Mountain State Medical Policy Bulletin |
Section: | Orthotic & Prosthetic Devices |
Number: | O-28 |
Topic: | Knee Orthosis |
Effective Date: | October 11, 2010 |
Issued Date: | October 11, 2010 |
Date Last Reviewed: |
Indications and Limitations of Coverage
An orthosis (brace) is a rigid or semi-rigid device which is used for the purpose of supporting a weak or deformed body member or restricting or eliminating motion in a diseased or injured part of the body. It must provide support and counterforce (i.e., a force in a defined direction of a magnitude at least as great as a rigid or semi-rigid support) on the limb or body part that it is being used to brace. An orthosis can be either prefabricated or custom-fabricated. Prefabricated Knee Orthoses (L1810, L1820, L1830-L1832, L1836, L1843, L1845, L1847, L1850) A knee flexion contracture is a condition in which there is shortening of the muscles and/or tendons with the resulting inability to bring the knee to 0 degrees extension or greater (i.e., hyperextension) by passive range of motion. (0 degrees knee extension is when the femur and tibia are in alignment in a horizontal plane). A knee extension contracture is a condition in which there is shortening of the muscles and/or tendons with the resulting inability to bring the knee to 80 degrees flexion or greater by passive range of motion. A contracture is distinguished from the temporary loss of range of motion of a joint following injury, surgery, casting or other immobilization. A knee orthosis with joints (L1810) or knee orthosis with condylar pads and joints with or without patellar control (L1820) are covered for ambulatory patients who have weakness or deformity of the knee and require stabilization. If an L1810 or L1820 is provided but the criteria above are not met, the orthosis will be denied as not medically necessary. A knee orthosis with a locking knee joint (L1831, L1847) or a rigid knee orthosis (L1836) is covered for patients with flexion or extension contractures of the knee with movement on passive range of motion testing of at least 10 degrees (i.e., a nonfixed contracture). If an L1831, L1836, or L1847 orthosis is provided but the criterion above is not met, the orthosis will be denied as not medically necessary. There is no proven clinical benefit to the inflatable air bladder incorporated into the design of code L1847; therefore, if the criterion above is met, payment will be based on the allowance for the least costly medically appropriate alternative, code L1831. A knee immobilizer without joints (L1830) or a knee orthosis with adjustable knee joints (L1832) is covered if the patient has had recent injury to or a surgical procedure on the knee(s) and has one of the following diagnoses:
An L1832 knee orthosis is also covered for a patient who is ambulatory and has knee instability due to a condition specified in one of the following diagnoses: Any diagnosis listed above; or:
A knee orthosis, with an adjustable flexion and extension joint that provides both medial-lateral and rotation control (L1843, L1845) is covered for a patient who is ambulatory and has knee instability due to a condition specified by one of the diagnoses for L1832 listed above. A knee orthosis, Swedish type, prefabricated (L1850) is covered for a patient who is ambulatory and has knee instability due to genu recurvatum - hyperextended knee. For codes L1832, L1843, L1845 and L1850, knee instability must be documented by examination of the member and objective description of joint laxity (e.g., varus/valgus instability). Claims for L1832, L1843, L1845, or L1850 will be denied as not medically necessary when the patient does not meet the above criteria for coverage. For example, they will be denied if only pain or a subjective description of joint instability is documented. “Addition” codes are grouped into four (4) categories in relation to knee orthosis base codes.
Addition codes in the first two categories are addressed in the following tables of the policy. Addition codes in the latter two categories are addressed in the Coding Guidelines section of the policy. The following table lists addition codes which describe components or features that can be and frequently are physically incorporated in the specified prefabricated base orthosis. Addition codes may be separately payable if:
Addition codes will be denied as not medically necessary if the base orthosis is not medically necessary or the addition is not medically necessary.
