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Try CasePilotCPT 84450 covers any quantitative AST measurement performed on serum or plasma, regardless of setting (office lab, independent reference lab, hospital outpatient, or inpatient). The test is ordered in three broad contexts.
Liver disease workup and monitoring: AST elevation is a sensitive indicator of hepatocellular injury. The code supports claims for viral hepatitis (acute and chronic), alcoholic liver disease, non-alcoholic steatohepatitis (NASH/NAFLD), cirrhosis, drug-induced hepatotoxicity, and ischemic hepatitis. The AST to ALT ratio adds diagnostic weight: a ratio greater than 2:1 with both enzymes elevated is a classic marker for alcoholic liver disease, while an isolated AST elevation disproportionate to ALT points toward muscle or cardiac sources rather than hepatocellular injury [1].
Pre-treatment baseline and medication monitoring: AST must be documented before and during therapy with hepatotoxic agents including statins, methotrexate, isoniazid, antiepileptics, and antifungals. Serial monitoring of a patient on atorvastatin every 3 to 6 months is a high-volume billing scenario. Each date of service requires a documented clinical rationale tying the test to the specific agent being monitored.
Muscle and cardiac injury: AST is not liver-specific. Myocardial infarction, rhabdomyolysis, and myositis all release AST into circulation. When the clinical context points to muscle rather than liver, the diagnosis code must reflect that source and support the medical necessity of the test.
Scope note: The blood draw is separately reportable by the drawing facility using 36415 (venipuncture, age 3 and older) or 36416 (capillary collection). The laboratory performing the analysis bills 84450; the ordering physician does not.
| Code | Description | When to Use Instead |
|---|---|---|
| 84450 | Transferase; aspartate amino (AST) (SGOT) | Standalone AST when a panel is not ordered or not fully performed |
| 84460 | Transferase; alanine amino (ALT) (SGPT) | Standalone ALT; pair with 84450 when only AST and ALT are ordered, not the full hepatic panel |
| 80076 | Hepatic function panel | All 7 components performed: albumin, total and direct bilirubin, alkaline phosphatase, total protein, ALT, and AST |
| 80053 | Comprehensive metabolic panel | All 14 CMP components performed; subsumes both 84450 and 84460 |
| 80050 | General health panel | All components of 80053 plus CBC and TSH; subsumes 84450 |
The critical differentiator is component count. If a provider orders AST and ALT only, bill 84450 and 84460 separately. If the same provider orders the full hepatic panel and all 7 analytes are resulted, 80076 replaces the individual codes. Billing individual components when the complete panel was performed is just as problematic as unbundling; it undercodes revenue and often reflects a chargemaster configuration gap [4].
Modifier QW: Any facility holding a CLIA Certificate of Waiver must append QW when billing Medicare for 84450 performed on an FDA-approved waived analyzer. Omitting QW on a waived-device claim triggers denial because the payer cannot confirm the facility holds the appropriate CLIA certificate level [5].
Modifier 91: The MUE for 84450 is 1 under normal circumstances [4]. When serial AST monitoring is medically necessary on the same calendar day (e.g., every 6 hours in suspected acetaminophen toxicity), append modifier 91 to each subsequent unit. Modifier 91 is not appropriate when the first result was unsatisfactory due to equipment failure or specimen quality.
Modifiers that do not apply:
Panel bundling [4]:
Hospital outpatient (OPPS): APC Status Indicator = "Conditionally packaged laboratory tests." In an OPPS setting, 84450 may be packaged into the payment for the primary service; it is only paid separately when it is the primary or sole service billed on the claim [2].
Venipuncture billing: The entity that performs the draw bills 36415. If a physician office draws and sends to a reference lab, the office bills 36415 and the reference lab bills 84450. Neither bills the other's component.
