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HMI Cor poration First Quarter 2010 March 31, 2010 C O D I N G & B I L L I N G F O R P R O S P E C T I V E P Y M E N T S Y S T E M S Inside This Issue: Procedure and Device Edits for pril 2010 Editing of Hospital Part B Inpatient Services Clarification to Coding Requirements for Pulmonary Rehabilitation Services Warfarin Testing 2 Reporting of Outpatient Diagnostic Nuclear Medicine Procedures Human Immunodeficiency Virus (HIV) Screening Tests Coverage Determinations 3 Billing for Drugs, Biologicals and Radiopharmaceuticals Drugs and Biologicals with Payments Based on the SP Effective pril 1, 2010 Drugs and Biologicals with OPPS Pass- Through Status Effective pril 1, 2010 Correct Reporting of Biologicals When Used as Implants Correct Report of Units for Drugs Q& 6 1 1 1 2 3 4 4 4 5 5 pril 2010 Update of the Hospital Outpatient Prospective Payment System (OPPS) PROCEDURE TO DEVICE EDITS FOR PRIL 2010 Procedure-to-device edits require that when a particular procedural HCPCS code is billed, the claim must also contain an appropriate device code. Failure to pass these edits will result in the claim being returned to the provider. Device-to procedure edits require that a claim that contains one of a specific set of devices codes be returned to the provider if it fails to contain an appropriate procedure code. The updated lists of both types of edits can be found under the Device, Radiolabeled Product, and Procedure Edits subheading at: http://www.cms.hhs.gov/hospitaloutpatientpps/ EDITING OF HOSPITL PRT B INPTIENT SERVICES Blood and blood products are not included in the list of services that may be covered when furnished to persons who are inpatients but for whom no Medicare inpatient coverage is available and therefore, no Part B payment may be made for them. CMS is updating the Medicare Claims Processing Manual, Pub. 100-04, Chapter 4 Section 240.1 to add revenue codes 038X (Blood and Blood Components) and 039X (dministration, Processing and Storage for Blood and Blood Components) to the table of revenue codes that are not allowed to be reported on a claim for payment of services furnished for these patients. They also revised the instruction to indicate that these edits are currently controlled by the MC or FI and are not imbedded in the FISS. To read Transmittal 1924: go to http://www.cms.hhs.gov/transmittals/downloads/r1924cp.pdf To read MM6857: go to: http://www.cms.hhs.gov/mlnmattersrticles/downloads/mm6857.pdf CLRIFICTION TO CODING REGUIREMENTS FOR PULMORY REHBILITTION SERVICES FURNISHED ON OR FTER JNURY 1, 2010 CMS is revising Section 140.4.1 (Coding Requirements for Pulmonary Rehabilitation Services Furnished On or fter January 1, 2010), Chapter 32 in the Medicare Claims Processing Manual, Pub. 100-04. This update reflects instructions to hospitals and practitioners offices for reporting respiratory or pulmonary services furnished to a patient when those services do not meet the diagnosis and coverage criteria for pulmonary rehabilitation services. To read the changes in total go to: http://www.cms.hhs.gov/manuals/downloads/clm104c32.pdf Continued on page 2

First Quarter 2010 Page 2 pril 2010 OPPS Update cont WRFRIN TESTING Effective ugust 3, 2009, Medicare began coverage of pharmacogenomic testing to predict warfarin responsiveness only in the context of an approved, clinical study, in addition to the coverage criteria outlined in the Medicare National Coverage Determinations (NCD) Manual, Pub. 100-03, Chapter 1, Section 90.1, and in the Medicare Claims Processing Manual, Pub. 100.04, Chapter 32, Section 240. New Level II HCPCS code G9413 was developed to enable implementation of this new coverage policy. This testing is a once-in-a-lifetime test. Coding & Billing for Prospective Payment Systems Newsletter contributors and editorial board: Thomas P. Holliday, RN, P, MH G. Maria Caston, CCS, CPC-H, CCS-P, CPC, CPS, CFS Mary Quimby, CPC-H, CPS, CFS Vickie Faler, RHIT, CPC Under the hospital OPPS, HCPCS code G9143 will be assigned status indicator effective pril 2010 and payment for this lab test will be made under the clinical lab fee schedule (CLFS). However, because of CLFS payment requirements and the timing of the creation of the new code, HCPCS G9143 does not appear in the CY 2010 CLFS with an assigned rate and therefore, its CY 2010 payment shall be determined by Medicare FIs and/or /B MCs. They shall determine the hospital outpatient payment rate for HCPCS code G9143 in the same manner that payment rates for unlisted laboratory codes are currently determined. HCPCS Long Descriptor PC SI G9143 Warfarin responsiveness testing by genetic technique using any method, any number of specimen(s) REPORTING OF OUTPTIENT DIGNOSTIC NUCLER MEDICINE PROCEDURES Hospitals should only report HCPCS codes for products they provide in the hospital outpatient department and should not report a HCPCS code and charge for a radiolabeled product on the nuclear medicine procedure-to-radiolabeled product edit list solely for the purpose of bypassing those edits present in the I/OCE. The only exception to this is HCPCS code C9898 (Radiolabeled product provided during a hospital inpatient stay) which indicates that the procedure was provided during a hospital inpatient stay. s previously stated in the October 2009 update, in the rare instance when a diagnostic radiopharmaceutical may be administered to a beneficiary in a given calendar year, prior to a hospital furnishing an associated nuclear medicine procedure in the subsequent calendar year, hospitals are instructed to report the date the radiolabeled product is furnished to the beneficiary as the same date that the nuclear medicine procedure is performed. It is believed that this situation is extremely rate and it is expected that the majority of hospitals will not encounter this situation. Continued on page 3

