Tryvio (aprocitentan) — United Healthcare
resistant hypertension
Initial criteria
- Diagnosis of resistant hypertension
- Systolic blood pressure ≥ 130 mm Hg on two consecutive measurements despite maximally tolerated antihypertensive treatment OR Diastolic blood pressure ≥ 80 mm Hg on two consecutive measurements despite maximally tolerated antihypertensive treatment
- Patient has been previously treated with all of the following antihypertensive classes for an adequate duration (minimum 4 weeks each) at a maximally tolerated dose: 1) Maximally tolerated blocker of the renin-angiotensin system [ACE inhibitor (e.g., enalapril, lisinopril) or ARB (e.g., candesartan, valsartan)] 2) Maximally tolerated calcium channel blocker (e.g., amlodipine, diltiazem, verapamil) 3) Maximally tolerated diuretics (e.g., hydrochlorothiazide) 4) Maximally tolerated mineralocorticoid receptor antagonist (e.g., spironolactone, eplerenone)
- Provider attests other causes of hypertension have been excluded (e.g., secondary causes, white coat effect, medication nonadherence)
- Used as an adjunct to lifestyle modification (e.g., dietary or caloric restriction, exercise, behavioral support, community-based program)
- Tryvio will be used in combination with at least 3 antihypertensive medications from different classes at maximally tolerated doses
- Prescribed by or in consultation with a specialist experienced in the treatment of resistant hypertension (e.g., cardiologist, nephrologist)
Reauthorization criteria
- Documentation the patient is receiving clinical benefit to Tryvio therapy
- Tryvio will be used in combination with at least 3 antihypertensive medications from different classes at maximally tolerated doses
Approval duration
12 months