[Federal Register: November 2, 2001 (Volume 66, Number 213)]
[Rules and Regulations]
[Page 55857-55866]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr02no01-24]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
42 CFR Part 419
[CMS-1159-F1]
RIN 0938-AK54
Medicare Program; Announcement of the Calendar Year 2002
Conversion Factor for the Hospital Outpatient Prospective Payment
System and a Pro Rata Reduction on Transitional Pass-Through Payments
AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION: Final rule.
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SUMMARY: This final rule announces the Medicare hospital outpatient
prospective payment system conversion factor for calendar year (CY)
2002. In addition, it describes the Secretary's estimate of the total
amount of transitional pass-through payments for CY 2002 and the
implementation of a uniform reduction in each of the pass-through
payments for that year.
EFFECTIVE DATE: This final rule is effective January 1, 2002 and
applies to services furnished on or after January 1, 2002. This rule is
a major rule as defined in 5 U.S.C. 804(2). According to 5 U.S.C.
801(a)(1)(A), we are submitting a report to the Congress on this rule
on November 1, 2001.
FOR FURTHER INFORMATION CONTACT: Anne Tayloe, (410) 786-0600.
SUPPLEMENTARY INFORMATION:
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Register
[[Page 55858]]
online database through GPO Access, a service of the U.S. Government
Printing Office. The Web site address is: http://www.access.gpo.gov/
nara/index.html.
I. Background
Section 1833(t) of the Social Security Act (the Act), as added by
section 4523 of the Balanced Budget Act of 1997 (BBA), Pub. L. 105-133,
provided for implementation of a prospective payment system (PPS) for
hospital outpatient services furnished to Medicare beneficiaries. The
Medicare, Medicaid, and SCHIP Balanced Budget Refinement Act of 1999
(BBRA), Pub. L. 106-113, amended section 1833(t) of the Act to make
major changes that affected the new prospective payment system. On
April 7, 2000, we published a final rule with comment period in the
Federal Register (65 FR 18434) to implement the new PPS for hospital
outpatient services. The new system established payment rates for each
service paid under this system using ambulatory payment classification
(APC) groups. On June 30, 2000, we published a notice in the Federal
Register (65 FR 40535) announcing a delay in the effective date of the
hospital outpatient PPS (OPPS) from July 1, 2000 (as set forth in the
April 7, 2000 final rule) until August 1, 2000. Therefore, OPPS became
effective on August 1, 2000. The regulations implementing the payment
system appear at 42 CFR part 419.
On August 3, 2000, we published an interim final rule with comment
period (65 FR 47670) that modified criteria that we use to determine
which medical devices are eligible for transitional pass-through
payments. On November 13, 2000, we published an interim final rule with
comment period in the Federal Register (65 FR 67798) that provided for
the annual update to the amounts and factors for OPPS payment rates
effective for services furnished on or after January 1, 2001. We also
responded to public comments on those portions of the April 7, 2000
final rule that implemented related provisions of the BBRA and public
comments on the August 3, 2000 rule.
On August 24, 2001, we published a proposed rule in the Federal
Register (66 FR 44672) that set forth proposed changes to the OPPS to
implement applicable statutory requirements, including relevant
provisions of the Medicare, Medicaid, and SCHIP Benefits Improvement
and Protection Act of 2000 (BIPA) (Pub. L. 106-554), enacted on
December 21, 2000, as well as changes arising from our continuing
experience with the system. That document described proposed changes to
the amounts and factors used to determine the payment rates for
services paid under the hospital OPPS for CY 2002. These amounts and
factors include the updated conversion factor, APC classifications and
relative weights, wage index values, copayment amounts, and the
discussion of a possible pro rata reduction to be applied to the
transitional pass-through payments for certain drugs, biologicals, and
medical devices.
We received approximately 400 timely items of correspondence
containing multiple comments on the August 24, 2001 proposed rule. In
this final rule, we will respond to those comments addressing the
Secretary's estimate of the total amount of pass-through payments for
CY 2002 and the need for a uniform reduction to those payments in 2002
as well as the determination of the OPPS conversion factor for CY 2002.
In a subsequent final rule to be published by December 1, 2001, we
will address the remainder of the comments and include the tables
necessary to calculate CY 2002 payment rates and beneficiary copayment
amounts.
II. Transitional Pass-Through Payments
A. Background
Section 1833(t)(6) of the Act provides for temporary additional
payments or "transitional pass-through payments" for certain
innovative medical devices, drugs, and biologicals. As originally
enacted by the BBRA, this provision required the Secretary to make
additional payments to hospitals for current orphan drugs, as
designated under section 526 of the Federal Food, Drug and Cosmetic
Act; current drugs, biologicals, and brachytherapy devices used for the
treatment of cancer; and current radiopharmaceutical drugs and
biologicals. Transitional pass-through payments are also required for
new medical devices, drugs, and biologicals that were not being paid
for as a hospital outpatient service as of December 31, 1996 and whose
cost is "not insignificant" in relation to the OPPS payment for the
procedures or services associated with the new device, drug, or
biological. Under the statute, transitional pass-through payments for
any given device, drug, or biological are to be made for at least 2
years but not more than 3 years.
Section 1833(t)(6)(D)(i) of the Act sets the payment rate for drugs
and biologicals eligible for a transitional pass-through payment as the
amount by which the amount determined under section 1842(o) of the Act
(that is, 95 percent of the applicable average wholesale price) exceeds
the portion of the otherwise applicable fee schedule amount (that is,
the APC payment rate) that the Secretary determines is associated with
the drug or biological. Section 1833(t)(6)(D)(ii) of the Act sets the
transitional pass-through payment for a medical device at the amount by
which the hospital's charges, adjusted to cost, exceeds the portion of
the otherwise applicable fee schedule amount (that is, the APC payment
rate) that the Secretary determines is associated with the device.
B. Pro Rata Reductions
Section 1833(t)(6)(E) of the Act limits the total projected amount
of transitional pass-through payments for a given year to an
"applicable percentage" of projected total payments under the
hospital OPPS. For a year before 2004, the applicable percentage is 2.5
percent; for 2004 and subsequent years, the applicable percentage is a
percentage specified by the Secretary up to 2.0 percent. If the
Secretary estimates before the beginning of the calendar year that the
total amount of pass-through payments in that year would exceed the
applicable percentage, section 1833(t)(6)(E)(iii) of the Act requires a
uniform prospective reduction in the amount of each of the transitional
pass-through payments for that year to ensure that the limit is not
exceeded.
