Implantable testosterone hormone pellets (e.g., Testopel)
Defines medical necessity and prior authorization requirements for implantable testosterone pellets as replacement therapy in males with testosterone deficiency; governs reimbursement and documentation submission procedures for Culinary Health Fund members.
No material clinical or coverage changes in this revision.
Medical necessity — implantable testosterone pellets
Medical necessity — implantable testosterone pellets (initial coverage)
Implantable testosterone pellets are considered medically necessary as replacement therapy in males with testosterone deficiency when ALL of the following are met:
ALL of the following
ONE of the following diagnoses
- Congenital or acquired primary hypogonadism (e.g., testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testes syndrome or orchidectomy)
- Congenital or acquired hypogonadotrophic hypogonadism (e.g., idiopathic or gonadotropic LHRH deficiency, or pituitary–hypothalamic injury from tumors, trauma or radiation)
- Failure or intolerance of topical/gels, transdermal patches, and injectable testosterone
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