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Quick Reference: CPT 85610

  • Definition: Prothrombin Time (PT) test. Includes the calculated INR result. Do not bill INR separately.
  • Coverage: Covered for warfarin monitoring, bleeding disorders, and liver disease. Routine pre-op screening is generally not covered without risk factors.
  • Medicare Rule: For warfarin, code Z79.01 as primary, followed by the condition (e.g., Atrial Fibrillation). Stable patients are limited to testing every 2-3 weeks.
  • Point-of-Care: Must bill as 85610-QW if using a CLIA-waived device (e.g., fingerstick) in the office.
  • Reimbursement: Approx. $4.29 (Medicare National Avg), paid under the Clinical Lab Fee Schedule.

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).

Common Indications for PT/INR and Associated ICD-10 Codes

Medical necessity for CPT 85610 must be supported by an appropriate diagnosis code on the claim, or insurers will deny coverage. Common indications include:

  • Monitoring of Anticoagulation: For patients on warfarin (Coumadin), Medicare instructs providers to use Z79.01 (Long term current use of anticoagulants) as the primary diagnosis. This should be paired with the underlying condition code, such as:
    • Atrial fibrillation (e.g., I48.91, I48.20).
    • History of venous thromboembolism/DVT (e.g., Z86.711, Z86.718).
    • Mechanical heart valve (Z95.2).
  • Bleeding or Clotting Disorders: For patients with abnormal bruising, bleeding, or thrombosis. Codes include:
    • Coagulation defect, unspecified (D68.9).
    • Disseminated intravascular coagulation (D65).
    • Abnormal coagulation profile (R79.1).
  • Liver Disease and Vitamin K Deficiency: Since clotting factors are produced in the liver and are Vitamin K dependent, indicated codes include:
    • Unspecified cirrhosis of liver (K74.60).
    • Vitamin K deficiency (E56.1).
  • Pre-Operative Assessment: Medicare only covers pre-op PT testing if specific risk factors exist (e.g., history of bleeding). Routine screening using Z01.812 is generally not covered without an additional risk diagnosis.

Medicare Coverage (NCD 190.17) and Frequency Limitations

Medicare coverage is strictly governed by National Coverage Determination (NCD) 190.17. Key rules include:

  • Frequency Limits: For patients on stable warfarin therapy, testing is typically covered every 2-3 weeks. More frequent testing (e.g., weekly) requires documentation of instability or dose changes.
  • ESRD Patients: Testing more often than weekly for ESRD patients on heparin requires documentation of necessity beyond ESRD alone.
  • Acute Evaluation: If an initial test is normal, repeat testing is not covered unless the clinical status changes.
  • Non-Covered: Medicare does not pay for routine screening or home self-testing under CPT 85610 (home testing uses G0250/93793).

Medicaid and Commercial Payer Considerations

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.

Documentation and Billing Requirements

To withstand audits and ensure payment:

  • Order and Signature: There must be a signed physician order for the test.
  • Diagnosis Linking: The claim diagnosis must match the documented indication. Do not use a "routine exam" code for a diagnostic test.
  • CLIA Number: Claims must include the CLIA number. For waived tests, this allows payment for 85610-QW.
  • ABN: For Original Medicare, obtain an Advance Beneficiary Notice (ABN) if you suspect the test (e.g., routine pre-op) will be denied. Use modifier GA if an ABN is on file.
  • Bill the Correct Entity: Only the entity performing the test bills 85610. If you draw blood and send it to LabCorp, LabCorp bills 85610; you bill only the draw fee (36415).

Point-of-Care (POC) Testing vs. Laboratory Testing

Coding differs based on the setting:

  • CLIA Waived (Office/Clinic): If using a fingerstick device (e.g., CoaguChek), you must append Modifier QW (85610-QW). This tells Medicare it was a waived test.
  • Reagents/Supplies: You cannot bill separately for test strips or cartridges; these costs are included in the 85610 reimbursement.
  • Home Self-Testing: Do not use 85610 for patients testing themselves at home. Use codes G0250 (review) or 93793 (management) instead.

