to
avoid any perceived or real conflicts of interest that might bias the
external review decision in favor of the health plan.
Exhausting Internal Review.
Should
the patient or their advocate always have to exhaust the health plan
internal appeals process before filing an external appeal? Should the
patient have the right to skip right to external review? The Kennedy
Forum recommends that the patient be permitted to skip the internal UM
appeals process and go right to external review if that is their
decision.
However, once this decision is made, the patient or
their advocate loses the right to use the health plan’s internal appeal
system for that particular issue under dispute.
Filing An Appeal Based On a Parity Violation The Kennedy Forum • 7.
File More Appeals.
While
working to lower the number of denials issued on claims, stakeholders
should simultaneously work to ensure that every questionable denial is
subjected to the appeals process so that enrollees receive the care they
are entitled to.
Each stakeholder group should do the following to promote the filing of appeals: n Consumer/Provider.
Every
patient who has experienced a denial or care restriction of mental
health or addiction services should file a complaint at and/or with the
applicable government agency.
Filing a complaint will help us develop comprehensive data to better understand the different types of parity denials.
Industry.
When an appeal is filed, health plan personnel must make a good faith effort to respond in a timely and meaningful manner.
Health
plans and medical management organizations must ensure they are
complying with existing regulations and the patient’s plan documents on
how these appeals should be processed (e g , timeframes, disclosure
requirements).
n Policymakers/Regulators.
Policymakers
and public officials must ensure they enforce existing state and federal
regulations on how appeals should be filed and processed.
In
addition, the current regulatory and accreditation requirements should
be updated to create a more efficient and effective appeals process for
all parties.
8.
Leverage Technology to Improve the Efficiency of the Appeals Process.
Much like TurboTax has helped tax filers, it is time to leverage technology to promote a more efficient appeals process.
All too often, the appeals process is still paper-based or otherwise very fragmented.
While is one step in the right direction, more can be done.
9.
Update Regulatory Oversight Mechanisms.
It is time to update regulations to capture recent trends in how best to monitor and promote the appeals process.
This
could include updating the model laws, regulations and accreditation
standards covering utilization management, grievance procedures,
external review and mental health parity compliance, both at the federal
and state levels.
It also could include promoting value-based and outcome measures.
Regulations need to keep pace with changes in health care delivery, technology capabilities, and communication platforms.
Filing An Appeal Based On a Parity Violation The Kennedy Forum • 10.
Promote Advocacy and Sponsor Education Programs.
States
should sponsor and subsidize experts who can help patients understand,
file, and process appeals by creating consumer advocate offices, like
the Office of the Health Care Advocate in Connecticut or Health Law
Advocates in Massachusetts.
Regulators and health insurers can
support this effort through customer service lines, supplemental
educational programs, broker materials and other resources that are
specific to their agency or plan.
These agencies should also
actively connect consumers interested in filing an appeal with
non-profits capable of supporting individuals throughout the process.
Final
Thoughts The appeals process, especially for parity violations, remains
a complex and confusing system for most stakeholders.
It is
time to rethink and improve on existing appeal systems with an eye
towards making the appeals process more efficient, transparent and
meaningful.
The impact of doing so will be meaningful for
individuals—and their families—who need and deserve care and are
entitled to services.
For more information on this topic,
contact Garry Carneal, JD, Senior Policy Advisor, The Kennedy Forum, at
info@thekennedyforum.org. See also Organize Your Materials What papers
do I need? Keep copies of all information related to your claim and the
denial.
This includes information your insurance company
provides to you, and information you provide to your insurance company,
such as: The Explanation of Benefits (EOB) forms or letters showing what
payment(s or service(s were denied A copy of the request for an
internal appeal that you send to your insurance company Any additional
information you send to the insurance company (such as a letter or other
information from your doctor) A copy of any letter or form you are
required to sign, if you choose to have your doctor or anyone else file
an appeal for you.
Keep a diary of phone conversations you have
with your insurance company or your doctor that relate to your appeal
(include the date, time, name, and title of the person you talked to, as
well as details about the conversation) Keep your original documents
and submit copies to your insurance company.
You will need to
send your insurance company the original request for an internal appeal,
and your request to have a third party (such as your doctor) file an
internal appeal for you.
Make sure you keep copies of all documents for your records.
What
kinds of denials can be appealed? You can file an internal appeal if
your health plan won’t pay some or all of the cost for health care
services you believe should be covered.
The plan might issue a
denial because: The benefit is not offered under your health plan Your
medical problem began before you joined the health plan You received
health services from a health provider or facility that is not in your
health plan’s approved network Your health plan determines the requested
service or treatment is “not medically necessary” Your health plan
determines the requested service or treatment is an “experimental” or
“investigative” treatment You are no longer enrolled or eligible to be
enrolled in a health plan Your health plan revokes or cancels your
coverage, going back to the date you enrolled, because the insurance
company claims you gave false or incomplete information when you applied
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The class counsel would like to hear from you if you believe you are a class member or you are impacted by this lawsuit.
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LA Health Care Services Division
Agency Description The LSU Health Care Services Division (LSU HCSD)
includes Executive Administration and General Support (Central Office)
and six (6) hospitals that have entered into cooperative endeavor
agreements (CEA) for public-private partnerships and the Lallie Kemp
Regional Medical Center.
The six hospitals that currently have
CEAs are the Earl K Long Medical Center, University Medical Center, W O
Moss Regional Medical Center, Washington-St.
Tammany Regional
Medical Center, Leonard J Chabert Medical Center, and the Medical Center
of Louisiana at New Orleans LSU A M LSU Agricultural Center LSU
Alexandria LSU Eunice LSU Shreveport LSU Health Sciences Center, New
Orleans LSU Health Sciences Center, Shreveport LSU Pennington Biomedical
Research Center The Hospital and Central Office of the LSU Health Care
Services Division Commitment authorizations for $1,964,876,382 LA Health
Care Services Division Lallie Kemp Regional Medical Center HCSD - 8
Executive Budget Supporting Document [FY 2016-2017] DHHS Centers for
Medicaid and Medicare Services online survey, certification and
reporting database.
Medicare metrics tied to reimbursement.
Clinical
quality measures hospitals submit patient record data MyQualityNetís
(Hospital Consumer Assessment of Healthcare Providers and Systems)
HCAPHS survey.
experiences with medical, surgical, or maternity
care quarterly benchmark ourselves against other similar hospitals
towards meeting national standards of care, maintaining patient safety,
providing quality care, efficient use of federal and state budgeted
resources.
An emergency room visit is an immediate treatment of treated by ER staff/associates to be counted as an ER visit.
ED visits include ER visits (ED Encounters) plus ER admits.
Patient
satisfaction The Myers Group Centers for Medicare and Medicaid Services
(CMS) approved vendor, and is summarized in overall rating of hospital
and willingness to recommend hospital.
It should be noted that
CMS' patient satisfaction survey is a standardized instrument which
measures inpatient care across the United States.
The LSU Health
System is working with the University Healthsystem Consortium to
further define performance indicators and peer group comparisons.
Patient
satisfaction is measured using The Myers Group, a Centers for Medicare
and Medicaid Services (CMS) approved vendor, and is summarized in
overall rating of hospital and willingness to recommend hospital.
LSU-HCSD has set its performance standards above the state, national and west south regional averages.
LSU-HCSD
will follow the CMS rules for reporting; which represents data from a
prior quarter being reported due to timing 1: the several campuses as
defined below (Sec.
2B).
The President and the academic officers of the University 2: fulfill the duties of the faculty.
