February 6, 2007 Part B Medicare Bulletin
Posted February 6, 2007
Table of Contents
- 2007 Annual Update for Clinical Laboratory Fee Schedule and Laboratory Services Subject to Reasonable Charge Payment
- 2007 Medicare Physician Fee Schedule
- 2007 Physician Fee Schedule Payment Policies
- 2007 Update of HCPCS Codes and Payments for Ambulatory Surgical Centers (ASCs)
- Cardiac Output Monitoring by Thoracic Electrical Bioimpedance (TEB)
- Cardiac Output Monitoring by Thoracic Electrical Bioimpedance (TEB)
- Cavernous Nerves Electrical Stimulation with Penile Plethysmograph
- Competitive Acquisition Program (CAP) - Claim Processing for Not Otherwise Classified ("NOC") Drugs
- Comprehensive Error Rate Testing (CERT)
- Emergency Update to the 2007 Medicare Physician Fee Schedule Database (MPFSDB)
- FDA Alert: Erythropoiesis Stimulating Agents (ESA)
- Fee Schedule Update for 2007 for Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS)
- Implementation of a One-Time Only Ultrasound Screening for Abdominal Aortic Aneurysms (AAA), Resulting from a Referral from an Initial Preventive Physicial Examination
- Implementation of Revised Fee Schedule Amounts for New Healthcare Common Procedure Coding System (HCPCS) Codes for Power Mobility Devices (PMDs)
- Implementation of Revised Fee Schedule Amounts for New Healthcare Common Procedure Coding System (HCPCS) Codes for Power Mobility Devices (PMDs)
- Infrared Therapy Devices
- January 2007 Quarterly Average Sales Price (ASP) Medicare Part B Drug Pricing File, Effective January 1, 2007, and Revisions to April 2006, July 2006 and October 2006 Quarterly ASP Medicare Part B Drug Pricing Files
- Laboratory Competitive Bidding Demonstration
- Legislative Change to the Update Factor for the 2007 Medicare Physician Fee Schedule (MPFS) and Extension of the Participating Enrollment Period
- Medical Review Frequently Asked Questions
- Medically Unlikely Edits (MUEs)
- Medicare Payment for Preadministration-Related Services Associated with IVIG Administration - Payment Extended through CY 2007
- Most Common EDI Errors and How to Correct Those Errors
- NPI: Get it. Share it. Use it
- Outpatient Therapy Cap Exceptions Clarifications
- Payment Allowances for the Influenza Virus Vaccine (CPT Codes 90655, 90656, 90657, and 90658) and the Pneumoccocal Vaccine (CPT 90732) When Payment is Based on 95 Percent of the Average wholesale Price (AWP)
- Private Contracting - Definition of Physician/Practitioner
- Quarterly Update to Correct Coding Initiative (CCI)Edits, Version 13.0, Effective Janaury 1, 2007
- Reasonable Charge Update for 2007 for Splints, Casts, Dialysis Supplies, Dialysis Equipment, and Certain Intraocular Lenses
- Remittance Advice Remark Code and Claim Adjustment Reason Code Update
- Revisions to Procedures to Establish Good Cause and Qualified Independent Contractor (QIC) Jurisdictions
- Tennessee PR Will Host a Medicare Beyond the Basics Intermediate Workshop (102)
- The 2007 CIGNA Governemnt Services Holiday Schedule Is As Follows:
- Unsolicited/Voluntary Refunds
2007 Annual Update for Clinical Laboratory Fee Schedule and Laboratory Services Subject to Reasonable Charge Payment
Provider Types Affected
Clinical laboratories billing Medicare carriers, intermediaries, or Part
A/B Medicare Administrative Contractors (A/B MACs)
Provider Action Needed
This article and related CR5362 contain important information
regarding:
- The 2007 annual updates to the clinical laboratory fee schedule
- Mapping for new codes for clinical laboratory tests, and
- Laboratory costs related to services subject to reasonable charge payments.
It is important that affected laboratories understand these changes to ensure correct and accurate payments from Medicare.
Key Points
Update to Fees
In accordance with §1833(h)(2)(A)(i) of the Social Security
Act (the Act), as amended by Section 628 of the Medicare Prescription
Drug, Improvement, and Modernization Act (MMA) of 2003, the annual update
to the local clinical laboratory fees for 2007 is zero (0) percent.
Section 1833(a)(1)(D) of the Act provides that payment for a clinical laboratory test is the lesser of the actual charge billed for the test, the local fee, or the National Limitation Amount (NLA).
The Part B deductible and coinsurance do not apply for services paid under the clinical laboratory fee schedule.
National Minimum Payment Amounts
For a cervical or vaginal smear test (pap smear), §1833(h)(7)
of the Act requires payment to be the lesser of the local fee or the
NLA, but not less than a national minimum payment amount. Also, payment
may not exceed the actual charge.
The 2007 national minimum payment amount is $14.76 ($14.76 plus zero percent update for 2007). The affected codes for the national minimum payment amount include the following Current Procedure Terminology (CPT) codes:
| 88142 | 88143 | 88147 | 88148 | 88150 | 88152 | 88153 |
| 88154 | 88164 | 88165 | 88166 | 88167 | 88174 | 88175 |
| G0123 | G1043 | G1044 | G1045 | G0147 | G0148 | P3000 |
National Limitation Amounts (Maximum)
For tests for which NLAs were established before January 1,
2001, the NLA is 74 percent of the median of the local fees. For tests
for which NLAs are first established on or after January 1, 2001, the
NLA is 100 percent of the median of the local fees in accordance with §1833(h)(4)(B)(viii)
of the Act.
Access to 2007 Clinical Laboratory Fee Schedule
Internet access to the 2007 clinical laboratory fee schedule data file
should be available after November 20, 2006, at http://www.cms.hhs.gov/ClinicalLabFeeSched on
the Centers for Medicare & Medicaid Services (CMS) Web site.
Medicaid State agencies, the Indian Health Service, the United Mine Workers, Railroad Retirement Board, and other interested parties should use the Internet to retrieve the 2007 clinical laboratory fee schedule. It will be available in multiple formats: Excel, text, and comma delimited.
Public Comments
On July 17, 2006, CMS hosted a public meeting to solicit input
on the payment relationship between 2006 codes and new 2007 Current Procedural
Terminology codes. Notice of the meeting was published in the Federal
Register on May 26, 2006 and on the CMS Web site on June 19,
2006.
Recommendations were received from many attendees, including individuals representing laboratories, manufacturers, and medical societies. CMS posted a summary of the meeting and the tentative payment determinations on the Web site http://www.cms.hhs.gov/ClinicalLabFeeSched. Additional written comments from the public were accepted until September 26, 2006.
Additional Pricing Information
The 2006 laboratory fee schedule includes separately payable
fees for certain specimen collection methods (codes 36415,
P9612, and P9615).
For dates of service January 1, 2007 through December 2007, the fee for
clinical laboratory travel code P9603 is $0.935 per mile and for code
P9604 is $9.35 per flat rate trip basis. The clinical laboratory travel
codes are billable only for traveling to perform a specimen collection
for either a nursing home or homebound patient. The standard mileage
rate for transportation costs was increased by the Federal Government's
Treasury Department to 48.5 cents a mile and this amount is incorporated
into the fees for travel codes P9603 and P9604.
The 2007 laboratory fee schedule also includes codes that have a 'QW'
modifier to both identify codes and determine payment for tests performed
by a laboratory registered with only a certificate of waiver under the
Clinical Laboratory Improvement Amendments (CLIA).
Based on comments and data submitted, codes 83037 and 83037QW
are priced by crosswalking to code 82985.
Organ or Disease Oriented Panel Codes
Similar to prior years, the 2006 pricing amounts for certain organ or
disease panel codes and evocative/suppression test codes were determined
by Medicare by summing the lower of the fee schedule amount or the NLA
for each individual test code included in the panel code.
Mapping Information
CMS advises the following:
- New code 80178QW is priced at the same rate as code 80178.
- New code 82107 is priced at the same rate as code 83950.
- New code 83698 is priced at the same rate as code 83880.
- New code 83913 is priced at the same rate as code 83907.
- New code 84443QW is priced at the same rate as code 84443.
- New code 86788 is priced at the same rate as code 86645.
- New code 86789 is priced at the same rate as code 86644.
- New code 86901 is priced at the same rate as code 86900.
- New code 87305 is priced at the same rate as code 87327.
- New code 87498 is priced at the same rate as code 87496.
- New code 87640 is priced at the same rate as code 87651.
- New code 87641 is priced at the same rate as code 87651.
- New code 87653 is priced at the same rate as code 87651.
- New code 87808 is priced at the same rate as code 87802.
- New code 87808 QW is priced at the same rate as code 87808.
- New code G0394 is priced at the same rate as code 82270.
Laboratory Costs Subject to Reasonable Charge Payment in 2006
For outpatients, the following codes are paid under a reasonable charge
basis. In accordance with 42 CFR 405.502 – 405.508, the reasonable
charge may not exceed the lowest of the actual charge or the customary
or prevailing charge for the previous 12-month period ending June 30,
updated by the inflation-indexed update. The inflation-indexed update
is calculated using the change in the applicable Consumer Price Index
for the 12-month period ending June 30 of each year as prescribed by §1842(b)(3)
of the Act and 42 CFR 405.509(b)(1). The inflation-indexed update for
year 2007 is 4.3 percent.
Manual instructions for determining the reasonable charge payment can
be found in the Medicare Claims Processing Manual, Chapter 23, §80-80.8.
If there is insufficient charge data for a code, the instructions permit
considering charges for other similar services and price lists. The
Medicare Claims Processing Manual, is located at http://www.cms.hhs.gov/Manuals/IOM/list.asp#TopOfPage on
the CMS Web site.
