Archive for: The RAISE Family Caregiver Resource and Dissemination Center
What Family Caregivers Need: Findings from Listening Sessions
/in The RAISE Act Family Caregiver Resource and Dissemination Center Featured News Home, Reports The RAISE Family Caregiver Resource and Dissemination Center /by University of Massachusetts at Boston and Community Catalyst
The family caregiver listening sessions included a range of diverse caregivers, from teen caregivers to grandparents providing care, and caregivers of varying racial and ethnic backgrounds. The listening sessions directly captured the emotional and financial stresses caregivers experience, and their priorities and concerns, including respite, caregiving education and training, and financial considerations, including direct pay for caregiving, workplace flexibility, and tax policy changes that support caregivers.
This report is a publication of NASHP’s RAISE Family Caregiver Resource and Dissemination Center and was made possible by funding from The John A. Hartford Foundation in collaboration with ACL.
RAISE Family Caregiving Advisory Council Votes the Report to Congress into Clearance
/in The RAISE Act Family Caregiver Resource and Dissemination Center Council Meeting Materials and Resources /by NASHP StaffPaying Family Caregivers through Medicaid Consumer-Directed Programs: State Opportunities and Innovations
/in The RAISE Act Family Caregiver Resource and Dissemination Center Connecticut, Florida, Virginia Featured News Home, Reports Chronic and Complex Populations, Chronic Disease Prevention and Management, Consumer Affordability, Cost, Payment, and Delivery Reform, Health Coverage and Access, Health System Costs, Long-Term Care, Medicaid Managed Care, Population Health, State Resources, The RAISE Family Caregiver Resource and Dissemination Center, Workforce Capacity /by Salom Teshale, Wendy Fox-Grage and Kitty PuringtonFamily members provide significant amounts of care to relatives with complex needs, including those who are Medicaid enrollees.
Individuals may hesitate about receiving care in congregate care settings, particularly during the COVID-19 pandemic, but many face home-based care service workforce shortages. Programs that incorporate family members who provide care can help support person-centered care for Medicaid enrollees and also help states address the demand for long-term services and supports. States have the opportunity to use Medicaid to support enrollees with long-term care needs and their families by developing consumer direction programs that allow family members to be hired to provide care. This report explores how Connecticut, Florida, and Virginia developed consumer-directed care programs to serve older adults and people with physical disabilities.
Introduction
COVID-19 has upended states’ long-term services and supports (LTSS) systems and strained congregate care facilities. A recent report suggests virtually all states have seen a significant drop in skilled nursing facility occupancy rates . The increasing demand for home-based care is exacerbating underlying challenges, such as long-standing LTSS direct care workforce shortages and gaps in meeting the needs of communities of color and speakers of different languages.
Medicaid consumer–directed care programs are an alternative way individuals can receive home-based services. Consumers choose and hire their care providers rather than having an agency dictate who delivers care.
To address these challenges, states are exploring how Medicaid options can support enrollees with long-term care needs through consumer direction programs (also called consumer-directed care programs, participant direction programs, or self-direction programs) that allow family members to be paid for providing care. States have developed and expanded consumer direction programs over the past decades. Given increasing interest in home-and community-based care over institutional care, consumer direction programs are a growing option to offer older adults and people with disabilities an alternative to institutionalization. This report highlights three states’ self-directed care programs that include older adults and people with physical disabilities.
Findings suggest consumer-directed programs can improve quality of life and health outcomes and can help meet participant needs without increasing Medicaid fraud.
Medicaid-funded consumer direction- programs allow enrollees to directly hire people, including some family members, to provide personal care, such as bathing, dressing, and toileting. According to the National Council on Disability, consideration of consumer-directed personal care options began in the late 1960s and 1970s with calls for increased autonomy and independence by and for people with disabilities. While early pilot programs focused on people with disabilities, the model – and its core values of autonomy and dignity – have since been applied to programs for older adults. Findings from the Cash and Counseling Demonstration Program suggest consumer-directed programs can improve quality of life and health outcomes and can help meet participant needs without increasing Medicaid fraud. While small-scale studies have shown savings, states can also incorporate cost-containment mechanisms into these models through waiver enrollment or spending caps, or reimbursement methodologies that limit consumer-directed care payment to a percentage of agency rates.
States are increasingly using consumer-directed models; according to Applied Self-Direction, all 50 states and Washington, DC have at least one consumer direction LTSS option. Several federal initiatives, Centers for Medicare & Medicaid Services (CMS) guidance beginning in the early 2000s, the Deficit Reduction Act of 2005, and creation of the Community First Choice state plan option under the Affordable Care Act have expanded states’ ability to provide these programs. This trend is likely to continue as states:
- Seek to address issues raised by the COVID-19 pandemic;
- Promote equity and access to services in underserved communities; and
- Address growing work force shortages.
Modifying or expanding consumer-directed programs can be an important strategy.
How States Can Develop Consumer-Directed Programs
States have multiple decision points when developing a Medicaid consumer-directed program.
Medicaid Authority: States can use various Medicaid authorities to support consumer-directed options that allow family members to receive reimbursement for providing care. Policymakers have many factors to consider when designing these waivers and/or state plan amendments, such as whether to expand Medicaid eligibility, whether to target specific populations or geographic areas, and what services and supports should be provided.
The majority of states operate consumer-directed programs through the Medicaid 1915(c) home- and community-based waiver (HCBS) authority. Using 1915(c) waivers, states can modify eligibility requirements, target services to particular areas of the state, and/or limit or tailor services to certain populations, such as older adults or adults with physical disabilities who are at risk of institutionalization. States can, depending on the authority, add self-direction options for different services into a single waiver.
