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Federal Policy Updates

For state specific policy head to State Policy Updates


Senators Capito and Manchin Reintroduce the Protecting Jessica Grubb's Legacy Act

The PCC is excited to sign on to the a letter supporting Senators Shelley Moore Capito (R-WV) and Joe Manchin (D-WV) and their efforts to reintroduce the Protecting Jessica Grubb's Legacy Act.  This bipartisan legislation will modernize patient privacy protections and allow for appropriate access to patient information. This will allow the patient to receive safe, effective, whole person care. 

Multi-Stakeholder Coalition Applauds Congress for Bill to Increase Access to Preventative Treatments

June 25, 2019

The Honorable John Thune
511 Dirksen Senate Office Building
Washington, DC 20510

The Honorable Tom Carper
513 Hart Senate Office Building
Washington, DC 20510

The Honorable Earl Blumenauer
1111 Longworth House Office Building
Washington, DC 20515

The Honorable Tom Reed
2263 Rayburn House Office Building
Washington, DC 20515

Dear Congressmen,

On behalf of the Smarter Health Care Coalition (the Coalition) and the undersigned organizations, we are writing to applaud the introduction of the Chronic Disease Management Act of 2019. The Coalition represents a broad-based, diverse group of health care stakeholders, including consumer groups, employers, health plans, life science companies, provider organizations, and academic centers. The Coalition is squarely focused on achieving “smarter health care” by removing barriers to clinically-nuanced health care services and medications. Our goal is to better align health care spending with value, improve the patient experience, and lower health care costs by supporting innovative benefit design that encourages the use of high valuecare, and discourages the use of low-value care.

As such, the Coalition supports your legislation, which would help patients with chronic illness access high-value health care services and medications that ensure optimal health and wellbeing. As you know, approximately half of all Americans have at least one chronic condition and millions struggle to receive the appropriate care due to onerous cost burdens. Studies show that chronic conditions account for $.90 of every dollar spent on health care and, without appropriate management, lead to adverse effects on quality of life. As such, the management of chronic conditions and the prevention of further complications is not only essential to improving health but would ensure a more rational and sustainable health care system.

Yet certain health benefit arrangements face regulatory barriers to ensure patients have access to critical, high-value care. Specifically, when a health savings account (HSA) is paired with a high deductible health plan (HDHP), these plans are generally prohibited from offering services and medications to manage chronic conditions on a pre-deductible basis. This problem is exacerbated by the fact that the HSA-HDHP marketplace is expanding rapidly. Studies show the percentage of employers offering HDHPs grew by 25 percent between 2005 and 2018, and the percentage of employees covered by HDHPs over the same period grew by 25 percent.1 Additionally, the Kaiser Family Foundation’s 2018 Employer Health Benefits Survey shows the average annual deductibles for all plan types have increased 212 percent since 2008.1

The legislation addresses this problem by allowing HSA-eligible HDHPs to provide access to health care services and medications that manage chronic conditions on a pre-deductible basis. Simultaneously, the Coalition continues to work with the Administration by encouraging the Department of the Treasury to utilize existing authority to include chronic disease management as part of the preventive care definition, which would make it possible for employers and health plans to decrease out-of-pocket spending for millions of Americans with chronic conditions.

Enacting this legislation or updating existing guidance would yield enormous benefits to consumers, employers, and payers alike including better health, enhanced workplace productivity, and the avoidance of unnecessary emergency care visits and hospitalizations to the benefit of patients and our health care system overall. Thank you for introducing this important legislation and we look forward to working with you.

Sincerely,

America’s Health Insurance Plans
American Benefits Council
American Osteopathic Association
Amgen
Blue Cross Blue Shield Association
Eli Lilly
Families USA
Juvenile Diabetes Research Foundation
Merck
National Coalition on Health Care
Patient-Centered Primary Care Collaborative
Public Sector Health Care Roundtable
Sanofi
University of Michigan V-BID Center
U.S. Chamber of Commerce


1 Kaiser Family Foundation, 2018 Employer Health Benefits Survey, September 2018, available at, https://www.kff.org/report-section/2018-employer-health-benefits-survey-section-8-high-deductible-health-plans-with-savings-option/

Health Organizations Support Removing Cost-sharing from Chronic Care Management

June 25, 2019

The Honorable Suzan DelBene
2330 Rayburn House Office Building
Washington, DC 20515

Dear Representative DelBene,

We the undersigned organizations are writing to offer our strong endorsement of your legislation to ensure that more chronically ill Medicare patients receive access to the best care. By removing the costsharing obligations from the Chronic Care Management (CCM) code, more chronically ill Medicare beneficiaries will benefit from the care coordination and case management services the code supports.

CCM is a critical part of coordinated care, and as a result, Medicare began reimbursing physicians for CCM under a separate code in the Medicare Physician Fee Schedule. This code is designed to reimburse providers for non-face-to-face care management. We support this initiative to further manage chronic care conditions to improve the health of patients.

The creation of a separately billable code, however, created a beneficiary cost-sharing obligation for care management services. Under current policy, Medicare beneficiaries are subject to a 20% coinsurance requirement to receive the service. This cost-sharing requirement creates a barrier to care, as
beneficiaries are not accustomed to cost-sharing for care management services. Consequently, only 684,000 patients out of 35 million Medicare beneficiaries with two or more chronic conditions benefitted from CCM services over the first two years of the payment policy.