When these services are performed for independent dialysis facility patients,
Medicare Claims Processing Manual, Chapter 8, §60.3 instructs
the reasonable charge basis applies. However, when these services are
performed for hospital based renal dialysis facility patients, payment
is made on a reasonable cost basis. Also, when these services are performed
for hospital outpatients, payment is made under the hospital outpatient
prospective payment system (OPPS).
Blood Products
| P9010 | P9011 | P9012 | P9016 | P9017 | P9019 | P9020 |
| P9021 | P9022 | P9023 | P9031 | P9032 | P9033 | P9034 |
| P9035 | P9036 | P9037 | P9038 | P9039 | P9040 | P9044 |
| P9050 | P9051 | P9052 | P9053 | P9054 | P9055 | P9056 |
| P9057 | P9058 | P9059 | P9060 |
Also, the following codes should be applied to the blood deductible, as instructed in the Medicare General Information, Eligibility and Entitlement Manual, (also available at http://www.cms.hhs.gov/Manuals/IOM/list.asp#Top OfPage) Chapter 3, Section 20.5-20.54:
| P9010 | P9011 | P9016 | P9021 | P9022 | P9038 | P9039 |
| P9040 | P9051 | P9054 | P9056 | P9057 | P9058 |
NOTE: Biologic products not paid on a cost or prospective payment basis are paid based on §1842(o) of the Act. The payment limits based on section 1842(o), including the payment limits for codes P9041, P9043, P9045, P9046, P9047, and P9048, should be obtained from the Medicare Part B Drug Pricing Files.
Transfusion Medicine
| 86850 | 86860 | 86870 | 86880 | 86885 | 86886 | 86890 |
| 86891 | 86900 | 86901 | 86903 | 86904 | 86905 | 86906 |
| 86920 | 86921 | 86922 | 86923 | 86927 | 86930 | 86931 |
| 86932 | 86945 | 86950 | 86960 | 86965 | 86970 | 86971 |
| 86972 | 86975 | 86976 | 86977 | 86978 | 86985 | G0267 |
Reproductive Medicine Procedures
| 89250 | 89251 | 89253 | 89254 | 89255 | 89257 | 89258 |
| 89259 | 89260 | 89261 | 89264 | 89268 | 89272 | 89280 |
| 89281 | 89290 | 89291 | 89335 | 89342 | 89343 | 89344 |
| 89346 | 89352 | 89353 | 89354 | 89356 |
Additional Information
If you have questions, please contact your Medicare fiscal intermediary
(FI), carrier or A/B MAC at their toll-free number which may be found
at: http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on
the CMS Web site.
For complete details regarding CR5362, please see the official instruction
issued to your Medicare FI, Carrier or A/B MAC. That instruction may
be viewed by going to http://www.cms.hhs.gov/Transmittals/downloads/R1122CP.pdf on
the CMS Web site.
Instructions for calculating reasonable charges are located in the Medicare
Claims Processing Manual (Pub. 100-04) Chapter 23, Sections 80-80.8 at
http://www.cms.hhs.gov/manuals/downloads/clm104c23.pdf on
the CMS Web site
2007 Medicare Physician Fee Schedule
The Tax Relief and Health Care Act of 2006 set the 2007 Conversion Factor for physician payment at the same level as in 2006 ($37.8975), reversing the statutorily mandated 5.0 percent negative update. However, it does not maintain 2007 physician payments at 2006 levels. There are a number of other factors that may affect payment rates for 2007.
Medicare Physician Fee Schedule amounts are calculated based on a specific methodology. With the reversal of the 5.0 percent reduction in the Conversion Factor, there have been numerous questions regarding the 2007 Physician Fee Schedule. The correct 2007 Physician Fee Schedule has been posted to the CIGNA Government Services Web site at the following link: http://www.cignagovernmentservices.com/partb/fsch/index.html#2007updates.
The 2007 Medicare Physician Fee Schedule amounts may or may not match the amounts from 2006. Differences occur as a result of 2007 changes to the Relative Value Units (RVUs) and/or Geographic Practice Cost Indices (GPCIs) for a specific procedure or service.
The Physician Fee Schedule formula to calculate allowable amounts uses RVUs and GPCIs multiplied by the annual Conversion Factor to equal the allowed amounts.
Relative Value Units (RVUs)
Three RVUs are set for each procedure code. Each procedure code has an
RVU for:
- Physician Work (RVUw) - includes:
- Time required to furnish the service
- Intensity of the effort
- Technical skills required
- Practice Expense (RVUpe) - includes costs for:
- Office rent
- Employee salaries
- Supplies
- Malpractice Expense (RVUm)
- Based on historical data
- Weighted by specialty
Geographic Practice Cost Indices (GPCIs)
RVUs are adjusted to reflect the variation in practice costs
from area to area. Each payment locality has three separate GPCIs:
- Physician Work (GPCIw)
- Practice Expense (GPCIpe)
- Malpractice Insurance (GPCIm)
National Conversion Factor (CF)
The National Conversion Factor is a multiplier that transforms
relative values into payment amounts.
Calculation and Payment Information
The calculation for the Medicare Physician Fee Schedule is:
[(RVUw X GPCIw) + (RVUpe X GPCIpe) + (RVUm X GPCIm) X CF]=MPFS Amount
Medicare's approved amount would be the lower of the:
- Physicians actual charge, or
- Medicare Physician Fee Schedule amount
Medicare's payment is generally 80% of the approved amount after the annual deductible has been met.
For more information regarding updates to the 2007 Medicare Physician Fee Schedule, see MLN Matters article 5443, available at: http://www.cms.hhs.gov/MLNMattersArticles/downloads/MM5443.pdf.
2007 Physician Fee Schedule Payment Policies
Provider Types Affected
Physicians and other providers who bill Medicare carriers, fiscal intermediaries
(FI) and A/B MACs for services, including ambulance and telehealth
services.
What you Need to Know
CR 5443, from which this article was taken:
- Summarizes significant issues contained in the Medicare Physician Fee Schedule Regulation for 2007 (including publishing the Ambulance Inflation Factor (AIF) for CY 2007); and
- Announces the telehealth originating site facility fee for 2007. CR5443 also discusses several provisions of the recently-enacted Tax Relief and Health Care Act of 2006. You should refer to the Background and Additional Information sections, below, for more details and information on how to find the background/reference documents.
Background
Tax Relief and Health Care Act of 2006
The Tax Relief and Health Care Act of 2006 set the 2007 conversion
factor for physician payment at the same level as in 2006 ($37.8975),
reversing the statutorily mandated 5.0 percent negative update. However,
it does not maintain 2007 physician payments at 2006 levels. There are
a number of other factors that affect payment rates for 2007 and this
article discusses several of those factors. The legislation also extends
the 1.0 floor on work Geographic Practice Cost Indices (GPCIs) through
December 31, 2007. Practice expense GPCIs and malpractice GPCIs are not
affected by this provision.
Section 202 of this act mandates that Medicare Part B will cover, for 2007 only, the administration of vaccines that are covered under Part D of Medicare. A new G code (G0377) has been created for the administration of Part D vaccines and payment for G0377 will be crosswalked to CPT code 90471 for one year. When a physician administers a Part D vaccine, the physician should use G0377 to bill the local carrier for the administration of the vaccine. Payment to the physician will be on an assigned basis only. Normal beneficiary deductible and coinsurance requirements apply to the administration. Payment for Part D covered vaccines is made solely by the participating Prescription Drug Plan. Medicare Part B will not pay for the vaccine itself.
Medicare Physician Fee Schedule Regulation for 2007
Section 1848(b)(1) of the Social Security Act requires the Centers for
Medicare and Medicaid Services (CMS) to establish (by regulation, before
November 1 of each year) fee schedules that establish payment amounts
for physicians' services for the subsequent year.
Accordingly, on November 1, 2006, the Centers for Medicare & Medicaid
Services (CMS) released the Medicare Physician Fee Schedule (MPFS) final
rule for calendar year 2007. In this rule (effective January 1, 2007)
Medicare:
- Will increase physician payment for the time spent talking with Medicare beneficiaries about their health care. The 2007 final rule significantly increases the Relative Value Units' (RVU) work component for the face-to-face visits (evaluation and management or "E&M services"), during which the physician and patient discuss the patient's health status and the steps that can be taken to maintain or improve the patient's health.
- Adopts work values for CPT codes 97802, 97803, 97804, G0270, and G0271.
- Expands its preventive services benefits to include:
- Adding a one-time preventive ultrasound screening for abdominal aortic aneurysms (AAA), for at risk beneficiaries, only available as part of the Initial Preventive Physical Examination (also referred to as the Welcome to Medicare physical);
- Insuring more accurate and reliable bone mass measurements are performed for Medicare beneficiaries; and
- Exempting the colorectal cancer screening benefit from the Part B deductible.
- Adjusts the methodology for determining practice expense (such as
office overhead) RVUs. As part of the methodology, CMS will use a bottom-up
methodology for direct costs, use supplementary survey data for indirect
costs, and eliminate the non-physician workpool. This methodology (to
be phased over a four-year period), will be more transparent than the
existing methodology, allowing specialties and other stakeholders to
predict the effects of proposals
to improve accuracy of practice expense payments. - Adds diabetes outpatient self-management training and medical nutrition therapy services to the list of covered and separately payable services included in the Federally Qualified Health Center benefit, making these services more available to beneficiaries in both rural and urban underserved areas.