The
Board, the President, and the Chancellors will rely on those elected 3:
which, in the judgment of the Chancellor, or of the President, is
administrative or which seriously affects 4: or of the University
itself, may be suspended by the President and such action shall be
reported to the Board 5: or, for LSU or in inter-campus situations, by
the President.
4.
Meetings.
Each faculty, or its
representative 6: for that purpose may be called at the request of the
President as chair or of the Chancellor of the campus or, 7: shall be
given.
It shall be the prerogative of the President to preside;
otherwise, the Chancellor of the 8: officer concerned, shall be reported
to the President.
The President may then refer any such action on 9: concerned, shall be reported to the President.
The President may then refer any such action on academic 10: the several campuses as defined below (Sec.
2B).
The President and the academic officers of the University 11: fulfill the duties of the faculty.
The
Board, the President, and the Chancellors will rely on those elected
12: which, in the judgment of the Chancellor, or of the President, is
administrative or which seriously affects 13: or of the University
itself, may be suspended by the President and such action shall be
reported to the Board 14: or, for LSU or in inter-campus situations, by
the President.
a Minutes of all actions taken by the faculties 15: officer concerned, shall be reported to the President.
The President may then refer any such action on 16: concerned, shall be reported to the President.
The
President may then refer any such action on academic 17: purpose may be
called at the call request of the President as chair or of the
Chancellor of the campus or, 18: shall be given.
It shall be the
prerogative of the President to preside; otherwise, the Chancellor of
the 19: officer concerned, shall be reported to the President.
The President may then refer any such action on 20: concerned, shall be reported to the President.
The
President may then refer any such action on academic 21: that should be
brought to the attention of the President and Board 5.
An explanation of any significant 22: to the reporting format will be approved by the President with notification to the Board.
ARTICLE I ACADEMIC AND ADMINISTRATIVE ORGANIZATION Section 2.
Academic
Organizational Units A The Faculty of the University The faculty of the
University shall consist of the faculties of the several campuses as
defined below (Sec.
2B).
The President and the academic
officers of the University shall be members of the University faculty
and the former shall be its highest officer.
B The Faculties of the Several Campuses 1.
Membership.
Full-time
members of the academic staff having the rank of Instructor or higher
(or equivalent ranks) shall constitute the faculty of the campus on
which they are appointed.
As a class, part-time members of the
academic staff having the rank of Instructor or higher (or equivalent
ranks) may be enfranchised to the degree deemed appropriate by the
faculties of the several campuses.
2.
Duties.
Under
the Constitution of the State of Louisiana, the Board of Supervisors of
Louisiana State University and Agricultural & Mechanical College
has the authority to organize and manage the university.
The
Board authorizes the general body of the faculty, or its representative
body, to establish curricula, fix standards of instruction, determine
requirements for degrees, make recommendations for the granting of
degrees through its respective colleges or schools not within a college
and generally determine educational policy, subject to the authority of
the Board.
Except as otherwise provided, each faculty shall establish its own educational policies.
The
Board authorizes the faculty to establish admissions criteria for
graduate and professional programs, however, standards for undergraduate
admission to the University shall be approved by the Board.
3.
Faculty Representative Body.
Except as otherwise provided, the faculty of each campus shall establish its own governance policies.
The
faculty may establish one representative body, such as a Senate or
committee, to represent the will of the faculty and exercise legislative
power to conduct its own meetings and fulfill the duties of the
faculty.
The Board, the President, and the Chancellors will rely
on those elected representative bodies as the voice of the general
faculty.
Any action a faculty representative body which, in the
judgment of the Chancellor, or of the President, is administrative or
which seriously affects the interests of faculty of the University or of
the University itself, may be suspended by the President and such
action shall be reported to the Board at its next meeting.
All
questions of jurisdiction among colleges, schools not within colleges,
or divisions shall be determined by the Chancellor, or, for LSU or in
inter-campus situations, by the President.
4.
Meetings.
Each faculty, or its representative body, shall meet at least once each academic year.
For
the purpose of replacing or reconstituting the representative body, a
meeting of the general faculty for that purpose may be called at the
request of the President as chair or of the Chancellor of the campus or,
for LSU, the President’s designee, as vice-chair, or upon the written
request of 50 members or 20 percent of the membership, whichever is the
fewer.
The written request must be received within a 14-day period from the time of original solicitation.
At least five days notice of meeting shall be given.
It
shall be the prerogative of the President to preside; otherwise, the
Chancellor of the campus or, for LSU, the President’s designee, will
preside.
Minutes of all actions taken by the representative
bodies, together with appropriate recommendations of the major
administrative officer concerned, shall be reported to the President.
The
President may then refer any such action on academic matters of general
University concern to the appropriate council, or a committee thereof,
for consideration.
1.
Quorum.
Not less than 25
percent of the membership of the faculty or Faculty Council shall be
necessary to constitute a quorum, provided, however, that any faculty or
Faculty Council (at a meeting at which a quorum of 25 percent of the
members is present) may, by majority vote, establish a higher percentage
of the membership as a quorum for future meetings.
BE IT
FURTHER RESOLVED, the Board does hereby amend Article V Section 12B of
the Regulations approved on August 6, 2021 to read: Article V Section 12
a Consolidated Financial Report (the annual financial report shall
suffice as the report for the second-half of the year) NOW BE IT FURTHER
RESOLVED, the revised Regulation adopted on September 10, 2021 will be
effective on September 13, 2021.
BE IT FURTHER RESOLVED, the
Secretary is authorized to make technical adjustments for the
appropriate and accurate codification of these Rules and Regulations.
REGULATIONS OF THE BOARD OF SUPERVISORS ARTICLE I ACADEMIC AND ADMINISTRATIVE ORGANIZATION Section 1.
Order
of Communications and Reports The official recommendations and
communications of any member of the academic or nonacademic staff shall
be sent through channels to the appropriate officer.
An
administrative officer shall, when so requested, promptly transmit any
such recommendations or communications, with the officer's own comments
and recommendations thereon, to the next higher office.
Section 2.
Academic
Organizational Units A The Faculty of the University The faculty of the
University shall consist of the faculties of the several campuses as
defined below (Sec.
2B).
The President and the academic
officers of the University shall be members of the University faculty
and the former shall be its highest officer.
B The Faculties of the Several Campuses 1.
Membership.
Full-time
members of the academic staff having the rank of Instructor or higher
(or equivalent ranks1) shall constitute the faculty of the campus on
which they are appointed.
The faculty may organize itself into a
Faculty Council which shall include all full-time members of the
faculty and members of the Administrative Council (see sec.
1-3.1).
As a class, part-time members of the academic staff having the rank of
Instructor or higher (or equivalent ranks) may be enfranchised to the
degree deemed appropriate by the faculties of the several campuses.
Members of the Administrative Council, not holding academic rank, shall be non-voting members of the Faculty Council.
2.
Duties.
Under
the Constitution of the State of Louisiana, the Board of Supervisors of
Louisiana State University and Agricultural & Mechanical College
has the authority to organize and manage the university.
The
Board authorizes the general body of the faculty, or its representative
body, Faculty Council2 shall to establish curricula, fix standards of
instruction, determine requirements for degrees, make recommendations
for the granting of degrees through its respective colleges or schools
not within a college and generally determine educational policy, subject
to the authority of the Board.
Except as otherwise provided, each faculty shall establish its own educational policies.
It
shall, within the framework of the educational policy of the
University, have legislative power over all matters pertaining to its
own meetings and may delegate its own authority to an elected Senate
and/or to standing committees, whose authority shall be limited to
matters which are proper to the faculty and which have been specifically
delegated by the faculty.
