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Test Code ESR Erythrocyte Sedimentation Rate

Additional Codes

Cerner

NextGen

ESR

Erythrocyte Sedimentation Rate

Alternate Name(s)

ESR

Sed Rate

Useful For

The erythrocyte sedimentation rate (ESR) is a nonspecific indicator of inflammation or infection. Sedimentation is accelerated by an increase in the plasma concentration of acute phase proteins, which are increased in acute tissue damage, chronic inflammation, chronic infection, and pregnancy. The ESR reflects both the increase in certain accelerating proteins, such as fibrinogen and gamma globulins, and the decrease in retarding proteins, such as albumin. Conditions that promote the formation of rouleaux produce an elevated ESR result.

ESR is useful in diagnosing some diseases, such as polymyalgia rheumatica, temporal arteritis, rheumatoid arthritis and Hodgkin’s disease, and is useful as an effective marker of pharmacological treatment in some diseases including rheumatoid arthritis, vasculitis, collagenosis, and septic arthritis. ESR is usually higher in females compared to males, increases in pregnancy, and tends to rise with age in both genders.

Methodology

The MINI-CUBE is an automated ESR analyzer that accurately and precisely measures the sedimentation rate of erythrocytes based upon the principle of the Westergren method. Anticoagulated blood is placed into a vertical column that remains undisturbed for a specified amount of time. At the end of the period, the distance the red cells have settled is measured in mm per hour. The instrument compensates for temperatures above 18 °C according to Manley’s Nomogram.

Patient Preparation

None

Collection Instructions

  • Maximum of two labels to prevent damage to instruments.
  • The bottom of the tube must be free of labels, with no folding over, to prevent erroneous results.
  • Straight, label free gap on side of tube needed for instrument to read values. 
  • Avoid over or under filling.

Specimen Requirements

Preferred Volume

Standard 13 x 75 mm K2EDTA Lavender tubes (BD 3 mL, BD 4 mL, Greiner 3 mL) with Hemogard or conventional stoppers filled to capacity

Minimum Volume

2.0mL of EDTA whole blood in standard 13 x 75 mm K2EDTA Lavender tubes (BD 3 mL, BD 4 mL, Greiner 3 mL) with Hemogard or conventional stoppers

Container

Standard 13 x 75 mm K2EDTA Lavender tubes (BD 3 mL, BD 4 mL, Greiner 3 mL) with Hemogard or conventional stoppers.

Stability

  • ≤ 4 hours at room temperature (18-25 °C)
  • Refrigerated (2-8°C): ≤ 24 hrs

Rejection Criteria

  • Under- or overfilled Specimens.
  • Clotted specimens

Result Reporting and Reference Values

Reference Range

  • Male: 0-10 mm/hr.
  • Female: 0-20 mm/hr.

Critical Ranges

None

Reflex Testing

None

Limitations

  • Specimens labeled with more than two labels are at risk for being stuck in the instrument and for producing erroneous results.
  • The clinical significance of an ESR result obtained from an abnormal specimen including, but not limited to, icteric, lipemic, cold agglutinins, anemic conditions, low hemoglobin concentrations, hemolysis, or any pathological condition that interferes or prevents a clear red blood cell to plasma interface, should be determined by the clinician ordering the test.
  • Manual and automated ESR measurements in samples without a clear interface are subject to a high degree of variability.