- Caps payment rates for imaging services under the physician fee schedule at the amount paid for the same services when performed in hospital outpatient departments; includes a list of codes to which the outpatient prospective payment system (OPPS) cap would apply; and reduces the payment for certain multiple imaging procedures on contiguous body parts by 25% after full payment for the first procedure. Note: CMS will apply the multiple imaging reductions first, followed by the OPPS imaging cap, if applicable.
The final rule also:
- Finalizes drug manufacturer reporting requirements and addresses a number of technical average sales price (ASP) issues such as the treatment of bona fide service fees in the context of the ASP calculation and the definition of nominal sales;
- Codifies the public consultation process for developing payment amounts for new clinical laboratory tests;
- Adopts supplier standards for independent diagnostic testing facilities (IDTFs);
- Continues the temporary intravenous immune globulin preadministration-related services fee into 2007;
- Addresses the final regulations affecting ambulance payment policy under the ambulance fee schedule, which will improve the accuracy of payments for ambulance services and incorporate changes in geographic adjustments based on the most recent census data.
- Announces an Ambulance Inflation Factor (AIF) for CY 2007 of 4.3%, and further 1) Clarifies the designation of areas as urban or rural to incorporate changes made by the Office of Management and Budget to the Metropolitan Statistical Areas (MSAs); 2) Replaces the Goldsmith Modification (identifying rural census tracts within MSAs) with the most recent version based on Rural Urban Commuting Areas; and 3) Discontinues formal annual reviews of "low billers" and air ambulances to determine whether adjustments are needed in the ambulance fee schedule conversion factors.
- Includes a discussion of exceptions to the therapy cap for CY2006 and 2007 and announces that the 2007 therapy cap is $1,780. (Note that Section 201 of the Tax Relief and Health Care Act of 2006 extended the exceptions process until December 31, 2007.)
- Amends the reassignment of payment regulations to state that an individual supplier furnishing a service has unrestricted access to the billings submitted by the entity receiving Medicare payment for services furnished by that supplier, irrespective of whether the supplier is an employee or independent contractor.
- Announces that the drug add-on adjustment to the end stage renal diseased (ESRD) composite payment rate for 2007 will increase from 14.5 percent to 15.1 percent.
Lastly, the final rule addresses comments received on the separate notice published June 29, 2006 (Five Year Review of Work Relative Value Units Under the Physician Fee Schedule and Proposed Changes to the Practice Expense Methodology (CMS-1521-PN)), which is contained in an attachment to CR 5443. Further discussion of the above summarized items is in that same attachment to CR5443.
Telehealth originating site facility fee for 2007
Section 1834(m) of the Social Security Act established the Medicare
telehealth originating site facility fee payment amount for telehealth
services provided from October 1, 2001, through December 31, 2002, at
$20.
For telehealth services provided on or after January 1 of each subsequent calendar year, the telehealth originating site facility fee is increased as of the first day of the year by the percentage increase in the Medicare Economic Index (MEI).
The MEI increase for 2007 is 2.1%. Thus for calendar year 2007, the payment amount for HCPCS code "Q3014, telehealth originating site facility fee" is 80%t of the lesser of the actual charge, or $22.94.
Note that the beneficiary is responsible for any unmet deductible amount or coinsurance.
The Medicare telehealth originating site facility fee and MEI increase
by applicable time period is shown in Table 1, below.
Table 1
| Medicare Telehealth Originating site Facility Fee and MEI by Time Period Facility Fee MEI Time Period | ||
| Facility Fee | MEI | Time Period |
| $20.00 | N/A | 10/01/2001-12/31/2002 |
| $20.60 | 3.0% | 01/01/2003-12/31/2003 |
| $21.20 | 2.9% | 01/01/2004-12/31/2004 |
| $21.86 | 3.1% | 01/01/2005-12/31/2005 |
| $22.47 | 2.8% | 01/01/2006-12/31/2006 |
| $22.94 | 2.1% | 01/01/2007-12/21/2007 |
Additional Information
You can find more information about the 2007 Physician Fee Schedule
Payment Policies by going to CR 5443, located at http://www.cms.hhs.gov/Transmittals/downloads/R258OTN.pdf on
the CMS Web site.
Please see, as an attachment to that CR, a document entitled Revisions to Payment Policies and Five-Year Review of Work Relative Value Units Under the Physician Fee Schedules for CY 2007, and Other Changes to Payment Under Part B; Revisions to the Payment Policies of Ambulance Services Under the Fee Schedule for Ambulance Services; Ambulance Inflation Factor Update for CY 2007, for more details on the significant issues discussed in the final rule.
You can find the November 1, 2006 CMS press release entitled MEDICARE ANNOUNCES FINAL RULE SETTING PHYSICIAN PAYMENT RATES AND POLICIES FOR 2007, by going to http://cms.hhs.gov/apps/media/press/release.asp?Counter=2044; and other information about the physician fee schedule by going to the CMS Physician Center Web site at http://cms.hhs.gov/center/physician.asp.
If you have any questions, please contact your carrier, FI, or A/B MAC at their toll-free number, which may be found at http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip.
Flu Shot Reminder
As a respected source of health care information, patients trust their
doctors' recommendations. If you have Medicare patients who haven't
yet received their flu shot, help protect them by recommending an annual
influenza and a one time pneumococcal vaccination. Medicare provides
coverage for flu and pneumococcal vaccines and their administration.
And don't forget to immunize yourself and your staff. Protect yourself,
your patients, and your family and friends. Get Your Flu Shot. Remember – Influenza
vaccination is a covered Part B benefit. Note that influenza vaccine
is NOT a Part D covered drug. For more information about Medicare's
coverage of adult immunizations and educational resources, go to CMS's
Web site:
http://www.cms.hhs.gov/MLNMattersArticles/downloads/SE0667.pdf
Cardiac Output Monitoring by Thoracic Electrical Bioimpedance (TEB)
Note: This article was revised on December 29, 2006, to correct, on page 2, the Web address for accessing CR5414. All other information remains the same.
Provider Types Affected
Physicians who bill Part A/B Medicare Administrative Contractors
(A/B MACs), or Medicare carriers for services to Medicare beneficiaries.
Background
The Centers for Medicare & Medicaid Services (CMS) reconsidered
the Medicare coverage policy for TEB for drug-resistant hypertension
and decided to retain current coverage as written in section 20.16 of
the National Coverage Determinations (NCD) Manual.
Effective for dates of service on and after November 24, 2006, the current policies for cardiac output monitoring by TEB listed at section 20.16 of the NCD Manual will remain the same. Medicare A/B MACs and carriers will continue to make reasonable and necessary determinations for the use of TEB related to drug-resistant hypertension only. All other coverage and non-coverage policies at section 20.16 remain in effect.
Additional Information
If you have questions, please contact your Medicare A/B MAC
or carrier at their toll-free number which may be found at: http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on
the CMS Web site.
For complete details regarding this Change Request (CR) including the revised section of 20.16 of the NCD manual, please see the official instruction (CR5414) issued to your Medicare A/B MAC or carrier. That instruction may be viewed by going to http://www.cms.hhs.gov/Transmittals/downloads/R63NCD.pdf on the CMS Web site.
Cardiac Output Monitoring by Thoracic Electrical Bioimpedance (TEB)
Cardiac Ouput Monitoring by Thoracic Electrical Bioimpedance
Cavernous Nerves Electrical Stimulation with Penile Plethysmograph
Note: This article was changed on December 6, 2006 to correct the HCPCS code for the test. The article had incorrectly stated to use HCPCS code 58899 (page 3), but it should have stated HCPCS code 55899. The reference to carriers and FIs was also changed to add a reference to A/B MACs. All other information remains the same.
Provider Types Affected
Physicians and hospitals who bill Medicare fiscal intermediaries
(FI) and carriers for performing Cavernous Nerves Electrical Stimulation
with Penile Plethysmography in Medicare beneficiaries undergoing nerve-sparing
prostatic or colorectal surgical procedures.
Provider Action Needed
STOP – Impact to You
Effective for claims with dates of service on or after August
24, 2006, Medicare will not pay for performing Cavernous Nerves Electrical
Stimulation with Penile Plethysmography in Medicare beneficiaries undergoing
nerve-sparing prostatic or colorectal surgical procedures.
CAUTION – What You Need to Know
CR 5294, from which this article is taken, announces` the results
of a national coverage determination (NCD) addressing Cavernous Nerves
Electrical Stimulation with Penile Plethysmography performed for Medicare
beneficiaries undergoing nerve-sparing prostatic or colorectal surgical
procedures. It states that CMS, after reviewing the evidence, has determined
that this test is not reasonable and necessary for Medicare beneficiaries
undergoing these procedures.
GO – What You Need to Do
Make sure that your billing staffs are aware of this NCD.
Background
The direct application of electrical stimulation with penile
plethysmography (also referred to as cavernosal nerve mapping) may be
performed, in nerve-sparing prostatic and colorectal surgical procedures,
to assess the integrity and function of the cavernous nerves.
Through either an open or laparoscopic approach, the surgeon can assess
the function of the cavernous nerves by stimulating, with an electrical
nerve stimulator, the most distal end of the nerve that can be located.
A functioning and stimulated nerve will trigger blood flow either into
or out of the penis, which can be detected via a penile plethysmography
sensor fitted around the penis and connected to a nerve stimulator control
unit. If the nerves are intact, cavernous blood flow will cause slight
changes in penile girth, which the sensor can detect.
The presence (and degree) of a response may be used to provide the surgeon
with a more realistic assessment of the chance of the patient regaining
potency and assist in choosing appropriate therapy.
Heretofore, local Medicare carriers/FIs had the discretion to cover
this test whenever it was determined to be medically necessary for the
individual patient, because a national coverage determination (NCD) or
national Medicare coverage policy had not been issued. However, on December
9, 2005, a request for review of this test initiated a national coverage
analysis.
