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To detect the presence of inflammation caused by one or more conditions such as infections, tumors or autoimmune diseases; to help diagnose and monitor specific conditions such as temporal arteritis, systemic vasculitis, polymyalgia rheumatica, or rheumatoid arthritis
When your health practitioner thinks that you might have a condition causing inflammation; when you have signs and symptoms associated with temporal arteritis, systemic vasculitis, polymyalgia rheumatica, or rheumatoid arthritis such as headaches, neck or shoulder pain, pelvic pain, anemia, poor appetite, unexplained weight loss, and joint stiffness
A blood sample drawn from a vein in your arm
Erythrocyte sedimentation rate (ESR or sed rate) is a test that indirectly measures the degree of inflammation present in the body. The test actually measures the rate of fall (sedimentation) of erythrocytes (red blood cells) in a sample of blood that has been placed into a tall, thin, vertical tube. Results are reported as the millimeters of clear fluid (plasma) that are present at the top portion of the tube after one hour.
When a sample of blood is placed in a tube, the red blood cells normally settle out relatively slowly, leaving little clear plasma. The red cells settle at a faster rate in the presence of an increased level of proteins, particularly proteins called acute phase reactants. The level of acute phase reactants such as C-reactive protein (CRP) and fibrinogen increases in the blood in response to inflammation.
Inflammation is part of the body's immune response. It can be acute, developing rapidly after trauma, injury or infection, for example, or can occur over an extended time (chronic) with conditions such as autoimmune diseases or cancer.
The ESR is not diagnostic; it is a non-specific test that may be elevated in a number of these different conditions. It provides general information about the presence or absence of an inflammatory condition.
There have been questions about the usefulness of the ESR in light of newer tests that have come into use that are more specific. However, ESR test is typically indicated for the diagnosis and monitoring of temporal arteritis, systemic vasculitis and polymyalgia rheumatica. Extremely elevated ESR is useful in developing a rheumatic disease differential diagnosis. In addition, ESR may still be a good option in some situations, when, for example, the newer tests are not available in areas with limited resources or when monitoring the course of a disease.
The erythrocyte sedimentation rate (ESR or sed rate) is a relatively simple, inexpensive, non-specific test that has been used for many years to help detect inflammation associated with conditions such as infections, cancers, and autoimmune diseases.
ESR is said to be a non-specific test because an elevated result often indicates the presence of inflammation but does not tell the health practitioner exactly where the inflammation is in the body or what is causing it. An ESR can be affected by other conditions besides inflammation. For this reason, the ESR is typically used in conjunction with other tests, such as C-reactive protein.
ESR is used to help diagnose certain specific inflammatory diseases, including temporal arteritis, systemic vasculitis and polymyalgia rheumatica. (For more on these, read the article on Vasculitis.) A significantly elevated ESR is one of the main test results used to support the diagnosis.
This test may also be used to monitor disease activity and response to therapy in both of the above diseases as well as some others, such as lupus.
An ESR may be ordered when a condition or disease is suspected of causing inflammation somewhere in the body. There are numerous inflammatory conditions that may be detected using this test. For example, it may be ordered when arthritis is suspected of causing inflammation and pain in the joints or when digestive symptoms are suspected to be caused by inflammatory bowel disease.
A health practitioner may order an ESR when an individual has symptoms that suggest polymyalgia rheumatica, systemic vasculitis, or temporal arteritis, such as headaches, neck or shoulder pain, pelvic pain, anemia, poor appetite, unexplained weight loss, and joint stiffness. The ESR may also be ordered at regular intervals to assist in monitoring the course of these diseases.
Before doing an extensive workup looking for disease, a health practitioner may want to repeat the ESR.
The result of an ESR is reported as the millimeters of clear fluid (plasma) that are present at the top portion of the tube after one hour (mm/hr).
Since ESR is a non-specific marker of inflammation and is affected by other factors, the results must be used along with other clinical findings, the individual's health history, and results from other laboratory tests. If the ESR and clinical findings match, the health practitioner may be able to confirm or rule out a suspected diagnosis.
A single elevated ESR, without any symptoms of a specific disease, will usually not give enough information to make a medical decision. Furthermore, a normal result does not rule out inflammation or disease.
Moderately elevated ESR occurs with inflammation but also with anemia, infection, pregnancy, and with aging.