In the August 24, 2001 proposed rule setting out the proposed
changes for CY 2002 in the OPPS, we described the extensive data base
that we have constructed in order to prepare for making an estimate of
pass-through payments for 2002. This data base includes outpatient
claims data submitted by hospitals for services furnished on or after
July 1, 1999 and before July 1, 2000, as well as device cost and
utilization data extracted from applications for pass-through status
submitted by manufacturers, hospitals, specialty societies, and other
entities. In their applications for pass-through status, manufacturers
have supplied information on the expected cost to hospitals of devices
and the procedures with which the devices are commonly used.
In the August 24, 2001 proposed rule, we indicated that the
information collected to that time suggested that a significant pro
rata reduction might be required for 2002 in order to meet the
statutory limit on the amount of the pass-through payments. We also
announced that we were considering the appropriateness of a number of
possible alternative approaches that would have the effect of
minimizing the amount of any potential reduction in these
[[Page 55859]]
payments. Finally, we presented a discussion of the methodology that we
contemplate using in the development of our estimate.
We announced in the August 24, 2001 proposed rule that we were
considering a number of possible approaches to different technical
aspects of estimating payments. We also indicated that, as is always
the case in making these types of estimates, it would be necessary to
make a number of assumptions in interpreting the data. We were
tentatively contemplating using the following assumptions and
techniques in developing our methodology:
1. Data and Procedures for Estimation
We planned to base the estimate of 2002 pass-through expenditures
on the claims we would use to set payment rates for 2002; 2001 pass-
through amounts for drugs and radiopharmaceuticals; and device cost and
use data from pass-through applications submitted by manufacturers,
hospitals, specialty societies, and other entities. We proposed to make
projections to CY 2002 on the basis of price, volume, and service-mix
inflators consistent with our baseline for OPPS spending. Estimates for
drugs, radiopharmaceuticals, and devices would be made separately and
combined for the final projection of pass-through spending.
2. Drug Estimate
We also proposed to identify those drugs eligible for pass-through
status that have been separately billed to the Medicare program on the
claims that we intend to employ for the estimate. We proposed to
multiply the frequency of use for each of these drugs (that is, the
number of line items multiplied by the number of units billed as shown
in the claims data) by its 2001 pass-through payment amount. We would
determine a reasonable adjustment to account for those drugs that do
not appear in the claims data. Such an adjustment might take into
account the extent to which the noncoded items were classified as
orphan drugs and therefore to be used infrequently.
3. Radiopharmaceutical Estimate
As in the case of the drug estimates, we proposed to identify those
radiopharmaceuticals eligible for pass-through status that were
separately billed to Medicare in the claims data file. We proposed to
estimate expenditures for these radiopharmaceuticals directly as
described above. For radiopharmaceutical drugs, we would multiply the
frequency of use for each item by the 2001 pass-through amount. We
would estimate expenditures for the remaining items by using the
frequency counts for all nuclear medicine procedures not billed with
one of these radiopharmaceuticals.
4. Device Estimate
We proposed to estimate the transitional pass-through payments
attributable to devices by linking the frequencies for all device-
related procedures in the claims data file with the cost and use data
supplied by the manufacturers or other entities as part of their
applications for pass-through status. We proposed to match each device
eligible as of January 2001 with the procedures with which it would be
used. We would then calculate an average cost for each device or device
package associated with a procedure.
The statute requires that we calculate transitional pass-through
payments for devices by adjusting the hospital's charge for the device
to cost and then subtracting an amount that reflects the device costs
already included in the payment for the associated APC. As we explained
in the April 7, 2000 final rule (65 FR 18481), we were not able to
implement these subtractions at the time of implementation of the
system. For 2001, we made these deductions for pacemakers and
neurostimulators. In the August 24, 2001 proposed rule, we proposed to
make these subtractions for most other devices beginning in 2002. For
the purpose of doing this estimation, we proposed to deduct these
amounts from each device package before multiplying that cost by the
procedure frequencies.
5. Projecting to 2002
We planned to project prices and quantities in the estimates
determined as above to 2002 using actuarial projections of price and
enrollee volume and service increase consistent with the OPPS baseline.
We then proposed to add the three separate results in an estimate of
total pass-through spending.
We received over 80 comments in response to our proposal, including
comments from national provider associations, hospitals, device and
drug manufacturers, and their representative associations.
Comment: Many commenters expressed concern about the data and the
methodology that we proposed to use in developing an estimate of pass-
through spending for 2002. A number of these commenters specifically
cited the lack of actual claims data under the OPPS as one major
concern. Commenters doubted that claims from the period before
implementation of the OPPS would contain sufficiently accurate coding
or adequately reflect utilization of pass-through items to allow us to
make an accurate estimate.
Response: We believe that the outpatient claims data submitted by
hospitals for services furnished on or after July 1, 1999 and before
July 1, 2000 provide adequate information for use in projecting pass-
through spending for 2002. These claims are the most recent outpatient
data available to us, and we are also using these claims for the
purpose of recalibrating the APC relative weights for 2002. These data
provide useful information on the frequencies of the procedures in
which pass-through items are used, as well as of the utilization
frequencies of some of the pass-through items themselves (especially
drugs). Claims data for the period after the implementation of the
prospective payment system are not at present available for analysis.
Under the best of circumstances, we would only expect data from the
prior calendar year to be available. Thus, only data from the first 5
months under the OPPS (August to December 2000) might be available at
this point in the update cycle. However, the extent to which these
data, were they available, would offer any significant improvement for
these purposes is unclear. Those claims data would not contain
information on most of the devices approved for pass-through payment in
2002 because those items became eligible for payment after January 1,
2001. It would still be necessary to use a crosswalk that maps devices
to procedures in order to project spending for pass-through devices in
2002.