Chart: Medicaid Authorities and Consumer-Direction Options
| Medicaid authority | Is institutional level of care required? | Can states waive comparability? | Can states waive statewideness? | Financial management services required? | Budget authority/
cash payments allowed? |
Limits on reimbursing family caregivers |
| 1905 (a) (24) state plan personal care services | As medically necessary | No | No | Only fiscal employer agent required | Neither budget authority nor cash payments are allowed | Excludes “legally responsible individuals” |
| 1915(c) Home and Community-Based Services | Yes | Yes | Yes | Yes | Budget authority is allowed, but cash payments are not | Allows relatives, legally responsible individuals, and legal guardians |
| 1915 (i) Home and Community-Based Services state plan option | No (allows individuals with less than institutional level-of-care requirements depending on certain types of eligibility) | Yes | No | Yes | Budget authority is allowed but cash payments are not | Allows relatives, legally responsible individuals, and legal guardians |
| 1915(j) self-directed personal assistance services state plan option | No, if receiving services through state plan and state plan does not require it
Yes, if receiving services through a 1915 (c) waiver |
Yes | Yes | Yes, unless participants choose to receive cash directly | Budget authority is required, cash payments are allowed | Allows legally responsible relatives |
| 1915(k) Community First Choice State Plan Option | Yes | No | No | Yes, depending on the model selected | States may allow budget authority and cash payments to participants depending on the model selected | Allows legally responsible individuals, relatives |
| 1115 Demonstration Waiver | Determined by state | Determined by state | Yes | Yes, when incorporating participant- direction | States may allow budget authority and cash payments to participants | Allows legally responsible individuals, relatives |
Sources:
Authority Comparison Chart. HCBS Technical Assistance Web Site. Center for Medicare and Medicaid Services. Accessed Dec. 31, 2020.
Home and Community Based Services Authorities. Medicaid.gov. Centers for Medicare and Medicaid Services. Accessed Dec. 31, 2020.
Self-Directed Services, Medicaid.gov (Centers for Medicare and Medicaid Services), accessed Dec. 31, 2020.
Participant Direction Features of the Optional Medicaid Authorities, Table 7-1, p. 182. O’Keeffe, Janet, Paul Saucier, Beth Jackson, Robin Cooper, Ernest McKenney, Suzanne Crisp, and Charles Moseley. Understanding Medicaid home and community services: A primer, 2010 edition. Washington DC: US Department of Health and Human Services and RTI International, 2010.
Wolff, Jennifer, Karen Davis, Mark Leeds, Lorraine Narawa, Ian Stockwell, and Cynthia Woodcock. Family Caregivers as Paid Personal Care Attendants in Medicaid. Baltimore, MD: Johns Hopkins Bloomberg School of Public Health, 2016.
Enrollee authority: States can determine how care recipients manage their budgets, caregivers, and services:
- Employer authority permits recipients to directly recruit and manage their service providers. Employer authority is integral to the consumer direction model. Depending on the authority, states have some flexibility to determine which employer responsibilities can be consumer-directed.
- Budget authority allows enrollees to manage their budgets and purchase other goods and services. States also have flexibility in determining what types of goods and services can be purchased under budget authority.
Enrollee supports: States are required to provide supports for enrollees in managing the consumer-direction process, which can include training and assistance, information about responsibilities, or access to financial management services. For example, Virginia’s 1915(c) waivers include a “services facilitator” to support individuals in managing consumer-directed services.
Definition of “family:” States have discretion to determine who may provide HCBS under consumer direction. Under most authorities, states have flexibility to allow services to be provided by family members, including “legally responsible individuals” such as spouses or parents of minor children under specific circumstances. Within the 1915(c) waiver, for example, states have the option to allow relatives to provide waiver services, and/or allow legally responsible individuals, such as spouses and parents of minor children, to provide personal care services. When delivering personal care-related services, the legally responsible person must be providing care that is beyond the care normally expected of a spouse or parent. In defining family for reimbursement, the state plan personal care option is the exception: legally responsible individuals may not be paid under this authority to provide personal care services.
Training and workforce requirements: State Medicaid agencies often require background checks or certification requirements for caregivers.
- States vary in the specifics of the training requirements for caregivers hired under consumer direction. Florida does not require licensing or certification to provide personal care, homemaker, or adult companion services, but does require licensure for attendant care.
- States can, through legislation, specify the types of tasks that can be delegated by a nurse to an unlicensed caregiver who receives training, as in the example of Virginia’s regulations on nurse delegation. The AARP 2020 LTSS Scorecard found that 26 states allow nurses to delegate at least 14 health maintenance tasks to be performed by a direct care aide, such as medication administration, respiratory care, tube feeding/gastric care, and/or bladder regimen and skin/appliance care-related tasks.
Use of representatives: Participants can choose to have a representative assist them with managing their consumer-directed services. Individuals may appoint a family member as a representative, but that family member cannot be paid to be the participant’s representative, or provide paid care to the participant. (Note: Due to the COVID-19 emergency, emergency flexibilities may allow states to waive certain requirements during the public health emergency. For example, West Virginia’s Appendix K for its 1915[c] waivers allows legal representatives to receive payment for certain personal care-related services under specific circumstances during the emergency.)
Three State Approaches
States can structure consumer-directed program options in a variety of ways, reflecting the needs of their residents. After a nationwide scan of Medicaid waivers and state plan options for older adults and adults with physical disabilities, the National Academy for State Health Policy (NASHP) identified three states — Connecticut, Florida, and Virginia — that have long-standing consumer-directed care programs and illustrate the various policy strategies available to states to help Medicaid enrollees (and their family caregivers) who are older adults or have physical disabilities live in their communities.
Connecticut’s 1915(k) Community First Choice (CFC) State Plan Amendment was approved in 2015. Enrollees in Connecticut’s CFC option may hire, supervise, and train their own staff and manage their budgets themselves or with support of an individual other than a spouse or legally liable individual.
- Medicaid authority: 1915(k) Community First Choice (CFC) state plan option
- Services: Attendant care, transitional services, home-delivered meals, environmental accessibility adaptations, assistive technology, and voluntary training on how to hire/manage/dismiss staff
- Family caregivers: Enrollees in the CFC option can hire family members or other individuals as long as they meet qualification requirements. (Excludes spouses and legally responsible individuals, health care representatives, conservators, or guardians.) Caregivers may live in the home.
Enrollees create job descriptions. Participants who choose to hire an attendant can request a pay rate subject to approval of the state. They can offer a particular wage if they believe the job description merits it (e.g., special skills, fluency in a particular language, etc.). In its 1915(k) SPA, Connecticut recommends that attendants, “be at least 16 years of age; have experience providing personal care; be able to follow written or verbal instructions given by the individual or the individual’s representative or designee; be physically able to perform the services required; and be able to receive and follow instructions given by the individual or the individual’s representative or designee.” Connecticut provides access to additional employee training opportunities, such as coordinating with a community college to provide personal attendant training certification or certified nursing assistant (CNA) training for personal care assistants (PCAs).
