THEVP - Fees: Thalassemia and Hemoglobinopathy Evaluation

Test Catalog

Test ID: THEVP    
Thalassemia and Hemoglobinopathy Evaluation

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Test Classification Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer's instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR), Investigation Use Only (IUO) product, or a Research Use Only (RUO) product.

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CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

Thalassemia and Hemoglobinopathy Evaluation

82728-Ferritin

83020-Hemoglobin electrophoresis

83021-Hemoglobin A2 and F

 

IEF Confirms

82664 (if appropriate)

 

Hemoglobin, Unstable, Blood

83068 (if appropriate)

 

Hemoglobin Variant by Mass Spectrometry

83789 (if appropriate)

 

Hemoglobin Electrophoresis, Molecular

81257-HBA1/HBA2 (alpha globin 1 and alpha globin 2) (eg, Alpha thalassemia, Hb Bart hydrops fetalis syndrome, HBH disease) gene analysis for common deletions or variant (eg, Southeast Asian, Thai, Filipino, Mediterranean, alpha3.7, alpha4.2, alpha20.5, and Constant Spring) (if appropriate)

81401-HBB (hemoglobin, beta) (eg, sickle cell anemia, hemoglobin C, hemoglobin E), common variants (eg, HbS, HbC, HbE) (if appropriate)

81403-HBB (hemoglobin, beta, beta-globin) (eg, beta thalassemia), duplication/deletion analysis (if appropriate)

81404-HBB (hemoglobin, beta, beta-globin) (eg, thalassemia), full gene sequence (if appropriate)

 

Alpha Globin Gene Analysis

81257 x 2-HBA1/HBA2 (alpha globin 1 and alpha globin 2) (eg, Alpha thalassemia, Hb Bart hydrops fetalis syndrome, HBH disease) gene analysis for common deletions or variant (eg, Southeast Asian, Thai, Filipino, Mediterranean, alpha3.7, alpha4.2, alpha20.5, and Constant Spring) (if appropriate)

 

Hemoglobin S, Screen, Blood

85660 (if appropriate)

 

Hemoglobin F, Red Cell Distribution, Blood

88184 (if appropriate)

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and result codes of this test.

LOINC codes are provided by the performing laboratory.

Test IDTest Order NameOrder LOINC Value
THEVPThalassemia and Hemoglobinopathy EvIn Process

 

Result IDTest Result NameResult LOINC Value
2380Hemoglobin A20572-4
FERRFerritin, S20567-4
2381Hemoglobin A24551-8
583Hemoglobinopathy Interpretation59466-3
2382Hemoglobin F4576-5
2383Variant32017-6
29224Variant 232017-6
29225Variant 332017-6
2101Interpretation49316-3