June 2004 Part B Medicare Bulletin
Table of Contents
- 2004 Not Otherwise Classified Drug Pricing File - 2nd Quarter
- 2004 Jurisdiction List
- Adjudication of Reference Laboratory Service Claims
- Arrangements for Physical, Occupational, and Speech-Language Pathology Services
- Beneficiary Eligibility Options
- Electrical Stimulation and Electromagnetic Therapy for the Treatment of Wounds
- E/M Coding: Volume of Documentation versus Medical Necessity
- Emergency Correction Regarding Correction to Healthcare Common Procedure Coding System (HCPCS) Codes for Low-Osmolar Contrast Material
- G Code Error
- Incident to Services
- Manulization of POS Code Set Program Memorandum; Revision to Group Home Code Description
- Manulization of NCD: Acupuncture for Fibromyalgia / Osteroarthritis
- Medical Review Frequently Asked Questions - April 2004
- Medicare Providers: Their Vendors, Clearinghouses, or Other Third-Party Billers and the HIPAA/Medicare Contingency plan
- (MMA) - Clarifications to Certain Exceptions to Medicare Limits on Physician Referrals
- MMA - New Medicare-Approved Drug Discount Cards and Transitional Assistance Program: A Summary for Pharmacists and Other Pharmacy Professionals
- MMA - New Medicare-Approved Drug Discount Cards and Transitional Assistance Program: A Summary for Physicians and Other Health Care Professionals
- Not Otherwise Classified Drugs/Biologicals Claim Filing Instructions
- Ocular Photodynamic Therapy (OPT) with Verteporfin for Age-Related Macular Degeneration (AMD)
- Progressive Corrective Action on HCPCS code J9310, Rituxan®
- Refiling Denied Claims for Payment
- Reminder to Stop Duplicate Billings
- Update to the Health Care Provider Taxonomy Codes (HPTCs)Version 4.0
- Update to PT Re-Certification Dates
Part B Not Otherwise Classified Drug Fee Schedule
The most current version of this document is available on the Part B Fee Schedule Index. If you need a copy of the document as it was originally published, please refer to the PDF copy of this Medicare Bulletin.
2004 Jurisdiction List
| HCPCS | DESCRIPTION | JURISDICTION |
| A0021 - A0999 | Ambulance Services | Local Carrier |
| A4206 - A4209 | Medical, Surgical, and Self-Administered Injection Supplies | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4210 | Needle Free Injection Device | DME REGIONAL Carrier |
| A4211 | Medical, Surgical, and Self-Administered Injection Supplies | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4212 | Non Coring Needle or Stylet with or without Catheter | Local Carrier |
| A4213 - A4215 | Medical , Surgical, and Self-Administered Injection Supplies | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4216 - A4217 | Saline | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4220 | Refill Kit for Implantable Pump | Local Carrier |
| A4221 - A4250 | Medical, Surgical, and Self-Administered Injection Supplies | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4253 - A4259 | Diabetic Supplies | DME REGIONAL Carrier |
| A4260 | Levonorgestrel Implant | Local Carrier |
| A4261 | Cervical Cap for Contraceptive Use | Local Carrier |
| A4262 - A4263 | Lacrimal Duct Implants | Local Carrier |
| A4265 | Paraffin | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4266 - A4269 | Contraceptives | Local Carrier |
| A4270 | Endoscope Sheath | Local Carrier |
| A4280 | Accessory for Breast Prosthesis | DME REGIONAL Carrier |
| A4281 - A4286 | Accessory for Breast Pump | DME REGIONAL Carrier |
| A4290 | Sacral Nerve Stimulation Test Lead | Local Carrier |
| A4300 - A4301 | Implantable Catheter | Local Carrier |
| A4305 - A4306 | Disposable Drug Delivery System | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4310 - A4359 | Incontinence Supplies/Urinary Supplies | If provided in the physician's office for a temporary condition, the item is incident to the physician's service & billed to the Local Carrier. If provided in the physician's office or other place of service for a permanent condition, the item is a prosthetic device & billed to the DME REGIONAL Carrier. |
| A4361 - A4434 | Ostomy Supplies | If provided in the physician's office for a temporary condition, the item is incident to the physician's service & billed to the Local Carrier. If provided in the physician's office or other place of service for a permanent condition, the item is a prosthetic device & billed to the DME REGIONAL Carrier. |
| A4450 - A4455 | Tape;Adhesive Remover | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4458 | Enema Bag | DME REGIONAL Carrier |
| A4462 | Abdominal Dressing | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4465 | Non-elastic Binder for Extremity | DME REGIONAL Carrier |
| A4470 | Gravlee Jet Washer | Local Carrier |
| A4480 | Vabra Aspirator | Local Carrier |
| A4481 | Tracheostomy Supply | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4483 | Moisture Exchanger | DME REGIONAL Carrier |
| A4490 - A4510 | Surgical Stockings | DME REGIONAL Carrier |
| A4521 - A4538 | Diapers | DME REGIONAL Carrier |
| A4550 | Surgical Trays | Local Carrier |
| A4554 | Disposable Underpads | DME REGIONAL Carrier |
| A4556 - A4558 | Electrodes; Lead Wires; Con-ductive Paste | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4561 - A4562 | Pessary | Local Carrier |
| A4565 | Sling | Local Carrier |
| A4570 | Splint | Local Carrier |
| A4575 | Topical Hyperbaric Oxygen Chamber, Disposable | DME REGIONAL Carrier |
| A4580 - A4590 | Casting Supplies & Material | Local Carrier |
| A4595 | TENS Supplies | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4606 | Oxygen Probe for Oximeter | DME REGIONAL Carrier |
| A4608 | Transtracheal Oxygen Catheter | DME REGIONAL Carrier |
| A4609 - A4610 | Tracheal Suction Catheter | DME REGIONAL Carrier |
| A4611 - A4613 | Oxygen Equipment Batteries and Supplies | DME REGIONAL Carrier |
| A4614 | Peak Flow Rate Meter | Local Carrier if incident to a physician's service (not separately payable). If other DME Regional Carrier. |
| A4615 - A4629 | Oxygen & Tracheostomy Supplies | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4630 - A4640 | DME Supplies | DME REGIONAL Carrier |
| A4641 - A4646 | Imaging Agent; Contrast Material | Local Carrier |
| A4647 | Contrast Material | Local Carrier |
| A4649 | Miscellaneous Surgical Supplies | Local Carrier if incident to a physician's service (not separately payable). If other DME REGIONAL Carrier. |
| A4651 - A4932 | Supplies for ESRD | DME REGIONAL Carrier |
| A5051 - A5093 | Additional Ostomy Supplies | If provided in the physician's office for a temporary condition, the item is incident to the physician's service & billed to the Local Carrier. If provided in the physician's office or other place of service for a permanent condition, the item is a prosthetic device & billed to the DME REGIONAL Carrier. |
| A5102 - A5200 | Additional Incontinence and Ostomy Supplies | If provided in the physician's office for a temporary condition, the item is incident to the physician's service & billed to the Local Carrier. If provided in the physician's office or other place of service for a permanent condition, the item is a prosthetic device & billed to the DME REGIONAL Carrier. |