We support your legislation to waive the beneficiary co-insurance amount to facilitate further managing chronic care conditions to improve the health of patients. Providers and care managers report several positive outcomes for beneficiaries who receive CCM services, including improved patient satisfaction
and adherence to recommended therapies, improved clinician efficiency, and decreased hospitalizations and emergency department visits.

We appreciate your leadership on this issue. Please let us know how we can be a resource to ensure that this co-insurance requirement is repealed so that more Medicare beneficiaries gain access to providers who prioritize and coordinate care of the chronically ill.


Sincerely,

American Academy of Family Physicians
American College of Physicians
American Diabetes Association
American Medical Association
AMGA
American Osteopathic Association
America’s Physician Groups
Association of American Medical Colleges
Health Care Transformation Task Force
Healthcare Leadership Council
Medical Group Management Association
National Association of ACOs
Patient-Centered Primary Care Collaborative
Premier healthcare alliance

Multi-Stakeholder Coalition Applauds Congress for Bill to Continue Federal Funding for the National Quality Forum

June 20, 2019
The Honorable Judy Chu 2423 Rayburn House Office Bldg. Washington, DC 20515

The Honorable Eliot Engel 2426 Rayburn House Office Bldg. Washington, DC 20515

The Honorable Buddy Carter 2432 Rayburn House Office Bldg. Washington, DC 20515
Dear Representatives Chu, Engel and Carter,


As members of the Friends of NQF, we applaud your leadership and introduction of bipartisan legislation (H.R. 3031) continuing federal funding for the National Quality Forum.

Continued federal funding for the National Quality Forum (NQF) is foundational to efforts to achieve a cost-efficient, high-quality, value-based healthcare system that ensures the best care for Americans and the best use of the nation’s healthcare dollars. The introduction of your bill to reauthorize federal funding for NQF helps ensure that quality measures used in care delivery and payment reform continue to be reliable, effective and drive measurable improvements for our nation’s Medicare beneficiaries.

During the continued legislative process, we encourage the Committees on Energy and Commerce and Ways and Means to consider other changes to modernize and enhance the impact of NQF’s contribution to our nation’s continued commitment to value-based care. These changes would include:

• Improve public transparency and accountability regarding the use and implementation of measures, enabling public input into emerging Center for Medicare and Medicaid Innovation models;
• Advance quality improvement reforms that reduce administrative burden and foster alignment across programs and payers; and,
• Advance national health priorities and high-value, high-impact quality measures through innovations in measurement.

Thank you for your leadership and commitment to NQF. Continuing the nation’s work to advance quality, safety, and cost-effective healthcare is one objective we all share.
Sincerely,

The Friends of NQF

Academy of Managed Care Pharmacy
AdvaMed
Adventist Health System
AMDA - The Society for Post-Acute and Long-Term Care Medicine
America’s Physician Groups
American Academy of Dermatology
American Academy of Family Physicians
American Academy of Hospice and Palliative Medicine
American Academy of Ophthalmology
American Academy of Orthopaedic Surgeons
American Academy of Pediatrics
American Academy of Physical Medicine and Rehabilitation
American Association for Physician Leadership
American Association of Nurse Anesthetists
American Association on Health and Disability
American Board of Medical Specialties
American Cancer Society Cancer Action Network
American College of Cardiology
American College of Emergency Physicians
American College of Medical Quality
American College of Physicians
American College of Surgeons
American Geriatrics Society
American Health Quality Association
American Healthcare Association
American Heart Association/American Stroke Association
American Nurses Association
American Occupational Therapy Association
American Osteopathic Association
American Physical Therapy Association
American Psychiatric Association
American Society for Gastrointestinal Endoscopy
American Society of Anesthesiologists
American Society of Clinical Oncology
American Society of Colon and Rectal Surgeons
American Society of Health-System Pharmacists
American Society of Nephrology
America’s Essential Hospitals
America’s Health Insurance Plans
AmeriHealth Caritas
AMGA
Anthem, Inc.
Association for Community Affiliated Plans
Association for Professionals in Infection Control and Epidemiology
Association of American Medical Colleges
Association of periOperative Registered Nurses
BD
bioMérieux
Blue Cross Blue Shield Association
Blue Cross Blue Shield of North Carolina
CareFirst BlueCross Blue Shield
Carilion Clinic
Center to Advance Palliative Care
Children’s National Medical Center
Coalition to Transform Advanced Care
Compassus
Connecticut Center for Patient Safety
Consumer Coalition for Quality Health Care
Council of Medical Specialty Societies
Dental Quality Alliance
eHealth Initiative
ElevatingHOME
Eli Lilly and Company
Federation of American Hospitals
Focus on Therapeutic Outcomes
Fresenius Medical Care North America
Geisinger
Genetech, Inc.
GlaxoSmithKline
Greater Philadelphia Business Coalition on Health
Harborview Medical Center
HCA
Health Action Council
Health Care Service Corporation
Healthcare Leadership Council
HealthPartners, Inc., Bloomington Minnesota
HealthSouth
Henry Ford Health System
Hospice and Palliative Nurses Association
Human Services Research Institute
Humana
Informed Patient Institute
Integrated Healthcare Association
Intermountain Healthcare
Institute for Healthcare Improvement
Johns Hopkins Health System
Johns Hopkins Medicine Armstrong Institute for Patient Safety and Quality
Johnson & Johnson Health Care Systems, Inc.
Kaiser Permanente
Massachusetts General Hospital, Boston, MA
Medicare Rights Center
Memorial Hermann Health System
Memorial Sloan Kettering Cancer Center
Memphis Business Group on Health
Merck & Co.
Minnesota Health Action Group
MN Community Measurement
National Alliance of Healthcare Purchaser Coalitions
National Association of ACOs
National Association of Behavioral Healthcare
National Association of Pediatric Nurse Practitioners
National Business Group on Health
National Coalition for Hospice and Palliative Care
National Committee for Quality Assurance
National Council on Aging
National Health Policy Group
National Hospice and Palliative Care Organization
National Partnership for Hospice Innovation
National Partnership for Women and Families
National Patient Advocate Foundation
National Pressure Ulcer Advisory Panel
National Rural Health Association
National Sleep Foundation
Nemours Children’s Health System
Network for Regional Healthcare Improvement
New Jersey Health Care Quality Institute
New Jersey Hospital Association
Next Wave, Inc.
NICHE – Nurses Improving Care for Healthsystem Elders
Northeast Business Group on Health
Pacific Business Group on Health
Partners HealthCare
Patient-Centered Primary Care Collaborative
PCPI Foundation
PFCC Partners
Pharmacy Quality Alliance
PhRMA
Planetree International
Premier, Inc.
Press Ganey
Quality Insights, Inc.
SNP Alliance
Society for Maternal-Fetal Medicine
Society of Hospital Medicine
Society of Interventional Radiology
Society of Thoracic Surgeons
St. Louis Area Business Health Coalition
Suncoast RHIO
Tenet Healthcare, Inc.
The Alliance
The Council on Quality and Leadership
The Health Collaborative
The Joint Commission
The Leapfrog Group
University of Pennsylvania Health System Penn Medicine
University of Texas MD Anderson Cancer Center
Vizient, Inc.
Wisconsin Collaborative for Healthcare Quality
Women’s Care Florida


