• Prior Authorization For Perinatal Care

    For Services at: UnityPoint Health - Meriter Center for Perinatal Care
  • What type of prior authorization is being requested?
  • **GHC-SCW Care Management reserves the right to change referral type should the request not match definitions listed above.**

  • Patient Information

  • Patient's Date of Birth *
     / /
  • Referred by Provider

  • Format: (000) 000-0000.
  • Format: (000) 000-0000.
  • REFERRED TO FACILITY/PROVIDER

  • Facility Name: UnityPoint Health - Meriter Center for Perinatal Care [26628]

    Facility Address: 202 S. Park St. 

    City/State/Zip: Madison, WI 53715

    Facility NPI ID#: N/A 

    Facility Phone #: (608) 417-6667

    Facility Fax #: (608) 417-6364

    Facility Tax ID #: 390806367

  • Services Requested and Diagnosis Information

    Supporting clinical documentation must accompany this request.
  • What services are being requested for this prior authorization?*
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  • A referral is not a guarantee of eligibility or benefits under the member’s health plan. Payment will be made in accordance with the member’s plan benefits at the time the service is rendered. Please call Member Services at (800) 605-4327 if you have questions about benefits. Retrospective requests will not be accepted. 

    Prior Authorization and Clinical Information Fax Number: (608) 831-6099

  • Where should GHC-SCW members go for scans/services?

    Questions? Please call GHC Care Management at (608)831-6099
  • Where GHC-SCW members should go for scans/services:

  • Service Location
     Amniotic Fluid   Index (AFI)

    GHC-SCW Radiology

     20-week Anomaly
     Scan/Anatomy Scan
     (Level I Ultrasound)
    GHC-SCW Radiology EXCEPT for patients with a pre-pregnancy BMI ≥ 30 (with no rounding) or risk factors in List 1 below
     Targeted Ultrasound* Unity Point Health - Meriter Center for Perinatal Care (one follow-up allowed to complete the targeted exam if anatomic assessment was not complete). *See List 1 below for covered indications
     Growth Scan /   Follow- Up Scan GHC-SCW Radiology. EXCEPT for patients who have transferred care to MFM, or patients who have abnormal fetal ultrasound findings, then follow-up should be at UPH - Meriter Center for Perinatal Care
     Biophysical Profile
     (BPP)
    GHC-SCW Radiology
     Cervical Length GHC-SCW Radiology. EXCEPT for diagnoses of incompetent cervix or cerclage, which should be at UPH - Meriter Center for Perinatal Care
     Dating Ultrasound GHC-SCW Medical Imaging
     Non-Stress Tests   (NST) Ok to take place at the office of the Primary OB provider
     12- to 14-Week   Ultrasound GHC-SCW Radiology (including dichorionic twin gestation). EXCEPT twins with unknown chronicity, monochorionic twin pregnancies, abnormal NIPS results, previous abnormal ultrasound findings in current pregnancy, then should be at Unity Point Health - Meriter Center for Perinatal Care. With full transfer of care to MFM, this can be at GHC or MFM per MFM provider recommendation
     NT ultrasound NT ultrasound has been replaced by NIPS. NT ultrasound is not authorized. EXCEPT for situations of twin demise, repeated non-reportable NIPS testing, or visibly abnormal nuchal area; in those cases, NT ultrasound as part of the first trimester screen should be done at UPH - Meriter Center for Perinatal Care, with Meriter genetic counseling
     Genetic Counseling GHC-SCW for prenatal genetic counseling (e.g. NIPS, abnormal quad, family history, carrier screening). Meriter genetic counselors when member has transferred care to MFM, with abnormal ultrasound findings, or in conjunction with CVS or amniocentesis. UW genetic counselors for oncology indications.
     NIPS/ NIPT GHC-SCW labs. Genetic counseling is required prior to testing
     Carrier screening GHC-SCW labs. Expanded carrier screening is available and requires pre-test genetic counseling at GHC, refer patient to GHC genetic counselor for coordination. If only cystic fibrosis and spinal muscular carrier screening desired, fax orders to GHC labs (no prior auth required).
    Genetic Testing GHC-SCW Labs. Prior auth is required for all genetic testing other than CF, SMA, NIPS and any other carrier screening not ordered by the GHC genetic counselor
     Genetic Testing on   Fetus UnityPoint Health - Meriter Center for Perinatal Care for CVS and amniocentesis. Prior auth is not needed for CVS or amnio samples for karyotype, microarray, FISH prenatal panel or in cases of echogenic bowel cystic fibrosis mutation panel. Prior auth is needed for any other genetic testing from fetal samples. Parental blood samples can be collected same day as procedure at MFM clinic to accompany fetal samples as needed.
     Non-Genetic Lab Tests If patient has GHC-SCW Primary Care Provider (PCP): labs at GHC-SCW. If patient has UW or Meriter primary care provider: non-genetic labs can be at the PCP office, OB office or at GHC-SCW labs. For full transfer of care to MFM: routine labs (not genetic testing) can be done at MFM clinic. If a lab is needed for same day care (e.g. antibody screen for a procedure happening that day): labs can be done at the specialist’s office that day, regardless of PCP.
     Diabetes Management Pregnant patients: Unity Point Health - Meriter center for perinatal care for pregnant patients with type 1, pre-existing type 2, pre-diabetes, gestational diabetes and preconception consult for type 1 or 2 diabetes. If patient has GHC-SCW PCP, GHC-SCW nutrition can see patients with gestational diabetes for nutrition consults and meter training, but these are also allowed at Meriter.
  • Table 2: Indications for a Targeted Ultrasound at Perinatal Center