| A5500 - A5511 | Therapeutic Shoes | DME REGIONAL Carrier |
| A6000 | Non-Contact Wound Warming Cover | DME REGIONAL Carrier |
| A6010-A6024 | Surgical Dressing | Local Carrier if incident to a physician's service (not separately payable) or if supply for implanted prosthetic device or implanted DME. If other DME REGIONAL Carrier. |
| A6025 | Silicone Gel Sheet | Local Carrier if incident to a physician's service (not separately payable) or if supply for implanted prosthetic device or implanted DME. If other DME REGIONAL Carrier. |
| A6154 - A6411 | Surgical Dressing | Local Carrier if incident to a physician's service (not separately payable) or if supply for implanted prosthetic device or implanted DME. If other DME REGIONAL Carrier. |
| A6412 | Eye Patch | Local Carrier if incident to a physician's service (not separately payable) or if supply for implanted prosthetic device or implanted DME. If other DME REGIONAL Carrier. |
| A6441 - A6512 | Surgical Dressings | Local Carrier if incident to a physician's service (not separately payable) or if supply for implanted prosthetic device or implanted DME. If other DME REGIONAL Carrier. |
| A6550 - A6551 | Supplies for Negative Pressure Wound Therapy Electrical Pump | DME REGIONAL Carrier |
| A7000 - A7039 | Accessories for Nebulizers, Aspirators, and Ventilators | DME REGIONAL Carrier |
| A7042 - A7043 | Pleural Catheter | Local Carrier |
| A7044 - A7046 | Respiratory Accessories | DME REGIONAL Carrier |
| A7501-A7526 | Tracheostomy Supplies | DME REGIONAL Carrier |
| A9150 | Non-Prescription Drugs | Local Carrier |
| A9270 | Noncovered Items or Services | DME REGIONAL Carrier |
| A9280 | Alarm Device | DME REGIONAL Carrier |
| A9300 | Exercise Equipment | DME REGIONAL Carrier |
| A9500 - A9700 | Supplies for Radiology Procedures | Local Carrier |
| A9900 | Miscellaneous DME Supply or Accessory | Local Carrier if used with implanted DME. If other, DME REGIONAL Carrier. |
| A9901 | Delivery | DME REGIONAL Carrier |
| A9999 | Miscellaneous DME Supply or Accessory | Local Carrier if used with implanted DME. If other, DME REGIONAL Carrier. |
| B4034 - B9999 | Enteral and Parenteral Therapy | DME REGIONAL Carrier |
| D0120 - D9999 | Dental Procedures | Local Carrier |
| E0100 - E0105 | Canes | DME REGIONAL Carrier |
| E0110 - E0118 | Crutches | DME REGIONAL Carrier |
| E0130 - E0159 | Walkers | DME REGIONAL Carrier |
| E0160 - E0175 | Commodes | DME REGIONAL Carrier |
| E0176 - E0199 | Decubitus Care Equipment | DME REGIONAL Carrier |
| E0200 - E0239 | Heat/Cold Applications | DME REGIONAL Carrier |
| E0240 - E0248 | Bath and Toliet Aids | DME REGIONAL Carrier |
| E0249 | Pad for Heating Unit | DME REGIONAL Carrier |
| E0250 - E0304 | Hospital Beds | DME REGIONAL Carrier |
| E0305 - E0326 | Hospital Bed Accessories | DME REGIONAL Carrier |
| E0350 - E0352 | Electronic Bowel Irrigation System | DME REGIONAL Carrier |
| E0370 | Heel Pad | DME REGIONAL Carrier |
| E0371 - E0373 | Decubitus Care Equipment | DME REGIONAL Carrier |
| E0424 - E0484 | Oxygen and Related Respiratory Equipment | DME REGIONAL Carrier |
| E0500 | IPPB Machine | DME REGIONAL Carrier |
| E0550 - E0585 | Compressors/Nebulizers | DME REGIONAL Carrier |
| E0590 | Drug Dispensing Fee | DME REGIONAL Carrier |
| E0600 | Suction Pump | DME REGIONAL Carrier |
| E0601 | CPAP Device | DME REGIONAL Carrier |
| E0602 - E0604 | Breast Pump | DME REGIONAL Carrier |
| E0605 | Vaporizer | DME REGIONAL Carrier |
| E0606 | Drainage Board | DME REGIONAL Carrier |
| E0607 | Home Blood Glucose Monitor | DME REGIONAL Carrier |
| E0610 - E0615 | Pacemaker Monitor | DME REGIONAL Carrier |
| E0616 | Implantable Cardiac Event Recorder | Local Carrier |
| E0617 | External Defibrillator | DME REGIONAL Carrier |
| E0618 - E0619 | Apnea Monitor | DME REGIONAL Carrier |
| E0620 | Skin Piercing Device | DME REGIONAL Carrier |
| E0621 - E0636 | Patient Lifts | DME REGIONAL Carrier |
| E0637 - E0638 | Standing Devices | DME REGIONAL Carrier |
| E0650 - E0675 | Pneumatic Compressor and Appliances | DME REGIONAL Carrier |
| E0691 - E0694 | Ultraviolet Light Therapy Systems | DME REGIONAL Carrier |
| E0700 | Safety Equipment | DME REGIONAL Carrier |
| E0701 | Helmet | DME REGIONAL Carrier |
| E0710 | Restraints | DME REGIONAL Carrier |
| E0720 - E0745 | Electrical Nerve Stimulators | DME REGIONAL Carrier |
| E0746 | EMG Device | Local Carrier |
| E0747 - E0748 | Osteogenic Stimulators | DME REGIONAL Carrier |
| E0749 | Implantable Osteogenic Stimulators | Local Carrier |
| E0752 | Implantable Nerve Stimulator Electrodes | Local Carrier |
| E0754 | Patient Programmer for use with IPG | Local Carrier |
| E0755 | Reflex Stimulator | DME REGIONAL Carrier |
| E0756 - E0759 | Implantable Nerve Stimulator | Local Carrier |
| E0760 | Ultrasonic Osteogenic Stimulator | DME REGIONAL Carrier |
| E0761 | Electromagnetic Treatment Device | DME REGIONAL Carrier |
| E0765 | Nerve Stimulator | DME REGIONAL Carrier |
| E0776 | IV Pole | DME REGIONAL Carrier |
| E0779 - E0780 | External Infusion Pumps | DME REGIONAL Carrier |
| E0781 | Ambulatory Infusion Pump | Billable to both the local carrier and the DME REGIONAL Carrier. This item may be billed to the DME REGIONAL Carrier whenever the infusion is initiated in the physician's office but the patient does not return during the same business day. |
| E0782 - E0783 | Infusion Pumps, Implantable | Local Carrier |
| E0784 | Infusion Pumps, Insulin | DME REGIONAL Carrier |
| E0785 - E0786 | Implantable Infusion Pump Catheter | Local Carrier |
| E0791 | Parenteral Infusion Pump | DME REGIONAL Carrier |
| E0830 | Ambulatory Traction Device | DME REGIONAL Carrier |
| E0840 - E0900 | Traction Equipment | DME REGIONAL Carrier |
| E0910 - E0930 | Trapeze/Fracture Frame | DME REGIONAL Carrier |
| E0935 | Passive Motion Exercise Device | DME REGIONAL Carrier |
| E0940 | Trapeze Equipment | DME REGIONAL Carrier |
| E0941 | Traction Equipment | DME REGIONAL Carrier |
| E0942 - E0945 | Orthopedic Devices | DME REGIONAL Carrier |
| E0946 - E0948 | Fracture Frame | DME REGIONAL Carrier |
| E0950 - E1298 | Wheelchairs | DME REGIONAL Carrier |
| E1300 - E1310 | Whirlpool Equipment | DME REGIONAL Carrier |
| E1340 | Repair or Non-routine Service | Local Carrier if repair of implanted DME. If other, DME REGIONAL Carrier. |
| E1353 - E1391 | Additional Oxygen Related Equipment | DME REGIONAL Carrier |
| E1399 | Miscellaneous DME | Local Carrier if implanted DME. If other, DME REGIONAL Carrier. |
| E1405 - E1406 | Additional Oxygen Equipment | DME REGIONAL Carrier |
| E1500 - E1699 | Artificial Kidney Machines and Accessories | DME REGIONAL Carrier |
| E1700 - E1702 | TMJ Device and Supplies | DME REGIONAL Carrier |
| E1800 - E1840 | Dynamic Flexion Devices | DME REGIONAL Carrier |
| E1902 | Communication Board | DME REGIONAL Carrier |
| E2000 | Gastric Suction Pump | DME REGIONAL Carrier |
| E2100 - E2101 | Blood Glucose Monitors with Special Features | DME REGIONAL Carrier |
| E2120 | Pulse Generator for Tympanic Treatment of Inner Ear | DME REGIONAL Carrier |
| E2201 - E2399 | Wheelchair Accessories | DME REGIONAL Carrier |
| E2402 | Negative Pressure Wound Therapy Pump | DME REGIONAL Carrier |
