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Diagnosis & Evaluation

A. Examination of the Patient

Two helpful clinical clues for diagnosing arthritis are the joint pattern and the presence or absence of extra-articular manifestations. The joint pattern is defined by the answers to three questions: (1) Is inflammation present? (2) How many joints are involved? and (3) What joints are affected? Joint inflammation manifests as warmth, swelling, and morning stiffness of at least 30 minutes' duration. Overlying erythema occurs with the intense inflammation of crystal-induced and septic arthritis. Both the number of affected joints and the specific sites of involvement affect the differential diagnosis (Table 22-1. Diagnostic Value of the Joint Pattern). Some diseases-gout, for example-are characteristically monoarticular, whereas other diseases, such as rheumatoid arthritis (RA), are usually polyarticular. The location of joint involvement can also be distinctive. Only two diseases frequently cause prominent involvement of the distal interphalangeal (DIP) joint: osteoarthritis and psoriatic arthritis. Extra-articular manifestations such as fever (eg, gout, Still disease, endocarditis, vasculitis, SLE), rash (eg, SLE, psoriatic arthritis, inflammatory myositis), nodules (eg, RA, gout), or neuropathy (eg, vasculitis) narrow the differential diagnosis further.

Table 22-1. Diagnostic value of the joint pattern.
CharacteristicStatusRepresentative Disease
Inflammation

Present

Absent

Rheumatoid arthritis, SLE, gout

Osteoarthritis

Number of involved joints

Monoarticular

Oligoarticular (2-4 joints)

Polyarticular ( 5 joints)

Gout, trauma, septic arthritis, Lyme disease, osteoarthritis

Reactive arthritis, psoriatic arthritis, IBD

Rheumatoid arthritis, SLE

Site of joint involvement

Distal interphalangeal

Metacarpophalangeal, wrists

First metatarsal phalangeal

Osteoarthritis, psoriatic arthritis (not rheumatoid arthritis)

Rheumatoid arthritis, SLE, calcium pyrophosphate deposition disease (not osteoarthritis)

Gout, osteoarthritis

B. Arthrocentesis and Examination of Joint Fluid

If the diagnosis is uncertain, synovial fluid should be examined whenever possible (Table 22-2. Examination of Joint Fluid). Most large joints are easily aspirated, and contraindications to arthrocentesis are few (eFigures 22-1, 22-2, 22-3, 22-4, 22-5, 22-6, 22-7). The aspirating needle should never be passed through an overlying cellulitis or psoriatic plaque because of the risk of introducing infection. For patients who are receiving DOACs or long-term anticoagulation therapy with warfarin, joints can be aspirated with a small-gauge needle (eg, 22F); the INR should be less than 3.0 for patients taking warfarin.

Table 22-2. Examination of joint fluid.
Measure(Normal)Group I (Noninflammatory)Group II (Inflammatory)Group III (Purulent)
Volume (mL) (knee)<3.5Often >3.5Often >3.5Often >3.5
ClarityTransparentTransparentTranslucent to opaqueOpaque
ColorClearYellowYellow to opalescentYellow to green
WBC per mcL<200 (0.2 × 109 /L)<2000 (2.0 × 109 /L)2000-75,0001 (2.0-75.0 × 109 /L)>100,0002 (100 × 109 /L)
Polymorphonuclear leukocytes<25%<25%50% or more75% or more
CultureNegativeNegativeNegativeUsually positive2

1 Gout, rheumatoid arthritis, and other inflammatory conditions occasionally have synovial fluid WBC counts >75,000/mcL (75 × 109 /L) but rarely >100,000/mcL (100 × 109 /L).

2 Most purulent effusions are due to septic arthritis. Septic arthritis, however, can present with group II synovial fluid, particularly if infection is caused by organisms of low virulence (eg, Neisseria gonorrhoeae) or if antibiotic therapy has been started.

eFigure 22-1. A: Lateral View of the Ankle




A: Lateral view of the ankle. B: Injection of the true ankle joint, just medial to the extensor hallucis longus. C: Injection of the subtalar joint, just inferior and anterior to the tip of the lateral malleolus. (Used, with permission, from Imboden JB et al. Current Diagnosis & Treatment: Rheumatology, 3e. McGraw-Hill, 2013.)

eFigure 22-2. A: Anterior View of the Shoulder





A: Anterior view of the shoulder. B: Technique for infiltration of the bicipital groove of the humerus with a glucocorticoid preparation (treatment for biceps tendinitis). C: Injection of the glenohumeral joint from the anterior position. D: Injection of the shoulder just inferior to the acromion (the preferred approach to shoulder injection). (Used, with permission, from Imboden JB et al. Current Diagnosis & Treatment: Rheumatology, 3e. McGraw-Hill, 2013.)

