Effective January 1, 2020, our medical policy on
hyaluronate acid (HA) products will reflect new coverage criteria, including
the addition of Monovisc® as a fourth preferred product in the
HA class, along with Orthovisc®, Synvisc®, and
Synvisc-One®. As a result, Monovisc will no
longer require precertification for AmeriHealth members.
Medical Policy #11.14.07u: Intra-Articular Injection of Hyaluronan for the
Treatment of Osteoarthritis was posted as a Notification on October 3, 2019,
and will go into effect January 1, 2020.
Background
There are 16 HA products that have been approved by the U.S. Food and Drug
Administration to treat osteoarthritis of the knee:
- Durolane®
- Euflexxa®
- Gel-One®
- Gelsyn-3™
|
- GenVisc 850®
- Hyalgan®
- Hymovis®
- Monovisc®
|
- Orthovisc®
- Supartz®
- Synojoynt™
- Synvisc®
|
- Synvisc-One®
- Triluron™
- TriVisc®
- VISCO-3™
|
Although there are many
hyaluronate acid products on the market for the treatment of osteoarthritis of
the knee, there is no reliable evidence of the superiority of any one brand
compared to the others.
Coverage criteria
All HA products are eligible for coverage in accordance
with the member’s benefit plan and the criteria listed in our medical
policy.
Cost-sharing (e.g., copayment, deductible,
and coinsurance) applies to all HA products for members who are enrolled in
Commercial FLEX products and select plans that have a cost-share component.
Learn more
To view the Notification for this medical policy, visit our Medical Policy Portal.