Hyaluronic Acid Derivatives

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Hyaluronic Acid Derivatives

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Federal Employee Program 1310 G Street, N.W. Washington, D.C. 20005 202.942.1000 Fax 202.942.1125 5.11.04 Subject: Hyaluronic Acid Page: 1 of 6 Last Review Date: March 13, 2014 Hyaluronic Acid Derivatives Description Euflexxa (sodium hyaluronate) / Hyalgan (sodium hyaluronate) / Gel-ONE/ Orthovisc / Monovisc (hyaluronan) / Supartz (sodium hyaluronate) / Synvisc (hylan G-F 20) / Synvisc - One (hylan G-F 20) Background Osteoarthritis of the knee is a disease in which the elastoviscous property of the synovial fluid in the knee joint becomes diminished, resulting in less protection and shock absorption. Orthovisc, Monovisc, Euflexxa, Supartz, Gel-ONE, Hyalgan, Synvisc and Synvisc-One are hyaluronan derivatives that are injected into the knee joints to increase the elastoviscous properties of arthritic joint fluid and slow its outflow from the joint. The goal of therapy is to restore the viscoelasticity in the affected joints, thereby decreasing pain, improving mobility, and restoring the natural protective functions (1). The American College of Rheumatology (ACR) updated its guidelines for the treatment of osteoarthritis (OA) of the knee in 2012. In mild symptomatic OA, treatment may be limited to patient education, physical and occupational therapy and other non-pharmacologic modalities. Nonpharmacologic modalities strongly recommended for the management of knee OA were aerobic, aquatic, and/or resistance exercises as well as weight loss for overweight patients. Nonpharmacologic modalities conditionally recommended for knee OA included medial wedge insoles for valgus knee OA, subtalar strapped lateral insoles for varus knee OA, medially directed patellar taping, manual therapy, walking aids, thermal agents, tai chi, self-management

Subject: Hyaluronic Acid Page: 2 of 6 programs, and psychosocial interventions. Pharmacologic modalities conditionally recommended for the initial management of patients with knee OA included acetaminophen, oral and topical NSAIDs, tramadol, and intraarticular corticosteroid injections (1). Regulatory Status FDA-approved indication: Hyaluronic acid derivatives are indicated for the treatment of pain in osteoarthritis (OA) of the knee in patients who have failed to respond adequately to conservative non-pharmacologic therapy, simple analgesics (e.g., acetaminophen), NSAIDs, tramadol, or intra-articular steroid injections (2-9). The hyaluronic acid derivatives are contraindicated for use in patients with known hypersensitivity to hyaluronan (sodium hyaluronate) preparations. Orthovisc lists hypersensitivity to gram positive bacterial proteins as an additional contraindication (4). Caution should be exercised when Gel-One, Hyalgan, Synvisc, Synvisc-One and Supartz are administered to patients with allergies to avian proteins, feathers, and egg products (3,5,6,7,8). Hyaluronic acid derivatives are contraindicated to treat patients with knee joint infections, infections or skin diseases in the area of the injection site (2-8). A treatment cycle for most of the hyaluronan derivatives typically involves multiple weekly injections. Euflexxa and Synvisc are given for a total of three injections. Orthovisc is given for three or four injections. Supartz and Hyalgan are given for a total of three or five injections. Gel-One and Synvisc-One differ from the other hyaluronan derivatives in that it only requires one injection. Repeat courses of hyaluronan derivatives may be administered if symptoms return (2-9). Upon the basis of high quality supporting evidence, the American Academy of Orthopedic Surgeons cannot recommend using hyaluronic acid for patients with symptomatic osteoarthritis of the knee (10). Related policies Policy