The Medicaid enrollee is considered the employer. The state’s Division of Health Services (DHS) establishes the budget and determines how much of the budget can be spent each month. If participants continually exceed their budget, they may lose access to the option, and DHS also tracks underutilization. While DHS does not specifically track the use of paid family personal care providers, a state official estimates that approximately 30 percent of the roughly 4,000 individuals who use the service engage family caregivers as PCAs. Connecticut’s CFC option can include older adults and people with physical disabilities, and Medicaid enrollees who require institutional levels of care are eligible.
Monitoring for fraud and abuse. Connecticut’s Quality Assurance unit examines referrals and has systems and controls in place to examine and flag PCA hours. One example of a system control is related to the state’s policy that disallows PCA services while a member is hospitalized. To disallow payments to PCAs submitting claims during their employer’s hospitalization, Connecticut’s Medicaid Management Information System (MMIS) compares PCA claims for the enrollee to hospital claims for the enrollee. If there is a hospital claim on the same day as a PCA’s claim, the PCA claim is not paid. In addition, the fiscal intermediary monitors for fraud and abuse. The state also established a fraud and abuse hotline and online reporting capacity to encourage public reporting.
Reimbursement. Connecticut established a universal assessment to evaluate levels of care for all Medicaid enrollees with HCBS needs in 2015, at the same time as the CFC option was being developed. Data from this universal needs assessment has been used since then to determine tiered budget groupings within the CFC option as well. Because CFC budgets are driven by the universal assessment — as are its other HCBS programs – a Connecticut state official reported costs did not differ greatly across programs. The state is in the process of working with consultants, including the University of Connecticut, to review the tool and the data collected from the universal assessment and to revise the current budget groupings.
Payment. The fiscal intermediary pays the PCA, then submits claims for reimbursement through the Medicaid Management Information System (MMIS). The state sends information about individual budgets to the fiscal intermediary. If enrollees want to pay their PCAs a different payment rate than listed in their individual budgets, they must submit documents about how risk would be managed. This is because individual budgets are based on needed hours at the minimum wage rate. While it is permissible for participants to request higher wages, this decision decreases the number of hours available within the budget. In 2020, Connecticut selected Allied Community Resources as its fiscal intermediary through a request for proposals. The provider fee schedule is posted at ctdssmap.com. As of 2020, PCAs in Connecticut are unionized and their minimum payment rate has increased. Some program costs also have increased accordingly.
Florida
In Florida’s participant-directed option (PDO), the managed care plan sets the fee schedule and makes payments. The PDO, which is provided by Florida’s Statewide Medicaid Managed Long-Term Care program, can serve both older adults and people with physical disabilities. The enrollee has responsibility for finding, training, and managing workers, setting hours, reporting fraud or abuse, and submitting timesheets to the managed care plan, among other responsibilities.
- Medicaid authority: Statewide Medicaid Managed Care Long-Term Care (LTC) 1915(b)/(c) waiver, which includes a participant-directed option (PDO)
- Services: Allows five services through PDO: adult companion, homemaker, attendant care, intermittent and skilled nursing, and personal care services
- Family caregivers: Legally responsible individuals, including spouses, can provide PDO services as long as the caregiver is qualified, has executed a PDO work agreement, and has passed the necessary background checks; the enrollee can live in their own home or in a family member’s home.
The PDO initially began as a consumer direction pilot in 2000 administered by the state’s Agency for Health Care Administration (AHCA) and the Department of Elder Affairs (DOEA). In 2013, the participant-directed option was transitioned into the Statewide Medicaid Managed Care Long-Term Care (SMMC-LTC) program. Eight managed care plans offer PDOs. As of June 2020, slightly more than 119,000 enrollees were enrolled in the SMMC-LTC program overall. According to state data, out of 51,848 HCBS enrollees, 7,841 were participating in the PDO as of June 2020.
Specific family caregiver hiring information is not reported in the care plan, although all care is documented in the care plan, including whether services are administered through the PDO or traditional options. Because the PDO offers flexibility in hiring caregivers, the option can be used by enrollees who desire culturally competent caregivers, or who are not satisfied with other available options. Legally responsible individuals, including spouses, can receive reimbursement. In 2020, Florida included a caregiver training benefit as part of its LTC Waiver. Training is available based on a caregiver assessment administered through the managed care plan. Each managed care plan has its own training program. This caregiver training support can be utilized only for unpaid caregivers, however.
Monitoring for fraud and abuse. The Agency for Health Care Administration (AHCA), Florida’s Medicaid agency, monitors for fraud and waste through the state’s contracted Medicaid managed care plans, which are required to provide fiscal/employer agent (F/EA) services. The managed care plan either operates as a F/EA, or subcontracts to an F/EA vendor. The managed care plan is responsible for fulfilling certain F/EA-related tasks, including reporting of underutilization to participants/case managers, and following up with timesheet issues. AHCA conducts a desk review every quarter, which involves an audit process for compliance.
Reimbursement. Each plan has a designated fee schedule, and there are no caps from AHCA on the number of PDO hours that can be received by an enrollee, which is determined by medical necessity. Managed care plans or their vendors who serve as F/EAs provide payroll and tax management services for participants and are responsible for processing and payment of all applicable taxes on behalf of participants and their workers.
Virginia
Virginia’s consumer-directed option began in the mid-1990s and was available only to individuals with physical disabilities. Virginia’s options expanded over time to include individuals with cognitive impairment, and additional services, such as companion services and respite. These consumer-directed program services have since been incorporated into Virginia’s HCBS waivers. Consumer direction for older adults and people with physical disabilities is part of the Commonwealth Coordinated Care Plus (CCC Plus) program operated under a 1915b/c waiver.
- Medicaid authority: Commonwealth Coordinated Care Plus 1915(b)/(c) waiver program
- Services: Participants have the option to self-direct personal care and respite services
- Family caregivers: As of 2020, relatives other than spouses or parents of minor children can be reimbursed for services, however, during the pandemic, spouses and parents of minor children can be reimbursed for care.
Enrollees selecting consumer direction are provided with a list of “services facilitators” as part of the screening process for level-of-care eligibility assessment (administered by local Virginia Department of Health nurses and physicians or local departments of social services’ family services specialists). Services facilitators are Medicaid-enrolled providers who support participants in managing their consumer directed services. Services facilitators can:
- Assess a participant for particular consumer-directed services;
- Help develop a plan of care; and
- Provide training and support to the participant in performing their role as employer.