First Quarter 2010 Page 3 pril 2010 OPPS Update cont HUMN IMMUNODEFICIENCY VIRUS (HIV) SCREENING TEST Effective December 8, 2009, Medicare covers HIV screening test for beneficiaries that are at increased risk for HIV infection per the U. S. Preventive Services Task Force (USPSTF) guidelines and beneficiaries that are pregnant whose diagnosis of pregnancy is know, during the third trimester, and at labor. Three new Level II HCPCS G-codes were created to implement this new coverage decision. The three HCPCS G-codes (G0432, G0433 and G0435) describe both standard and FD-approved rapid HIV screening tests. Under OPPS these codes will be assigned status indicator effective pril 2010 and payment for these test will be made under the clinical lab fee schedule (CLFS). However, because of CLFS payment requirements and the timing of the creation of these new codes, G0432, G0433 and G0435 do not appear in the CY 2010 CLFS with an assigned rate and therefore, their CY 2010 payment shall be determined by Medicare FIs and/or /B MCs. They shall determine the hospital outpatient payment rate for these HCPCS codes in the same manner that payment rates for unlisted laboratory codes are currently determined. HCPCS Long Descriptor PC SI G0432 G0433 G0435 Infections agent antigen detection by enzyme immunoassay (EI) technique, qualitative or semi-quantitative, multiple step method, HIV-I or HIV-2, screening Infectious agent antigen detection by enzyme-linked immunosorbent assay (ELIS) technique, antibody, HIV-1 or HIV- 2, screening Infectious agent antigen detection by rapid antibody test of oral mucosa transudate, HIV-1 or HIV-2, screening COVERGE DETERMITIONS CMS is reminding everyone in this update that the fact that a drug, device, procedure or services is assigned a HCPCS code and a payment rate under the OPPS this does not imply coverage by the Medicare program. It only indicates how the product, procedure or service may be paid if it was covered by the program. Fiscal Intermediaries (FIs)/Medicare dministrative Contractors (MCs) determine whether a drug, device, procedure, or other service meets all program requirements for coverage. Continued on page 4

First Quarter 2010 Page 4 January 2010 OPPS Update cont BILLING FOR DRUGS, BIOLOGICLS ND RDIOPHRMCEUTICLS Hospitals are strongly encouraged to report charges for all drugs, biologicals, and radiopharmaceuticals, regardless of whether the items are paid separately or packaged, using the correct HCPCS codes for the items used. It is also of great importance that hospitals billing for these products make certain that the reported units of service of the reported HCPCS codes are consistent with the quantity of a drug, biological, or radiopharmaceutical that was used in the care of the patient. Hospitals are reminded that under the OPPS, if two or more drugs or biologicals are mixed together to facilitate administration, the correct HCPCS codes should be reported separately for each product used in the care of the patient. The mixing together of two or more products does not constitute a new drug as regulated by the FD under the New Drug pplication (ND) process. DRUGS ND BIOLOGICLS WITH PYMENTS BSED ON VERGE SLES PRICE (SP) EFFECTIVE PRIL 1, 2010 For CY 2010, payment for non-pass-through drugs, biologicals and therapeutic radiopharmaceuticals is made at a single rate of SP + 4 percent, which provides payment for both the acquisition and pharmacy overhead costs associated with the drug, biological or therapeutic radiopharmaceutical. In CY 2010, a single payment of SP + 6 percent for pass-through drugs, biologicals and radiopharmaceuticals is made to provide payment for both the acquisition and pharmacy overhead costs of these pass-through items. It was noted in the second quarter of CY 2010, payment for drugs and biologicals with pass-through status is not made at the Part B Drug Competitive cquisition Program (CP) rate, as the CP program was suspended beginning January 1, 2009. Should the Part B Drug CP program be reinstituted sometime during CY 2010, you would again use the Part B drug CP rate for pass-through drugs and biologicals if they are part of the Part B drug CP program, as required by statute. DRUGS ND BIOLOGICLS WITH OPPS PSS-THROUGH STTUS EFFECTIVE PRIL 1, 2010 Six drugs and biologicals have newly been granted OPPS pass-through status effective pril 1, 2010. These items, along with their descriptors and PC assignments, are identified in the table below. HCPCS CODE LONG DESCRIPTOR PC STTUS INDICTOR EFFECTIVE 4/1/10 C9258 Injection, telavancin, 10 mg 9258 G C9259 Injection, pralatrexate, 1 mg 9259 G C9260 Injection, ofatumumab, 10 mg 9260 G C9261 Injection, ustekinumab, 1 mg 9261 G C9262 Fludarabine phosphate, oral, 1 mg 9262 G C9263 Injection, ecallantide, 1 mg 9263 G Continued on page 5

