03-32322. Medicare Program; Hospital Outpatient Prospective Payment System; Payment Reform for Calendar Year 2004
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AGENCY:
Centers for Medicare & Medicaid Services (CMS), HHS.
ACTION:
Interim final rule with comment period.
SUMMARY:
This interim final rule with comment period implements provisions of the Medicare Prescription Drug, Improvement, and Modernization Act (DIMA) of 2003 that affect the Medicare outpatient prospective payment system (OPPS) that become effective January 1, 2004. Sections 303 and 621 of the DIMA include provisions that alter the methods for drug payment in hospital outpatient departments, some of which become effective January 1, 2004. These provisions affect the methodology for paying for pass-through and non-pass-through drugs under the OPPS. Further, the new law includes a requirement that all brachytherapy sources be paid separately. Section 411 of the DIMA reinstates the hold-harmless protection for small rural hospitals with fewer than 100 beds and extends that protection to sole community hospitals in rural areas.
DATES:
Effective date: January 1, 2004.
Comment date: We will consider comments if we receive them at the appropriate address, as provided below, no later than 5 p.m. on March 8, 2004.
ADDRESSES:
In commenting, please refer to file code CMS-1371-IFC. Because of staff and resource limitations, we cannot accept comments by facsimile (FAX) transmission or e-mail.
Mail written comments (one original and two copies) to the following address ONLY: Centers for Medicare & Medicaid Services, Department of Health and Human Services, Attention: CMS-1371-IFC, P.O. Box 8018, Baltimore, MD 21244-8018.
Please allow sufficient time for mailed comments to be timely received in the event of delivery delays.
If you prefer, you may deliver (by hand or courier) your written comments (one original and two copies) to one of the following addresses: Room 445-G, Hubert H. Humphrey Building, 200 Independence Avenue, SW., Washington, DC 20201, or Room C5-14-03, 7500 Security Boulevard, Baltimore, MD 21244-1850.
(Because access to the interior of the HHH Building is not readily available to persons without Federal Government identification, commenters are encouraged to leave their comments in the CMS drop slots located in the main lobby of the building. A stamp-in clock is available for persons wishing to retain a proof of filing by stamping in and retaining an extra copy of the comments being filed.)
Comments mailed to the addresses indicated as appropriate for hand or courier delivery may be delayed and could be considered late.
For information on viewing public comments, see the beginning of the SUPPLEMENTARY INFORMATION section.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Dana Burley, (410) 786-0378.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
Inspection of Public Comments: Comments received timely will be available for public inspection as they are received, generally beginning approximately 3 weeks after publication of a document, at the headquarters of the Centers for Medicare & Medicaid Services, 7500 Security Boulevard, Baltimore, Maryland 21244, Monday through Friday of each week from 8:30 a.m. to 4 p.m. To schedule an appointment to view public comments, call (410) 786-7195.
Availability of Copies and Electronic Access
Copies: To order copies of the Federal Register containing this document, send your request to: New Orders, Superintendent of Documents, P.O. Box 371954, Pittsburgh, PA 15250-7954. Specify the date of the issue requested and enclose a check or money order payable to the Superintendent of Documents, or enclose your Visa or Master Card number and expiration date. Credit card orders can also be placed by calling the order desk at (202) 512-1800 (or toll-free at 1-888-293-6498) or by faxing to (202) 512-2250. The cost for each copy is $10. As an alternative, you can view and photocopy the Federal Register document at most libraries designated as Federal Depository Libraries and at many other public and academic libraries throughout the country that receive the Federal Register.
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I. Background
A. Authority for the Outpatient Prospective Payment System
When the Medicare statute was originally enacted, Medicare payment for hospital outpatient services was based on hospital-specific costs. In an effort to ensure that Medicare and its beneficiaries pay appropriately for services and to encourage more efficient delivery of care, the Congress mandated replacement of the cost-based payment methodology with a prospective payment system (PPS). The Balanced Budget Act of 1997 (BBA) (Pub. L. 105-33), enacted on August 5, 1997, added section 1833(t) to the Social Security Act (the Act) authorizing implementation of a PPS for hospital outpatient services. The Balanced Budget Refinement Act of 1999 (BBRA) (Pub. L. 106-113), enacted on November 29, 1999, made major changes that affected the hospital outpatient PPS (OPPS). The Medicare, Medicaid, and SCHIP Benefits Improvement and Protection Act of 2000 (BIPA) (Pub. L. 106-554), enacted on December 21, 2000, made further changes in the OPPS. The OPPS was first implemented for services furnished on or after August 1, 2000.
The Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (DIMA) (Pub. L. 108-173), enacted on December 8, 2003, made additional changes to the Act relating to the OPPS and calendar year 2004 payment rates to be implemented January 1, 2004.
We would ordinarily publish a notice of proposed rulemaking in the Federal Register and invite public comment on the proposed rule. This procedure can be waived, however, if an agency finds good cause that a notice-and-comment procedure is impracticable, unnecessary, or contrary to the public interest and incorporates a statement of the finding and its reasons in the rule issued. We find good cause to waive notice and comment procedures for this correction notice as set forth in section IV, “Waiver of Proposed Rulemaking and Waiver of 30-Day Delay in the Effective Date,” below.
B. Summary of Relevant Provisions of the DIMA
The DIMA, enacted December 8, 2003, made the following changes to the Act that relate to the OPPS:
1. Transitional Corridor Payments Extended
Section 411 of the DIMA amends section 1833(t)(7)(D)(i) of the Act and extends the hold-harmless provision for small rural hospitals. The hold harmless Start Printed Page 821transitional corridor payments will continue through December 31, 2005 for small rural hospitals having 100 or fewer beds. Section 411 of the DIMA further amends section 1833(t)(7) of the Act to provide that hold-harmless transitional corridor payments shall apply to sole community hospitals as defined in section 1886(d)(5)(D)(iii) of the Act and will continue through December 31, 2005.
2. Payment for “Specified Covered Outpatient Drugs”
Section 621(a)(1) of the DIMA amends the Act by adding section 1833(t)(14) that requires classification of separately paid radiopharmaceutical agents and drugs or biologicals that had transitional pass-through status on or before December 31, 2002, into 3 categories: innovator multiple source drugs; noninnovator multiple source drugs; and sole source drugs. Payment levels based on the reference average wholesale price are specified for each category.
3. Payment for Drug or Biological Before HCPCS Code Assigned
Section 621(a)(1) of the DIMA amends the Act by adding section 1833(t)(15), which requires that payment be made at 95 percent of the average wholesale price (AWP) for new drugs and biologicals until a HCPCS code is assigned.
4. Payment for Pass-Through Drugs
Section 303(b) of the DIMA amends section 1842(o) of the Act. As a result, certain pass-through drugs are to be paid at 95 percent, and others at 85 percent, of the AWP. Drugs and biologicals furnished during 2004 for which pass-through payment was first made on or after January 1, 2003 (which removes them from application of section 621 of the DIMA) and were approved by the FDA for marketing as of April 1, 2003, will be paid 85 percent of AWP pursuant to section 1842(o)(1)(B) and 1842(o)(4)(A), unless sections 1842(o)(4)(B), (C) or (D) apply. Blood clotting factors furnished during 2004, drugs or biologicals furnished during 2004 that were not available for payment as of April 1, 2003, vaccines furnished on or after January 1, 2004, and drugs or biologicals furnished during 2004 in connection with the renal dialysis services if billed by renal dialysis facilities, are paid at 95 percent of the reference AWP. Drugs or biologicals that were paid on a pass-through basis under the OPPS on or after January 1, 2003 and that were available for payment as of April 1, 2003 are paid at 85 percent of the reference AWP rather than 95 percent as was previously the policy under section 1842(o) of the Act.
5. Exclude Separately Payable Drugs and Biologicals From Outlier Payments
Section 621(a)(3) amends section 1833(t)(5) of the Act to require that separately paid drugs and biologicals be excluded from outlier payments.
6. Brachytherapy Sources Are To Be Paid Separately
Section 621(b) amends the Act by adding section 1833(t)(16)(C) which requires that all devices of brachytherapy consisting of a seed or seeds (or radioactive source) be paid based on the hospital's charge for each device adjusted to cost. Also included in the new provision is a requirement that all such brachytherapy sources be excluded from outlier payments.
Payment Methodology That Applied Prior To Enactment
In the hospital outpatient prospective payment update final rule published in the Federal Register on November 7, 2003, CMS announced payments for 2004 under the Medicare hospital outpatient prospective payment system (68 FR 63398). The provisions of that final rule with regard to payment for brachytherapy sources, for separately payable drugs, biologicals and radiopharmaceutical agents and for pass-through drugs and biologicals is superceded in part with enactment of the DIMA, effective for services furnished on or after January 1, 2004. This interim final rule with comment presents the payment amounts that apply in 2004 that result from the changes made by DIMA.
The following is a summarization of the payment policies that we published for the 2004 OPPS before enactment of the new law.
Drugs and biologicals that were within the 2-3 year pass-through payment period were paid amounts as specified in section 1842(o) of the Act. Under the November 7 final rule, that payment was 95 percent of AWP.
Under the provisions of the November 7 OPPS final rule, payment for non-pass-through drugs, biologicals and radiopharmaceutical agents with per day median costs greater than $50 was based on data compiled from hospital claims submitted on or after April 1, 2002 through December 31, 2002. Those data were used to set median costs which were converted to relative weights, scaled for budget neutrality, and multiplied by the 2004 conversion factor, the same methodology used to set relative weights for procedural ambulatory payment classifications (APCs) under the OPPS. A detailed discussion of the rate setting methodology for the 2004 OPPS update is provided in the November 7, 2003 final rule (68 FR 63416).
Payment for drugs, biologicals and radiopharmaceutical agents that had per day median costs less than $50 and drugs, biologicals and radiopharmaceutical agents for which there was no HCPCS code, was included in the rate for the service in which the item was used. There were no separate payments for these drugs, biologicals and radiopharmaceutical agents.
Changes Required Under the DIMA
a. Changes in Payment for “specified covered outpatient drugs”: radiopharmaceutical agents and drugs or biologicals that were paid as pass-throughs under the OPPS on or before December 31, 2002. The DIMA amends the Act by adding section 1833(t)(14) which states that payment for specified covered outpatient drugs is to be based on its “reference average wholesale price,” that is, the average wholesale price for the drug as determined under section 1842(o) of the Act as of May 1, 2003 (1833(t)(14)(G)).
Under new section 1833(t)(14)(B)(i) a “specified covered outpatient drug” is a covered outpatient drug as defined in 1927(k)(2) of the Act, for which a separate ambulatory payment classification group (APC) exists and that is a radiopharmaceutical agent or a drug or biological for which payment was made on a pass-through basis on or before December 31, 2002.
Under section 1833(t)(14)(B)(ii) of the Act, certain drugs and biologicals are designated as exceptions, which are not included in the definition of “specified covered outpatient drugs.” These exceptions are the following:
- A drug or biological for which payment is first made on or after January 1, 2003 under the transitional pass-through payment provision in section 1833(t)(6) of the Act.
- A drug or biological for which a temporary HCPCS code has not been assigned.
- During 2004 and 2005, an orphan drug (as designated by the Secretary).
Section 1833(t)(14)(A)(i) specifies payment limits for 3 categories of “specified covered outpatient drugs” in 2004. Section 1833(t)(14)(F) defines the 3 categories of “specified covered outpatient drugs” based on sections 1861(t)(1) and 1927(k)(7)(A)(ii), (iii) and (iv) of the Act. The categories of drugs are “sole source drugs”, “innovator multiple source drugs” and “noninnovator multiple source drugs.” Start Printed Page 822
b. Definitions and payment rates for DIMA-specified categories for drugs, biologicals, and radiopharmaceutical agents. Section 1927(k) of the Act pertains to the Medicaid drug rebate program. In order to administer the Medicaid drug rebate program, CMS gathers information from manufacturers and classifies drugs into categories that are defined in sections 1927(k)(7)(A)(ii), (iii) and (iv) of the Act. We are using these category designations to guide our classification of covered OPPS drugs in order to implement the changes in payment under the OPPS that are required by DIMA in section 1833(t)(14) of the Act. The classifications are listed in the Medicaid average manufacturer price (AMP) database, which can be found at http://www.cms.gov/medicaid/drugs/drug6.asp. In cases when the AMP database does not provide a classification for an affected drug or biological, we relied on our clinical and pharmaceutical experts to determine the appropriate classification. Further, when there are conflicting or incomplete designations in the AMP, we assigned drugs to the noninnovator multiple-source category for payment effective January 1, 2004, until we can resolve the conflicts and make a definitive classification. Classification changes will be implemented April 1, 2004 effective for services furnished on or after January 1, 2004. We invite comments regarding the appropriate classification of the drugs listed in Table 2.
The Medicaid AMP database is updated on a quarterly basis. However, we believe that midyear changes in the classification of drugs could be confusing and burdensome for providers to administer. Therefore, the final category designations used to determine 2004 OPPS drug payments for the “specified covered outpatient drugs” to which section 1833(t)(14)(A)(i) of the Act applies, will remain in effect through December 31, 2004. We will update the category designations through rulemaking as part of the annual OPPS update for 2005.
The sole source category is defined in section 1833(t)(14)(F)(i) of the Act as a biological product (as defined under section 1861(t)(1) of the Act) or a single source drug (as defined in section 1927(k)(7)(A)(iv)) of the Act). Section 1927(k)(7)(A)(iv) of the Act defines the term “single source drug” to mean a covered outpatient drug which is produced or distributed under an original new drug application (NDA) approved by the Food and Drug Administration (FDA), including a drug product marketed by any cross-licensed producers or distributors operating under the NDA. Based on this definition, in effect, single source drugs are brand name drugs for which there is no FDA generic approval, and the term is used interchangeably with “sole source drug” in this preamble.
Section 621(a) of the DIMA, amends the Act by adding section 1833(t)(14)(A)(i)(I), which provides that a sole source drug shall, in 2004, be paid no less than 88 percent and no more than 95 percent of the reference AWP.
Innovator multiple source drugs are defined in section 1833(t)(14)(F)(ii) of the Act according to the definition provided in section 1927(k)(7)(A)(ii) of the Act. Section 1927(k)(7)(A)(ii) of the Act defines an innovator multiple source drug as a multiple source drug that was originally marketed under an original NDA approved by the FDA. Under this definition, these drugs were originally sole source drugs for which FDA subsequently approved a generic alternative(s). An innovator multiple source drug first must be a sole source drug.
Section 621(a) of the DIMA, amends the Act by adding section 1833(t)(14)(A)(i)(II), which provides that an innovator multiple source drug shall, in 2004, be paid no more than 68 percent of the reference AWP.
Section 1833(t)(14)(F)(III) defines a noninnovator multiple source drug according to the definition of the term in 1927(k)(7)(A)(iii). Section 1927(k)(7)(A)(iii) defines noninnovator multiple source drug as a multiple source drug that is not an innovator multiple source drug. Under this definition, noninnovator multiple source drugs are, in effect, generic drugs approved by the FDA.
Section 621(a) of the DIMA, amends the Act by adding section 1833(t)(14)(A)(i)(III), which provides that a noninnovator multiple source drug shall, in 2004, be paid no more than 46 percent of the reference AWP.
There are several drugs that are classified in the AMP database as qualifying for all three categories. A drug that meets the criteria for all 3 categories has FDA approval as an innovator drug. A generic version of the drug, the noninnovator, also has received FDA approval. In addition, there is an FDA approval for a different indication for use under a different NDA for which the drug is the sole source. When a single drug, biological or radiopharmaceutical agent that meets the definition of a single HCPCS code qualifies for all of the 3 categories in the AMP file, we are recognizing the product only as an innovator multiple source and noninnovator multiple source drug. That is, once a drug qualifies as a multiple source drug, we will not recognize it as a sole source drug for payment under the OPPS. We believe that it would be impossible to operationalize a system in which the same drug would be paid differently according to the clinical indication for its use. Medicare makes payment for a drug or biological that is reasonable and necessary to treat an illness or disease. Medicare does not base payment for drugs and biologicals according to their indicated uses, except when required by a national coverage decision. Further, to do so would circumvent the payment limitation that the law requires for drugs, biologicals and radiopharmaceutical agents that have generic competition by allowing payment for a drug that has generic competition at the sole source rate (88 to 95 percent of AWP) rather than at the limit for innovator multiple source (68 percent of AWP) or noninnovator multiple source (46 percent of AWP) drugs.
c. Definition of “reference AWP” and determination of payment amounts. Section 1833(t)(14)(G) of the Act defines reference AWP as the AWP determined under section 1842(o) as of May 1, 2003. We interpret this to mean the AWP set under the CMS single drug pricer (SDP) based on prices published in the Red Book on May 1, 2003.