Comment: Some commenters questioned the appropriateness of using
data on cost, utilization, and coding derived from applications from
device manufacturers for pass-through status in developing the
estimate. These commenters specifically contended that these data were
not collected for the purpose of establishing payment amounts. They
also contended that the cost, utilization, and coding information were
not requested in a specific format on the applications, and that this
information was therefore not presented in an appropriately consistent
manner for the requisite level of analysis.
Response: The assertions of the commenters are incorrect. We were
aware that we would have to develop estimates of pass-through costs for
the purposes of applying the statutory limit on these costs when we
developed the applications for pass-through status. We also knew at
that time that we needed cost data in order to apply the cost
significance eligibility criteria for pass-
[[Page 55860]]
through status. We deliberately developed the applications in order to
generate reliable information on the cost, coding, and use of devices.
We specifically requested that the following information be
uniformly provided: "Current cost of the item or service to hospitals
(i.e., actual cost paid by hospitals net of all discounts, rebates, and
incentives in cash or in-kind)." We also specifically asked applicants
to identify the Healthcare Common Procedure Coding System (HCPCS) or
American Medical Association Current Procedural Terminology (CPT)
service codes associated with each device application. We certainly
assume that the manufacturers would be reliable sources of this
information. We did not derive information on utilization frequencies
solely from the manufacturers' applications for pass-through status.
Rather, we calculated our projections of utilization by analyzing the
claims at our disposal using a crosswalk of pass-through items to
procedure codes that our clinical staff developed from the information
supplied by manufacturers. The crosswalk established the CPT codes and
the APCs with which the particular devices are used, while the claims
data provided the frequency of use for devices in those APCs.
Comment: Many commenters questioned the validity of matching items
eligible for pass-through payment with the procedures with which they
would be used, citing the complexity of the CPT coding system and the
variety and number of pass-through items that could be associated with
particular procedure codes. The commenters asserted that a crosswalk
that matched pass-through items and codes would require external review
and validation. One commenter expressed concern that this crosswalk
could overstate the frequencies of device use, since devices may not
actually be used in every procedure where they could have been used.
Response: Using the information from the applications, our clinical
staff (including physicians, nurses, and coding specialists) developed
the device-to-procedure crosswalk. The staff employed a rigorous
process of analysis and verification in developing this crosswalk. All
members of the staff reviewed each tentative assignment of pass-through
items to procedures. In order to minimize the use of individual
clinical judgement, the staff made final decisions only after reaching
a consensus on the assignment of pass-through items to each procedure.
We are confident that the crosswalk reflects an appropriate level of
analytical rigor and independent validation.
The clinical staff also followed a conservative approach in
matching devices to procedures. Specifically, they assigned pass-
through items only to procedures for those pass-through items that
would be typically used, even if there were other procedures in which
those items might occasionally be used. Moreover, the crosswalk
specifically accounts for procedures where a device or devices might be
used less than 100 percent of the time. We are confident that the
crosswalk procedure itself has not in any way led to an overstatement
of pass-through costs.
Comment: Many commenters asserted that the method described in the
August 24, 2001 proposed rule is necessarily flawed because we excluded
multiple service claims from the data.
Response: We use only single service claims in calibrating the APC
weights because we have no way of allocating ancillary service costs
among the various procedures on multiple service claims. However, for
all other facets of our annual calculation of OPPS payment amounts and
factors (for example, our estimate of outlier spending and resulting
thresholds), we use both single and multiple service claims. Similarly,
we included both single service and multiple service claims in
developing our estimate of pass-through costs and the pro rata
reduction. Specifically, we used both types of claims in developing the
count of the procedures associated with the use of pass-through items.
Comment: Several commenters questioned whether we had provided
sufficient notice of a possible pro rata reduction to comply with the
requirements of the Administrative Procedure Act. These commenters
contended that the description of the proposed method for calculating a
pro rata reduction was too general to allow for adequate public comment
and that the data supporting the need for such a reduction should have
been published to allow for public review and analysis. One commenter
argued that a pro rata reduction cannot be implemented legally without
specifying the size of the reduction in a proposed rule with an
adequate comment period. A commenter from the drug industry stated that
data on utilization should be released in time for review and analysis
so that the industry could have sufficient opportunity to assess the
contribution of its products to pass-through spending and to develop
options and recommendations for legislative and administrative action.
Response: At the time the August 24, 2001 proposed rule was
published, we had assembled a data base and developed a preliminary
methodology for making an estimate of pass-through spending in 2002.
Our best judgment was that further review and analysis of the data and
methodology were warranted before we announced a specific estimate of
2002 pass-through spending and any requisite pro rata reduction. We
therefore confined our discussion in the proposed rule to the
information that was then clearly known to us, namely the general
methodology that we proposed to employ, and the likely magnitude of a
pro rata reduction.
We believe that our description of our data sources and methodology
allowed ample opportunity for substantive comment, and we did receive
numerous substantive comments on both the data sources and the
methodology. Furthermore, our notice that a "significant pro rata
reduction could be required for 2002" provided interested parties
sufficient opportunity to assess the situation and to develop options
and recommendations for both legislative and administrative action. We
received many comments with proposals and recommendations for
administrative action, as well as proposals for possible legislative
measures that commenters have urged us to bring to the attention of the
Congress. (We respond to these comments below.) Finally, we note that
section 1833(t)(12) of the Act provides that there "shall be no
administrative or judicial review * * * of the application of any pro
rata reduction * * *."
Based on the methodology described above, we estimate that the
total amount of transitional pass-through payments for 2002 would
exceed the limit of 2.5 percent of total spending under the OPPS.
Specifically, we estimate that total transitional pass-through payments
for 2002 would be about $2.26 billion, of which about $1.89 billion is
attributable to devices and about $0.37 billion is attributable to
drugs and radiopharmaceuticals. (Of the latter number,
radiopharmaceuticals account for about $0.17 billion, and drugs account
for about $0.20 billion.) Estimated total pass-through payments would
thus be approximately 13 percent of the baseline projection of $17.5
billion in total payments (including both program and beneficiary
payments) to hospitals in 2002 under the OPPS, and pass-through
payments for devices are approximately 11 percent total of OPPS
payments in 2002. Based on this estimate, a pro rata reduction of 80.7
percent would be required by the statute.