CR 5294, from which this article is taken, announces the results of this
NCD. It provides that CMS has reviewed the evidence and determined that:
1) Cavernous Nerves Electrical Stimulation with Penile Plethysmography
is not reasonable and necessary for Medicare beneficiaries undergoing
nerve-sparing prostatic or colorectal surgical procedures, and 2) this
test is noncovered under Medicare (as specified the Medicare National
Coverage Manual (100-03, Section 160.26 (Cavernous Nerves Electrical
Stimulation with Penile Plethysmography).
Effective with claims with dates of service on or after August 24, 2006,
your FIs and carriers will not pay for these services.
Physicians should use HCPCS code 55899 to bill
this for test. Your FIs and carriers will suspend claims containing this
code to determine whether this test is the service being billed, and
will deny the line item associated with it, using Medicare Summary Notice
21.11 (This test was not covered by Medicare at the time you received
it).
You should be aware that your FIs, A/B MACs and carriers will not search for, and adjust, claims for tests that have been paid prior to January 8, 2007, but they will adjust claims brought to their attention. Further, physicians and hospitals should, as appropriate:
1. Issue the appropriate liability notice for Medicare beneficiaries
having this test;
2. Include the following language when issuing an Advanced Beneficiary
Notice (ABN):
- Under "Items or Service" Section: Cavernous Nerves Electrical Stimulation with Penile Plethysmography.
- Under "Because" Section: As specified in section 160.26
of Medicare NCD Manual, Medicare will
not pay for this test as it is not reasonable and necessary for Medicare beneficiaries undergoing nerve-sparing prostatic or colorectal surgical procedures. and/or
3. Issue a hospital Issued Notice of Noncoverage (HINN).
If a physician does not issue an ABN, the physician is liable for the
service.
Additional Information
You can find more information about payment for Cavernous Nerves
Electrical Stimulation with Penile Plethysmography by going to CR5294,
which is available at http://www.cms.hhs.gov/Transmittals/downloads/R61NCD.pdf on
the CMS site. You will find revised section 160.26 (Cavernous Nerves
Electrical Stimulation with Penile Plethysmography) of the Medicare National
Coverage Manual (Publication 100-03) as an attachment to this CR.
If you have any questions, please contact your FI or carrier at their toll-free number, which may be found at http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on the CMS Web site.
Competitive Acquisition Program (CAP) – Claim Processing for Not Otherwise Classified ("NOC") Drugs
Note: This article was revised on December 14, 2006, to correct the Web address on page 4 for accessing CR5079. All other information remains the same.
Provider Types Affected
Physicians participating in the Medicare Part B Drug CAP.
Impact on Providers
This article is based on Change Request (CR) 5259, which describes
the process for adding Not Otherwise Classified (NOC) Drugs to the CAP
beginning in 2007. It provides additional details, information and instructions
for the implementation of the CAP as outlined previously in CRs 4064,
4306, 4309 and 5079 and the MLN Matters articles related to those CRs.
Background
As discussed in the November 21, 2005 CAP final rule (http://www.access.gpo.gov/su_docs/fedreg/a051121c.html)
and in response to public comments about beneficiary access to new medications,
CMS provided for the addition of NOC drugs to the CAP beginning in 2007.
CMS believes that the addition of NOC drugs to the CAP will improve beneficiaries'
access to newly marketed drugs that have a national sales price, will
decrease the reliance on buy and bill acquisition and will further simplify
the drug acquisition process for physicians who have elected to participate
in the CAP.
PROCESS TO ADD NOC DRUGS TO A CAP VENDOR'S DRUG LIST
The process for adding NOC drugs to the CAP will basically follow
the process for adding other drugs to the CAP as described in CR5079.
An approved CAP vendor will be required to submit a written request to
add specific NOC drugs to the CAP designated carrier. The request must
include:
- A rationale for the proposed change,
- A discussion of the impact on the CAP (including safety, waste, etc.), and
- The potential for cost savings.
CMS will define a list of CAP NOC drugs that the approved CAP vendor
must use when requesting the addition of NOC drugs to the CAP. The
CAP NOC drug list will be based on the ASP NOC list, but will include
only drugs that are both likely to fit the existing CAP drug category
(or categories) and drugs that have a single national ASP-based payment
amount. The CAP NOC drug list will be posted on the CMS CAP Web site
and updated quarterly.
If approved, changes will become effective at the beginning of the following quarter. CMS will post the changes on the CMS Web site (http://www.cms.hhs.gov/CompetitiveAcquisforBios/ ) and notify the carriers and participating CAP physicians of any changes on a quarterly basis. Participating CAP physicians will be notified of changes to their approved CAP vendor's CAP drug list on a quarterly basis and at least 30 days before the approved changes are due to take effect. CAP drug list approvals apply only to the CAP vendor who submitted the request and to the category identified on the request. Therefore, each vendor's drug list may contain different drugs after changes to the initial drug list are approved. The CAP NOC drug payment amount will be at the same rate as published on the ASP NOC file consistent with the next quarterly update, and the payment amount will be updated annually as for other CAP drugs.
CAP NOC CLAIMS SUBMISSION REQUIREMENTS
CMS requires the use of a CAP-specific Q code (Q4082 Drug/bio NOC part
B drug CAP) for CAP NOC drug claims in order to distinguish CAP NOC
drug claims from ASP NOC claims and to prevent the CAP claims from
being paid outside the Medicare Part B drug CAP. Physician drug administration
claims for CAP NOC drugs are required to
- use the CAP-specific NOC Q-code: Q4082 Drug/bio NOC part B drug CAP
- and identify the specific NOC drug that had been administered in Item 19 on paper claims or Loop 2300 Segment NTE on electronic claims
- Physician claims must also contain the appropriate CAP modifiers (J1, J2, J3) All other CAP claim parameters will remain the same
Note: Physicians who have elected to participate in the CAP should continue to use ASP NOC codes when billing for NOC drugs that are outside the CAP. Also remember that physicians who participate in the CAP are required to obtain all CAP drugs on the updates from the approved CAP vendor unless medical necessity requires the use of a formulation not supplied by the vendor.
RETURNED CAP NOC CLAIMS
For the following three situations, if:
- The claim is submitted with a CAP NOC code, but the description does not match a CAP NOC drug on the approved list; or
- The claim is submitted with a CAP NOC code by a non-CAP physician; or
- The claim is submitted with a J NOC code with a description of a CAP approved NOC drug.
Then:
- Claims will be returned to physicians with a reason code of 16 (Claim/service lacks information needed for adjudication) and remark code MA 130 (Your claims contain incomplete and/or invalid information, and no appeals rights are afforded because the claim is unprocessable).
- Remark code N350 (Missing/incomplete/invalid description of a service for a NOC code or unlisted procedure) will also appear in the first situation.
- Remark code N56 (Procedure code billed is not correct/valid for the services billed or the date of service billed) will appear in the second and third situations.
Implementation
The implementation date for CR5259 is January 2, 2007.
Additional Information
Section 303 (d) of the Medicare Prescription Drug Improvement
and Modernization Act (MMA) of 2003, requires the implementation of a
competitive acquisition program (CAP) for Medicare Part B drugs and biologicals
("drugs") not paid on a cost or prospective payment system
basis. Beginning with drugs administered on or after July 1, 2006, physicians
will be given a choice between buying and billing these drugs under the
average sales price (ASP) system, or obtaining these drugs from vendors
selected in a competitive bidding process. A participating CAP physician
will submit a claim for drug administration to the Medicare local carrier.
An approved CAP vendor will submit a claim for the drug product to the
CAP Medicare designated carrier.
Change Request (CR) 5259 is not a stand-alone CR. It provides additional
details, information, and instructions for the implementation of the
Competitive Acquisition Program (CAP) as outlined in:
CR 4064 (http://www.cms.hhs.gov/transmittals/downloads/R777CP.pdf; http://www.cms.hhs.gov/MLNMattersArticles/downloads/MM4064.pdf),
CR4306 (http://www.cms.hhs.gov/transmittals/downloads/R841CP.pdf),
CR4309 (http://www.cms.hhs.gov/transmittals/downloads/R866CP.pdf; http://www.cms.hhs.gov/MLNMattersArticles/downloads/MM4309.pdf)
and
CR 5079 (http://www.cms.hhs.gov/Transmittals/downloads/R1055CP.pdf; http://www.cms.hhs.gov/MLNMattersArticles/downloads/MM5079.pdf).
For complete details, please see the official instruction issued to your
carrier regarding this change. That instruction may be viewed at http://www.cms.hhs.gov/Transmittals/downloads/R1034CP.pdf on
the CMS Web site.
If you have any questions, please contact your carrier at their toll-free number, which may be found on the CMS Web site at: http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip
Flu Shot Reminder
As a respected source of health care information, patients trust
their doctors' recommendations. If you have Medicare patients who haven't
yet received their flu shot, help protect them by recommending an annual
influenza and a one time pneumococcal vaccination. Medicare provides
coverage for flu and pneumococcal vaccines and their administration.
And don't forget to immunize yourself and your staff. Protect yourself,
your patients, and your family and friends. Get Your Flu Shot. Remember – Influenza
vaccination is a covered Part B benefit. Note that influenza vaccine
is NOT a Part D covered drug. For more information about Medicare's coverage
of adult immunizations and educational resources, go to CMS's Web site:
http://www.cms.hhs.gov/MLNMattersArticles/downloads/SE0667.pdf.
Comprehensive Error Rate Testing (CERT)
Remember the importance to complying with requests from the CERT Documentation Contractor (CDC) office for medical records needed for the CERT program.