It shall make recommendations for the
granting of degrees through its respective colleges or schools not
within a college.The Board authorizes the faculty to establish
admissions criteria for graduate and professional programs, however,
standards for undergraduate admission to the University shall be
approved by the Board.
1See Section 2-6.
2The terms faculty and Faculty Council are used interchangeably in this Section (2).
3.
Faculty Representative Body.
Except as otherwise provided, the faculty of each campus shall establish its own governance policies.
The
faculty may establish one representative body, such as a Senate or
committee, to represent the will of the faculty and exercise legislative
power to conduct its own meetings and fulfill the duties of the
faculty.
The Board, the President, and the Chancellors will rely
on those elected representative bodies as the voice of the general
faculty.
Actions.
Any action of a faculty or Faculty
Council which faculty representative body which, in the judgment of the
Chancellor, or of the President, is administrative or which seriously
affects the interests of another faculty of the University or of the
University itself, may be suspended by the President and such action
shall be reported to the Board at its next meeting.
All
questions of jurisdiction among colleges, schools not within colleges,
or divisions shall be determined by the Chancellor, or, for LSU or in
inter-campus situations, by the President.
a Minutes of all
actions taken by the faculties or Faculty Councils, together with
appropriate recommendations of the major administrative officer
concerned, shall be reported to the President.
The President may
then refer any such action on academic matters of general University
concern to the appropriate council, or a committee thereof, for
consideration.
4.
Meetings.
Each faculty, or its representative body, or Faculty Council shall meet at least once each academic year.
For
the purpose of replacing or reconstituting the representative body, a
meeting of the general faculty for that purpose may be called at the
call request of the President as chair or of the Chancellor of the
campus or, for LSU, the President’s designee, as vice-chair, or upon the
written request of 50 members or 20 percent of the membership,
whichever is the smaller number fewer.
The written request must be received within a 14-day period from the time of the original solicitation.
At least five days notice of meeting shall be given.
It
shall be the prerogative of the President to preside; otherwise, the
Chancellor of the campus or, for LSU, the President’s designee, will
preside.
Minutes of all actions taken by the representative
bodies, together with appropriate recommendations of the major
administrative officer concerned, shall be reported to the President.
The
President may then refer any such action on academic matters of general
University concern to the appropriate council, or a committee thereof,
for consideration.
5.
Quorum.
Not less than 25
percent of the membership of the faculty or Faculty Council shall be
necessary to constitute a quorum, provided, however, that any faculty or
Faculty Council (at a meeting at which a quorum of 25 percent of the
members is present) may, by majority vote, establish a higher percentage
of the membership as a quorum for future meetings.NOW, THEREFORE, BE IT
RESOLVED that the Board of Supervisors of Louisiana State University
and Agricultural & Mechanical College does hereby approve the
operating budget for the fiscal year ending June 30, 2022, providing: (a
Final approval and commitment authorization of funds for unrestricted
educational and general, medical, and related expenses in the amount of
$1,190,016,205 for the campuses shown below.
LSU A M LSU
Agricultural Center LSU Alexandria LSU Eunice LSU Shreveport LSU Health
Sciences Center, New Orleans LSU Health Sciences Center, Shreveport LSU
Pennington Biomedical Research Center The Hospital and Central Office of
the LSU Health Care Services Division (b Commitment authorizations for
auxiliary enterprises, grants and contracts, and other restricted funds
estimated to be $1,964,876,382.
(c Transactions included or
referred to in the operating budget that otherwise require Board
approval are not approved by mere inclusion in the operating budget.
BE IT FURTHER RESOLVED that each campus shall prepare a semi-annual financial report.
The format of the report will include the following: 1.
Budget and actual for unrestricted revenues by source of funds 2.
Actual for unrestricted expenditures by object and by function 3.
Beginning account balances and actual revenues and expenditures/transfers for restricted operations 4.
Any significant changes in the budget that should be brought to the attention of the President and Board 5.
An
explanation of any significant reduction in anticipated revenues or
significant increase in expenditures Any subsequent modification to the
reporting format will be approved by the President with notification to
the Board.
•
Keeping a cell phone readily available, • Scheduling sessions at a time
when colleagues are also seeing patients in the office suite or clinic,
• Forming a safety network among colleagues, and • Planning an escape
route (Manca, 2005; Pinals et al., 2007).
B Prevention and
Intervention Carr and colleagues outline a model of primary, secondary,
and tertiary prevention for both the individual psychiatrist and the
healthcare setting (e g , university, hospital, private clinic, etc.)
(Carr et al., 2013).
Primary strategies can be routinely
incorporated into clinical care; secondary strategies may be considered
when the psychiatrist has concerns about patient behavior, such as when
expected boundaries are tested; and tertiary strategies become important
when stalking behaviors may include actual threats to cause harm or
actions resulting in harm.
Examples of primary prevention
measures include: • Providing detailed information at the outset of
treatment regarding how therapy will work, the frame of the therapeutic
setting and context, and the importance of collaboration in a way that
helps maximize a sense of safety for all parties, • Minimizing one’s
online presence (e g , social media).
This particularly applies
to personal information, such as one’s private phone number, home
address, details about personal or family schedules, or even online
photos that might easily identify these details, • Using post office
boxes and answering services, and • Becoming familiar with telephone
services (e g , the procedure to block caller ID when making outgoing
calls from a cell phone) (Manca, 2005).
Periodic reviews of basic security measures at home and at work are also important.
These
measures could include: • Checking the proper functioning of any locks,
alarm systems, motion sensors, and security monitors, • Training video
cameras on entryways and having peepholes on office or clinic doors
(Manca, 2005), • Participating in self-defense classes (Pinals et al.,
2007), • Consulting with private security services or local law
enforcement for specific safety strategies (Pinals et al., 2007).
While
outside the scope of this document, psychiatrists may also consider
consulting with hospital or private cyber security experts.
Examples
of secondary measures that might be taken by psychiatrists include: •
Providing and seeking supervision and consultation as soon as possible
in a potential escalating situation and informing other members of the
patient’s treatment team, • Thoroughly documenting boundary violations,
problematic behavior, and attempted interventions.
Finally,
examples of tertiary measures that might be taken by psychiatrists
include: • Seeking consultation with experts in behavioral threat
assessment and management (see “Consultation” below), • Participating in
ongoing risk assessment, especially at critical junctures such as
anniversaries and court dates, which may elevate the potential for the
stalker to become violent, and • Careful consideration of whether, when,
and how to terminate patient care and provision of thoughtful referrals
(of the patient) to an appropriate provider (see “Legal and Ethical
Issues” below) (Carr et al., 2013).
A special note about
boundary-setting: in general, in any therapeutic relationship, setting
firm limits and establishing clear boundaries is important (Manca,
2005).
Psychiatrists should examine boundary testing by patients with the possibility that they may progress to stalking.
If
a patient violates expected prosocial behaviors and there is a specific
concern for stalking behavior, the psychiatrist may consider sending
one clear, unambiguous message to the patient to change this behavior
(Sandberg et al., 2002; Pinals et al., 2007; McIvor et al., 2008).
However, this approach can require a more nuanced consideration of when and whether to do so.
Caution
related to this communication is advised because this may escalate the
behavior and increase the risk of retaliation from the stalker in some
situations (Sandberg et al., 2002; Pinals et al., 2007).
After a
careful weighing of the facts, a decision to “do nothing” may be as
impactful and helpful as proactive measures, but each situation requires
individualized planning and direction.
Also, victims or
identified stalking targets must often make their own decision
(preferably with support and guidance) as to what intervention, if any,
to take, early in the course of the stalking behavior.
Regardless,
if the patient’s behavior persists after reasonable attempts at limit
setting, the psychiatrist should try to avoid any direct subsequent
engagement with the patient until consultation has been sought (McIvor
et al., 2008) (See “Consultation” below).
