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Wheeless' Textbook of Orthopaedics
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Laboratory Studies for Gout



  - Hyperuricemia:
          - biochemical hallmark of gout is hyperuricemia, but not by itself diagnostic for gout;
          - risk of gout increases with the degree and duration of hyperuricemia;
          - more than 95% of pts w/ gout have primary hyperuricemia;
                - these pts exhibit overproduction of endogenous urate regardless of dietary intake;
                - pts w/ primary gout also have defect excreting urate;
          - note that the presence hyperuricemia in a patient with arthritis does not necessarily establish the dx of gout;
          - w/ serum urate concentrations of 9.0 mg per deciliter (540 µmol / lit), incidence of acute gout is only about 5 % / year;

  - Leukocytosis:
          - there may be a left shift of immature PMNs & elevated sed rate;
  - Synovial Fluid:
          - synovial fluid leukocyte counts may approach counts seen in septic arthritis;
          - viscosity of synovial fluid is < that seen in septic or inflammatory arthritis;
          - crystals:
                - crystal examination of synovial fluid:
                - needle-like intracellular & extracellular monosodium urate crystals are seen under compensated polarized light microscopy;
                      - crystals are brightly birefringent and have negative elongation
                      - dx is made by observing negatively birefringent, needle-shaped MSU crystals engulfed by PMNs;
  - Urine Analysis:
          - note that the excretion rate of urate in these patients is usually within the normal range'
          - references:
                - Gutman AB, Yu TF. Renal function in gout. Am J Med 1957;23:600-22.
                - Simkin PA. Uric acid excretion in patients with gout. Arthritis Rheum 1979;22:98-9.












Original Text by Clifford R. Wheeless, III, MD.