[[Page 55861]]
Many commenters recommended measures to delay or mitigate the
effects of any pro rata reduction. These comments and our responses are
set forth below.
Comment: A number of commenters requested a 1-year delay in
implementing a pro rata reduction, citing their concerns about data
limitations and methodological weaknesses as reasons for such a delay.
Other commenters recommended that any pro rata reduction should be
phased in over a period of several years in order to allow vendors and
hospitals adequate time to adjust to the reduced payment.
Response: The statute specifically requires that, if the Secretary
estimates before the beginning of a year that the amount of the pass-
through payments for that year will exceed the limit, "the Secretary
shall reduce pro rata the amount of each of the additional payments * *
* for that year." (Emphasis added.) Therefore, we can legally neither
delay the reduction until a later year nor spread the reduction over
the payments for several years. We now have an estimate of pass-through
spending for 2002, and we have explained above why we believe that our
methodology for determining it was reasonable.
Comment: Several commenters recommended that we use the amount
"reserved" for outlier payments (up to 2.5 percent of OPPS payments)
to increase the amount of money available for pass-through payments in
order to reduce the need for a pro rata reduction. (As we have
explained in other contexts, outlier payments are financed through a
prospective reduction to PPS rates. We do not "set aside" money in a
discrete fund to pay for outliers, and the same is true for pass-
through payments.) Another commenter advocated that we fold the pass-
through payments into the outlier "pool," and pay for the high costs
of new technology as part of our payment for high cost services of all
types. Other commenters contended that the 2.5 percent limit on pass-
through payments was inadequate to pay for the costs of new
technologies and recommended that the limit be raised.
Response: The statute provides for both the outlier and
transitional pass-through payments and establishes the 2.5 percent
limits on those payments for the years before 2004 (when the limit for
outliers increases to 3.0 percent and the limit for transitional pass-
throughs decreases to 2.0 percent). Thus, we do not have the
administrative authority to make any of the changes that these
commenters have recommended. Rather, legislative action would be
required to make any of these changes.
Comment: One commenter recommended that we move the procedures
associated with pass-through items to the inpatient list so that they
can be paid under the hospital inpatient PPS.
Response: We believe that the commenter is confused about the
purpose of the inpatient list. The inpatient list identifies procedures
that may not be paid under the OPPS. If medically necessary, any
procedure, including those not on the inpatient list, that is performed
in an inpatient setting may be paid under the hospital inpatient PPS.
We decide which procedures are included on the inpatient list on the
basis of clinical criteria alone. We believe that procedures should not
be included on the inpatient list for payment reasons.
Comment: Several commenters asserted that a pro rata reduction will
be necessary in 2002 only because we have failed to implement the
transitional pass-through program as the Congress intended it.
Specifically, these commenters contended that we have failed to
restrict the pass-through payments to the incremental costs of new
technologies by identifying the costs for predecessor technologies that
are already represented in the APC payment rates and subtracting those
amounts from the pass-through payments, as contemplated by the statute.
Response: Because of constraints on our data analysis before
implementation of the pass-through provision, we did have difficulty
initially in determining appropriate offsets for the technology costs
already represented in the payment rates for many APCs. However, in the
August 24, 2001 proposed rule, based on the updated claims data, we
proposed appropriate offset amounts for 25 APCs that are associated
with the use of pass-through devices. We will announce our final
computations of the offset amounts for the affected APCs in a
subsequent rule, which will be published before the beginning of the
year. We will thus have substantially accounted for the technology
costs that are already represented in APC payment rates, and,
therefore, the magnitude of the pro rata reduction cannot be attributed
to a failure to restrict pass-through payments to the incremental costs
of new technology.
Comment: Many commenters expressed their concern about the prospect
for a significant pro rata reduction, and the potential effect of such
a reduction on access of Medicare beneficiaries to necessary treatments
in the outpatient setting. These commenters therefore urged us not to
implement a pro rata reduction in 2002.
Response: A significant pro rata reduction could affect the
availability of improved medical technology for Medicare beneficiaries,
but the possibility of such a result is inherent in the statutory
scheme. The Congress has set up a scheme to limit the aggregate amount
of (projected) pass-through payments in a given year, including a
requirement for a pro rata reduction. The statute reflects a balance of
competing considerations-- providing pass-through payments for new
technologies but limiting the aggregate amount of those payments so
that payments for other services are not reduced significantly (if
there were no limit on projected pass-through payments, then, other
things being equal, we would be reducing the base payments by 13
percent rather than 2.5 percent to ensure budget neutrality). In order
to promote access to new technologies, we have decided to take a
significant administrative action in order to reduce the size of the
reduction. That action, which incorporates a portion of the pass-
through costs into the base APCs, is discussed below. We believe that
there are no other feasible and prudent administrative options
available to reduce the amount of a pro rata reduction.
Comment: Several commenters, including device manufacturers and the
associations that represent them, recommended that we fold the costs of
pass-through devices into the base APC rates. These commenters noted
that such a step would limit pass-through payments to the incremental
costs of new technologies, and at least reduce the size of a pro rata
reduction. Some of these commenters urged us not to implement any pro
rata reduction until we have revised the base rates to include these
costs.
Response: The transitional pass-through payment provision was
intended as an interim measure to allow for adequate payment of new,
innovative technology while we collected the necessary data to
incorporate the costs for these items into the base APC rates. The
statute and regulations specifically limit the payment for individual
pass-through items to at least 2 years but no more than 3 years, with
the intention that the costs for these items should be incorporated
into the APC rates for the procedures associated with these items after
that period. We agree with these commenters that we have the discretion
to fold some of these costs into the APC rates before the time period
for
[[Page 55862]]
transitional payment of specific devices has expired. (We cannot fold
all of the current pass-through costs into the APC rates at this time,
because the statute implies that pass-through payments for devices that
have been eligible for less than 2 years must continue to be made.)
We also agree with the commenters that it is reasonable and prudent
to incorporate some of the pass-through costs into the APC rates now,
before we are legally required to do so, in order to mitigate the
effects of the significant pro rata reduction that is mandated by the
statute. Prudence also dictates, however, that we take into account all
the other effects of incorporating these costs into the base rates at
this time in deciding how much of the costs to incorporate into the
base rates for 2002.