CC: Chairman Richard Neal House Committee on Ways and Means Washington, DC 20515
Ranking Member Kevin Brady House Committee on Ways and Means Washington, DC 20515
Chairman Frank Pallone, Jr. House Committee on Energy and Commerce Washington, DC 20515
Ranking Member Greg Walden House Committee on Energy and Commerce Washington, DC 20515

PCPCC and Others Call on Congress to Address Patient Matching in 2020 Appropriations Bills

June 3, 2019

The Honorable Richard Shelby, Chairman
Senate Committee on Appropriations
Room S-128, The Capitol
Washington, D.C. 20510

The Honorable Roy Blunt, Chairman
Subcommittee on Labor, Health and Human Services, Education, and Related Agencies
Senate Committee on Appropriations
131 Dirksen Senate Office Building
Washington, DC 20510

The Honorable Patrick Leahy, Vice Chairman
Senate Committee on Appropriations
S-146A, The Capitol
Washington, DC 20510

The Honorable Patty Murray, Ranking Member
Subcommittee on Labor, Health and Human Services, Education, and Related Agencies
Senate Committee on Appropriations
156 Dirksen Senate Office Building
Washington, DC 20510

Dear Chairman Shelby, Vice Chairman Leahy, Chairman Blunt and Ranking Member Murray:

On behalf of the undersigned organizations, we wish to urge inclusion of report language that seeks to end patient safety issues related to patient matching in the Senate Fiscal Year 2020 Labor, Health and Human Services, and Education and Related Agencies (Labor-HHS) Appropriations Bills.
For nearly two decades, innovation and industry progress has been stifled due to a narrow interpretation of the language included in Labor-HHS bills since FY1999, prohibiting the U.S. Department of Health and Human Services (HHS) from adopting or implementing a unique patient identifier. More than that, without the ability for clinicians to correctly connect a patient with their medical record, lives have been lost and medical errors have needlessly occurred. These are situations that could have been entirely avoidable had patients been able to have been accurately identified and matched with their records. This problem is so dire that one of the nation’s leading patient safety organization, the ECRI Institute, named patient identification among the top ten threats to patient safety.1

Importantly, recently proposed rulemakings by both the Centers for Medicare and Medicaid Services (CMS) and the Office of the National Coordinator for Health Information Technology (ONC) have referenced the existing funding prohibition and have cited the patient matching strategy appropriation report language included in previous Labor-HHS bills to explore new and innovative ways that the Administration can work with industry stakeholders on this critical patient safety and care issue. Moreover, the ability to accurately match patients to their records across the care continuum is an imperative for achieving greater value and better outcomes in our healthcare system and a critical piece of the interoperability puzzle.