| E2500 - E2599 | Speech Generating Device | DME REGIONAL Carrier |
| G0001 - G9016 | Misc. Professional Services | Local Carrier |
| J0120 - J0850 | Injection | Local Carrier if incident to a physician's service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| J0880 | Injection | Local Carrier |
| J0895 - J3570 | Injection | Local Carrier if incident to a physician's service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| J3590 | Unclassified Biologics | Local Carrier |
| J7030 - J7130 | Miscellaneous Drugs and Solutions | Local Carrier if incident to a physician's service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| J7190 - J7192 | Factor VIII | Local Carrier |
| J7193 - J7195 | Factor IX | Local Carrier |
| J7197 | Antithrombin III | Local Carrier |
| J7198 | Anti-inhibitor; per I.U. | Local Carrier |
| J7199 | Other Hemophilia Clotting Factors | Local Carrier |
| J7300 - J7303 | Intrauterine Copper Contraceptive | Local Carrier |
| J7308 | Aminolevulinic Acid HCL | Local Carrier |
| J7310 | Ganciclovir | Local Carrier if incident to a physician's service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| J7317 - J7320 | Injection | Local Carrier |
| J7330 | Autologous Cultured Chondrocytes, Implant | Local Carrier |
| J7340 - J7350 | Dermal and Epidermal - Tissue of Human Origin | Local Carriers |
| J7500 - J7599 | Immunosuppressive Drugs | Local Carrier if incident to a physician's service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| J7608 - J7699 | Inhalation Solutions | Local Carrier if incident to a physician's service. If other, DME REGIONAL Carrier. |
| J7799 | NOC, Other than Inhalation Drugs through DME | DME REGIONAL Carrier |
| J8499 | Prescription Drug, Oral, Non Chemotherapeutic | DME REGIONAL Carrier |
| J8510 - J8999 | Oral Anti-Cancer Drugs | DME REGIONAL Carrier |
| J9000 - J9999 | Chemotherapy Drugs | Local Carrier if incident to a physician's service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| K0001 - K0108 | Wheelchairs | DME REGIONAL Carrier |
| K0114 - K0116 | Spinal Orthotics | DME REGIONAL Carrier |
| K0195 | Elevating Leg Rests | DME REGIONAL Carrier |
| K0415 - K0416 | Antiemetic Drugs | DME REGIONAL Carrier |
| K0452 | Wheelchair Bearings | DME REGIONAL Carrier |
| K0455 | Infusion Pump used for Uninterrupted Administration of Epoprostenal | DME REGIONAL Carrier |
| K0462 | Loaner Equipment | DME REGIONAL Carrier |
| K0552 | External Infusion Pump Supplies | DME REGIONAL Carrier |
| K0601 - K0605 | External Infusion Pump Batteries | DME REGIONAL Carrier |
| K0606 - K0609 | Defibrilator Accessories | DME REGIONAL Carrier |
| K0618 - K0619 | TLSOs | DME REGIONAL Carrier |
| K0620 | Surgical Dressing | Local Carrier if incident to a physician's service (not separately payable) or if supply for implanted prosthetic device or implanted DME. If other DME REGIONAL Carrier. |
| L0100 - L2090 | Orthotics | DME REGIONAL Carrier |
| L2106 - L2116 | Orthotics | DME REGIONAL Carrier |
| L2126 - L4398 | Orthotics | DME REGIONAL Carrier |
| L5000 - L5999 | Lower Limb Prosthetics | DME REGIONAL Carrier |
| L6000 - L7499 | Upper Limb Prosthetics | DME REGIONAL Carrier |
| L7500 - L7520 | Repair of Prosthetic Device | Local Carrier if repair of implanted prosthetic device. If other, DME REGIONAL Carrier. |
| L7900 | Vacuum Erection System | DME REGIONAL Carrier |
| L8000 - L8490 | Prosthetics | DME REGIONAL Carrier |
| L8499 | Unlisted Procedure for Miscellaneous Prosthetic Services | Local Carrier if implanted prosthetic device. If other, DME REGIONAL Carrier. |
| L8500 - L8501 | Artificial Larynx; Tracheostomy Speaking Valve | DME REGIONAL Carrier |
| L8505 | Artificial Larynx Accessory | DME REGIONAL Carrier |
| L8507 - L8514 | Voice Prosthesis | DME REGIONAL Carrier |
| L8600 - L8699 | Prosthetic Implants | Local Carrier |
| L9900 | Miscellaneous Orthotic or Prosthetic Component or Accessory | Local Carrier if used with implanted prosthetic device. If other, DME REGIONAL Carrier. |
| M0064 - M0301 | Medical Services | Local Carrier |
| P2028 - P9615 | Laboratory Tests | Local Carrier |
| Q0035 | Influenza Vaccine; Cardio-kymography | Local Carrier |
| Q0081 | Infusion Therapy | Local Carrier if incident to a physicians service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| Q0083 - Q0085 | Chemotherapy Administration | Local Carrier if incident to a physicians service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| Q0091 | Smear Preparation | Local Carrier |
| Q0092 | Portable X-ray Setup | Local Carrier |
| Q0111 - Q0115 | Miscellaneous Lab Services | Local Carrier |
| Q0136 | Injection, Epoetin Alpha | Local Carrier if incident to a physician's service. If other, DME REGIONAL Carrier. |
| Q0137 | Injection Darbepoetin | Local Carrier if incident to a physician's service. If other, DME REGIONAL Carrier. |
| Q0144 | azithromycin dihydrate | Local Carrier if incident to a physician's service. If other, DME REGIONAL Carrier. |
| Q0163 - Q0181 | Anti-emetic | DME REGIONAL Carrier |
| Q0182 - Q0183 | Artificial Skin | Local Carrier |
| Q0187 | Factor VIIA | Local Carrier |
| Q1001 - Q1005 | New Technology IOL | Local Carrier |
| Q2022 | Von Willebrand Factor | Local Carrier |
| Q3014 | Telehealth Originating Site Facility Fee | Local Carrier |
| Q3019 - Q3020 | ALS Transport | Local Carrier |
| Q3025 - Q3026 | Vaccines | Local Carrier |
| Q3031 | Collagen Skin Test | Local Carrier |
| Q4001 - Q4051 | Splints and Casts | Local Carrier |
| Q4054 - Q4055 | Injection | DME REGIONAL Carrier when for Method II ESRD beneficiaries. If other, Local Carrier. |
| Q4075 - Q4077 | Injection | Local Carrier if incident to a physicians service or used in an implanted infusion pump. If other, DME REGIONAL Carrier. |
| R0070 - R0076 | Diagnostic Radiology Services | Local Carrier |
| V2020 - V2025 | Frames | DME REGIONAL Carrier |
| V2100 - V2513 | Lenses | DME REGIONAL Carrier |
| V2520 - V2523 | Hydrophilic Contact Lenses | Local Carrier if incident to a physician's service. If other, DME REGIONAL Carrier. |
| V2530 - V2531 | Contact Lenses, Scleral | DME REGIONAL Carrier |
| V2599 | Contact Lens, Other Type | Local Carrier if incident to a physician's service. If other, DME REGIONAL Carrier. |
| V2600 - V2615 | Low Vision Aids | DME REGIONAL Carrier |
| V2623 - V2629 | Prosthetic Eyes | DME REGIONAL Carrier |
| V2630 - V2632 | Intraocular Lenses | Local Carrier |
| V2700 - V2780 | Miscellaneous Vision Service | DME REGIONAL Carrier |
| V2781 | Progressive Lens | DME REGIONAL Carrier |
| V2782 - V2784 | Lenses | DME REGIONAL Carrier |
| V2785 | Processing--Corneal Tissue | Local Carrier |
| V2786 | Lense | DME REGIONAL Carrier |
| V2790 | Amniotic Membrane | Local Carrier |
| V2797 | Vision Supply | DME REGIONAL Carrier |
| V2799 | Miscellaneous Vision Service | DME REGIONAL Carrier |
| V5008 - V5299 | Hearing Services | Local Carrier |
| V5336 | Repair/Modification of Augmentative Communicative System or Device | DME REGIONAL Carrier |
| V5362 - V5364 | Speech Screening | Local Carrier |
| Revised: February 2004 | ||
(04-0883)
Adjudication of Reference Laboratory Service Claims
Provider Types Affected
Independent clinical diagnostic laboratories.
