Summary & Overview
CPT 82633: 11–Desoxycorticosterone Measurement in Serum/Plasma/Urine
CPT code 82633 denotes a laboratory assay for 11–desoxycorticosterone measured in serum, plasma, or urine. The test assesses adrenal corticosteroid production and can inform evaluation of mineralocorticoid-related disorders and physiologic changes that occur in pregnancy. Nationally, lab-based endocrine assays like this code are important for diagnostic pathways, guiding further endocrine evaluation and management.
Key payers covered in the analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find context on the clinical utility of the assay, typical sites of service, and payer considerations relevant to laboratory billing. The publication also summarizes expected service classification, common billing modifiers (list provided in input), and where to find related clinical and coding references.
The content is intended to help clinicians, billing staff, and policy analysts understand the code’s clinical role, typical use cases, and payer landscape at a national level. Data not available in the input is noted explicitly where applicable.
Billing Code Overview
CPT code 82633 measures the level of 11–desoxycorticosterone in serum, plasma, or urine. This laboratory assay detects a steroid hormone produced by the adrenal cortex that normally rises during the last half of pregnancy. The test is a diagnostic laboratory service used to evaluate adrenal steroid production and electrolyte or blood pressure abnormalities potentially related to mineralocorticoid activity.
Service Type: Laboratory diagnostic test
Typical Site of Service: Clinical laboratory or hospital laboratory; specimen collection may occur in outpatient clinics or inpatient settings
Clinical & Coding Specifications
Clinical Context
A typical patient is a pregnant woman in her second or third trimester referred by her obstetrician for laboratory measurement of 11‑desoxycorticosterone (DOC) to evaluate suspected disorders of mineralocorticoid synthesis or placental/adrenal steroid metabolism. Common clinical presentations prompting this test include refractory maternal hypertension in pregnancy, unexplained hypokalemia, features suggestive of congenital adrenal hyperplasia variants, or investigation of abnormal fetal growth with concern for endocrine causes. The clinical workflow begins with the ordering clinician documenting the indication and pregnancy status, collection of a timed blood or urine specimen (serum, plasma, or 24‑hour urine as indicated), proper labeling with patient identifiers and pregnancy gestational age, transport to the clinical laboratory, analytic measurement by immunoassay or mass spectrometry, result verification by a laboratory professional, and transmission of results to the ordering obstetrician or maternal‑fetal medicine specialist for interpretation in context of other steroid panels and clinical findings. Typical site of service is an outpatient laboratory or hospital clinical laboratory supporting obstetrics clinics and maternal‑fetal medicine units.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when only the physician professional interpretation or reading of the test result is reported separately from the technical laboratory component. |