What is the CPT code for a PKU?

What is the CPT code for a PKU?

Also the addition of 83516 as the CPT code for this test.

What is the CPT code for newborn screening?

81406
CPT Codes: 81406 Fees: See Laboratory Fee schedule.

What is newborn PKU testing?

A phenylketonuria (PKU) test is done to check whether a newborn baby has the enzyme needed to use phenylalanine in his or her body. Phenylalanine is an amino acid that is needed for normal growth and development.

What is CPT S3620?

HCPCS code S3620 for Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by the state for inclusion in this panel (e.g., galactose; hemoglobin, electrophoresis; hydroxyprogesterone, 17-D; phenylanine (PKU); and thyroxine, total) as maintained by CMS falls under Miscellaneous …

What does CPT code 83516 mean?

Immunoassay for analyte other
83516 – CPT® Code in category: Immunoassay for analyte other than infectious agent antibody or infectious agent antigen.

What is procedure code 99393?

99393 – CPT® Code in category: Periodic comprehensive preventive medicine reevaluation and management of an individual including an age and gender appropriate history, examination, counseling/anticipatory guidance/risk factor reduction interventions, and the ordering of laboratory/diagnostic procedures, established …

What is procedure code 99480?

Codes 99478-99480 each are described as, “Subsequent intensive care, per day, for the evaluation and management of the recovering low or very low birth weight infant” with the code selected based upon the present body weight of the infant as below.

How do you test for PKU?

A PKU test is done a day or two after your baby’s birth. The test is done after your baby is 24 hours old and after your baby has ingested some protein in the diet to ensure accurate results. A nurse or lab technician collects a few drops of blood from your baby’s heel or the bend in your baby’s arm.

What is a positive PKU test?

Ask the healthcare provider what the test results mean for your child. The test screens for blood levels of phenylalanine. Normal levels of phenylalanine in the blood are less than 2 milligrams per deciliter (mg/dL). More than 4 mg/dL of phenylalanine in the blood is considered high and may mean your child has PKU.

What is procedure code 81479?

According to the AMA, code 81479, unlisted molecular pathology procedure, should only be used for a unique. procedure that is not adequately addressed by any other CPT code. It should be reported only once per patient, per. specimen and date of service to identify the services provided.

What is procedure code 81420?

81420: Fetal chromosomal aneuploidy (e.g., trisomy 21, monosomy X) genomic sequence analysis panel, circulating cell-free fetal DNA in maternal blood, must include analysis of chromosomes 13, 18, and 21.

When to take a blood test for PKU?

Specimen Requirements. A blood specimen must be collected for screening when the baby is between 24 and 48 hours old. If the specimen is collected from an infant before 24 hours of age, a second specimen must be collected no later than the 14th day of life. Collect specimen on “Minnesota Department of Health PKU Filter Paper” as follows: 1.

What does PKU stand for in medical terms?

PKU stands for phenylketonuria, a rare disorder that prevents the body from properly breaking down a substance called phenylalanine (Phe). Phe is part of proteins that are found in many foods and in an artificial sweetener called aspartame.

What to do if your baby has PKU?

If your baby was diagnosed with PKU, he or she can drink formula that does not contain Phe. If you would like to breastfeed, talk your health care provider. Breast milk does contain Phe, but your baby may be able to have a limited amount, supplemented by the Phe-free formula.

When to take blood test for newborn metabolic screening?

The blood is tested for multiple disorders unless the parent refuses in writing. A blood specimen must be collected for screening when the baby is between 24 and 48 hours old. If the specimen is collected from an infant before 24 hours of age, a second specimen must be collected no later than the 14th day of life. 1.