Medicare Program; Update to the Required Prior Authorization List of Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Items That Require Prior Authorization as a Condition of Payment

Published date22 April 2019
Citation84 FR 16616
Record Number2019-08031
SectionRules and Regulations
CourtCenters For Medicare & Medicaid Services
Federal Register, Volume 84 Issue 77 (Monday, April 22, 2019)
[Federal Register Volume 84, Number 77 (Monday, April 22, 2019)]
                [Rules and Regulations]
                [Pages 16616-16617]
                From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
                [FR Doc No: 2019-08031]
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                DEPARTMENT OF HEALTH AND HUMAN SERVICES
                Centers for Medicare & Medicaid Services
                42 CFR Part 414
                [CMS-6080-N2]
                Medicare Program; Update to the Required Prior Authorization List
                of Durable Medical Equipment, Prosthetics, Orthotics, and Supplies
                (DMEPOS) Items That Require Prior Authorization as a Condition of
                Payment
                AGENCY: Centers for Medicare & Medicaid Services (CMS), HHS.
                ACTION: Update to list.
                -----------------------------------------------------------------------
                SUMMARY: This document announces the addition of 12 Healthcare Common
                Procedure Coding System (HCPCS) codes to the Required Prior
                Authorization List of Durable Medical Equipment, Prosthetics,
                Orthotics, and Supplies (DMEPOS) Items that require prior authorization
                as a condition of payment.
                DATES: Phase one of implementation is effective on July 22, 2019. Phase
                two of implementation is effective on October 21, 2019.
                FOR FURTHER INFORMATION CONTACT:
                 Virginia Boulin, (410) 786-1079.
                 Erica Ross, (410) 786-7480.
                SUPPLEMENTARY INFORMATION:
                I. Background
                 Sections 1832, 1834, and 1861 of the Social Security Act (the Act)
                establish that the provision of durable medical equipment, prosthetics,
                orthotics, and supplies (DMEPOS) are covered benefits under Part B of
                the Medicare program.
                 Section 1834(a)(15) of the Act authorizes the Secretary to develop
                and periodically update a list of DMEPOS items that the Secretary
                determines, on the basis of prior payment experience, are frequently
                subject to unnecessary utilization and to develop a prior authorization
                process for these items.
                 In the December 30, 2015 final rule (80 FR 81674) titled ``Medicare
                Program; Prior Authorization Process for Certain Durable Medical
                Equipment, Prosthetics, Orthotics, and Supplies,'' we implemented
                section 1834(a)(15) of the Act by establishing an initial Master List
                (called the Master List of Items Frequently Subject to Unnecessary
                Utilization) of certain DMEPOS that the Secretary determined, on the
                basis of prior payment experience, are frequently subject to
                unnecessary utilization and by establishing a prior authorization
                process for these items. In the same final rule, we also stated that we
                would inform the public of those DMEPOS items on the Required Prior
                Authorization List in the Federal Register with 60-day notice before
                implementation. The Required Prior Authorization List specified in
                Sec. [thinsp]414.234(c)(1) is selected from the Master List of Items
                Frequently Subject to Unnecessary Utilization (as described in Sec.
                [thinsp]414.234(b)(1)), and items on the Required Prior Authorization
                List require prior authorization as a condition of payment.
                 In addition to the prior authorization process for certain DMEPOS
                items that we established under section 1834(a)(15) of the Act, on
                September 1, 2012, we implemented the Medicare Prior Authorization for
                Power Mobility Devices (PMDs) Demonstration that would operate for a
                period of 3 years (September 1, 2012 through August 31, 2015). This
                demonstration was established under section 402(a)(1)(J) of the Social
                Security Amendments of 1967 (42 U.S.C. 1395b-1(a)(1)(J)), which
                authorizes the Secretary to conduct demonstrations designed to develop
                or demonstrate improved methods for the investigation and prosecution
                of fraud in the provision of care or services provided under the
                Medicare program. The demonstration was initially implemented in
                California, Florida, Illinois, Michigan, New York, North Carolina, and
                Texas. These states were selected for the demonstration based upon
                their history of having high levels of improper payments and incidents
                of fraud related to PMDs. On October 1, 2014, we expanded the
                demonstration to 12 additional states (Pennsylvania, Ohio, Louisiana,
                Missouri, Washington, New Jersey, Maryland, Indiana, Kentucky, Georgia,
                Tennessee, and Arizona) that had a history of high expenditures and
                improper payments for PMDs based on 2012 billing data. On July 15,
                2015, we announced we were extending the demonstration for 3 years,
                through August 31, 2018. The demonstration ended as scheduled on August
                31, 2018.
                 In a June 5, 2018 Federal Register document, we announced that,
                effective September 1, 2018, we would add 31 HCPCS codes that were a
                part of the PMD demonstration to the Required Prior Authorization List
                (83 FR 25947).
                II. Provisions of the Document
                 The purpose of this document is to inform the public that we are
                updating the Required Prior Authorization List of DMEPOS items that
                require prior authorization as a condition of payment to include seven
                additional power mobility devices and five pressure reducing support
                surfaces. These 12 items are on the Master List of Items Frequently
                Subject to Unnecessary Utilization. To assist stakeholders in preparing
                for implementation of the prior authorization program, we are providing
                90 days' notice.
                 The following seven HCPCS codes for PMDs are being added to the
                Required Prior Authorization List:
                ------------------------------------------------------------------------
                 HCPCS code Description
                ------------------------------------------------------------------------
                K0857........................ Power wheelchair, group 3 standard,
                 single power option, captains chair,
                 patient weight capacity up to and
                 including 300 pounds.