In addition to reducing the size of the pro rata reduction,
incorporating a portion of the cost of pass-through devices into the
basic APC costs has an effect on the APC relative weights. This is
because the costs to be incorporated are not evenly distributed among
the APCs, but are rather concentrated in a relatively small number of
APCs that include the procedures that use pass-through devices. The
effect of incorporating pass-through costs into the APCs is thus to
decrease the APC weights for services such as clinic visits, preventive
care, and diagnostic tests, while the weights for the APCs into which
the pass-through costs are incorporated generally increase, often by
large percentages.
In addition, increases in the relative weights for some APCs can
lead to increases in beneficiary copayments because, by statute, the
coinsurance rate cannot be less than 20 percent of the payment rate for
an APC. We note, however, that beneficiaries are protected from much of
this increase on an individual APC basis because section 1833(t)(8)(C)
of the Act limits the copayment for a procedure performed in a year to
no more than the amount of the inpatient hospital deductible for that
year. For CY 2002, that amount is $812.
Accordingly, choosing a percentage of the estimated pass-through
costs for devices to fold into the APCs associated with the use of
those devices requires us to balance several considerations. We must be
mindful not only of the effect on transitional pass-through payments
for drugs and devices, but also on the payments for other services and
on beneficiary copayments. In addition, we note that, in CY 2003,
almost all of the items currently receiving transitional pass-through
payments will have reached the end of their eligibility for this
payment status, and their costs must be folded into the APCs at that
time. Changes made in CY 2002 will thus provide a transition to rates
in CY 2003. After weighing these factors, and considering the potential
impacts of a variety of options, we have concluded it is appropriate to
incorporate 75 percent of the estimated pass-through costs for devices
into the procedure APCs associated with these devices. We are
incorporating 75 percent of the device pass-through payments, or
approximately $1.4 billion, into the costs that are used to establish
the APC relative weights for 2002.
We are not incorporating any of the current drug and biological
pass-through costs into the APCs for two reasons. First, the costs for
drugs and biologicals are already incorporated to a large extent into a
base APC rate. As discussed more fully in the August 24, 2001 proposed
rule (66 FR 44701), we assume that, for most drugs, 68 percent of the
AWP is acquisition costs of the drug or biological that is already
recognized in the base costs. Thus, the pass-through payment for those
drugs and biologicals is 27 percent of the AWP. Second, it is generally
not feasible to determine which APCs are associated with the use of
drugs and biologicals from our current claims data. Unlike devices,
which are used solely in the performance of certain procedures, drugs
and biologicals can be provided in connection with almost any
outpatient service. Thus, we are postponing the incorporation of these
costs until we have data that allow us to determine the APCs with which
the use of these items is associated. We note, however, that the pro
rata reduction will be applied to the pass-through payment for drugs
and biologicals as well as devices.
To incorporate 75 percent of the device payments, we are employing
the following methodology. We use the crosswalk that we developed as
part of the methodology for estimating total pass-through spending as
the basis for determining the device costs that we include in setting
the relative weight for each APC. As we have discussed above, this
crosswalk matches devices to the typical procedures in which they are
used.
In developing the total pass-through estimate, we used this
crosswalk to produce a device package for each CPT code associated with
device use, based on the device or devices used in each procedure
included in an APC. We adjusted the costs of each package by
subtracting the device costs already represented in the payment amount
for the APC. (These are the costs that we deduct from each pass-through
payment to ensure that the pass-through payments are limited to the
incremental costs of the new technologies. The principle for making
this subtraction is the same in each case: to avoid double-counting
costs already represented in the APC rates.) We then add 75 percent of
these adjusted costs of the package to the costs at the claim level for
each device-related procedure in the APC. At this point, we determine a
revised median cost for the APC. That new median cost in turn is the
basis for the APC's new relative weight.
The costs folded in will affect the relative weights of the APCs.
The resulting APC payment rates will not increase on a dollar-for-
dollar basis with the device costs folded into the APCs. In most cases,
the device costs folded into an APC will not be uniformly distributed
among the procedures in that APC. This is because procedures in an APC
may require different types or numbers of devices and some procedures
may not require devices at all. Therefore, the increase in median cost
for an affected APC is unlikely to exactly equal the amount of the cost
folded in. Furthermore, the statute requires that APC recalibration and
reclassification changes be made in a manner that assures that
aggregate payments will be neither greater nor less than they would
have been without the changes. Changes in an APC's payment rate
therefore cannot be expected to vary on a dollar-for-dollar basis with
changes in the costs used to determine the APC's relative weight.
Finally, we note that the initial payments under the OPPS were
calculated to be budget neutral to the methodology in use before the
implementation of the OPPS. The prior payment methodology paid
hospitals, on average, approximately 83 percent (the actual payment-to-
cost ratio under the prior system) of their costs for furnishing
outpatient services. Under the pass-through payment methodology,
eligible devices are paid at 100 percent of their costs. Once these
costs are incorporated into the APCs, they will also be paid at rates
calculated to reflect these reductions.
The increase in APC rates due to the incorporation of these pass-
through costs will be offset against the estimated 2002 pass-through
payments. (As discussed above, we subtract the amount of the pass-
through costs represented in the rate for the associated APC from each
pass-through payment.) The remaining amount of estimated pass-through
spending for 2002, once we have applied these offsets, will be subject
to the pro rata reduction. Because we have not completed the
recalculation of the adjusted APC payments, we are unable to provide
the
[[Page 55863]]
specific amount of the pro rata reduction at this time. We will
announce the exact amount of the reduction that will be required before
the beginning of 2002. In the meantime, we are announcing that we
expect the required reduction will be in the range of 65 to 70 percent.
As can be seen from this estimate, folding in 75 percent of the device
costs into the APCs does not reduce the pro rata by 75 percent. The
following is a simplified illustration of the process.