    Questions? Please call GHC Care Management at (608)831-6099
  • List 1: Indications for a Targeted Ultrasound at Perinatal Center

    1. Previous fetus or child with a congenital, genetic, or chromosomal abnormality, with potential for prenatal ultrasound findings
    2. Known or suspected fetal anomaly or known or suspected fetal growth restriction in the current pregnancy
    3. Fetus at increased risk for a congenital anomaly, genetic, or chromosomal condition, such as the following:
      a. Maternal pregestational diabetes or gestational diabetes diagnosed before 24 weeks’ gestation
      b. Pregnancy conceived via in vitro fertilization (IVF)
      c. Pre-pregnancy maternal body mass index of 30 kg/m2 or higher
      d. Multiple gestations
      e. Abnormal maternal serum analytes, abnormal or indeterminate NIPS/cell free DNA results
      f. Teratogen exposure
      g. First-trimester cystic hygroma or nuchal translucency measurement of 3.0 mm or greater
      h. Parental carrier of a chromosomal or genetic abnormality with potential for prenatal ultrasound findings
      i. Maternal age of 35 years or older at delivery without normal NIPS results (Note that if a patient has normal NIPS, GHC-SCW does not consider targeted ultrasound medically necessary for the indication of advanced maternal age)
      j. Positive screening test results for aneuploidy
      k. Aneuploidy marker noted on an ultrasound examination (excluding isolated finding of choroid plexus cyst, intracardiac echogenic focus or pyelectasis)
      l. First-trimester cystic hygroma or nuchal translucency measurement of 3.0 mm or greater
      m. Family history of 1st or 2nd degree relative to the fetus of congenital anomaly when both an increased risk to the fetus and potential for prenatal ultrasound detection are present (e.g. open neural tube defect, cleft lip/palate, congenital heart defect)
    4. Other conditions affecting the fetus, including the following:
      a. Congenital infections with known teratogenic effects
      b. Maternal drug use
      c. Alloimmunization
      d. Oligohydramnios / Polyhydramnios
    5. Suspected placenta accreta spectrum (PAS) or risk factors for PAS such as placenta previa in the third trimester or placenta overlying a prior cesarean scar site
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