CPT code 85610 refers to the Prothrombin Time (PT) test, a clinical laboratory test that measures how long it takes blood plasma to clot. In practice, a sample of the patient's plasma is mixed with reagents (such as calcium and tissue factor) and the clotting time is recorded.
The PT/INR primarily evaluates the extrinsic (tissue factor-dependent) and common coagulation pathways. It is commonly used to assess anticoagulation therapy (especially warfarin), which affects vitamin K-dependent clotting factors.
Importantly, when a PT test is performed, the International Normalized Ratio (INR) is a calculated value and is not separately billable; it is considered part of the PT test itself (i.e., you should not code an INR separately from CPT 85610).
Medical necessity for CPT 85610 must be supported by an appropriate diagnosis code on the claim, or insurers will deny coverage. Common indications include:
Medicare coverage is strictly governed by National Coverage Determination (NCD) 190.17. Key rules include:
Medicaid: Most states follow Medicare's medical necessity principles. For example, New York Medicaid lists 85610 as covered when medically necessary. Reimbursement is often lower (e.g., $3-$5).
Commercial: Plans like UnitedHealthcare and Blue Cross typically cover PT/INR for the same indications (AFib, liver disease, etc.). However, Medicare Advantage plans will strictly follow the NCD rules. Always verify specific payer policies regarding pre-op testing.
To withstand audits and ensure payment:
Coding differs based on the setting:
INR vs PT: INR is a calculation included in 85610. Never bill a separate code for INR.
PTT (85730): Can be billed with 85610 if medically necessary (e.g., heparin + warfarin). There is no NCCI edit bundling these two.
Specimen Collection:
The 99211 Issue: CMS considers the work of drawing blood and running the test to be included in the lab code. Do not bill 99211 for a simple INR check where no separate evaluation occurs. A CMS compliance officer stated that "all work performed by the nurse is part of the blood draw and is encompassed in that code."
| Modifier | Usage Description |
|---|---|
| QW | CLIA Waived Test. Required for Medicare when using waived devices (fingerstick). |
| 91 | Repeat Test. Use if the test is repeated on the same day for medical necessity (e.g., 8 AM high INR, repeat at 4 PM). Do not use for lab errors. |
| 25 | Separate E/M. Append to E/M code (e.g., 99213-25) if a significant visit occurred alongside the lab. While 85610 has no global period, many payers require this modifier to prevent bundling. |
| 26/TC | Do Not Use. CPT 85610 is not split into professional/technical components. Physician review is part of the E/M. |
CPT 85610 has no global period and is paid under the Clinical Laboratory Fee Schedule (CLFS), not the Physician Fee Schedule.
Scenario 1: Routine Warfarin Clinic (Office)
Patient on warfarin for AFib comes in. Nurse performs fingerstick INR (2.5, stable). Physician briefly reviews and says "continue dose."
Bill: 85610-QW.
Do NOT Bill: 99211 (bundled) or 36416.
Diagnosis: Z79.01 + I48.91.
Scenario 2: High INR with Evaluation
Patient INR is 4.5; reports bleeding gums. Physician evaluates, examines, holds dose, and counsels (15 mins).
Bill: 85610-QW AND 99213-25.
The E/M is justified by the significant separate evaluation and management of the complication.
Scenario 3: Repeat Testing Same Day
INR is 9.0 at 8 AM. Vitamin K given. Repeat test ordered at 1 PM shows INR 5.0.
Bill:
Line 1: 85610-QW
Line 2: 85610-QW-91
Modifier 91 indicates a medically necessary repeat, distinct from a duplicate error.
Scenario 4: Pre-Operative Clearance
Healthy 60-year-old for hernia repair. No risk factors. Surgeon orders PT/INR.
Coding: Medicare will likely deny this as not medically necessary. An ABN should be signed, and the claim billed with Modifier GA to transfer liability to the patient.
flowchart TD
A[PT/INR Test Ordered] --> B{Where is the test performed?}
B -->|Office/Clinic POC device| C{Is the device CLIA-waived?}
B -->|Reference laboratory| D[Bill 85610 without QW]
B -->|Patient home self-test| E[Do not use 85610 - Use G0250/93793]
C -->|Yes| F[Bill 85610-QW]
C -->|No| G[Bill 85610 - Ensure moderate/high complexity CLIA certificate]
© Copyright 2026 American Medical Association. All rights reserved.
Prothrombin time (PT) is a laboratory test that measures the duration it takes for blood to clot. This test evaluates the functionality of prothrombin, also known as factor II, which is a crucial protein produced by the liver. The synthesis of prothrombin is dependent on adequate levels of vitamin K, which is essential for the liver to generate sufficient amounts of this clotting factor. The prothrombin time test serves multiple purposes in clinical practice. It is primarily utilized to identify the underlying causes of abnormal bleeding or bruising in patients. Additionally, it is instrumental in monitoring the effectiveness of anticoagulant therapy, particularly for patients taking blood-thinning medications such as warfarin (Coumadin). Furthermore, the test can help assess the levels of various blood-clotting factors, specifically factors I, II, V, VII, and X, as well as evaluate vitamin K levels and liver function. The procedure for measuring prothrombin time involves the use of electromagnetic mechanical clot detection, which accurately determines the clotting time of the blood sample. In cases where the prothrombin time is found to be elevated and the patient is not currently on anticoagulant therapy, a follow-up test known as a prothrombin time mixing study may be indicated. This secondary test involves mixing the patient's plasma with normal plasma in a 1:1 ratio, incubating the mixture, and measuring the clotting time again. The results of this mixing study can provide further insights into whether the patient has an inhibitor, such as lupus anticoagulant, or a coagulation factor deficiency, guiding appropriate clinical management.
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