Provider Action Needed
An independent laboratory may bill for services they refer to another laboratory no matter where the
reference laboratory is located, as long as it is within any Medicare claims processing jurisdiction. When billing for reference laboratory services, independent clinical diagnostic laboratories must submit the zip code of the location where the laboratory service was actually performed. The carriers’ standard billing systems will now price the payment of referred laboratory services based on the zip code where the service was performed.
Any independent laboratories that were assigned a Provider Identification Number (PIN) for the purposes of reimbursement of reference laboratory services in a payment jurisdiction other than one they have a physical presence will have those PINs revoked. The Independent Laboratory will not need to take any action. Carriers will revoke the PIN and notify the appropriate Independent Laboratory. The following requirements apply when billing for reference laboratory services for dates of service, July 1, 2004, and later:
Electronic Claim Submission Requirements
ANSI format:
- Will require the presence of the performing and billing laboratory’s CLIA number.
- If tests are referred to another laboratory, the CLIA number of the laboratory where the testing is rendered must also be on the claim.
- The clinical diagnostic laboratory will not have to submit separate claims for referred and performed services under the ANSI format.
- An independent clinical diagnostic laboratory submits a 90 modifier on the line item when billing a reference laboratory service and the CLIA number assigned to the reference laboratory in X12N 837 (HIPAA version) loop 2400, REF02. REF01 = F4.
NSF format:
- Suppliers may not combine services that they performed themselves and any that they referred to another laboratory on the same NSF claim form.
- If a billing laboratory performs some testing and refers the remaining tests to another (reference) laboratory to perform, the laboratory must segment the services and submit two separate claims.
- If services are referred to more than one laboratory, a separate claim must be submitted for each reference laboratory to which services were referred.
- The CLIA number assigned to the performing laboratory shall be reported in FA0 – 34.0.
- An NSF electronic claim for laboratory testing requires the presence of the performing and billing laboratory’s name and address.
- The billing laboratory for a service with a line item CPT ‘90’ modifier requires the address information of the performing lab to be submitted in the following NSF record and fields:
EA1 Field 06 Facility/Lab ADDR1 EA1 Field 09 Facility/Lab State
EA1 Field 07 Facility/Lab ADDR2 EA1 Field 10 Facility/Lab Zip Code
Paper Claim Submission Requirements
- Suppliers that submit claims in the paper format (CMS-1500) may not combine services that they performed themselves and any that they referred to another laboratory on the same CMS-1500 claim form.
- If a billing laboratory performs some testing and refers the remaining tests to another (reference) laboratory to perform, the laboratory must separate the services and submit two separate claims.
- If services are referred to more than one laboratory a separate claim must be submitted for each reference laboratory to which services were referred.
- Paper claims will be returned as unprocessable if billing providers combine clinical laboratory services performed themselves and any referred to another laboratory on the same CMS-1500.
- The line items submitted for referred laboratory test must contain a modifier 90.
- The performing laboratory’s name and address must be reported in item 32 on the CMS-1500 form to show where the service (test) was actually performed. A paper claim for laboratory testing requires the presence of the CLIA number of the laboratory actually performing the testing in item 23 of the CMS-1500 billing form.
- An NSF electronic claim for laboratory testing requires the presence of the performing and billing laboratory’s name and address.
- The performing laboratory for a service with a line item CPT ‘90’ modifier requires provider information to be submitted in the item 32 of the CMS-1500.
Sometimes a clinical diagnostic laboratory will refer a specimen to another laboratory for testing. In most cases the laboratory that furnishes the service will bill for the service. But it’s also possible for one laboratory to bill for a service performed by another laboratory. Medicare uses certain terms of art in describing laboratories in this context. “Referring laboratory” is defined as the laboratory that refers a specimen to another laboratory for testing. “Reference laboratory” is defined as the laboratory that receives a specimen from another laboratory and performs one or more tests on such specimen.
Medicare’s payment policy for laboratory services is generally based on fee schedules specific to each carrier jurisdiction. Previously, some carriers have been unable to process a claim for a laboratory test performed in another jurisdiction because they did not possess the fee schedule of that other jurisdiction. Thus, some carriers paid for referred services performed outside of their jurisdiction and based payment on the fee schedule for that jurisdiction.
Other carriers attempted to overcome the difficulty by enrolling the laboratory outside their jurisdiction as a reference laboratory. These carriers issued a Provider Identification Number (PIN) for the reference laboratory as a “reference-use-only” PIN. However, not every carrier has been willing to issue “reference use- only” PINs.
Implementation
This change resolves the issues by requiring that:
- An independent clinical laboratory may bill only the carrier in which it is enrolled by location.
- An independent clinical laboratory may not enroll with a carrier as a “reference-use-only” laboratory.
- Every carrier must settle a claim for a referred service submitted by a laboratory located in its
jurisdiction, regardless of where the service was performed. - Every carrier must pay for a referred service on the basis of the fee schedule in effect in the jurisdiction where the test was performed.
- Every carrier must cancel all existing “reference- use-only” enrollments and “reference-use-only”
PINs and refrain from making any further “reference-use-only” enrollments. - The referring laboratory must identify a referred service as such on the claim and identify reference
laboratory performing that test and correctly entering the zip code of such laboratory. - Both the referring laboratory and the reference laboratory must be enrolled in Medicare.
When a billing laboratory is the referring laboratory it must identify the referred service as such by use of modifier 90 and must identify the reference laboratory by specifying its CLIA number and the address, including the correct zip code, where the service was actually performed. Also, the referring laboratory must meet one of the following conditions:
- It must be located in, or be part of, a rural hospital;
- It must be wholly-owned by the reference laboratory; or both it and the reference laboratory are wholly owned subsidiaries of the same entity; or
- It refers no more than thirty (30) percent of the clinical laboratory tests annually to other laboratories (not including referrals made under the wholly- owned proviso stated above).
