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Author Topic: FREE Electric Wheelchair or at No Cost to You! (it is true or false ?)  (Read 762 times)
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The MOBILITY Center
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« on: January 18, 2009, 02:36:27 AM: GMT-2 »

We hear a lot of; "FREE Electric Wheelchair" or "Electric Wheelchair at NO COST", especially on TV.

That is Absolutely FALSE, someone has to pick up the bill or the company giving out the equipment would be out of business or they will simply be a non-profit organization.

What happens in most cases someone gets the bill for the electric wheelchair in most cases your insurance carrier(s). There is a medical requirement behind there decision.

There for "FREE Electric Wheelchair" or "Electric Wheelchair at NO COST" is a myth.

the link below is straight from the Medicare and their documentation requirements.

Here is a link to Centers for Medicare & Medicaid Services:
http://www.cms.hhs.gov/mcd/viewncd.asp?ncd_id=280.3&ncd_version=2&basket=ncd%3A280%2E3%3A2%3AMobility+Assistive+Equipment+%28MAE%29

this expert is from the link above:

NCD for Mobility Assistive Equipment (MAE) (280.3)
Publication Number
100-3

Manual Section Number
280.3

Version Number
2

Effective Date of this Version
5/5/2005

Implementation Date
7/5/2005

Benefit Category
Durable Medical Equipment


Note: This may not be an exhaustive list of all applicable Medicare benefit categories for this item or service.

Coverage Topic
Durable Medical Equipment
Motorized/Power Wheelchairs
Wheelchair Options and Accessories
Wheelchairs


Item/Service Description

A. General

The Centers for Medicare & Medicaid Services (CMS) addresses numerous items that it terms “mobility assistive equipment” (MAE) and includes within that category canes, crutches, walkers, manual wheelchairs, power wheelchairs, and scooters. This list, however, is not exhaustive.

Medicare beneficiaries may require mobility assistance for a variety of reasons and for varying durations because the etiology of the disability may be due to a congenital cause, injury, or disease. Thus, some beneficiaries experiencing temporary disability may need mobility assistance on a short-term basis, while in contrast, those living with chronic conditions or enduring disabilities will require mobility assistance on a permanent basis.

Medicare beneficiaries who depend upon mobility assistance are found in varied living situations. Some may live alone and independently while others may live with a caregiver or in a custodial care facility. The beneficiary's environment is relevant to the determination of the appropriate form of mobility assistance that should be employed. For many patients, a device of some sort is compensation for the mobility deficit. Many beneficiaries experience co-morbid conditions that can impact their ability to safely utilize MAE independently or to successfully regain independent function even with mobility assistance.

The functional limitation as experienced by a beneficiary depends on the beneficiary's physical and psychological function, the availability of other support, and the beneficiary's living environment. A few examples include muscular spasticity, cognitive deficits, the availability of a caregiver, and the physical layout, surfaces, and obstacles that exist in the beneficiary's living environment.

Indications and Limitations of Coverage

B. Nationally Covered Indications

Effective May 5, 2005, CMS finds that the evidence is adequate to determine that MAE is reasonable and necessary for beneficiaries who have a personal mobility deficit sufficient to impair their participation in mobility-related activities of daily living (MRADLs) such as toileting, feeding, dressing, grooming, and bathing in customary locations within the home. Determination of the presence of a mobility deficit will be made by an algorithmic process, Clinical Criteria for MAE Coverage, to provide the appropriate MAE to correct the mobility deficit.

Clinical Criteria for MAE Coverage

The beneficiary, the beneficiary’s family or other caregiver, or a clinician, will usually initiate the discussion and consideration of MAE use. Sequential consideration of the questions below provides clinical guidance for the coverage of equipment of appropriate type and complexity to restore the beneficiary’s ability to participate in MRADLs such as toileting, feeding, dressing, grooming, and bathing in customary locations in the home. These questions correspond to the numbered decision points on the accompanying flow chart. In individual cases where the beneficiary’s condition clearly and unambiguously precludes the reasonable use of a device, it is not necessary to undertake a trial of that device for that beneficiary.

