Medicaid Managed Care - U.S. Senate Special Committee on Aging

Medicaid Managed Care - U.S. Senate Special Committee on Aging Medicaid Managed Care - U.S. Senate Special Committee on Aging

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744 Tn Uvman 1usoUU - Ya..e. PeMh ith M. Wi (Ane...g. W. N- l.W5u,1 I I;! THE URBAN INSTITUTE Younger People with Disabilities and State Health Policy bv Joshua M Wener The views expressed are those of the authors and do not necessarily reflect those of the Urban Institute, its board, its sponsors, or other authors in the series Services to younger persons with disabilities (children and adults under 65 years of age) form a substantial share of overall state health spending and are an important part of the Medicid program. This population accounted for 16 percent of all ong>Medicaidong> beneficiaries in 1995 (about3.7 millon persons), but 32 percent of ong>Medicaidong> expenditures (almost $50 billion). Younger persons with disabilities also accounted for nearly one-third of the extraordinary growth in ong>Medicaidong> spending over the 1988-1995 period. 1 Thus, this population is critical to state efforts to control ong>Medicaidong> expenditures and to reform health care generally. This brief discusses a variety of delivery and financing issues that states are facing as they rethink ong>Medicaidong> and other health programs. A brief overview of the population and the costs associated with health services provided to this group helps set the stage for the discussion. The Population and Its Service Costs - Younger people with disabilities are a very heterogeneous group, consisting of individuals with physical disabilities, mental illnesses, and mental retardation/developmental disabilities. The number of younger people with substantial disabilities living in the community ranged from 1.0 to 14:1 million people in 1995, depending on the definition used. 2 In addition, about 500,000 younger people with disabilities were in institutions: 13 5,OOCin intermediate care facilities for the mentally retarded (ICF/MRs), 220,000 inpatients in psychiatric institutions, and 150,000 in nursing homes. 1 There is an ongoing trend away from institutional use. As noted above, the ong>Medicaidong> program served about 5.7 millon younger persons with disabilities in 1995. Spending on blind and disabled ong>Medicaidong> beneficiaries averaged $8,685 per person in 1995, compared to $1,728 for younger beneficiaries who are not disabled. 4 For the very'severely disabled, the cost can be much higher. For example, the average cost of a year's institutional care in an ICF/MR was almost $71,000 in 1995. 1 These institutional costs are particularly high because of extensive quality standards, use of (relatively expensive) unionized state employees in public facilities, and low occur y rates resulting from the deinstitutionalization movement. The average ong>Medicaidong> cost of serv;people with mental retardation/developmental disabilities in home and community-ba- ong>Medicaidong> waivers was just over $24,000 in 1996. ong>Medicaidong> expenditures for younger persons with disabilities historically have been about evenly split between acute and long-term care services, but in recent years the balance has shifted toward acute care expenditures. In 1994, 57 percent of ong>Medicaidong> expenditures for blind and disabled beneficiaries were for

2of II 745 acute care, while 43 percent were for long-term care (figure I). Service Delivery States play a much larger role in the direct provision of services for younger people with disabilities than they do for the elderly. They are especially important providers of institutional services for younger persons with mental retardation/developmental disabilities and with chronic-mental illnesses. Two major issues concern states as they review their delivery of services to younger people with disabilities: the balance between institutional and home and community-based care and the integration of acute and long-term care services within a managed care system. Both are important features of ongoing debates about cost and appropriateness of care with respect to this population. Balance Between Institutional and Noninstitutional Services There is an extremely widespread, although not unchallenged, policy consensus among state policymakers and disability advocates that institutions should play a far smaller role in providing services to younger persons with disabilities than has traditionally been the case. Many advocates go further than policymakers and are unwilling to grant even a residual role for institutional care (which sharply distinguishes the disability movement from-advocates for the elderly). There have been numerous lawsuits forcing deinstitutionalizati6n at many state mental hospitals and ICF/MRs. As a result of transferring less disabled individuals to other settings, the remaining residents of state institutions are very severely disabled; moving them to less structured environments may be more difficult and expensive than past shifts. Although the institutionalized population has declined, funds and services have not always followed individuals from the institution to the community. Home and community-based services are expanding rapidly and embrace an increasingly wide range of services, including home health, personal care, homemaker services, assisted living, adult-foster care, day habilitation, prevocational services, supported employment, supported living, chore service, homemaker - services, meals-on-wheels, respite care, family training, modifications to the home, and personal emergency response systems. Many of these services are beyond the traditional definition of "medical . care," but are important supports for people with disabilities. As a sign of the shifting balance of care, in 1994 for the first time the number of ong>Medicaidong> beneficiaries with mental retardation or developmental disabilities receiving home and community-based services exceeded the number of persons receiving care in ICF/MRs. 6 For home and community-based services, two key issues are the flexibility and scope of services and the use of"personal assistance services." Advocates argue that because each person is differentpeople with disabilities should be able to tailor services to their own needs by choosing from a very broad There is increasing state policy interest array of services. In the most far-reaching - in integrating acute and long-term formulation of this argument, some advocates have proposed "cashing out" services and care services through managed care giving individual consumers total freedom to organiatons. But debate rages over spend the money as they see fit. Although whether managed care is appropriate supporting increased flexibility, federal aind state officials worry that, with an for people with disabilifiis. ever-widening array of services on the list of offerings, more and more persons with disabilities will come forward to claim services. In an Lpen-ended program like ong>Medicaidong>, according to this view, people cannot be entitled to "everything" without expenditures increasing greatly.

