Effective Date:
a) This policy will apply to all services performed on or after the above revision date which will become the new effective date.
b) For all services referred to in this policy that were performed before the revision date, contact customer service for the rules that would apply.
1) Cinryze, Takhzyro, and Haegarda require prior authorization for use as prophylaxis therapy in hereditary angioedema (HAE).
2) Berinert, Firazyr, Kalbitor, and Ruconest are covered to treat acute attacks of hereditary angioedema (HAE) based on the criteria in this policy.
Coverage of all products in this policy requires a diagnosis of hereditary angioedema (HAE) based on the following criteria demonstrated on two separate occasions:
· Low C4 level (C4 < 14mg/dl; normal range 14-40mg/dl or C4 below the lower limit of normal as defined by the laboratory performing the test, plus:
a. A low C1 inhibitor (C1INH) antigenic level (C1INH < 19mg/dl; normal range 19-37mg/dl, or C1INH antigenic level below the lower limit of normal as defined by the laboratory performing the test, OR
b. A normal C1INH antigenic level (C1INH > or = to 19mg/dl) and a low C1INH functional level (functional C1INH < 50%) or below the lower limit of normal as defined by the laboratory performing the test.
A. Cinryze (J0598), Takhzyro (J0593), and Haegarda (J0599) is considered medically necessary for prophylaxis against angioedema attacks in adolescents and adults when the following criteria are met. Haegarda is preferred over Cinryze and Takhzyro for members age > 6 years. Haegarda must be tried first before Cinryze or Takhzyro will be approved. Haegarda and Cinryze are FDA-approved for patients age 6 and older; Takhzyro is FDA-approved for patients age 2 and older.
1) Member has no signs of current acute angioedema; AND
2) Member has a history of at least 1 HAE attack per month; AND
3) Diagnosis of HAE (see above); AND
4) Medications known to cause angioedema (i.e. ACE-inhibitors, estrogens, angiotensin II receptor antagonists) have been evaluated and discontinued when appropriate; AND
5) Member has tried and failed or is intolerant to or has a contraindication to 17 alpha-alkylated androgens (e.g. Danazol, Stanozolol) or anti-fibrinolytic agents (e.g. aminocaproic acid or tranexamic acid) for HAE prophylaxis.
B. The following products are covered for the treatment of acute moderate to severe attacks of hereditary angioedema (HAE) based on the diagnosis criteria above, and subject to the additional criteria below for each drug.
1) Berinert (J0597) for the treatment of a HAE acute attack of abdominal, facial, or laryngeal areas in adolescents and adults.
2) Kalbitor (J1290) for the treatment of acute attacks of HAE in patients 16 years of age and older.
3) Firazyr (J1744) for the treatment of acute attacks of HAE in patients 18 years of age or older.
4) Ruconest (J0596) for the treatment of acute attacks of HAE in adolescents and adults.
Codes Used In This BI:
ACTIVE
J0593
J0596
Injection, lanadelumab-flyo, 1mg
Injection, C-1 esterase inhibitor (recombinant), Ruconest, 10 units
J0597
Injection, C-1 esterase inhibitor (human), Berinert, 10 units
J0598
Injection, C-1 esterase inhibitor (human), Cinryze, 10 units
J0599
Injection, C-1 esterase inhibitor (human), Haegarda, 10 units (new code 1/1/19)
J1290
Injection, ecallantide, 1 mg
J1744
Injection, icatibant, 1 mg
DELETED
C9015
Injection, C-1 esterase inhibitor (human), Haegarda, 10 units (code deleted 1/1/19)
1) Effective 01/01/2018: Added Haegarda to coverage policy.
2) Effective 01/01/2019: Added Takhzyro to coverage policy.
2019 Code Updates. HCPCS code C9015 deleted and replaced with new HCPCS code J0599.
3) Effective 10/01/2019: Added J0593 to coverage policy.
4) Effective 06/01/2023: Updated Takhzyro to reflect FDA-approval for age 2 and older.