Participants can select workers and are considered the employer, but do not have decision-making authority over the budget. Within CCC Plus, a legally responsible relative can serve as the participant’s representative and be the employer if the participant is not independently able to self-direct care, but this relative cannot also be a services facilitator, paid caregiver, or attendant. Spouses and parents of children cannot be paid to provide personal care services, but other relatives can be paid under specific circumstances. Currently, flexibilities instituted due to COVID-19 under Virginia’s Appendix K waiver allow spouses and parents of children to provide services during the public health emergency.
Consumer direction is available for members living in their own homes or in family members’ homes. An estimated 40 percent of caregivers are family members, according to key informant estimates.
Monitoring for fraud and abuse. Payments to family caregivers under the CCC Plus program are monitored through the Quality Management review process in the Department of Medical Assistance Services (DMAS) using the same processes used to monitor other home-based and personal care services. However, if payments are made to a family member living in the same home as the participant, the member must provide documentation to justify hiring the relative who lives in the same home as an “option of last resort.” There are no limits that are specific to relatives on the number of hours of services that can be furnished.
Reimbursement. Participants in Virginia’s consumer-directed option must use a fiscal/employer agent, who conducts payroll functions on the participant’s behalf, including payment and withholding. DMAS issued a request for proposals to select the state’s fiscal/employer agent. The fiscal/employer agent must also process background checks. Managed care organizations in CCC Plus contract with a fiscal/employer agent, and follow the same processes as the state for consumer-direction. In the 2020 budget, a 5 percent increase beginning July 2020 and a 2 percent increase beginning in July 2021 to the salary rate for attendants was approved. Time and a-half payment up to 16 hours was also approved for attendants working over 40 hours per week providing Medicaid consumer-directed personal assistance, respite, and companion services.
Lessons Learned
State policy leaders interviewed for this report all expressed value for program flexibility and choice for enrollees receiving care. They also noted the broader state goals of providing home- and community-based services alternatives over institutional services as a critical factor in supporting self-direction for people requiring institutional levels of care, and paying family caregivers. Across the highlighted states, additional themes emerged:
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- Consumer direction provides an important opportunity to support health equity and culturally competent care. By giving enrollees flexibility to select caregivers and employ family members, states enhanced their ability to support the needs of underserved populations. Both Florida and Connecticut officials highlighted that the consumer-directed option allowed participants to hire caregivers who met their cultural and linguistic needs. Connecticut’s Community First Choice state plan option allows enrollees, as the hiring employer, to develop job descriptions that can include speaking a specific language or possessing a particular type of certification.
- Paying family caregivers can be a cost-neutral Medicaid rebalancing strategy. States can set comparable (or lower) rates for family caregivers, manage service utilization, and support more individuals in home and community settings. Connecticut state health officials anticipated a shift from institutional care toward community-based services through use of its Community First Choice (CFC) option, and results are tracking accurately to the state’s initial estimates. Connecticut also reports a lower dependence on home health agencies. Utilization of Connecticut’s CFC program has grown since 2015, but a state official noted significant savings in other services. The CFC option also benefits from a 6 percent enhanced federal match. A state official in Florida also noted that the state PDO’s lower service costs make the program competitive when compared to similar services provided by a traditional vendor.
- Outreach to Medicaid enrollees is critical. States noted that the complexity of these programs can be a challenge to enrollment, particularly among participants who are uncertain about whether they would be required to manage their own budgets. Due to the COVID-19 pandemic and interest in avoiding facility-based care, states may have a heightened opportunity to raise awareness about consumer-directed options for personal care-related services.
Effects of COVID-19
Enrollment support for consumer-directed programs in the three states has increased as reliance on family caregivers grew during the pandemic:
- Within a week of declaring the emergency, Connecticut permitted expedited enrollment so enrollees could hire family caregivers, and the state also allowed overtime. Connecticut has commissioned a report from the University of Connecticut to examine the impact of COVID-19 on LTSS.
- Florida encouraged enrollment in its PDO to obtain or provide care during COVID-19, and the state has since documented an increase in new enrollees. State administrators report they are not concerned about sustaining their managed care PDO option because the option is cost-effective.
- Virginia officials noted that family members have been designating themselves as live-in caregivers in response to COVID-19. Virginia used CARES Act funding to provide personal protective equipment (PPE) to caregivers and advocate in particular for caregivers of color. CARES Act funding was also used to provide COVID-19-related hazard pay to consumer-directed caregivers who worked during the first few months of the pandemic.
- States may want to consider enhancing data collection to better identify family caregivers who are reimbursed through consumer-directed programs. States do not currently track whether enrollees in consumer-directed programs hire family members. States can consider tracking data on family caregivers within consumer-directed options to better understand the fiscal and health impact of incorporating family caregivers within these programs. Virginia officials are interested in developing mechanisms to encourage individuals who provide care to identify themselves as family caregivers. States could also support data collection to better analyze whether services are reaching at-risk populations and to better support underserved populations, including caregivers of different ethnic or racial backgrounds.
- States have a number of strategies they can use to prevent fraud and abuse. A 2017 GAO report notes that personal care services are particularly prone to incomplete data, overbilling, and risk of neglect for vulnerable enrollees. States can incorporate a range of policies that can mitigate the risk of fraud while improving the quality of care, such as:
- Criminal background checks;
- Service provider requirements and training; and
- Use of care managers.
States can also leverage electronic visit verification (EVV) technology (mandated by the 21st Century Cures Act for personal care and home-based services) to mitigate fraud and abuse. Anticipating the particular needs of consumer-directed enrollees and family caregivers can help. Also, flexible scheduling, user-friendly technology, and active engagement of stakeholders in implementation can avoid challenges. Florida noted that some MCOs provide tablets to family caregivers to utilize for EVV.
- Understand how employment and scope-of-practice laws can affect family caregivers receiving reimbursement through a consumer-directed option. Family caregivers can be considered employees and subject to a range of state and federal regulations that can impact state Medicaid programs. When the US Department of Labor issued a Final Rule regarding the Fair Labor Standards Act (FLSA) that live-in caregivers for specific services could be included in receiving overtime, Florida noted that overtime hour claims increased. Plans subsequently required use of in-network providers for service hours over 40 hours per week. While Virginia’s program focuses on caregivers who do not provide services that licensed or certified professionals provide, Virginia’s Nurse Practice Act has been amended to allow a nurse to delegate authority to caregivers to render certain tasks without violation of licensing regulations under specific circumstances.
