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Procainamide is a medication classified as a cardiac antidysrhythmic agent, primarily utilized to manage and treat abnormal heart rhythms, particularly ventricular tachycardia. The CPT® Code 80192 specifically refers to a laboratory test that quantifies the levels of procainamide in the blood, along with its metabolites, notably n-acetyl procainamide. This test is crucial for monitoring the concentration of the drug in the bloodstream to ensure that therapeutic levels are maintained, thereby optimizing treatment efficacy and minimizing potential toxicity. The measurement of procainamide and its metabolites is essential, as it helps healthcare providers assess the patient's response to the medication and make necessary adjustments to the dosage. The test is performed on a blood sample obtained through venipuncture, which is a standard procedure for collecting blood for laboratory analysis. The analysis is conducted using a fluorescence polarization immunoassay, a sensitive and specific method that allows for accurate detection of drug levels. Monitoring procainamide levels is particularly important due to the risk of adverse effects, including the formation of antinuclear antibodies, which can lead to symptoms resembling systemic lupus erythematosus. Regular testing ensures that patients receive the appropriate therapeutic benefits while minimizing the risk of complications associated with improper dosing.
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Procainamide testing is indicated for patients who are undergoing treatment with procainamide to monitor drug levels and ensure therapeutic efficacy. The following conditions and symptoms may warrant this testing:
The procedure for testing procainamide levels involves several key steps that ensure accurate measurement of the drug and its metabolites:
After the blood sample has been collected and sent for analysis, patients may be advised to resume their normal activities unless otherwise directed by their healthcare provider. It is important for patients to follow up with their physician to discuss the test results and any necessary adjustments to their procainamide therapy. If elevated levels of procainamide or its metabolites are detected, the healthcare provider may consider modifying the dosage or frequency of administration to mitigate potential side effects. Additionally, patients should be monitored for any adverse reactions associated with procainamide therapy, including symptoms indicative of antinuclear antibody formation. Regular follow-up testing may be recommended to ensure ongoing monitoring of drug levels and patient safety.
| Short Descr | ASSAY OF PROCAINAMIDE | Medium Descr | DRUG SCREEN QUANTITATIVE PROCAINAMIDE METABOLITE | Long Descr | Procainamide; with metabolites (eg, n-acetyl procainamide) | 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 | 2 | CCS Clinical Classification | 235 - Other Laboratory |
| 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. |
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| 2013-01-01 | Changed | Medium description changed per AMA 2013 corrections document dated January 25, 2013. |
| 1993-01-01 | Added | First appearance in code book in 1993. |
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