C Consultation Seeking
consultation, particularly from a multi-disciplinary team, is one of
the early steps a psychiatrist should consider in situations involving
stalking.
Even for experienced psychiatrists, getting another
perspective about their level of concern (e g , “Am I overreacting or
underreacting?”) can be very helpful.
It is also important to
acknowledge that each consultation requires a risk assessment and that
the facts can evolve, especially as new information about a case becomes
available.
Thus, it can be helpful to have a consultant
available for the duration of the stalking situation, which may be brief
or extend for years.
The specific make-up of the
multi-disciplinary team may vary, but often includes law enforcement,
hospital security, legal counsel, forensic psychiatric experts, and
other hospital or administrative and personal victim supports.
Depending
on the setting, a hospital or university may have a threat management
team or a forensic psychiatry service (Binder et al., 2017) that can be
particularly useful in scenarios that take place in an institutional
context.
In a private setting, psychiatrists may consider
contacting the nearest university’s forensic psychiatry program,
professional organizations like the Association of Threat Assessment
Professionals (ATAP), or local law enforcement that has specialized
services (e g , San Diego County District Attorney’s Stalking Unit).
• How dangerous is the stalker? • How can the
behavior be stopped? • How do I protect myself? • Will the behavior
stop, or get worse? • If [the behavior] stops, is it going to come back
again? (Binder, 2006; Mackenzie et al., 2011).
While further
research is needed regarding the management of stalking behaviors and
the effectiveness of specific interventions, (Mullen et al., 2006;
Binder, 2006; Mackenzie et al., 2011), a multi-disciplinary consultation
approach can systematically assess prevention and risk management
strategies.
For example: • Community law enforcement may have
seen many stalking cases, have experience or even actuarial knowledge
about stalking behaviors, easier access to legal records (e g , court
documents) that could be useful in risk assessment, and understanding of
local practices and enforcement regarding anti-stalking laws (Mullen et
al., 2006; Binder, 2006), • Hospital security can help plan on-site
safety measures, and • A private attorney, hospital legal counsel,
and/or attorney from a malpractice insurance provider can provide input
regarding local criminal stalking laws and about privacy laws related to
the release of medical records and pursuit of criminal charges related
to one’s patient.
A forensic psychiatric team can help determine
what types of risk assessment (e g , HCR-20, SAM, or RSP [Carr,
Goranson, & Drammond, 2013; Binder, 2006]) and management options (e
g , psychotherapeutic who, medications, etc.) are reasonable (Mackenzie
et al., 2011) for the patient who remains in the care of the
psychiatrist or in the care of other psychiatric personnel.
A
forensic team may also help balance relevant clinical and legal
considerations (e g , confidentiality, duty to third parties,
termination of patient care, impact on therapeutic relationship, etc.).
Furthermore, a clinical forensic psychiatric consultation service,
especially within the same institution, may not require patient consent
to review protected health information (though each institution may have
unique policies that should be reviewed prior to accessing a patient
record).
D Mental Health Counseling Psychiatrists who are being stalked may also consider seeking personal mental health counseling.
Situations
involving stalking can be intense, anxiety-provoking, and potentially
lengthy (on average two years) (Carr, Goranson, & Drummond, 2013;
Mullen et al., 2009).
Though further research is needed on the
impact of stalking among physicians, in a questionnaire completed by 274
psychiatrists in Ireland, of those who were stalked (n 69), 85%
reported suffering psychological distress as a result of their
experience (Nwachukw et al., 2012).
Another survey of 1190
physicians, including 117 psychiatrists (Abrams and Robinson, 2013)
found feelings of anger (73.8%) frustration (73.1%), anxiety (69.7%),
fear (67.6%), helplessness (44.8%) and loss of control (52.4%). A UK
study of 10,424 psychiatrists with 2,585 responses found a variety of
impacts on psychiatrists, including feeling anxious and afraid (80.65%),
having difficulty sleeping (52.19%) and ceasing to enjoy life’s
enjoyment (11%) (Whyte et al.
2011).
Regardless of the
basis for the stalking behaviors, the consequences “personally and
professionally, can be disruptive and potentially devastating”
(MacKenzie et al., 2011).
Many victims of stalking may feel or
actually be alienated, blamed, and criticized by supervisors and
colleagues (Mackenzie et al., 2011; Carr et al., 2013).
respondents
described variability of support from supervisors, colleagues, and law
enforcement; some respondents felt very well supported, and others
encountered a dismissive attitude that being stalked is inevitable for
psychiatrists.
Those who received help experienced less distress than those who did not (Maclean et al., 2013).
E
Documentation Detailed documentation of a patient’s stalking behavior
toward the psychiatrist or staff is useful for both future legal
interventions as well as behavioral management.
Victims of
stalking are advised to maintain detailed records of any communication
attempts on behalf of the stalker, such as emails and phone calls,
including dates, times, recordings, and fear about safety (some stalking
laws are based on the victim’s sense of fear) (Manca 2005).
Whether
to keep such detailed records separate from the official patient
medical record can be complex, and psychiatrists should seek further
advice (e g , from legal counsel, administration, and supervisors) about
which details should be part of the medical record and which should be
kept as a separate file.
In general, clinically relevant
information, such as behaviors (e g , gifts, boundary testing, breaches
of privacy etc.), risk assessments, diagnoses, interventions, and issues
surrounding termination, can be important to document in the medical
record, especially to communicate to the treatment team or other
providers involved in the patient’s care.
F Civil Protection
Orders Protection orders are also known by a variety of other names,
including restraining orders (Benitez et al., 2010) and intervention
orders (Mackenzie et al., 2011).
Though the U S Interstate
Stalking Punishment and Prevention Act of 1996 established that
protection orders issued in one state are enforceable in other states
(Benitez et al., 2010), the effectiveness of protection orders can vary
greatly across jurisdiction.
For example, some statessprotection
orders are designed for specific types of relationships such as
domestic or interfamilial violence only whereas other statessorders can
be more expansive (Knight, 2014).
Moreover, the utility of
protection orders is debated and may not be helpful in every stalking
scenario as they may fail to protect the potential victim, have high
rates of violation, may provide a false sense of security, or even
exacerbate the stalking behavior (Ostermeyer et al., 2016).
Police
and court responses to protection orders may vary considerably since
interpreting the point at which patterns of behavior cross the legal
threshold and become criminal can be complicated (Mackenzie, et al.,
2011).
Nonetheless, while they may not necessarily deter
stalking behavior, protection orders may give law enforcement leverage
to take the stalker into custody (Binder, 2006).
Thus,
consultation may be particularly useful to draw on experiences,
knowledge of the perpetrator’s prior response to such orders, and any
available scientific literature to make recommendations.
For
example, in a review of 15 publications, factors such as timing,
potential escalation of behaviors, victim characteristics, perpetrator
characteristics, abuser-victim relationships, and the context of the
legal system were useful to consider in determining whether a protection
order can be useful (Benitez et al., 2010).
Some additional
considerations with protection orders are that they may be more
effective earlier than later (Ostermeyer et al., 2016; Pinals, 2007), a
stalker’s reaction to any previous protection order may be useful to
guide decisions, and, if agreed to be ordered, the psychiatrist must
make a commitment to report all violations to the appropriate
authorities (Pinals et al., 2007).
Overall, even if protection orders are in place, they do not replace other personal protection and safety measures.
order
might be issued so that they are aware of the protection order and the
psychiatrist has points of contact in case of an untoward situation.
IV)
Healthcare Setting Obligations Organizations and businesses generally
have a legal and ethical responsibility to ensure workplace safety.