Does the beneficiary have a mobility limitation that significantly impairs his/her ability to participate in one or more MRADLs in the home? A mobility limitation is one that:


Prevents the beneficiary from accomplishing the MRADLs entirely, or,
Places the beneficiary at reasonably determined heightened risk of morbidity or mortality secondary to the attempts to participate in MRADLs, or,
Prevents the beneficiary from completing the MRADLs within a reasonable time frame.


Are there other conditions that limit the beneficiary’s ability to participate in MRADLs at home?


Some examples are significant impairment of cognition or judgment and/or vision.
For these beneficiaries, the provision of MAE might not enable them to participate in MRADLs if the comorbidity prevents effective use of the wheelchair or reasonable completion of the tasks even with MAE.


If these other limitations exist, can they be ameliorated or compensated sufficiently such that the additional provision of MAE will be reasonably expected to significantly improve the beneficiary’s ability to perform or obtain assistance to participate in MRADLs in the home?


A caregiver, for example a family member, may be compensatory, if consistently available in the beneficiary's home and willing and able to safely operate and transfer the beneficiary to and from the wheelchair and to transport the beneficiary using the wheelchair. The caregiver’s need to use a wheelchair to assist the beneficiary in the MRADLs is to be considered in this determination.

If the amelioration or compensation requires the beneficiary's compliance with treatment, for example medications or therapy, substantive non-compliance, whether willing or involuntary, can be grounds for denial of MAE coverage if it results in the beneficiary continuing to have a significant limitation. It may be determined that partial compliance results in adequate amelioration or compensation for the appropriate use of MAE.


Does the beneficiary or caregiver demonstrate the capability and the willingness to consistently operate the MAE safely?


Safety considerations include personal risk to the beneficiary as well as risk to others. The determination of safety may need to occur several times during the process as the consideration focuses on a specific device.
A history of unsafe behavior in other venues may be considered.


Can the functional mobility deficit be sufficiently resolved by the prescription of a cane or walker?


The cane or walker should be appropriately fitted to the beneficiary for this evaluation.
Assess the beneficiary’s ability to safely use a cane or walker.


Does the beneficiary’s typical environment support the use of wheelchairs including scooters/power-operated vehicles (POVs)?


Determine whether the beneficiary’s environment will support the use of these types of MAE.
Keep in mind such factors as physical layout, surfaces, and obstacles, which may render MAE unusable in the beneficiary’s home.


Does the beneficiary have sufficient upper extremity function to propel a manual wheelchair in the home to participate in MRADLs during a typical day? The manual wheelchair should be optimally configured (seating options, wheelbase, device weight, and other appropriate accessories) for this determination.


Limitations of strength, endurance, range of motion, coordination, and absence or deformity in one or both upper extremities are relevant.
A beneficiary with sufficient upper extremity function may qualify for a manual wheelchair. The appropriate type of manual wheelchair, i.e. light weight, etc., should be determined based on the beneficiary’s physical characteristics and anticipated intensity of use.

The beneficiary's home should provide adequate access, maneuvering space and surfaces for the operation of a manual wheelchair.
Assess the beneficiary’s ability to safely use a manual wheelchair.

NOTE: If the beneficiary is unable to self-propel a manual wheelchair, and if there is a caregiver who is available, willing, and able to provide assistance, a manual wheelchair may be appropriate.


Does the beneficiary have sufficient strength and postural stability to operate a POV/scooter?


A POV is a 3- or 4-wheeled device with tiller steering and limited seat modification capabilities. The beneficiary must be able to maintain stability and position for adequate operation.

The beneficiary's home should provide adequate access, maneuvering space and surfaces for the operation of a POV.
Assess the beneficiary’s ability to safely use a POV/scooter.


Are the additional features provided by a power wheelchair needed to allow the beneficiary to participate in one or more MRADLs?


The pertinent features of a power wheelchair compared to a POV are typically control by a joystick or alternative input device, lower seat height for slide transfers, and the ability to accommodate a variety of seating needs.

The type of wheelchair and options provided should be appropriate for the degree of the beneficiary’s functional impairments.
The beneficiary's home should provide adequate access, maneuvering space and surfaces for the operation of a power wheelchair.
Assess the beneficiary’s ability to safely use a power wheelchair.

NOTE: If the beneficiary is unable to use a power wheelchair, and if there is a caregiver who is available, willing, and able to provide assistance, a manual wheelchair is appropriate. A caregiver’s inability to operate a manual wheelchair can be considered in covering a power wheelchair so that the caregiver can assist the beneficiary.

