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Official Description

Procainamide; with metabolites (eg, n-acetyl procainamide)

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

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.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

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:

  • Ventricular Tachycardia - A condition characterized by an abnormally fast heart rate originating from the ventricles, which may require the use of procainamide for management.
  • Monitoring Therapeutic Drug Levels - Regular assessment of procainamide and its metabolites is essential to maintain appropriate drug concentrations in the bloodstream, ensuring effective treatment while minimizing toxicity.
  • Adverse Reactions - Patients experiencing side effects or complications related to procainamide therapy may require testing to evaluate drug levels and adjust dosages accordingly.

2. Procedure

The procedure for testing procainamide levels involves several key steps that ensure accurate measurement of the drug and its metabolites:

  • Step 1: Patient Preparation - Prior to the blood draw, the patient may be instructed to avoid certain medications or substances that could interfere with the test results. It is important to gather a thorough medication history to ensure accurate interpretation of the results.
  • Step 2: Venipuncture - A qualified healthcare professional performs a venipuncture to obtain a blood sample. This involves inserting a needle into a vein, typically in the arm, to collect the necessary volume of blood for testing. The procedure is performed using sterile techniques to minimize the risk of infection.
  • Step 3: Sample Handling - Once the blood sample is collected, it is properly labeled and transported to the laboratory for analysis. Care is taken to ensure that the sample is handled according to laboratory protocols to maintain its integrity.
  • Step 4: Laboratory Analysis - The blood serum is tested using fluorescence polarization immunoassay, a method that allows for the specific detection and quantification of procainamide and its metabolites in the sample. This technique utilizes the principles of fluorescence to measure the concentration of the drug accurately.
  • Step 5: Result Interpretation - After the analysis is complete, the results are reviewed by a qualified healthcare professional. The procainamide levels are compared against established therapeutic ranges to determine if the patient is within the appropriate dosing parameters.

3. Post-Procedure

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.
Date
Action
Notes
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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Description
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