Related Tests and Bundling Considerations

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:

  • Venous (36415): Billable if drawing venous blood to send out.
  • Capillary (36416): Generally bundled into 85610 by Medicare and not separately payable.

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."

Proper Use of Modifiers

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.

Reimbursement and RVU Benchmarks

CPT 85610 has no global period and is paid under the Clinical Laboratory Fee Schedule (CLFS), not the Physician Fee Schedule.

  • Medicare Allowable (2025/2026): Approximately $4.29 per test. This has decreased from ~$5.39 in previous years due to PAMA adjustments.
  • RVUs: 0.00 Work RVU (no physician work component).
  • Medicaid Rates: Varies by state (e.g., FL ~$2.31, NY ~$3.95).
  • Commercial Rates: Typically range from $4.00 to $7.00.

Real-World Clinical Billing Scenarios

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.

Decision Logic: When to Use Modifier QW

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]

Official Description

Prothrombin time;

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

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.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The prothrombin time (PT) test is indicated for several clinical scenarios, including:

  • Abnormal Bleeding or Bruising The test is performed to help identify the underlying causes of unexplained bleeding or bruising in patients.
  • Monitoring Anticoagulant Therapy It is used to check the effectiveness of blood-thinning medications, such as warfarin (Coumadin), ensuring that the dosage is appropriate for the patient's needs.
  • Assessment of Clotting Factors The PT test helps evaluate for low levels of blood-clotting factors I, II, V, VII, and X, which are essential for normal coagulation.
  • Vitamin K Levels It is utilized to check for low levels of vitamin K, which is necessary for the synthesis of certain clotting factors.
  • Liver Function Evaluation The test assesses liver function by determining how quickly the body is utilizing its clotting factors, providing insights into the liver's ability to produce these proteins.

2. Procedure

The prothrombin time test involves several procedural steps to ensure accurate measurement of clotting time:

  • Sample Collection A blood sample is drawn from the patient, typically from a vein in the arm, using standard venipuncture techniques. The collected blood is then placed into a tube containing an anticoagulant to prevent clotting prior to testing.
  • Preparation of Plasma The blood sample is centrifuged to separate the plasma from the cellular components. This plasma is what will be used for the prothrombin time measurement.
  • Clot Detection The plasma is subjected to a clot detection method, specifically electromagnetic mechanical clot detection, which measures the time it takes for the plasma to clot after the addition of a thromboplastin reagent.
  • Result Interpretation The time measured is reported as the prothrombin time, which is typically expressed in seconds. This result is then compared to a normal range to determine if the patient's clotting time is prolonged.
  • Follow-Up Testing (if necessary) If the prothrombin time is elevated and the patient is not on anticoagulant therapy, a prothrombin time mixing study may be performed. This involves mixing the patient's plasma with normal plasma in a 1:1 ratio, incubating the mixture, and measuring the clotting time again to assess for inhibitors or coagulation factor deficiencies.

3. Post-Procedure

After the prothrombin time test is completed, there are generally no specific post-procedure care requirements for the patient. However, patients may be advised to monitor for any unusual bleeding or bruising, especially if the test results indicate prolonged clotting times. If a mixing study is performed, the results will guide further clinical management, which may include additional testing or adjustments to anticoagulant therapy. It is important for healthcare providers to communicate the results of the test to the patient and discuss any necessary follow-up actions based on the findings.

