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The CPT® Code 85301 refers to the assay for antithrombin III, which is a critical component in the body's coagulation system. Antithrombin III is a protein that helps regulate blood clotting by inhibiting thrombin and other clotting factors, thereby preventing excessive clot formation. The procedure involves taking a diluted blood sample and mixing it with antithrombin-deficient plasma, which lacks the necessary antithrombin III to facilitate normal coagulation. This mixture is then treated with intrinsic coagulation enzymes, an augmenting compound such as heparin, phospholipids, and an activator that initiates the contact phase of the intrinsic coagulation pathway. After these components are combined, calcium ions are added to the mixture to trigger the coagulation process. The time it takes for coagulation to occur is measured and compared to a reference standard, allowing for the determination of the antithrombin III activity level in the sample. In the specific method described for CPT® Code 85301, serum is added to a thrombin solution, and after a predetermined incubation period, the remaining thrombin activity in the plasma is measured. This assay is essential for diagnosing and managing conditions related to abnormal blood clotting, such as thrombosis or bleeding disorders.
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The CPT® Code 85301 is indicated for use in various clinical scenarios where the assessment of antithrombin III levels is necessary. This includes:
The procedure for CPT® Code 85301 involves several critical steps to accurately assess the level of antithrombin III activity in the blood sample. The first step is the collection of a diluted blood sample from the patient, which is essential for the subsequent analysis. This sample is then mixed with antithrombin-deficient plasma, which lacks the antithrombin III necessary for normal coagulation processes. The addition of intrinsic coagulation enzymes, an augmenting compound such as heparin, phospholipids, and an activator initiates the contact phase of the intrinsic coagulation pathway, setting the stage for the coagulation reaction. Following the preparation of this mixture, calcium ions are introduced to trigger the coagulation process. The time taken for coagulation to occur is meticulously measured and compared against a reference standard. This comparison allows for the determination of the antithrombin III activity level in the sample. In the specific method outlined for CPT® Code 85301, serum is added to a thrombin solution, and after a fixed incubation period, the residual thrombin activity in the plasma is measured. This step is crucial as it provides a direct assessment of the antithrombin III levels, which is vital for diagnosing and managing coagulation disorders.
After the completion of the CPT® Code 85301 procedure, the patient may not require any specific post-procedure care, as the assay is typically performed on an outpatient basis. However, it is essential for healthcare providers to monitor the patient for any potential adverse reactions, particularly if anticoagulant therapy is being adjusted based on the results of the assay. The results of the antithrombin III assay will be analyzed and interpreted by the healthcare provider, who will then discuss the findings with the patient and determine any necessary follow-up actions or treatments based on the antithrombin levels measured. It is also important to ensure that the patient understands the significance of the results and any implications for their ongoing management of coagulation disorders.
Short Descr | ANTITHROMBIN III ANTIGEN | Medium Descr | CLOTTING INHIBITRS ANTITHROMBN III ANTIGEN ASSAY | Long Descr | Clotting inhibitors or anticoagulants; antithrombin III, antigen assay | 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 |
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. | 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. |
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2013-01-01 | Changed | Short Descriptor changed. |
Pre-1990 | Added | Code added. |
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