Unfortunately,
many healthcare settings and organizations do not have well-defined
procedures on how to handle stalking situations (Carr, Goranson, &
Drummond, 2013).
First and foremost, organizations should strive
to create and maintain work environments that are conducive to persons
reporting concerns and receiving supports.
In addition, there is
a progressive escalation of interventions which organizations might
undertake.2 Examples of primary prevention measures that might be taken
by institutions include: • Educating providers around issues such as the
importance of setting and maintaining appropriate boundaries in a
therapeutic relationship even when those boundaries are challenged or
tested; • Ensuring that healthcare providers are educated about
community contacts and support, such as law enforcement, so as to be
able to readily seek assistance for any concerning patient behaviors,
and • Establishing and educating staff about policies and procedures
with regard to stalking behaviors by patients.
An important
consideration for risk management personnel in universities, hospitals,
and healthcare settings is what policies and/or procedures are needed to
handle situations involving stalking.
These types of protocols would be separate and distinct from a sexual harassment type protocol or policy.
A
stalking-related protocol or policy would include safety measures,
expected legal responses, and a mechanism to provide staff with
emotional support, resources, and multi-disciplinary consultation
(McIvor et al., 2008).
Provisions for staff to take a leave of
absence to address any psychological distress and to tend to practical
matters, such as court appearances, may be necessary.
It is also
important for administrative supports to be prepared to step in to
manage communication with the patient and assist in the transfer of care
when clinically appropriate (Mackenzie et al., 2011).
The
healthcare setting may additionally consider a standardized debriefing
with staff - with appropriate discretion regarding victim and patient
privacy - regarding what patterns or conduct has occurred, how the
clinic responded, what risks may persist, and what is needed from the
rest of the clinical staff.
Creating this culture and
establishing related policies can provide an opportunity to educate
staff about preventative measures, such as boundary and transference
issues, and violence risk assessment and management resources.
On
a practical level, creating a collegial atmosphere that facilitates the
disclosure of problematic patient behavior may allow earlier
recognition, assessment, and treatment of the potential stalker, while
also protecting co-workers and other clients (Mackenzie et al., 2011).
V
Legal and Ethical Issues 2 As already noted, this document focuses on
safety pertaining to patients as potential stalking perpetrators, and
does not address workplace safety related to co-workers or domestic
partners who may pose separate risks in a workplace setting.
Legal
and ethical issues, such as concerns regarding breach of
confidentiality and abandonment when terminating patient care, often
arise when psychiatrists are concerned about being stalked.
Psychiatrists
may be in a “double bind,” in which taking appropriate steps may result
in a violation of confidentiality or even result in negative
consequences for the patient (Carr, Goranson, & Drummon, 2013).
Seeking
consultation, and proactively establishing appropriate procedures in
healthcare settings for such situations, can help address some of these
concerns.
In some settings, for example, psychiatrists may
establish a zero-tolerance termination policy (Manca 2005), though legal
and risk management guidance for such considerations is strongly
advised.
Specific administrative strategies for termination and
referrals should also be considered, such as, if indicated, provisions
for clear communication to the patient that any contact with the
previous psychiatrist (who was stalked) may be criminally prosecuted.
If
a termination letter is sent, it should be by certified mail and
include referrals to another professional, and might be better to come
from the administrative director or clinic rather than the psychiatrist
who was stalked (Pinals et al., 2007).
However, there should
also be a careful determination of what if any final contact should be
generated from the psychiatrist with clear instruction that leaves no
room for ambiguity.
If the patient is being referred to an out-of-system provider, then ethical and legal transfer of information is important.
The
psychiatrist (who was stalked) should develop a strategy to manage any
future contacts - for example, one way to address the issues is that
once the patient care has been terminated, it might be prudent for the
psychiatrist who was stalked to not respond directly to the ex-patient’s
future contacts.
Instead the hospital risk management division
should send a clear and polite letter stating that it is hospital policy
for the psychiatrist not to respond to the ex-patient, but to address
the ex-patient’s needs through the hospital system (e g , a request for a
release of records).
The psychiatrist who will be taking on the
treatment of the patient should also carefully consider unique
challenges in these situations, such as “stalking by proxy,” which in
this case reflects when the patient passes notes or communication to
their previous psychiatrist through their new psychiatrist (Carr et al.,
2013).
VI) Special Considerations involving Medical Students
and Psychiatric Residents Given the higher prevalence of psychopathology
in individuals who stalk medical professionals (McIvor, Petch, 2006)
and the higher prevalence of stalking victimization amongst
psychiatrists as compared to other physicians (Abrams, Robinson 2011),
trainees in psychiatry, from medical students in clinical clerkships to
fellows in subspecialty fields, might be at risk for becoming stalking
victims in these contexts.
To these authorssknowledge, there
have been no published reports or protocols about how psychiatry
residency training programs approach this issue.
Unlike
practitioners already in independent practice, psychiatric students and
trainees may not be as skilled at picking up any early warning signs of
stalking.
Stalking may escalate from repeated phone calls to
showing up to appointments outside of a scheduled session (Lee, Missett
1994).
Such behaviors may be minimized as part of the patient’s psychopathology and not reported quickly to a supervisor.
There
may be a sense, too, that the professional role offers protection when
care is delivered objectively (MacKenzie et al., 2011).
Trainees
who are just learning about the boundaries of a treatment relationship
may inadvertently encourage behavior that may lead to stalking.
For
an example, a boundary crossing (aimed at enhancing the therapist’s
treatment efforts), such as giving a hug instead of a handshake at the
end of a particularly difficult session could be misinterpreted by a
particular patient (Marshall, Teston 2008).
The
American College of Graduate Medical Education (ACGME) Common Program
Requirements stipulate that accredited residency programs monitor
residentsswell-being, evaluate workplace safety data, and address “the
safety of residents and faculty members.”3 They also have requirements
about supervision and progressive independence over the course of the
residency.
The ACGME makes clear that “at each participating
site, there must be a sufficient number of faculty with documented
qualifications to instruct and supervise all residents at that location
(ACGME, 2019).” The presence of a readily-available and approachable
supervisor is a critical component in reassuring trainees that they are
not alone in their work, that they have a safe space in which to discuss
the dynamics of a wide variety of therapeutic relationships, and that
they have someone to whom they can go when they have concerns.
Unfortunately,
many supervisors themselves are unfamiliar with how to best to handle,
or possibly even identify, a stalking situation.
In addition,
trainees may not report problematic behavior to their supervisor for
fear of being perceived as a failure in the treatment relationship,
shame, or a misplaced sense of a duty to treat the patient despite risk
to the resident (Appel, Kleinman 2012).
Supervisors should be educated about steps to take in the event that a supervisee reports concerning patient behavior.
Program
directors should have a protocol in place that addresses such issues by
bringing in additional faculty supports, consulting with in-house
forensic psychiatrists or even consulting with other programs,
determining when to notify law enforcement and the risk management
division of the resident’s training institution, and how to prioritize
resident health and safety in the context of the stalking situation.
Residents
should also be instructed on careful risk assessments and warning signs
about problematic behavior to ensure their safety early as part of
preventive strategic planning.
Recommended Elements of a
Stalking Prevention and Response Program for Trainees Examples of
measures that might be taken by institutions include: • Didactics early
in training regarding boundary crossings, boundary violations, patient
stalking and other behaviors are important to increase knowledge about
such issues.
Didactics should include: o Definitions of Stalking
o Clear guidance indicating that psychiatrists are responsible for
managing transference and boundary issues as well as safely navigating
patient relationships, and as such they may need assistance when their
capacity to cope or manage is outweighed by their concerns and fears
related to patient behavior.
