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Official Description

Russell viper venom time (includes venom); undiluted

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 85612 refers to the Russell viper venom time (RVVT) test, which is a specialized laboratory procedure used to assess blood coagulation. This test involves obtaining a blood sample from the patient, which is then subjected to analysis using undiluted Russell viper venom as an activating agent. The primary purpose of the RVVT is to detect deficiencies in specific blood clotting factors that are crucial for normal coagulation processes. By measuring the clotting time, healthcare professionals can identify potential bleeding disorders or coagulation abnormalities. The undiluted nature of the venom used in this test distinguishes it from the diluted version, CPT® Code 85613, which is designed to detect the presence of lupus anticoagulants—nonspecific inhibitors that can interfere with the clotting process. The RVVT is an important diagnostic tool in the evaluation of patients with unexplained bleeding or thrombotic events, providing critical information for appropriate management and treatment strategies.

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

The Russell viper venom time (RVVT) test, coded as CPT® 85612, is indicated for the evaluation of patients who may have bleeding disorders or abnormalities in blood coagulation. The specific indications for performing this test include:

  • Assessment of Coagulation Disorders The RVVT is utilized to detect deficiencies in certain blood clotting factors, which can lead to bleeding complications.
  • Evaluation of Unexplained Bleeding This test is performed in patients presenting with unexplained bleeding episodes, helping to identify underlying coagulation issues.
  • Preoperative Assessment The RVVT may be indicated as part of a preoperative workup to ensure that patients do not have undiagnosed bleeding disorders that could complicate surgical procedures.

2. Procedure

The procedure for conducting the Russell viper venom time (RVVT) test involves several key steps, which are outlined as follows:

  • Step 1: Blood Sample Collection A blood sample is obtained from the patient, typically via venipuncture. This sample is essential for the subsequent analysis and must be collected in a manner that prevents contamination and ensures accurate results.
  • Step 2: Preparation of the Sample The collected blood sample is processed to separate the plasma, which is the liquid component needed for the RVVT. This step is crucial as the test specifically evaluates the plasma's coagulation properties.
  • Step 3: Addition of Undiluted Russell Viper Venom The undiluted Russell viper venom is then added to the patient’s plasma. This venom acts as an activating agent, initiating the coagulation process and allowing for the measurement of clotting time.
  • Step 4: Measurement of Clotting Time The clotting time is measured using photo-optical methods, which provide a precise assessment of how long it takes for the blood to clot in the presence of the venom. This measurement is critical for determining the presence of deficiencies in clotting factors.

3. Post-Procedure

After the RVVT test is completed, the patient may be monitored for any immediate reactions, although the procedure is generally safe and well-tolerated. The results of the test will be analyzed and interpreted by a qualified healthcare professional, who will consider the findings in conjunction with the patient's clinical history and other diagnostic tests. Depending on the results, further testing or treatment may be recommended to address any identified coagulation issues. It is important for healthcare providers to communicate the results to the patient and discuss any necessary follow-up actions or interventions.

Short Descr VIPER VENOM PROTHROMBIN TIME
Medium Descr RUSSELL VIPER VENON TIME UNDILUTED
Long Descr Russell viper venom time (includes venom); undiluted
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) T1H - Lab tests - other (non-Medicare fee schedule)
MUE 1
CCS Clinical Classification 233 - Laboratory - Chemistry and Hematology
GA Waiver of liability statement issued as required by payer policy, individual case
Date
Action
Notes
Pre-1990 Added Code added.
Code
Description
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