We determined the payment amount for specified covered outpatient drugs under the provisions of the DIMA by comparing the payment amount calculated under the median cost methodology in effect prior to enactment of the DIMA to the percentages specified in new section 1833(t)(14)(A) of the Act.
Specifically, for sole source drugs, we compared the payments established in the November 7, 2003 final rule for the HCPCS code for the drug to its reference AWP. When the payment fell below 88 percent of the reference AWP, we increased the payment to 88 percent of the reference AWP. When the payment exceeded 95 percent of the reference AWP, we reduced the payment to 95 percent of the reference AWP. When the payment was no lower than 88 percent and no higher than 95 percent of reference AWP, we made no change. To receive payment for sole source drugs on or after January 1, 2004, hospitals should continue to bill the appropriate HCPCS code for the drug. Table 1 lists the payment amounts for sole source drugs, biologicals and radiopharmaceutical agents effective January 1, 2004 through December 31, 2004. Start Printed Page 823
There are a few drugs for which we cannot find an AWP rate. We are working to resolve this on a case-by-case basis for each of the drugs. The drugs are: Technetium TC 99M Sodium Glucoheptonate (C1200), Cobalt Co 57 cobaltous chloride (C9013), I-131 tositumomab, diagnostic (C1080) and I-131 tositumomab, therapeutic (C1081).
With regard to C1080 and C1081, there is no AWP available because this drug did not receive FDA approval until June, 2003 and so could not be in the May 1, 2003 Red Book (AWP) that we have identified as the source of the reference AWP. We presented an in-depth discussion of our policy for payment of this drug, Bexxar, in our November 7 final rule. In that rule we explain our rationale for making payment for Bexxar parallel to that for another radiopharmaceutical called Zevalin. In order to set the payment rate for Bexxar in accordance with DIMA, we also have adhered to the policy regarding the pricing of Bexxar established in the November 7 final rule.
For the remaining drugs for which we could not identify a May 1, 2003 AWP amount, we will continue our research to find an AWP. If we are able to identify the AWP established on dates other than May 1, 2003, we will use whichever is closest to May 2003. In the interim, we will implement the payment rates published in the November 7 final rule to make payments for these drugs for January 1, 2004 through March 31, 2004. We will address our findings regarding development of payment rates for these drugs in our April update.
APC 9024 is made up of 3 sole source drugs: Amphotericin B lipid complex (J0287); Amphotericin B cholesteryl sulfate (J0288); and Amphotericin B liposome injection (J0289). To comply with the statute, these 3 drugs must all be paid separately under the OPPS and that will require that we create an APC for each of the drugs. Due to the limited time available to implement the changes required for January 1, 2004, we will not be able to implement the new APCs until April 1, 2004. We will continue to pay for these drugs in APC 9024 at the rate published in the November 7 final rule. The new APCs will be implemented April 1, 2004 and will be effective for services furnished on or after January 1, 2004.
Table 1.—Sole Source Drugs
HCPCS Status indicator Description APC OPPS CY 2004 November 7, 2003 rate DIMA final rate A4642 K Satumomab pendetide per dose 0704 $124.46 $1,474.00 A9500 K Technetium TC 99m sestamibi 1600 64.28 112.73 A9502 K Technetium TC99M tetrofosmin 0705 58.06 665.28 A9507 K Indium/111 capromab pendetid 1604 687.71 2,030.60 A9511 K Technetium TC 99m depreotide 1095 37.87 704.00 A9521 K Technetiumtc-99m exametazine 1096 210.65 825.00 A9524 K Iodinated I-131 serumalbumin, per 5uci 9100 0.36 48.58 A9600 K Strontium-89 chloride 0701 402.85 892.43 C1079 K CO 57/58 per 0.5 uCi 1079 68.51 235.14 C1080 K I-131 tositumomab, dx 1080 2,260.00 2,565.55 C1081 K I-131 tositumomab, tx 1081 19,565.00 22,210.19 C1082 K In-111 ibritumomab tiuxetan 9118 2,260.00 2,565.55 C1083 K Yttrium 90 ibritumomab tiuxetan 9117 19,565.00 22,210.19 C1092 K IN 111 pentetate per 0.5 mCi 1092 217.45 237.60 C1122 K Tc 99M ARCITUMOMAB PER VIAL 1122 534.77 1,144.00 C1166 K CYTARABINE LIPOSOMAL, 10 mg 1166 278.99 344.08 C1167 K EPIRUBICIN HCL, 2 mg 1167 20.43 25.60 C1178 K BUSULFAN IV, 6 Mg 1178 299.70 27.87 C1200 K TC 99M Sodium Glucoheptonat 1200 30.28 30.28 C1201 K TC 99M SUCCIMER, PER Vial 1201 80.24 125.66 C1305 K Apligraf 1305 822.19 1,199.00 C9003 K Palivizumab, per 50 mg 9003 344.15 611.24 C9008 K Baclofen Refill Kit-500mcg 9008 6.90 73.92 C9009 K Baclofen Refill Kit-2000mcg 9009 40.92 40.92 C9010 K Baclofen Refill Kit—4000mcg 9010 42.22 79.82 C9109 K Tirofiban hcl, 6.25 mg 9109 118.60 218.33 C9202 K Octafluoropropane 9202 118.60 137.28 J0130 K Abciximab injection 1605 289.44 475.22 J0207 K Amifostine 7000 289.40 419.59 J0287 K Amphotericin b lipid complex 9024 20.86 20.86 J0288 K Ampho b cholesteryl sulfate 9024 20.86 20.86 J0289 K Amphotericin b liposome inj 9024 20.86 20.86 J0350 K Injection anistreplase 30 u 1606 1,516.46 2,495.31 J0585 K Botulinum toxin a per unit 0902 3.21 4.58 J0587 K Botulinum toxin type B 9018 6.98 8.14 J0637 K Caspofungin acetate 9019 29.64 30.52 J0850 K Cytomegalovirus imm IV /vial 0903 291.18 659.60 J1327 K Eptifibatide injection 1607 7.99 11.88 J1438 K Etanercept injection 1608 102.37 143.73 J1440 K Filgrastim 300 mcg injection 0728 123.48 172.20 J1441 K Filgrastim 480 mcg injection 7049 175.96 290.93 J1565 K RSV-ivig 0906 48.61 16.55 J1626 K Granisetron HCl injection 0764 5.70 17.18 J1830 K Interferon beta-1b / .25 MG 0910 100.51 67.22 J1950 K Leuprolide acetate /3.75 MG 0800 182.92 479.20 Start Printed Page 824 J2020 K Linezolid injection 9001 15.12 34.09 J2353 K Octreotide injection, depot 1207 65.74 73.62 J2354 K Octreotide inj, non-depot 7031 1.44 3.94 J2788 K Rho d immune globulin 50 mcg 9023 1.69 32.21 J2790 K Rho d immune globulin inj 0884 10.16 92.93 J2792 K Rho(D) immune globulin h, sd 1609 9.76 19.03 J2820 K Sargramostim injection 0731 16.32 26.92 J2941 K Somatropin injection 7034 41.18 297.79 J2993 K Reteplase injection 9005 568.33 1,263.90 J3100 K Tenecteplase injection 9002 1,296.75 2,492.60 J3245 K Tirofiban hydrochloride 7041 227.85 436.66 J3305 K Inj trimetrexate glucoronate 7045 61.36 132.00 J3395 K Verteporfin injection 1203 897.20 1,350.80 J7191 K Factor VIII (porcine) 0926 1.52 1.89 J7195 K Factor IX recombinant 0932 1.01 1.04 J7320 K Hylan G-F 20 injection 1611 123.46 215.97 J7504 K Lymphocyte immune globulin 0890 127.89 258.17 J7505 K Monoclonal antibodies 7038 320.84 792.33 J7507 K Tacrolimus oral per 1 MG 0891 1.34 3.24 J7511 K Antithymocyte globuln rabbit 9104 163.56 331.23 J7520 K Sirolimus, oral 9020 2.89 6.60 J7525 K Tacrolimus injection 9006 5.72 110.04 J8510 K Oral busulfan 7015 1.57 1.93 J8520 K Capecitabine, oral, 150 mg 7042 1.65 3.14 J8700 K Temozolmide 1086 3.76 6.81 J9001 K Doxorubicin hcl liposome inj 7046 256.34 364.49 J9010 K Alemtuzumab injection 9110 424.88 541.46 J9017 K Arsenic trioxide 9012 26.91 34.32 J9020 K Asparaginase injection 0814 16.13 58.00 J9045 K Carboplatin injection 0811 86.47 137.79 J9098 K Cytarabine liposome 1166 278.99 344.08 J9151 K Daunorubicin citrate liposom 0821 163.55 64.60 J9170 K Docetaxel 0823 220.97 331.53 J9178 K Inj, epirubicin hcl, 2 mg 1167 20.43 25.60 J9185 K Fludarabine phosphate inj 0842 205.74 329.83 J9201 K Gemcitabine HCl 0828 80.43 112.09 J9202 K Goserelin acetate implant 0810 285.16 413.59 J9206 K Irinotecan injection 0830 100.55 135.00 J9213 K Interferon alfa-2a inj 0834 20.61 32.31 J9214 K Interferon alfa-2b inj 0836 10.93 13.78 J9215 K Interferon alfa-n3 inj 0865 79.65 8.17 J9216 K Interferon gamma 1-b inj 0838 180.15 290.70 J9217 K Leuprolide acetate suspnsion 9217 312.37 576.47 J9219 K Leuprolide acetate implant 7051 3,666.71 5,001.92 J9245 K Inj melphalan hydrochl 50 MG 0840 254.90 389.14 J9268 K Pentostatin injection 0844 965.98 1,784.64 J9270 K Plicamycin (mithramycin) inj 0860 15.42 86.89 J9293 K Mitoxantrone hydrochl / 5 MG 0864 173.68 332.87 J9310 K Rituximab cancer treatment 0849 306.40 464.20 J9320 K Streptozocin injection 0850 65.19 131.05 J9350 K Topotecan 0852 433.41 739.80 J9355 K Trastuzumab 1613 40.56 53.85 J9357 K Valrubicin, 200 mg 1614 461.78 487.87 J9390 K Vinorelbine tartrate/10 mg 0855 64.79 100.97 J9600 K Porfimer sodium 0856 1,594.30 2,411.82 Q0136 K Non esrd epoetin alpha inj 0733 9.83 11.76 Q0137 K Darbepoetin alfa, non esrd 0734 3.24 3.88 Q0166 K Granisetron HCl 1 mg oral 0765 34.49 171.78 Q0180 K Dolasetron mesylate oral 0763 41.00 152.38 Q0187 K Factor viia recombinant 1409 1,083.93 1,495.30 Q2003 K Aprotinin, 10,000 kiu 7019 1.17 13.26 Q2005 K Corticorelin ovine triflutat 7024 224.91 375.00 Q2006 K Digoxin immune fab (ovine) 7025 271.14 1.79 Q2007 K Ethanolamine oleate 100 mg 7026 27.82 67.10 Q2008 K Fomepizole, 15 mg 7027 7.23 10.65 Q2009 K Fosphenytoin, 50 mg 7028 4.88 5.63 Q2011 K Hemin, per 1 mg 7030 0.64 6.86 Q2013 K Pentastarch 10% solution 7040 26.40 139.94 Q2017 K Teniposide, 50 mg 7035 137.41 238.49 Start Printed Page 825 Q2018 K Urofollitropin, 75 iu 7037 63.48 63.48 Q3000 K Rubidium-Rb-82 9025 143.89 162.63 Q3003 K Technetium tc99m bicisate 1620 183.69 392.93 Q3005 K Technetium tc99m mertiatide 1622 20.63 1,650.00 Q3008 K Indium 111-in pentetreotide 1625 449.84 1,144.00 Q4052 K Octreotide injection, depot 1207 65.74 73.62 Start Printed Page 826Table 2.—Multisource Drugs
HCPCS Status indicator Description APC OPPS CY 2004 November 7, 2003 rate DIMA final rate A9505 K Thallous chloride TL 201/mci 1603 $19.89 $18.29 A9508 K Iobenguane sulfate I-131, per 0.5 mCi 1045 165.82 165.82 A9517 K Th I131 so iodide cap millic 1064 5.48 5.48 A9528 K Dx I131 so iodide cap millic 1064 5.48 5.48 A9529 K Dx I131 so iodide sol millic 1065 6.49 6.49 A9530 K Th I131 so iodide sol millic 1065 6.49 6.49 A9605 K Samarium sm153 lexidronamm 0702 874.44 493.89 C1091 K IN111 oxyquinoline, per0.5mCi 1091 224.52 224.52 C1775 K FDG, per dose (4-40 mCi/ml) 1775 324.48 324.48 C9013 K Co 57 cobaltous chloride 9013 56.67 56.67 C9105 K Hep B imm glob, per 1 ml 9105 71.33 65.58 J1190 K Dexrazoxane HCl injection 0726 112.48 112.48 J1563 K Immune globulin, 1 g 0905 43.96 37.95 J1564 K Immune globulin 10 mg 9021 0.44 0.41 J1745 K Infliximab injection 7043 38.86 31.81 J1825 K Interferon beta-1a 0909 184.79 123.77 J2430 K Pamidronate disodium /30 MG 0730 174.32 128.74 J7190 K Factor viii 0925 0.51 0.42 J7192 K Factor viii recombinant 0927 1.01 0.61 J7193 K Factor IX non-recombinant 0931 0.51 0.51 J7194 K Factor ix complex 0928 0.51 0.18 J7198 K Anti-inhibitor 0929 1.01 0.69 J7310 K Ganciclovir long act implant 0913 86.54 86.54 J7317 K Sodium hyaluronate injection 7316 138.78 67.16 J7502 K Cyclosporine oral 100 mg 0888 2.56 2.41 J7517 K Mycophenolate mofetil oral 9015 2.04 1.36 J8560 K Etoposide oral 50 MG 0802 27.37 21.91 J9000 K Doxorubic hcl 10 MG vl chemo 0847 6.61 4.69 J9031 K Bcg live intravesical vac 0809 103.75 77.54 J9040 K Bleomycin sulfate injection 0857 160.56 88.32 J9060 K Cisplatin 10 MG injection 0813 21.74 7.73 J9065 K Inj cladribine per 1 MG 0858 37.82 24.84 J9070 K Cyclophosphamide 100 MG inj 0815 4.74 2.77 J9093 K Cyclophosphamide lyophilized 0816 4.50 2.36 J9100 K Cytarabine hcl 100 MG inj 0817 5.07 1.55 J9130 K Dacarbazine 100 mg inj 0819 5.31 5.31 J9150 K Daunorubicin 0820 73.97 35.94 J9181 K Etoposide 10 MG inj 0824 4.56 0.83 J9200 K Floxuridine injection 0827 114.19 66.24 J9208 K Ifosfomide injection 0831 106.04 72.81 J9209 K Mesna injection 0732 28.43 17.66 J9211 K Idarubicin hcl injection 0832 178.21 178.21 J9218 K Leuprolide acetate injection 0861 43.60 14.48 J9265 K Paclitaxel injection 0863 112.14 79.04 J9280 K Mitomycin 5 MG inj 0862 53.03 30.91 J9340 K Thiotepa injection 0851 59.93 45.31 Q2022 K VonWillebrandFactr CmplxperIU 1618 1.01 0.46 Q3002 K Gallium ga 67 1619 11.22 11.22 Q3007 K Sodium phosphate p32 1624 70.61 66.44 Q3011 K Chromic phosphate p32 1628 98.52 81.27 Q3012 K Cyanocobalamin cobalt co57 1089 57.07 47.38 Q3025 K IM inj interferon beta 1-a 9022 61.60 13.36 Coding for Specified Outpatient Drugs
In order to implement these provisions timely on January 1, 2004, we are instructing hospitals to use the existing HCPCS code that describes the drug for services furnished on or after January 1, 2004. For sole source drugs, the existing HCPCS code is priced in accordance with the provisions of section 1833(t)(14)(A)(i) of the Act as indicated in Table 1. However, existing HCPCS codes do not allow us to differentiate payment amounts for innovator multiple source and noninnovator multiple source forms of the drug.
Therefore, for implementation January 1, 2004, we set payment rates for all multiple source innovator and noninnovator drugs, biologicals and radiopharmaceutical agents at the lower of the payment rate in the November 7, 2003 final rule or 46 percent of the reference AWP. These rates are shown in Table 2.
