SafeRide Health (SRH) is the new provider for all NEMT rides to doctor appointments and pharmacy visits.
Depending on your needs, rides may include wheelchair-lift-equipped vehicles, stretcher vans, minivans, or ambulatory vans. Please let SRH know what type of ride you need when scheduling.
SafeRide Health (SRH) es el nuevo proveedor de todos los servicios de transporte médico que no son de emergencia (NEMT, por sus siglas en inglés) hacia consultas médicas y farmacias.
Según tus necesidades, los servicios de transporte pueden incluir vehículos con elevador para sillas de ruedas, camionetas con camilla, minivans o camionetas ambulatorias. Por favor, informa a SRH qué tipo de transporte necesitas al programar tu traslado.
Effective date for benefit: April 1, 2026 Effective date for Prior Authorization: May 1, 2026
Call to action: Texas Children’s Health Plan (TCHP) would like to inform providers that Texas Health and Human Services Commission (HHSC) will add Zevaskyn (procedure code J3389) as a benefit for Medicaid and CHIP, effective April 1, 2026, and will require prior authorization for those programs, effective May 1, 2026.
Zevaskyn (prademagene zamikeracel) is an autologous cell sheet-based gene therapy indicated for the treatment of wounds in adult and pediatric patients with recessive dystrophic epidermolysis bullosa (RDEB).
Authorization requirements
HHSC requires prior authorization for Zevaskyn (prademagene zamikeracel).
The prior authorization request for this surgical topical application may be approved for 12 months for patients who meet the following requirements:
Patient is at least 6 years and older.
Patient has a confirmed diagnosis of RDEB (diagnosis code: Q81.2), confirmed by biopsy and genetic testing detecting biallelic mutation(s) in the COL7A1 gene.
Patient has chronic cutaneous stage 2 wound(s) adequate for treatment which meets the following:
Cutaneous wound open/present for at least 6 months.
Stage 2 wounds with an area of greater than or equal to 20 cm2.
Wound has not previously been treated with Zevaskyn.
Patient’s target wound(s) is not infected.
Patient’s wound area shows no current evidence or history of squamous cell carcinoma.
Patient does not have severe hypersensitivity (i.e., anaphylaxis) to vancomycin or amikacin.
Authorization will not be approved for administration to wounds previously treated with Zevaskyn.
For continued therapy, patient must meet the following requirements:
Re-authorization for the same wound is not permitted. Patient must meet the initial approval criteria if the request is for previously untreated or newly developed wounds.
Absence of unacceptable toxicity from Zevaskyn (e.g., severe hypersensitivity reactions and development of new malignancies).
Patient shows positive response to treatment as defined by improvement (healing) of treated wound sites and/or reduction in skin infections.
Next step for providers: Providers should share this communication with their staff.
