Description

Immunoassays are subject to a number of interferences that can cause false positive or false negative test results. The clinician should be willing to question a laboratory test result that does not match the clinical picture. If a cause for the discrepancy is found, then it should be documented in the medical record to prevent problems in the future.


 

A patient at increased risk for interference in an immunoassay:

(1) multiply transfused patient

(2) patient with a history of previous false positive or negative assay

(3) multiparous woman

(4) patient with autoimmune disorder, especially rheumatoid arthritis

(5) patient with an acute infection, often viral

(6) recent immunization

(7) malignant disorder, especially multiple myeloma, malignant lymphoma, or CLL

(8) immunosuppression or immunodeficiency

 

Clinical features:

(1) A test finding does not match the clinical findings.

(2) The unexpected test finding is seen in a repeat specimen.

(3) The test utilizes an antibody in the detection system (to drug, serum protein, hormone, tumor marker, antibody to an infectious agent).

 

Possible solutions:

(1) Test for possible interfering compound (rheumatoid factor, heterophile antibody, etc.).

(2) Modify the test protocol (alter steps, switch to antibody from different species, use a blocking agent).

(3) Repeat testing later, if associated with a period of activity in an autoimmune disease or if suspect an infection with prior to development of the immune response.

(4) Perform serial dilutions of the specimen. Dilution of an interfering substance may give nonlinear results (a small dilution can result in the interference disappearing).

(5) Perform the assay using a different immunoassay platform.

 


To read more or access our algorithms and calculators, please log in or register.