                K0858........................ Power wheelchair, group 3 heavy duty,
                 single power option, sling/solid set/
                 back, patient weight 301 to 450 pounds.
                K0859........................ Power wheelchair, group 3 heavy duty,
                 single power option, captains chair,
                 patient weight capacity 301 to 450
                 pounds.
                K0860........................ Power wheelchair, group 3 heavy duty,
                 single power option, sling/solid seat/
                 back, patient weight capacity 451 to 600
                 pounds.
                K0862........................ Power wheelchair, group 3 heavy duty,
                 multiple power option, sling/solid seat/
                 back, patient weight capacity 301 to 450
                 pounds.
                K0863........................ Power wheelchair, group 3 heavy duty,
                 multiple power option, sling/solid seat/
                 back, patient weight capacity 451 to 600
                 pounds.
                K0864........................ Power wheelchair, group 3 extra heavy
                 duty, multiple power option, sling/solid
                 seat/back, patient weight capacity 601
                 pounds or more.
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                [[Page 16617]]
                 In phase one of implementation, which begins as specified in the
                DATES section of this document, we will implement a prior authorization
                program for these seven HCPCS codes for PMDs nationwide. The nationwide
                prior authorization program for these seven HCPCS codes will continue
                during phase 2. We believe prior authorization of these seven
                additional HCPCS codes for PMDs will help further our program integrity
                goals of reducing fraud, waste, and abuse, while protecting access to
                care.
                 The following five HCPCS codes for Support Surfaces are also being
                added to the Required Prior Authorization List:
                ------------------------------------------------------------------------
                 HCPCS code Description
                ------------------------------------------------------------------------
                E0193.................................. Powered Air Flotation Bed (Low
                 Air Loss Therapy).
                E0277.................................. Powered pressure-reducing air
                 mattress.
                E0371.................................. Nonpowered advance pressure
                 reducing overlay for mattress
                 length and width.
                E0372.................................. Powered air overlay for
                 mattress, standard mattress
                 length and width.
                E0373.................................. Nonpowered advanced pressure
                 reducing mattress.
                ------------------------------------------------------------------------
                 The CMS' Comprehensive Error Rate Testing (CERT) program continues
                to estimate high rates of improper payments for support surface codes.
                Since 2015, the estimated improper payment rate for these codes is over
                59 percent, with an estimated improper payment rate of 75.2 percent, or
                over $18 million in projected improper payments for fiscal year 2018.
                 We will implement a prior authorization program for these five
                HCPCS codes for Support Surfaces in two phases. This phased-in approach
                will allow us to identity and resolve any unforeseen issues by using a
                smaller claim volume in phase one before nationwide implementation
                occurs in phase two. In phase one of implementation, which begins as
                specified in the DATES section of this document, we will limit the
                prior authorization requirement to one state in each of the four DME
                Medicare Administrative Contractors (MAC) geographic jurisdictions, as
                follows: California, Indiana, New Jersey, and North Carolina. In phase
                two, which begins as specified in the DATES section of this document,
                we will expand the program to the remaining states.
                 We believe prior authorization of these five HCPCS codes for
                Support Surfaces will help further our program integrity goals of
                reducing fraud, waste, and abuse, while protecting access to care.
                 These additional 12 HCPCS codes will be subject to the requirements
                of the prior authorization program for certain DMEPOS items as outlined
                in Sec. 414.234. All 33 HCPCS codes currently on the Required Prior
                Authorization List (81 FR 93636 and 83 FR 25947) will continue to be
                subject to the requirements of prior authorization as well.
                 Prior to furnishing the item to the beneficiary and prior to
                submitting the claim for processing, a requester must submit a prior
                authorization request that includes evidence that the item complies
                with all applicable Medicare coverage, coding, and payment rules.
                Consistent with Sec. 414.234(d), such evidence must include the order,
                relevant information from the beneficiary's medical record, and
                relevant supplier-produced documentation. After receipt of all
                applicable required Medicare documentation, CMS or one of its review
                contractors will conduct a medical review and communicate a decision
                that provisionally affirms or non-affirms the request.
                 We will issue specific prior authorization guidance in
                subregulatory communications, including final timelines, which are
                customized for the DMEPOS items subject to prior authorization, for
                communicating a provisionally affirmed or non-affirmed decision to the
                requester. In the December 30, 2015 final rule (80 FR 81694), to allow
                us to safeguard beneficiary access to care, we stated that this
                approach to final timelines provides the flexibility to develop a
                process that involves fewer days, as may be appropriate. If at any time
                we become aware that the prior authorization process is creating
                barriers to care, we can suspend the program.
                 The updated Required Prior Authorization list is available in the
                download section of the following CMS website: https://www.cms.gov/Research-Statistics-Data-and-Systems/Monitoring-Programs/Medicare-FFS-Compliance-Programs/DMEPOS/Prior-Authorization-Process-for-Certain-Durable-Medical-Equipment-Prosthetic-Orthotics-Supplies-Items.html. We
                will post additional educational resources to the website.
                III. Collection of Information Requirements
                 This document announces the addition of DMEPOS items on the
                Required Prior Authorization List and does not impose any new
                information collection burden under the Paperwork Reduction Act of
                1995. However, there is an information collection burden associated
                with this program that is currently approved under OMB control number
                0938-1293 which expires on March 31, 2022.
                 Dated: March 19, 2019.
                Seema Verma,
                Administrator, Centers for Medicare & Medicaid Services.
                [FR Doc. 2019-08031 Filed 4-18-19; 4:15 pm]
                 BILLING CODE 4120-01-P
                

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