The CERT program produces national, contractor-specific and service-specific paid claim error rates, as well as a provider compliance error rate. The paid claim error rate is a measure of the extent to which the Medicare program is paying claims correctly. The provider compliance error rate is a measure of the extent to which providers are submitting claims correctly. A portion of this error rate was due to providers not sending requested supporting documentation to the designated CERT contractor.
REMINDER
- Medicare physicians, providers and suppliers must provide documentation and medical records that support their claims for covered Medicare services to the designated CERT contractor upon request. Providers who fail to submit medical documentation will receive requests for refunds from CIGNA Government Services for those services where no documentation is received
- The provider agreement to participate in the Medicare program requires providers to submit all information necessary to support the services billed on claims. If services were rendered at another facility, the billing provider is responsible for obtaining those records for review.
- Medicare contractors do not need to obtain a patient's authorization to release medical information to the CDC. Medicare patients have already given authorization to release necessary medical information in order to process claims.
The CDC sends a written request for medical records to an individual provider that includes a checklist of the types of documentation required. Medical records should be submitted to the CDC within 75 days from the receipt date of the initial letter or the claim will be denied.
Providers should submit this documentation to the CDC via fax or mail at the number/address specified below:
FAX: 240.568.6222
CERT Documentation Office
Attn: CID #: (Claim Identifier listed at the top of the checklist)
9090 Junction Drive, Suite 9
Annapolis Junction, MD 20701
Providers may call the CDC at 301.957.2380 with questions regarding specific documentation to submit.
Emergency Update to the 2007 Medicare Physician Fee Schedule Database (MPFSDB)
Provider Types Affected
Physicians and other providers who bill Medicare contractors (carriers,
fiscal intermediaries (FIs), or Part A/B Medicare administrative contractors
(A/B MACs)) for professional services paid under the Medicare Physician
Fee Schedule (MPFS).
Background
This article and related Change Request (CR) 5459 wants providers to
know that payment files were issued to contractors based upon the December
1, 2006, MPFS Final Rule. CR5459 amends those payment files.
Key Points http://www.cms.hhs.gov/MLNMattersArticles/downloads/SE0667.pdf
You may wish to review Attachment 1 of the CR5459, which is located at http://www.cms.hhs.gov/Transmittals/downloads/R1143CP.pdf on
the CMS Web site. The following key points summarize the specifics that
are identified in the attachment to CR5459.
- The physician fee schedule status indicators for oncology demonstration
codes G9050 to G9062
for 2007 are "I"; these codes are invalid for Medicare use in 2007, thus, payment will not be made for these codes in 2007. (For more details on the Oncology Demonstration, see the
MLN Matters article at http://www.cms.hhs.gov/MLNMattersArticles/downloads/MM4219.pdf on the CMS site.) - Oncology demonstration codes G9076, G9081, G9082, G9118, G9119, G9120, G9121, G9122, and G9127 are deleted and will not be paid for services provided after December 31, 2006 in 2007.
- Active Oncology demonstration codes in the range G9063 to G9139
have status indicators of "M" on the Medicare physician fee
schedule database.
(Note: See requirement above for discontinued oncology demonstration codes within this range). Those filing claims may report these codes for oncology disease status in 2007, but payment will not be made for these codes for services provided after December 31, 2006. - Category II codes 3047F and 3076F and Category III code 0152T have been deleted for 2007.
- G codes G0377 and G8348 through G8368 will be added to the 2007 HCPCS file.
- Q codes Q4083, Q 4084, Q4085, and Q4086 will be added, even though they are not on the 2007 HCPCS file. Note that corresponding ASP amounts will be reflected in updated 2007 ASP pricing files to be posted to the CMS Web site.
- Incorrect Diagnostic Supervision Indicators were assigned to some codes and these codes and correct indicators are listed in the attachment to CR5459.
- Corrected Multiple Procedure Codes of 0 and Diagnostic Family Imaging Indicators of 99 have been assigned to codes G0389, G0389-TC, 70554, 70554-TC, 70555, 70555-TC, 76776, and 76776-TC.
- As identified in the attachment to CR5459, correct work, practice expense, and/or malpractice relative value units (RVUs) have been assigned for codes 44180, 44186, 73223, 73223-26, 76775, 76775-TC, 76775-26, 93503, 93539, 93540, 93541, 93542, 93543, 93544, 93545, 95060, 95065, G0389, G0389-TC, and G0389-26.
- As a result of the Tax Relief and Health Care Act of 2006, effective January 1, 2007, G0377 (Administration of vaccine for Part D drug) is added to the MPFS with a status indicator of X. Payment for HCPCS code G0377 is linked to CPT code 90471 (just as payment is made for G0008, G0009, and G0010). For 2007 only, the legislation provides for Part B to pay for the administration of a covered Part D vaccine. When a physician administers a Part D vaccine, the physician should use G0377 to bill the local carrier for the administration of the vaccine. Payment to the physician will be on an assigned basis only. Normal beneficiary deductible and coinsurance requirements apply to this administration. Payment for Part D covered vaccines is made solely by the participating Prescription Drug Plan. Medicare will not pay for the vaccine itself.
- Effective January 1, 2007, the following G codes are added to the MPFSDB with a status indicator of M: G8348, G8349, G8350, G8351, G8352, G8353, G8354, G8355, G8356, G8357, G9358, G8359, G8360, G8361, G8362, G8363, G8364, G8365, G8366, G8367, and G8368.
- CMS has established separate payment for sodium hyaluronate products that have come on the market since October 2003. Four interim Q codes are in effect for these products as of January 1, 2007, i.e., Q4083 (Hyalgan/supartz inj per dose), Q4084 (Synvisc inj per dose), Q4095 (Euflexxa inj per does), and Q4086 (Orthovisc inj per dose).
- Procedure status I is assigned toJ7319, effective January 1, 2007.
- Effective January 1, 2007, the HCPCS codes Q9958, Q9959, Q9960, Q9961, Q9962, Q9963, and Q9964 will be assigned to procedure status indicator E.
- As a courtesy to the public, CMS has established RVUs for a number of codes, even though the codes are either bundled or not valid for Medicare purposes. These codes are 38204, 38207, 38208, 38209, 38210, 38211, 38212, 38213, 38214, and 38215. The RVUs are listed for these codes in the attachment to CR5459.
Additional Information
For complete details regarding this Change Request (CR) please see the
official instruction (CR5459) issued to your Medicare carrier, FI or
A/B MAC. That instruction may be viewed by going to http://www.cms.hhs.gov/Transmittals/downloads/R1143CP.pdf on
the CMS Web site.
If you have questions, please contact your Medicare carrier, FI or A/B
MAC, at their toll-free number which may be found at: http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on
the CMS Web site.
Flu Shot Reminder
As a respected source of health care information, patients trust
their doctors' recommendations. If you have Medicare patients who haven't
yet received their flu shot, help protect them by recommending an annual
influenza and a one time pneumococcal vaccination. Medicare provides
coverage for flu and pneumococcal vaccines and their administration.
And don't forget to immunize yourself and your staff. Protect yourself,
your patients, and your family and friends. Get Your
Flu Shot. Remember – Influenza vaccination is a covered Part B
benefit. Note that influenza vaccine is NOT a Part D covered drug. For
more information about Medicare's coverage of adult immunizations and
educational resources, go to CMS's Web site: http://www.cms.hhs.gov/MLNMattersArticles/downloads/SE0667.pdf.
2007 Update of HCPCS Codes and Payments for Ambulatory Surgical Centers (ASCs)
Note: This article was revised on December 21, 2006, to reflect changes made to CR5211. CR5211 was amended to provide the Web address for accessing the "2007 ASC Approved HCPCS Codes and Payment Rates." That address is in the Additional Information section of this article. The article was also revised to reflect the new CR release date, transmittal number, and Web address for accessing the revised CR5211. All other information remains the same.
Provider Types Affected
Ambulatory surgical centers (ASCs) submitting claims to Medicare carriers
or fiscal intermediaries (FIs) for ASC services provided to Medicare
beneficiaries.
Impact on Providers
This article is based on Change Request (CR) 5211, which updates the
2007 HCPCS codes and ASC payment rates, effective for services furnished
on or after January 1, 2007.
Background
Section 5103 of the Deficit Reduction Act of 2005 (DRA) limits ASC payments
to:
- The lesser of the Medicare Hospital Outpatient Prospective Payment System (OPPS) payment amount; or
- The ASC payment amount for services furnished on or after January 1, 2007.
Also, §1833(i)(1) of the Social Security Act requires that the list of payable ASC procedures be updated as least every two years.
\CR5211, from which this article is taken, implements the required biennial ASC update, which includes changes made by the American Medical Association for the CY 2007 Common Procedural Terminology (CPT). These changes include replacing the ASC 2-digit payment group code designation next to the ASC-approved Healthcare Common Procedure Coding System (HCPCS) codes with a "yy" designation for these codes, which will be defined as "the procedure is approved to be performed in an ambulatory surgical center."
CR5211 also revises the manner in which ASC payment groups are defined.
The number of ASC payment groups that carriers and fiscal intermediaries
(FI) currently use to identify ASC payment amounts for individual HCPCS
codes is being expanded in order to accommodate the new payment amounts
that will be assigned to certain ASC services in Calendar Year (CY) 2007
under the DRA requirement. The ASC payment groups will now be called
ASC PRICER groups.
The additional ASC PRICER groups reflect the DRA-driven payment amounts,
which will be included in the ASC PRICER files that carriers, and certain
FIs, use to process ASC facility claims.
And lastly, CR5211 includes payment file retrieval instructions that your carriers and FIs will use to access the final payment files on, or after, the specified retrieval date provided in CMS's notification.