The patient matching report language below, which has been included in the House FY20 Labor-HHS bill, clarifies Congress’ intent while ensuring that the federal government does not impede private-sector efforts to solve this serious problem. The language enables HHS, acting through ONC and CMS, to provide technical assistance to private-sector led initiatives that support a coordinated national strategy to promote patient safety by accurately identifying patients and matching them to their health information. Allowing ONC and CMS to offer this type of technical assistance will help accelerate and scale safe and effective patient matching solutions.
The absence of a consistent approach to accurately identifying patients has resulted in significant costs to hospitals, health systems, physician practices, long-term post-acute care (LTPAC) facilities, and other providers, as well as hindered efforts to facilitate health information exchange. According to a 2016 study of healthcare executives, misidentification costs the average healthcare facility $17.4 million per year in denied claims and potential lost revenue. More importantly, there are patient safety implications when data is matched to the wrong patient and when essential data is lacking from a patient’s record due to identity issues. The 2016 National Patient Misidentification Report cites that 86 percent of respondents said they have witnessed or know of a medical error that was the result of patient misidentification.

Patient identification errors often begin during the registration process and can initiate a cascade of errors, including wrong site surgery, delayed or lost diagnoses, and wrong patient orders, among others. These errors not only impact care in hospitals, medical practices, LTPAC facilities, and other healthcare organizations, but incorrect or ineffective patient matching can have ramifications well beyond a healthcare organization’s four walls. As data exchange increases among providers, patient identification and data matching errors will become exponentially more problematic and dangerous. Precision medicine and disease research will continue to be hindered if records are incomplete or duplicative. Further, as our nation combats a growing opioid epidemic, successfully matching patients with their records is critical. Accurately identifying patients and matching them to their data is essential to coordination of care and is a requirement for health system transformation and the continuation of our substantial progress towards nationwide interoperability, a goal of the landmark 21st Century Cures Act.

The ability to identify patients across the care continuum is critical in our efforts to fight the opioid epidemic. Patients being treated for opioid use disorder and patients who have experienced an opioid overdose, for example, may be especially vulnerable and need careful monitoring to help them continue in their recovery and avoid new overdose episodes, both of which hinge in part on the ability to link patients with their complete health data. Appropriately-obtained accurate and complete health data can improve prescribing decisions and help clinicians avoid inadvertently prescribing opioid analgesics to patients with these risk factors. Risk factors could be identified and tracked over time and could enable clinicians to take steps to reduce overdose risks, such as prescribing naloxone, as well as to ensure timely follow-up and save lives.

The quality, safety and cost-effectiveness of healthcare across the nation will improve if a national strategy to accurately identify patients and match those patients to their health information is achieved. Clarifying Congress’ commitment to ensuring patients are consistently matched to their healthcare data is a key barrier that needs to be addressed if we are to solve this problem, but not the only one. We the undersigned are committed to working together to identify and address, the various barriers that prevent patient matching today.

We respectfully request that you include the report language below in any FY20 appropriations bill:

Clarifying the Unique Patient Identifier Ban to Enable Patient Matching
The Committee is aware that one of the most significant challenges inhibiting the safe and secure electronic exchange of health information is the lack of a consistent patient data matching strategy. With the passage of the HITECH Act, a clear mandate was placed on the Nation’s healthcare community to adopt electronic health records and health exchange capability. Although the Committee continues to carry a prohibition against HHS using funds to promulgate or adopt any final standard providing for the assignment of a unique health identifier for an individual until such activity is authorized, the Committee notes that this limitation does not prohibit HHS from examining the issues around patient matching. Accordingly, the Committee encourages the Secretary, acting through the Office of the National Coordinator for Health Information Technology and CMS, to provide technical assistance to private-sector led initiatives in support of a coordinated national strategy for industry and the federal government that promote patient safety by accurately identifying patients to their health information.

We appreciate your consideration and inclusion of this report language and we look forward to working with you to pursue an appropriate solution to enable accurate patient identification and data matching in our nation’s healthcare system.

Sincerely,

American Health Information Management Association (AHIMA)
America’s Health Insurance Plans (AHIP)
American Medical Association (AMA)
American Medical Informatics Association (AMIA)
Blue Cross Blue Shield Association (BCBSA)
College of Healthcare Information Management Executives (CHIME)
eHealth Initiative (eHI)
EP3 Foundation
Federation of American Hospitals (FAH)
Health Innovation Alliance
Healthcare Information and Management Systems Society (HIMSS)
Healthcare Leadership Council (HLC)
himagine solutions, Inc.
Imprivata
Intermountain Healthcare
Just Associates, Inc.
LTPAC Health IT Collaborative
4medica
Medical Group Management Association (MGMA)
Nemours Children’s Health System
NextGate
Patient-Centered Primary Care Collaborative
Premier healthcare alliance
The Sequoia Project
Strategic Health Information Exchange Collaborative (SHIEC)
Trinity Health
Verato
WebShield

 

UPDATE:  On July 11, many of the same organizations came together to support an amendment being offered by Representative Bill Foster (IL) and Representative Mike Kelly (PA) to HR 2740.  The Amendment strikes Section 510 of the Labor-HHS Appropriations bill which currently prohibits the US Department of Health and Human Services from spending any federal dollars to promulgate or adopt a national patient identifier.

