Horizon Blue Cross Blue Shield of New Jersey · Apnea obstructiva del sueño (indicación Zepbound SURMOUNT-OSA) · Versión completa en inglés: /pa-letter/horizon-bcbs--osa/

Carta de PA para Horizon Blue Cross Blue Shield of New Jersey: Apnea obstructiva del sueño (indicación Zepbound SURMOUNT-OSA).

Plantilla defensible de carta para Zepbound (tirzepatide). FDA expanded Zepbound's label in December 2024 to include moderate-to-severe obstructive sleep apnea in adults with obesity. This is the first GLP-1 indication for OSA and opens a coverage path under Medicare.

La carta misma está en inglés porque el revisor del plan la lee en inglés. La envuelve y la firma su clínico.

Plan
Horizon Blue Cross Blue Shield of New Jersey
Commercial / Medicare Advantage / Medicaid managed care (New Jersey)
Enviar a través de
NaviNet provider portal or fax 1-800-682-9510
Tiempo de respuesta
5 business days standard, 72 hours expedited
Plazo de apelación
180 days from denial notice
Cita de política: Horizon BCBSNJ Medical Policy 117, Anti-Obesity Pharmacotherapy.
Nota del plan: Horizon BCBS covers Wegovy and Zepbound at BMI greater than or equal to 30 (or 27 with weight-related comorbidity). Six months of lifestyle intervention required. Prime Therapeutics is the PBM for most Horizon commercial lines. Horizon NJ Health (Medicaid managed care) follows the New Jersey FamilyCare PDL, which has historically excluded GLP-1 for obesity indication; route T2D or CV indication for Medicaid members. Verify your specific plan's policy.

La carta (copiar y editar)

Copie el cuerpo a continuación y péguelo en el portal de su clínico o procesador de textos. Reemplace cada marcador de posición entre [CORCHETES] con datos específicos del paciente antes de enviar. La carta es de su clínico al plan, firmada por su clínico.

Enviar esta página a mi médico
[Today's date]

Horizon Blue Cross Blue Shield of New Jersey
Prior Authorization Department
Submitted via: NaviNet provider portal or fax 1-800-682-9510

Re: Prior Authorization Request, Zepbound (tirzepatide)
Patient: [Patient full name]
Member ID: [Plan member ID]
Date of birth: [Patient DOB]
Group number: [Group number if applicable]
Prescriber: [Prescriber full name, NPI, DEA]
Prescriber contact: [Phone, fax, email]

To the Horizon Blue Cross Blue Shield of New Jersey Prior Authorization Reviewer,

I am the treating clinician for [Patient name]. I am writing to request prior authorization for Zepbound (tirzepatide) for treatment of Obstructive sleep apnea (Zepbound SURMOUNT-OSA indication) (ICD-10: G47.33).

Clinical justification

FDA approved Zepbound (tirzepatide) for the treatment of moderate-to-severe obstructive sleep apnea in adults with obesity in December 2024, based on the SURMOUNT-OSA trial program. SURMOUNT-OSA enrolled adults with moderate-to-severe OSA (AHI greater than or equal to 15 events per hour) and BMI greater than or equal to 30. At week 52, Zepbound reduced the apnea-hypopnea index by 25 to 29 events per hour versus 5 events per hour for placebo, with approximately 43 to 52 percent of treated patients achieving disease resolution (AHI less than 5 or AHI 5 to 14 with no daytime symptoms). This is the first GLP-1 indication for OSA and is a Medicare-eligible indication unlike pure obesity.

Patient-specific findings

  - [Insert current measurements: weight, height, BMI, blood pressure]
  - [Insert relevant lab values with dates: A1c, lipid panel, kidney function]
  - [Insert documentation of comorbidities with ICD-10]
  - [Insert documentation of prior treatment history, including any prior GLP-1 trials, anti-obesity medication trials or lifestyle intervention]

Criteria met per Horizon Blue Cross Blue Shield of New Jersey policy

This request meets the criteria set out in Horizon BCBSNJ Medical Policy 117, Anti-Obesity Pharmacotherapy:

  - OSA diagnosed by polysomnography or home sleep apnea test with AHI greater than or equal to 15 (moderate to severe)
  - BMI greater than or equal to 30
  - Documentation of CPAP intolerance, non-adherence or patient preference (some plans require CPAP failure first; the FDA label does not require it)
  - Sleep medicine specialist involvement if the plan requires it
  - Most recent sleep study report attached

Supporting evidence

The clinical case for Zepbound (tirzepatide) in this indication is supported by the following registration trials and outcomes data:

  - SURMOUNT-OSA Study 1 (Zepbound in OSA patients on PAP therapy)
  - SURMOUNT-OSA Study 2 (Zepbound in OSA patients not on PAP therapy)

Plan-specific note

Horizon BCBS covers Wegovy and Zepbound at BMI greater than or equal to 30 (or 27 with weight-related comorbidity). Six months of lifestyle intervention required. Prime Therapeutics is the PBM for most Horizon commercial lines. Horizon NJ Health (Medicaid managed care) follows the New Jersey FamilyCare PDL, which has historically excluded GLP-1 for obesity indication; route T2D or CV indication for Medicaid members. Verify your specific plan's policy.

Requested action

I am requesting prior authorization for Zepbound (tirzepatide) at the [insert starting dose] starting dose, with planned titration per FDA labeling. I am also requesting that this authorization be granted for a continuous 12-month period subject to documented clinical response, per standard formulary practice.

If additional information is required, please contact me directly at [Prescriber phone] or [Prescriber email]. I am available to discuss this case with your medical director if helpful.

Thank you for your attention to this request.

Sincerely,

[Prescriber full signature]
[Prescriber printed name, credentials]
[Prescriber NPI]
[Practice name and address]

Attachments:
  - Current vital signs and BMI calculation
  - Most recent relevant labs
  - Documentation of comorbidities
  - Documentation of prior treatment trials
  - Sleep study report (if OSA indication)
  - Cardiac history documentation (if CV indication)

Plantillas educativas únicamente. No constituyen asesoramiento legal ni médico. Las cartas deben ser firmadas por el clínico tratante (MD, DO, NP, PA) con autoridad de prescripción. Cada plan cambia los criterios trimestralmente. Verifique con el boletín de política de PA más reciente de su plan antes de enviar. No invente hallazgos clínicos. No altere la firma de un clínico.

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