• A clear protocol about potential
notifications which should include: o Direct supervisors (senior
resident, chief resident, or attending resident), o Program Directors o
Hospital Safety Officer and Security (if available) to consider security
measures for the resident while they are in the hospital, o
Multidisciplinary threat management team if one exists (including the
police, who can do a search regarding that individual’s legal history),
Institutional police who may be able to research the perpetrator’s legal
history, put an institutional restraining order in place, and contact
the local police department in the jurisdiction of the resident’s home
to provide extra protection.
The recommendations above with
regard to Consultation, Mental Health Counseling, Documentation and
Protection Orders may be equally applicable to scenarios involving
psychiatrists in training.
Resources
for the Patient A final issue of paramount importance is how to
continue providing care in some way for the patient or how to safely
refer the patient to the next psychiatrist who may need information as
to the reason for the transfer.
There is a fiduciary duty on the part of the physician that needs to be balanced against concerns for their safety.
Depending
on the location where the stalking is occurring, several options for
patient care include transferring to a different provider in the same
location (but possibly in another building) or transferring the patient
to another provider altogether.
These can also be items for consideration in Consultation.
8 More than half of patients with mental illness and substance use disorders also have an underlying physical illness.
For example, people with diabetes or heart disease often suffer from depression.
The
complex interactions between mental and physical health conditions and
the medications used to treat them require advanced medical training in
order to ensure high-quality clinical care through adherence to best
practices, which typically leads to highly positive health outcomes.
We know that mental health and substance use related conditions can compromise outcomes and drive costs of medical care.
Efforts
at integrated care models are increasing, with funding streams being
designed to help improve quality while containing costs.
These models depend on thoughtful clinical judgment and proper management of complex conditions.
A
physician who provides oversight or collaborative consultation, with
comprehensive knowledge of clinical needs, is essential to achieve these
aims.
As such, PAs should be authorized to provide patient care
services only so long as the PA is functioning under the direction and
supervision of a physician or group of physicians.
The training
PAs receive does not substitute for the comprehensive knowledge and
skills physicians acquire as a function of their medical school
education and experience.
The key difference between medical and
physician assistant education and training is the fact that medical
students spend four years focusing on the entire human body and all of
its systems—organ, endocrine, biomedical, neuropsychiatric, and
more—before undertaking three to seven years of residency training to
further develop and refine their ability to safely evaluate, diagnose,
treat, and manage a patient’s full range of medical conditions and
needs.
By gradually allowing residents to practice those skills
with greater independence, residency training prepares physicians for
the independent practice of medicine.
Combined, the most basic
medical school and residency training total more than 10,000 hours of
clinical education and supervised training experience, including basic
course work as well as years of practical supervised experience with
patients.
The very nature of physician assistant training
involves working with physicians; physician assistants are not trained
to provide patient care without physician supervision.
Even
physicians do not work independently before the end of their residency,
even though at that point they have much more education and training
than physician assistants.
Physician assistants just do not have
extensive training in pharmacology, differential diagnoses, or the
years of education and training regarding the human body and its systems
that physicians have.
The vast majority of statess regulations reflect the necessity for oversight of PAs and the importance of physician-led care.
In 48 states a PA’s scope of practice is determined with the supervising or collaborating physician at the practice site.
Moreover,
in 34 states PAs are supervised by physicians and in 16 other states
PAs are subject to other forms of collaborative or alternative
agreements.
Thus, as the billing abilities of PAs change it is
important to ensure that this change does not impact the care the
patients receive or the scope of practice requirements that are in
place.
Rural Health Clinics (RHCs) and Federally Qualified
Health Centers (FQHCs) (sections III.A , III.B , and III.C ) APA fully
supports CMSsproposal to allow RHCs, FQHCs, and Critical Access
Hospitals to provide audio- only services, in a patient centered-manner
and based on the clinical judgement of the clinician.
As we
stated previously with regard to expanded telehealth services, APA is
concerned about any requirement 9 for a patient to be seen in-person by a
practitioner in order to be eligible for any telehealth encounter.
Again, implementing requirements such as this may dilute the benefits of the expanded policy.
We also encourage CMS to expand audio-only coverage to include treating patients with substance use disorders.
We
support RHCs and FQHCs receiving their usual PPS or AIR rates for
audio-only telehealth services and support the billing for both G0511
and G0512 in the same month for the same patient as long as the time and
effort is not counted more than once.
Medicare Shared Savings
Program (section III.J APA is supportive of the Medicare Shared Savings
Program and the Accountable Care Organization concept; facilitating
better coordination and integration of care is critical to improving the
quality of mental and behavioral health care, and the Shared Savings
program is an important step in promoting these goals.
However,
we are concerned that some of CMS’s proposed policies may undermine the
ability of ACOs to meet requirements under the program.
Electronic
clinical quality measures are important for reducing data collection
burdens and incorporating clinically-enriched data into measurement
activities, but a continued lack of EHR standardization raises concerns
about the feasibility of aggregating data from diverse and disparate
systems that may be in use across an ACO.
Furthermore, the
practice of introducing new measures on a pay-for-reportingsbasis before
incorporating them into payment calculations is an important step in
the process of building a valid and feasible measure set, allowing
participants to identify potential problems or unintended consequences
that may arise with measure implementation.
We would encourage
CMS to continue consulting with the ACO and clinician communities and
patient representatives to determine the best-balanced measure set and
measurement approach for the Medicare Shared Savings Program.
APA
also supports the inclusion of the Behavioral Health Integration codes
(99492-99494, G2214, and 99484) in the definition of primary care
services for the Shared Savings Program.
Modifications Related
to Medicare Coverage for Opioid Use Disorder (OUD) Treatment Services
Furnished by Opioid Treatment Programs (OTPs) (section III.O).
We
appreciate the two proposed changes included in this section to improve
access to care for patients with opioid use disorder by allowing payment
for a recently FDA-approved higher dose of naloxone hydrochloride nasal
spray product to treat opioid overdose.
We also support
allowing the therapy and counseling portions of the weekly bundles, and
any additional counseling or therapy provided by opioid treatment
programs, to be furnished using audio-only telephone calls rather than
via two-way interactive audio/ video communication technology for the
duration of the PHE for COVID–19.
This is important given many patients do not have smart phones that allow for two- way communication.
Requirement
for Electronic Prescribing for Controlled Substances for a Covered Part
D Drug under a Prescription Drug Plan or an MA-PD Plan (section 2003 of
the SUPPORT Act) (section III.Q APA appreciates CMS continued
flexibility around the compliance date requiring the electronic
prescription of controlled substances (ECPS) for Part D clinicians in
light of the PHE.
As noted in this 10 proposed rule, and in
APA’s previous letters to the Administration, the PHE resulted in
numerous practical and administrative constraints of physicians in
transitioning to ECPS by the original date of January 2021, and we
appreciate CMS's previous action in moving the compliance date to January
2022.
APA supports CMSs current proposal to move compliance to January 2023.
APA
also supports the proposed compliance threshold that would apply to all
ECPS for Part D clinicians, including:
When it would be impractical for
the patient to obtain medication (prescribed by electronic
prescription in a timely manner and such delay would adversely impact
the patient’s medical condition.
When the National Council for
Prescription Drug Programs (NCPDP) standard does not support
transmitting the prescription, APA also recommends that CMS consider an
additional compliance threshold based on clinician practice size, such
as used in the MIPS Promoting Interoperability program.
Updates
to the Quality Payment Program(section IV.)
APA appreciates CMS’s
effort to make minimal changes to the QPP program in light of the
COVID-19 Public Health Emergency and the unique pressures our health
care systemcontinues to be under at this time.