Custom Fabricated Knee Orthoses (L1834, L1840, L1844, L1846, L1860) A custom fabricated orthosis is covered when there is a documented physical characteristic which requires the use of a custom fabricated orthosis instead of a prefabricated orthosis. Examples of situations which meet the criterion for a custom fabricated orthosis include, but are not limited to:
Although these are examples of potential situations where a custom fabricated orthosis may be appropriate, suppliers must consider prefabricated alternatives such as pediatric knee orthoses in patients with small limbs, straps with additional length for large limbs, etc. If the medical necessity for a custom fabricated orthosis is not met, but the criteria for a prefabricated orthosis is met, payment will be based on the allowance for the least costly medically appropriate alternative, a prefabricated orthosis. If a claim for a custom fabricated orthosis is not supported by a written order specifying custom fabricated, payment will be based on the allowance for the least costly medically appropriate alternative, a prefabricated orthosis. Custom fabricated orthoses are not medically necessary in the treatment of knee contractures in cases where the patient is nonambulatory. If a custom fabricated knee orthosis (L1834, L1840, L1844, L1846, L1860) is used in the treatment of a contracture in a nonambulatory patient and criterion for a prefabricated knee orthosis with a locking joint (L1831) is met, payment will be based on the allowance for the least costly medically appropriate alternative, L1831. A custom fabricated knee immobilizer without joints (L1834) is covered if criteria 1 and 2 are met:
If an L1834 orthosis is provided and both criteria 1 and 2 are not met, the orthosis will be denied as not medically necessary. If an L1834 orthosis is provided and criterion 1 is met but criterion 2 is not met, payment will be based on the allowance for the least costly medically appropriate alternative, L1830. A custom fabricated derotation knee orthosis (L1840) is covered for instability due to internal ligamentous disruption of the knee. A custom fabricated knee orthosis with an adjustable flexion and extension joint (L1844, L1846) is covered if criteria 1 and 2 are met:
If an L1844 or L1846 orthosis is provided and both criteria 1 and 2 are not met, the orthosis will be denied as not medically necessary. If an L1844 or L1846 orthosis is provided and criterion 1 is met but criterion 2 is not met, payment will be based on the allowance for the least costly medically appropriate alternative, L1843 or L1845, respectively. A custom fabricated knee orthosis with a modified supracondylar prosthetic socket (L1860) is covered for a patient who is ambulatory and has knee instability due to genu recurvatum - hyperextended knee. The following table lists addition codes which describe components or features that can be and frequently are physically incorporated in the specified custom fabricated base orthosis. Addition codes may be separately payable if:
Addition codes will be denied as not medically necessary if the base orthosis is not medically necessary or the addition is not medically necessary.
Miscellaneous Heavy duty knee joint codes (L2385, L2395) are covered only for patients who weigh more than 300 pounds. Coverage of a removable soft interface (K0672) is limited to a maximum of two (2) per year beginning one (1) year after the date of service for initial issuance of the orthosis. Additional replacement interfaces will be denied as not medically necessary. Refer to the Coding Guidelines section of the policy for information on denial of removable soft interfaces that are billed separately at the time of initial issue of the orthosis. Reasons for Noncoverage For an item to be considered for coverage under the Brace benefit category, it must be a rigid or semi-rigid device which is used for the purpose of supporting a weak or deformed body member or restricting or eliminating motion in a diseased or injured part of the body. It must provide support and counterforce (i.e., a force in a defined direction of a magnitude at least as great as a rigid or semi-rigid support) on the limb or body part that it is being used to brace. Items that do not meet the definition of a brace are non-covered. A participating, preferred, or network provider can bill the member for the non-covered device. Effective 1/1/2010, elastic support garments do not meet the statutory definition of a brace because they are not rigid or semi-rigid devices. Devices that are not rigid or semi-rigid must be coded A4466. Code A4466 will be denied as non-covered. A participating, preferred, or network provider can bill the member for the non-covered device. The following chart reflects the reasonable useful lifetime of prefabricated knee orthoses: L1810 – 1 year L1820 – 1 year L1830 – 1 year L1831 – 2 years L1832 – 2 years L1836 – 3 years L1843 – 3 years L1845 – 3 years L1847 – 2 years L1850 – 2 years The reasonable useful lifetime of custom fabricated orthoses is three years. Replacement during the “reasonable useful lifetime,” is covered if the item is lost or irreparably damaged. Replacement for other reasons, including but not limited to irreparable wear, during the period of reasonable useful lifetime is denied as non-covered. The provider can bill the member for the denied service. L-coded additions to knee orthoses (L2275 - L2830, K0672) will be denied as non-covered when the base orthosis is non-covered. A participating, preferred, or network provider can bill the member for the non-covered