Conclusion
The COVID-19 pandemic is reinvigorating long-standing state efforts to support older adults and others with LTSS needs while reducing reliance on congregate settings of care. Reimbursing family members to provide some services can help states rebalance long-term care toward more home- and-community-based options and promote more person-centered long-term care, especially for underserved populations. These considerations are particularly important as states consider winding down various program changes put in place in response to the pandemic. As policymakers consider ways to support enrollees while balancing financial considerations, robust consumer-directed options that engage family caregivers can provide important and person-centered strategies for long-term care.
Acknowledgements: The National Academy for State Health Policy (NASHP) thanks Dawn Lambert, Co-Leader, Community Options Unit, Division of Health Services (CT), Karen Kimsey, Director, Department of Medical Assistance Services (VA), and Eunice Medina, Bureau Chief, Medicaid Plan Management Operations, Agency for Health Care Administration (FL) for sharing their time, expertise, and input on this report. NASHP also greatly appreciates The John A. Hartford Foundation for its support of NASHP’s work related to family caregiving and state policy.
Spotlight on Home- and Community-Based Services: New Federal Opportunities?
/in COVID-19 Relief and Recovery Resource Center Blogs, Featured News Home Chronic and Complex Populations, Chronic Disease Prevention and Management, COVID-19, Health Coverage and Access, Medicaid Managed Care, Population Health, Relief and Recovery, Social Determinants of Health, State Resources, The RAISE Family Caregiver Resource and Dissemination Center, Workforce Capacity /by Kitty PuringtonOlder adults, people with disabilities, and their family caregivers have been hard hit by COVID 19. As states reel from the pandemic’s human and fiscal toll, policymakers are increasingly looking to home- and community-based services (HCBS) to address the pressing need for alternatives to nursing home care and supporting family caregivers who can help loved ones age in place.
Recent actions signal that the importance of HCBS is gaining traction at the federal level, and may receive significant attention in the coming months:
- The American Rescue Act, passed last month, includes a one-year, 10-point boost in Federal Medical Assistance Percentage (FMAP) for HCBS delivered between April, 2021 and March, 2022. The funding must supplement – not supplant – current state expenditures, and can be used for an expansive list of HCBS. These include Medicaid waiver services, but also case management and rehabilitative services, which are often used to support people with serious mental illness. The Centers for Medicare & Medicaid Services recently held a “listening session” to gather input for guidance that will be issued in the near future.
- The American Jobs Act, released by the White House on March 31, 2021, has been touted by the Biden Administration as an historic opportunity to rebuild America’s infrastructure. Interestingly, a full quarter of the total $1.2 billion proposed expenditure would go to “expanding access to quality, affordable home- or community-based care for aging relatives and people with disabilities.” The plan targets expansion of Medicaid HCBS and would improve wages and conditions for the nation’s direct care workforce, a majority of whom are women of color.
- Also last month, a group of members of Congress – Rep. Debbie Dingell (D-MI), Sen. Maggie Hassan (D-NH), Sen. Bob Casey (D-PA), and Sen. Sherrod Brown (D-OH) – sought input on the HCBS Act of 2021, draft legislation that would make HCBS a mandatory benefit in state Medicaid plans and expand the kinds of services offered, among other changes.
In the short term, states will need to act quickly to develop time-limited strategies to take advantage of the Federal Medical Assistance Percentage (FMAP) enhancement offered by the American Rescue Plan, and be prepared for other funding and policy opportunities as they emerge. States may choose to add enrollees to their existing HCBS programs, expand access by enhancing direct care workforce pay, focus on services to support family caregivers, and/or build on existing programs.
Explore the National Academy for State Health Policy’s (NASHP) State PACE Action Network for a new technical assistance opportunity for states to enhance or expand this home- and community-based services model. NASHP will continue to track these issues, and provide updates on state and federal initiatives that reflect the growing importance of HCBS.
Request for Applications for NASHP’s Second Health and Housing Institute – Due April 30, 2021
/in Policy Featured News Home Chronic and Complex Populations, State Resources, The RAISE Family Caregiver Resource and Dissemination Center /by NASHP StaffThe National Academy for State Health Policy (NASHP), with support from the Health Resources and Services Administration (HRSA) through the National Organizations of State and Local Officials (NOSLO) program, invites states to apply to its second Health and Housing Institute. The goal of the Institute is to break down inter-agency silos and strengthen services and supports to help low-income and vulnerable populations become and remain successfully housed.
With newly available American Rescue Plan resources, this is an opportune time for states to build capacity to address housing affordability, home- and community-based services, permanent supportive housing and other related topics.
States participating in institute will receive two years of targeted technical assistance to support the development and/or implementation of sustainable financing of health and housing programs. This may include guidance on how to equitably and efficiently allocate new federal resources to address an increase in housing instability and homelessness arising from COVID-19.
What States Will Gain
Institute participants will have access to facilitated peer learning opportunities, subject matter experts, and state-specific technical assistance. Participating states may also have the opportunity to shine a national spotlight on their work during NASHP’s annual state health policy conference in September, 2021. Institute activities include:
- Access to expert consultants from federal agencies and nationally recognized housing policy organizations;
- Quarterly individualized technical assistance calls;
- Quarterly state-to-state learning calls;
- Expense-paid, in-person meetings held in conjunction with the annual NASHP state health policy conference, when in-person meetings are held again; and
- An opportunity to be showcased in NASHP’s Housing and Health Resources page and a final report on institute activities featured prominently on the NASHP website.
• The institute will run for two years and is open to five states.
• Expression of interest form are due April, 30, 2021.
• Selected state teams will be notified May 14, 2021.
• The institute begins in June, 2021.
From 2018 to 2020, NASHP convened multi-agency teams from Illinois, Louisiana, New York, Oregon, and Texas for its first Health and Housing Institute. The second institute will draw on lessons learned from NASHP’s first institute.
Detailed information on the first institute’s is in its final report, Five States Break Down Interagency Silos to Strengthen their Health and Housing Initiatives.
State Teams
Teams must include:
- One person from senior Medicaid leadership;
- One person from senior state housing agency leadership; and
- [Optional] Others based on the state’s project focus. For example, public health, state education, transportation or social service agency representatives, other payers, Medicaid managed care organizations, state data analytics staff, legislators, local officials, community-based partner organizations, governors’ health policy advisors, and individuals with lived experience.
Each state team will be expected to:
- Maintain a core team of at least two members, including participants from the state’s Medicaid agency and a housing agency should have decision-making authority within their respective agencies. States are welcome to include additional team members.