Initially, we will implement sections 1833(t)(14)(A)(i)(II) and (III) of the Act in this manner because we are unable to compile a definitive list of the innovator multiple source drugs in time for January 1, 2004 implementation. On April 1, 2004, CMS will implement new HCPCS codes that providers may use to bill for innovator multiple source drugs in order to receive appropriate payment in accordance with section 1833(t)(14)(A)(i)(II) of the Act, that is, the payment amount established in the November 7, 2003 final rule or 68 percent of the reference AWP, whichever is lower. The new codes will be effective January 1, 2004 so that providers may submit adjustment bills after April 1, 2004 to receive appropriate payment for multiple source innovator drugs furnished on or after January 1, 2004 through March 31, 2004.
Beginning April 1, 2004, innovator multiple source drugs will be paid at the statutory rate as long as the new codes are used. The multiple source noninnovator rate will be the default payment rate for the existing HCPCS code assigned to the drug, and providers will continue to use the current HCPCS codes to bill for noninnovator multiple source drugs after March 31, 2004. The new HCPCS codes will be very similar to the current codes with only the distinction that the drug being billed is an innovator multiple source drug eligible for payment of as much as 68 percent of the AWP.
We recognize that creation and use of a new code to designate a drug to be an innovator multiple source drug creates burden for hospitals. However, the law provides different payment rules based on the category into which the drug falls and therefore, to ensure correct payment, hospitals must report a code for the drug that identifies the category into which it falls. We request comments on ways that we can reduce the reporting burden on hospitals that results from the law's imposing different payment limitations on brand name and generic versions of the same drug.
Table 2 lists the drugs for which the new HCPCS codes will be implemented April 1, 2004 to distinguish innovator multiple source from noninnovator multiple source drugs.
Other changes in payment methodology effective January 1, 2004 as a result of enactment of the Medicare Prescription Drug, Improvement and Modernization Act of 2003
Payment for Pass-Through Drugs, Biologicals, and Radiopharmaceuticals
Drugs and biologicals that are within the 2-3 year pass-through payment period in 2004 continue to be paid pursuant to section 1842(o) of the Act. However, section 1842(o) of the Act has been revised by section 303(b) of the DIMA and those revisions change the way that these drugs are paid.
Drugs and biologicals furnished during 2004 that are approved for pass-through payment under the OPPS and that were not approved by the FDA for marketing as of April 1, 2003 will be paid 95 percent of AWP pursuant to section 1842(o)(1)(A)(iii). See Table 3b for a list of these pass-through drugs.
Drugs and biologicals furnished during 2004 for which pass-through payment was first made on or after January 1, 2003 (which removes them from application of section 621 of the DIMA) and were approved by the FDA for marketing as of April 1, 2003, will be paid 85 percent of AWP pursuant to section 1842(o)(1)(B) and 1842(o)(4)(A), unless sections 1842(o)(4)(B), (C) or (D) apply. See Table 3a for a list of these pass-through drugs.
Table 3c lists 10 drugs and biologicals with pass-through status in 2004 that also meet the criteria for “specified covered outpatient drugs” under section 1833(t)(14). That is, the drugs in Table 3c are pass-through drugs in 2004 that were available for payment before April 1, 2003 and would therefore be paid 85 percent of AWP (determined as of April 1, 2003) under the cross reference in section 1833(t)(6)(D)(i) to section 1842(o). Separate APCs have been established for these drugs and they were paid as pass-through drugs on or before December 31, 2002. Therefore, these pass-through drugs qualify under section 1833(t)(14)(B) as “specified covered outpatient drugs.” As specified covered outpatient drugs, the ten drugs would be categorized as “sole source” drugs.
Sole source drugs, under section 1833(t)(14)(A)(i)(I) are paid no less than 88 percent nor more than 95 percent of the reference AWP. To the extent that the ten drugs listed in Table 3c qualify as both pass-through drugs and sole source drugs under the DIMA, it appears that they are subject to two different payment provisions. We have reconciled the two apparently conflicting payment provisions in a way that we believe results in the fewest anomalies. The drugs will retain their pass-through status, and therefore, the rules and policies that otherwise apply to pass-through drugs continue to apply to them. They will also be considered sole source drugs for purposes of section 1833(t)(14). We will pay for the drugs as follows.
First, because the drugs are pass-through drugs, we will give them pass-through payments. The pass-through payments will equal 85 percent of AWP (determined as of April 1, 2003) under section 1833(t)(6)(D)(i). However, because the drugs are also sole source drugs, we will also apply the payment methodology set forth in section 1833(t)(14)(A)(i)(I), and raise the payment to 88 percent of the reference AWP (the AWP determined as of May 1, 2003).
Under the payment methodology that we are applying to sole source drugs, we look at the payment that would otherwise be made and if it is less than 88 percent or greater than 95 percent of reference AWP, we adjust it as minimally as necessary to ensure that it is within the required range. In the case of these drugs, absent the provisions of 1833(t)(14)(i)(I), we would pay 85 percent of AWP (determined as of April 1, 2003). Therefore adjusting the payment that would otherwise be made results in payment at 88 percent of reference AWP.
In light of the total revamping of the methodology for payment for drugs and biologicals under OPPS, we revisited the adjustment that we made under our authority in section 1833(t)(2)(E) of the Act to ensure equitable payments in 2003 and in the November 7 final rule for the 2004 update of the OPPS. After considering the nature of the DIMA payment changes, we have concluded that it is still appropriate to apply this adjustment to the methodology discussed in the previous two paragraphs for the reasons we stated in the OPPS rulemaking during the past two years. Therefore, for darbepoetin alpha (Q0137 and C1774), we are Start Printed Page 827making an adjustment in accordance with section 1833(t)(2)(E) of the Act (which was unaffected by DIMA) to the combined pass-through amount and 3 percent additional payment provided under section 1833(t)(14)(A)(i)(I) of DIMA, resulting in a payment rate of $3.88 per unit. This payment rate is budget neutral.
Table 3a.—Pass-Through Drugs Reimbursed at 85% of AWP
HCPCS APC Long description 2004 Payment amount 2004 Co-payment amount J9395 9120 Injection, Fulvestrant, per 25 mg $78.36 $13.09 C9121 9121 Injection, Argotroban, per 5 mg 14.63 2.44 C9123 9123 TransCyte, per 247 sq cm 689.78 115.23 C9205 9205 Injection, Oxaliplatin, per 5 mg 8.45 1.41 C9203 9203 Injection, Perflexane lipid microspheres, per single use vial 127.50 21.30 J3315 9122 Injection, Triptorelin pamoate, per 3.75 mg 356.66 59.58 J3486 9204 Injection, Ziprasidone mesylate, per 10 mg 18.60 3.11 C9211 9211 Injection, IV, Alefacept, per 7.5 mg 595.00 99.40 C9212 9212 Injection, IM, Alefacept, per 7.5 mg 422.88 70.65 Table 3b.—Pass-Through Drugs Paid at 95% of AWP
HCPCS APC Long description Amount Amount C9207 9207 Injection, IV, Bortezomib, per 3.5 mg 1,039.68 155.40 C9208 9208 Injection, IV, Agalsidase beta, per 1 mg 123.78 18.50 C9209 9209 Injection, IV, Laronidase, per 2.9 mg 644.10 96.28 C9210 9210 Injection, IV, Palonosetron HCI, per 0.25 mg (250 micrograms) 307.80 46.01 Table 3c.—Pass-Through Drugs Paid as Sole Source Drugs at 88% of AWP
HCPCS APC Long description OPPS CY2004 November 7 rate DIMA final rate J0583 9111 Injection, Bivalirudin, per 1 mg $1.43 $1.61 C9112 9112 Injection, Perflutren lipid microsphere, per 2 ml 132.60 137.28 C9113 9113 Injection, Pantoprazole sodium, per vial 22.44 23.23 J1335 9116 Injection, Ertapenem sodium, per 500 mg 21.24 21.99 J2505 9119 Injection, Pegfilgrastim, per 6 mg single dose vial 2,507.50 2,596.00 C9200 9200 Orcel, per 36 sqare centimeters 1,015.75 1,051.60 C9201 9201 Dermagraft, per 37.5 square centimeters 516.80 535.04 J2324 9114 Injection, Nesiritide, per 0.5 mg 135.66 140.45 J3487 9115 Injection, Zoledronic acid, per 1 mg 194.52 211.07 Payment for New Drugs and Biologicals Before a HCPCS Code Is Assigned
Under new section 1833(t)(15) of the Act, as added by section 621(a)(1) of the DIMA a drug or biological that is furnished as part of covered outpatient department services for which a HCPCS codes has not been established, is to be paid at 95 percent of the AWP for the drug or biological.
We are in the process of determining how hospitals would bill Medicare for a drug prior to assignment of a HCPCS code. We will issue instructions once we have determined how to make this requirement operational.
Payment for Orphan Drugs as Designated by the Secretary
Section 1833(t)(14)(C) as added by section 621(a)(1) of the DIMA, provides that the amount of payment for orphan drugs designated by the Secretary shall, for 2004 and 2005, equal the amount the Secretary shall specify. We have determined that single indication orphan drugs as designated by the Secretary will be paid at the rates published in the November 7, 2003 Federal Register (68 FR 63398). Neither the definition nor the 2004 payment amounts for single indication orphan drugs under the OPPS have changed from what was published in the November 7 final rule.
Brachytherapy
Section 621(b)(1) of the DIMA of 2003 amends the Act by adding section 1833(t)(16)(C) and section 1833(t)(2)(H) which establish separate payment for devices of brachytherapy consisting of a seed or seeds (or radioactive source) based on a hospital's charges for the service, adjusted to cost. Further, charges for the brachytherapy devices shall not be used in determining any outlier payments and consistent with our practice under OPPS to exclude items paid at cost from budget neutrality consideration, these items will be excluded from budget neutrality as well. The period of payment under this provision is for brachytherapy sources furnished from January 1, 2004 through December 31, 2006.
We will pay for the brachytherapy sources listed in Table 4 on a cost basis, as required by the statute. The status indicator for brachytherapy sources is changed to “H.” The definition of status indicator “H” is currently for pass-through payment for devices, but the brachytherapy sources affected by new sections 1833(t)(16)(C) and 1833(t)(2)(H) are not pass-through device categories. Therefore, we are also changing, for 2004, the definition of payment status indicator “H” to include non-pass-through brachytherapy sources paid for on a cost basis. This use of status indicator “H” is a pragmatic decision that allows us to pay for brachytherapy sources in accordance with new section 1833(t)(16)(C) effective January 1, 2004 Start Printed Page 828without having to modify our claims processing systems. We will revisit the use and definition of status indicator “H” for this purpose for the OPPS update for 2005. Table 4 provides a complete listing of the HCPCS codes, descriptors, APC assignments and status indicators for brachytherapy sources.
Table 4.—Brachytherapy Sources To Be Paid Separately, Using Charges Reduced to Cost
HCPCS Descriptor APC APC title New status indicator C1716 Brachytx source, Gold 198 1716 Brachytx source, Gold 198 H C1717 Brachytx source, HDR Ir-192 1717 Brachytx source, HDR Ir-192 H C1718 Brachytx source, Iodine 125 1718 Brachytx source, Iodine 125 H C1719 Brachytx sour, Non-HDR Ir-192 1719 Brachytx source, Non-HDR Ir-192 H C1720 Brachytx source, Paladium 103 1720 Brachytx source, Paladium 103 H C2616 Brachytx source, Yttrium-90 2616 Brachytx source, Yttrium-90 H C2632 Brachytx solution, I-125, per mCi 2632 Brachytx sol, I-125, per mCi H C2633 Brachytx source, Cesium-131 2633 Brachytx source, Cesium-131 H C2632 Brachytx sol, I-125, per mCi 2632 Brachytx sol, I-125, per mCi H As indicated in Table 4, brachytherapy source in HCPCS code C1717 will be paid based on the hospital's charge reduced to cost beginning January 1, 2004. Prior to enactment of DIMA, these sources were paid as packaged services in APC 0313. As a result of the requirement to pay for C1717 separately, we are adjusting the payment rate for APC 0313 to reflect the unpackaging of the brachytherapy source. The new rate is listed in Addendum A.
Section 1833(t)(2)(H) is added by section 621(b)(2)(C) of DIMA, mandating the creation of separate groups of covered OPD services that classify brachytherapy devices separately from other services or groups of services. The additional groups shall be created in a manner reflecting the number, isotope and radioactive intensity of the devices of brachytherapy furnished, including separate groups for palladium-103 and iodine-125.
We invite the public to submit recommendations for new codes to describe brachytherapy sources in a manner reflecting the number, radioisotope, and radioactive intensity of the sources. We request that commenting parties provide a detailed rationale to support recommended new codes. We will propose appropriate changes in codes for brachytherapy sources in the 2005 OPPS update.
Continuation of Transitional Corridor Payments for CY 2004
Since the inception of the OPPS, providers have been eligible to receive additional transitional payments if the payments they received under the OPPS were less than the payments they would have received for the same services under the payment system in effect before the OPPS. Under 1833(t)(7) of the Act, most hospitals that realize lower payments under the OPPS received transitional corridor payments based on a percent of the decrease in payments. However, rural hospitals having 100 or fewer beds, as well as cancer hospitals and children's hospitals described in section 1886(d)(1)(B)(iii) and (v) of the Act, were held harmless under this provision and paid the full amount of the decrease in payments under the OPPS.
Transitional corridor payments were intended to be temporary payments to ease providers' transition from the prior cost-based payment system to the prospective payment system. In accordance with section 1833(t)(7) of the Act, transitional corridor payments were to be eliminated January 1, 2004, for all providers other than cancer hospitals and children's hospitals. Cancer hospitals and children's hospitals are held harmless permanently under the transitional corridor provisions of the statute.
Section 411 of the DIMA amends section 1833(t)(7) of the Act to provide that hold harmless transitional corridor payments will continue through December 31, 2005 for rural hospitals having 100 or fewer beds.
Section 411 of the DIMA further amends section 1833(t)(7) of the Act to provide that hold harmless transitional corridor payments shall apply to sole community hospitals, as defined in section 1886(d)(5)(D)(iii) of the Act, which are located in rural areas, with respect to services furnished during cost reporting periods beginning on or after January 1, 2004, and continuing through December 31, 2005. For purposes of this provision, a sole community hospital's location in a rural area will be determined as it is under the inpatient PPS, in 42 CFR 412.63(b).
II. Provisions of the Interim Final Rule With Comment Period
The Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (DIMA), enacted December 8, 2003 makes changes to the Social Security Act (the Act) relating to calendar year 2004 payments under the Hospital Outpatient Prospective Payment System. This interim final rule with comment period implements changes resulting from enactment of the DIMA that are effective January 1, 2004, as follows:
Transitional Corridor Payments Extended
Hold harmless transitional corridor payments are continued through December 31, 2005 for small rural hospitals having 100 or fewer beds. In addition, hold-harmless transitional corridor provisions shall apply to sole community hospitals as defined in section 1886(d)(5)(D)(iii) of the Act with respect to cost reporting periods beginning on or after January 1, 2004 and will continue through December 31, 2005.
Payment for “Specified Covered Outpatient Drugs”
Separately paid radiopharmaceutical agents and drugs or biologicals that had transitional pass-through status on or before December 31, 2002, are classified into 3 categories: innovator multiple source drugs; noninnovator multiple source drugs; and sole source drugs. Payment levels based on the reference average wholesale price as of May 1, 2003 are specified for each category.
Payment for Pass-Through Drugs
Drugs and biologicals furnished during 2004 for which pass-through payment was first made on or after January 1, 2003 (which removes them from application of section 621 of the Start Printed Page 829DIMA) and were approved by the FDA for marketing as of April 1, 2003, will be paid 85 percent of AWP pursuant to section 1842(o)(1)(B) and 1842(o)(4)(A), unless sections 1842(o)(4)(B), (C) or (D) apply.
Certain drugs, biologicals and radiopharmaceutical agents that are pass-through drugs in 2004 and that also meet the definition of “specified covered outpatient drugs”, except as otherwise specified, are paid 88 percent of the reference AWP. Those drugs, biologicals, and radiopharmaceutical agents remain pass-through drugs and all policies that apply to them as pass-through drugs continue to apply.
Exclude Separately Payable Drugs and Biologicals From Outlier Payments
Separately paid drugs and biologicals are excluded from outlier payments.
Brachytherapy Sources Are To Be Paid Separately
All devices of brachytherapy consisting of a seed or seeds (or radioactive source) are paid based on the hospital's charge for the device adjusted to cost. All such brachytherapy sources are excluded from outlier payments.