service. Brace sleeves (A9270) used in conjunction with orthoses are non-covered because they are not used to support a weak or deformed body member or to restrict or eliminate motion in a diseased or injured part of the body (i.e., it does not meet the definition of a brace). A participating, preferred, or network provider can bill the member for the non-covered service. Repairs to a covered orthosis are covered when they are necessary to make the orthosis functional. The reason for the repair must be documented in the supplier’s record. If the expense for repairs exceeds the estimated expense of providing another entire orthosis, no payment will be made for the amount in excess. Services that do not meet the medical necessity guidelines of this policy will be denied as not medically necessary. A participating, preferred, or network provider cannot bill the member for the denied service unless the provider has given advance written notice, informing the member that the service may be deemed not medically necessary and providing an estimate of the cost. The member must agree in writing to assume financial responsibility, in advance of receiving the service. The signed agreement should be maintained in the provider's records. Documentation Requirements It is expected that the patient’s medical records will reflect the need for the care provided. The patient’s medical records include the physician’s office records, hospital records, nursing home records, home health agency records, records from other healthcare professionals and test reports. This documentation must be available upon request. An order for all items must be signed and dated by the treating physician, kept on file by the supplier, and made available upon request. Items billed before a signed and dated order has been received by the supplier must be submitted with an EY modifier added to each affected procedure code. Orders must be sufficiently detailed including all options or additional features that will be separately billed. Written orders for custom fabricated orthoses must specifically state “custom fabricated” or specify a brand name and model that is only available as a custom fabricated product. The diagnosis code that justifies the need for the item must be included on the claim. KX, GA, GZ Modifiers Suppliers must add a KX modifier to knee orthosis, base and addition codes only if all of the coverage criteria in the “Indications and Limitations of Coverage” section of this policy have been met and evidence of such is retained in the supplier’s files and available upon request. If all of the criteria in the "Indications and Limitations of Coverage " section have not been met, the GA or GZ modifier must be added to the code. When there is an expectation of a medical necessity denial, suppliers must enter GA on the claim line if they have obtained a signed agreement from the member and the waiver of liability statement is on file. Suppliers must enter GZ on the claim line if they have not obtained a signed agreement from the member. Services submitted with a GA modifier will be denied as not medically necessary and are billable to the member. Services submitted with a GZ modifier will be denied as not medically necessary and are not billable to the member. Claim lines billed with codes without a KX, GA or GZ modifier will be rejected as missing information. For custom fabricated orthoses (L1834, L1840, L1844, L1846), there must be detailed documentation in the (no spelling suggestions) records to support the medical necessity of custom fabricated rather than a prefabricated orthosis. This information must be available upon request. When billing L2999, the following information should accompany the claim: manufacturer's name; product name; justification of patient's medical necessity for the item. In addition, if the item is custom fabricated, a complete and clear description of the item, including what makes this item unique, and a breakdown of charges (material and labor used in fabrication) must be included with the claim. An order is not necessary for the repair of an orthosis; however, claims for code L4210 must be accompanied by a description of the part that is being repaired or replaced. This information should be entered into the narrative field on an electronic claim. Coding Guidelines “Addition” codes are grouped into four (4) categories in relation to knee orthosis base codes.
Addition codes in the first two categories are addressed in the policy. Addition codes that are not separately payable are addressed in the tables below. The following table lists addition codes which describe components or features that can be physically incorporated in the specified prefabricated base orthosis but are considered to be included in the allowance for the orthosis. The addition codes will be denied as not separately payable if they are billed with the related base code.