Flow chart    
C. Nationally Non-Covered Indications

Medicare beneficiaries not meeting the clinical criteria for prescribing MAE as outlined above, and as documented by the beneficiary’s physician, would not be eligible for Medicare coverage of the MAE.

D. Other

All other durable medical equipment (DME) not meeting the definition of MAE as described in this instruction will continue to be covered, or noncovered, as is currently described in the NCD Manual, in Section 280, Medical and Surgical Supplies. Also, all other sections not altered here and the corresponding policies regarding MAEs which have not been discussed here remain unchanged.

(This NCD last reviewed May 2005).

Cross Reference

See Section 280.1 Durable Medical Equipment (DME) Reference List.


Transmittal Number
37

Transmittal Link
http://www.cms.hhs.gov/transmittals/downloads/R37NCD.pdf

Revision History
06/2005 - Determined MAE is reasonable and necessary for beneficiaries who have personal mobility deficit sufficient to impair their performance of mobility-related activities of daily living such as toileting, feeding, dressing, grooming, and bathing in customary locations in home. Effective date 05/05/2005. Implementation date 07/05/2005. (TN 37 ) (CR 3791)

Claims Processing Instructions
TN 574 Medicare Claims Processing  
National Coverage Analyses (NCAs)
This NCD has been or is currently being reviewed under the National Coverage Determination process. The following are existing associations with NCAs, from the National Coverage Analyses database.

Page Last Modified: 11/14/2008 11:24:36 AM
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« Reply #1 on: June 26, 2009, 07:06:03 PM: GMT-2 »

Here is an Update

Documentation Requirements For K0823 Power Wheelchair Claims

Recently NAS began monitoring HCPCS code K0823 (Power wheelchair, group 2 standard, captain's chair) due to a high volume of claim errors found by the Comprehensive Error Rate Testing (CERT) contractor. NAS has found the documentation received for these developed K0823 claims is insufficient to support medical necessity as noted in Power Mobility Devices Local Coverage Determination (LCD).

The documentation guidelines for K0823 can be found in the Power Mobility Devices LCD (L23598) located at: https://www.noridianmedicare.com/dme/coverage.

As a result of K0823 claim monitoring, NAS found the documentation submitted is insufficient to support even the basic coverage criteria for a power mobility device, namely:

Mobility-related activities of daily living (MRADLs) limitations are not provided in detail. Documentation should identify the beneficiary's specific limitations and clearly indicate what they can and cannot complete in terms of MRADLs. MRADLs are such things as bathing, grooming, eating, transferring, and walking.
The beneficiary's mobility cannot be sufficiently and safely resolved by the use of an appropriately fitted cane or walker. Documentation should identify specifically why the cane or walker is insufficient.
The beneficiary does not have sufficient upper extremity function to self-propel an optimally-configured manual wheelchair in the home in order to perform his/her MRADLs during a typical day.
A walker or manual wheelchair has been tried and the results of this trial are documented.
Why is this beneficiary unable to use a scooter?
In addition to addressing the MRADLs in detail, the medical documentation should include the following:

Strength levels and degrees of range of motion (ROM) of the beneficiary's upper and lower extremities
Coordination
Transferring abilities: self, assist of how many, or use of assistive devices
Endurance level
Pain rating and how performance of MRADLs impacts this pain rating
Supplier Generated Reports of Face-to-Face Mobility Examination:

NAS is seeing the use of supplier generated forms. Forms produced by the supplier for the face-to-face mobility exam do not record a complete medical examination and thus do not provide enough detailed information to adequately describe the medical necessity for the power mobility device in the beneficiary's home and are insufficient to meet the statutory requirements. The Power Mobility Devices LCD states:

"Many suppliers have created forms which have not been approved by CMS which they send to physicians and ask them to complete. Even if the physician completes this type of form and puts it in his/her chart, this supplier-generated form is not a substitute for the comprehensive medical record as noted above. Suppliers are encouraged to help educate physicians on the type of information that is needed to document a beneficiary's mobility needs."

These forms are vague in the areas addressed with no detailed objective documentation to support the items marked. Check marks in boxes are insufficient to support the statutory requirements.