Example: Assume there is only one device eligible for a pass-
through and only one associated APC. That APC has a payment rate of
$3,000, of which $1,000 is associated with device costs already in
the APC. If a hospital bills a device with that APC whose charge
adjusted to cost is $9,000, the payment for the pass-through is
$9,000 minus $1,000, or $8,000. Thus, the payment for the entire
service is $3,000 for the base APC and $8,000 for the device, for a
total payment of $11,000. The pro rata reduction would be applied to
the $8,000. If we were to implement the 80.7 percent reduction, the
total payment would be $4,544 ($3,000 + $8,000 (0.193)).
For the 75 percent fold-in, we would first adjust the $9,000 device
cost to account for the $1,000 in device costs already represented in
the APC rate. The remaining $8,000 represents the adjusted costs for
the device. We would then incorporate $6,000 of the $8,000 in adjusted
costs into the APC rate. As discussed above, the increase in the APC
rate is not a dollar-for-dollar match with the amount folded in.
Therefore, assume that the APC rate increases by $3,500, for a total of
$6,500. The $6,500 payment rate now reflects $4,500 in device costs "
the original $1,000 plus the difference between the original APC
payment ($3,000) and the APC payment rate after the fold-in ($6,500),
or $3,500. The increase in the amount of device costs reflected in the
APC is a dollar-for-dollar match with the increase in the payment rate.
The total payment for the service is now $6,500 for the base APC and
$4,500 for the device ($9,000 minus $4,500), for a total payment of
$11,000. Even though 75 percent of the $8,000, or $6,000, has been
folded into the APC rate, the pass-through payment (before any pro rata
reduction) is reduced by only $4,500, to $4,500. Thus, folding in 75
percent of the device costs does not reduce the total pass-through
estimate by that same 75 percent. However, any remaining pro rata
reduction would be applied only to the $4,500. Based on an expected
reduction of between 65 and 70 percent, total payment would be between
$8,075 and $7,850, respectively.
Comment: Several commenters requested that we clarify how the
incorporation of pass-through costs into the associated APCs would
affect the APC payments. Specifically, some of these commenters
requested that we clarify whether there would be a dollar-for-dollar
match between the costs incorporated into an APC and the resulting
increase in the APC's rate. Others asked whether there would be a
dollar-for-dollar match between the increase in the APC's rate and the
increase in the reduction in the pass-through payments to account for
the device costs incorporated into the APC.
Response: As discussed in the response immediately preceding, there
is not a dollar-for-dollar match between the costs incorporated into an
APC and the resulting increase in the APC's payment rate. There is,
however, a dollar-for-dollar match between the increase in an APC's
rate and the increase in the reduction for the pass-through payment for
devices associated with that APC. This is because the additional
payment for a pass-through item equals the amount by which the
hospital's cost for the item exceeds the portion of the applicable APC
payment amount that is associated with the item. There is thus
necessarily a dollar-for-dollar match between the increase in the APC's
rate that is due to the new costs being incorporated into the APC, and
the reduction applied to the pass-through payments.
Comment: Several commenters made specific requests for data files
and other information related to any possible pro rata reduction. These
requests included the following:
The data files used to estimate pass-through spending,
including claims data from the period July 1, 1999 and July 1, 2000.
A comprehensive description of the methods used to
identify gaps in the reporting of drugs, biologicals, and devices, and
the assumptions used to estimate utilization of pass-through items.
An estimate of projected pass-through payments for 2002,
including breakdowns by category (orphan drugs, cancer drugs, devices,
etc.).
An estimate of the magnitude of any proposed reduction in
pass-through payments to meet the 2.5 percent statutory cap.
A detailed description of how any pro rata reduction would
be implemented.
Response: It is our general practice to release the data we use in
setting Medicare payment amounts to the public when we announce
proposed payment amounts. Some of the data requested by these
commenters, especially the relevant claims data for the period July 1,
1999 and July 1, 2000, were in fact released at the time of the August
24, 2001 proposed rule because these data were used in developing the
proposed APC payment rates in that rule. We did publish a substantive
description of the methodology that we were proposing to use in
developing an estimate of pass-through costs, and we received numerous
comments on that proposed methodology. To the degree that we did not
release some of the other information requested by these commenters,
such as an estimate of a proposed pro rata reduction and a breakdown of
pass-through costs by category, it was because we were still reviewing
our methodology and analyzing the data. We did, however, present the
public with the likely magnitude of a reduction at that time.
In this final rule, in response to the comments, we are providing
more information on the methodology that we have used to determine the
pro rata reduction. We are also providing a detailed account of our
calculation of 2002 pass-through costs. We plan to release additional
information when we announce the exact percentage of the required pro
rata reduction before the beginning of the year. The pro rata reduction
will be implemented by our systems as a uniform reduction to every
pass-through payment.
Comment: The Medicare Payment Assessment Commission commented that
the transitional pass-through provision has three flaws:
The use of categories to determine the eligibility of
devices allows devices the costs of which had already been taken into
account in setting the base rates to qualify for pass-through payments.
The pass-through payments for drugs and biologicals are
set at 95 percent of average wholesale cost, thus creating an incentive
to increase Medicare payments by raising prices for these items.
Pass-through payment rates are based on hospital-specific
cost-to-charge ratios, allowing hospitals to increase their payments by
raising the charges for eligible items.
The Commission recommended that the Congress enact three statutory
changes to improve the transitional pass-through provision:
Restrict the eligibility for pass-through payments to
technologies that are new or substantially improved and that add
substantially to the cost of care.
Allow for the costs of pass-through items to be completely
incorporated into the base APC rates more quickly than the current
statutory eligibility period of 2 to 3 years allows.
[[Page 55864]]
Replace the facility-specific payments for devices with
national payments.
Response: We appreciate the Commission's comments about flaws in
the transitional pass-through provision. We will be available to
provide technical assistance to the appropriate congressional
committees in developing measures to improve the provision. We do note,
however, that although the use of categories allows devices whose costs
had previously been included in the calculation of the APC payment
rates to qualify for pass-through payments, those payments will be
reduced by the amount that we have calculated to be reflected in that
APC. However, this subtraction of the costs in the APC may not reduce
the pass-through payment for those devices to zero.