A very high ESR usually has an obvious cause, such as a severe infection, marked by an increase in globulins, polymyalgia rheumatica or temporal arteritis. A health practitioner will typically use other follow-up tests, such as blood cultures, depending on the person's symptoms. People with multiple myeloma or Waldenstrom's macroglobulinemia (tumors that make large amounts of immunoglobulins) typically have very high ESRs even if they don't have inflammation.
When monitoring a condition over time, rising ESRs may indicate increasing inflammation or a poor response to a therapy; normal or decreasing ESRs may indicate an appropriate response to treatment.
That depends on the laboratory performing the test. Results may be available the same day or, if the sample is sent to a reference laboratory, it may take a day or two for your results.
Traditional ESR tests are read by a technician one hour after the test is started. Newer methods can be read at 20-30 minutes; and there are now commercial rapid tests available that use a centrifugal method and can be read five minutes after setup. This new method is being used more widely to shorten waiting times for patients, particularly in emergency departments.
Inflammation can occur over the short term (acute) or over a long period of time (chronic) and can be caused by a variety of conditions and disease. Some examples include:
Your health practitioner may order the C-reactive protein (CRP) test as well as other general tests, such as a comprehensive metabolic panel (CMP) or a complete blood count (CBC), at the same time as the ESR. ESR and C-reactive protein (CRP) are both markers of inflammation. Generally, ESR does not change as rapidly as does CRP, either at the start of inflammation or as it resolves. CRP is not affected by as many other factors as is ESR, making it a better marker of inflammation. However, because ESR is an easily performed test, many healthcare practitioners still use ESR as an initial test when they think a patient has inflammation.
Examples of other tests that may be ordered based on your symptoms include antinuclear antibody (ANA), rheumatoid factor (RF), fibrinogen or serum protein electrophoresis. An elevated ESR is typically a result of two types of proteins, globulins or fibrinogen. Depending on your medical history, signs, symptoms and what your health practitioner suspects is the cause, he or she may order a fibrinogen level (a clotting protein that is another marker of inflammation) and a serum protein electrophoresis to determine which of these (or both) is causing the elevated ESR. If severe infection is suspected, a blood culture may be done.
Changes in the ESR may indicate the presence or abatement of infection or inflammation. If you have a chronic inflammatory disease, the ESR may fluctuate with the degree of severity or clinical course of your condition.
A low ESR can be seen with conditions that inhibit the normal sedimentation of red blood cells, such as a high red blood cell count (polycythemia), significantly high white blood cell count (leukocytosis), and some protein abnormalities. Some changes in red cell shape (such as sickle cells in sickle cell anemia) also lower the ESR.
Women tend to have a higher ESR, and menstruation and pregnancy can cause temporary elevations.
In a pediatric setting, the ESR test is used for the diagnosis and monitoring of children with rheumatoid arthritis or Kawasaki disease.
LOINC Observation Identifiers Names and Codes (LOINC®) is the international standard for identifying health measurements, observations, and documents. It provides a common language to unambiguously identify things you can measure or observe that enables the exchange and aggregation of clinical results for care delivery, outcomes management, and research. Learn More.
Listed in the table below are the LOINC with links to the LOINC detail pages. Please note when you click on the hyperlinked code, you are leaving Lab Tests Online and accessing Loinc.org.
|LOINC||LOINC Display Name|
|30341-2||ESR (Bld) [Velocity]|
|43402-7||ESR 15 minute reading (Bld) [Velocity]|
|82477-1||ESR Photometric method (Bld) [Velocity]|
|18184-2||ESR 2H Westergren method (Bld) [Velocity]|
|4537-7||ESR Westergren method (Bld) [Velocity]|
|4538-5||ESR Wintrobe method (Bld) [Velocity]|
|4539-3||Erythrocyte sedimentation rate Zeta Zetafuge (Bld) [Velocity]|
Sources Used in Current Review
(Aug 1, 2014) Kellner C, Erythrocyte Sedimentation Rate, Medscape Reference. Available at
https://emedicine.medscape.com/article/2085201-overview#a4. Accessed March 2018
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(October 2017) Giant Cell Arteritis - Temporal Arteritis, Arup Consult. Available online at
https://arupconsult.com/content/giant-cell-arteritis. Accessed March 2018
(Dec 30, 2017) Mayo Clinic, Sed Rate (Erythrocyte Sedimentation Rate),
https://www.mayoclinic.org/tests-procedures/sed-rate/about/pac-20384797. Accessed March 2018
(©2018) Quest Diagnostics, Sed Rate by Modified Westergren. Available at
Accessed March 2018
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