Important Dates
These changes will be implemented by Medicare on July 6, 2004, and will apply to services rendered on or after July 1, 2004.
Related Instructions
If you need further clarification, background, details or just want to see the original change request
implementing these changes, you can find it at:
http://www.cms.hhs.gov/manuals/pm_trans/R85CP.pdf
[EM 2004-0081/3090]
(04-0898)
Arrangements for Physical, Occupational, and Speech-Language Pathology Services
Provider Types Affected
Physicians, therapists, providers, clinics.
Provider Action Needed
Physicians, suppliers, and providers should note that this instruction clarifies information regarding arrangements for Medicare Part B outpatient physical therapy, occupational therapy, and speech-language pathology services furnished under arrangements with providers and clinics. Revisions have been made to Chapter 15, Section 220.1 of the Medicare Benefits Policy Manual (Pub 100-02). Section 220.1 Therapy Services Furnished Under Arrangements with Providers and Clinics is included in this article for informational purposes. Please note that this information is for clarification purposes only and should not represent any change for providers.
Background
The excerpt from the manual itself is as follows:
“A provider or clinic may have others furnish outpatient physical therapy, occupational therapy, or speech language pathology services through arrangements under which receipt of payment by the provider or clinic for the services discharges the liability of the beneficiary or any other person to pay for the service.”
However, it is not intended that the provider or clinic merely serve as a billing mechanism for the other party. The provider’s or clinics professional supervision over the services requires application of many of the same controls as are applied to services furnished by salaried employees. The provider or clinic must:
- Accept the patient for treatment in accordance with its admission policies;
- Maintain a complete and timely clinical record on the patient which includes diagnosis, medical history, physician’s orders, and progress notes relating to all services received;
- Maintain liaison with the attending physician or non- physician practitioner with regard to the progress of the patient and to assure that the required plan of
treatment is periodically reviewed by the physician; - Secure from the physician the required certifications and recertifications; and
- See to it that the medical necessity of such service is reviewed on a sample basis by the agency’s staff an outside review group.
In addition, when a clinic provides outpatient physical therapy, occupational therapy, or speech-language pathology services under an arrangement with others, such services must be furnished in accordance with the terms of a written contract, which provides for retention by the clinic of responsibility for and control and supervision of such services. The terms of the contract should include at least the following:
- Provide that the therapy or speech-language pathology services are to be furnished in accordance with the plan of care established by the physician after any necessary consultation with the physical therapist, occupational therapist, or speech-language pathologist as appropriate, the physical therapist who will provide the physical therapy services, the occupational therapist who will provide the occupational therapy services, or the speech- language pathologist who will provide the speech language pathology services;
- Specify the geographical areas in which the services are to be furnished;
- Provide that personnel and services contracted for meet the same requirements as those which would be applicable if the personnel and services were furnished directly by the clinic;
- Provide that the therapist will participate in conferences required to coordinate the care of an individual patient;
- Provide for the preparation of treatment records, with progress notes and observations, and for the prompt incorporation of such into the clinical records of the clinic;
- Specify the financial arrangements. The contracting organization or individual may not bill the patient the health insurance program; and
- Specify the period of time the contract is to be in effect and the manner of termination or renewal.
Additional Information
To view Chapter 15 of the Medicare Benefits Policy Manual, visit: http://www.cms.hhs.gov/manuals/102_policy/bp102index.asp
Once at that site, scroll down to Chapter 15 and select the file version you wish to receive. The official instruction issued to your carrier regarding this change may be found by going to: http://www.cms.hhs.gov/manuals/transmittals/comm_date_dsc.asp
From that web page, look for CR3134 in the CR NUM column on the right, and click on the file for that CR. If you have any questions, please contact your carrier/intermediary at their toll-free number, which may be found at: http://www.cms.hhs.gov/MedlearnProducts/downloads/CallCenterTollNumDirectory.pdf
(04-0896)
Electrical Stimulation and Electromagnetic Therapy for the Treatment of Wounds
Provider Types Affected
Physicians, Therapists, Federally Qualified Health Centers, Rural Health Clinics, Hospitals, and Critical Access Hospitals.
Provider Action Needed
STOP – Impact to You
Effective July 1, 2004, under specific conditions Medicare will cover electromagnetic therapy for wound treatment for the same settings and conditions in which electrical stimulation (ES) for wound treatment is currently covered.
CAUTION – What You Need to Know
Be aware of the conditions under which Medicare will cover this procedure.
GO – What You Need to Do
You may file claims with Medicare for electromagnetic therapy for the treatment of certain wounds for services rendered on or after July 1, 2004. Be sure to use the correct HCPCS and revenue codes as specified below to assure timely and correct payment.
Background
Medicare conducted a reconsideration review of electromagnetic therapy used for the treatment of certain wounds. They found that wounds treated using either electrical stimulation (ES) therapy or electromagnetic therapy resulted in similar improvements. Therefore, CMS decided to cover electromagnetic therapy for wound treatment for the same settings and conditions in which electrical stimulation for wound treatment is currently covered.
Effective July 1, 2004, Medicare will cover ES or electromagnetic therapy for chronic stage III or stage IV pressure ulcers (ulcers that have not healed within 30 days of occurrence), arterial ulcers, diabetic ulcers, and venous stasis ulcers. Electromagnetic therapy services will be covered only when performed by a physician, physical therapist, or incident to a physician service. No other wound treatment using electromagnetic therapy will be covered.
ES and electromagnetic therapy for wound treatment will be covered only after appropriate standard wound treatment has been tried for at least 30 days with no measurable signs of healing. Additionally, wounds undergoing treatment by electromagnetic therapy must be evaluated at least monthly by the treating physician.
Medicare will not continue to cover the treatment if the wound shows no measurable signs of improvement within any 30 day period of treatment. Additionally, ES or electromagnetic therapy must be discontinued when the wound demonstrates a 100% epitheliliazed wound bed. Unsupervised therapy for wound treatment will not be covered, nor will ES and electromagnetic therapy be covered as an initial treatment modality.
Additional Information
The applicable Healthcare Common Procedure Coding System (HCPCS) code for Electromagnetic.
Therapy is as follows:
HCPCS G0329 – Electromagnetic Therapy, to one or more areas for chronic stage III and stage IV
pressure ulcers, arterial ulcers, diabetic ulcers, and venous stasis ulcers not demonstrating measurable
signs of healing after 30 days of conventional care as part of a therapy plan of care. Effective date: July 1, 2004. Note: Medicare will not cover the device (Code E0761) used for electromagnetic treatment of wounds, nor will Medicare cover unsupervised home use of electromagnetic therapy.
The following revenue codes must be used in conjunction with the HCPCS code identified:
| Revenue Code | Description |
|---|---|
| 420 | Physical Therapy |
| 430 | Occupational Therapy |
| 520 | Federal Qualified Health Center |
| 521 | Rural Health Center |
| 977,978 | Critical Access Hospital - method II CAH professional services only |
The official instruction issued to your carrier regarding this change may be found by going to:
http://www.cms.hhs.gov/manuals/transmittals/comm_date_dsc.asp
From that web page, look for CR 3149 in the CR NUM column on the right, and click on the file for that CR. The CR includes the revised portions of the Medicare National Coverage Determinations Manual, which further explain this change.
[EM 2004-0344/3149]
(04-0899)
E/M Coding: Volume of Documentation versus Medical Necessity
The Social Security Act, Section 1862 (a)(1)(A) states: “No payment will be made … for items or services … not reasonable and necessary for the diagnosis or treatment of an injury or illness or to improve the functioning of a malformed body member.” This medical reasonableness and necessity standard is the overarching criterion for the payment for all services billed to Medicare.
