http://www.nationalmssociety.org/Research-2002Jan11.asp
January 11, 2002
Summary:
A study by investigators at the Center
for Health Economics Research and the University of California, San Diego
indicates that health care expenditures among persons with MS are two to
three times higher than those among individuals without MS. The study
was supported in part by the Health Care Delivery and Policy Research Program
of the National MS Society.
The authors utilized three insurer
administrative billing datasets (private insurance, Medicare, and Medicaid
for disabled individuals).
Researchers have reported that health
care expenditures and utilization among persons with MS who are covered
by private or governmental insurance are two to three times higher than
among individuals without MS having the same types of coverage. The comparison
group used in this study included both healthy individuals as well as those
with other chronic or acute conditions. Gregory Pope and colleagues at
the Center for Health Economics Research (Waltham, MA) and the University
of California at San Diego reported their findings in the January 8, 2002
issue of Neurology. The study was supported in part by the Health Care
Delivery and Policy Research Program of the National MS Society
Background:
Individuals with chronic conditions
such as MS tend to utilize health care services more than healthy people.
As a result, persons with MS are more expensive both for insurers and for
health care providers in managed care plans who receive a fixed monthly
fee per patient to cover all health care services. Understanding the level
of health care expenditures and utilization among persons with MS can help
in setting appropriate insurance premiums and provider payments that take
these higher costs into account. When the actual costs of health care are
taken into account it may help to ensure that individuals with a chronic
condition such as MS have access to appropriate specialists and services.
Failure to take these higher costs into account encourages insurers and
providers to regard the person with MS as a financial drain and to attempt
to restrict their access to needed services.
Study:
Gregory Pope and colleagues used
three insurer administrative billing datasets (privately insured, Medicare,
and Medicaid for disabled individuals in six states) to generate samples
of persons with MS between the ages of 18 and 64 and to calculate their
expenditures for, and utilization of, health care services. These same
data were used to generate comparative information on individuals without
MS, including healthy individuals and those with other medical conditions.
Persons with MS were included on the basis of the diagnostic codes that
providers are required to enter on claim forms. Using this method, the
investigators were able to obtain data on 7,477 individuals with MS who
were privately insured, 5,755 who were covered by Medicare, and 3,681 who
were covered by Medicaid. Since the three datasets contained no identifying
information such as names, addresses, or Social Security numbers, the privacy
of all persons was protected.
The expenditure data included both
the insurer’s component (the amount the insurer pays) and any cost-sharing
on the part of the insured such as deductibles and co-payments (the amount
the patient pays). It did not include out-of-pocket expenditures for goods
or services not covered by the insured’s plan or indirect costs of illness
such as lost wages.
The chart below summarizes the findings
concerning average annual insured medical expenditures across the three
plans. Because much of this information was collected prior to the widespread
use of disease-modifying drugs in MS and because Medicare does not cover
prescription medications, the dollar figures shown here exclude costs associated
with prescription drugs. Compared to other persons in the same insurance
plans, average annual insured expenditures for persons with MS were 3.2
times higher among the privately insured ($6,329 vs. $2,001), 1.9 times
higher among Medicare beneficiaries ($11,230 vs. $6,006), and 2.5 times
higher among Medicaid recipients ($10,358 vs. $4,111).
Expenditures were not evenly distributed
across the MS population. Instead, as is generally true of such costs in
the general population, expenditures for health care among persons with
MS tended to be concentrated among a small proportion of individuals. For
example, 20% of the costs were accounted for by the most expensive 1% of
those with MS
Conclusion:
This study found that health care
expenditures and utilization were higher among persons with MS than among
persons without MS across three important third-party payers: private insurers,
Medicare, and Medicaid. The authors conclude that these higher costs need
to be taken into account in payments made to health care providers. Not
taking these higher costs into account could adversely affect the access
that persons with MS have to needed services. Particularly in managed care
plans where providers are paid a fixed monthly fee to provide health care
to enrollees, the higher costs associated with MS could discourage providers
from serving those with MS.
The authors suggest that “diagnostic
risk adjustment” (adjusting payments based on costs associated with a specific
medical diagnosis) should be more widely utilized than at present. Diagnostic
risk adjustment could result in reimbursement levels that more accurately
reflect the costs associated with MS and help to ensure that persons with
MS have access to the specialized services they need. The authors further
suggest that since health care costs are not evenly distributed across
the MS population, an additional adjustment based on MS severity could
further refine reimbursement procedures. Many third party payers have already
begun to move in the direction of utilizing diagnostic risk adjustment.
The authors endorse this trend and suggest that it needs to be expanded
in the future not only for MS but for other chronic conditions with similarly
elevated expenditures and rates of utilization.
Details:
and 82.5% of the costs were accounted
for by the most expensive 25% of those with MS. The least expensive 50%
of those with MS accounted for less than 5% of costs. Because administrative
billing data do not include information on type or severity of MS, the
investigators were not able to identify the type or severity of MS represented
in these breakdowns.
© 2002 The National Multiple
Sclerosis Society