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The CPT® Code 80081 refers to an obstetric panel that encompasses a series of laboratory tests performed on maternal blood, typically prior to or during pregnancy. This panel is essential for identifying and monitoring various medical conditions that could potentially impact the health of both the mother and the developing fetus. The tests included in this panel are designed to screen for infections, anemia, coagulopathy, and immune disorders, which are critical for ensuring a healthy pregnancy outcome. The panel specifically includes a complete blood count (CBC) with either an automated differential white blood cell (WBC) count or a manual differential WBC count. A CBC provides vital information about the blood's components, including hemoglobin (Hgb), hematocrit (Hct), red blood cell (RBC) count, WBC count, and platelet count. Hematocrit measures the proportion of blood volume occupied by red blood cells, while the RBC count indicates the number of erythrocytes present in a specified volume of blood. The WBC count reflects the number of white blood cells, which are crucial for the immune response, and includes five distinct types: neutrophils, eosinophils, basophils, monocytes, and lymphocytes, each counted separately in a differential analysis. The platelet count assesses the number of thrombocytes, which play a key role in blood clotting. In addition to the CBC, the obstetric panel mandates the inclusion of several specific tests: Hepatitis B surface antigen (HBsAg), which screens for Hepatitis B infection; human immunodeficiency virus-1 (HIV-1) antigen along with antibodies for both HIV-1 and HIV-2; rubella antibody testing; a qualitative syphilis test for non-treponemal antibodies (such as VDRL, RPR, or ART); an antibody screen for red blood cells; and blood typing for both ABO and Rh D factors. Collectively, these tests provide comprehensive insights into the maternal health status and help guide appropriate clinical management during pregnancy.
© Copyright 2025 Coding Ahead. All rights reserved.
The obstetric panel (CPT® Code 80081) is indicated for use in pregnant women to screen for various medical conditions that may affect maternal and fetal health. The specific indications for performing this panel include:
The procedure for conducting the obstetric panel (CPT® Code 80081) involves several key steps, each critical for obtaining accurate laboratory results. The first step is the collection of maternal blood, which is typically drawn from a vein in the arm using a sterile technique to ensure sample integrity. Following blood collection, the sample is processed in a laboratory setting. The complete blood count (CBC) is performed, which includes measuring various components of the blood. This involves automated analysis to determine hemoglobin (Hgb) levels, hematocrit (Hct) percentages, red blood cell (RBC) counts, white blood cell (WBC) counts, and platelet counts. If an automated differential WBC count is not performed, a manual differential count may be conducted to categorize the five types of white blood cells. In addition to the CBC, the laboratory will conduct specific tests for Hepatitis B surface antigen (HBsAg) to screen for Hepatitis B infection, and for HIV-1 antigen along with antibodies for both HIV-1 and HIV-2 to assess the risk of HIV transmission. The rubella antibody test is performed to determine immunity to rubella, which is crucial for preventing congenital rubella syndrome. A qualitative syphilis test is also included to detect non-treponemal antibodies, which can indicate syphilis infection. Furthermore, an antibody screen for red blood cells is conducted to identify any potential incompatibilities between maternal and fetal blood types. Finally, blood typing for both ABO and Rh D factors is performed to ensure proper management of any blood type-related issues during pregnancy. Each of these steps is essential for providing a comprehensive assessment of the mother's health and ensuring appropriate prenatal care.
After the obstetric panel tests are completed, the results are typically reviewed by a healthcare provider. Depending on the findings, further action may be required. For instance, if any infections are detected, appropriate treatment or monitoring may be initiated to protect both the mother and the fetus. If anemia is identified, dietary changes or supplementation may be recommended. The healthcare provider will discuss the results with the patient, addressing any concerns and outlining the next steps in prenatal care. It is important for the patient to follow up with their healthcare provider to ensure that any identified issues are managed effectively throughout the pregnancy. Additionally, routine follow-up testing may be scheduled as part of ongoing prenatal care to monitor the health of both the mother and the developing baby.
Short Descr | OBSTETRIC PANEL INC HIV TSTG | Medium Descr | OBSTETRIC PANEL INCLUDES HIV TESTING | Long Descr | Obstetric panel (includes HIV testing) This panel must include the following: Blood count, complete (CBC), and automated differential WBC count (85025 or 85027 and 85004) OR Blood count, complete (CBC), automated (85027) and appropriate manual differential WBC count (85007 or 85009) Hepatitis B surface antigen (HBsAg) (87340) HIV-1 antigen(s), with HIV-1 and HIV-2 antibodies, single result (87389) Antibody, rubella (86762) Syphilis test, non-treponemal antibody; qualitative (eg, VDRL, RPR, ART) (86592) Antibody screen, RBC, each serum technique (86850) Blood typing, ABO (86900) AND Blood typing, Rh (D) (86901) | Status Code | Statutory Exclusion (from MPFS, may be paid under other methodologies) | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 9 - Not Applicable | Multiple Procedures (51) | 9 - Concept does not apply. | Bilateral Surgery (50) | 9 - Concept does not apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 9 - Concept does not apply. | Co-Surgeons (62) | 9 - Concept does not apply. | Team Surgery (66) | 9 - Concept does not apply. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | CLIA Waived (QW) | No | APC Status Indicator | Conditionally packaged laboratory tests | Type of Service (TOS) | 5 - Diagnostic Laboratory | Berenson-Eggers TOS (BETOS) | T1B - Lab tests - automated general profiles | MUE | 1 |
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2025-01-01 | Changed | Short and Medium Descriptions changed. |
2016-01-01 | Added | Added |