III. Conversion Factor Update for CY 2002
Section 1833(t)(3)(C)(ii) of the Act requires us to update the
conversion factor used to determine payment rates under the OPPS on an
annual basis. Section 1833(t)(3)(C)(iv) of the Act, as redesignated by
section 401 of the BIPA, provides that for 2002, the update is equal to
the hospital inpatient market basket percentage increase applicable to
hospital discharges under section 1886(b)(3)(B)(iii) of the Act,
reduced by one percentage point. Further, section 401 of the BIPA
increased the conversion factor for 2001 to reflect an update equal to
the full market basket percentage increase amount.
To set the proposed OPPS conversion factor for 2002, we increased
the 2001 conversion factor of $50.080, which reflects the BIPA
provision of the full market basket update, by 2.3 percent, that is,
the full market basket percentage increase of 3.3 percent minus 1
percentage point.
In accordance with section 1833(t)(9)(B) of the Act, we further
adjusted the conversion factor for 2002 to ensure that the revisions we
made to update the wage index are made on a budget-neutral basis. A
proposed budget neutrality factor of 0.9924 was calculated for wage
index changes by comparing total payments from our simulation model
using the proposed FY 2002 hospital inpatient PPS wage index values to
those payments using the current (FY 2001) wage index values.
The increase factor of 2.3 percent for 2002 and the required wage
index budget neutrality adjustment of 0.9924 resulted in a proposed
conversion factor for 2002 of $50.842.
Based on the 2.3 percent update factor and the final FY 2002
hospital inpatient wage index values, the final wage index budget
neutrality adjustment is 0.9936, which results in a final conversion
factor for 2002 of $50.904.
We received one comment on the calculation of the conversion
factor.
Comment: One commenter requested clarification of the methodology
used to calculate the conversion factor for CY 2002, particularly as it
relates to the payment update provided by section 401 of BIPA. The
commenter is concerned that we did not explain that the CY 2001
conversion factor we set forth in the August 24, 2001 proposed rule as
the basis for the CY 2002 conversion factor was never used to make
payment in CY 2001.
Response: Before the enactment of BIPA on December 21, 2000,
section 1833(t)(3)(C)(iii) of the Act provided for a 2001 update of the
market basket percentage increase reduced by 1 percentage point. This
is the update that was implemented by the November 13, 2000 final rule
(65 FR 67827).
Section 401(a) of BIPA amended section 1833(t)(3)(C)(iii)
(redesignated by section 401(b) of BIPA as section 1833(t)(3)(C)(iv))
of the Act to provide for a full market basket percentage increase for
CY 2001. However, section 401(c) of BIPA also provided a special
payment rule for CY 2001 that requires the payment rate for services
furnished under the OPPS on or after April 1, 2001 and before January
1, 2002 to be updated by an additional 0.32 percent to account for the
timing of the implementation of the full market basket update for 2001.
Thus, the conversion factor used to make payment on or after January 1
and before April 1, 2001 was based on a market basket percentage
increase minus 1 percentage point, and the conversion factor used to
make payment on or after April 1, 2001 was based on a full market
basket percentage increase increased by 0.32 percent. Payment was never
made in 2001 using a conversion factor based on a full market basket
percentage increase. However, it is this last conversion factor (which
is equal to $50.080) that must be used to update the conversion factor
for CY 2002.
IV. Collection of Information Requirements
This document does not impose information collection and
recordkeeping requirements. Consequently, it need not be reviewed by
the Office of Management and Budget under the authority of the
Paperwork Reduction Act of 1995 (44 U.S.C. 35).
V. Regulatory Impact Analysis
A. General
We have examined the impacts of this final rule as required by
Executive Order 12866 (September 1993, Regulatory Planning and Review)
and the Regulatory Flexibility Act (RFA) (September 19, 1980 Public Law
96-354). Executive Order 12866 directs agencies to assess all costs and
benefits of available regulatory alternatives and, if regulation is
necessary, to select regulatory approaches that maximize net benefits
(including potential economic, environmental, public health and safety
effects, distributive impacts, and equity). A regulatory impact
analysis (RIA) must be prepared for major rules with economically
significant effects ($100 million or more annually).
The statutory effects of the provisions that are implemented by
this final rule result in expenditures exceeding $100 million per year.
We estimate the total impact of these changes for CY 2002 payments
compared to CY 2001 payments to be approximately a $400 million
increase. Therefore, this final rule is an economically significant
rule under Executive Order 12866, and a major rule under 5 U.S.C.
804(2).
The RFA requires agencies to determine whether a rule will have a
significant economic impact on a substantial number of small entities.
For purposes of the RFA, small entities include small businesses,
nonprofit organizations, and government agencies. Most hospitals and
most other providers and suppliers are small entities, either by
nonprofit status or by having revenues of $5 to $25 million or less
annually (see 65 FR 69432). For purposes of the RFA, all providers of
hospital outpatient services are considered small entities. Individuals
and States are not included in the definition of a small entity.
In addition, section 1102(b) of the Act requires us to prepare a
regulatory impact analysis if a rule may have a significant impact on
the operations of a substantial number of small rural hospitals. This
analysis must conform to the provisions of section 604 of the RFA. With
the exception of hospitals located in certain New England counties, for
purposes of section 1102(b) of the Act, we define a small rural
hospital as a hospital that is located outside of a Metropolitan
Statistical Area (MSA) and has fewer than 100 beds, or New England
County Metropolitan Area (NECMA). Section 601(g) of the Social Security
Amendments of 1983 (Pub. L. 98-21) designated hospitals in certain New
[[Page 55865]]
England counties as belonging to the adjacent NECMA. Thus, for purposes
of the OPPS, we classify these hospitals as urban hospitals.
It is clear that the changes in this final rule affect both a
substantial number of rural hospitals as well as other classes of
hospitals, and the effects on some may be significant. The discussion
below, in combination with the rest of this final rule, constitutes a
regulatory impact analysis.
Section 202 of the Unfunded Mandates Reform Act of 1995 (Pub. L.
104-4) also requires that agencies assess anticipated costs and
benefits before issuing any rule that may result in an expenditure in
any one year by State, local, or tribal governments, in the aggregate,
or by the private sector, of $110 million. This final rule does not
mandate any requirements for State, local, or tribal governments.