A replacement removable soft interface for a knee orthosis is billed with code K0672 (lower extremity orthosis, not otherwise specified). One unit of service includes all the components that are used at the same time on a single orthosis. Either a nonremovable soft interface (L2820, L2830) or two (2) removable soft interfaces (K0672) are included in the allowance for a knee orthosis. Soft interfaces billed separately at the time of initial issue will be denied as not separately payable. Codes L2320 and L2330 (non-molded and molded lacers, respectively) may only be billed as replacement items. Claims for prefabricated or custom-fabricated devices that contain a concentric adjustable torsion style mechanism in the knee joint should be coded as E1810 (dynamic adjustable knee extension/flexion device, includes soft interface material). All lines on claims billed with L-codes for devices incorporating a concentric adjustable torsion style mechanism in the knee joint will be rejected as incorrect coding. The allowance for the labor involved in replacing/repairing an orthotic component that is coded with a specific L code is included in the allowance for that component. The allowance for the labor (L4205) involved in replacing/repairing an orthotic component that is coded with the miscellaneous code L4210 is separately payable in addition to the allowance for that component. The right (RT) and/or left (LT) modifiers must be used when billing for orthosis base codes, additions and replacement parts. When the same code for bilateral items (left and right) is billed on the same date of service, bill for both items on the same claim line using the RTLT modifiers and 2 units of service. Claims billed without modifiers RT and/or LT will be denied or rejected as incorrect coding. Code L2999 (lower extremity orthosis, not otherwise specified) should be used only when billing for item(s) that do not meet the definition of an existing code(s). Code L4205 (Repair of orthotic device, labor component, per 15 minutes) may only be billed for time involved with the actual repair of an orthosis or for medically necessary adjustments made more than 90 days after delivery. Code L4205 must not be used to bill for time involved with other professional services including, but not limited to:
Reimbursement for these services is included in the allowance for the procedure codes which describe the orthosis. Similarly, code L4210 (Repair of orthotic device, repair or replace minor parts) must not be used for casting supplies or other materials used in the fitting or fabrication of an orthosis. Should a supplier wish to submit a claim for services/items that are included in the allowance for the orthosis, code L9900 (Orthotic and prosthetic supply, accessory and/or service component of another L code) must be used. Code L9900 is denied as not separately payable. Coverage for orthotics is determined according to individual or customer benefits. |
A4466 | A9270 | K0672 | L1810 | L1820 | L1830 |
L1831 | L1832 | L1834 | L1836 | L1840 | L1843 |
L1844 | L1845 | L1846 | L1847 | L1850 | L1860 |
L2275 | L2320 | L2330 | L2385 | L2390 | L2395 |
L2397 | L2405 | L2415 | L2425 | L2430 | L2492 |
L2750 | L2755 | L2780 | L2785 | L2795 | L2800 |
L2810 | L2820 | L2830 | L2999 | L4205 | L4210 |
L9900 |
This medical policy may not apply to FEP. Medical policy is not an authorization, certification, explanation of benefits, or a contract. Benefits are determined by the Federal Employee Program. |
DME MAC Jurisdiction A - L27263 Medicare Coverage Database LCD for DME MAC Regions A, B, C, and D Anderson D, Samuelson K, Karlson J. Treatment of anterior cruciate ligament injuries with special reference to surgical technique and rehabilitation: an assessment of randomized controlled trials. Arthroscopy. 2009; 2596):653-685. Birmingham TB, Bryant DM, Giffin Jr, et al. A randomized controlled trial comparing the effectiveness of functional knee brace and neoprene sleeve use after anterior cruciate ligament reconstruction. AM J Sports Med. 2008; 36(4):648-655. Brouwer RW, van Raaij TM, Verharr JA, et al. Brace treatment for osteoarthritis of the knee: a prospective randomized multi-centre trial. Osteoarthritis Cartilage. 2006; 14(8):777-783. Chew KT, Lew HL, Date E, Fredericson M. Current evidence and clinical applications of therapeutic knee braces. AM J Phys Med Rehabil. 2007; 86(8):678-686. Wright, FW, Fetzer GB. Bracing after ACL reconstruction: a systematic review. Clin Orthop Relat Res. 2007;455:162-168. Beaudreuil J. Clinical practice guidelines for rest orthosis, knee sleeves and unloading knee braces in knee osteoarthritis. Joint Bone Spine. 01 Dec 2009; 76(6):629-36. Hiemstra LA. Knee immobilization for pain control after a hamstring tendon anterior cruciate ligament reconstruction: a randomized clinical trial. AM J Sports Med. 01 Jan 2009; 37(1):56-64. |
[Version 003 of O-28] |
[Version 002 of O-28] |
[Version 001 of O-28] |
For procedure codes L1831, L1836 and L1847:
718.46 |
For procedure codes L1830 and L1834:
714.0-714.4 | 715.16 | 715.26 | 715.36 |
715.96 | 717.0-717.5 | 717.7 | 717.81-717.9 |
727.65 | 733.15 | 733.16 | 733.49 |
733.93 | 755.64 | 821.20-821.39 | 822.0-822.1 |
823.00-823.42 | 836.0-836.69 | 844.0-844.2 | 966.40-996.49 |
996.66 | 996.77 | V43.65 |
For procedure code L1840:
718.81-717.9 |
For procedures codes L1832, L1843, L1844, L1845 and L1846:
340 | 342.90 | 343.9 | 344.1 |
355.0 | 355.2 | 714.0-714.4 | 715.16 |
715.26 | 715.36 | 715.96 | 717.0-717.5 |
717.7 | 717.81-717.9 | 727.65 | 733.15 |
733.16 | 733.49 | 733.93 | 755.64 |
821.20-821.39 | 822.0-822.1 | 823.00-823.42 | 836.0-836.69 |
844.0-844.2 | 996.40-996.49 | 996.66 | 996.77 |
V43.65 |
For procedure codes L1850 and L1860:
736.5 |
Term | Description |
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Prefabricated Orthosis | A prefabricated orthosis is one which is manufactured in quantity without a specific patient in mind. A prefabricated orthosis may be trimmed, bent, molded (with or without heat), or otherwise modified for use by a specific patient (i.e., custom fitted). An orthosis that is assembled from prefabricated components is considered prefabricated. Any orthosis that does not meet the definition of a custom-fabricated orthosis is considered prefabricated.
