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Serum complements. Inappropriate use in patients with suspected rheumatic disease

T M Bush1, T L Shlotzhauer, W Grove

  • 1Department of Medicine, Santa Clara Valley Medical Center, San Jose, Calif.

Insights

Serum complement testing offers limited diagnostic value for suspected rheumatic diseases. Clinicians should consider judicious use of complement assays, potentially starting with a single C3 test, to improve cost-effectiveness.

Area of Science:

  • Rheumatology
  • Immunology
  • Clinical Diagnostics

Background:

  • Serum complement testing is established for inherited deficiencies and glomerulonephritis, but its utility in rheumatic diseases is less certain.
  • Complement tests were frequently ordered for patients referred to a rheumatology clinic.
  • The study aimed to clarify the rationale and impact of complement testing in rheumatic disease patients.

Purpose of the Study:

  • To determine the clinical rationale for ordering serum complement tests in a hospital setting.
  • To evaluate the effect of complement test results on the diagnosis of rheumatic diseases.
  • To assess the diagnostic utility of complement screening in patients with suspected rheumatic conditions.

Main Methods:

  • Retrospective review of medical charts for patients with serum complement tests (C3, C4, or total hemolytic complement).
  • Identification of cases where tests were ordered for suspected rheumatic diseases.
  • Correlation of complement test results with eventual patient diagnoses.

Main Results:

  • Of 130 patients and 307 assays, 68% were for diagnostic reasons, often by nonspecialists.
  • In 28 patients with suspected rheumatic diseases, none with hypocomplementemia had connective tissue disease.
  • Rheumatic disease patients (10) had normal complement levels; 77% had multiple assays, with 24% discordant results.

Conclusions:

  • Complement screening lacks significant diagnostic value for most patients with suspected rheumatic disease.
  • Frequent performance of these tests, despite limited utility, suggests potential for cost savings through judicious use.
  • When indicated, consider a single C3 assay initially, avoiding multiple assays unless hereditary deficiency is suspected.
Abstract

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