NAS has noted that these forms can be in contradiction with the physician's or other Licensed Certified Medical Professional (LCMP) documentation. The forms have also been noted to conflict within itself from page to page.
The documentation submitted should provide a clear concise picture of the beneficiary's status.

Is the beneficiary able to ambulate?
What type of assistance is needed including the assistive device used?
How many caregivers are required to provide assistance?
What distance can the beneficiary ambulate?
If no, why is the beneficiary unable to ambulate?
How long will ambulation be a problem?
Is this a short term non-weight bearing issue?
Is the assistive device currently being used safe for the beneficiary?
If no, why is the beneficiary not safe?
How does the beneficiary transfer in and out of bed and to and from toilet?
What equipment or physical assistance is needed for transfers from bed to chair and chair to toilet?
Can the beneficiary perform pressure relief or weight shifting?
What is the beneficiary's sitting and standing balance?
What is the objective functional assessment of the beneficiary's strength and range of motion?
Statements of moderate weakness are vague and subjective and insufficient to meet statutory requirements.
Does the beneficiary have abnormal sensation or difficulties with coordination?
Does the beneficiary have abnormal tone or a deformity of the arms, legs, or trunk, including spasticity?
What interventions have been tried, and what were the results?
Sequence of Events for Power Mobility Devices:

1. The beneficiary goes to his/her physician to discuss the need for a power wheelchair.

2. The beneficiary is seen by the physician for a face-to-face mobility examination.

The physician shall document the examination in a detailed narrative note in the beneficiary's chart in the format used for other entries.
The note must clearly indicate that a major reason for the visit was a mobility examination.
The physician may also write an additional order for a wheelchair evaluation to be performed by PT/OT personnel who have experience and training in mobility evaluations to perform part of the face-to-face examination.
This could be the specialty evaluation as required in LCD L23598 for group 2 single and multiple power wheelchairs, all group 3 and 4 power wheelchairs, and the push-rim activated power assist device.
The physician then reviews the written report of the LCMP examination, signs and dates that report, and states concurrence or any disagreement with that examination.
The physician must send a copy of the note from his/her initial visit to evaluate the patient plus the annotated, signed, and dated copy of the LCMP examination to the supplier. The 45-day period begins when the physician signs and dates the LCMP examination.
3. The physician writes a seven element order for a power wheelchair which includes the following items:

Beneficiary's name
Description of the item that is ordered, general or specific
Date of the face-to-face mobility examination
Pertinent diagnoses or conditions that relate to the need for the power mobility device
Length of need
Physician's signature
Date of signature
4. This seven element order written by the physician is submitted to the supplier.

The written order is completed after the in-person visit and medical evaluation.
The supplier should date stamp or have an equivalent way to document the date this order is received.
The supplier must receive this order within 45 from the days after completion of the face-to-face exam and prior to delivery of the power mobility device.
5. The supplier determines the appropriate wheelchair and accessories for the beneficiary based on the mobility needs of the patient. A detailed product description is then created.

This form includes the HCPCS codes, billed amount, and Medicare fee schedule amount for the wheelchair and all options and accessories.
This form is submitted to the physician for his/her signature and date.
Date stamp or equivalent documenting date the supplier received detailed product description back from physician
6. The supplier completes a home evaluation to determine:

The power mobility device can access all rooms of the home.
The beneficiary is able to use the wheelchair to assist with MRADLS in the home.
The home evaluation must be dated and completed prior to delivery.
7. Additional documentation should be sent as requested in the claim development letter or as the physician or supplier deem necessary to assist in determining medical necessity and coverage criteria were met.

Sources:

Power Mobility Devices LCD (L23598)
Power Mobility Devices Policy Article (A41127)

 


 


Posted: 6/8/2009

Resources: https://www.noridianmedicare.com/cgi-bin/coranto/viewnews.cgi%3fid=EkuuuyVlZZKLdUlCab&tmpl=dme_viewnews&style=part_ab_viewnews
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« Reply #2 on: January 21, 2010, 09:08:43 PM: GMT-2 »

I found this on BrokenCountry.com

http://www.brokencountry.com/index.php/2008/02/01/the-scooter-store-scam/
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sufjanart98
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« Reply #3 on: December 08, 2010, 07:01:31 AM: GMT-2 »

such a helpful post. thanks Smiley
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