Short Descr PROTHROMBIN TIME
Medium Descr PROTHROMBIN TIME
Long Descr Prothrombin time;
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 4
CCS Clinical Classification 233 - Laboratory - Chemistry and Hematology
QW Clia waived test
GA Waiver of liability statement issued as required by payer policy, individual case
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.
GW Service not related to the hospice patient's terminal condition
GZ Item or service expected to be denied as not reasonable and necessary
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.
Q4 Service for ordering/referring physician qualifies as a service exemption
CR Catastrophe/disaster related
X1 Continuous/broad services: for reporting services by clinicians, who provide the principal care for a patient, with no planned endpoint of the relationship; services in this category represent comprehensive care, dealing with the entire scope of patient problems, either directly or in a care coordination role; reporting clinician service examples include, but are not limited to: primary care, and clinicians providing comprehensive care to patients in addition to specialty care
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.
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.
Q1 Routine clinical service provided in a clinical research study that is in an approved clinical research study
X2 Continuous/focused services: for reporting services by clinicians whose expertise is needed for the ongoing management of a chronic disease or a condition that needs to be managed and followed with no planned endpoint to the relationship; reporting clinician service examples include but are not limited to: a rheumatologist taking care of the patient's rheumatoid arthritis longitudinally but not providing general primary care services
GV Attending physician not employed or paid under arrangement by the patient's hospice provider
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
AY Item or service furnished to an esrd patient that is not for the treatment of esrd
GC This service has been performed in part by a resident under the direction of a teaching physician
XE Separate encounter, a service that is distinct because it occurred during a separate encounter
XU Unusual non-overlapping service, the use of a service that is distinct because it does not overlap usual components of the main service
24 Unrelated evaluation and management service by the same physician or other qualified health care professional during a postoperative period: the physician or other qualified health care professional may need to indicate that an evaluation and management service was performed during a postoperative period for a reason(s) unrelated to the original procedure. this circumstance may be reported by adding modifier 24 to the appropriate level of e/m service.
25 Significant, separately identifiable evaluation and management service by the same physician or other qualified health care professional on the same day of the procedure or other service: it may be necessary to indicate that on the day a procedure or service identified by a cpt code was performed, the patient's condition required a significant, separately identifiable e/m service above and beyond the other service provided or beyond the usual preoperative and postoperative care associated with the procedure that was performed. a significant, separately identifiable e/m service is defined or substantiated by documentation that satisfies the relevant criteria for the respective e/m service to be reported (see evaluation and management services guidelines for instructions on determining level of e/m service). the e/m service may be prompted by the symptom or condition for which the procedure and/or service was provided. as such, different diagnoses are not required for reporting of the e/m services on the same date. this circumstance may be reported by adding modifier 25 to the appropriate level of e/m service. note: this modifier is not used to report an e/m service that resulted in a decision to perform surgery. see modifier 57 for significant, separately identifiable non-e/m services, see modifier 59.
51 Multiple procedures: when multiple procedures, other than e/m services, physical medicine and rehabilitation services or provision of supplies (eg, vaccines), are performed at the same session by the same individual, the primary procedure or service may be reported as listed. the additional procedure(s) or service(s) may be identified by appending modifier 51 to the additional procedure or service code(s). note: this modifier should not be appended to designated "add-on" codes (see appendix d).
52 Reduced services: under certain circumstances a service or procedure is partially reduced or eliminated at the discretion of the physician or other qualified health care professional. under these circumstances the service provided can be identified by its usual procedure number and the addition of modifier 52, signifying that the service is reduced. this provides a means of reporting reduced services without disturbing the identification of the basic service. note: for hospital outpatient reporting of a previously scheduled procedure/service that is partially reduced or cancelled as a result of extenuating circumstances or those that threaten the well-being of the patient prior to or after administration of anesthesia, see modifiers 73 and 74 (see modifiers approved for asc hospital outpatient use).