PCPCC Joins Other Stakeholders in Commenting on Pediatric EHRs

June 3, 2019

Donald Rucker, MD
National Coordinator
Office of the National Coordinator for Health Information Technology
Department of Health and Human Services
Mary E. Switzer Building
330 C Street SW
Washington, DC 20201

RE: RIN 0955-AA01: 21st Century Cures Act: Interoperability, Information Blocking, and the ONC Health IT Certification Program

Dear National Coordinator Rucker:

Our organizations—which represent physicians, nurses, hospitals, public health professionals, and other stakeholders—encourage the Office of the National Coordinator for Health Information Technology (ONC) to prioritize patient safety as part of its efforts to implement new criteria for electronic health records (EHRs) used in the care of children.

Given that the care of children can differ significantly from that of adults, the technology used by clinicians should account for that variation. For example, children often receive medication doses based on their weight. Similarly, chronological or gestational age may be used for medication dosing in highly vulnerable premature infants. The EHRs used to prescribe those drugs should account for these critical dosing differences, which—coupled with the use of technology that is not geared towards these unique variations—can contribute to medical errors in pediatric care.

Safety problems associated with the use of EHRs in pediatrics often stem from system usability, which refers to how the technology can be effectively and efficiently used by clinicians. System layout, customizations, facility workflows, and many other factors can affect EHR usability for pediatric providers.

Poor usability can have significant negative consequences. It can contribute to clinician burden when using systems, which can harm the efficiency and quality of care. Poor usability can also contribute to medical errors. Research published in the November 2018 edition of Health Affairs showed that EHR usability contributed to medication errors in 3,243 of 9,000 safety events examined across just three health care organizations that care for children.1 Additionally, recent examples of EHR usability-related medical errors showcased pediatric-specific challenges, such as with newborn care and weight-based dosing.2

Recognizing this challenge, Congress—via the 21st Century Cures Act (Cures) passed in 2016—required ONC to establish voluntary certification criteria for EHRs used in pediatric settings. To implement this provision, the ONC proposed rule identifies 10 clinical priorities for pediatric care. ONC also included worksheets to map each of these clinical priorities to existing and proposed requirements for EHRs. For example, ONC proposes that EHRs used in pediatric care should have the ability to compute the weight-based dosage of a medication and could use EHR functions for electronic drug prescribing with pediatric vital signs to meet this clinical priority.

While we generally support the 10 clinical priorities identified by ONC for pediatric care, including weight-based drug dosing, tools to support growth charts for children, and age-based dose checking, we
assert the agency can take additional steps to improve patient safety and system usability for EHRs used in the care of children. These include:

  • Mapping additional existing EHR certification requirements to pediatrics - ONC should further extend the approach taken in the proposed rule to map the agency’s existing EHR certification requirements to pediatric care. For example, ONC currently requires that all EHR developers test their system using predefined scenarios that mimic real-world situations. ONC should clarify that demonstrating adherence to the 10 clinical priorities must involve pediatric-focused scenarios. Similarly, ONC currently requires that EHR developers test their system with end-users, such as physicians and nurses. ONC should clarify that EHR developers must involve end-users that care for children—such as pediatricians and pediatric nurses—in the testing of the identified clinical priorities in pediatric care.
  • Providing additional pediatric-focused resources - ONC should ensure that the appropriate resources are available to support meeting pediatric-focused criteria. For example, ONC should develop specific and detailed guidance for each proposed pediatric clinical priority. In addition, ONC should involve pediatric usability experts in the development of implementation guides and test procedures for the pediatric clinical priorities.

Conclusion

Cures directed ONC to address deficiencies in the use of technology in pediatric settings. By incorporating these additional recommendations into its development of a pediatric EHR certification program, ONC can take concrete steps to improve the usability of EHRs used in pediatric care to both reduce clinician burden and prevent medical errors.

Thank you for the opportunity to comment on the proposed rule to implement new criteria for EHRs used in the care of children. Should you have any questions or if we can be of further assistance, please contact Ben Moscovitch, director, health information technology, The Pew Charitable Trusts at bmoscovitch@pewtrusts.org or 202.540.6333.

Sincerely,

American Academy of Pediatrics
American Nurses Association
Arkansas Children’s Hospital
Children’s Hospital Association
Drummond Group
Medical Group Management Association
MedStar Health
Patient-Centered Primary Care Collaborative
The Pew Charitable Trusts
The University of Texas, UT Health Austin

 

PCPCC and Others Support CMS Proposal For Information Sharing With Community Practitioners

June 3, 2019

Submitted via www.regulations.gov
Ms. Seema Verma
Administrator
Centers for Medicare & Medicaid Services
7500 Security Boulevard
Baltimore, MD 21244

RE: CMS–9115–P; Medicare and Medicaid Programs; Patient Protection and Affordable Care Act; Interoperability and Patient Access for Medicare Advantage Organization and Medicaid Managed Care Plans, State Medicaid Agencies, CHIP Agencies and CHIP Managed Care Entities, Issuers of Qualified Health Plans in the Federally Facilitated Exchanges and Health Care Providers

Dear Administrator Verma,

We write to express strong support for CMS’ proposal to require hospitals participating in Medicare and Medicaid to send event notifications – also known as admission/discharge/transfer or ADT feeds – to community practitioners. These notifications are critical to improving patient safety through better care transitions and are key to enabling value-based care at scale.

Although our organizations play different roles in the health care system, we are united in a common commitment to realizing the promise of health care data through increased information sharing. We believe that advancing regulations that lead hospitals to share information with community practitioners is a transformative step toward greater data liquidity that will enable better decision-making, reduce waste, and improve outcomes for patients. The benefits of such notifications are evident in states and localities where this information is shared today, and CMS’ proposal will ensure that they are experienced by all patients regardless of where they live.