Our comments focus on the MIPS Value Pathways (MVPs) program and efforts to incorporate cost measures into the MIPS program.
Cost
measures APA continues to have strong concerns about application of
episode-based cost measures (ECBMs) to individual clinicians, both as
part of the overall MIPS program and through MVPs specifically.
As
APA has expressed previously, existing and proposed ECBMs, as applied
to psychiatrists, present serious challenges across multiple dimensions,
including but not limited to:
Psychiatrist control over key
cost-related factors There is a limited range of costs that are directly
within the control of individual psychiatrists, particularly those
practicing in the inpatient environment, and minimal opportunities to
exert indirect control over many of the costs included as part of the
current ECBM attribution methodology.
This undermines both the
validity of the measures and their effectiveness of measures as
incentives for behavioral change, as clinicians will find it difficult
to understand how their behavior is connected to increases or decreases
in cost measure scores.
Potential for unintended consequences
Without a full understanding of contributors to the varying costs of
psychosis related care, emphasizing cost reduction creates a significant
likelihood of unintended consequences, including potential for the
measure to exacerbate problems with access to care.
Many
psychiatrists care for a highly vulnerable population of patients who
experience high rates of unemployment high and where socioeconomic
challenges are common.
We know that individuals with serious
mental illness have substantial physical health comorbidities and a
lifespan that is as much as 20 years less than that of the population as
a 11 whole.
Cognitive aspects of aging also appear to be accelerated in these individuals.
Efforts
to reduce costs of care in these individuals may place them at even
further disadvantage, with even greater disparities among Blacks,
Latinx, and Indigenous People as has been starkly evident in health care
delivery during the pandemic.
We urge CMS to avoid implementing measures or policies that have the potential to deepen inequities in access to care.
Transforming
MIPS: MIPS Value Pathways APA supports the concept of MVPs and applauds
CMS’s efforts to develop a measurement program that is more
conceptually coherent, focused on improvement, and relevant to specialty
practices than past activities.
However, as expressed above,
there remain serious practical concerns about the implementation of cost
measures, which are a key component of MVPs.
We are concerned
that use of problematic cost measures will undermine the intent and
effectiveness of the MVP program, and could lead to unintended
consequences, such as cherry-picking of patients who are likely to be
lower-cost, or further reduction in the number of psychiatrists willing
to accept Medicare patients.
There also continues to be gaps in
clinically-relevant quality measures for psychiatrists; we hope and
expect that this will be improved over time, but at present, the set of
measures available for mental and behavioral health is limited and is
focused largely on process metrics that have not been demonstrated to
have a high impact on patient outcomes.
CMS requests comment on what should happen when specialty clinicians cannot identify an applicable and relevant MVP.
APA
would suggest that CMS slow the transition from traditional MIPS to
MVPs to accommodate clinicians who cannot identify MVPs that are
directly relevant to their clinical practices, allowing those clinicians
to continue their participation in traditional MIPS until an
appropriate MVP is available.
Other CMS measurement policies In
addition to our comments on the proposed rule, APA would like to note
that having a sufficient number of quality measures available for
psychiatrists and members of the mental health care team is a priority
for APA.
We anticipate that this will likely involve developing
and then moving QCDR measures through the Measures Under Consideration
process and into the MIPS program.
Over the course of the last
four years, the number of measures approved via the MUC has declined
precipitously, from several dozen measures to only four quality measures
last year.
Combined with measure attrition, the availability of quality measures for groups to report has become much tighter.
CMS
should rebuild the library of MIPS measures available for reporting by
encouraging the submission of QCDR measures through the MUC process.
However, rebuilding a library of quality measures will be challenged by regulations finalized by CMS last year.
We are very concerned about CMS’s policy on measure testing for 2023 and beyond.
In
the 2021 quality payment program rule, CMS finalized a proposal to
require face validity testing for measures in 2022 and then “full
testing” for measures submitted as part of the QCDR in 2023.
Because
data to fully test a quality measure for validity is difficult to
capture, we cannot support requirements that each measure be tested for
validity beyond face validity.
12 We recognize that CMS will attempt to implement these testing requirements over the next year.
In
2020 and again in 2021, CMS rightly allowed groups that were disrupted
by the COVID-19 pandemic to apply for and receive a hardship exemption.
That policy, however, reduced the amount of data available for measure testing.
Because
the extreme and uncontrollable circumstances policy decreased the
number of groups able to report quality data, we ask that measure
testing requirements (not including face validity testing) be delayed
until two years after the end of the public health emergency (PHE).
In
addition, CMS should approve an improvement activity for groups that
assist measure stewards with measure development and testing efforts.
Measure
development requires a significant amount of time, money, and analysis
to complete, and often relies on volunteers to collect and report data
to help assess measure feasibility, reliability, and validity.
Offering
MIPS eligible clinicians and groups opportunities to earn improvement
activities credit for helping improve the measures offered in MIPS is a
worthwhile and meaningful action CMS can take immediately.
Proposed
Changes to the Medicare Promoting Interoperability Program The APA
appreciates the continued flexibility in reporting requirements under
the Promoting Interoperability program for Eligible Clinicians (ECs),
including options surrounding measure choice, scoring, and opportunities
for bonus points.
Please find feedback regarding the proposed
changes below: 4(b ...the performance period for the Promoting
Interoperability performance category is a minimum of any continuous
90-day period within CY 2022...we are not proposing any changes to the
Promoting Interoperability performance category... APA appreciates that
CMS has maintained the 90-day reporting period for these electronic
measures since the inception of MACRA in 2015.
APA supports maintaining this reporting period window, keeping consistent with previous reporting years.
Proposed
Changes to the Query of Prescription Drug Monitoring Program Measure
Under the Electronic Prescribing Objective (4 (c (i ) APA supports
maintaining the PDMP measure as optional for CY2022, and also supports
increasing the bonus for reporting on this measure from 5 points to 10.
As
we have stated in previous letters to CMS, it is still premature to
require the Query of PDMP measure and then include it in the Promoting
Interoperability score.
As CMS has acknowledged, there are still technical challenges associated with connecting PDMPs with various EHR systems.
Our
membership remains affected by these technical challenges, which
include: a a lack of standards connecting PDMPs and EHRs, b the policy
(e g , statutory) and other technical challenges around integrating
state PDMPs with HIEs and hospitals, c addressing the challenges in
integrating PDMP queries seamlessly into physician workflows, d the cost
and time required for developers—and subsequent downstream financial
impact on physicians/hospitals—to develop standards and technological
solutions to better integrating PDMPs with other health IT software and
finally, e the burden in tracking and calculating numerator/denominator
requirements for the PDMPs.
13 Moreover, not only do these
challenges remain, but they were difficult to address during the PHE by
healthcare organizations, as they shifted resources to mitigate the
ongoing public health crisis.
Additionally, as ONC and CMSs Final
Rule around Interoperability and Information Blocking were released in
2020, with the revised Applicability Date of April 2021, clinicians sand vendors priorities had to be adjusted to meet the expectations around
complying with these regulations.
Thus, waiting to require the
Query PDMP measure under the Electronic Prescribing Objective would give
hospitals and vendors more time to adapt their systems accordingly.
As the technology necessary to connect PDMPs with HIT systems matures, requiring this measure will become less burdensome.
For
example, the 2020 PFS outlined a transition to the updated CEHRT 2015
Edition standard and a transition for CEHRT to use the NCPDP SCRIPT
2017071 standard for electronic prescribing; the ONC, in its 21st
Century Cures Final Rule, requires those vendors developing CEHRT for
Promoting Interoperability will use FHIR open APIs to connect providers
and other users of HIT.