Subject: Hyaluronic Acid Page: 3 of 6 This policy statement applies to clinical review performed for pre-service (Prior Approval, Precertification, Advanced Benefit Determination, etc.) and/or post-service claims. Hyaluronic acid derivatives may be considered medically necessary for the treatment of osteoarthritis of the knee when conservative non-pharmacologic therapy and simple analgesic therapy have failed to provide relief. Hyaluronic acid derivatives may be considered investigational for all other indications. Prior-Approval Requirements Age 18 years or older (22 or older for Synvisc and Synvisc-One) Diagnosis Patient must have the following: Osteoarthritis of the knee AND BOTH of the following: 1. NO adequate response to ONE or more of the following conservative nonpharmacologic therapy: a. Cardiovascular (aerobic) activity, such as: walking, biking, stationary bike, aquatic exercise b. Resistance exercise c. Weight reduction (for persons who are overweight) d. Participation in self-management programs e. Wear of medially directed patellar taping f. Wear of wedged insoles g. Thermal agents h. Walking aids i. Physical therapy j. Occupational therapy 2. NO adequate response to ONE or more of the following: (unless clinically contraindicated or intolerant) a. Acetaminophen

Subject: Hyaluronic Acid Page: 4 of 6 b. Oral NSAIDs c. Topical NSAIDs d. Tramadol e. Intra-articular steroid injections Prior Approval Renewal Requirements Diagnosis Patient must have the following: Osteoarthritis of the knee AND ALL of the following: 1. Documentation of improvement in pain with previous course of treatment 2. At least 6 months has elapsed since last injection of the prior treatment cycle 3. Documentation of reduction of dosing of NSAIDs or other analgesics during the 6 month period following the last injection of the prior treatment cycle. Policy Guidelines Pre - PA Allowance None Prior - Approval Limits Duration Quantity 12 months Two courses of therapy for each knee Prior Approval Renewal Limits Duration Quantity 12 months Two courses of therapy for each knee

Subject: Hyaluronic Acid Page: 5 of 6 Rationale Summary Osteoarthritis of the knee is a disease in which the elastoviscous property of the synovial fluid in the knee joint becomes diminished, resulting in less protection and shock absorption. Orthovisc, Monovisc, Euflexxa, Supartz, Gel-One, Hyalgan, Synvisc and Synvisc-One are hyaluronan derivatives that are injected into the knee joints to increase the elastoviscous properties of arthritic joint fluid and slow its outflow from the joint. The goal of therapy is to restore the viscoelasticity in the affected joints, thereby decreasing pain, improving mobility, and restoring the natural protective functions. Prior approval is required to ensure the safe, clinically appropriate and cost effective use of the hyaluronic acid derivatives while maintaining optimal therapeutic outcomes. References 1. American College of Rheumatology, Subcommittee on Osteoarthritis Guidelines. Recommendations for the medical management of osteoarthritis of the hip and knee: 2012 update. Arthritis Care & Research 2012; 64(4):465-474. 2. Euflexxa [package insert]. Suffern, NY: Ferring Pharmaceuticals Inc; September 2011. 3. Hyalgan [package insert]. New York, NY: Sanofi-Synethelabo, Inc; June 2011. 4. Orthovisc [package insert]. Raynham, MA: Anika Therapeutics; June 2005. 5. Supartz [package insert]. Memphis, TN: Smith & Nephew; June 2012. 6. Synvisc [package insert]. Ridgefield, NJ: Genzyme Corp; March 2010. 7. Synvisc-One [package insert]. Ridgefield, NJ: Genzyme Corp; January 2010 8. Gel-One [package insert]. Warsaw. IN. Zimmer Inc. May 2011. 9. Monovisc [package insert]. Bedford, MA: Anika Therapeutics;December 2013 10. American Academy of Orthopaedic Surgeons. Treatment of Osteoarthritis of the Knee. Evidence-based guideline 2 nd Edition. May 2013. Policy History Date Action Reason

Subject: Hyaluronic Acid Page: 6 of 6 January 2012 December 2012 December 2013 March 2014 April 2014 Keywords Added minimum age - only approved for adults. Annual editorial review and reference update Annual editorial review and reference update Annual editorial review Addition of examples of non-pharmacological agents and agents of prior failure medications. Line-Addition of Monovisc to PA This policy was approved by the FEP Pharmacy and Medical Policy Committee on March 13, 2014 and is effective April 1, 2014. Signature on File Deborah M. Smith, MD, MPH