Required elements for 84450:
Audit red flags for this code specifically:
For medication monitoring claims: The medical record must identify the specific drug (e.g., "atorvastatin 40 mg"), the duration of therapy, and the clinical rationale for testing frequency. Z79.899 (long-term use of other medication) is the appropriate diagnosis when no hepatic disease has been diagnosed, but it must be supported by documentation of the specific agent [3].
Medicare:
84450 carries Statutory Exclusion status from the MPFS; payment flows through the CLFS with rates updated annually under the PAMA methodology. CMS uses private payer rate data to set CLFS rates; current-year rates require verification at the CMS CLFS page [2].
Most Medicare Administrative Contractors have issued LCDs covering automated chemistry tests. Common covered indications include liver disease monitoring, viral hepatitis management, suspected drug hepatotoxicity, pre-operative evaluation, alcohol use disorder monitoring, and metabolic syndrome assessment [3]. There is no universal frequency limitation for 84450 under Medicare; coverage is determined claim by claim on medical necessity. Some MACs include specific frequency guidance in their LCD articles; the applicable MAC's LCD article should be reviewed for the beneficiary's jurisdiction.
ABN requirements: If 84450 is ordered and there is reason to believe Medicare will not cover it (no qualifying diagnosis, screening context without documented risk factors), issue an Advance Beneficiary Notice of Non-Coverage before the test is performed. File modifier GA (ABN on file) or GY (service meets a statutory exclusion) as appropriate [6].
Commercial payers:
Commercial payer policies generally mirror the panel bundling logic, but prior authorization requirements and frequency limitations vary significantly. Standalone 84450 for medication monitoring is typically covered without prior authorization when accompanied by an appropriate diagnosis code, but documentation requirements mirror Medicare's medical necessity standard.
Medicaid:
Medicaid and managed Medicaid plans may apply state-specific frequency caps or require a qualifying ICD-10-CM code from a defined covered diagnosis list. Verify with the applicable state fee schedule and any contracted managed care plan policies.
Unbundled panel component
Panel NCCI edits fire automatically when 84450 appears on the same claim as 80053 or 80076 [4]. This occurs when laboratory information systems generate charges at the analyte level and the billing system does not roll up to the panel code. Prevention: configure the chargemaster or LIS to suppress individual analyte codes automatically when all panel components are resulted on the same accession. For post-payment denials, appeal is unlikely to succeed unless documentation shows only partial panel components were performed; if that is the case, refile with individual analyte codes and attach the original order.
Missing or incorrect CLIA modifier
Medicare denies 84450 when a CLIA-waived facility omits modifier QW [5]. Prevention: build QW into the charge description master for all analytes performed on waived devices, keyed to the specific analyzer. Corrected claims with QW added timely are generally accepted within the filing limit.
Insufficient medical necessity
The claim passes NCCI but denies at the LCD level because no covered diagnosis appears on the claim or the record lacks a documented clinical indication. Prevention: ensure the ordering provider links 84450 to a specific ICD-10-CM code from the MAC's covered diagnosis list at the time of order. R74.01 (elevation of liver transaminase levels) is acceptable when a specific etiology is not yet confirmed, but the most specific available code should be used when a diagnosis is established [3].
Ordering provider billing the lab analyte
Physician offices that send specimens to reference labs and then also bill 84450 create duplicate claim scenarios. Prevention: implement a billing policy restricting 84450 to the performing laboratory. The ordering physician's reimbursement for clinical review of lab results is captured through the E/M, not a separate lab code.
Same-day repeat without modifier 91
A second 84450 on the same date without modifier 91 triggers the MUE of 1 and is denied [4]. Prevention: append modifier 91 to every subsequent same-day unit and attach documentation of the clinical rationale at claim submission, particularly for inpatient or observation claims where serial monitoring is common.
Scenario 1: Standalone AST and ALT for statin monitoring
A 58-year-old patient on atorvastatin presents for a 3-month follow-up. The provider orders AST and ALT only to screen for statin-induced hepatotoxicity. Both tests are resulted.
