Synonym/Acronym
N/A
Rationale
To detect antibodies to the organism that causes Lyme disease.
Patient Preparation
There are no food, fluid, activity, or medication restrictions unless by medical direction.
Normal Findings
(Method: Enzyme immunoassay [EIA]) Negative; positives are confirmed either by an FDA approved EIA test that has been cleared for use in the serodiagnosis of Lyme disease or by Western blot analysis (immunoblot). The criterion for interpretation of a positive immunoblot test requires the identification of at least five specific bands.
Specific infectious organisms are required to be reported to local, state, and national departments of health. Lists of specific organisms may vary among facilities. State health departments provide information regarding reportable diseases, which can be accessed at each state health department Web site. The CDC provides information regarding national notifiable diseases at https://ndc.services.cdc.gov /search-results-year/.
Study type: Blood collected in a gold-, red-, or red/gray-top tube; related body system: .
Borrelia burgdorferi, a deer tickborne spirochete, is the organism that causes Lyme disease. Lyme disease affects multiple systems and is characterized by fever, arthralgia, and arthritis. The circular, red rash characterizing erythema migrans can appear 3 to 30 days after the tick bite. About one-half of patients in the early stage of Lyme disease (stage 1) and generally all of those in the advanced stage (stage 2, with cardiac, neurological, and rheumatoid manifestations) will have a positive test result. Some laboratories perform IgG and IgM specific testing, other laboratories use a combined method (total or IgG and IgM). Patients in remission will also have a positive test response. The presence of immunoglobulin M (IgM) antibodies indicates acute infection. The presence of IgG antibodies indicates current or past infection. However, other diseases such as anaplasmosis (formerly granulocytic ehrlichiosis), autoimmune disorders (e.g., lupus erythematosus, rheumatoid arthritis), endocarditis (bacterial), Epstein-Barr virus infection, Helicobacter pylori infection, leptospirosis, syphilis, tick-borne relapsing fever, or Treponema denticola infection can produce a positive EIA test, when the patient does not have Lyme disease.
Up until recently, the Centers for Disease Control and Prevention (CDC) had recommended a two-step testing process that begins with an EIA test and is confirmed by using a Western blot test. On July 29, 2019, the FDA cleared several newer EIA-based assays with performance characteristics that surpass those of the standard screening serologic test kits on the market. The FDA deemed the new assays appropriate for use in a modified two-step testing process that uses a second EIA test in place of the more time-consuming Western blot assay. The specific assays recently cleared by the FDA can be considered as CDC-recommended procedures indicated for the serodiagnosis of Lyme disease.
Potential Nursing Problems: Assessment & Nursing Diagnosis
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Before the Study: Planning and Implementation
Teaching the Patient What to Expect
Potential Nursing Actions
After the Study: Implementation & Evaluation Potential Nursing Actions
Treatment Considerations
Infection
Clinical Judgement
Follow-Up and Desired Outcomes