III. 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.
IV. Waiver of Notice of Proposed Rulemaking and the 30-Day Delay in the Effective Date
We ordinarily publish a notice of proposed rulemaking in the Federal Register and invite public comment on the proposed rule in accordance with 5 U.S.C. section 553(b) of the Administrative Procedure Act (APA). The notice of proposed rulemaking includes a reference to the legal authority under which the rule is proposed, and the terms and substances of the proposed rule or a description of the subjects and issues involved. This procedure can be waived, however, if an agency finds good cause that a notice-and-comment procedure is impracticable, unnecessary, or contrary to the public interest and incorporates a statement of the finding and its reasons in the rule issued.
In this case, we believe that it is in the public interest to comply with the statutory requirement to implement these changes effective January 1, 2004. Failure to meet this deadline would cause a delay in payment increases for many drugs and biologicals and brachytherapy sources.
Section 1871 of the Act also provides for publication of a notice of proposed rulemaking and opportunity for public comment before CMS issues a final rule. However, section 1871(b)(2)(B) provides an exception when a law establishes a specific deadline for implementation of a provision and the deadline is less than 150 days after the law's date of enactment. The DIMA was enacted by the Congress on November 25, 2003 and signed into law by the President on December 8, 2003. The provisions of this rule that amend the Medicare hospital outpatient prospective payment system are required to be implemented January 1, 2004. Therefore, these provisions are subject to waiver of proposed rulemaking in accordance with section 1871(b)(2)(B) of the Act.
In addition, we ordinarily provide a 30-day delay in the effective date of the provisions of an interim final rule. Section 553(d) of the APA (5 U.S.C. section 553(d)) ordinarily requires a 30-day delay in the effective date of final rules after the date of their publication in the Federal Register. This 30-day delay in effective date can be waived, however, if an agency finds for good cause that the delay is impracticable, unnecessary, or contrary to the public interest, and the agency incorporates a statement of the finding and its reasons in the rule issued.
In this case, we believe that it is in the public interest to comply with the statutory requirement to implement these changes effective January 1, 2004 without the 30-day delay in effective date. Failure to meet this deadline would cause a delay in payment increases for many drugs and biologicals and brachytherapy sources.
In addition to the APA requirements, section 1871(e)(1), as amended by section 903(b)(1) of DIMA also requires that a substantive change in a regulation shall not become effective before the end of the 30-day period that begins on the date that the Secretary has issued or published the substantive change. Section 903(b)(1) provides an exception to the requirement of a 30-day delay in the effective date if the Secretary finds that the waiver of such 30-day period is necessary to comply with statutory requirements or that the application of such 30-day period is contrary to the public interest.
For purposes of DIMA, we believe that it is in the public interest to comply with the statutory requirement to implement these changes effective January 1, 2004 without the 30-day delay in effective date for the same reasons stated above—failure to meet this deadline would cause a delay in payment increases for many drugs and biologicals and brachytherapy sources. In addition, we find it is necessary to waive the 30-day delay period in order to timely comply with the statutory requirement that new payment rates be effective on January 1, 2004. We are providing a 60-day public comment period.
V. Regulatory Impact Analysis
A. Overall Impact
We have examined the impacts of this rule as required by Executive Order 12866 (September 1993, Regulatory Planning and Review), the Regulatory Flexibility Act (RFA) (September 16, 1980, Pub. L. 96-354), section 1102(b) of the Social Security Act, the Unfunded Mandates Reform Act of 1995 (Pub. L. 104-4), and Executive Order 13132.
Executive Order 12866 (as amended by Executive Order 13258, which merely reassigns responsibility of duties) 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 in any 1 year).
We estimate the effects of the provisions that will be implemented by this final rule will result in expenditures exceeding $100 million in any 1 year. Our Office of the Actuary estimates that the total change in expenditures under the OPPS for CY 2004 as a result of the changes made by DIMA to be approximately $150 million. Therefore, this final rule with comment is an economically significant rule under Executive Order 12866, and a major rule under 5 U.S.C. 804(2). Therefore the discussion below, in combination with the rest of this final rule constitutes a regulatory impact analysis. The RFA requires agencies to analyze options for regulatory relief of small businesses. However a regulatory flexibility analysis is not required for an interim final rule because no proposed rule is being issued.
Therefore the discussion below constitutes a regulatory impact analysis but no regulatory flexibility analysis is provided. Start Printed Page 830
Unfunded Mandates
Section 202 of the Unfunded Mandates Reform Act of 1995 also requires that agencies assess anticipated costs and benefits before issuing any rule that may result in expenditure in any 1 year by State, local, or tribal governments, in the aggregate, or by the private sector, of $110 million. This interim final rule will not mandate any requirements for State, local or tribal governments. This interim final rule will not impose unfunded mandates on the private sector of more than $110 million dollars.
Federalism
Executive Order 13132 establishes certain requirements that an agency must meet when it promulgates a proposed rule (and subsequent final rule) that imposes substantial direct requirement costs on State and local governments, preempts State law, or otherwise has Federalism implications.
We have examined this interim final rule in accordance with Executive Order 13132, Federalism, and have determined that it will not have an impact on the rights, roles, and responsibilities of State, local or tribal governments.
B. Anticipated Effects of Changes in This Interim Final Rule and Alternatives Considered for Each Change
All of the changes made in this interim final rule with comment are required by DIMA. We are required under section 621 of the DIMA to revise payments for certain drugs and biologicals and for radiopharmaceuticals. We are also required under section 621 of the DIMA to pay for brachytherapy sources on the basis of application of a cost to charge ratio to the charges for the sources. In addition, we are required under section 621 of the DIMA to continue transitional outpatient payment for certain hospitals.
Impact on Drugs and Biologicals That Will Be Paid Under Pass-Through Provisions in 2004
Four of the drugs and biologicals that will be paid under pass-through provisions in 2004 will be paid at 95 percent of AWP. Nine of the drugs and biologicals that will be paid under pass-through provisions in 2004 will be paid at 85 percent of AWP in 2004. This is a reduction of 10 percent of AWP compared to the payment that would have been made for these drugs and biologicals before passage of the DIMA.
As discussed previously in this rule, some pass-through drugs and biologicals also meet the criteria for “specified covered outpatient drugs” under 1833(t)(14) and, except as specified in this rule, will be paid 88 percent of the reference AWP. Notwithstanding the payment amount, however, they remain pass-through drugs.
Hospitals that provide drugs paid at 85 percent of AWP will be paid less than they would have been paid absent passage of the new law.
It is unclear whether the reduction in payments for these drugs will have any effect on beneficiary access to them. Hospitals consider many factors when they determine whether they choose to provide the drugs and it is unclear whether the reduction in payment for Medicare will result in impaired access. However, reduction in the payment amounts for some drugs means that beneficiaries will have lower copayments for those drugs and that they, and complementary insurers who pay beneficiary cost sharing, will have reduced expenses. Hospitals, however, will clearly be paid reduced amounts by Medicare for these drugs compared to the amounts that would be paid had the statute not imposed these changes. Manufacturers and distributors of the pass-through drugs that will be paid at 85 percent of AWP will be under increased pressure to reduce the price of the drugs since the hospitals to which they sell the items will be paid lower amounts by Medicare for them when used in hospital outpatient departments.
We considered setting payment at 85 percent for pass-through drugs that also meet the definition of “specified covered outpatient drugs” as allowed in the cross reference from 1833(t)(6) to 1842(o). However, given that the drugs are eligible for payment under both sets of criteria, we chose to increase their payment to 88 percent of reference AWP, except as otherwise specified. We believe that this choice will result in the least possible disruption to beneficiary access to these drugs.
We considered no alternatives with regard to payment for pass-through drugs that did not meet the definition of “specified covered outpatient drugs” because the law provides only one payment methodology for these drugs.
Impact of Changes for “Specified Covered Outpatient Drugs”
Radiopharmaceutical agents and drugs or biologicals for which payment was made on a pass-through basis on or before December 31, 2002, are now to be paid under section 1833(t)(14) of the Act as added by DIMA. Under these provisions, radiopharmaceuticals and drugs and biologicals that meet the criteria, are paid amounts that must be limited as specified in the law. Specifically, items that meet the definition of sole source drugs must be paid no less than 88 percent of reference AWP nor more than 95 percent of reference AWP. Items that meet the definition of innovator multiple source drugs must be paid no more than 68 percent of AWP and items that meet the definition of noninnovator multiple source drugs must be paid no more than 46 percent of AWP.
As described previously, these categories are defined in section 1927(k)(7) of the Act. That section classifies drugs, biologicals and radiopharmaceuticals for purposes of the Medicaid drug rebate program. CMS has a database in which these items are categorized to which we looked to seek the classification of each drug, biological and radiopharmaceutical paid under pass-through provisions before December 31, 2002. Table 1 shows those items that we believe meet the definition of sole source drug. Table 2 shows those items for which it is not clear to us whether the item should be classified as a sole source drug or as both an innovator multiple source and a noninnovator multiple source drug and which we will pay as noninnovator multiple source drugs until we receive comments and determine the classification into which the drug falls. Paying for those drugs with questionable classification as noninnovator multiple source drugs allows payment to be made to hospitals for these drugs when they are furnished and also protects hospitals from incurring overpayments. Once we review the public comments and establish the correct classification and codes for the billing of innovator multiple source drugs, hospitals may subject adjustment bills to be paid the additional amounts due.
We will pay the 121 drugs in Table 1 at the amounts shown, as previously discussed. Six of these drugs will have no payment change from the payment announced in the November 7, 2003 final rule. Six of these drugs will receive decreases in payment compared to the final rule because the payment established in the November 7, 2003 final rule exceeded 95 percent of the reference AWP. The payment amounts for these drugs are now set at 95 percent of the reference AWP in accordance with the law. One hundred nine of these drugs will receive increases in payment compared to the final rule because the payment established in the November 7, 2003 final rule was less than 88 percent of reference AWP. The payment amounts for these drugs, biologicals and radiopharmaceuticals is now set at 88 percent of the reference AWP. Start Printed Page 831
We will temporarily pay the 52 drugs in Table 2 at the amounts shown, as previously discussed. Thirteen of these items will be paid the amount that was published in the November 7, 2003 final rule. Thirty-eight of these items will receive payment decreases. One of these items did not have a reference AWP under the SDP and will require further research to determine the correct payment amount. Until we determine a reference AWP for this item it will be paid at the amount that was published in the November 7, 2003 final rule.
It is unclear what the final overall impact of these changes will be because we are, as yet, unable to determine into which categories 52 items in dispute will fall. Moreover, once they are categorized, we do not anticipate that we will know the frequency with which hospitals will use the innovator multiple source drug versus the noninnovator multiple source drug in the outpatient department. Moreover, it is not clear to what extent hospitals may change their behavior with regard to which type of a drug they choose to purchase and whether their purchasing decisions will be affected by whether they furnish the item to hospital outpatient departments or inpatient departments.
We considered whether to classify the 52 items with questionable category assignment as both innovator multiple source and noninnovator multiple source drugs and to create HCPCS codes to be used when innovator multiple source drugs are administered. However, we believe that public comment is necessary to determine the correct classification of these items. Similarly, we believe that, given the burden the law imposes on hospitals for reporting drugs by the category into which they fall, it was important to receive public comment regarding whether new codes should be created and regarding ways we can reduce the reporting burden on hospitals. Hence, until we receive and review the comments, we will not be able to assess the impact of these requirements of the law.
We do acknowledge, however, that for the 52 drugs that are not sole source drugs, the temporary payments to hospitals at the noninnovator multiple source drug rate will be less than the payment that would have been made under the November 7, 2003 final rule. For those drugs that are sole source drugs, the payment will increase in most cases.
Hospitals that provide sole source drugs will be paid more for these drugs under these provisions than they would have been paid before enactment of the DIMA. Hospitals that provide innovator multiple source drugs and noninnovator multiple source drugs will be paid less for these items than they would have been before enactment of the DIMA. This may encourage use of sole source drugs and discourage use of multiple source drugs. As a result, beneficiaries may have greater access to sole source drugs but will also incur greater copayments because those payment rates are higher than they would have been before enactment of DIMA. In turn, there may be increased payment by complementary insurers for these items. Manufacturers of sole source drugs may realize increased sales and manufacturers of generic drugs may see reduced sales.
We considered whether to permit a drug that is classified by AMP as a sole source drug, an innovator multiple source drug and a noninnovator multiple source drug to be paid under all three classifications. We decided not to pay a drug as a sole source drug if it is also a multiple source drug for reasons described previously in this interim final rule. We considered no alternatives because the law is quite specific with regard to the classification of drugs and the payment rules that apply to each class of drug.
Impact of Cost-Based Payment for Sources of Brachytherapy
The law provides that sources of brachytherapy will be paid an amount equal to the hospital's charge for the source adjusted by the applicable cost to charge ratio. It is unclear whether this will result in an increase or decrease in payment for brachytherapy sources. However, removing the brachytherapy source from packaged payment for the services with which it is furnished removes incentives for using the least number of sources needed for the therapeutic purpose. There is no evidence that packaged payment for brachytherapy sources resulted in inappropriately low utilization of brachytherapy, nor that separate payment will result in any change in availability of the service. We are unable to estimate the impact of this change on utilization and program payment.
We considered no alternatives to this policy because the statute was specific with regard to how payment for brachytherapy sources must be made.
Impact of Continuation of Transitional Outpatient Payments for Certain Hospitals
The law provides that transitional outpatient payments must continue for rural hospitals with 100 or fewer beds and be provided for sole community hospitals in rural areas through December 31, 2005. There are approximately 600 sole community hospitals and approximately 1150 rural hospitals with 100 beds or fewer that may be affected by this provision. These hospitals will continue to receive transitional corridor payments in addition to the payments they will receive under OPPS. These payments should continue to strengthen the ability of these hospitals to furnish services to beneficiaries who reside in the areas served by these hospitals. Beneficiaries should be better assured of access to services in these hospitals. These hospitals will be assured of payment for the reasonable costs of providing outpatient services.
We considered no alternatives because the statute is quite directive with regard to the extension of hold harmless protection to these hospitals.
C. Conclusion
We have prepared the analysis above because we have determined that this interim final rule will have a significant economic impact. In accordance with the provisions of Executive Order 12866, this interim final rule was reviewed by the Office of Management and Budget.
Publication of Addenda
The addenda included in this interim final rule, Addenda A and D1 replace the addenda in the November 7, 2003 Federal Register (68 FR 63478). The revised addenda reflect changes required by the DIMA as well as corrections to minor errors contained in the addenda published November 7, 2003.
In addition to the addenda included here, we will post the updated Addenda B and C on our Web site at http://www.cms.hhs.gov/regulations/hopps/.
Start List of SubjectsList of Subjects in 42 CFR Part 419
- Hospitals
- Medicare
- Reporting and recordkeeping requirements
For the reasons set forth in the preamble, the Centers for Medicare & Medicaid Services amends 42 CFR chapter IV as set forth below:
End Amendment Part Start PartPART 419—PROSPECTIVE PAYMENT SYSTEM FOR HOSPITAL OUTPATIENT DEPARTMENT SERVICES
End Part Start Amendment Part1. The authority citation for part 419 continues to read as follows:
End Amendment Part Start Printed Page 832Subpart C—Basic Methodology for Determining Prospective Payment Rates for Hospital Outpatient Services
Start Amendment Part2. Section 419.32 is amended by revising paragraph (d) to read as follows:
End Amendment PartCalculation of prospective payment rates for hospital outpatient services.* * * * *(d) Budget neutrality. (1) CMS adjusts the conversion factor as needed to ensure that updates and adjustments under § 419.50(a) are budget neutral.
(2) In determining adjustments for 2004 and 2005, CMS will not take into account any additional expenditures per section 1833(t)(14) of the Act that would not have been made but for enactment of section 621 of the Medicare Prescription Drug, Improvement, and Modernization Act of 2003.
Subpart D—Payments to Hospitals
Start Amendment Part3. Section § 419.43 is amended as follows:
End Amendment Part Start Amendment PartA. Paragraph (d)(1) introductory text is revised.
End Amendment Part Start Amendment PartB. Paragraph (e) is revised.
End Amendment Part Start Amendment PartC. New paragraph (f) is added.
End Amendment PartThe revisions and additions read as follows:
Adjustments to national program payments and beneficiary copayment amounts.* * * * *(d) Outlier adjustment—(1) General rule. Subject to paragraph (d)(4) of this section, CMS provides for an additional payment for a hospital outpatient service (or group of services) not excluded under paragraph (f) of this section for which a hospital's charges, adjusted to cost, exceed the following:
* * * * *(e) Budget neutrality. CMS establishes payment under paragraph (d) of this section in a budget-neutral manner excluding services and groups specified in paragraph (f) of this section.
