Normally, about 1 mL of SF is present in each large joint:
knee, ankle, hip, elbow, wrist, and shoulder (Table 12.3).
Clinical Indications for Aspiration
¾ Arthritis of unknown etiology, manifested by effusion.
¾ Possible infectious arthritis, with or without effusion, to
¾ Effusions of known etiology, to relieve pain or to allow
Aspiration must be done under absolute aseptic
conditions. Since effusion often exists when aspiration is
indicated, 10–20 mL of fluid may usually be obtained. The
specimen is collected in 3 to 4 sterile tubes.
1. Plain tube for gross examination, evaluation of viscosity,
2. EDTA tube for cell counts and microscopic study.
3. A sterile, plain or preferably heparinized tube (precludes
clot formation) for microbiologic study.
heparinized tube for total protein, oxalate fluoride
When normal fluid drips from a syringe, a tenacious ‘string’
at least 4 cm long forms with each drop. This provides an
estimate of whether viscosity is normal, decreased (string
less than 4 cm in length), or markedly decreased (string
Another method for evaluating viscosity is to see how
far a drop of fluid can be stretched between the thumb and
index finger before breaking: fluids with very low viscosity
will behave like water. Decreased viscosity reflects
decreased hyaluronate in the synovial fluid.
This is done by adding 1 mL of synovial fluid to 20 mL of 5%
(v/v) acetic acid in a small breaker. Normally, a compact
TABLE 12.2: Grades of syphilitic spinal fluid
Investigation Grade I Grade II Grade III
Number of WBCs/cu mm 5–25 25–100 70–100
Colloidal gold curve 0000000000 0023454310 5555554310
TABLE 12.3: Presence of synovial fluid
Synovial fluid Findings SI units
Appearance Clear or colorless to pale
Transudate < 10 mg/dL lower than blood
Exudate Lower than whole blood
Transudate < Client’s serum LD
Transudate < 100/mm3 < 100 × 109
Exudate > 1000/mm3 > 1000 × 109
Cerebrospinal and Other Body Fluids 389
large clot will form, surrounded by clear solution, this is
graded as ‘good’. If a soft clot forms in a turbid solution,
this is graded as fair. A friable clot with cloudy surrounding
fluid is graded as ‘poor’ or ‘fragile’. No clot formation, with
flakes in a cloudy suspension, is graded as ‘very poor’.
Good clots do not break up when agitated, while poor clots
break up into small shreds. This procedure actually is an
estimate of synovial hyaluronate and not mucin, which is
Total and differential counts as for CSF. But the usual
leukocyte diluent with 1% glacial acetic acid precipitates
synovial fluid hyaluronate and is unsatisfactory, instead
methylene blue in saline can be used. If the fluid is very
turbid, use saline dilution or digestion with hyaluronidase
(2 mL SF incubated with 150 IU hyaluronidase for 1 hour at
37oC) may be helpful. Differential count can be done from
EDTA sample (sediment) that has been centrifuged, a film
made and stained as for peripheral blood.
LE cells are frequently seen in stained SF from patients
with systemic lupus erythematosus (SLE). Sometimes,
they can be seen in cases of rheumatoid arthritis. Large
phagocytes containing neutrophils may be found in SF
and are called ‘Reiter cells’, they are nonspecific and
may be present in effusions of varying etiology. RA cells
or ‘Ragocytes’ are neutrophils containing 0.5 µ to 1.5 µ
inclusions better seen with phase contrast microscopy.
They are seen in 94% cases of rheumatoid joint fluids
but are nonspecific for they can also be found in septic
Both wet preparation (a drop of SF put on a slide and
coverslipped) and stained films should be studied for
crystals, using polarized light to detect monosodium urate
(MSU) or calcium pyrophosphate dihydrate (CPPD). MSU
crystals appear birefringent and needle or rod shaped;
while CPPD crystals will appear birefringent and rhomboid
or rod shaped. MSU crystals are found in acute/chronic
gout joints. CPPD crystals are found in pseudogout or
Seronegative rheumatoid arthritis may have a positive
joint fluid, but this is not very specific. Decreased synovial
fluid complement (under 30% of serum level) occurs in
rheumatoid arthritis and SLE (Table 12.4).
The pleural surfaces are normally moistened by 1 to 10 mL
of fluid derived by ultrafiltration of plasma. Normal protein
concentration of this fluid is 1–2 g% with no fibrinogen
Appearance Viscosity White cells Mucin clot Protein total (Avg-g%)
Normal Straw-colored, High 200–600/25% poly’s Good 1.36 0.05
Traumatic Yellow to bloody High ± 2000/30% poly’s Good 4.27
Osteoarthritis Yellow, clear High ± 1000/20% poly’s Good 3.08 0.75 Cartilage fibrils
Low ± 10,000/50% poly’s Good 3.74 1.07
Systemic lupus Straw-colored, High ± 5000/10% poly’s Good
Low ± 12,000/60% poly’s Fragile 4.18 1.54 Urate
Tuberculous Yellow, cloudy Low ± 25,000 Fragile 5.3 2.0 Tubercle
arthritis 50–60% poly’s bacilli
Septic arthritis Grayish or bloody, Low ± 80,000/90% poly’s Fragile 5.64 2.45 Bacteria
Rheumatoid Yellow to greenish, Low ± 15,000 Fragile 4.74 1.79 Rheumatoid
arthritis cloudy 65% ± poly’s factor
TABLE 12.4: Synovial analysis in arthritis
Pleural fluid Observation SI units parameter
Appearance Clear, slightly amber
Transudate < 60 mg/dL < 1. 55 mmol/L
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