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Custom-fabricated Orthosis | A custom-fabricated orthosis is one which is individually made for a specific patient (no other patient would be able to use this orthosis) starting with basic materials including, but not limited to, plastic, metal, leather, or cloth in the form of sheets, bars, etc. It involves substantial work such as vacuum forming, cutting, bending, molding, sewing, etc. It may involve the incorporation of some prefabricated components. It involves more than trimming, bending, or making other modifications to a substantially prefabricated item.
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Molded-to-Patient-Model Orthosis | A molded-to-patient-model orthosis is a particular type of custom fabricated orthosis in which either: a) An impression of the specific body part is made (usually by means of a plaster or fiberglass cast) and this impression is then used to make a positive model (usually of plaster) of the body part; or b) Detailed measurements are taken of the patient's extremity and are used to modify a positive model (which has been selected from a large library of models) to make it conform to the patient's body shape and dimensions; or c) A digital image of the patient's extremity is made using computer (CAD-CAM) software which then directs the carving of a positive model. The orthosis is then individually fabricated and molded over the positive model of the patient.
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L1810 | Code L1810 describes a prefabricated knee orthosis constructed of latex, neoprene, spandex or other elastic material. There are no condylar pads. There are hinges or joints.
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L1820 | Code L1820 describes a prefabricated knee orthosis with hinges or joints, constructed of latex, neoprene, spandex or other elastic material. There are medial and lateral condylar pads.
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L1830 | Code L1830 describes a prefabricated knee orthosis immobilizer, with rigid metal or plastic stays placed laterally and posteriorly. The interface material is constructed of canvas, closed cell foam or equal. The thigh and calf cuffs are one-piece construction held in place by velcro straps or equal. The orthosis immobilizes the knee joint and prevents flexion or extension. There are no hinges or joints.
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L1831, L1847 | Codes L1831 and L1847 describe prefabricated knee orthoses with joint(s) which lock the knee into a particular position. Code L1847 is distinguished from L1831 by the addition of an air bladder in the space behind the knee. These orthoses are designed for patients who are nonambulatory. They are typically used to treat flexion / extension contractures of the knee. An adjustable flexion and extension joint is one which enables the practitioner to set limits on flexion and extension but allows the patient free motion of the knee within those limits. The increments of adjustability must be, at a minimum, 15 degrees. The joint may be either unicentric or polycentric.
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L1832 | Code L1832 describes a prefabricated knee orthosis that has double uprights and adjustable flexion and extension joints. Medial-lateral control of the knee is accomplished by the solid metal (or similar material) structure of the double uprights. It may have condylar pads. This orthosis is designed for a patient who can bear weight on the knee and is capable of ambulation. It is typically used for early rehabilitation following knee surgery.
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L1834, L1836 | Codes L1834 and L1836 describe rigid knee orthosis without a knee joint. Both are designed to prevent knee motion. These orthoses are designed for patients who can bear weight on the knee, are capable of ambulating, and need additional support provided through immobilization of the knee joint. Code L1834 refers to a custom fabricated knee orthotic while L1836 refers to one that is pre-fabricated.
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L1840 | Code L1840 describes a custom fabricated knee orthosis with knee joints designed to protect the ligaments of the knee through medial-lateral torsion, providing stability and preventing rotation.
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L1843, L1844 | Codes L1843 and L1844 describe prefabricated and custom fabricated (respectively) knee orthoses which are constructed of rigid thigh and calf cuffs and a single upright with an adjustable flexion and extension knee joint. It must have condylar pads. Through a series of straps/supports that cross over and around the knee joint, rotational control and varus or valgus force is exerted on the knee joint. These orthoses are designed to open the medial or lateral compartment of the knee to provide pain relief due to osteoarthritis. These orthoses are designed for patients who are fully ambulatory.
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L1845, L1846 | Codes L1845 and L1846 describe prefabricated and custom fabricated (respectively) knee orthoses that have double uprights, condylar pads, and an adjustable flexion and extension joint and provide both medial-lateral and rotation control. Medial-lateral control of the knee is accomplished by the solid metal (or similar material) structure of the double uprights. Rotation control is accomplished by the combination of (1) solid metal (or similar material) in the anterior portion of the thigh and calf cuffs and (2) the condylar pads. These orthoses are designed for patients who are fully ambulatory.
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L1850 | L1850 describes a prefabricated orthosis with double uprights and thigh and calf pads. It may or may not have joints. These orthoses are used to prevent hyperextension of the knee joint in ambulatory patients.
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L1860 | L1860 describes a custom fabricated orthosis without joints, constructed of plastic or other similar material. These orthoses are used to prevent hyperextension of the knee joint in ambulatory patients. |