New York State Department of Social Services, DAB No. 905 (1987)

DEPARTMENTAL GRANT APPEALS BOARD

Department of Health and Human Service

SUBJECT: New York State  Department of Social Services

Docket No. 87-69
Decision No. 905

DATE:  October 7, 1987

DECISION

The New York State Department of Social Services (State) appealed a
decision by the Health Care Financing Administration (HCFA, Agency)
disallowing federal financial participation (FFP) in the amount of
$2,489,194 claimed by the State under title XIX (Medicaid) of the Social
Security Act (Act) for the period July 1 through December 31, 1985.  The
costs represented supplemental malpractice insurance purchased by
hospitals for their affiliated physicians and dentists pursuant to a
State law which became effective July 1, 1985.  The costs were included
in calculating the rates paid to the hospitals.

The disallowance was taken on the ground that the costs were not
allowable under the terms of a demonstration project approved by HCFA
for the three-year period ending December 31, 1985.  This demonstration
project was authorized by 42 U.S.C. 1395b-1, which gives the Secretary
authority to conduct experiments relating to the administration of the
Medicare program, and, in conjunction with such experiments, to waive
compliance with certain requirements of titles XVIII (Medicare) and XIX
relating to reimbursement.  The major feature of the State's project was
the setting of Medicare rates on a prospective rather than a
retrospective basis in order to bring Medicare into conformity with the
rest of the State reimbursement system.  The project also modified the
prospective reimbursement system then in place. The project affected
Medicaid reimbursement since the State apparently used the Medicare
principles of reimbursement to determine Medicaid per diem rates.

The State took the position that the costs were allowable under the
demonstration project.  It did not argue that the costs were ordinarily
allowable under its Medicaid program. 1/

For the reasons discussed below, we conclude that the costs were not
authorized under the demonstration project.  Accordingly, we sustain the
disallowance.


Changes in Project Methodology

The State's application for a waiver under 42 U.S.C. 1395b-1 was
entitled "A Proposal for the Development of Hospital Reimbursement
Methodology for New York State for the 1980's." This proposal was
approved by HCFA subject to terms and conditions in a letter from HCFA
to the State dated December 14, 1982.  The letter stated in pertinent
part that--

       Any changes in the demonstration methodology shall be subject to
       approval by the Health Care Financing     Administration (HCFA)
       Project Officer prior to       implementation of the changes.

(State's appeal file, Ex. 1, p. 1)

The Agency argued that the inclusion of the supplemental malpractice
insurance costs in determining the rates paid to hospitals constituted a
change in the demonstration methodology for which prior approval was
required.  The Agency advised the State in letters dated August 29 and
September 13, 1985 that the costs would not be allowed if claimed.
(Agency's appeal file, Exs. 1 and 2)  (The letters indicated that they
were in response to inquiries concerning the allowability of the costs.
There is no request for prior approval in the record, however.)   In its
appeal of the disallowance, the State took the position that there was
no change in methodology involved.  We conclude that the addition of the
supplemental malpractice insurance costs in determining the rates was a
change in methodology.  The approved project proposal identifies certain
generally unallowable costs which are to be reimbursable under the
project.  The proposal states:

     The reimbursement system attempts to provide
sufficient operating funds based upon allowable costs       which are
supplemented with allowances for                discretionary funds, bad
debts and charity care.      (Proposal, pp. 2-3)  Significantly, the
references to the allowability of these additional costs frequently
appear in the context of discussions of project methodology.    The
"Executive Summary" includes a section headed "Proposed Methodology"
which states in part:

     The hospital's fiscal base is strengthened with     allowances for
       bad debt, charity care and     discretionary purposes. . . . This
       methodology will      produce a predictable revenue base for both
providers      and payors over three years.

(Proposal, p. vi)  Chapter III of the proposal, captioned "Research and
Demonstration Methodology," states in part:

     Institutional and systemwide fiscal viability will be strengthened
       under a uniform reimbursement methodology that recognizes the
costs of bad debt and charity care and that provides hospitals with a
discretionary and working capital allowance.

(Proposal, p. 48)  Elsewhere, the proposal states:

       These savings, however, are offset by other changes to Medicare's
       current methodology:  These would be  two allowances added to
       third party rates--an annual  average of 3.23 percent for bad
       debt/charity care and 2 percent for discretionary purposes. . . .

(Proposal, p. 43)  Furthermore, the use of the term "methodology" in the
proposal's title indicates that all elements of the proposal--including
the provisions quoted above--were considered part of the demonstration
methodology within the meaning of the prior approval requirement.

Thus, the methodology for the demonstration project provided for
reimbursement of some generally unallowable costs, i.e., bad debts,
charity, working capital and costs paid out of the discretionary fund.
Supplemental malpractice insurance costs were not among these costs (and
could not have been, since the law requiring hospitals to pay such costs
was not effective until July 1, 1985, long after the January 1, 1983
beginning date of the demonstration project).  Accordingly, the
inclusion of such costs in calculating the hospitals' per diem rates was
a change in methodology for which prior approval was required.  Since
the State did not obtain prior approval, the costs are unallowable.

Rate Increases to Meet State Requirements

The State also argued that the supplemental malpractice insurance costs
were allowable under a provision of State law, incorporated in the
approved project proposal, allowing rate increases based on "additional
costs to be incurred in meeting state or federal requirements. . . ."
(Public Health Law, section 2807- a(5)(b)(iii))  The State noted that
another State law required that hospitals have qualified physicians
available for emergency service, and argued that the malpractice
insurance legislation assured the availability of physicians in
accordance with this law.  The malpractice insurance legislation
provided in effect for a rate increase on the basis stated in section
2807- a(5)(b)(iii).