eFigure 22-3. A: Dorsum of the Left Wrist



A: Dorsum of the left wrist. B: Injection of the radiocarpal joint. (Used, with permission, from Imboden JB et al. Current Diagnosis & Treatment: Rheumatology, 3e. McGraw-Hill, 2013.)

eFigure 22-4. A: Lateral View of the Knee




A: Lateral view of the knee. B: Optimal positioning of the knee for joint injection. C: Optimal positioning of the knee for joint aspiration. (Used, with permission, from Imboden JB et al. Current Diagnosis & Treatment: Rheumatology, 3e. McGraw-Hill, 2013.)

eFigure 22-5. A: Lateral View of the Elbow Flexed to 90 Degrees




A: Lateral view of the elbow flexed to 90 degrees. B: Injection of the ulnohumeral joint, into the olecranon fossa. C: Injection of the lateral epicondyle, just proximal to the radial head. (Used, with permission, from Imboden JB et al. Current Diagnosis & Treatment: Rheumatology, 3e. McGraw-Hill, 2013.)

eFigure 22-6. Injection of the Metacarpophalangeal Joint


Injection of the metacarpophalangeal joint. (Used, with permission, from Imboden JB et al. Current Diagnosis & Treatment: Rheumatology, 3e. McGraw-Hill, 2013.)

eFigure 22-7. Injection of the Trochanteric Bursa


Injection of the trochanteric bursa. (Used, with permission, from Imboden JB et al. Current Diagnosis & Treatment: Rheumatology, 3e. McGraw-Hill, 2013.)

1. Types of Studies

A. GROSS EXAMINATION- Clarity is an approximate guide to the degree of inflammation. Noninflammatory fluid is transparent, mild inflammation produces translucent fluid, and purulent effusions are opaque. Traumatic taps, trauma, and bleeding disorders are the most common causes of bloody effusions.
B. CELL COUNT- Normal synovial fluid contains less than 200 white cells/mcL (0.2 × 109 /L). Higher synovial fluid white cell counts can discriminate between noninflammatory (less than 2000 white cells/mcL [2.0 × 109 /L]), inflammatory (2000-75,000 white cells/mcL [2.0-75 × 109 /L]), and purulent (greater than 100,000 white cells/mcL [100 × 109 /L]) joint effusions. Synovial fluid glucose and protein levels add little information and should not be ordered.
C. MICROSCOPIC EXAMINATION- Compensated polarized light microscopy distinguishes monosodium urate (gout, negatively birefringent) and calcium pyrophosphate (pseudogout, positive birefringent) crystals. Gram stain has specificity but limited sensitivity (50%) for septic arthritis.
D. CULTURE- Bacterial cultures and special studies for gonococci, tubercle bacilli, or fungi are ordered as appropriate.

2. Interpretation

Synovial fluid analysis is diagnostic in infectious or microcrystalline arthritis. Although the severity of inflammation in synovial fluid can overlap among various conditions, the synovial fluid white cell count is a helpful guide to diagnosis (Table 22-3. Differential Diagnosis by Joint Fluid Groups).

Table 22-3. Differential diagnosis by joint fluid groups.
Noninflammatory (< 2000 white cells/mcL [< 2 × 109 /L])Inflammatory (2000-75,000 white cells/mcL [2.0-75.0 × 109 /L])Purulent (>100,000 white cells/mcL [>100 × 109 /L])Hemorrhagic

Osteoarthritis

Traumatic arthritis

Osteonecrosis

Charcot arthropathy

Rheumatoid arthritis

SLE

Polymyositis or dermatomyositis

Systemic sclerosis

Systemic vasculitides

Polychondritis

Gout

Calcium pyrophosphate deposition disease

Hydroxyapatite deposition disease

Juvenile rheumatoid arthritis

Ankylosing spondylitis

Psoriatic arthritis

Reactive arthritis

IBD arthritis

Hypogammaglobulinemia

Sarcoidosis

Rheumatic fever

Indolent/low virulence infections (viral, mycobacterial, fungal, Whipple disease, Lyme disease)

Septic arthritis (bacterial)

Trauma

Pigmented villonodular synovitis

Tuberculosis

Neoplasia

Coagulopathy

Charcot arthropathy

Reproduced with permission from JH Klippel, JH Stone et al. Primer on the Rheumatic Diseases, 13th ed. Springer, 2008.

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