Below we put forth several recommendations designed to further strengthen and refine CMS’ approach based on our real-world experience.

1. Hospitals are able to send ADT notifications today without any new standards or use of certified EHRs to collect data.
While there are many hospitals that have chosen not to share ADT feed alerts with community providers for competitive or other reasons, states such as Connecticut, Iowa, Wisconsin, Florida, Tennessee, Maryland and New York have already taken steps to encourage hospitals to share ADT feeds with community providers. In other localities, many hospitals are sharing alerts with accountable care organizations (ACOs) and other providers, on their own or through intermediaries.
We stress that hospitals are able to share ADT notifications today using their existing systems, and by working with a health information exchange (HIE) or health information network (HIN), contracting with a vendor that can send the alerts on their behalf, or building their own interfaces. As evidenced by the widescale adoption of this use case today, new standards efforts are not needed for the successful, immediate implementation of the proposed requirements. In numerous conversations with HIEs, other intermediaries and providers, we were unable to find a single example where a hospital was unable to send an ADT notification today due to lack of standards. For the future, further development of ADT messaging standards could be useful to support inclusion of new data elements and/or types of notifications.

2. CMS should strike language limiting proposed requirements to hospitals with EHR systems, recognizing that many facilities use other types of systems to send notifications.
While CMS proposed to limit the new requirements to hospitals that currently possess an EHR system with the capacity to generate the basic information needed for the notification, it is not necessary to use an EHR to gather the required information or send the notification. In fact, many hospitals use administrative IT systems for this purpose. We encourage CMS to strike this language and instead allow hospitals the flexibility to choose how to comply with the new requirement.

3. Event notifications should be shared for patients who present in the ED regardless of whether they are subsequently admitted as an inpatient, and the minimum information included in the notification should be expanded to include discharge disposition.
We strongly encourage CMS to expand the patient population to whom this requirement applies to include patients who present in the ED and are subsequently discharged without being admitted, as well as those patients who are admitted in observational status. Planning for a safe care transition begins when a patient presents in the ED regardless of whether they are admitted to the facility. In addition, notifying the community practitioner when a patient visits the ED enables them to intervene immediately which can improve outcomes for the patient and result in better coordination that reduces costs and prevents waste.
We also recommend that CMS expand the minimum information in the notification to include the discharge disposition data field. This information is critical for community providers because it gives insight into the outpatient care recommended to the patient and better enables the provider to follow-up with the patient on their hospital visit and coordinate any additional care.

4. CMS should consider other policy options for replacing and/or augmenting what constitutes “reasonable certainty” with respect to receipt of notifications.
We appreciate the need for CMS to establish parameters around a hospital’s responsibility for sharing information with community practitioner. While we agree that an exception may be needed when technical issues beyond a hospital’s control prevent successful receipt and use of a notification, we are concerned that the “reasonable certainty” standard may not be specific enough to ensure the requirement has the intended effect on information sharing.

Accordingly, we recommend that CMS consider other policy options for replacing and/or augmenting the “reasonable certainty” standard included in the proposed regulation. For example, we encourage CMS to deem a hospital compliant if they send the required information to an intermediary for distribution to their provider networks if the intermediary is covered by the prohibition on information blocking. A hospital would be compliant with the new requirement if they: 1) attest that they are not information blocking through the Promoting Interoperability Program; and 2) generate a notification and share it with the intermediary, but it is not ultimately sent because there is no subscribing provider.

This is an important clarification that ensures hospitals receive credit if they are unable to comply through no fault of their own. It also reinforces that hospitals have discretion in determining the technological mechanism through which they will share notifications; we urge CMS to further clarify this point in the final rule.

5. CMS should implement a feedback mechanism for community providers to report issues receiving ADT notifications.

We encourage CMS to consider creating a feedback mechanism for community providers that have the ability to receive notifications yet get incomplete, unreasonably delayed, or no data at all to log or report these issues.

Conclusion

Advancing regulatory levers to promote Medicare and Medicaid-participating hospitals to share ADT feeds has the potential to significantly improve care for patients across the country. CMS’ proposed rule is a significant first step on the path to greater information sharing and interoperability. We encourage CMS to implement this new requirement expeditiously (e.g., within months) given that there are no technical barriers to doing so.

Sincerely,

Aledade
American Academy of Home Care Medicine
Audacious Inquiry
Beth Israel Deaconess Care Organization
Biden Cancer Initiative
Blue Shield of California
Caregiver Action Network
Community Care Collaborative of Pennsylvania and New Jersey
Elation Health
Florida Association of ACOs
Greater Houston Healthconnect
Healthix
Iora Health
Keystone ACO
Lahey Clinical Performance ACO
Lahey Clinical Performance Network
MaineHealth Accountable Care Organization
Manifest Medex
Mental Health America
Missouri Health Connection
National Association of Accountable Care Organizations
National Council for Behavioral Health
National Partnership for Women & Families
NEQCA Accountable Care, Inc.
Network ACO
OneHealth Nebraska
Partnership to Empower Physician-Led Care
Patient-Centered Primary Care Collaborative
PatientPing
Rhode Island Quality Institute
RGV ACO Health Providers, LLC
Saint Francis Healthcare Partners
The Health Collaborative

Geographic Population-Based Payment (PBP) Model Option Request for Information (RFI)

May 30, 2019

Submitted via DPC@cms.hhs.gov Mr. Adam Boehler

Centers for Medicare & Medicaid Services 7500 Security Boulevard
Baltimore, MD 21244

Re: Geographic Population-Based Payment (PBP) Model Option Request for Information (RFI)

Dear Deputy Administrator Boehler:

Thank you for the opportunity to respond to the RFI on Direct Contracting – Geographic PBP Model Option. We applaud your commitment to pursuing payment and delivery system reform through innovative demonstration programs.