Even assuming that the increased rates resulting from the inclusion of
supplemental malpractice insurance costs were permitted by the terms of
section 2807-a(5)(b)(iii), we conclude that the costs were not allowable
under the demonstration project.  To allow the costs under this
provision would violate the requirement for prior approval of changes in
the project methodology.  Under the State's reading of section 2807-
a(5)(b)(iii), the State could add new costs to its Medicaid program
virtually without limitation, as long as it found that they were
incurred to meet the requirements of State law.  This would make the
prior approval requirement meaningless.  Thus, where the addition of
costs involves a change in project methodology, section
2807-a(5)(b)(iii) must be read to allow rate increases only where the
additional costs have been approved by the Agency.

In any event, it is not clear that the supplemental malpractice
insurance costs were allowable under section 2807-a(5)(b)(iii) since the
State did not provide any support for its allegation that these costs
assured the availability of qualified physicians for emergency service.

Other Arguments

The State also asserted that language in the approved project proposal
providing for "a payment level reflecting allowable, reasonable and
justifiable costs of the efficient production of necessary inpatient
services" (Proposal, p. 25) governed here. The State argued that
limitations on reimbursable costs were specified in the approved
proposal, and that any costs not specified--including the supplemental
malpractice insurance costs--were thus allowable within the meaning of
the quoted provision.  As discussed previously, however, rather than
allowing any costs not specifically prohibited, the proposal identifies
those costs ordinarily not allowable which will be reimbursed.  The
supplemental malpractice insurance costs are not among them and are
therefore not allowable.  The State further argued that the costs were
reasonable within the meaning of this provision since they assured
compliance with the requirement of section 1902(a)(13)(A) of the Act to
"assure. . . reasonable access to. . . inpatient hospital services. . .
."  We need not address this argument, however, since we find that the
quoted language does not render the costs allowable.

The State asserted in addition that the approval of the demonstration
project "gave the State additional discretion in its administration of
the hospital reimbursement portion of the Medicaid program by removing
the restrictions imposed by Section 1902 of the Act. . . ."   (State's
brief, p. 4)  The State identified neither the alleged restrictions in
section 1902 nor the language in the approved project proposal waiving
the restriction, however.

The State also argued that the allowance for a discretionary fund was
evidence of the State's "increased autonomy" under the demonstration
project.  (State's brief, p. 5)  The hospitals were free to use this
fund to support a range of activities.  The supplemental malpractice
insurance costs were not paid out of this fund, however.  The State's
point appears to be that the existence of the discretionary fund was
evidence that it was intended to have a sufficiently broad range of
discretion under the project to treat the supplemental malpractice
insurance costs as allowable.  This argument has no merit.  We see no
basis for inferring from the fact that hospitals were given a limited
amount of funds to pay any costs they deemed necessary that the payment
of any costs from sources outside of this fund was within their
discretion.

The State further contended that the cap on Medicare liability included
in the approved project proposal was not exceeded by amounts claimed for
supplemental malpractice insurance.  The provision referred to requires
that costs under the waiver not exceed expenditures that would otherwise
have been incurred under the Medicare program.  This point is
irrelevant, however, since even costs which do not exceed the cap may be
unallowable on some other basis.

The State also asserted that the provision of supplemental malpractice
insurance was in keeping with the stated purpose of the project to
contain costs.  It asserted that the malpractice legislation as a
whole--which included certain reforms in addition to requiring the
purchase of supplemental malpractice insurance--was intended to reduce
overall malpractice costs (although the supplemental malpractice
insurance itself represented an increased cost).  However, this does not
change the fact that the costs were unallowable absent prior approval.

Finally, the State argued that the supplemental malpractice insurance
costs were allocated using the same methodology required by the approved
project proposal for allocating hospitals' malpractice insurance.
However, the allowability of the costs, and not their allocability, is
at issue here. 2/      .Conclusion

For the foregoing reasons, we sustain the disallowance in the amount of
$2,489,194.

 

 

                            ________________________________ Donald F.
                            Garrett

 

                            ________________________________ Alexander
                            G. Teitz

 

                            ________________________________ Norval D.
                            (John) Settle Presiding Board Member

 


1.     The Agency asserted that the supplemental malpractice insurance
costs were personal costs of physicians and dentists and, as such, were
not reasonable and necessary costs under either the generally applicable
cost principles in OMB Circular A-87 or the demonstration project.  The
State asserted that the costs in question were hospital costs, not
personal costs. However, it did not dispute the statement in HCFA's
brief that the State "does not maintain that . . . [the costs] were ever
approved under its prior state plan(s) or that they are allowable under
generally applicable cost principles."  (Agency's brief, p.  6, n. 4)
Furthermore, the State did not claim the costs beyond the end date of
the demonstration project.

2.    The Agency stated, however, that the supplemental malpractice
insurance covered "medical and dental malpractice occurrences from the
entirety of the physician's or dentist's practice, not solely his
hospital practice," and that "if these costs were finally determined to
be Medicaid-allowable, they would include. . . costs clearly not
allocable to Medicaid, and which the Federal government would have to
refuse to pay." (Agency's brief, p. 2 and p. 9, n.