Complement Assay
Test Description:
The term complement refers to the 20 serum beta-globulin protein enzymes which
are a part of the immune system response to antigen-antibody reactions. The complement
system is necessary for phagocytosis, destruction of foreign bacteria, and
mediation of the overall inflammatory response. Activation of the complement cascade
may occur by way of the classic pathway, in which activation is stimulated by
an antigen-antibody response, or by the alternate pathway, in which polysaccharides,
endotoxins, or immunoglobulins are the stimulating forces. Regardless of the
stimulus, the final product of the complement cascade’s work is a complex protein
capable of destroying the cell membrane of the antigen.
To assess the functioning of the complement system and to determine whether
deficiencies of these proteins are contributing to increased infections or increased
autoimmune activity, two of the components are typically measured. C3 is involved
in both the classic and alternate pathways and composes about 70% of the total
complement protein. C4 is involved in only the classic pathway. Individuals found to
be deficient in C4 have a lowered resistance to infection.
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Normal Values
C3: 83–177 mg/dL (0.83–1.77 g/L SI units)
C4: 15–45 mg/dL (0.15–0.45 g/L SI units)
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Possible Meanings of Abnormal Values
C3 Complement
Increased Decreased
Infection Anemia
Inflammatory Acute glomerulonephritis
Malignancy with metastasis Anorexia nervosa
Necrotizing disorders Arthralgias
Rheumatic fever Celiac disease
Rheumatoid arthritis Chronic active hepatitis
Chronic liver disease
Cirrhosis
Congenital C3 deficiency
Disseminated intravascular coagulation
Immune complex disease
Malnutrition
Multiple myeloma
Multiple sclerosis
Renal transplant rejection
Septicemia
Serum sickness
Subacute bacterial endocarditis
Systemic lupus erythematosus
Uremia
C4 Complement
Increased Decreased
Cancer Chronic active hepatitis
Juvenile rheumatoid arthritis Congenital C4 deficiency
Rheumatoid spondylitis Cryoglobulinemia
Glomerulonephritis
Hereditary angioedema
Immune complex disease
Lupus nephritis
Renal transplant rejection
Serum sickness
Subacute bacterial endocarditis
Systemic lupus erythematosus
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Contributing Factors to Abnormal Values
• Hemolysis of the sample may alter test results.
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Interventions/Implications
Pretest
• Explain to the patient the purpose of the test and the need for a blood sample to be drawn.
• No fasting is required before the test.
Procedure
• A 7-mL blood sample is drawn in a red-top collection tube.
• Gloves are worn throughout the procedure.
Posttest
• Apply pressure at venipuncture site. Apply dressing, periodically assessing for continued
bleeding.
• Label the specimen and transport it to the laboratory.
• Report abnormal findings to the primary care provider.
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Clinical Alerts
• Risk of infection at venipuncture site due to possible immunocompromised state.
Teach patient to notify health-care provider if drainage, redness, warmth, edema,
or pain at the site or fever occur.
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