Our organizations are deeply committed to value-based care. We believe that effective, efficient primary care is key to improving outcomes and reducing costs, and we were pleased to see the Center for Medicare and Medicaid Services (CMS) focus on these critical health care services in its new models.

As you move forward in implementing this model, we strongly urge you to consider the impact on provider competition. As required by the Executive Order on Healthcare Choice and Competition, the Administration released a report in November 2018 outlining key recommendations for strengthening our health care system through increased competition.1 The report recommended that the Administration ensure that delivery system reform models “foster collaboration across systems within a geographic area and do not produce harmful consolidation..., ” and that the Administration ensure that smaller physician and provider practices are not “unduly harmed” by delivery system reform requirements.

We are pleased that you intend to give preference to direct contracting entities (DCEs) in target regions with more than one DCE, but believe that additional guardrails may be necessary to preserve choice and competition for traditional Medicare beneficiaries. For example, geographic DCEs should not be allowed to use their market power to mandate or require providers in a specific area to contract with them, or to require patients to see providers with whom they have a negotiated relationship. Any geographic demonstration should be closely monitored for unintended consequences and shifting competitive dynamics to ensure that it does not fuel provider consolidation trends already contributing to high costs in the commercial market.

We also strongly urge you to consider the implications of model overlap in a particular region. Geographic DCEs should not displace or take precedence over existing risk-taking entities working to achieve value- based care such as accountable care organizations (ACOs) and professional or global DCEs. Participants in existing models, including many physician-led groups, have made significant investments to shift to value- based care. These investments should be recognized by new models and model participants coming into a target region. We encourage CMS to continue to directly contract with ACOs in the Medicare Shared

 

Deputy Administrator for Innovation & Quality

Director, Center for Medicare and Medicaid Innovation

Savings Program, the Next Generation ACO Program and other CMMI models. Any disruption in an existing model inevitably distracts from the important work of creating more value for Medicare beneficiaries.

Thank you again for the opportunity to provide input. We look forward to working with CMS as you further develop this model.

Sincerely,

Alliance for Innovative Primary Care

American Academy of Family Physicians

Medical Group Management Association

National Association of Accountable Care Organizations Next Generation ACO Coalition

National Coalition on Health Care Partnership to Empower Physician-Led Care Patient-Centered Primary Care Collaborative

 

1 U.S. Departments of Health and Human Services, Labor and Treasury, “Reforming America’s Healthcare System Through Choice and Competition.” Available here: https://www.hhs.gov/sites/default/files/Reforming-Americas- Healthcare-System-Through-Choice-and-Competition.pdf

Community Statement on Medicare Coverage for Medically Necessary Oral and Dental Health Therapies

Community Statement on Medicare Coverage for Medically Necessary Oral and Dental Health Therapies
 
(The PCPCC joined the Community in 2019)
 
The undersigned organizations are proud to join in support of Medicare coverage for medically-necessary oral/dental health therapies.
 
It is well established that chronic diseases disproportionately impact Medicare beneficiaries and impose a substantial cost on the federal government. It is also well established that untreated oral microbial infections are closely linked to a wide range of costly chronic conditions, including diabetes, heart disease, dementia, and stroke. In addition, oral diseases have been documented by researchers and medical specialty societies as precluding, delaying, and even jeopardizing medical treatments such as organ and stem cell transplantation, heart valve repair or replacement, cancer chemotherapies, placement of orthopedic prostheses, and management of autoimmune diseases.
 
Despite these factors, most Medicare beneficiaries do not currently receive oral/dental care even when medically necessary for the treatment of Medicare-covered diseases. In fact, Medicare coverage extends to the treatment of all microbial infections except for those relating to the teeth and periodontium. There is simply no medical justification for this exclusion, especially in light of the broad agreement among health care providers that such care is integral to the medical management of numerous diseases and medical conditions. Moreover, the lack of medically necessary oral/dental care heightens the risk of costly medical complications, increasing the financial burden on Medicare, beneficiaries, and taxpayers.
 
A number of major insurance carriers provide medically-necessary oral and dental coverage to targeted enrollees with conditions such as diabetes, heart disease, stroke, head/neck cancers, and transplants. According to some reports, such coverage has realized important benefits, including markedly lower hospitalization and emergency department admission rates as well as substantial cost reductions. On a further note, veterans getting care through the Veterans Health Administration receive medically adjunctive oral/dental treatment in many instances when a dental diagnosis affects their medical prognosis. These are all important steps forward, and medically necessary oral/dental healthcare should be provided in traditional Medicare as well.
 