First Quarter 2010 Page 5 pril 2010 OPPS Update cont CORRECT REPORTING OF BIOLOGICLS WHEN USED S IMPLNTBLE DEVICES When billing for biologicals where the HCPCS code describes a product that is solely surgically implanted or inserted, whether the HCPCS code is indentified as having pass-through status or not, hospitals are to report the appropriate HCPCS code for the product. In circumstances where the implanted biological has pass-through status, either as a biological or a device, a separate payment for the biological or device is made. In circumstances where the implanted biological does not have pass-through status, the OPPS payment for the biological is packaged into the payment for the associated procedure. When billing for biologicals where the HCPCS code describes a product that may either be surgically implanted or inserted or otherwise applied in the care of a patient, hospitals should not separately report the biological HCPCS codes, with the exceptions of biologicals with pass-through status when using these items as implantable devices (including as a scaffold or an alternative to human or nonhuman connective tissue or mesh used in a graft) during surgical procedures. Under the OPPS, hospitals are provided a packaged PC payment for surgical procedures that includes the cost of supportive items, including implantable devices without pass-through status. When using biologicals during surgical procedures as implantable devices, hospitals may include the charges for these items in their charge for the procedure, report the change on an uncoded revenue center line, or report the charged under a device HCPCS code (if one exists) so these codes would appropriately contribute to the future median setting for the associated surgical procedure. CORRECT REPORTING OF UNITS FOR DRUGS Hospitals and providers are reminded to ensure that units of drugs administered to patients are accurately reported in terms of the dosage specified in the full HCPCS code descriptor. That is, units should be reported in multiples of the units included in the HCPCS descriptor. For example, if the description for the drug code is 6 mg, and 6 mg of the drug was administered to the patient, the units would be billed as 1. nother example would be, if the description for the drug code is 50 mg, but 200 mg of the drug was administered to the patient, the units billed would be 4. CMS reminds providers and hospitals to not bill the units based on the way the drug is packaged, stored or stocked. If the HCPCS descriptor for the drug code specifies 1mg and a 10 mg vial was administered then the units billed would be 10 and not 1, even though only 1 vial was administered.

First Quarter 2010 Newsletter Prepared By: 155 Franklin Road, Suite 100 Brentwood, TN 37027 Phone: (800) 659-5145 Fax: (615) 661-5147 http://www.hmi-corp.com/ Page 6 Since 1989 HMI Corporation, a Healthcare Management Company, has been assisting acute care, teaching, critical access, long term care, nursing home, home health, and skilled nursing facilities, as well as physician groups, with clinical reimbursement through accurate coding and billing for all financial classes as well as maintaining compliance with Federal payers. HMI s consultant specialists perform compliance reviews, billing, and coding medical reviews, as well as other revenue improvement services, utilizing the provider s chargemaster. HMI also provides physician education to strengthen the medical staff's E/M coding for compliance and to improve reimbursement. HMI offers a full-service program to assist providers in positioning themselves to meet federal compliance guidelines, with an emphasis on PPS reimbursement. This process also includes inpatient and outpatient record review, on-going chargemaster maintenance, and on-site education/training of clinical staff and physicians. Our fifteen-year success has been primarily founded on facilitating quality consulting service, on-going accountability through management plan objectives and guaranteed service based on our ability to deliver results. Q & Corner HMI would like to express our gratitude to those serving our country here and abroad. Thank you! The information contained herein is solely for the purpose of informing you the health care professional of current changes. Every effort has been made to ensure the accuracy of the contents. However, this newsletter does not replace policies or guidelines set by your Medicare FI or replace the ICD-9-CM or CPT/ HCPCS coding manuals. It serves only as a resource. Q: re hospitals required to report HCPCS codes on outpatient claims processed by Medicare? : Yes. ccording to the Medicare Claims Processing Manual, Chapter 4, Section 20, Reporting of HCPCS codes is required of acute care hospitals including those paid under alternate payment systems, e.g., Maryland, long-term care hospitals. HCPCS codes are also required of rehabilitation hospitals, psychiatric hospitals, hospital-based RHCs, hospital-based FQHCs, and CHs reimbursed under Method II (HCPCS required to be billed for fee reimbursed services). This also includes all-inclusive rate hospitals.