- Develop a project plan and work toward accomplishing goals and actionable steps to achieve these goals.
- Participate in quarterly individual team technical assistance calls with NASHP staff to identify progress and barriers as well as identify any emerging technical assistance needs.
- Revise project plans as necessary to improve your state’s initiative during the two-year technical assistance period.
- Participate in group activities as planned, including the annual meetings and quarterly state-to-state learning calls.
To apply: Each state team must complete an Expression of Interest Form (linked above) and submit it to Allie Atkeson (aatkeson@oldsite.nashp.org) by COB on Friday, April 30, 2021.
More information: Any questions about the Health and Housing Institute application process should be directed to Allie Atkeson (aatkeson@oldsite.nashp.org).
Overview of Health and Housing Institute Opportunity
Evidence shows a strong association between access to safe, affordable, and stable housing and positive health outcomes. At the beginning of the COVID-19 pandemic, states moved to rapidly rehouse individuals in congregate and institutionalized settings to slow the spread of the virus. As rapid rehousing is a temporary solution, states identified a need to provide individuals with additional wraparound and supportive services to maintain housing.
States have the opportunity to shift investments from episodic emergency and institutional care to more sustainable community and supportive housing solutions. States can also capitalize on newly available federal resources through the American Rescue Plan and American Jobs Plan to support their efforts. Housing is an essential social determinant of health and there is a demonstrated need for equitable and targeted access for populations, such as those experiencing homelessness, housing instability, behavioral health needs, and chronic conditions and those transitioning out of institutions.
Through the institute, NASHP will work with state Medicaid and housing agencies and other state policymakers from five states to address the challenges of sustainably financing health and housing initiatives. Discussions will also address related challenges of measuring program outcomes, ensuring equitable access to housing-related services, demonstrating return on investment, collecting and sharing data among agencies and providers, and determining effective governance structures for cross-sector housing and health initiatives.
Acknowledgement: This project is supported by the Health Resources and Services Administration (HRSA) of the US Department of Health and Human Services (HHS) under grant number U2MOA394670100, National Organizations of State and Local Officials. This information or content and conclusions are those of the author and should not be construed as the official position or policy of, nor should any endorsements be inferred by HRSA, HHS or the US government.
NASHP State PACE Action Network Request for Applications – Due April 15
/in Policy Featured News Home Chronic and Complex Populations, State Resources, The RAISE Family Caregiver Resource and Dissemination Center /by NASHP StaffThe National Academy for State Health Policy (NASHP) is seeking applications to participate in its State Program of All-Inclusive Care for the Elderly (PACE) Action Network. The network will engage up to five teams of state leaders to expand access to their existing PACE programs. Lessons learned and best practices from this effort will be shared with other states. NASHP is convening the network in partnership with the National PACE Association and with generous support from The John A. Hartford Foundation, the Gary and Mary West Foundation, and the Harry and Jeanette Weinberg Foundation.
What’s in it for states? Each state team will receive technical support during an eight-month period. The network will provide team members with opportunities for peer-to-peer discussion, targeted support for their state policy strategies, and access to national experts. The support period will conclude with a next-steps virtual or in-person meeting to launch network participants into their future work. (If face-to-face meetings are safe, it will be held in-person in Washington, DC.)
Team composition: State applications may include a team of up to four members. The team must include at least one Medicaid official and one PACE representative, such as a representative of a PACE program or state PACE association. (The PACE representative requirement may be waived in extenuating circumstances. Please contact Luke Pluta-Ehlers to request a waiver of the requirement.) The team may include additional state or PACE staff and others who can directly support team goals (e.g., aging agency administrators, managed care enrollment counselors, etc.)
To apply: NASHP will select up to five state teams. Applications should be emailed to Luke Pluta-Ehlers at lpehlers@oldsite.nashp.org by 5 p.m. (ET) Thursday, April 15, 2021.
More information: Interested state officials are encouraged to participate in an informational webinar about the PACE Action Network RFA from 2 to 3 p.m. (ET) Tuesday, March 30, 2021. Register here.
Overview of PACE Action Network RFA Opportunity
PACE programs are designed to benefit very frail elders by enabling them to stay in their communities as long as safely possible. The services are very comprehensive, including and extending beyond traditional Medicare and Medicaid services. PACE programs directly provide the majority of covered services, including primary care and transportation. PACE participants experience fewer hospitalizations, unmet needs, and emergency room visits than older adults in other programs.
Research also shows that care coordination and supports provided by PACE interdisciplinary teams reduce caregiver burden and stress — enabling families and caregivers to maintain frail elders more effectively at home or in a community-based setting. About 58 percent of caregivers experience a reduced burden after their family member enrolled in PACE, and 97.5 percent of family caregivers would recommend PACE to someone in a similar situation.
To date, 31 states have implemented 138 PACE programs that serve more than 55,000 elders. However, even in those states, some elders and families who would benefit from PACE are not able to participate due to a lack of access to a PACE site or lack of knowledge about the PACE program. The network is intended to help states with existing PACE programs increase Medicaid enrollees’ access to PACE programs so more individuals who would benefit from PACE can participate in the program.
The network is designed to help states develop and implement policies that efficiently achieve their visions of PACE programs’ role within their HCBS and MLTSS portfolios.
State PACE Action Network states will:
Participate in an in-person or virtual next- steps meeting in December. The meeting will offer opportunities to consult with national and federal experts and share challenges and lessons learned with your peers. If the meeting is in-person, NASHP will fund travel for two team members, others may participate at their own expense.
Develop a PACE Access work plan to support key state priorities.
Participate in one individualized work plan development call with NASHP to identify and plan to meet priority technical assistance needs.
Attend three technical assistance webinars with facilitated discussions, open to members of all state teams.
Engage in two individualized technical support calls to each state from NASHP, with expert consultation from national, state, and federal leaders
PACE can also bring benefits to state Medicaid programs. PACE integrates and coordinates all medical and long-term care services and supports for enrollees across both community and institutional settings. The program is especially valuable for the high-need, high-cost segment of the home- and community-based services (HCBS) recipient population. Because PACE is a capitated program it, like managed care programs, limits Medicaid’s financial risk. With its focus on a challenging segment of the Medicaid population, PACE can help state Medicaid programs ensure that these enrollees have ready access to a range of coordinated, high-quality services and supports that can be critical to maintaining individuals in the community. The access to a consistent set of providers may be especially helpful to the 46 percent of PACE members who have dementia. Some states have found that PACE can complement other HCBS and managed long-term care services and support (MLTSS) programs.