2of II<br />

745<br />

acute care, while 43 percent were for l<strong>on</strong>g-term care (figure I).<br />

Service Delivery<br />

States play a much larger role in the direct provisi<strong>on</strong> of services for younger people with disabilities than<br />

they do for the elderly. They are especially important providers of instituti<strong>on</strong>al services for younger<br />

pers<strong>on</strong>s with mental retardati<strong>on</strong>/developmental disabilities and with chr<strong>on</strong>ic-mental illnesses. Two major<br />

issues c<strong>on</strong>cern states as they review their delivery of services to younger people with disabilities: the<br />

balance between instituti<strong>on</strong>al and home and community-based care and the integrati<strong>on</strong> of acute and<br />

l<strong>on</strong>g-term care services within a managed care system. Both are important features of <strong>on</strong>going debates<br />

about cost and appropriateness of care with respect to this populati<strong>on</strong>.<br />

Balance Between Instituti<strong>on</strong>al and N<strong>on</strong>instituti<strong>on</strong>al Services<br />

There is an extremely widespread, although not unchallenged, policy c<strong>on</strong>sensus am<strong>on</strong>g state policymakers<br />

and disability advocates that instituti<strong>on</strong>s should play a far smaller role in providing services to younger<br />

pers<strong>on</strong>s with disabilities than has traditi<strong>on</strong>ally been the case. Many advocates go further than<br />

policymakers and are unwilling to grant even a residual role for instituti<strong>on</strong>al care (which sharply<br />

distinguishes the disability movement from-advocates for the elderly). There have been numerous lawsuits<br />

forcing deinstituti<strong>on</strong>alizati6n at many state mental hospitals and ICF/MRs. As a result of transferring less<br />

disabled individuals to other settings, the remaining residents of state instituti<strong>on</strong>s are very severely<br />

disabled; moving them to less structured envir<strong>on</strong>ments may be more difficult and expensive than past<br />

shifts. Although the instituti<strong>on</strong>alized populati<strong>on</strong> has declined, funds and services have not always<br />

followed individuals from the instituti<strong>on</strong> to the community.<br />

Home and community-based services are expanding rapidly and embrace an increasingly wide range of<br />

services, including home health, pers<strong>on</strong>al care, homemaker services, assisted living, adult-foster care, day<br />

habilitati<strong>on</strong>, prevocati<strong>on</strong>al services, supported employment, supported living, chore service, homemaker -<br />

services, meals-<strong>on</strong>-wheels, respite care, family training, modificati<strong>on</strong>s to the home, and pers<strong>on</strong>al<br />

emergency resp<strong>on</strong>se systems. Many of these services are bey<strong>on</strong>d the traditi<strong>on</strong>al definiti<strong>on</strong> of "medical .<br />

care," but are important supports for people with disabilities. As a sign of the shifting balance of care, in<br />

1994 for the first time the number of <str<strong>on</strong>g>Medicaid</str<strong>on</strong>g> beneficiaries with mental retardati<strong>on</strong> or developmental<br />

disabilities receiving home and community-based services exceeded the number of pers<strong>on</strong>s receiving care<br />

in ICF/MRs. 6<br />

For home and community-based services, two key issues are the flexibility and scope of services and the<br />

use of"pers<strong>on</strong>al assistance services." Advocates argue that because each pers<strong>on</strong> is differentpeople with<br />

disabilities should be able to tailor services to<br />

their own needs by choosing from a very broad There is increasing state policy interest<br />

array of services. In the most far-reaching - in integrating acute and l<strong>on</strong>g-term<br />

formulati<strong>on</strong> of this argument, some advocates<br />

have proposed "cashing out" services and care services through managed care<br />

giving individual c<strong>on</strong>sumers total freedom to organiat<strong>on</strong>s. But debate rages over<br />

spend the m<strong>on</strong>ey as they see fit. Although whether managed care is appropriate<br />

supporting increased flexibility, federal aind<br />

state officials worry that, with an for people with disabilifiis.<br />

ever-widening array of services <strong>on</strong> the list of<br />

offerings, more and more pers<strong>on</strong>s with<br />

disabilities will come forward to claim services. In an Lpen-ended program like <str<strong>on</strong>g>Medicaid</str<strong>on</strong>g>, according to<br />

this view, people cannot be entitled to "everything" without expenditures increasing greatly.

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