You should be aware that final ASC payment rates are established after publication of the OPPS final rule and the code change update will be published as part of the OPPS final rule in the Federal Register. This publication usually occurs in late October. Shortly after publication, you can reach this rule through a link at http://www.cms.hhs.gov/center/asc.asp on the CMS Web site.
Also note that your carriers and FIs will continue
to use the wage index values contained in Transmittal 51, dated February
4, 2004, to calculate payment amounts for all type of service F Healthcare
Common Procedural Coding System (HCPCS) codes until further notice.
This transmittal is available at http://www.cms.hhs.gov/Transmittals/downloads/R51OTN.pdf on
the CMS site.
Additional Information
For complete details, please see CR 5211, the official instruction
issued to your carrier/intermediary regarding this change, located
at http://www.cms.hhs.gov/Transmittals/downloads/R1134CP.pdf on
the CMS Web site. The "2007 ASC Approved HCPCS Codes and Payment
Rates" changes are available at http://www.cms.hhs.gov/ASCPayment/01_Overview.asp on
the CMS site.
If you have any questions, please contact your carrier at their toll-free number, which may be found at http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on the CMS Web site.
Flu Shot Reminder
As a respected source of health care information, patients trust their
doctors' recommendations. If you have Medicare patients who haven't
yet received their flu shot, help protect them by recommending an annual
influenza and a one time pneumococcal vaccination. Medicare provides
coverage for flu and pneumococcal vaccines and their administration.
And don't forget to immunize yourself and your staff. Protect yourself,
your patients, and your family and friends. Get Your Flu Shot. Remember – Influenza
vaccination is a covered Part B benefit. Note that influenza vaccine
is NOT a Part D covered drug. For more information about Medicare's
coverage of adult immunizations and educational resources, go to CMS's
Web site: http://www.cms.hhs.gov/MLNMattersArticles/downloads/SE0667.pdf
FDA Alert: Erythropoiesis Stimulating Agents (ESA)
[Aranesp (darbepoetin), Epogen (epoetin alfa), and Procrit (epoetin alfa)]
FDA ALERT [11/16/2006]: FDA is issuing this alert to advise you of a newly published clinical study showing that patients treated with an erythropoiesis-stimulating agent (ESA) and dosed to a target hemoglobin concentration of 13.5 g/dL are at a significantly increased risk for serious and life threatening cardiovascular complications, as compared to use of the ESA to target a hemoglobin concentration of 11.3 g/dL. The "Correction of Hemoglobin and Outcomes in Renal Insufficiency" (CHOIR) study, published November 16, 2006 in the New England Journal of Medicine, reports the adverse cardiovascular complications as a composite of the occurrence of one of the following events: death, myocardial infarction, hospitalization for congestive heart failure, or stroke.
The CHOIR study findings underscore the importance of following the currently approved prescribing information for Procrit, Epogen, and Aranesp, including the dosing recommendation that the target hemoglobin not exceed 12 g/dL.
This information reflects FDA's current analysis of data available to FDA concerning these drugs. FDA intends to update this sheet when additional information or analyses become available.
To report any serious adverse events associated with the use of these drugs, please contact the FDA MedWatch program using the contact information at the bottom of this sheet.
Considerations
Physicians and other healthcare professionals should consider the following
when using erythropoiesis stimulating agents:
- For all patients:
- Adhere to dosing to maintain the recommended target hemoglobin range of 10 to12 g/dL.
- Measure hemoglobin twice a week for 2 to 6 weeks after any dosage adjustment to ensure that hemoglobin has stabilized in response to the dose change.
- Decrease the dose of the ESA if the hemoglobin increase exceeds 1g/dL in any 2 week period.
- For chronic renal failure (CRF) patients: Measure hemoglobin twice a week after initiating treatment until hemoglobin has stabilized
- For cancer patients and zidovudine-treated HIV patients: Measure hemoglobin once a week after initiating treatment until hemoglobin has stabilized
- For patients with a history of cardiovascular disease or hypertension: Closely monitor and control blood pressure
Information for the Patient
Physicians and other healthcare professionals should discuss
the following with their patients:
- The goal of treatment with erythropoiesis stimulating agents (ESA) is to increase the number of red blood cells which can help them in treating their anemia.
- Treatment with an ESA can be harmful if not closely monitored.
- The importance of keeping their appointments for their blood tests
- The need to monitor their blood pressure every day (if appropriate) and call you if there are any changes outside of the range established for the patient.
- To call you if they experience any of the following symptoms:
- Pain and/or swelling in the legs
- Worsening in shortness of breath
- Increases in blood pressures
- Dizziness or loss of consciousness
- Extreme tiredness
- Blood clots in hemodialysis vascular access ports
Data Summary
Safety concerns related to the use of erythropoiesis-stimulating
agents in the treatment of the anemia of chronic renal failure (CRF)
is the topic of two clinical studies and an editorial published in The
New England Journal of Medicine on November, 16, 2006. The 1,432 subject
CHOIR study demonstrated increases in serious and potentially life threatening
cardiovascular events when epoetin alfa (Procrit) is administered to
reach higher target hemoglobin levels than lower target hemoglobin levels.
The 603 subject CREATE study showed a trend toward more cardiovascular
events in a pattern similar to the CHOIR study, thus supporting the findings
of the CHOIR study. The CREATE study examined the use of epoetin beta,
a product not approved in the USA.
- The CHOIR study was a randomized, open label design in which anemic chronic kidney disease (CKD) subjects were randomized to be dosed to either a higher average target hemoglobin (13.5 g/dL) or a lower average target hemoglobin (11.3 g/dL). All subjects received Procrit. The primary endpoint was a time to event analysis for a composite cardiovascular endpoint (all cause mortality, congestive heart failure (CHF) hospitalization, non-fatal MI, or non-fatal stroke).
- Procrit was administered as 10,000 Units SC weekly and titration allowed to a maximum dose of 20,000 Units weekly.
- Overall, 715 subjects were randomized to the high target hemoglobin (13.5 g/dL) and 717 randomized to the low target hemoglobin (11.3 g/dL). At the end of the study, the average hemoglobin was 12.6 g/dL for the high group and 11.3 g/dL for the low group.
- The composite cardiovascular endpoint was statistically worse in the higher target hemoglobin group with a hazard ratio of 1.3 [95% CI 1.03, 1.74] (p = 0.03 by log rank test).
- The rates for the individual components of the composite primary
endpoint were (high target vs. low):
- Death: 7.3% vs 5.0% (p = 0.07)
CHF hosp: 9.0% vs 6.6% (p = 0.07)
Non-fatal MI: 2.5% vs 2.8%
Non-fatal stroke: 1.7% vs 1.7%
- Death: 7.3% vs 5.0% (p = 0.07)
- The analyses for this study found no correlation between rate of rise of hemoglobin and adverse cardiovascular events. However, the relationship between seizures and the rate of rise of hemoglobin as reported in the labeling for all three products remains a concern.
The CHOIR and CREATE study findings underscore the importance of the existing warnings regarding cardiovascular risks that include thrombotic events and increased mortality observed in hemodialysis patients with cardiac disease targeted to higher hemoglobin levels (~14 g/dL), and recommendations not to exceed hemoglobin levels of 12 g/dL in approved labeling for Procrit, Epogen, and Aranesp. Please refer to the full prescribing information for additional information. Internet links to the full prescribing information for all approved ESA products may be found at the FDA page for this alert.
Report serious adverse events to FDA's MedWatch reporting system by completing a form on line at http://www.fda.gov/medwatch/report.htm, by faxing (1.800.FDA.0178), by mail using the postage-paid address form provided online (5600 Fishers Lane, Rockville, MD 20852-9787), or by telephone (1.800.FDA.1088).
Fee Schedule Update for 2007 for Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS)
Do you have your NPI? National Provider Identifiers (NPIs) will be required
on claims sent on or after May 23, 2007. Every health care provider needs
to get an NPI. Learn more about the NPI and how to apply for an NPI by
visiting http://www.cms.hhs.gov/NationalProvIdentStand/ on
the CMS Web site.
Provider Types Affected
Physicians, suppliers, and providers who bill Medicare contractors
(Part A/B Medicare Administrative Contractors (A/B MACs), durable medical
equipment regional carriers (DMERCs), DME Medicare administrative contractors
(DME MACs), fiscal intermediaries (FIs), carriers, and/or regional home
health intermediaries (RHHIs)), for services paid under the DMEPOS Fee
Schedule.
Provider Action Needed
This article is based on Change Request (CR) 5417, and it provides
specific information regarding the annual update for the 2007 DMEPOS
Fee Schedule. Be sure billing staff are aware of this update.
Background
The DMEPOS fee schedules are updated on a quarterly basis in
order to:
- Implement fee schedule amounts for new codes; and
- Revise any fee schedule amounts for existing codes that were calculated in error.
Payment on a fee schedule basis is required for:
- Durable Medical Equipment (DME), prosthetic devices, orthotics, prosthetics, and surgical dressings by the Social Security Act (Sections 1834(a), (h), and (i)); and
- Parenteral and Enteral Nutrition (PEN) by
regulations contained in the Code of Federal Regulations (42 CFR 414.102).
| A4348 | L0100 | L6745 | L6825 | L6872 |
| A4359 | L0110 | L6750 | L6830 | L6873 |
| A4462 | L3902 | L6755 | L6835 | L6875 |
| A4632 | L3914 | L6765 | L6840 | L6880 |
| E0164 | L6700 | L6770 | L6845 | L7010 |
| E0166 | L6705 | L6775 | L6850 | L7015 |
| E0180 | L6710 | L6780 | L6855 | L7020 |
| E0701 | L6715 | L6790 | L6860 | L7025 |
| E0977 thru E0999 | L6725 | L6795 | L6865 | L7030 |
| E2320 | L6730 | L6800 | L6867 | L7035 |
| K0090 thru K0097 | L6735 | L6806 thru L6809 | L6868 | |
| K0099 | L6740 | L6830 | L6870 |
Note: DMERCs and DME MACS will use the 2007 PEN fee schedule payment amounts to pay claims for items furnished from January 1, 2007 through December 31, 2007
Deleted HCPCS Codes
The following codes are being deleted from the HCPCS effective
January 1, 2007, and are therefore being removed from the DMEPOS and
PEN fee schedule files.
