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Infant Formula Recall Retirada del mercado de fórmula infantil

ALERT: ByHeart Recalls Whole Nutrition Infant Formula. Read more

AVISO IMPORTANTE: ByHeart retira del mercado su fórmula infantil Whole Nutrition. Aprender más

Transportation Update Actualización de transporte

Starting December 15, 2025, SafeRide Health will become the new provider for all member rides to doctor appointments and pharmacy visits. After this date, Texas Children’s Health Plan will no longer use MTM for Non Emergency Medical Transportation (NEMT) services.

Learn more here

For other questions, please call Member Services at the number on the back of your member ID card.

A partir del 15 de diciembre de 2025, SafeRide Health será el nuevo proveedor para todos los viajes de los miembros a citas médicas y visitas a la farmacia. Después de esta fecha, Texas Children’s Health Plan ya no usará MTM para los servicios de Transporte Médico No Urgente (NEMT).

Obtenga más información AQUI

Si tiene otras preguntas, llame a Servicios para Miembros al número que aparece en la parte posterior de su tarjeta de identificación del miembro.

Texas Medicaid Prior Authorization Criteria for Emapalumab-Lzsg (Gamifant)

Date: October 8, 2025

Attention: All Providers

Effective date: October 1, 2025

Call to action: Effective for dates of service on or after October 1, 2025, providers must meet updated prior authorization requirements for emapalumab-lzsg (Gamifant) (procedure code J9210).

Emapalumab-lzsg (Gamifant) is an interferon gamma (IFNy)-blocking antibody that is indicated for the treatment of the following:

  • Primary hemophagocytic lymphohistiocytosis (HLH) in patients who have refractory, recurrent, or progressive disease or intolerance of conventional HLH therapy
  • HLH or macrophage activation syndrome (MAS) in patients who have known or suspected Still’s disease (including systemic juvenile idiopathic arthritis [sJIA]) and an inadequate response to or intolerance of glucocorticoids or recurrent MAS

Authorization Requirements

Texas Medicaid will approve prior authorization requests for up to six months of initial therapy if the patient has one of the diagnoses listed below:

  • Primary HLH (diagnosis code D761), diagnosed based on one of the following:
    • Genetic mutation of the gene known to cause primary HLH (e.g., PRF1, UNC13D, STX11, or STXBP2) or a family history consistent with primary HLH
    • Confirmation of at least five of the following criteria:
      • Fever ≥ 101.3 °F
      • Splenomegaly
      • Cytopenia defined by at least two of the following: Hemoglobin < 9 g/dl, platelet count < 100 x 109 /L, or neutrophils < 1 x 109
      • Fasting triglycerides > 265 mg/dl or fibrinogen ≤ 1.5 g/L
      • Hemophagocytosis in the liver, bone marrow, spleen, or lymph node
      • Low or absent natural killer (NK) cell activity
      • Serum ferritin concentration ≥ 500 mg/L
      • High plasma concentration of soluble CD25 (i.e., soluble interleukin-2 receptor) > 2,400 U/mL
  • HLH or MAS in Still’s disease, diagnosed based on the following:
    • A diagnosis of HLH along with a confirmed or suspected diagnosis of systemic juvenile idiopathic arthritis or adult onset of Still’s disease
    • A diagnosis of active MAS with ferritin level greater than 684 ng/mL and any of two of the four laboratory criteria listed below:
      • Platelet count ≤ 181 x 109/L
      • Aspartate aminotransferase (AST) > 48 U/L
      • Triglycerides > 156 mg/dL
      • Fibrinogen levels ≤ 360 mg/dL
  • An inadequate response to high-dose IV glucocorticoids
  • No active infections caused by specific pathogens favored by IFNy neutralizations (such as mycobacteria and Histoplasma capsulatum).

Providers must submit prior authorization requests for procedure code J9210 with one or more of the following diagnosis codes:

Diagnosis Codes
D761M061M0820M08211M08212M08219M08221
M08222M08229M08231M08232M08239M08241M08242
M08249M08251M08252M08259M08261M08262M08269
M08271M08272M08279M0828M0829  

 

Renewal or Continuation Therapy

Prior authorization requests for renewal or continuation therapy with emapalumab-lzsg (Gamifant) must include documentation that the patient:

  • Continues to meet the initial approval criteria.
  • Continues to require emapalumab-lzsg (Gamifant) as HLA treatment.

Texas Medicaid will not approve prior authorization for renewal or continuation therapy after the initiation of hematopoietic stem cell transplant (HSCT) or if the treatment for HLH or MAS becomes unnecessary.

Next step for providers: Providers should share this communication with their staff.

If you have any questions, please email Provider Relations at providerrelations@texaschildrens.org

For access to all provider alerts: www.texaschildrenshealthplan.org/provideralerts.