Hep virus ab igm

CPT codes are provided only as guidance to assist clients with billing. CPT coding is the sole responsibility of the billing party. Click here for your pricing. Components Components of test. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases Other names that describe the test. First Name. Last Name. Client ID. Leave this field blank. ARUP Consult. Increasing levels of anti-HAV IgM are detectable approximately three weeks after challenge with the highest titer after four to six weeks later.

Within six months of infection, the IgM concentration drops to undetectable levels. You save. Rating Required Select Rating 1 star worst 2 stars 3 stars average 4 stars 5 stars best.

Name Required. Email Required. Review Subject Required. Comments Required. Search Cancel. Home Test Catalog Overview. Test Catalog. Order This Test. Useful For Suggests clinical disorders or settings where the test may be helpful. Viral Hepatitis Serologic Profiles. Method Name A short description of the method used to perform the test. Reporting Name Lists a shorter or abbreviated version of the Published Name for a test. Aliases Lists additional common names for a test, as an aid in searching.

Specimen Type Describes the specimen type validated for testing. Date of draw is required. Specimen Required Defines the optimal specimen required to perform the test and the preferred volume to complete testing. Specimen Minimum Volume Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory.

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected. Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included.

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test. Reference Values Describes reference intervals and additional information for interpretation of test results.

May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this. Interpretation Provides information to assist in interpretation of the test results. Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances. Clinical Reference Recommendations for in-depth reading of a clinical nature.

Rev ; 3. Method Description Describes how the test is performed and provides a method-specific reference. PDF Report Indicates whether the report includes an additional document with charts, images or other enriched information.