Correct coding: 84450 + 84460; diagnosis Z79.899
Why: Only two analytes were ordered and performed. Billing 80076 when only AST and ALT were performed is upcoding; all 7 panel components must be resulted to report the hepatic function panel.
Scenario 2: Full hepatic function panel for hepatitis C monitoring
A 45-year-old with chronic hepatitis C presents for quarterly liver function assessment. The provider orders albumin, total bilirubin, direct bilirubin, alkaline phosphatase, total protein, ALT, and AST. All 7 analytes are resulted.
Correct coding: 80076 only; diagnosis B18.2
Why: All 7 components of the hepatic function panel were performed. Billing 84450 and 84460 alongside 80076 constitutes unbundling and triggers NCCI edit denial [4].
Scenario 3: Serial AST monitoring in acetaminophen toxicity
A hospitalized patient with suspected acetaminophen overdose has an initial AST drawn at 8:00 AM. The hepatologist documents the clinical necessity for serial AST every 6 hours to detect progression to fulminant hepatic failure. A second draw is performed at 2:00 PM.
Correct coding: 84450 at 8:00 AM; 84450-91 at 2:00 PM; diagnosis K71.10
Why: The MUE of 1 applies to the first unit. Modifier 91 supports the second unit by indicating a medically necessary subsequent result rather than a repeated test due to specimen failure. Documentation must explicitly state why same-day serial testing was clinically necessary [4].
Scenario 4: CLIA-waived CMP on point-of-care analyzer
An outpatient clinic holds a CLIA Certificate of Waiver and performs a CMP on an FDA-approved waived analyzer for a patient with type 2 diabetes on metformin. All 14 CMP components, including AST and ALT, are resulted.
Correct coding: 80053-QW; diagnosis E11.9
Why: The QW modifier applies to the panel code because the waived device performed all panel components. Neither 84450 nor 84460 should be billed alongside 80053 on the same date [5].
© Copyright 2026 American Medical Association. All rights reserved.
The CPT® Code 84450 refers to the measurement of aspartate aminotransferase (AST), an enzyme that plays a crucial role in amino acid metabolism. This enzyme, which was formerly known as serum glutamic oxaloacetic transaminase (SGOT), is predominantly located in liver and muscle cells. The presence of AST in the bloodstream is typically low; however, elevated levels can indicate various medical conditions, particularly those related to liver health. Conditions such as liver disease, hepatitis, cirrhosis, and ischemia can lead to increased AST levels. Additionally, muscle damage, including that from myocardial infarction, can also result in elevated AST. The AST test is frequently ordered alongside alanine transferase (ALT) tests, as well as other liver function tests, to provide a comprehensive assessment of liver function and to monitor patients who are undergoing treatment with cholesterol-lowering medications. The procedure involves obtaining a blood sample through venipuncture, which is reported separately, and the serum or plasma is then analyzed using a quantitative enzymatic method to determine the AST levels.
© Copyright 2026 Coding Ahead. All rights reserved.
The aspartate aminotransferase (AST) test, represented by CPT® Code 84450, is indicated for the following conditions:
The procedure for obtaining the aspartate aminotransferase (AST) test involves several key steps:
After the procedure, patients may experience minor discomfort or bruising at the venipuncture site, which typically resolves quickly. There are generally no specific post-procedure care instructions required for the AST test, but patients should be advised to report any unusual symptoms or prolonged discomfort. The results of the AST test are usually available within a few hours to a few days, depending on the laboratory's processing time. Healthcare providers will discuss the results with the patient and may recommend further testing or treatment based on the findings.