The Medicare program and all its beneficiaries should not be without the vital clinical and fiscal benefits of coverage for medically necessary oral/dental health therapies. Given the significant potential to improve health outcomes and reduce program costs, we urge Congress and the Administration to explore options for extending such evidence-based coverage for all Medicare beneficiaries.
 
 
AARP
Acuity Specialists
Adenoid Cystic Carcinoma Research Foundation
AIDS Foundation of Chicago
Allies for Independence
American Academy of Maxillofacial Prosthetics American Academy of Nursing
American Academy of Periodontology
American Association for Dental Research
American Association of Clinical Endocrinologists American Association of Colleges of Nursing
American Association of Diabetes Educators
American Association of Hip and Knee Surgeons American Association of Kidney Patients
American Association of Oral and Maxillofacial Surgeons American Association of Nurse Practitioners
American Autoimmune Related Diseases Association American College of Cardiology
American College of Emergency Physicians
American College of Gastroenterology
American College of Physicians
American College of Prosthodontists
American College of Rheumatology
American Dental Association
American Dental Education Association
American Dental Hygienists’ Association
American Diabetes Association
American Geriatrics Society
American Head and Neck Society
American Kidney Fund
American Liver Foundation
American Network of Oral Health Coalitions
American Nurses Association
American Parkinson Disease Association
American Psychiatric Association
American Public Health Association
American Society for Radiation Oncology
American Society of Clinical Oncology
American Society of Nephrology
American Society of Transplant Surgeons
American Society of Transplantation
American Thoracic Society
Arcora Foundation
Arthritis Foundation
Association of Community Cancer Centers
Association of Dental Support Organizations
Association of State and Territorial Dental Directors
Autistic Self Advocacy Network
Brain Injury Association of America
California Dental Association
California Medical Association
Catholic Health Association of the United States
Center for Health Law and Policy Innovation
Center for Medicare Advocacy
Children’s Dental Health Project
Cornerstone Dental Specialties
Crohn’s and Colitis Foundation of America
Dental Lifeline Network
Dental Trade Alliance
DentaQuest Partnership for Oral Health Advancement Disability Rights Education and Defense Fund
Eating Disorders Coalition
Epilepsy Foundation
Families USA
Georgia AIDS Coalition
Gerontological Advanced Practice Nurses Association Hartford Institute for Geriatric Nursing
Head and Neck Cancer Alliance
Henry Schein Cares Foundation
HIV Medicine Association
International Pemphigus and Pemphigoid Foundation John A. Hartford Foundation
Justice in Aging
Leukemia and Lymphoma Society
Lupus and Allied Diseases Association, Inc.
Lupus Foundation of America
Medicare Rights Center
Mending Hearts
Mental Health America
National Alliance of State & Territorial AIDS Directors National Alliance on Mental Illness
National Association of Area Agencies on Aging National Association of Community Health Centers National Association of Dental Plans
National Association of Nutrition and Aging Services Programs
National Association of Social Workers
National Association of States United for Aging and Disabilities
National Comprehensive Cancer Network
National Committee to Preserve Social Security and Medicare
National Council for Behavioral Health
National Forum for Heart Disease and Stroke Prevention
National Health Law Program
National Interprofessional Initiative on Oral Health National Kidney Foundation
National League for Nursing
National Multiple Sclerosis Society
National Network for Oral Health Access
National Osteoporosis Foundation
National Rural Health Association
National Stroke Association
Oral Cancer Foundation
Oral Health America
Oral Health Nursing Education and Practice Program Pacific Dental Services Foundation
Parkinson’s Foundation
Patient-Centered Primary Care Collaborative
PEW Dental Campaign
Preventive Cardiovascular Nurses Association ProHEALTH Dental
Renal Physicians Association
Santa Fe Group
School-Based Health Alliance
Scleroderma Foundation
Sjogren’s Syndrome Foundation
Society for Transplant Social Workers
Support for People with Oral and Head and Neck Cancer The AIDS Institute
The Arc of the United States
The Gerontological Society of America
The Michael J. Fox Foundation
The Society for Thoracic Surgeons
The TMJ Association

 

Primary Care Community Urges Congress to Allocate $5 Million for AHRQ’s CPCR

On April 2, 2019, in an effort initiated by the Patient-Centered Primary Care Collaborative (PCPCC) and the Council for Academic Family Medicine (CAFM), more than 20 of our nation’s leading organizations, associations, foundations, and institutions supporting primary care research, delivered a letter to the House and Senate Appropriations Committees requesting $5 million for FY2020 to fund the Center for Primary Care Research (CPCR) at the Agency for Healthcare Research and Quality (AHRQ).

Since 1999, CPCR has had a statutorily-authorized home at AHRQ. The Center, however, does not receive dedicated funding to conduct the essential research needed to support the complex and multifaceted discipline of primary care. As a nation, investment in primary care is paramount in order to ensure a more efficient, equitable, higher quality health system for all Americans.

The letter emphasizes that, with appropriate funding, the CPCR will improve coordination and emphasize the need for expanded primary care research—both in the clinical and health services spheres. The requested $5 million establishes a funding foothold and is a first-step supporting AHRQ’s unique role to conduct and expand primary care research, furthering the mission of PCPCC’s Shared Principles of Primary Care

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