Added HCPCS
The HCPCS codes listed below are being added to the HCPCS on
January 1, 2007:
| A4461 | A8003 | L1001 | L6639 |
| A4463 | A004 | L3806 | L6703 |
| A4559 | A9279 | L3808 | L6704 |
| A4600 | E0676 | L3915 | L6706 |
| A4601 | E0936 | L5993 | L6707 thru L6709 |
| A8000 | E2373 thru E2377 | L5994 | L7007 thru L7009 |
| A8001 | E2381 thru E2396 | L661 | L8690 |
| A8002 | K0733 thru K0737 | L6624 | L8691 |
| L8695 |
Payment Rates for Oxygen and Oxygen Equipment
As part of this fee schedule update, the Centers for Medicare & Medicaid
Services (CMS) is implementing national monthly payment rates for oxygen
and oxygen equipment effective for claims with dates of service on or
after January 1, 2007. The 2007 national monthly payment rates are listed
in the table below. As a result of these changes, CMS is revising the
fee schedule amounts for codes E1405 and E1406. Since 1989, the fees
for E1405 and E1406 have been established based on a combination of the
Medicare payment amounts for stationary oxygen equipment and nebulizer
codes E0585 and E0570, respectively.
As part of these changes, suppliers must submit claims with both the
code for stationary oxygen contents (E0441 or E0442) and the code for
portable oxygen contents (E0443 or E0444) when billing for payment for
furnishing both stationary and portable oxygen contents for beneficiary-owned
gaseous or liquid stationary and portable oxygen equipment.
| HCPCS Codes | Amount | Class |
| E0424, E0439, E1390, and E1391 | $198.40 | Stationary Oxygen Equipment (including stationary concentrator, liquid and gaseous equipment) and Oxygen Contents (stationary and portable) |
| E0431 and E0434 | $31.79 | Portable Equipment Only (gaseous or liquid tanks) |
| E1392 and K0738 | $51.63 | Oxygen Generating Portable Equipment (OGPE) Only |
| E0441 and E0442 | $77.45 | Oxygen Contents for Beneficiary-Owned Stationary Gaseous or Liquid Oxygen Equipment |
| E0443 and E0444 | $77.45 | Oxygen Contents for Beneficiary-Owned Portable Gaseous or Liquid Oxygen Equipment |
The fee schedules for HCPCS code E0461 (Volume Control Ventilator, Without
Pressure Support Mode, May Include Pressure Control Mode, Used with Non-Invasive
Interface (E.G. Mask)) are being revised as part of this update to correct
calculation errors and are effective for dates of service on or after
January 1, 2007.
Gap-Fill Items
The Medicare DMERCS and DME MACs will gap-fill base fee schedule
amounts for each State in their region for the following new and revised
HCPCS codes that will be subject to the DMEPOS fee schedules in 2007:
- Inexpensive or routinely purchased DME for codes A8002, A8003, A8004,
E2373, E2374, E2375,
E2376, E2377, E2388, E2389, E2390, E2391, E2392, E2393, E2394, E2395 - Capped rental DME codes of E0639 and E0640 • Prosthetics and Orthotics codes of L1001, L3806, L3808, L3915, L5993, L5994, L6611, L6624, L6639 • Surgical Dressings codes of A4463
- DME supplies codes of A4559
Additional Information
If you have questions, please contact your Medicare A/B MAC,
FI, DMERC, DME/MAC, RHHI or carrier at their toll-free number which may
be found at: http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on
the CMS Web site.
For complete details regarding this Change Request (CR) please see the official instruction (CR5417) issued to your Medicare A/B MAC, DMERC, DME MAC, FI, RHHI, or carrier. That instruction may be viewed by going to http://www.cms.hhs.gov/Transmittals/downloads/R1125CP.pdf on the CMS Web site.
Flu Shot Reminder
As a respected source of health care information, patients
trust their doctors' recommendations. If you have Medicare patients
who haven't yet received their flu shot, help protect them by recommending
an annual influenza and a one time pneumococcal vaccination. Medicare
provides coverage for flu and pneumococcal vaccines and their administration.
And don't forget to immunize yourself and your staff. Protect yourself,
your patients, and your family and friends. Get Your Flu Shot. Remember — Influenza
vaccination is a covered Part B benefit. Note that influenza vaccine
is NOT a Part D covered drug. For more information about Medicare's coverage
of adult immunizations and educational resources, go to CMS's Web site: http://www.cms.hhs.gov/MLNMattersArticles/downloads/SE0667.pdf.
Implementation of a One-Time Only Ultrasound Screening for Abdominal Aortic Aneurysms (AAA), Resulting from a Referral from an Initial Preventive Physical Examination
Note: This article was changed on December 8, 2006 to emphasize that this coverage is for a one-time only service and it must also be as a result of a referral from an initial preventive physical exam and is also subject to other limitations as discussed in this article and in CR5235.
Provider Types Affected
All physicians and providers who bill Medicare carriers, fiscal
intermediaries (FIs), and Medicare Administrative Contractors (MACs)
for subject services
Background
This article and related CR5235 highlight the fact that section
5112 of the Deficit Reduction Act (DRA) of 2005 allows for one ultrasound
screening for Abdominal Aortic Aneurysms (AAA) under Medicare Part B,
effective for services furnished on or after January 1, 2007, as a result
of a referral from an Initial Preventive Physical Examination (IPPE)
and subject to certain eligibility and other limitations. This provision
also waives the annual Part B deductible for the AAA screening test.
Key Points
Effective for dates of service on and after January 1, 2007
Medicare will pay for a one-time ultrasound screening for AAA, for beneficiaries
who meet the following criteria:
- Receives a referral for such an ultrasound screening as a result of an initial preventive physical examination (IPPE) (See MLN Matters article MM3638 at http://www.cms.hhs.gov/ MLNMattersArticles/downloads/MM3638.pdf for more details on the IPPE.)
- Receives such ultrasound screening from a provider or supplier who is authorized to provide covered ultrasound diagnostic services.
- Has not been previously furnished such an ultrasound screening under the Medicare Program
- Is included in at least one of the following risk categories:
- Has a family history of abdominal aortic aneurysm;
- Is a man age 65 to 75 who has smoked at least 100 cigarettes in his lifetime;
- Is a beneficiary, who manifests other risk factors in a beneficiary category recommended for screening by the United States Preventive Services Task Force regarding AAA, as specified by the Secretary of Health and Human Services, through the national coverage determinations process.
Payment
- The Part B deductible for screening AAA is waived effective January 1, 2007, but coinsurance is applicable.
- If the screening is provided in a physician office, the service is billed to the carrier using the HCPCS code G0389: Ultrasound, B-scan and/or real time with image documentation; for abdominal aortic aneurysm (AAA) screening.
- Short Descriptor: Ultrasound exam AAA screen
- Modifiers: TC, 26 (modifiers are optional)
- Payment is under the Medicare Physician Fee Schedule (MPFS).
FIs will pay for the AAA screening only when the services are performed in a hospital, including a CAH, IHS facility, an SNF, RHC, or FQHC and submitted on one of the following types of bills (TOBs): 12X, 13X, 22X, 23X, 71X, 73X, 85X. - The following table describes the payment methodology Medicare will use for AAA Screening:
| Facility | Type of Bill | Payment |
| Hospitals subject to OPPS | 12X, 13X | OPPS |
| Method I and Method II Critical Access Hospitals (CAHs) | 12x and 85X | 101% of reasonable cost |
| IHS providers | 13X, revenue code 051X | OMB-approved outpatient per visit all inclusive rate (AIR) |
| IHS providers | 12X, revenue code 024X | All inclusive inpatient ancillary per diem rate |
| IHS CAHs | 85X, revenue code 051X | 101% of the all-inclusive facility specific per visit rate |
| IHS CAHs | 12X, revenue code 024X | 101% of the all -inclusive facility specific per diem rate |
| SNFs** | 22X, 23X | Non-facility rate on the MPFS |
| RHCs* | 71X, revenue code 052X | All-inclusive encounter rate |
| FQHCs* | 73X, revenue code 052X | All inclusive encounter rate |
| Maryland Hospitals under jurisdication of the Health Services Cost Review Commission (HSCRC) | 12X, 13X | 94% of provider submitted charges or according to the terms of the Maryland Waiver |
*If the screening is provided in an RHC or FQHC, the professional portion
of the service is billed to the FI using TOBs 71x and 73x, respectively,
and the appropriate site of service revenue code in the 052x revenue
code series. If the screening is provided in an independent RHC or freestanding
FQHC, the technical component of the service can be billed by the practitioner
to the carrier under the practitioner's ID following instructions for
submitting practitioner claims to the Medicare carrier. If the screening
is provided in a provider-based RHC/FQHC, the technical component of
the service can be billed by the base provider to the FI under the base
provider's ID, following instructions for submitting claims to the FI
from the base provider.
** The SNF consolidated billing provision allows separate part B payment
for screening services for beneficiaries that are in skilled Part A SNF
stays, however, the SNF must submit these services on a 22x bill type.