Executive Order 13132 establishes certain requirements that an
agency must meet when it publishes a proposed rule (and subsequent
final rule) that imposes substantial direct costs on State and local
governments, preempts State law, or otherwise has Federalism
implications. We have examined this final rule in accordance with
Executive Order 13132, Federalism, and have determined that it will not
have any negative impact on the rights, roles, and responsibilities of
State, local, or tribal governments.
B. Changes in This Final Rule
This final rule implements changes to the OPPS that are required by
the statute. We are required under section 1833(t)(3)(C)(ii) of the Act
to update annually the conversion factor used to determine the APC
payment rates. In addition, section 1833(t)(6)(E)(iii) of the Act
requires a uniform reduction in the amount of each of the transitional
pass-through payments made in a year if the Secretary estimates, before
the beginning of that year, that the total pass-through payments will
exceed an applicable percentage of total payments estimated to be made
under OPPS in that year. For CY 2002, the applicable percentage is 2.5
percent.
The projected aggregate impact of updating the conversion factor is
to increase total payments to hospitals by 2.3 percent. As described in
the preamble, a budget neutrality adjustment is made to the conversion
factor to assure that the revision in the wage index does not affect
aggregate payments.
C. Estimated Impacts of This Final Rule
The 2.3 percent update in the conversion factor results, in the
aggregate, in an increase in payments for hospitals under the OPPS of
approximately $400 million.
As discussed above in section II of this preamble, we have
estimated that the total amount of pass-through payments for CY 2002
would be $2.26 billion if we did not fold in costs of pass-through
devices into the base APC rates. Of that amount, approximately $0.37
million represents payments for drugs and biologicals and $1.89 billion
represents payments for medical devices. Total OPPS payments in CY 2002
are estimated to be $17.5 billion. Because the estimate of pass-through
payments exceeds 2.5 percent of estimated total payments, which is
approximately $437 million (2.5 percent of $17.5 billion), we must
implement a uniform reduction of all pass-through payments. Absent any
administrative action, the estimate of the reduction necessary to
account for the full pass-through estimate would be 80.7 percent. That
is, we would pay 19.3 percent of the otherwise applicable pass-through
payment for drugs, biologicals, and devices.
As further discussed above in section II of this preamble, in order
to mitigate the effects of this significant pro rata reduction, we are
incorporating, into the base APC costs, 75 percent of the cost of the
devices currently eligible for pass-through payment. In the proposed
rule, we estimated for most APCs that involve devices, an amount that
represents the cost of devices already included in the APC payments.
Those amounts would be subtracted from any pass-through payments
associated with those APCs (before the pro rata reduction). That policy
reduced the total estimate of pass-through payments by approximately
$450 million. Because we are now incorporating additional device costs
into the base APC costs, those subtraction amounts will increase to
reflect the additional amounts included in the device-related APC
payments. Thus, the total amount of pass-through payments estimated to
be made in CY 2002 will be reduced, which will, in turn, reduce the
amount of the pro rata reduction necessary to meet the 2.5 percent
limit. As noted above in this preamble, because we have not yet
completed our analysis and computations related to the fold in, we
cannot yet announce the exact size of the pro rata reduction. However,
we estimate that the amount of the reduction will be between 65 and 70
percent. The incorporation of costs into the base APCs results in the
pro rata reduction being applied only to the marginal costs of the
pass-through devices not incorporated into the APCs.
We believe that the changes we have made in this final rule will
lessen the impact on hospitals of the required pro rata reduction on
pass-through payments.
We estimate that the implementation of the pro rata reduction on
pass-through payments for devices will affect urban hospitals more than
rural hospitals and, in urban areas, large urban and teaching hospitals
will be affected more than other urban hospitals. This is due to the
fact that the types of outpatient procedures that use the pass-through
devices are more frequently performed in large urban hospitals,
particularly teaching hospitals. We estimate that the effect of the
reduction on pass-through payments for drugs and biologicals may be
more uniform across types of hospitals. Use of these items is more
widespread among hospitals, although hospitals that furnish
chemotherapy may be affected to a greater degree than others.
In accordance with the provisions of Executive Order 12866, this
final rule was reviewed by the Office of Management and Budget.
List of Subjects in 42 CFR Part 419
Hospitals, Medicare, Reporting and recordkeeping requirements.
For the reasons set forth in the preamble, 42 CFR part 419 is
amended as follows:
PART 419--PROSPECTIVE PAYMENT SYSTEM FOR HOSPITAL OUTPATIENT
DEPARTMENT SERVICES
1. The authority citation continues to read as follows:
Authority: Secs. 1102, 1833(t), and 1871 of the Social Security
Act (42 U.S.C. 1302, 1395l(t), and 1395hh).
2. In Sec. 419.62, paragraph (c) is republished and a new paragraph
(d) is added to read as follows:
Sec. 419.62 Transitional pass-through payments: General rules.
* * * * *
(c) Uniform prospective reduction of pass-through payments. (1) If
CMS estimates before the beginning of a calendar year that the total
amount of pass-through payments under Secs. 419.64 and 419.66 for the
year would exceed the applicable percentage (as described in paragraph
(c)(2) of this section) of the total amount of Medicare payments under
the outpatient prospective payment system. CMS will reduce, pro rata,
the amount of each of the additional payments under Secs. 419.64 and
419.66 for that year to ensure that the applicable percentage is not
exceeded.
[[Page 55866]]
(2) The applicable percentages are as follows:
(i) For a year before CY 2004, the applicable percentage is 2.5
percent.
(ii) For 2004 and subsequent years, the applicable percentage is a
percentage specified by CMS up to (but not to exceed) 2.0 percent.
(d) CY 2002 incorporated amount. For CY 2002, CMS incorporated 75
percent of the estimated pass-through costs (before the incorporation
and any pro rata reduction) for devices into the procedure APCs
associated with these devices.
(Catalog of Federal Domestic Assistance Program No. 93.773,
Medicare--Hospital Insurance; and Program No. 93.774, Medicare--
Supplementary Medical Insurance Program)
Dated: October 30, 2001.
Thomas A. Scully,
Administrator, Centers for Medicare & Medicaid Services.
Approved: October 26, 2001.
Tommy G. Thompson,
Secretary.
[FR Doc. 01-27659 Filed 10-31-01; 12 pm]
BILLING CODE 4120-01-P