53 Discontinued procedure: under certain circumstances, the physician or other qualified health care professional may elect to terminate a surgical or diagnostic procedure. due to extenuating circumstances or those that threaten the well being of the patient, it may be necessary to indicate that a surgical or diagnostic procedure was started but discontinued. this circumstance may be reported by adding modifier 53 to the code reported by the individual for the discontinued procedure. note: this modifier is not used to report the elective cancellation of a procedure prior to the patient's anesthesia induction and/or surgical preparation in the operating suite. for outpatient hospital/ambulatory surgery center (asc) reporting of a previously scheduled procedure/service that is partially reduced or cancelled as a result of extenuating circumstances or those that threaten the well being of the patient prior to or after administration of anesthesia, see modifiers 73 and 74 (see modifiers approved for asc hospital outpatient use).
76 Repeat procedure or service by same physician or other qualified health care professional: it may be necessary to indicate that a procedure or service was repeated by the same physician or other qualified health care professional subsequent to the original procedure or service. this circumstance may be reported by adding modifier 76 to the repeated procedure or service. note: this modifier should not be appended to an e/m 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.
95 Synchronous telemedicine service rendered via a real-time interactive audio and video telecommunications system: synchronous telemedicine service is defined as a real-time interaction between a physician or other qualified health care professional and a patient who is located at a distant site from the physician or other qualified health care professional. the totality of the communication of information exchanged between the physician or other qualified health care professional and the patient during the course of the synchronous telemedicine service must be of an amount and nature that would be sufficient to meet the key components and/or requirements of the same service when rendered via a face-to-face interaction. modifier 95 may only be appended to the services listed in appendix p. appendix p is the list of cpt codes for services that are typically performed face-to-face, but may be rendered via a real-time (synchronous) interactive audio and video telecommunications system.
AI Principal physician of record
AQ Physician providing a service in an unlisted health professional shortage area (hpsa)
CC Procedure code change (use 'cc' when the procedure code submitted was changed either for administrative reasons or because an incorrect code was filed)
CG Policy criteria applied
CS Cost-sharing waived for specified covid-19 testing-related services that result in and order for or administration of a covid-19 test and/or used for cost-sharing waived preventive services furnished via telehealth in rural health clinics and federally qualified health centers during the covid-19 public health emergency
FQ The service was furnished using audio-only communication technology
GE This service has been performed by a resident without the presence of a teaching physician under the primary care exception
GX Notice of liability issued, voluntary under payer policy
JZ Zero drug amount discarded/not administered to any patient
KX Requirements specified in the medical policy have been met
LT Left side (used to identify procedures performed on the left side of the body)
MC Ordering professional is not required to consult a clinical decision support mechanism due to the significant hardship exception of electronic health record or clinical decision support mechanism vendor issues
MH Unknown if ordering professional consulted a clinical decision support mechanism for this service, related information was not provided to the furnishing professional or provider
PD Diagnostic or related non diagnostic item or service provided in a wholly owned or operated entity to a patient who is admitted as an inpatient within 3 days
PN Non-excepted service provided at an off-campus, outpatient, provider-based department of a hospital
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
Q5 Service furnished under a reciprocal billing 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
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
QE Prescribed amount of stationary oxygen while at rest is less than 1 liter per minute (lpm)
QT Recording and storage on tape by an analog tape recorder
RT Right side (used to identify procedures performed on the right side of the body)
SA Nurse practitioner rendering service in collaboration with a physician
SG Ambulatory surgical center (asc) facility service
SL State supplied vaccine
T1 Left foot, second digit
TC Technical component; under certain circumstances, a charge may be made for the technical component alone; under those circumstances the technical component charge is identified by adding modifier 'tc' to the usual procedure number; technical component charges are institutional charges and not billed separately by physicians; however, portable x-ray suppliers only bill for technical component and should utilize modifier tc; the charge data from portable x-ray suppliers will then be used to build customary and prevailing profiles
TR School-based individualized education program (iep) services provided outside the public school district responsible for the student
U7 Medicaid level of care 7, as defined by each state
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
XP Separate practitioner, a service that is distinct because it was performed by a different practitioner
XS Separate structure, a service that is distinct because it was performed on a separate organ/structure
Date
Action
Notes
2010-01-01 Changed Code description changed.
Pre-1990 Added Code added.
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Description
Code
Description
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