Screening services provided by other provider types must be reimbursed
by the SNF.
Implementation
The implementation date for this instruction is January 2, 2007.
Information Regarding Advanced Beneficiary Notices: Medicare contractors will deny an AAA screening service billed more than one in a beneficiary's lifetime.
If a second G0389 is billed for AAA for the same beneficiary or if any
of the other statutory criteria for coverage listed in Section 1861(s)(2)(AA)
of the Social Security Act are not met, the service would be denied as
a statutory (technical) denial under Section 1861(s)(2)(AA), not a medical
necessity denial.
If a provider cannot determine whether or not the beneficiary has previously
had an AAA screening, but all of the other statutory requirements for
coverage have been met, the provider should issue the ABN-G. Likewise,
if all of the statutory requirements for coverage have been met, but
a question of medical necessity still exists, the provider should issue
the ABN-G.
Additional Information
The official instructions for CR 5235, issued to your Medicare
carrier, FI, MAC, FQHC, RHC, SNF, or CAH regarding this change can be
found at http://www.cms.hhs.gov/Transmittals/downloads/R1113CP.pdf on
the CMS Web site. The Medicare Claims Processing Manual, Publication
100-04, Chapter 18, has been updated to include the requirements to implement
section 5112 of the DRA of 2005. The new sections of this chapter address
the payment and allowable settings for AAA and the sections are attached
to CR5235.
If you have questions, please contact your Medicare carrier, MAC, or FI at their toll-free number, which may be found at http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on the CMS Web site.
Flu Shot Reminder
Flu season is here! Medicare patients give many reasons for
not getting their flu shot, including—"It causes the flu;
I don't need it; it has side effects; it's not effective; I didn't think
about it; I don't like needles!" The fact is that out of the average
36,000 people in the U.S. who die each year from influenza and complications
of the virus, greater than 90 percent of deaths occur in persons 65 years
of age and older. You can help your Medicare patients overcome these
odds and their personal barriers through patient education. Talk to your
Medicare patients about the importance of getting their annual flu shot—and
don't forget to immunize yourself and your staff. Protect yourself, your
patients, and your family and friends. Get Your Flu Shot. Remember — Influenza
vaccination is a covered Part B benefit. Note that influenza vaccine
is NOT a Part D covered drug. For more information about Medicare's coverage
of adult immunizations and educational resources, go to CMS's Web site: http://www.cms.hhs.gov/MLNMattersArticles/downloads/SE0667.pdf
Implementation of Revised Fee Schedule Amounts for New Healthcare Common Procedure Coding System (HCPCS) Codes for Power Mobility Devices (PMDs)
Joint Signature Memorandum/Technical Direction Letter (JSM/TDL)-07074, issued on November 16, 2006, included instructions for implementation on November 15, 2006, of refined fee schedule amounts for HCPCS codes K0813 thru K0864. The revised fee schedule amounts for codes K0813 thru K0864 were transmitted to contractors in addendum Durable Medical Equipment Prosthetic, Orthotics, & Supplies (DMEPOS) fee schedule files on November 16, 2006.
This is to advise that the fee schedule amounts for codes K0813 thru
K0864 have been further refined and will be transmitted to contractors
in addendum DMEPOS fee schedule files by 8 pm EST on December 13, 2006.
Contractors must adjust previously processed claims for codes K0813 thru K0864 with dates of service on or after November 15, 2006, if they are resubmitted as adjustments.
As a result of the PMD revisions, a revised 2007 DMEPOS Fee Schedule file will be released to the Statistical Analysis Durable Medical Equipment Regional Carrier (SADMERC), the Durable Medical Equipment Medicare Administrative Contractors (DME MACs), DMERCS, and local Part B carriers via CMS' mainframe telecommunications system on December 13, 2006. A revised 2007 DMEPOS Fee Schedule file will also be released to the intermediaries, regional home health intermediaries, Railroad Retirement Board (RRB), Indian Health Service, and United Mine Workers on December 13, 2006.
Implementation of Revised Fee Schedule Amounts for New Healthcare Common Procedure Coding System (HCPCS) Codes for Power Mobility Devices (PMDs)
Joint Signature Memorandum/Technical Direction Letter (JSM/TDL)-07145, issued on December 13, 2006, included instructions for implementation on November 15, 2006, of refined fee schedule amounts for HCPCS codes K0813 thru K0864. The revised fee schedule amounts for codes K0813 thru K0864 were transmitted to contractors in addendum Durable Medical Equipment Prosthetic, Orthotics, & Supplies (DMEPOS) fee schedule files on December 13, 2006.
This is to advise that the fee schedule amounts for codes K0827, K0829 and K0864 have been further refined and will be transmitted to contractors in addendum DMEPOS fee schedule files by 8 pm EST on December 21, 2006.
Contractors must adjust previously processed claims for codes K0827,
K0829, and K0864 with dates of service on or after November 15, 2006,
if they are resubmitted as adjustments.
As a result of the PMD revisions, a revised 2007 DMEPOS Fee Schedule
file will be released to the Statistical Analysis Durable Medical Equipment
Regional Carrier (SADMERC), the Durable Medical Equipment Medicare Administrative
Contractors (DME MACs), DMERCS, and local Part B carriers via CMS' mainframe
telecommunications system on December 21, 2006. A revised 2007 DMEPOS
Fee Schedule file will also be released to the intermediaries, regional
home health intermediaries, Railroad Retirement Board (RRB), Indian Health
Service, and United Mine Workers on December 21, 2006.
Infrared Therapy Devices
Provider Types Affected
Physicians, suppliers, and providers who submit claims to Medicare carriers,
Part A/B Medicare Administrative Contractors (A/B MACs), durable medical
equipment regional carriers (DMERCs), DME Medicare administrative contractors
(DME/MACs), fiscal intermediaries (FIs), and/or regional home health
intermediaries (RHHIs), for the use of infrared therapy devices for
treatment of diabetic and/or non-diabetic peripheral sensory neuropathy,
wounds and/or ulcers of the skin and/or subcutaneous tissues in Medicare
beneficiaries.
Impact on Providers
This article is based on Change Request (CR) 5421. Effective for services
performed on or after October 24, 2006, the Centers for Medicare & Medicaid
Services (CMS) has made a National Coverage Determination (NCD) stating
the use of infrared and/or near-infrared light and/or heat, including
monochromatic infrared energy (MIRE), is non-covered for the treatment,
including symptoms such as pain arising from these conditions, of diabetic
and/or non-diabetic peripheral sensory neuropathy, wounds and/or ulcers
of the skin and/or subcutaneous tissues in Medicare beneficiaries.
Background
The use of infrared therapy devices has been proposed for a variety of
disorders, including treatment of diabetic neuropathy, other peripheral
neuropathy, skin ulcers and wounds, and similar related conditions,
including symptoms such as pain arising from these conditions. A wide
variety of devices are currently available. Previously there was no
NCD concerning the use of infrared therapy devices, leaving the decision
to cover or not cover up to local Medicare contractors.
The following requirements are in effect as of October 24, 2006:
- Effective for services performed on or after October 24, 2006, infrared therapy devices, HCPCS codes E0221 (infrared heating pad system) and A4639 (infrared heating pad replacement) are non-covered as DME or PT/OT services when used for the treatment of diabetic and/or non-diabetic peripheral sensory neuropathy, wounds, and/or ulcers of the skin and/or subcutaneous tissues.
- Claims will be denied with CPT 97026 (infrared therapy incident
to or as a PT/OT benefit) and HCPCS E0221 or A4639, if they are accompanied
by the following ICD-9 codes:
- 250.60-250.63,
- 354.4, 354.5, 354.9,
- 355.1-355.4,
- 355.6-355.9
- 356.0, 356.2-356.4, 356.8-356.9,
- 357.0-357.7,
- 674.10, 674.12, 674.14, 674.20, 674.22, 674.24,
- 707.00-707.07, 707.09-707.15, 707.19,
- 870.0-879.9,
- 880.00-887.79,
- 890.0-897.7, or
- 998.31-998.32.
- Note that denial of infrared therapy claims for the indications listed above applies to all settings, and affects Types of bills (TOBs) 12X, 13X, 22X, 23X, 34X, 74X, 75X and 85X.
- If you submit a claim for one of the non-covered services, your patient will receive the Medicare Summary Notice (MSN) message stating "This service was not covered by Medicare at the time you received it". The Spanish translation is: "Este servicio no estaba cubierto por Medicare cuando usted lo recibió."
- If you submit a claim for one of the non-covered services you will receive a remittance advice notice that reads: Claim Adjustment Reason Code 50, "These are non-covered services because this is not deemed a 'medical necessity' by the payer."
- Physicians, physical therapists, occupational therapists, outpatient rehabilitation facilities (ORFs), comprehensive outpatient rehabilitation facilities (CORFs), home health agencies (HHAs), and hospital outpatient departments should note that you are liable if the service is performed, unless the beneficiary signs an Advanced Beneficiary Notice (ABN).
- DME suppliers and HHA be aware that you are liable for the devices when they are supplied, unless the beneficiary signs an ABN.
Additional Information
If you have questions, please contact your Medicare A/B MAC,
FI, DMERC, DME/MAC, RHHI or carrier at their toll-free number which may
be found at:
http://www.cms.hhs.gov/MLNProducts/downloads/CallCenterTollNumDirectory.zip on
the CMS Web site.
For complete details regarding this Change Request (CR) please see the official instruction (CR5421) issued to your Medicare A/B MAC, FI, DME MAC, RHHI, or carrier. There are actually two transmittals associated with CR5421. The first is the national coverage determination transmittal, located at
