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Official Description

Estrogens; fractionated

© Copyright 2026 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 82671 refers to a laboratory test that quantifies the levels of fractionated estrogens in the blood, specifically measuring estradiol and estrone separately, while also calculating the total estrogen amount. Estrogens are a group of hormones that play a crucial role in the development and regulation of the female reproductive system and secondary sexual characteristics. The three primary estrogens measured in this test are estradiol, estriol, and estrone. A blood sample is collected through venipuncture, which is a standard procedure for obtaining blood for laboratory analysis. The test can be performed on either plasma or serum samples. The measurement of fractionated estrogens is particularly important for diagnosing various conditions related to hormonal imbalances. For instance, it can help identify precocious or delayed puberty in girls, assess disorders of sex steroid metabolism, and evaluate bone mineral density. Additionally, this test is instrumental in monitoring hormone replacement therapy in post-menopausal women, evaluating conditions such as hypogonadism and oligo-amenorrhea, and assessing ovarian function, including follicle development for assisted reproductive technologies like in-vitro fertilization. The methodology for measuring estradiol varies based on the patient's demographic; it is typically assessed using chemiluminescent immunoassay for pre-menopausal women, while tandem mass spectrometry is employed for males, children, and post-menopausal women. Estrone is also measured using tandem mass spectrometry, and the total estrogen level is derived from these measurements. In contrast, CPT® Code 82672 encompasses the measurement of total estrogens, which combines the values of all three estrogens into a single reportable figure. This total estrogen measurement is particularly useful for diagnosing estrogen-producing ovarian tumors in both pre-menarche and post-menopausal females, as well as for evaluating elevated estrogen levels in males. Furthermore, it can assist in determining the timing of ovulation, which is critical for optimizing conception efforts.

© Copyright 2026 Coding Ahead. All rights reserved.

1. Indications

The CPT® Code 82671 is indicated for use in various clinical scenarios where the measurement of fractionated estrogens is necessary. The following conditions and situations warrant this laboratory test:

  • Precocious Puberty - The test is utilized to diagnose early onset puberty in girls, which can indicate hormonal imbalances or other underlying conditions.
  • Delayed Puberty - It helps in assessing delayed puberty in girls, providing insights into potential hormonal deficiencies or disorders.
  • Disorders of Sex Steroid Metabolism - The test aids in diagnosing conditions that affect the metabolism of sex steroids, which can lead to various reproductive health issues.
  • Bone Mineral Density Assessment - Fractionated estrogens are measured to evaluate bone health, particularly in post-menopausal women who are at increased risk for osteoporosis.
  • Monitoring Hormone Replacement Therapy - The test is used to monitor the effectiveness of hormone replacement therapy in post-menopausal women, ensuring appropriate estrogen levels are maintained.
  • Evaluation of Hypogonadism - It assists in diagnosing hypogonadism in women, a condition characterized by insufficient hormone production.
  • Assessment of Oligo-Amenorrhea - The test is relevant for evaluating women with irregular menstrual cycles or absence of menstruation.
  • Ovarian Function Assessment - It is used to assess ovarian function, including monitoring follicle development for assisted reproductive techniques such as in-vitro fertilization.

2. Procedure

The procedure for obtaining the results associated with CPT® Code 82671 involves several key steps that ensure accurate measurement of fractionated estrogens. The following outlines the procedural steps:

  • Step 1: Patient Preparation - Prior to the blood draw, the patient may be instructed to avoid certain medications or supplements that could interfere with hormone levels. It is essential to ensure that the patient is adequately informed about the procedure and any necessary preparations.
  • Step 2: Venipuncture - A qualified healthcare professional performs venipuncture to collect a blood sample. This involves inserting a needle into a vein, typically in the arm, to draw blood into a collection tube. The procedure is performed under sterile conditions to minimize the risk of infection.
  • Step 3: Sample Processing - Once the blood sample is collected, it is processed in the laboratory. The sample may be separated into plasma or serum, depending on the testing requirements. This step is crucial for isolating the components needed for accurate hormone measurement.
  • Step 4: Hormone Measurement - The laboratory utilizes specific assays to measure the levels of estradiol and estrone. Estradiol is typically measured using chemiluminescent immunoassay for pre-menopausal women, while tandem mass spectrometry is used for males, children, and post-menopausal women. Estrone is also measured using tandem mass spectrometry.
  • Step 5: Calculation of Total Estrogen - After measuring estradiol and estrone, the total estrogen level is calculated based on the individual measurements. This total is reported alongside the separate values for estradiol and estrone.
  • Step 6: Reporting Results - The final results, including the individual measurements and the total estrogen value, are compiled and reported to the healthcare provider. This information is critical for making informed clinical decisions regarding the patient's health.

3. Post-Procedure

After the procedure associated with CPT® Code 82671, patients may experience minimal discomfort at the venipuncture site, which typically resolves quickly. There are no specific post-procedure care instructions required for this test, as it is a routine laboratory procedure. However, patients should be advised to monitor the site for any signs of excessive bruising or infection, such as redness, swelling, or discharge. The results of the test will be reviewed by the healthcare provider, who will discuss the findings with the patient and determine any necessary follow-up actions or treatments based on the results. It is important for patients to understand that the interpretation of the results should be done in conjunction with their clinical history and other diagnostic findings.

Short Descr ASSAY OF ESTROGENS
Medium Descr ASSAY OF ESTROGENS FRACTIONATED
Long Descr Estrogens; fractionated
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.
GY Item or service statutorily excluded, does not meet the definition of any medicare benefit or, for non-medicare insurers, is not a contract benefit
GA Waiver of liability statement issued as required by payer policy, individual case
GW Service not related to the hospice patient's terminal condition
Date
Action
Notes
2013-01-01 Changed Medium Descriptor changed.
Pre-1990 Added Code added.
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