| Short Descr | TRANSFERASE (AST) (SGOT) | Medium Descr | TRANSFERASE ASPARTATE AMINO AST SGOT | Long Descr | Transferase; aspartate amino (AST) (SGOT) | 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) | Yes | APC Status Indicator | Conditionally packaged laboratory tests | Type of Service (TOS) | 5 - Diagnostic Laboratory | Berenson-Eggers TOS (BETOS) | T1H - Lab tests - other (non-Medicare fee schedule) | MUE | 1 | CCS Clinical Classification | 233 - Laboratory - Chemistry and Hematology |
| QW | Clia waived test | Q4 | Service for ordering/referring physician qualifies as a service exemption | 90 | Reference (outside) laboratory: when laboratory procedures are performed by a party other than the treating or reporting physician or other qualified health care professional, the procedure may be identified by adding modifier 90 to the usual procedure number. | 59 | Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25. | Q1 | Routine clinical service provided in a clinical research study that is in an approved clinical research study | 91 | Repeat clinical diagnostic laboratory test: in the course of treatment of the patient, it may be necessary to repeat the same laboratory test on the same day to obtain subsequent (multiple) test results. under these circumstances, the laboratory test performed can be identified by its usual procedure number and the addition of modifier 91. note: this modifier may not be used when tests are rerun to confirm initial results; due to testing problems with specimens or equipment; or for any other reason when a normal, one-time, reportable result is all that is required. this modifier may not be used when other code(s) describe a series of test results (eg, glucose tolerance tests, evocative/suppression testing). this modifier may only be used for laboratory test(s) performed more than once on the same day on the same patient. | GA | Waiver of liability statement issued as required by payer policy, individual case | GZ | Item or service expected to be denied as not reasonable and necessary | XS | Separate structure, a service that is distinct because it was performed on a separate organ/structure | 26 | Professional component: certain procedures are a combination of a physician or other qualified health care professional component and a technical component. when the physician or other qualified health care professional component is reported separately, the service may be identified by adding modifier 26 to the usual procedure number. | GW | Service not related to the hospice patient's terminal condition | GV | Attending physician not employed or paid under arrangement by the patient's hospice provider | XU | Unusual non-overlapping service, the use of a service that is distinct because it does not overlap usual components of the main service | 77 | Repeat procedure by another physician or other qualified health care professional: it may be necessary to indicate that a basic procedure or service was repeated by another physician or other qualified health care professional subsequent to the original procedure or service. this circumstance may be reported by adding modifier 77 to the repeated procedure or service. note: this modifier should not be appended to an e/m service. | AY | Item or service furnished to an esrd patient that is not for the treatment of esrd | CA | Procedure payable only in the inpatient setting when performed emergently on an outpatient who expires prior to admission | CC | Procedure code change (use 'cc' when the procedure code submitted was changed either for administrative reasons or because an incorrect code was filed) | GY | Item or service statutorily excluded, does not meet the definition of any medicare benefit or, for non-medicare insurers, is not a contract benefit | KX | Requirements specified in the medical policy have been met | PO | Excepted service provided at an off-campus, outpatient, provider-based department of a hospital | Q0 | Investigational clinical service provided in a clinical research study that is in an approved clinical research study | Q3 | Live kidney donor surgery and related services | Q6 | Service furnished under a fee-for-time compensation arrangement by a substitute physician or by a substitute physical therapist furnishing outpatient physical therapy services in a health professional shortage area, a medically underserved area, or a rural area | QP | Documentation is on file showing that the laboratory test(s) was ordered individually or ordered as a cpt-recognized panel other than automated profile codes 80002-80019, g0058, g0059, and g0060. | Ordering professional consulted a qualified clinical decision support mechanism for this service and the related data was provided to the furnishing professional | X5 | Diagnostic services requested by another clinician: for reporting services by a clinician who furnishes care to the patient only as requested by another clinician or subsequent and related services requested by another clinician; this modifier is reported for patient relationships that may not be adequately captured by the above alternative categories; reporting clinician service examples include but are not limited to, the radiologist's interpretation of an imaging study requested by another clinician |
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| Pre-1990 | Added | Code added. |
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