Establishing and administering a PACE program can require significant Medicaid resources. States can, however, structure their PACE programs to minimize the resources needed. California, for example, has aligned PACE program policies with those of its other MLTSS programs in order to minimize the resources needed to administer the PACE program. States can also scale the program so it serves sufficient numbers of Medicaid enrollees to offset the required resources. While most PACE programs are small, six states have at least one PACE organization that serves more than 1,000 patients. Also, of the 138 PACE programs nationwide, 27 are serving an estimated 15 percent or more of the dual-eligible older adults in their service areas.
There are at least three ways to expand access to PACE that interested states could consider.
- Implement Medicaid policies that increase access to existing PACE sites. For example, states can modify managed care program enrollment material and policies to better explain PACE’s benefits, work with managed care organizations to better manage transitions between PACE and other managed care contractors, or speed the assessment and enrollment process.
- Enable existing PACE programs to serve more people in their current service areas. For example, states can achieve this by working with the program to establish a new site within an existing service area or by lifting a cap on enrollment.
- Enable existing PACE programs to serve people in more areas of the state. For example, by working with a PACE provider to establish a site in a new service area or expand an existing service area.
NASHP is launching this network to assist states in helping those who would benefit from PACE access the program. NASHP will serve as a resource and convener to help policymakers connect with peers and experts, identify and share strategies and solutions, and provide insights for other state leaders who are seeking to increase access to PACE. Participating states will achieve the following during this eight-month State PACE Action Network:
- Gain information and insights into policies and practices that:
- Efficiently identify those who would benefit from the program and speed their enrollment,
- Increase the number of people who existing PACE programs may serve, and
- Minimize the resources required to administer PACE
- Develop a work plan for implementing the state’s chosen approach.
- Achieve key milestones to increase access to PACE services.
About NASHP
NASHP is a non-partisan, nonprofit organization with over three decades of experience in helping state policymakers lead. NASHP provides expertise, convenes states, shares innovations and best practices, and supports state policymakers in making concrete and sustainable health system reform. For more information, visit NASHP’s website at www.oldsite.nashp.org
Application Guidelines
Team composition: State applicants may identify a core team of up to four members to participate in the network, including at least one state Medicaid official and one PACE representative. Additional members may include other state staff, key state contractor staff (e.g., managed care enrollment broker staff), or representatives from community-based organizations, family caregiver associations, providers, or other key stakeholder groups. Strong candidates will demonstrate existing working relationships among key partners.
Applicants should identify a team lead who can provide overall leadership and serve as the primary point of contact for the project. The team lead must be a Medicaid official. Applicants must describe why that official is the right choice to ensure the state achieves its goals — and commit to providing that individual with sufficient time to fulfill their project responsibilities.
State approach: Applicants will describe their selected approach to increasing access to PACE and explain why they selected that approach.
State goals and initial planning: Applicants should describe specific and measurable goals, and a realistic timeline and activities to achieve these goals.
Technical assistance needs: Applicants should describe what specific expertise, technical support, and other resources would be helpful in making progress.
Submission: To apply to participate in the State PACE Action Network, please complete the brief application.
The application must be submitted electronically to Luke Pluta-Ehlers at lpehlers@oldsite.nashp.org by 5 p.m. (ET) Thursday, April 15, 2021. NASHP will notify each state of the state of its application status no later than April 26, 2021.
NASHP State PACE Action Network Application for Technical Support May-December, 2021
/in Policy Chronic and Complex Populations, State Resources, The RAISE Family Caregiver Resource and Dissemination Center /by NASHP StaffThis application is designed to help the National Academy for State Health Policy (NASHP) understand each state applicant’s goals and objectives for participating in its State Program of All-Inclusive Care for the Elderly (PACE) Action Network. NASHP will select states for the network using the criteria described in the request for applications guidelines. Applications and any optional letters of support must be submitted by email to Luke Pluta-Ehlers (lpehlers@oldsite.nashp.org) by 5 p.m. (ET) Thursday, April, 15, 2021
Interested state teams are encouraged to participate in an informational webinar from 2 to 3 p.m. (ET) Tuesday, March 30, 2021. Register here. For more information, contact Luke Pluta-Ehlers (lpehlers@oldsite.nashp.org). NASHP will notify each state about the status of its application no later than April 26, 2021.
Team Composition
State applications may include a team of up to four members. The team must include at least one Medicaid official and one PACE representative (e.g., PACE program or state PACE association). The team lead must be a state Medicaid official. The team may include additional state or PACE staff and others who can directly support team goals (e.g., aging agency administrators, managed care enrollment counselors, family caregiver representative, etc.).
Team Roster
Please complete the core team roster below.
Team Member 1 (Team Lead: State Medicaid official)
| Name:
Title: |
Phone:
Email: |
| Agency/Organization: | |
| Assistant: | Assistant’s Email: |
Team Member 2 (PACE representative)
| Name: | Phone: |
| Title: | Email: |
| Agency/Organization: | |
| Assistant: | Assistant’s Email: |
Team Member 3
| Name: | Phone: |
| Title: | Email: |
| Agency/Organization: | |
| Assistant: | Assistant’s Email: |
Team Member 4
| Name: | Phone: |
| Title: | Email: |
| Agency/Organization: | |
| Assistant: | Assistant’s Email: |
Project Plans
Please respond to the following questions and limit your response to 200 words or less per question.)
- Team lead: Please describe why the identified team lead is the right choice to ensure that your team achieves its goals. Also, please specify the amount of time the lead will dedicate to this project.
- State approach: Please select one or more of the options below and briefly explain why you selected that approach.
_______ Implementing Medicaid policies that increase access to existing PACE sites
_______ Enabling existing PACE programs to serve more people in their current service areas
_______ Enabling existing PACE programs to serve people in more areas of the state.
_______ Other (please specify)
- State goals and initial planning: What specific goals do you hope to achieve within the network’s eight-month timeline? These goals should be specific, measurable, and attainable.
- Technical assistance needs: Please describe up to four topics that you would like learn about and discuss during a network technical assistance event. If there are particular experts you would like to hear from or other resources you need to address the topic, please identify those as well.
