Web33 rows · Nuchal Translucency: mm: 12146-7: 017500: First Trimester Screen w/NT: 017512: Nuchal Translucency MoM: 49035-9: 017500: First Trimester Screen w/NT: 018281: NT Twin B: mm: 12146-7: 017500: First Trimester Screen w/NT: 018282: NT … for trisomy 18 by fetal nuchal translucency and maternal serum free beta-hCG and … WebFirst-trimester screening test for trisomy 21 (Down syndrome), trisomy 18, and open neural tube defects. Risks determined using a combination of first and second-trimester serum markers, with or without first-trimester nuchal translucency measurement. Risks provided after testing is completed for second-trimester specimen, Maternal Serum Screening, …
Nuchal translucency scan FMF Certification - Fetal …
WebApr 11, 2024 · 76813 - CPT® Code in category: Ultrasound, pregnant uterus, real time with image documentation, first trimester fetal nuchal translucency measurement, transabdominal or transvaginal approach CPT Code information is available to subscribers and includes the CPT code number, short description, long description, … WebAccording to Cigna’s medical policy document, “Sequencing-based non-invasive prenatal testing (NIPT) (CPT® codes 81420, 81507) to screen for fetal trisomy 13, 18 and 21 is … table with green screen
76801 and 76813 Medical Billing and Coding Forum - AAPC
WebOBUS-2.13 Fetal Nuchal Translucency (NT or Nuchal Fold Scan) 12 ©2009 MedSolutions, Inc. RETURN Page 7 of 56 Obstetrical Ultrasound Medical Necessity Criteria ... pregnancy (report one of the following CPT codes: 76801 [plus 76802 if more than one fetus] if a complete ultrasound has not yet been performed, 76815 or 76816 if a ... Webdone routinely with an ultrasound for nuchal translucency (CPT® 76813/ CPT® 76814). In cases where there is either a maternal and/or fetal indication, then the CPT® 76801 code can indeed be billed along with the nuchal translucency screening (CPT® 76813/ CPT® 76814) (SMFM, 2024). Fetal Anatomic Scan (CPT® 76805). WebNov 17, 2024 · First-trimester nuchal translucency measurement of 3.0 mm or greater 17; Fetus at increased risk for a genetic or chromosomal abnormality, such as the following: Parental carrier of a chromosomal or genetic abnormality 1, 2; Maternal age of 35 years or older at delivery 1, 2; Positive screening test results for aneuploidy 1, 2; table with heated blanket