During repeated reviews, we have observed the tendency to “over document” and consequently to select and bill for a higher level E/M code than medically reasonable and necessary. Word processing software, the electronic medical record, and formatted note systems facilitate the “carry over” and repetitive “fill in” of stored information. Even if a “complete” note is generated, only the medically reasonable and necessary services for the condition of the particular patient at the time of the encounter as documented can be considered when selecting the appropriate level of an E/M service. Information that has no pertinence to the patient’s situation at that specific time cannot be counted.
(04-0853)
Beneficiary Eligibility Options
As many of our providers and software vendors know, the ASC X12 270/271 Health Care Eligibility Benefit Inquiry and Response (Real Time), version 4010A1 is not yet fully operational for Medicare. Pending the production use of that transaction, CMS has instructed the contractors to continue support of all current formats used for eligibility verification.
The formats that CIGNA Government Services Part B supports are the Beneficiary Direct Data Entry (DDE) and the National Standard Format (NSF) batch eligibility. The DDE allows a provider to enter an eligibility request and receive an eligibility response instantaneously through TCP/IP connectivity. The NSF batch eligibility requires the supplier to create a file containing an eligibility request with as many as 99 requests. The file is then uploaded into the Stratus Network, using the same process as uploading a claim file. A response file will be generated after the nightly batch job is completed and the supplier would download a response file just as they would an electronic report. The NSF batch version does require the use of software to create the eligibility request and to read the response file received from Medicare. Medicare does not provide this software.
If you would like to sign up for the Beneficiary Eligibility feature, please contact EDI Support at 1.866.520.4022.
(04-0885)
Emergency Correction Regarding Correction to Healthcare Common Procedure Coding System (HCPCS) Codes for Low-Osmolar Contrast Material
Provider Types Affected
All Medicare hospitals and physicians.
Provider Action Needed
Affected providers should note that this instruction provides additional information regarding coding under the Healthcare Common Procedure Coding System (HCPCS) for low-osmolar contrast material. It corrects the effective date for the reinstatement of selected HCPCS codes and the change in status of HCPCS code A9525.
Background
On January 23, 2004, Change Request 3053 - Emergency Correction to Healthcare Common Procedure Coding System (HCPCS) Codes for Low-Osmolar Contrast Material was issued, and it provided the following instructions:
- Reinstatement of Healthcare Common Procedure Coding System (HCPCS) codes A4644 through
A4646; and - Change in status of HCPCS code A9525 to “not payable by Medicare.”
The effective date for these changes was given as April 1, 2004.
This April 1, 2004, date was incorrect. These changes are to be made retroactive to January 1, 2004. Thus, codes A4644 through A4646 are reinstated as of January 1, 2004, and code A9525 is invalid for dates of service on or after January 1, 2004.
On February 20, 2004, Change Request 3128 was issued. It updated the Medicare Physician Fee Schedule Database as follows:
- Status indicator E was assigned to codes A4644 through A4646; and
- Status indicator I was assigned to code A9525
The effective date for these changes was given as January 1, 2004.
This is correct.
Codes A4644 thru A4646 have been reinstated in the HCPCS.
Implementation
The implementation date for this instruction is May 24, 2004.
Additional Information
The official instruction issued to your carrier regarding this change may be found by going to:
http://www.cms.hhs.gov/manuals/transmittals/comm_date_dsc.asp
From that Web page, look for CR3185 in the CR NUM column on the right and click on the file for that CR.
If you have any questions, please contact your carrier/intermediary at their toll-free number, which may be found at: http://www.cms.hhs.gov/MedlearnProducts/downloads/CallCenterTollNumDirectory.pdf
Change Request 3053 - Emergency Correction to Healthcare Common Procedure Coding ystem(HCPCS) Codes for Low-Osmolar Contrast Material, Transmittal 45, dated January 23, 2004, can be found at the following Centers for Medicare & Medicaid Services Medlearn Matters Web site:
http://www.cms.hhs.gov/MedlearnMattersArticles/downloads/MM3053.pdf
Also, Change Request 3128 - 1st Update to the 2004 Medicare Physician Fee Schedule Database Transmittal 105, dated February 20, 2004, can be found at the following CMS Web site:
http://www.cms.hhs.gov/manuals/pm_trans/R105CP.pdf
[EM 2004-0331/3187]
(04-0908)
Incident to Services
Provider Types Affected
Physicians, suppliers, and providers.
Provider Action Needed
STOP - Impact to You
This instruction clarifies and standardizes the method of indicating the ordering and supervising professionals on the Centers for Medicare & Medicaid Services Health Insurance Claim Form (CMS-1500). Note that the CMS-1500 is the paper form, however, and is superceded now by the electronic form.
Caution - What You Need to Know
This instruction and the CMS Claims Processing Manual update clarifies where physician’s Provider Information Numbers and names should be reported when both an ordering provider and a supervising provider are involved in a service.
GO - What You Need to Do
Please refer to the Background and Additional Information sections of this instruction for further details.
Background
The Centers for Medicare & Medicaid Services (CMS) Health Insurance Claim Form (CMS-1500) is the basic form prescribed by CMS for the submission of claims from physicians and suppliers for the Medicare program. It is used by non-institutional providers and suppliers to bill Medicare Part B covered services and it is also used for billing some Medicaid covered services. It answers the needs of many health insurers and is the basic form prescribed by CMS for the submission of claims on behalf of Medicare patients. (However, please note that the CMS-1500 paper form is superceded by HIPAA electronic formats.)
Because of the multiple requests in Open Door Forums and correspondence, CMS is issuing this instruction to clarify and standardize the method of indicating the ordering and supervising professionals on the CMS-1500.
The Preamble of the Proposed Rule for the Medicare Physician Fee Schedule on November 1, 2001 (66 Fed Reg. 55267) stated “the billing number of the ordering physician (or other practitioner) should not be used if that person did not directly supervise the auxiliary personnel.” This instruction incorporates the rule into the CMS Claims Processing Manual.
The update to the Medicare Claims Processing Manual (Pub 100-4) (referred to in the Web link below) further clarifies where physician’s Provider Information Numbers and names should be reported when both an ordering provider and a supervising provider are involved in a service.
Implementation
The implementation date is May 24, 2004.
Additional Information
The CMS Manuals Index can be found at the following CMS Web site: http://www.cms.hhs.gov/manuals/cmsindex.asp
Also, the Medicare Claims Processing Manual (Pub 100-4) which was revised can be found at:
http://www.cms.hhs.gov/manuals/104_claims/clm104index.asp
The official instruction issued to your carrier regarding this change may be found by going to:
http://www.cms.hhs.gov/manuals/transmittals/comm_date_dsc.asp
From that Web page, look for CR3138 in the CR NUM column on the right, and click on the file for that CR. If you have any questions, please contact your carrier/intermediary at their toll-free number, which may be found at: http://www.cms.hhs.gov/MedlearnProducts/downloads/CallCenterTollNumDirectory.pdf
If you need to contact your Medicaid State Agency for more details, a list of toll-free telephone numbers exists for each Medicaid State Agency at:
http://www.cms.hhs.gov/medicaid/tollfree.pdf
(04-0897)
G Code Error
On January 1, 2004, CMS implemented NCCI edits with column one codes G0308-G0327 each with column two codes of 90935, 90937, 90945, 90947, and 99201-99356.