Six States to Participate in NASHP’s Family Caregiving Institute
/in The RAISE Act Family Caregiver Resource and Dissemination Center Blogs, Featured News Home State Resources, The RAISE Family Caregiver Resource and Dissemination Center /by NASHP StaffThe National Academy for State Health Policy (NASHP) has selected six states (CT, DE, IL, MD, NY, and UT) to participate in its State Medicaid Policy Institute on Family Caregiving. State teams will work with state leaders, NASHP staff, and experts to develop and strengthen policies and strategies that support family caregivers, with a particular focus on home- and community-based approaches for older adults.
The institute’s focus will include peer-to-peer state learning, technical assistance, promising practices, and an award of $40,000. The initiative, supported by The John A. Hartford Foundation along with RRF Foundation for Aging and the Ralph C. Wilson, Jr Foundation, will contribute to a national discussion on family caregiving fostered by the RAISE Act, a federal initiative led by the US Administration on Community Living to develop the first national strategy on family caregiving.
The institute will also contribute to the development of a state policy roadmap to better support family caregivers.
RAISE Family Caregiving Advisory Council: January 2021 Meeting Summary
/in The RAISE Act Family Caregiver Resource and Dissemination Center Blogs, Featured News Home Chronic and Complex Populations, Council Meeting Materials and Resources, The RAISE Family Caregiver Resource and Dissemination Center /by Luke Pluta-Ehlers, Salom Teshale and Wendy Fox-GrageOn Jan. 19, 2021, the RAISE Family Caregiving Advisory Council convened to hear presentations on Medicaid supports for family caregivers, listening sessions with caregivers, and the compiling of a federal inventory of family caregiver resources and programs. The council also discussed the process for reviewing its initial report to Congress.
The meeting began with a recorded video message from the council chair, Administrator and Assistant Secretary for Aging at the Administration for Community Living (ACL) Lance Robertson. He reflected on the council’s progress and accomplishments in 2020 and shared parting words and well wishes, thanking the council for its commitment, along with that of the US Department of Health and Human Services (HHS), the ACL, and other partners that have supported the council’s work. The council also took a moment to share its gratitude for Robertson’s support and leadership.
Medicaid Supports for Family Caregivers Presentation
National Academy for State Health Policy (NASHP) Senior Program Director Kitty Purington delivered an informative presentation on ways state Medicaid programs could support family caregivers (read the full report). Purington noted family caregivers’ role in states that are conducting rebalancing efforts toward home- and community-based services (HCBS). Examples of HCBS that could support family caregivers include counseling and respite, education and training, care coordination, and state reimbursement options that could include family caregivers. Purington noted that policy levers, such as state plan options, 1915(c) waivers, 1115 waivers, and Medicaid managed care present opportunities to incorporate benefits for enrollees that support family caregivers.
Purington highlighted examples of states that have incorporated innovative supports for family caregivers and noted opportunities at the federal level to support states in implementing effective family caregiver strategies. Purington concluded by noting potential options to support family caregivers of Medicaid enrollees, such as:
- Partnerships with area agencies on aging (AAA), and similar organizations that offer training and counseling supports through waivers or managed care organizations; and
- Support infrastructure for caregiver assessment.
Purington also explained the importance of developing evidence-based practices to support programs and services, particularly in underserved communities.
Family Caregiver Listening Sessions Presentation
Eileen Tell, chief executive officer of ET Consulting and Fellow at LTSS LeadingAge Center at UMass Boston, presented an overview of the caregiver listening sessions. After receiving caregiver input from ACL’s Request for Information on behalf of the council, a series of virtual listening sessions were held that gathered detailed perspectives from caregivers. Listening sessions attendees included family caregivers of diverse age, race, ethnicity, employment status, and family structure, along with additional groups, such as Latinx, teen, and grandparent caregivers.
The presentation covered the major areas of inquiry from the listening sessions including:
- Respite
- Adult day care
- Information and referral
- Caregiver training and education
- Care transitions, and
- Financial well-being.
The presentation examined how caregivers expressed a strong desire for respite services but expressed concern about finding quality respite caregivers. Council members also discussed caregiver concerns with referral systems and how they can be changed to earn caregiver trust. The presentation also addressed different preferences for training and education of caregivers, including behavioral and medical training in a hands-on or online setting.
Another area of concern covered in the presentation was caregiver perspectives on different financial supports including:
- Workplace accommodations
- Direct pay, and
- Tax incentives.
Tell also addressed how the COVID-19 pandemic is impacting caregivers, describing both positives and negatives. While many caregivers appreciate additional workplace flexibility and the greater availability of family to assist with care, they cited isolation, stress, difficulty adapting some therapies to a virtual setting, and other new responsibilities as challenges.
Inventory of Federal Programs and Initiatives to Support Family Caregivers
Greg Link from ACL shared updates on the compilation of an inventory of federal programs and initiatives that could support family caregivers. Information within the inventory is intended to address family caregivers, kinship/grandparent caregivers, and other stakeholders. The inventory is currently planned to be made available to the public via a webpage in the future, with a high-level overview in the report to Congress.
Initial Report to Congress: Overview of Council Review Process
Sarah Markel of ACL explained the process for publishing the finalized first draft of the report to Congress. Council members will soon have the opportunity to review and provide edits to the first draft and collaboratively discuss changes. Once the report is finalized and passes clearance, the council will vote on final approval.
Closing Remarks
The meeting concluded with a discussion of the review process for the council’s initial report to Congress, and next steps involving development of the Family Caregiving National Strategy. The council subcommittees will meet in February 2021.
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For individuals living with complex, often chronic conditions, and their families, palliative care can provide relief from symptoms, improve satisfaction and outcomes, and help address critical mental and spiritual needs during difficult times. Now more than ever, there is growing recognition of the importance of palliative care services for individuals with serious illness, such as advance care planning, pain and symptom management, care coordination, and team-based, multi-disciplinary support. These services can help patients and families cope with the symptoms and stressors of disease, better anticipate and avoid crises, and reduce unnecessary and/or unwanted care. While this model is grounded in evidence that demonstrates improved quality of life, better outcomes, and reduced cost for patients, only a fraction of individuals who could benefit from palliative care receive it. 























































































































