(f) Excluded services and groups. Drugs and biologicals that are paid under a separate APC and devices of brachytherapy, consisting of a seed or seeds (including a radioactive source) are excluded from qualification for outlier payments.
Subpart G—Transitional Pass-Through Payments
Start Amendment Part4. Section 419.64 is amended by revising paragraph (d).
End Amendment PartTransitional pass-through payments: Drugs and biologicals.* * * * *(d) Amount of pass-through payment. (1) Subject to any reduction determined under § 419.62(b), the pass-through payment for a drug or biological as specified in section 1842(o)(1)(A) and (o)(1)(D)(i) of the Act is 95 percent of the average wholesale price of the drug or biological minus the portion of the APC payment CMS determines is associated with the drug or biological.
(2) Subject to any reduction determined under § 419.62(b), the pass-through payment for a drug or biological as specified in section 1842(o)(1)(B) and (o)(1)(E)(i) of the Act is 85 percent of the average wholesale price, determined as of April 1, 2003, of the drug or biological minus the portion of the APC payment CMS determines is associated with the drug or biological.
Subpart H—Transitional Corridors
Start Amendment Part5. Section 419.70 is amended as follows:
End Amendment Part Start Amendment PartA. Paragraph (d)(1) is amended by removing “2004” and adding “2006” in its place.
End Amendment Part Start Amendment PartB. A new paragraph (d)(3) is added to read as follows:
End Amendment PartTransitional adjustment to limit decline and payment.* * * * *(d) * * *
(3) Temporary treatment for sole community hospitals located in rural areas. For covered hospital outpatient services furnished during cost reporting periods beginning on or after January 1, 2004, and continuing through December 31, 2005, for which the prospective payment system amount is less than the pre-BBA amount, the amount of payment under this part is increased by the amount of that difference if the hospital—
(i) Is a sole community hospital, under § 412.92 of this chapter; and
(ii) Is located in a rural area as defined in § 412.63(b) of this chapter or is treated as being located in a rural area under section 1886(d)(8)(E) of the Act.
(Catalog of Federal Domestic Assistance Program No. 93.773, Medicare—Hospital Insurance; and Program No. 93.774, Medicare—Supplementary Medical Insurance Program)
Dated: December 23, 2003.
Dennis G. Smith,
Acting Administrator, Centers for Medicare & Medicaid Services.
Approved: December 23, 2003.End SignatureTommy G. Thompson,
Secretary.
Note:
The following addenda will not appear in the Code of Federal Regulations.
Addendum A.—List of Ambulatory Payment Classifications (APCS) With Status Indicators, Relative Weights, Payment Rates, and Copayment Amounts Calendar Year 2004
APC Group title Status indicator Relative weight Payment rate National unadjusted copayment Minimum unadjusted copayment 0001 Level I Photochemotherapy S 0.4237 $23.12 $7.09 $4.62 0002 Level I Fine Needle Biopsy/Aspiration T 0.8083 $44.10 $8.82 0003 Bone Marrow Biopsy/Aspiration T 2.3229 $126.74 $25.35 0004 Level I Needle Biopsy/ Aspiration Except Bone Marrow T 1.5882 $86.65 $22.36 $17.33 0005 Level II Needle Biopsy/Aspiration Except Bone Marrow T 3.2698 $178.40 $71.59 $35.68 0006 Level I Incision & Drainage T 1.6527 $90.17 $23.26 $18.03 0007 Level II Incision & Drainage T 11.8633 $647.27 $129.45 0008 Level III Incision and Drainage T 19.4831 $1,063.02 $212.60 0009 Nail Procedures T 0.6652 $36.29 $8.34 $7.26 0010 Level I Destruction of Lesion T 0.6480 $35.36 $10.08 $7.07 0011 Level II Destruction of Lesion T 2.2217 $121.22 $27.88 $24.24 0012 Level I Debridement & Destruction T 0.7612 $41.53 $11.18 $8.31 0013 Level II Debridement & Destruction T 1.1302 $61.66 $14.20 $12.33 0015 Level III Debridement & Destruction T 1.5968 $87.12 $20.35 $17.42 0016 Level IV Debridement & Destruction T 2.5724 $140.35 $57.31 $28.07 0017 Level VI Debridement & Destruction T 16.3697 $893.15 $227.84 $178.63 0018 Biopsy of Skin/Puncture of Lesion T 0.9178 $50.08 $16.04 $10.02 Start Printed Page 833 0019 Level I Excision/ Biopsy T 3.9493 $215.48 $71.87 $43.10 0020 Level II Excision/ Biopsy T 7.0842 $386.52 $113.25 $77.30 0021 Level III Excision/ Biopsy T 14.3594 $783.46 $219.48 $156.69 0022 Level IV Excision/ Biopsy T 18.7932 $1,025.38 $354.45 $205.08 0023 Exploration Penetrating Wound T 2.8141 $153.54 $40.37 $30.71 0024 Level I Skin Repair T 1.6850 $91.94 $33.10 $18.39 0025 Level II Skin Repair T 5.1912 $283.24 $107.00 $56.65 0027 Level IV Skin Repair T 15.8990 $867.47 $329.72 $173.49 0028 Level I Breast Surgery T 17.6584 $963.46 $303.74 $192.69 0029 Level II Breast Surgery T 30.1167 $1,643.20 $632.64 $328.64 0030 Level III Breast Surgery T 37.3083 $2,035.58 $763.55 $407.12 0032 Insertion of Central Venous/Arterial Catheter T 11.4907 $626.94 $125.39 0033 Partial Hospitalization P 5.2569 $286.82 $57.36 0035 Placement of Arterial or Central Venous Catheter T 0.1691 $9.23 $2.79 $1.85 0036 Level II Fine Needle Biopsy/Aspiration T 1.5170 $82.77 $16.55 0037 Level III Needle Biopsy/Aspiration Except Bone Marrow T 9.8921 $539.72 $237.45 $107.94 0039 Implantation of Neurostimulator S 235.1866 $12,832.02 $2,566.40 0040 Level II Implantation of Neurostimulator Electrodes S 52.1002 $2,842.64 $568.53 0041 Level I Arthroscopy T 27.3819 $1,493.98 $298.80 0042 Level II Arthroscopy T 43.0808 $2,350.53 $804.74 $470.11 0043 Closed Treatment Fracture Finger/Toe/Trunk T 1.9074 $104.07 $20.81 0045 Bone/Joint Manipulation Under Anesthesia T 13.5889 $741.42 $268.47 $148.28 0046 Open/Percutaneous Treatment Fracture or Dislocation T 32.5581 $1,776.40 $535.76 $355.28 0047 Arthroplasty without Prosthesis T 29.9582 $1,634.55 $537.03 $326.91 0048 Arthroplasty with Prosthesis T 51.4609 $2,807.76 $695.60 $561.55 0049 Level I Musculoskeletal Procedures Except Hand and Foot T 19.6046 $1,069.65 $213.93 0050 Level II Musculoskeletal Procedures Except Hand and Foot T 24.8651 $1,356.66 $271.33 0051 Level III Musculoskeletal Procedures Except Hand and Foot T 34.5144 $1,883.14 $376.63 0052 Level IV Musculoskeletal Procedures Except Hand and Foot T 42.7126 $2,330.44 $466.09 0053 Level I Hand Musculoskeletal Procedures T 14.8831 $812.04 $253.49 $162.41 0054 Level II Hand Musculoskeletal Procedures T 24.2456 $1,322.86 $264.57 0055 Level I Foot Musculoskeletal Procedures T 18.7205 $1,021.41 $355.34 $204.28 0056 Level II Foot Musculoskeletal Procedures T 25.3930 $1,385.47 $405.81 $277.09 0057 Bunion Procedures T 25.5035 $1,391.50 $475.91 $278.30 0058 Level I Strapping and Cast Application S 1.0931 $59.64 $11.93 0060 Manipulation Therapy S 0.2788 $15.21 $3.04 0068 CPAP Initiation S 1.0807 $58.96 $29.48 $11.79 0069 Thoracoscopy T 28.9392 $1,578.95 $591.64 $315.79 0070 Thoracentesis/Lavage Procedures T 3.0717 $167.60 $33.52 0071 Level I Endoscopy Upper Airway T 0.8799 $48.01 $12.89 $9.60 0072 Level II Endoscopy Upper Airway T 1.7613 $96.10 $26.68 $19.22 0073 Level III Endoscopy Upper Airway T 3.4541 $188.46 $73.38 $37.69 0074 Level IV Endoscopy Upper Airway T 13.9480 $761.02 $295.70 $152.20 0075 Level V Endoscopy Upper Airway T 20.3815 $1,112.04 $445.92 $222.41 0076 Level I Endoscopy Lower Airway T 9.2346 $503.85 $189.82 $100.77 0077 Level I Pulmonary Treatment S 0.2837 $15.48 $7.74 $3.10 0078 Level II Pulmonary Treatment S 0.7917 $43.20 $14.55 $8.64 0079 Ventilation Initiation and Management S 2.1494 $117.27 $23.45 0080 Diagnostic Cardiac Catheterization T 36.0160 $1,965.07 $838.92 $393.01 0081 Non-Coronary Angioplasty or Atherectomy T 35.0285 $1,911.19 $382.24 0082 Coronary Atherectomy T 110.2196 $6,013.69 $1,293.59 $1,202.74 0083 Coronary Angioplasty and Percutaneous Valvuloplasty T 59.2047 $3,230.27 $646.05 0084 Level I Electrophysiologic Evaluation S 10.5226 $574.12 $114.82 0085 Level II Electrophysiologic Evaluation T 35.4126 $1,932.15 $426.25 $386.43 0086 Ablate Heart Dysrhythm Focus T 44.9389 $2,451.91 $833.33 $490.38 0087 Cardiac Electrophysiologic Recording/Mapping T 39.8161 $2,172.41 $434.48 0088 Thrombectomy T 34.6942 $1,892.95 $655.22 $378.59 0089 Insertion/Replacement of Permanent Pacemaker and Electrodes T 117.1896 $6,393.98 $1,722.59 $1,278.80 0090 Insertion/Replacement of Pacemaker Pulse Generator T 96.8284 $5,283.05 $1,651.45 $1,056.61 0091 Level II Vascular Ligation T 28.8326 $1,573.14 $348.23 $314.63 0092 Level I Vascular Ligation T 25.0959 $1,369.26 $505.37 $273.85 0093 Vascular Reconstruction/Fistula Repair without Device T 21.3104 $1,162.72 $277.34 $232.54 0094 Level I Resuscitation and Cardioversion S 2.6345 $143.74 $48.58 $28.75 0095 Cardiac Rehabilitation S 0.5994 $32.70 $16.35 $6.54 Start Printed Page 834 0096 Non-Invasive Vascular Studies S 1.7176 $93.71 $46.85 $18.74 0097 Cardiac and Ambulatory Blood Pressure Monitoring X 1.0635 $58.03 $23.80 $11.61 0098 Injection of Sclerosing Solution T 1.0729 $58.54 $14.06 $11.71 0099 Electrocardiograms S 0.3703 $20.20 $4.04 0100 Cardiac Stress Tests X 1.5862 $86.54 $41.44 $17.31 0101 Tilt Table Evaluation S 4.4040 $240.29 $105.27 $48.06 0103 Miscellaneous Vascular Procedures T 11.6202 $634.01 $223.63 $126.80 0104 Transcatheter Placement of Intracoronary Stents T 82.6713 $4,510.63 $902.13 0105 Revision/Removal of Pacemakers, AICD, or Vascular T 19.1898 $1,047.01 $370.40 $209.40 0106 Insertion/Replacement/Repair of Pacemaker and/or Electrodes T 58.9719 $3,217.57 $643.51 0107 Insertion of Cardioverter-Defibrillator T 337.1304 $18,394.17 $3,699.14 $3,678.83 0108 Insertion/Replacement/Repair of Cardioverter-Defibrillator Leads T 452.6995 $24,699.74 $4,939.95 0109 Removal of Implanted Devices T 7.4705 $407.60 $131.49 $81.52 0110 Transfusion S 3.6718 $200.34 $40.07 0111 Blood Product Exchange S 13.1719 $718.67 $200.18 $143.73 0112 Apheresis, Photopheresis, and Plasmapheresis S 37.5832 $2,050.58 $612.47 $410.12 0113 Excision Lymphatic System T 19.9322 $1,087.52 $217.50 0114 Thyroid/Lymphadenectomy Procedures T 37.5963 $2,051.29 $485.91 $410.26 0115 Cannula/Access Device Procedures T 25.6437 $1,399.15 $459.35 $279.83 0116 Chemotherapy Administration by Other Technique Except Infusion S 0.7996 $43.63 $8.73 0117 Chemotherapy Administration by Infusion Only S 3.0360 $165.65 $42.54 $33.13 0119 Implantation of Infusion Pump T 134.7194 $7,350.43 $1,470.09 0120 Infusion Therapy Except Chemotherapy T 1.9114 $104.29 $28.21 $20.86 0121 Level I Tube changes and Repositioning T 2.1114 $115.20 $43.80 $23.04 0122 Level II Tube changes and Repositioning T 8.8621 $483.53 $99.16 $96.71 0123 Bone Marrow Harvesting and Bone Marrow/Stem Cell Transplant S 6.1499 $335.54 $67.11 0124 Revision of Implanted Infusion Pump T 23.8050 $1,298.82 $259.76 0125 Refilling of Infusion Pump T 2.1606 $117.88 $23.58 0130 Level I Laparoscopy T 32.7724 $1,788.09 $659.53 $357.62 0131 Level II Laparoscopy T 40.8064 $2,226.44 $1,001.89 $445.29 0132 Level III Laparoscopy T 57.2045 $3,121.13 $1,239.22 $624.23 0140 Esophageal Dilation without Endoscopy T 6.4525 $352.05 $107.24 $70.41 0141 Upper GI Procedures T 7.8206 $426.70 $143.38 $85.34 0142 Small Intestine Endoscopy T 8.7959 $479.91 $152.78 $95.98 0143 Lower GI Endoscopy T 8.2957 $452.62 $186.06 $90.52 0146 Level I Sigmoidoscopy T 3.9826 $217.29 $64.40 $43.46 0147 Level II Sigmoidoscopy T 7.6808 $419.07 $83.81 0148 Level I Anal/Rectal Procedure T 3.8320 $209.08 $63.38 $41.82 0149 Level III Anal/Rectal Procedure T 17.1425 $935.31 $293.06 $187.06 0150 Level IV Anal/Rectal Procedure T 22.1919 $1,210.81 $437.12 $242.16 0151 Endoscopic Retrograde Cholangio-Pancreatography (ERCP) T 17.9462 $979.16 $245.46 $195.83 0152 Percutaneous Abdominal and Biliary Procedures T 9.1474 $499.09 $125.28 $99.82 0153 Peritoneal and Abdominal Procedures T 20.8723 $1,138.81 $410.87 $227.76 0154 Hernia/Hydrocele Procedures T 26.9636 $1,471.16 $464.85 $294.23 0155 Level II Anal/Rectal Procedure T 10.0809 $550.02 $188.89 $110.00 0156 Level II Urinary and Anal Procedures T 2.4747 $135.02 $40.52 $27.00 0157 Colorectal Cancer Screening: Barium Enema S 2.5693 $140.18 $28.04 0158 Colorectal Cancer Screening: Colonoscopy T 7.4244 $405.08 $101.27 0159 Colorectal Cancer Screening: Flexible Sigmoidoscopy S 2.7823 $151.81 $37.95 0160 Level I Cystourethroscopy and other Genitourinary Procedures T 6.8801 $375.39 $105.06 $75.08 0161 Level II Cystourethroscopy and other Genitourinary Procedures T 16.8407 $918.85 $249.36 $183.77 0162 Level III Cystourethroscopy and other Genitourinary Procedures T 21.9098 $1,195.42 $239.08 0163 Level IV Cystourethroscopy and other Genitourinary Procedures T 33.8805 $1,848.55 $369.71 0164 Level I Urinary and Anal Procedures T 1.2021 $65.59 $17.59 $13.12 0165 Level III Urinary and Anal Procedures T 14.6838 $801.16 $160.23 0166 Level I Urethral Procedures T 16.7918 $916.18 $218.73 $183.24 0167 Level III Urethral Procedures T 30.0186 $1,637.84 $555.84 $327.57 0168 Level II Urethral Procedures T 30.0147 $1,637.63 $405.60 $327.53 0169 Lithotripsy T 45.1150 $2,461.52 $1,115.69 $492.30 0170 Dialysis S 5.9678 $325.61 $65.12 Start Printed Page 835 0180 Circumcision T 18.6176 $1,015.79 $304.87 $203.16 0181 Penile Procedures T 29.4217 $1,605.28 $621.82 $321.06 0183 Testes/Epididymis Procedures T 21.6724 $1,182.47 $236.49 0184 Prostate Biopsy T 3.8995 $212.76 $96.27 $42.55 0187 Miscellaneous Placement/Repositioning X 4.4288 $241.64 $90.71 $48.33 0188 Level II Female Reproductive Proc T 1.1365 $62.01 $12.40 0189 Level III Female Reproductive Proc T 1.4232 $77.65 $18.09 $15.53 0190 Level I Hysteroscopy T 19.6922 $1,074.43 $424.28 $214.89 0191 Level I Female Reproductive Proc T 0.1853 $10.11 $2.93 $2.02 0192 Level IV Female Reproductive Proc T 2.7121 $147.97 $39.11 $29.59 0193 Level V Female Reproductive Proc T 15.0453 $820.89 $171.13 $164.18 0194 Level VIII Female Reproductive Proc T 18.4286 $1,005.48 $397.84 $201.10 0195 Level IX Female Reproductive Proc T 25.6950 $1,401.94 $483.80 $280.39 0196 Dilation and Curettage T 16.1219 $879.63 $338.23 $175.93 0197 Infertility Procedures T 4.8280 $263.42 $52.68 0198 Pregnancy and Neonatal Care Procedures T 1.3578 $74.08 $32.19 $14.82 0199 Obstetrical Care Service T 17.2831 $942.98 $188.60 0200 Level VII Female Reproductive Proc T 17.9920 $981.66 $307.83 $196.33 0201 Level VI Female Reproductive Proc T 16.8660 $920.23 $329.65 $184.05 0202 Level X Female Reproductive Proc T 38.9821 $2,126.90 $1,042.18 $425.38 0203 Level IV Nerve Injections T 11.5969 $632.74 $276.76 $126.55 0204 Level I Nerve Injections T 2.1711 $118.46 $40.13 $23.69 0206 Level II Nerve Injections T 5.2875 $288.49 $75.55 $57.70 0207 Level III Nerve Injections T 6.4554 $352.21 $123.69 $70.44 0208 Laminotomies and Laminectomies T 40.2830 $2,197.88 $439.58 0209 Extended EEG Studies and Sleep Studies, Level II S 11.5435 $629.82 $280.58 $125.96 0212 Nervous System Injections T 2.9739 $162.26 $74.67 $32.45 0213 Extended EEG Studies and Sleep Studies, Level I S 2.9055 $158.53 $65.74 $31.71 0214 Electroencephalogram S 2.2176 $120.99 $58.12 $24.20 0215 Level I Nerve and Muscle Tests S 0.6457 $35.23 $15.76 $7.05 0216 Level III Nerve and Muscle Tests S 2.8535 $155.69 $67.98 $31.14 0218 Level II Nerve and Muscle Tests S 1.1404 $62.22 $12.44 0220 Level I Nerve Procedures T 16.5554 $903.28 $180.66 0221 Level II Nerve Procedures T 24.8875 $1,357.89 $463.62 $271.58 0222 Implantation of Neurological Device T 232.2024 $12,669.20 $2,533.84 0223 Implantation or Revision of Pain Management Catheter T 26.7610 $1,460.11 $292.02 0224 Implantation of Reservoir/Pump/Shunt T 34.1770 $1,864.73 $453.41 $372.95 0225 Level I Implementation of Neurostimulator Electrodes S 206.0034 $11,239.75 $2,247.95 0226 Implantation of Drug Infusion Reservoir T 136.2989 $7,436.60 $1,487.32 0227 Implantation of Drug Infusion Device T 160.8363 $8,775.39 $1,755.08 0228 Creation of Lumbar Subarachnoid Shunt T 52.2880 $2,852.89 $639.03 $570.58 0229 Transcatherter Placement of Intravascular Shunt T 61.9895 $3,382.21 $771.23 $676.44 0230 Level I Eye Tests & Treatments S 0.7619 $41.57 $14.97 $8.31 0231 Level III Eye Tests & Treatments S 2.1883 $119.40 $50.94 $23.88 0232 Level I Anterior Segment Eye Procedures T 4.9206 $268.47 $103.17 $53.69 0233 Level II Anterior Segment Eye Procedures T 14.4205 $786.80 $266.33 $157.36 0234 Level III Anterior Segment Eye Procedures T 21.4631 $1,171.05 $511.31 $234.21 0235 Level I Posterior Segment Eye Procedures T 5.0749 $276.89 $72.04 $55.38 0236 Level II Posterior Segment Eye Procedures T 18.6701 $1,018.66 $203.73 0237 Level III Posterior Segment Eye Procedures T 34.1784 $1,864.81 $818.54 $372.96 0238 Level I Repair and Plastic Eye Procedures T 3.1954 $174.34 $58.96 $34.87 0239 Level II Repair and Plastic Eye Procedures T 6.1331 $334.63 $66.93 0240 Level III Repair and Plastic Eye Procedures T 17.4535 $952.28 $315.31 $190.46 0241 Level IV Repair and Plastic Eye Procedures T 22.1969 $1,211.09 $384.47 $242.22 0242 Level V Repair and Plastic Eye Procedures T 29.4294 $1,605.70 $597.36 $321.14 0243 Strabismus/Muscle Procedures T 21.7323 $1,185.74 $431.39 $237.15 0244 Corneal Transplant T 37.6284 $2,053.04 $803.26 $410.61 0245 Level I Cataract Procedures without IOL Insert T 12.2973 $670.95 $222.22 $134.19 0246 Cataract Procedures with IOL Insert T 22.9755 $1,253.57 $495.96 $250.71 0247 Laser Eye Procedures Except Retinal T 4.9482 $269.98 $104.31 $54.00 0248 Laser Retinal Procedures T 4.8223 $263.11 $95.08 $52.62 0249 Level II Cataract Procedures without IOL Insert T 27.7406 $1,513.55 $524.67 $302.71 0250 Nasal Cauterization/Packing T 1.4697 $80.19 $28.07 $16.04 0251 Level I ENT Procedures T 1.7880 $97.56 $19.51 0252 Level II ENT Procedures T 6.4469 $351.75 $113.41 $70.35 0253 Level III ENT Procedures T 15.2249 $830.69 $282.29 $166.14 0254 Level IV ENT Procedures T 21.8901 $1,194.35 $321.35 $238.87 0256 Level V ENT Procedures T 35.1548 $1,918.08 $383.62 0258 Tonsil and Adenoid Procedures T 20.6265 $1,125.40 $437.25 $225.08 Start Printed Page 836 0259 Level VI ENT Procedures T 392.8622 $21,434.95 $9,394.83 $4,286.99 0260 Level I Plain Film Except Teeth X 0.7802 $42.57 $21.28 $8.51 0261 Level II Plain Film Except Teeth Including Bone Density Measurement X 1.3176 $71.89 $14.38 0262 Plain Film of Teeth X 0.7540 $41.14 $9.82 $8.23 0263 Level I Miscellaneous Radiology Procedures X 2.1883 $119.40 $43.58 $23.88 0264 Level II Miscellaneous Radiology Procedures X 3.0287 $165.25 $79.41 $33.05 0265 Level I Diagnostic Ultrasound Except Vascular S 1.0289 $56.14 $28.07 $11.23 0266 Level II Diagnostic Ultrasound Except Vascular S 1.6117 $87.94 $43.97 $17.59 0267 Level III Diagnostic Ultrasound Except Vascular S 2.4586 $134.14 $65.52 $26.83 0268 Ultrasound Guidance Procedures S 1.3081 $71.37 $14.27 0269 Level III Echocardiogram Except Transesophageal S 3.2309 $176.28 $87.24 $35.26 0270 Transesophageal Echocardiogram S 5.8546 $319.43 $146.79 $63.89 0271 Mammography S 0.6499 $35.46 $16.80 $7.09 0272 Level I Fluoroscopy X 1.4184 $77.39 $38.36 $15.48 0274 Myelography S 3.5931 $196.04 $93.63 $39.21 0275 Arthrography S 3.2775 $178.82 $69.09 $35.76 0276 Level I Digestive Radiology S 1.5906 $86.78 $41.72 $17.36 0277 Level II Digestive Radiology S 2.4444 $133.37 $60.47 $26.67 0278 Diagnostic Urography S 2.7012 $147.38 $66.07 $29.48 0279 Level II Angiography and Venography except Extremity S 10.7073 $584.20 $174.57 $116.84 0280 Level III Angiography and Venography except Extremity S 19.1015 $1,042.20 $353.85 $208.44 0281 Venography of Extremity S 6.6031 $360.27 $115.16 $72.05 0282 Miscellaneous Computerized Axial Tomography S 1.6834 $91.85 $44.51 $18.37 0283 Computerized Axial Tomography with Contrast Material S 4.6543 $253.94 $126.27 $50.79 0284 Magnetic Resonance Imaging and Magnetic Resonance Angiography with Contras S 7.1165 $388.28 $194.13 $77.66 0285 Myocardial Positron Emission Tomography (PET) S 14.1508 $772.08 $334.45 $154.42 0287 Complex Venography S 6.4923 $354.23 $111.33 $70.85 0288 Bone Density:Axial Skeleton S 1.2726 $69.43 $13.89 0289 Needle Localization for Breast Biopsy X 3.4900 $190.42 $44.80 $38.08 0296 Level I Therapeutic Radiologic Procedures S 2.8635 $156.24 $69.20 $31.25 0297 Level II Therapeutic Radiologic Procedures S 7.7145 $420.91 $172.51 $84.18 0299 Miscellaneous Radiation Treatment S 5.7618 $314.37 $62.87 0300 Level I Radiation Therapy S 1.4912 $81.36 $16.27 0301 Level II Radiation Therapy S 2.1340 $116.43 $23.29 0302 Level III Radiation Therapy S 6.3268 $345.20 $130.77 $69.04 0303 Treatment Device Construction X 2.8835 $157.33 $66.95 $31.47 0304 Level I Therapeutic Radiation Treatment Preparation X 1.6742 $91.35 $41.52 $18.27 0305 Level II Therapeutic Radiation Treatment Preparation X 3.6767 $200.60 $91.38 $40.12 0310 Level III Therapeutic Radiation Treatment Preparation X 13.7165 $748.39 $325.27 $149.68 0312 Radioelement Applications S 3.6637 $199.90 $39.98 0313 Brachytherapy S 13.8073 $753.34 $150.67 0314 Hyperthermic Therapies S 4.6041 $251.20 $101.77 $50.24 0320 Electroconvulsive Therapy S 5.3785 $293.46 $80.06 $58.69 0321 Biofeedback and Other Training S 1.4817 $80.84 $21.78 $16.17 0322 Brief Individual Psychotherapy S 1.2802 $69.85 $13.97 0323 Extended Individual Psychotherapy S 1.8689 $101.97 $21.26 $20.39 0324 Family Psychotherapy S 2.4473 $133.53 $26.71 0325 Group Psychotherapy S 1.4865 $81.10 $18.27 $16.22 0330 Dental Procedures S 0.5745 $31.35 $6.27 0332 Computerized Axial Tomography and Computerized Angiography without Contras S 3.3936 $185.16 $91.27 $37.03 0333 Computerized Axial Tomography and Computerized Angio w/o Contrast Material S 5.4241 $295.94 $146.98 $59.19 0335 Magnetic Resonance Imaging, Miscellaneous S 6.3499 $346.46 $151.46 $69.29 0336 Magnetic Resonance Imaging and Magnetic Resonance Angiography without Cont S 6.3897 $348.63 $174.31 $69.73 0337 MRI and Magnetic Resonance Angiography without Contrast Material followed S 9.2075 $502.37 $240.77 $100.47 0339 Observation S 6.6961 $365.35 $73.07 0340 Minor Ancillary Procedures X 0.6314 $34.45 $6.89 0341 Skin Tests X 0.1365 $7.45 $3.03 $1.49 0342 Level I Pathology X 0.2162 $11.80 $5.88 $2.36 0343 Level II Pathology X 0.4617 $25.19 $12.55 $5.04 0344 Level III Pathology X 0.6291 $34.32 $17.16 $6.86 0345 Level I Transfusion Laboratory Procedures X 0.2550 $13.91 $3.10 $2.78 0346 Level II Transfusion Laboratory Procedures X 0.3866 $21.09 $5.32 $4.22 0347 Level III Transfusion Laboratory Procedures X 0.9610 $52.43 $13.20 $10.49 Start Printed Page 837 0348 Fertility Laboratory Procedures X 0.8194 $44.71 $8.94 0352 Level I Injections X 0.1230 $6.71 $1.34 0353 Level II Allergy Injections X 0.3982 $21.73 $4.35 0355 Level III Immunizations K 0.2749 $15.00 $3.00 0356 Level IV Immunizations K 0.7698 $42.00 $8.40 0359 Level II Injections X 0.8000 $43.65 $8.73 0360 Level I Alimentary Tests X 1.7313 $94.46 $42.45 $18.89 0361 Level II Alimentary Tests X 3.5510 $193.75 $83.23 $38.75 0362 Level III Otorhinolaryngologic Function Tests X 2.6984 $147.23 $29.45 0363 Level I Otorhinolaryngologic Function Tests X 0.8641 $47.15 $17.44 $9.43 0364 Level I Audiometry X 0.4459 $24.33 $9.06 $4.87 0365 Level II Audiometry X 1.2132 $66.19 $18.95 $13.24 0367 Level I Pulmonary Test X 0.5887 $32.12 $15.16 $6.42 0368 Level II Pulmonary Tests X 0.9319 $50.85 $25.42 $10.17 0369 Level III Pulmonary Tests X 2.4984 $136.32 $44.18 $27.26 0370 Allergy Tests X 0.9185 $50.11 $11.58 $10.02 0371 Level I Allergy Injections X 0.4105 $22.40 $4.48 0372 Therapeutic Phlebotomy X 0.5607 $30.59 $10.09 $6.12 0373 Neuropsychological Testing X 2.3288 $127.06 $25.41 0374 Monitoring Psychiatric Drugs X 1.1252 $61.39 $12.28 0375 Ancillary Outpatient Services When Patient Expires T $1,150.00 $230.00 0376 Level II Cardiac Imaging S 4.4510 $242.85 $121.42 $48.57 0377 Level III Cardiac Imaging S 6.8830 $375.54 $187.76 $75.11 0378 Level II Pulmonary Imaging S 5.4852 $299.28 $149.63 $59.86 0379 Injection adenosine 6 Mg K 0.2078 $11.34 $2.27 0380 Dipyridamole injection K 0.2525 $13.78 $2.76 0384 GI Procedures with Stents T 36.5400 $1,993.66 $433.01 $398.73 0385 Level I Prosthetic Urological Procedures S 67.1530 $3,663.93 $732.79 0386 Level II Prosthetic Urological Procedures S 116.2382 $6,342.07 $1,268.41 0387 Level II Hysteroscopy T 28.1480 $1,535.78 $655.55 $307.16 0388 Discography S 11.6347 $634.80 $303.19 $126.96 0389 Non-imaging Nuclear Medicine S 1.6328 $89.09 $44.54 $17.82 0390 Level I Endocrine Imaging S 2.7907 $152.26 $76.13 $30.45 0391 Level II Endocrine Imaging S 3.1956 $174.36 $87.18 $34.87 0393 Red Cell/Plasma Studies S 4.4354 $242.00 $121.00 $48.40 0394 Hepatobiliary Imaging S 4.3714 $238.51 $119.25 $47.70 0395 GI Tract Imaging S 3.9536 $215.71 $107.85 $43.14 0396 Bone Imaging S 4.1883 $228.52 $114.26 $45.70 0397 Vascular Imaging S 2.2183 $121.03 $60.51 $24.21 0398 Level I Cardiac Imaging S 4.5091 $246.02 $123.01 $49.20 0399 Nuclear Medicine Add-on Imaging S 1.5273 $83.33 $41.66 $16.67 0400 Hematopoietic Imaging S 3.8242 $208.65 $104.32 $41.73 0401 Level I Pulmonary Imaging S 3.3736 $184.07 $92.03 $36.81 0402 