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[Use of rheumatoid factor IgM analysis. A questionnaire study among the users]
B Schiøttz-Christensen1, N Grunnet
1Klinisk immunologisk afdeling, Aalborg Sygehus.
Ugeskrift for Laeger
|January 16, 1995
Summary
Rheumatoid factor (RF-IgM) analysis is frequently used for case-finding by general practitioners. Optimizing its use and understanding cut-off influences could reduce testing frequency.
Area of Science:
- Clinical Chemistry
- Immunology
- Rheumatology
Background:
- Rheumatoid factor (RF-IgM) is an antibody associated with autoimmune diseases, particularly rheumatoid arthritis.
- Understanding the utilization patterns and clinical indications for RF-IgM testing is crucial for appropriate diagnostic strategies.
Purpose of the Study:
- To investigate the demographic and clinical characteristics of patients undergoing RF-IgM analysis.
- To compare the ordering patterns and clinical indications with the laboratory results of RF-IgM tests.
- To assess the impact of different cut-off values on the interpretation of RF-IgM results.
Main Methods:
- A retrospective analysis of all RF-IgM tests performed over a one-month period.
- Physician questionnaires to gather data on clinical symptoms, other laboratory results, and testing history.
- Analysis of positive ELISA results based on a standard cut-off of 6 IU/ml.
Main Results:
- 467 RF-IgM analyses were registered in a population of approximately 300,000.
- 21% of analyses yielded a positive RF-IgM result (cut-off: 6 IU/ml).
- Only 31% of patients presented with clinical symptoms suggestive of rheumatoid arthritis.
- 67% of tests were ordered by general practitioners, indicating significant use in case-finding.
- Altering the cut-off to 15 or 20 IU/ml drastically reduced positive results to 14 or 12, respectively.
Conclusions:
- The RF-IgM assay is often employed for broad case-finding, potentially leading to overuse.
- More specific utilization of RF-IgM testing could help reduce its frequency.
- Clinicians receiving RF-IgM results must be aware of the significant impact of the laboratory's chosen cut-off value on test interpretation.