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Official Description

Tapentadol

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 80372 refers to a laboratory test specifically designed to measure the presence and concentration of tapentadol in biological samples such as urine, serum, or plasma. Tapentadol, which is marketed under the brand name Nucynta, is classified as a central acting opioid analgesic. Its mechanism of action involves agonism of the opioid receptors, which helps to alleviate pain by inhibiting the reuptake of norepinephrine, thereby enhancing analgesic effects. This medication is primarily utilized for the management of moderate to severe acute pain, serving as an alternative to traditional opiate medications. Additionally, tapentadol may be prescribed in an extended-release formulation for the treatment of diabetic peripheral neuropathy, a condition characterized by nerve damage due to diabetes. The testing process for tapentadol involves obtaining a blood sample through a procedure known as venipuncture, which is separately reportable, or collecting urine via random voiding or catheterization. The analysis of urine, serum, and plasma samples is conducted using a sophisticated technique known as quantitative liquid chromatography-tandem mass spectrometry, which allows for precise measurement of the drug's concentration in the samples tested.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The laboratory test for tapentadol is indicated for the following conditions:

  • Moderate to Severe Acute Pain This test is performed to monitor the levels of tapentadol in patients who are being treated for moderate to severe acute pain, ensuring appropriate therapeutic dosing and effectiveness.
  • Diabetic Peripheral Neuropathy The test may also be indicated for patients prescribed the extended-release formulation of tapentadol for the management of diabetic peripheral neuropathy, allowing for assessment of drug levels in relation to treatment efficacy.

2. Procedure

The procedure for testing tapentadol involves several key steps that ensure accurate measurement of the drug in biological samples.

  • Step 1: Sample Collection The first step in the procedure is the collection of biological samples. For serum or plasma testing, a blood sample is obtained through venipuncture, which is a standard method of drawing blood from a vein. This step is crucial as it provides the necessary fluid for analysis. For urine testing, samples can be collected either through random voiding, where the patient simply provides a urine sample at any time, or through catheterization, which involves inserting a catheter into the bladder to obtain a urine sample. Each method of collection is designed to ensure that the samples are representative of the patient's current drug levels.
  • Step 2: Laboratory Analysis Once the samples are collected, they are sent to a laboratory for analysis. The testing utilizes quantitative liquid chromatography-tandem mass spectrometry, a highly sensitive and specific technique that allows for the precise quantification of tapentadol in the collected samples. This method separates the components of the sample and measures the concentration of tapentadol, providing accurate results that can inform clinical decisions regarding the patient's pain management regimen.

3. Post-Procedure

After the procedure, there are no specific post-procedure care requirements mentioned for the tapentadol testing. However, it is important for healthcare providers to review the test results promptly to assess the patient's tapentadol levels. This information can guide further treatment decisions, including adjustments to medication dosages or changes in therapy, based on the measured levels of the drug in the patient's system. Additionally, patients may be monitored for any side effects or adverse reactions related to tapentadol use, ensuring that their pain management strategy remains effective and safe.

Short Descr DRUG SCREENING TAPENTADOL
Medium Descr DRUG SCREENING TAPENTADOL
Long Descr Tapentadol
Status Code Not Valid for Medicare Purposes
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
APC Status Indicator Code Not Recognized by OPPS when submitted on Outpatient Hospital Part B Bill Type (12x/13x)
Type of Service (TOS) 5 - Diagnostic Laboratory
Berenson-Eggers TOS (BETOS) T2D - Other tests - other
MUE 1
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.
GZ Item or service expected to be denied as not reasonable and necessary
Date
Action
Notes
2015-01-01 Added Added
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