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Official Description

Sickling of RBC, reduction

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 85660 refers to the sickling of red blood cells (RBC), specifically the reduction of these cells during testing. This procedure involves analyzing a blood sample to detect the presence of hemoglobin S (HbS), which is an abnormal variant of hemoglobin. The sickling of RBC reduction test, commonly known as the HbS solubility test, is primarily utilized to screen for sickle cell anemia, a genetic disorder characterized by the transformation of normal round RBCs into a crescent or sickle shape. This condition predominantly affects individuals of African descent but can also be found in those of Mediterranean and Middle Eastern backgrounds. The sickled RBCs exhibit impaired flow through the circulatory system and are less effective in oxygen transport. Furthermore, these abnormal cells have a significantly reduced lifespan of approximately 10 to 20 days, compared to the normal lifespan of 120 days for healthy RBCs. As a result, individuals with sickle cell anemia may experience anemia due to the decreased number of circulating RBCs and may suffer from painful episodes caused by complications arising from the obstruction of small blood vessels by sickled cells. The HbS solubility test is performed by introducing a chemical agent to the blood sample, which diminishes the oxygen content. This reduction leads to the formation of polymers associated with hemoglobin S, causing the affected RBCs to sickle. The test is sensitive enough to identify even minimal quantities of hemoglobin S, making it a crucial tool for screening both sickle cell trait (where an individual carries one sickle cell gene) and sickle cell anemia (where an individual carries two sickle cell genes).

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

The sickling of RBC reduction test (CPT® Code 85660) is indicated for the following conditions:

  • Sickle Cell Anemia Screening This test is performed to identify individuals who may have sickle cell anemia, a hereditary condition that leads to the production of abnormal hemoglobin S.
  • Sickle Cell Trait Screening The test is also used to screen for sickle cell trait, which occurs in individuals who carry one copy of the sickle cell gene and may not exhibit symptoms but can pass the gene to offspring.
  • Family Planning Individuals with a family history of sickle cell disease may undergo this test to assess the risk of having children with the condition.

2. Procedure

The procedure for the sickling of RBC reduction test involves several key steps to ensure accurate results:

  • Step 1: Blood Sample Collection A blood sample is collected from the patient, typically via venipuncture. This sample serves as the basis for the subsequent testing.
  • Step 2: Chemical Addition A specific chemical reagent is added to the blood sample. This reagent is designed to reduce the oxygen content in the sample, which is critical for the next step of the test.
  • Step 3: Observation of Hemoglobin S Polymerization As the oxygen level decreases, hemoglobin S begins to polymerize, leading to the sickling of the RBCs. This change is observed and analyzed to determine the presence of hemoglobin S.
  • Step 4: Result Interpretation The results are interpreted based on the degree of sickling observed. A positive result indicates the presence of hemoglobin S, confirming either sickle cell trait or sickle cell anemia.

3. Post-Procedure

After the sickling of RBC reduction test is completed, the patient may be advised on the following post-procedure considerations: monitoring for any immediate reactions to the blood draw, understanding the implications of the test results, and discussing potential follow-up testing or genetic counseling if the results indicate the presence of hemoglobin S. It is important for patients to be informed about the significance of their results, especially in the context of family planning and potential health implications associated with sickle cell disease.

Short Descr RBC SICKLE CELL TEST
Medium Descr SICKLING RBC REDUCTION
Long Descr Sickling of RBC, reduction
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 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.
26 Professional component: certain procedures are a combination of a physician or other qualified health care professional component and a technical component. when the physician or other qualified health care professional component is reported separately, the service may be identified by adding modifier 26 to the usual procedure number.
59 Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25.
91 Repeat clinical diagnostic laboratory test: in the course of treatment of the patient, it may be necessary to repeat the same laboratory test on the same day to obtain subsequent (multiple) test results. under these circumstances, the laboratory test performed can be identified by its usual procedure number and the addition of modifier 91. note: this modifier may not be used when tests are rerun to confirm initial results; due to testing problems with specimens or equipment; or for any other reason when a normal, one-time, reportable result is all that is required. this modifier may not be used when other code(s) describe a series of test results (eg, glucose tolerance tests, evocative/suppression testing). this modifier may only be used for laboratory test(s) performed more than once on the same day on the same patient.
Q1 Routine clinical service provided in a clinical research study that is in an approved clinical research study
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