Given these advancements, APA is
optimistic that, in time, the data captured by PDMPs will be able to
flow through the HIT ecosphere without significant burden to hospitals
and providers.
We look forward to continuing to be part of the
conversation regarding how the Query PDMP measure can be successfully
implemented in the Medicare Promoting Interoperability Programs in the
future.
(B to modify the Provide Patient’s Electronic Access to
Their Health Information measure to establish a data availability
requirement beginning with encounters with a date of service on or after
January 1, 2016, beginning with the EHR reporting period in CY 2022
Currently, the Provide Patient Access to Their Health Information does
not specify how long MIPS eligible clinicians are required to make
patient data available, or to ensure that patient data remain available
to patients in the event that an EC switches EHR vendors.
APA
appreciates CMSsintent to align the Provide Patient Electronic Access to
Their Health Information measure with the look-back period finalized in
the Patient Access and Interoperability final rule.
While the
January 1, 2016 date seems reasonable for ECs, the APA recommends that
CMS delay enforcement discretion from July 1, 2021, to the end of CY
2021, to account for the ongoing COVID-19 PHE.
Moreover, APA
seeks clarification that, during this lookback period, and other
proposed future accessibility requirements around changes to the Provide
Patient Access PI measure, that ECs can exercise the pertinent
Exceptions under the Information Blocking and Interoperability Final
Rule.
Specifically, that the Infeasibility, Content and Manner,
and Health IT Performance Exceptions may be employed, when applicable,
by the EC, when maintaining patient data in near-perpetuity may not be
possible for MIPS- eligible clinicians.
Additionally, APA seeks
clarification on whether this change to the Provide Patient Access
measure will only apply to the reporting years for which the clinician
was eligible and did not meet any of the MIPS program exceptions, such
as the low-volume threshold.
Clarifying the above points will
help to reduce burden among solo and small group psychiatrist ECs who
may not participate in MIPS in consecutive years.
14 Reweighting
the Promoting Interoperability Performance Category for MIPS Eligible
Clinicians in Small Practices APA appreciates CMS scontinued efforts to
reduce administrative and financial reporting burden for small practices
endeavoring to participate in MIPS.
As noted in this Proposed
Rule, many small practices may be eligible for the LVT; or, qualify as
small practices (i e , under 15 ECs), and therefore can apply for an
Exception to the Promoting Interoperability category, when there are
“overwhelming barriers” to participating.
In response to the
questions posed in this Rule, APA is unable to ascertain the specific
reason(s as to why some small practices may fail to apply for the Small
Practice Hardship Exception for the Promoting Interoperability
performance category, while still participating in MIPS as a whole.
This
is possibly because many of our members in solo or small group
practices qualify for a total exemption for all of MIPS under the Low
Volume Threshold; or, as CMS contemplates in this rule, they may be
unaware of the Exception itself, or may believe that they do not meet
the requirements of “overwhelming barriers.”
Regardless of reason, APA
supports CMS recommendation to automatically redistribute points from
the PI performance category to other performance categories of MIPS for
small practices who do not apply for the Exception, but who would have
been eligible, in order to avoid receiving a score of zero for the PI
category.
(ii)
We are proposing to add a new SAFER Guides
measure to the Protect Patient Health Information objective...we are
proposing that a MIPS eligible clinician must attest to having conducted
an annual self assessment using the High Priority Practice Guide, at
any point during the calendar year...with one “yes/no” attestation
statement accounting for the complete self-assessment using the guide.
Generally,
the APA supports the use of the Safety Assurance Factors for EHR
Resilience (SAFER) Guides, particularly the High Priority Practices
Guide, as a part of the Promoting Interoperability performance category.
Requiring
ECs to attest to completing these guides has the potential to help many
clinicians enhance and optimize health IT, ensuring that they are
“responsible operators of technology tools,” as stated in this proposed
rule.
This attestation is reminiscent of the existing Security
Risk Assessment measure in its utility to safeguard patient information,
and in that it will not be scored for PI.
While we appreciate
CMS acknowledgement ECs (especially those in solo or small group
practice) vary in terms of resources with respect being able to complete
the SAFER attestation annually, APA recommends that, for the 2022 RY,
CMS conduct an audit of those entities that attest “no,” in order to
ascertain why they did not complete a SAFER attestation, to see if
additional resources might support them in doing so for future reporting
years.
We are also more broadly soliciting public comment to
help us better understand the resource costs for services involving the
use of innovative technologies, including but not limited to software
algorithms and AI.
In addition to this broader prompt, CMS poses
a list of questions for consideration regarding the use of innovative
technologies within physician practices.
For example, the Rule
considers how technologies, 15 such as AI, have affected physician work
time and intensity of furnishing services (e g , possibly reducing the
amount of time that a practitioner spends time reviewing and
interpreting results of diagnostic testing), or how technologies are
changing cost structures, affecting access to services for Medicare
beneficiaries, and more.
While APA and psychiatry continues
apace in adopting new technologies into clinical workflows—such as
adjunctive therapeutic mobile applications, and wearables—it is
qualitatively different from how other specialties are using it.
For
example, in the Rule, CMS uses examples such as a simulation software
analysis of functional data to assess the severity of coronary artery
disease and how trabecular bone score software can supplement physician
work to predict and detect fracture risk.
These examples might
be considered as straightforward use cases of emerging technology where
an attempt to codify and quantify their value to Medicare practitioners
and beneficiaries seems reasonable.
For psychiatry some
analogous use cases, such as various emerging technologies utilizing
focused on discrete physiological symptoms (e g , neuropsychiatry,
movement disorders, clinical decision support, work on neurolinguistics
in detecting changes in language use patterns in predicting psychopathy
or dementia); however, presently, there are too few data points and
replicated research into how AI or other technologies are or can affect
psychiatric work flows, physician time, and other considerations as
contemplated in this Rule.
The use of AI in healthcare is still nascent.
With
respect to psychiatry, most AI-driven tools are embedded within health
IT products more appropriately described as “augmented intelligence”
rather than “artificial intelligence.” The scope of this technology
tends to encompass features of electronic health records (EHRs), such as
electronic clinical decision support (eCDS), and in mHealth, such as
apps that rely on patients behavioral history to send warnings to the
patient about environmental factors that could potentially be triggering
for mental health conditions, such as substance use disorders.
While
APA is optimistic that the future of AI may improve patient care and
lead to better outcomes, we are concerned that there are presently very
few standards to which industry is being held in the development of AI
in healthcare.
For instance, standards around privacy, security, and confidentiality within health IT is currently in flux.
There
are also limited regulatory standards on the development and
implementation of AI tools, which further complicates how such tools may
be accounted for in terms of quality care and outcomes when integrated
into Medicare payment considerations.
ermination Do you have a
policy on circumstances that may lead to terminating the relationship
with a patient? Does the policy include the state requirements to
properly terminate the relationship? The APA is also concerned around
background development of AI systems that may not include specific
populations within standardization samples in AI beta testing/research
studies.
Presently, some algorithms may be based solely on a
certain population for various medical conditions (e g , men or women;
various ethnicities; various socioeconomic groups) resulting in
algorithms that may not compute the best treatment options or
interventions for patients with unique vulnerabilities (e g ,
developmental disorders, suicidal ideation, substance use disorders).
Before
the technology can be incorporated into Medicare payment models, there
needs to be a comprehensive examination (by CMS, the FDA, other
entities), of which data are being used to develop any algorithms that
influence physician decision-making and patient care.
There
needs to be an assurance that AI helps patients regardless of one’s
race/ethnicity or other social determinants of health and isn’t
introducing or magnifying disparities.