Brain Imaging S 5.4063 $294.97 $147.48 $58.99 0403 CSF Imaging S 3.8402 $209.53 $104.76 $41.91 0404 Renal and Genitourinary Studies Level I S 3.7303 $203.53 $101.76 $40.71 0405 Renal and Genitourinary Studies Level II S 4.3432 $236.97 $118.48 $47.39 0406 Tumor/Infection Imaging S 4.3955 $239.82 $119.91 $47.96 0407 Radionuclide Therapy S 3.5841 $195.55 $97.77 $39.11 0409 Red Blood Cell Tests X 0.1390 $7.58 $2.32 $1.52 0410 Mammogram Add On S 0.1523 $8.31 $1.66 0411 Respiratory Procedures S 0.4367 $23.83 $4.77 0412 IMRT Treatment Delivery S 5.3904 $294.11 $58.82 0415 Level II Endoscopy Lower Airway T 20.7348 $1,131.31 $459.92 $226.26 0600 Low Level Clinic Visits V 0.9278 $50.62 $10.12 0601 Mid Level Clinic Visits V 0.9816 $53.56 $10.71 0602 High Level Clinic Visits V 1.5041 $82.07 $16.41 0610 Low Level Emergency Visits V 1.3691 $74.70 $19.57 $14.94 0611 Mid Level Emergency Visits V 2.3967 $130.77 $36.16 $26.15 0612 High Level Emergency Visits V 4.1476 $226.30 $54.12 $45.26 0620 Critical Care S 8.9992 $491.01 $142.30 $98.20 0648 Breast Reconstruction with Prosthesis T 54.0165 $2,947.19 $589.44 0651 Complex Interstitial Radiation Source Application S 10.2314 $558.24 $111.65 0652 Insertion of Intraperitoneal Catheters T 27.0364 $1,475.13 $295.03 0653 Vascular Reconstruction/Fistula Repair with Device T 30.0334 $1,638.65 $327.73 0654 Insertion/Replacement of a permanent dual chamber pacemaker T 112.6957 $6,148.79 $1,229.76 0655 Insertion/Replacement/Conversion of a permanent dual chamber pacemaker T 142.7039 $7,786.07 $1,557.21 Start Printed Page 838 0656 Transcatheter Placement of Intracoronary Drug-Eluting Stents T 103.4907 $5,646.56 $1,129.31 0657 Placement of Tissue Clips S 1.5102 $82.40 $16.48 0658 Percutaneous Breast Biopsies T 5.5779 $304.34 $60.87 0659 Hyperbaric Oxygen S 3.0228 $164.93 $32.99 660 Level II Otorhinolaryngologic Function Tests X 1.7353 $94.68 $30.66 $18.94 0661 Level IV Pathology X 3.2576 $177.74 $88.87 $35.55 0662 CT Angiography S 5.8775 $320.68 $156.47 $64.14 0664 Proton Beam Radiation Therapy S 9.7295 $530.85 $106.17 0665 Bone Density: Appendicular Skeleton S 0.7257 $39.59 $7.92 0668 Level I Angiography and Venography except Extremity S 10.2660 $560.12 $237.76 $112.02 0669 Digital Mammography S 0.9009 $49.15 $9.83 0670 Intravenous and Intracardiac Ultrasound S 27.4483 $1,497.61 $542.37 $299.52 0671 Level II Echocardiogram Except Transesophageal S 1.6384 $89.39 $44.69 $17.88 0672 Level IV Posterior Segment Procedures T 38.9476 $2,125.02 $988.43 $425.00 0673 Level IV Anterior Segment Eye Procedures T 26.8390 $1,464.36 $649.56 $292.87 0674 Prostate Cryoablation T 119.9733 $6,545.86 $1,309.17 0675 Prostatic Thermotherapy T 49.3452 $2,692.32 $538.46 0676 Level II Transcatheter Thrombolysis T 2.7315 $149.03 $40.30 $29.81 0677 Level I Transcatheter Thrombolysis T 2.1805 $118.97 $23.79 0678 External Counterpulsation T 2.0659 $112.72 $22.54 0679 Level II Resuscitation and Cardioversion S 5.4887 $299.47 $95.30 $59.89 0680 Insertion of Patient Activated Event Recorders S 62.8252 $3,427.81 $685.56 0681 Knee Arthroplasty T 98.1613 $5,355.78 $2,131.36 $1,071.16 0682 Level V Debridement & Destruction T 8.0790 $440.80 $174.57 $88.16 0683 Level II Photochemotherapy S 1.5489 $84.51 $30.42 $16.90 0685 Level III Needle Biopsy/Aspiration Except Bone Marrow T 4.8100 $262.44 $115.47 $52.49 0686 Level III Skin Repair T 7.9247 $432.38 $198.89 $86.48 0687 Revision/Removal of Neurostimulator Electrodes T 20.4416 $1,115.31 $513.05 $223.06 0688 Revision/Removal of Neurostimulator Pulse Generator Receiver T 46.7347 $2,549.89 $1,249.45 $509.98 0689 Electronic Analysis of Cardioverter-defibrillators S 0.5533 $30.19 $6.04 0690 Electronic Analysis of Pacemakers and other Cardiac Devices S 0.4074 $22.23 $10.63 $4.45 0691 Electronic Analysis of Programmable Shunts/Pumps S 2.8066 $153.13 $76.56 $30.63 0692 Electronic Analysis of Neurostimulator Pulse Generators S 1.1057 $60.33 $30.16 $12.07 0693 Level II Breast Reconstruction T 39.0111 $2,128.48 $798.17 $425.70 0694 Mohs Surgery T 2.9752 $162.33 $64.93 $32.47 0695 Level VII Debridement & Destruction T 19.1849 $1,046.75 $266.59 $209.35 0697 Level I Echocardiogram Except Transesophageal S 1.4415 $78.65 $39.32 $15.73 0698 Level II Eye Tests & Treatments S 0.9599 $52.37 $18.72 $10.47 0699 Level IV Eye Tests & Treatments T 2.2303 $121.69 $47.46 $24.34 0700 Antepartum Manipulation T 2.4306 $132.62 $37.13 $26.52 0701 SR 89 chloride, per mCi K $892.43 $178.49 0702 SM 153 lexidronam, 50 mCi K $493.89 $98.78 0704 IN 111 Satumomab pendetide per dose K $1,474.00 $294.80 0705 Technetium TC99M tetrofosmin K 1.0642 $665.28 $133.06 0726 Dexrazoxane hcl injection, 250 mg K 2.0616 $112.48 $22.50 0728 Filgrastim 300 mcg injection K $172.20 $34.44 0730 Pamidronate disodium , 30 mg K $128.74 $25.75 0731 Sargramostim injection K $26.92 $5.38 0732 Mesna injection 200 mg K $17.66 $3.53 0733 Non esrd epoetin alpha inj, 1000 u K $11.76 $2.35 0734 Injection, darbepoetin alfa (for non-ESRD), per 1 mcg K $3.88 $0.78 0763 Dolasetron mesylate oral K $152.38 $30.48 0764 Granisetron HCl injection K $17.18 $3.44 0765 Granisetron HCl 1 mg oral K $171.78 $34.36 0800 Leuprolide acetate, 3.75 mg K $479.20 $95.84 0802 Etoposide oral 50 mg K $21.91 $4.38 0807 Aldesleukin/single use vial K $680.35 $136.07 0809 Bcg live intravesical vac K $77.54 $15.51 0810 Goserelin acetate implant 3.6 mg K $413.59 $82.72 0811 Carboplatin injection 50 mg K $137.79 $27.56 0813 Cisplatin 10 mg injection K $7.73 $1.55 0814 Asparaginase injection K $58.00 $11.60 0815 Cyclophosphamide 100 MG inj K $2.77 $0.55 0816 Cyclophosphamide lyophilized K $2.36 $0.47 0817 Cytarabine hcl 100 MG inj K $1.55 $0.31 0819 Dacarbazine 100 mg inj K 0.0974 $5.31 $1.06 Start Printed Page 839 0820 Daunorubicin 10 mg K $35.94 $7.19 0821 Daunorubicin citrate liposom 10 mg K $64.60 $12.92 0823 Docetaxel, 20 mg K $331.53 $66.31 0824 Etoposide 10 MG inj K $0.83 $0.17 0827 Floxuridine injection 500 mg K $66.24 $13.25 0828 Gemcitabine HCL 200 mg K $112.09 $22.42 0830 Irinotecan injection 20 mg K $135.00 $27.00 0831 Ifosfomide injection 1 gm K $72.81 $14.56 0832 Idarubicin hcl injection 5 mg K 3.2663 $178.21 $35.64 0834 Interferon alfa-2a inj K $32.31 $6.46 0836 Interferon alfa-2b inj recombinant, 1 million K $13.78 $2.76 0838 Interferon gamma 1-b inj, 3 million u K $290.70 $58.14 0840 Melphalan hydrochl 50 mg K $389.14 $77.83 0842 Fludarabine phosphate inj 50 mg K $329.83 $65.97 0844 Pentostatin injection, 10 mg K $1,784.64 $356.93 0847 Doxorubic hcl 10 MG vl chemo K $4.69 $0.94 0849 Rituximab, 100 mg K $464.20 $92.84 0850 Streptozocin injection, 1 gm K $131.05 $26.21 0851 Thiotepa injection K $45.31 $9.06 0852 Topotecan, 4 mg K $739.80 $147.96 0855 Vinorelbine tartrate, 10 mg K $100.97 $20.19 0856 Porfimer sodium, 75 mg K $2,411.82 $482.36 0857 Bleomycin sulfate injection 15 u K $88.32 $17.66 0858 Cladribine, 1mg K $24.84 $4.97 0860 Plicamycin (mithramycin) inj K $86.89 $17.38 0861 Leuprolide acetate injection 1 mg K $14.48 $2.90 0862 Mitomycin 5 mg inj K $30.91 $6.18 0863 Paclitaxel injection, 30 mg K $79.04 $15.81 0864 Mitoxantrone hcl, 5 mg K $332.87 $66.57 0865 Interferon alfa-n3 inj, human leukocyte derived, 2 K $8.17 $1.63 0884 Rho d immune globulin inj, 1 dose pkg K $92.93 $18.59 0888 Cyclosporine oral 100 mg K $2.41 $0.48 0890 Lymphocyte immune globulin 250 mg K $258.17 $51.63 0891 Tacrolimus oral per 1 mg K $3.24 $0.65 0900 Alglucerase injection, per 10 u K $37.13 $7.43 0901 Alpha 1 proteinase inhibitor, 10 mg K $3.43 $0.69 0902 Botulinum toxin a, per unit K $4.58 $0.92 0903 Cytomegalovirus imm IV/vial K $659.60 $131.92 0905 Immune globulin, 1g K $37.95 $7.59 0906 RSV-ivig, 50 mg K $16.55 $3.31 0907 Ganciclovir sodium injection K 0.5918 $32.29 $6.46 0909 Interferon beta-1a, 33 mcg K $123.77 $24.75 0910 Interferon beta-1b /0.25 mg K $67.22 $13.44 0911 Streptokinase per 250,000 iu K 1.5733 $85.84 $17.17 0913 Ganciclovir long act implant K 1.5861 $86.54 $17.31 0916 Imiglucerase injection/unit K $3.71 $0.74 0917 Adenosine injection K 1.0393 $56.71 $11.34 0925 Factor viii per iu K $0.42 $0.08 0926 Factor VIII (porcine) per iu K $1.89 $0.38 0927 Factor viii recombinant per iu K $0.61 $0.12 0928 Factor ix complex per iu K $0.18 $0.04 0929 Anti-inhibitor per iu K $0.69 $0.14 0931 Factor IX non-recombinant, per iu K $0.51 $0.10 0932 Factor IX recombinant, per iu K $1.04 $0.21 0949 Plasma, Pooled Multiple Donor, Solvent/Detergent K $124.31 $24.86 0950 Blood (Whole) For Transfusion K $87.93 $17.59 0952 Cryoprecipitate K $29.31 $5.86 0954 RBC leukocytes reduced K $119.26 $23.85 0955 Plasma, Fresh Frozen K $95.00 $19.00 0956 Plasma Protein Fraction K $92.98 $18.60 0957 Platelet Concentrate K $41.44 $8.29 0958 Platelet Rich Plasma K $53.56 $10.71 0959 Red Blood Cells K $86.41 $17.28 0960 Washed Red Blood Cells K $160.69 $32.14 0961 Infusion, Albumin (Human) 5%, 50 ml K 0.2802 $15.29 $3.06 0963 Albumin (human), 5%, 250 ml K 1.0901 $59.48 $11.90 0964 Albumin (human), 25%, 20 ml K 0.3741 $20.41 $4.08 0965 Albumin (human), 25%, 50ml K 0.8869 $48.39 $9.68 0966 Plasmaprotein fract,5%,250ml K $464.90 $92.98 Start Printed Page 840 1009 Cryoprecip reduced plasma K $37.39 $7.48 1010 Blood, L/R, CMV-neg K $121.78 $24.36 1011 Platelets, HLA-m, L/R, unit K $499.77 $99.95 1013 Platelet concentrate, L/R, unit K $49.52 $9.90 1016 Blood, L/R, froz/deglycerol/washed K $301.68 $60.34 1017 Platelets, aph/pher, L/R, CMV-neg, unit K $393.15 $78.63 1018 Blood, L/R, irradiated K $132.40 $26.48 1019 Platelets, aph/pher, L/R, irradiated, unit K $406.28 $81.26 1020 Pit, pher,L/R,CMV,irrad K $495.22 $99.04 1021 RBC, frz/deg/wsh, L/R, irrad K $336.04 $67.21 1022 RBC, L/R, CMV neg, irrad K $201.12 $40.22 1045 Iobenguane sulfate I-131per 0.5 mCi K 3.0392 $165.82 $33.16 1064 I-131 sodium iodide capsule K 0.1004 $5.48 $1.10 1065 I-131 sodium iodide solution K 0.1189 $6.49 $1.30 1079 CO 57/58 per 0.5 uCi K $235.14 $47.03 1080 I-131 tositumomab, dx K $2,565.55 $513.11 1081 I-131 tositumomab, tx K $22,210.19 $4,442.04 1084 Denileukin diftitox, 300 MCG K $1,232.88 $246.58 1086 Temozolomide,oral 5 mg K $6.81 $1.36 1089 Cyanocobalamin cobalt co57 K $47.38 $9.48 1091 IN 111 Oxyquinoline, per .5 mCi K 4.1151 $224.52 $44.90 1092 IN 111 Pentetate, per 0.5 mCi K $237.60 $47.52 1095 Technetium TC 99M Depreotide K $704.00 $140.80 1096 TC 99M Exametazime, per dose K $825.00 $165.00 1122 TC 99M arcitumomab, per vial K $1,144.00 $228.80 1166 Cytarabine liposome K $344.08 $68.82 1167 Epirubicin hcl, 2 mg K $25.60 $5.12 1178 Busulfan IV, 6 mg K $27.87 $5.57 1200 TC 99M Sodium Glucoheptonat K $30.28 $6.06 1201 TC 99M SUCCIMER, PER Vial K $125.66 $25.13 1203 Verteporfin for injection K $1,350.80 $270.16 1207 Octreotide injection, depd K $73.62 $14.72 1305 Apligraf K $1,199.00 $239.80 1409 Factor viia recombinant, per 1.2 mg K $1,495.30 $299.06 1501 New Technology - Level I ($0-$50) S $25.00 $5.00 1502 New Technology - Level II ($50-$100) S $75.00 $15.00 1503 New Technology - Level III ($100-$200) S $150.00 $30.00 1504 New Technology - Level IV ($200-$300) S $250.00 $50.00 1505 New Technology - Level V ($300-$400) S $350.00 $70.00 1506 New Technology - Level VI ($400-$500) S $450.00 $90.00 1507 New Technology - Level VII ($500-$600) S $550.00 $110.00 1508 New Technology - Level VIII ($600-$700) S $650.00 $130.00 1509 New Technology - Level IX ($700-$800) S $750.00 $150.00 1510 New Technology - Level X ($800-$900) S $850.00 $170.00 1511 New Technology - Level XI ($900-$1000) S $950.00 $190.00 1512 New Technology - Level XII ($1000-$1100) S $1,050.00 $210.00 1513 New Technology - Level XIII ($1100-$1200) S $1,150.00 $230.00 1514 New Technology - Level XIV ($1200-$1300) S $1,250.00 $250.00 1515 New Technology - Level XV ($1300-$1400) S $1,350.00 $270.00 1516 New Technology - Level XVI ($1400-$1500) S $1,450.00 $290.00 1517 New Technology - Level XVII ($1500-$1600) S $1,550.00 $310.00 1518 New Technology - Level XVIII ($1600-$1700) S $1,650.00 $330.00 1519 New Technology - Level IXX ($1700-$1800) S $1,750.00 $350.00 1520 New Technology - Level XX ($1800-$1900) S $1,850.00 $370.00 1521 New Technology - Level XXI ($1900-$2000) S $1,950.00 $390.00 1522 New Technology - Level XXII ($2000-$2500) S $2,250.00 $450.00 1523 New Technology - Level XXIII ($2500-$3000) S $2,750.00 $550.00 1524 New Technology - Level XIV ($3000-$3500) S $3,250.00 $650.00 1525 New Technology - Level XXV ($3500-$4000) S $3,750.00 $750.00 1526 New Technology - Level XXVI ($4000-$4500) S $4,250.00 $850.00 1527 New Technology - Level XXVII ($4500-$5000) S $4,750.00 $950.00 1528 New Technology - Level XXVIII ($5000-$5500) S $5,250.00 $1,050.00 1529 New Technology - Level XXIX ($5500-$6000) S $5,750.00 $1,150.00 1530 New Technology - Level XXX ($6000-$6500) S $6,250.00 $1,250.00 1531 New Technology - Level XXXI ($6500-$7000) S $6,750.00 $1,350.00 1532 New Technology - Level XXXII ($7000-$7500) S $7,250.00 $1,450.00 1533 New Technology - Level XXXIII ($7500-$8000) S $7,750.00 $1,550.00 1534 New Technology - Level XXXIV ($8000-$8500) S $8,250.00 $1,650.00 1535 New Technology - Level XXXV ($8500-$9000) S $8,750.00 $1,750.00 Start Printed Page 841 1536 New Technology - Level XXXVI ($9000-$9500) S $9,250.00 $1,850.00 1537 New Technology - Level XXXVII ($9500-$10000) S $9,750.00 $1,950.00 1538 New Technology - Level I ($0-$50) T $25.00 $5.00 1539 New Technology - Level II ($50-$100) T $75.00 $15.00 1540 New Technology - Level III ($100-$200) T $150.00 $30.00 1541 New Technology - Level IV ($200-$300) T $250.00 $50.00 1542 New Technology - Level V ($300-$400) T $350.00 $70.00 1543 New Technology - Level VI ($400-$500) T $450.00 $90.00 1544 New Technology - Level VII ($500-$600) T $550.00 $110.00 1545 New Technology - Level VIII ($600-$700) T $650.00 $130.00 1546 New Technology - Level IX ($700-$800) T $750.00 $150.00 1547 New Technology - Level X ($800-$900) T $850.00 $170.00 1548 New Technology - Level XI ($900-$1000) T $950.00 $190.00 1549 New Technology - Level XII ($1000-$1100) T $1,050.00 $210.00 1550 New Technology - Level XIII ($1100-$1200) T $1,150.00 $230.00 1551 New Technology - Level XIV ($1200-$1300) T $1,250.00 $250.00 1552 New Technology - Level XV ($1300-$1400) T $1,350.00 $270.00 1553 New Technology - Level XVI ($1400-$1500) T $1,450.00 $290.00 1554 New Technology - Level XVII ($1500-$1600) T $1,550.00 $310.00 1555 New Technology - Level XVIII ($1600-$1700) T $1,650.00 $330.00 1556 New Technology - Level XIX ($1700-$1800) T $1,750.00 $350.00 1557 New Technology - Level XX ($1800-$1900) T $1,850.00 $370.00 1558 New Technology - Level XXI ($1900-$2000) T $1,950.00 $390.00 1559 New Technology - Level XXII ($2000-$2500) T $2,250.00 $450.00 1560 New Technology - Level XXIII ($2500-$3000) T $2,750.00 $550.00 1561 New Technology - Level XXIV ($3000-$3500) T $3,250.00 $650.00 1562 New Technology - Level XXV ($3500-$4000) T $3,750.00 $750.00 1563 New Technology - Level XXVI ($4000-$4500) T $4,250.00 $850.00 1564 New Technology - Level XXVII ($4500-$5000) T $4,750.00 $950.00 1565 New Technology - Level XXVIII ($5000-$5500) T $5,250.00 $1,050.00 1566 New Technology - Level XXIX ($5500-$6000) T $5,750.00 $1,150.00 1567 New Technology - Level XXX ($6000-$6500) T $6,250.00 $1,250.00 1568 New Technology - Level XXXI ($6500-$7000) T $6,750.00 $1,350.00 1569 New Technology - Level XXXII ($7000-$7500) T $7,250.00 $1,450.00 1570 New Technology - Level XXXIII ($7500-$8000) T $7,750.00 $1,550.00 1571 New Technology - Level XXXIV ($8000-$8500) T $8,250.00 $1,650.00 1572 New Technology - Level XXXV ($8500-$9000) T $8,750.00 $1,750.00 1573 New Technology - Level XXXVI ($9000-$9500) T $9,250.00 $1,850.00 1574 New Technology - Level XXXVII ($9500-$10000) T $9,750.00 $1,950.00 1600 Technetium TC 99m sestamibi K $112.73 $22.55 1603 Thallous chloride TL 201/mci K $18.29 $3.66 1604 IN 111 capromab pendetide, per dose K $2,030.60 $406.12 1605 Abciximab injection, 10 mg K $475.22 $95.04 1606 Anistreplase, 30 u K $2,495.31 $499.06 1607 Eptifibatide injection, 5mg K $11.88 $2.38 1608 Etanercept injection K $143.73 $28.75 1609 Rho(D) immune globulin h, sd, 100 iu K $19.03 $3.81 1611 Hylan G-F 20 injection, 16 mg K $215.97 $43.19 1612 Daclizumab, parenteral, 25 mg K $393.78 $78.76 1613 Trastuzumab, 10 mg K $53.85 $10.77 1614 Valrubicin, 200 mg K $487.87 $97.57 1615 Basiliximab, 20 mg K $1,425.06 $285.01 1618 Vonwillebrandfactrcmplx, per iu K $0.46 $0.09 1619 Gallium ga 67 K 0.2056 $11.22 $2.24 1620 Technetium tc99m bicisate K $392.93 $78.59 1622 Technetium tc99m mertiatide K $1,650.00 $330.00 1624 Sodium phosphate p32 K $66.44 $13.29 1625 Indium 111-in pentetreotide K $1,144.00 $228.80 1628 Chromic phosphate p32 K $81.27 $16.25 1716 Brachytx source, Gold 198 H 1717 Brachytx source, HDR Ir-192 H 1718 Brachytx source, Iodine 125 H 1719 Brachytx source,Non-HDR Ir-192 H 1720 Brachytx source, Palladium 103 H 1775 FDG, per dose (4-40 mCi/ml) K 5.9471 $324.48 $64.90 1783 Ocular implant, aqueous drain device H $- 1814 Retinal Tamp, silicone oil H $- 1818 Integrated keratoprosthesis H $- 1819 Tissue localization-excision dev H $- Start Printed Page 842 1884 Embolization Protect syst H $- 1888 Catheter, ablation, non-cardiac, endovascular (implantable) H $- 1900 Lead coronary venous H $- 2614 Probe, percutaneous lumbar disc H $- 2616 Brachytx source, Yttrium-90 H 2632 Brachytx sol, I-125, per mCi H $- 2633 Brachytx source, Cesium-131 H 7000 Amifostine, 500 mg K $419.59 $83.92 7007 Inj milrinone lactate, per 5 mg K 0.2129 $11.62 $2.32 7011 Oprelvekin injection, 5 mg K $248.16 $49.63 7015 Busulfan, oral, 2 mg K $1.93 $0.39 7019 Aprotinin, 10,000 kiu K $13.26 $2.65 7024 Corticorelin ovine triflutat K $375.00 $75.00 7025 Digoxin immune FAB (ovine) K $1.79 $0.36 7026 Ethanolamine oleate 100 mg K $67.10 $13.42 7027 Fomepizole, 15mg K $10.65 $2.13 7028 Fosphenytoin, 50 mg K $5.63 $1.13 7030 Hemin, per 1 mg K $6.86 $1.37 7031 Octreotide acetate injection K $3.94 $0.79 7034 Somatropin injection K $297.79 $59.56 7035 Teniposide, 50 mg K $238.49 $47.70 7036 Urokinase 250,000 iu inj K 3.7855 $206.54 $41.31 7037 Urofollitropin, 75 iu K 1.1634 $63.48 $12.70 7038 Muromonab-CD3, 5 mg K $792.33 $158.47 7040 Pentastarch 10% solution K $139.94 $27.99 7041 Tirofiban hydrochloride 12.5 mg K $436.66 $87.33 7042 Capecitabine, oral, 150 mg K $3.14 $0.63 7043 Infliximab injection 10 mg K $31.81 $6.36 7045 Trimetrexate glucoronate K $132.00 $26.40 7046 Doxorubicin hcl liposome inj 10 mg K $364.49 $72.90 7048 Alteplase recombinant K 0.2856 $15.58 $3.12 7049 Filgrastim 480 mcg injection K $290.93 $58.19 7051 Leuprolide acetate implant, 65 mg K $5,001.92 $1,000.38 7316 Sodium hyaluronate injection K $67.16 $13.43 9001 Linezolid injection K $34.09 $6.82 9002 Tenecteplase, 50mg/vial K $2,492.60 $498.52 9003 Palivizumab, per 50mg K $611.24 $122.25 9004 Gemtuzumab ozogamicin inj,5mg K $2,022.90 $404.58 9005 Reteplase injection K $1,263.90 $252.78 9006 Tacrolimus injection K $110.04 $22.01 9008 Baclofen Refill Kit-500mcg K $73.92 $14.78 9009 Baclofen refill kit - per 2000 mcg K 0.7499 $40.92 $8.18 9010 Baclofen refill kit - per 4000 mcg K $79.82 $15.96 9012 Arsenic Trioxide K $34.32 $6.86 9013 Co 57 cobaltous chloride K $56.67 $11.33 9015 Mycophenolate mofetil oral 250 mg K $1.36 $0.27 9018 Botulinum toxin B, per 100 u K $8.14 $1.63 9019 Caspofungin acetate, 5 mg K $30.52 $6.10 9020 Sirolimus tablet, 1 mg K $6.60 $1.32 9021 Immune globulin 10 mg K $0.41 $0.08 9022 IM inj interferon beta 1-a K $13.36 $2.67 9023 Rho d immune globulin 50 mcg K $32.21 $6.44 9024 Amphotericin B, lipid formulation K $20.86 $4.17 9025 Radiopharms Used to Image Perfusion of Heart K $162.63 $32.53 9100 Iodinated I-131albumin, per 5 uci K $48.58 $9.72 9104 Anti-thymocycte globulin rabbit K $331.23 $66.25 9105 Hep B imm glob, per 1 ml K $65.58 $13.12 9108 Thyrotropin alfa, per 1.1 mg K $572.00 $114.40 9109 Tirofliban hcl, per 6.25 mg K $218.33 $43.67 9110 Alemtuzumab, per 10 mg K $541.46 $108.29 9111 Inj, bivalirudin, per 250 mg vial G $1.61 $0.32 9112 Perflutren lipid micro, per 2ml G $137.28 $27.46 9113 Inj, pantoprazole sodium, vial G $23.23 $4.65 9114 Nesiritide, per 0.5 mg vial G $140.45 $28.09 9115 Inj, zoledronic acid, per 1 mg G $211.07 $42.21 9116 Inj, Ertapenem sodium, per 500 mg G $21.99 $4.40 9117 Yttrium 90 ibritumomab tiuxetan K $22,210.19 $4,442.04 9118 In-111 ibritumomab tiuxetan K $2,565.55 $513.11 Start Printed Page 843 9119 Pegfilgrastim, per 1 mg G $2,596.00 $519.20 9120 Inj, Fulvestrant, per 50 mg G $78.36 $13.09 9121 Inj, Argatroban, per 5 mg G $14.63 $2.44 9122 Inj, Triptorelin pamoate, per 3.75 mg G $356.66 $59.58 9123 Transcyte, per 247 sq cm G $689.78 $115.23 9200 Orcel, per 36 cm2 G $1,051.60 $210.32 9201 Dermagraft, per 37.5 sq cm G $535.04 $107.01 9202 Octafluoropropane K $137.28 $27.46 9203 Perflexane lipid micro G $127.50 $21.30 9204 Ziprasidone mesylate G $18.60 $3.11 9205 Oxaliplatin G $8.45 $14.12 9207 Injection, bortezomib G $1,039.68 $155.40 9208 Injection, agalsidase beta G $123.78 $18.50 9209 Injection, laronidase G $644.10 $96.28 9210 Injection, palonosetron HCL G $307.80 $46.01 9211 Inj, alefacept, IV G $595.00 $99.40 9212 Inj, alefacept, IM G $422.88 $70.65 9217 Leuprolide acetate suspnsion, 7.5 mg K $576.47 $115.29 9500 Platelets, irradiated K $74.79 $14.96 9501 Platelets, pheresis K $408.81 $81.76 9502 Platelet pheresis irradiated K $443.68 $88.74 9503 Fresh frozen plasma, ea unit K $69.74 $13.95 9504 RBC deglycerolized K $183.44 $36.69 9505 RBC irradiated K $108.65 $21.73 9506 Granulocytes, pheresis K $1,248.66 $249.73 End Supplemental InformationAddendum D1.—Payment Status Indicators for the Hospital Outpatient Prospective Payment System
Indicator Item/Code/Service Explanation A Services furnished to a Hospital Outpatient that are paid under a Fee Schedule/Payment System other than OPPS, e.g.: • Ambulance Services • Clinical Diagnostic Laboratory Services • Non-Implantable Prosthetic and Orthotic Devices • EPO for ESRD Patients • Physical, Occupational and Speech Therapy • Routine Dialysis Services for ESRD Patients Provided in a Certified Dialysis Unit of a Hospital • Screening Mammography Not paid under OPPS. Paid by Intermediaries under a Fee Schedule/Payment System other than OPPS. B Codes that are not recognized by OPPS when submitted on an Outpatient Hospital Part B bill type (12x, 13x, and 14x) Not paid under OPPS. • May be paid by Intermediaries when submitted on a different bill type, e.g., 75x (CORF), but not paid under OPPS. • An alternate code that is recognized by OPPS when submitted on an Outpatient Hospital Part B bill type (12x, 13x, and 14x) may be available. C Inpatient Procedures Not paid under OPPS. Admit patient; Bill as Inpatient. D Deleted Codes Not paid under OPPS. Not paid under Medicare. E Items, Codes, and Services: • That are not covered by Medicare based on Statutory Exclusion • That are not covered by Medicare for reasons other than Statutory Exclusion • That are not recognized by Medicare but for which an alternate code for the same item or service may be available • For which separate payment is not provided by Medicare Not paid under OPPS F Corneal Tissue Acquisition; Certain CRNA Services Not paid under OPPS. Paid at reasonable cost. G Drug/Biological Pass-Through Paid under OPPS; Separate APC payment includes Pass-Through amount. H Device Category Pass-Through and Brachytherapy Source Paid under OPPS; Separate cost-based K Non Pass-Through Drugs and Biologicals; Radiopharmaceutical Agents Paid under OPPS; Separate APC payment. L Influenza Vaccine; Pneumococcal Pneumonia Vaccine Not paid under OPPS. Paid at reasonable cost; Not subject to deductible or coinsurance. N Items and Services packaged into APC Rates Paid under OPPS. However, payment is packaged into payment for other services, including Outliers. Therefore, there is no separate APC payment. Start Printed Page 844 P Partial Hospitalization Paid under OPPS; Per diem APC payment. S Significant Procedure, Not Discounted when Multiple Paid under OPPS; Separate APC payment. T Significant Procedure, Multiple Procedure Reduction Applies Paid under OPPS; Separate APC payment. V Clinic or Emergency Department Visit Paid under OPPS; Separate APC payment. Y Non-Implantable Durable Medical Equipment Not paid under OPPS. All institutional providers other than Home Health Agencies bill to DMERC. X Ancillary Service Paid under OPPS; Separate APC payment. [FR Doc. 03-32322 Filed 12-31-03; 12:00 pm]
BILLING CODE 4120-01-P
Document Information
- Published:
- 01/06/2004
- Department:
- Centers for Medicare & Medicaid Services
- Entry Type:
- Rule
- Action:
- Interim final rule with comment period.
- Document Number:
- 03-32322
- Pages:
- 819-844 (26 pages)
- Docket Numbers:
- CMS-1371-IFC
- RINs:
- 0938-AM96
- Topics:
- Hospitals, Medicare, Reporting and recordkeeping requirements
- PDF File:
- 03-32322.pdf
- CFR: (4)
- 42 CFR 419.32
- 42 CFR 419.43
- 42 CFR 419.64
- 42 CFR 419.70