As a result of the way these edits were set up, claims have been denied by Carriers during the period from January 1, 2004, until now. These edits will be suspended effective July 1, 2004, and the changes will appear in NCCI version 10.2 scheduled for July 1, 2004. For dates of service between January 1, 2004 and June 30, 2004, providers can bypass these edits by appending modifier -59 when appropriate to CPT codes 90935, 90937, 90945, or 90947 or modifier -25 when appropriate to CPT codes 99201-99356. (The suspension of the edits cannot occur earlier because NCCI version 10.1 scheduled for April 1, 2004, is already completed.) Please use this “modifier workaround” until July 1, 2004, when applicable.
Please note: Providers that have received demand letters in error should notify Recovery @ 1.877.286.6801, Option 2. If the overpayment has been satisfied please contact the Appeals Department.
The basis for these edits remains unchanged. In order to report codes in the range, G0308-G0319, the provider must determine the number of face to face physician visits per month. In determining this number, the physician should not include face to face visits reported as 90935, 90937, 90945, 90947, or 99201-99356.
CMS will suspend these edits indefinitely unless evidence of improper billing is subsequently identified.
(04-0845)
Not Other Wise Classified Drugs/Biologicals Claim Filing Instructions
When billing for a Not Otherwise Classified Drug, the name of the drug and exact dosage administered must be entered in block 19 of the CMS-1500 claim form or as an attachment for paper claims. For claims submitted electronically, this information would be entered in the narrative field (the electronic equivalent of block 19 of the paper form). The allowed amount for the drug will be based on the information entered in these fields.
Once the drug has been issued a specific procedure code, the assigned procedure code should be used and your number of services should be adjusted based on the description and the dosage of the assigned procedure code. If the miscellaneous code continues to be billed after a specific procedure code has been assigned, your claim may be denied as a billing error. This does not apply to the compounded drugs billed under J3490. Compounded drugs shall continue to be billed under J3490 and the purchase information included with the claim.
(04-0912)
Medicare Providers: Their Vendors, Clearinghouses, or Other Third-Party Billers and the HIPAA/Medicare Contingency Plan
Provider Types Affected
All Medicare physicians, providers, and suppliers who use a vendor, clearinghouse, or other third-party billing agent to submit Medicare claims.
Provider Action Needed
Understand the requirements of HIPAA, the Medicare HIPAA contingency plan, its impact, and the need to verify HIPAA compliance by those who bill Medicare on your behalf.
Background
In a recent Medlearn Matters article (see MM2981, which may be found at:
http://www.cms.hhs.gov/MedlearnMattersArticles/downloads/MM2981.pdf the Centers for Medicare & Medicaid Services (CMS) announced a modification of the HIPAA contingency plan implemented by Medicare on October 16, 2003. Specifically, CMS announced on February 27, 2004, that Medicare would continue to accept claims electronically in a pre-HIPAA format on or after July 1, 2004, but such claims would not be eligible for Medicare payment until the 27th day after receipt, at the earliest. All electronic claims today are eligible for payment at 14 days after receipt.
This modification of the HIPAA contingency plan was intended to give providers additional time to become HIPAA compliant, but was also a measured step toward ending the contingency plan for all incoming Medicare claims.
CMS understands that many physicians, providers, and suppliers do not submit claims directly to Medicare, but submit their claims through a third party, such as a billing vendor, clearinghouse or other third-party billing agent. CMS recognizes the importance of these third parties to many providers and the extent to which providers rely on those entities to meet HIPAA requirements in a cost-effective manner with minimal impact on the provider’s most important mission, i.e., delivering high quality medical care to those who need such care.
Each provider has made a business decision to use these agents and is therefore best positioned to
assess the value of that decision.
CMS urges Medicare providers to understand the following issues, to assess their impact on the provider’s business and determine what, if any, steps need to be taken.
Issue # 1- Understand where your vendor, clearinghouse, or other third party biller stands in terms of HIPAA compliance.
Providers are required by statute to achieve compliance and to bill Medicare electronically in a HIPAA compliant manner. Thus, it is crucial for providers to assure themselves of their third-party partner’s readiness. It is especially important to remember that, at the time Medicare’s contingency plan is terminated, providers who remain non-compliant will face significant problems.
So, what steps might providers take to assure that they AND their partners are ready?
- Check with your clearinghouse, vendor, or other third party biller.
- Ask them about their readiness.
- Ask them how they have determined their readiness.
- Make sure they are aware of the Medicare contingency plan and the modification announced on
February 27th. - Ask them if your claims will continue to be eligible for payment on the 14th day after receipt, as of
July 1, 2004. Or, will your claims not qualify for such prompt payment from Medicare? - If your agent indicates that the Medicare contingency plan will affect your claims, ask them when they will correct the problem so your claims are eligible for prompt payment and ask when that will happen.
As stated earlier, CMS’s business relationship is with providers and we look to the provider to meet
requirements for correct submission of claims in HIPAA compliant formats. We also know that every piece of the process, and every entity involved, must be ready. That is why it is important for providers to question their agents, obtain assurances, and keep abreast of HIPAA developments. Ultimately, the benefits of compliance or the consequences of non-compliance will fall on the provider. Remember that continued timely payment of Medicare claims is closely linked to HIPAA readiness.
Issue #2- Make sure your agent builds on the HIPAA compliance you have achieved.
There have been instances where some third-party billers are taking claims submitted to them by Medicare providers that are HIPAA compliant and then converting them to a non-compliant format before sending them to a Medicare claims processing contractor. Such vendors and agents may be doing this because some of their providers are still not HIPAA compliant and the vendor has chosen to submit non-compliant formats for all their provider customers until all customers are compliant.
These decisions may make good business sense to the vendor, clearinghouse or other third party biller, but their decision may adversely affect providers who are compliant. That will certainly be the case for such claims submitted to Medicare on or after July 1, 2004, when Medicare deems such claims do not qualify for the prompt payment afforded to electronic claims that are HIPAA compliant. At the time Medicare ends its contingency plan, the consequences for non-compliant claims could be even more severe, e.g., a complete stoppage of payments for such claims.
What can providers do? The answer is similar to the one presented for the first issue, i.e., talk with your vendor, clearinghouse, or other third party biller. Ask them about their readiness. Ask them if they are altering your HIPAA compliant input to them into a non-compliant format before sending to Medicare. Ask them to assure you that your claims will remain eligible for payment on the 14th day after receipt on and after July 1, 2004.
As mentioned before, it is the provider’s ultimate responsibility to assure they are HIPAA compliant and that means assuring that your claims meet the transaction code set and format standards.
Issue # 3- Understand when your vendor, clearinghouse, or other third party biller will stop
accepting non-compliant transactions.
While CMS implemented a contingency plan on October 16, 2003, which allows Medicare providers,
suppliers, and other electronic billers to continue sending pre-HIPAA formats, that plan is not binding on other entities. At any time, vendors, clearinghouses, and other third party billers could decide to limit or discontinue supporting pre-HIPAA formats.
We encourage providers and suppliers using a third party entity for sending their electronic claims to work closely with that entity to understand the HIPAA electronic claims requirements. Verify that you are submitting the data required under HIPAA and that your claims are being transmitted in the standard HIPAA format.
In conclusion, the bottom line is that, in order to protect your interests and ensure uninterrupted cash
flow, begin immediately to work toward meeting the HIPAA standard requirements.
Additional Information
For additional information on HIPAA, visit the CMS Web site at: http://www.cms.hhs.gov/HIPAAGenInfo/default.asp
(04-0864)
Manualization of POS Code Set Program Memorandum; Revision to Group Home Code Description
Provider Types Affected
Physicians, suppliers, and providers who bill Medicare carriers.
Provider Action Needed
Physicians, suppliers, and providers should note that this article addresses only a new definition for the Place of Service (POS) Code for Group Homes. Other POS code set information was issued on May 16, 2003, in CMS Program Memorandum/Transmittal B-03-040 and Change Request 2730, “Update of the Place of Service (POS) Code Set.” That other information remains unchanged.
Background
Effective April 1, 2004, the description of POS code 14 (Group Home) will be as follows:
“A residence, with shared living areas, where clients receive supervision and other services, such as social and/or behavioral services, custodial services, and minimal services (e.g. medical administration).”
Once again, the remainder of the updated POS code set remains as presented in Program Memorandum B-03-040, which may be found at: http://www.cms.hhs.gov/manuals/pm_trans/B03040.pdf.
Additional Information
The official instruction issued to your carrier regarding this change may be found by going to:
http://www.cms.hhs.gov/manuals/pm_trans/R121CP.pdf.
If you have any questions, please contact your carrier/intermediary at their toll-free number, which may be found at: http://www.cms.hhs.gov/MedlearnProducts/downloads/CallCenterTollNumDirectory.pdf.
[EM 2004-0211/3087]
(04-0839)
Manualization NCD: Acupuncture for Fibromyalgia /Osteroarthritis
Provider Types Affected
Physicians, suppliers, and providers.
Provider Action Needed
STOP – Impact to You
Physicians, suppliers, and providers should note that this instruction relates to acupuncture for the treatment of fibromyalgia and osteoarthritis.
CAUTION – What You Need to Know
The Centers for Medicare & Medicaid Services (CMS) concludes that acupuncture is not reasonable and necessary for the treatment of fibromyalgia and osteoarthritis within the meaning of Section 1862(a)(1) of the Social Security Act. Therefore, CMS continues its national noncoverage determination for acupuncture.
GO – What You Need to Do
Refer to the Background and Additional Information sections of this instruction for further details regarding these changes.
Background
After reconsideration of the national noncoverage determination for acupuncture, the Centers for Medicare & Medicaid Services (CMS) concludes that acupuncture is not reasonable and necessary for the treatment of fibromyalgia and osteoarthritis within the meaning of Section 1862(a)(1) of the Social Security Act. Therefore, CMS continues its national noncoverage determination for acupuncture.
This revision is a national coverage determination (NCD), and NCDs are binding on all carriers, fiscal intermediaries, quality improvement organizations, health maintenance organizations, competitive medical plans, and health care prepayment plans. Under 42 Code of Federal Regulations (CFR) 422.256(b), an NCD that expands coverage is also binding on Medicare+Choice Organizations.
In addition, an administrative law judge may not review an NCD. (See §1869(f)(1)(A)(i) of the Social Security Act.)
Implementation
The implementation date for this instruction is April 16, 2004.
Related Instructions
The following Internet Only Medicare Manual (IOM) has been edited with revised and new sections to reflect changes implemented with this instruction.
The Medicare National Coverage Determinations Manual (Pub. 100-3), Chapter 1 (Coverage
Determinations)
- Table of Contents - revised
- Section 30.3.1 (Acupuncture for Fibromyalgia) – revised
- Section 30.3.2 (Acupuncture for Osteoarthritis) – revised
Changes to sections of the Medicare National Coverage Determinations Manual are included in CR3250 referenced below in the Additional Information section. These revised instructions briefly explain the process CMS used in reaching this decision.
Additional Information
The official instruction issued to your carrier regarding this change may be found by going to:
http://www.cms.hhs.gov/manuals/transmittals/comm_date_dsc.asp.
From that Web page, look for CR3250 in the CR NUM column on the right, and click on the file for that CR.
[EM 2004-0344/3250]
(04-0900)
Medical Review Frequently Asked Questions - April 2004
The following represent a variety of questions the Medical Review department has received. CIGNA Government Services will address at least quarterly “Frequently Asked Questions” related to coverage and local medical review policy issues. The previous issue was published in the January 2004 Web site bulletin. Providers may submit questions to the Web site at http://www.cignamedicare.com/customer_service/disclaimer.html.
1. Unna Boots
Q: When are Unna boots separately payable? Can an evaluation and management visit with modifier 25 also be billed?
A: Per the NCCI rebundling table, the code for Unna boots (CPT code 29580) is component to many other comprehensive surgeries (e.g. tendon sheath injections, joint aspiration/injection, etc.) unless a modifier is appended to reflect the Unna boot was used in a distinct, separate service. Unna boots applied as dressings would not be considered a separately reimbursable service apart from surgical procedure as payment for surgical dressings applied by the physician during his/her encounter with the patient is included in the fee schedule payment for the physician’s service. For medically necessary Unna boots not applied as post operative dressings, CPT code 29580 may be billed; but an evaluation and management visit should not be billed unless there is a distinct, separately identifiable reason for the E&M service. It would be inappropriate to bill an E&M service for the assessment related to Unna boot application. The assessment would be considered part of the pre-procedural evaluation that is component to the procedure/service. This is reflected in the following link to CMS Publication 100-4, The Medicare Claims Processing, Chapter 12, and Section 30.6.6. It explains that each procedure includes a pre-procedural evaluation that should not be separately billed as a distinct, separately payable E&M visit http://www.cms.hhs.gov/manuals/104_claims/clm104c12.pdf.
2. ASC
Q: Does Medicare reimburse ASC facilities for a covered procedure rate and implant cost? Many orthopedic cases involve implants that are substantially more in cost than the group rate fee that is paid.
A: According to CMS Publication 100-4, the Medicare Claims Processing Manual, Chapter 14, Section 10.4, prosthetic devices, other than intraocular lenses (IOLs), whether implanted, inserted, or otherwise applied by covered surgical procedures, are covered; but these are not included in the ASC facility payment amount. These items may be filed separately from the surgery using the appropriate HCPCS code; and if there is no specific code for the implant or prosthesis, providers should use an unlisted HCPCS code. In the latter case, these services would be reviewed to determine whether they fall under Part B or DMERC jurisdiction, if they should be separately paid from the surgery, and if separately paid then how much. Our interpretation for separately payable implants are those that can be set apart from items usually needed to perform the surgery (e.g. wires, screws, clips, tapes, etc.), and we use resources such as the AMA’s Relative Value Update Committee notes in making such determinations. http://www.cms.hhs.gov/manuals/104_claims/clm104c14.pdf
3. ASC
Q: How do ambulatory surgical centers get paid for procedures not on the approved list?
A: Generally, for CPT codes not on the ASC reimbursable list and that do have facility and non-facility prices, the physician gets reimbursed at a nonfacility level. There may be an arrangement between the physician and ASC where the physician might forward some of the differential amount to the ASC. For CPT codes that have identical reimbursements in and outside a facility, this may or may not be feasible and depends on the arrangement and ownership relationship that the physician and ASC might have. It may not be feasible to perform this procedure in an ASC, but this is not within our judgment and jurisdiction. The carrier does not determine when there is a facility/non-facility fee for a given procedure or what procedures are on the approved list. We receive these instructions from CMS. This list can be seen on the CMS Web site through the following link under “Ambulatory Surgical Center (ASC) Base Eligibility File”: http://www.cms.hhs.gov/providers/pufdownload/default.asp?#asc
4. 99211
Q: Can this code be billed at the same time an injection is given or a protime or urinalysis is collected? Can it be billed for assessment of vital signs?
A: CPT code 99211 cannot be billed solely for the purpose of administering an injection or collecting a specimen for a diagnostic test. Furthermore, it should not be billed for routine vital signs that would not impac
