Polyarthritis



by Nathan Wei, MD, FACP, FACR

Nathan Wei is a nationally known board-certified rheumatologist and author of the Second Opinion Arthritis Treatment Kit. It's available exclusively at this website... not available in stores.

Click here: Second Opinion Arthritis Treatment Kit




The term “polyarthritis” means inflammation of more than one joint. (Technically, the term “oligoarticluar arthritis “is used when 4 or fewer joints are inflamed.)

Patients with inflammatory polyarthritis (i.e., inflammation in more than 4 joints) are a diagnostic and management challenge.

When symptoms are of recent onset, the range of possible diagnoses is great. Certain viruses including those that cause rubella, and mumps, human parvovirus B19 and some enteroviruses can cause acute polyarthritis; however, these viral arthritides normally subside within 6 weeks without residual complications.

The beginning stages of acute hepatitis B infection and infection with the Lyme disease agent, Borrelia burgdorferi, may include polyarthritis. The former is recognized by the signs of hepatitis, while the latter requires a high index of suspicion (i.e., a history of tick bite or a typical rash on a patient from an endemic area) and often involves only 1 or 2 large joints.

In patients who are under 50 years of age with joint pain and swelling lasting longer than 6 weeks the diagnoses to be considered include rheumatoid arthritis, psoriatic arthritis, other seronegative spondyloarthropathies and SLE.

In patients past the age of 50 years, crystal-induced synovitis should also be considered. Osteoarthritis may also cause considerable inflammation in the affected joints. For most of these conditions specific therapies aimed at controlling inflammation, preserving range of motion in the joint and preventing joint damage are successful in decreasing morbidity and improving quality of life.

The patient with symptoms in many joints requires a careful history and physical examination. If there is morning stiffness lasting more than 30 minutes or stiffness after sitting, the joint complaints are likely to be caused by inflammation; a history of joint swelling can confirm the presence of inflammation.

However, this is not an absolute since patients with fibromyalgia, a disease that is not associated with inflammation may have prolonged morning stiffness and pain and also have subjective joint swelling.

A history of psoriasis in the patient or a family member is an important clue to the possibility of psoriatic arthritis. A history of iritis or inflammatory bowel disease, both of which are associated with seronegative spondyloarthropathies may be detected.

A recent episode of infectious diarrhea or genitourinary infection are clues to possible Reiter's syndrome. Does the patient have symptoms suggestive of SLE (e.g., photosensitive or malar rash, alopecia or pleurisy)? Is there a past history of acute episodes of arthritis or gout? Are the joints tender or swollen? Is movement limited? The choice of laboratory tests that may help depend on the differential diagnosis.

The typical patient with rheumatoid arthritis has inflammation in the wrist and MCP or metatarsophalangeal (MTP) joints, or both, that persists beyond 6 weeks. Among patients under 50 years of age more women are affected, but after age 50 incidence is equal for men and women. Morning stiffness and "gelling" (stiffness during the day with prolonged sitting) are almost always present, and swelling of affected joints is clear with careful examination. The condition may be intermittent at the start, but within weeks to months the symptoms become persistent and more disabling.

A positive rheumatoid factor test supports the diagnosis; however, as many as 30% of those affected have negative test results. A positive test for anti-CCP can help because it is more specific for RA. Early inflammatory changes in the small joints can be detected on both diagnostic ultrasound as well as MRI. If the patient has had active polyarthritis for more than 1 year, joint erosion may be seen on x-rays of the hand or foot.

Useful laboratory tests for patients with recent onset inflammatory polyarthritis may include complete blood count, erythrocyte sedimentation rate, C-reactive protein, rheumatoid factor test, anti-CCP, serum chemistries, and urinalysis. Erythrocyte sedimentation rate is an inexpensive measure of disease activity in those with rheumatoid arthritis; however, the test is not diagnostic and rates are not elevated in all patients affected. A positive test result for rheumatoid factor is helpful but not essential to confirm the clinical impression of rheumatoid arthritis in the setting of symmetric inflammatory polyarthritis.

The importance of diagnosing rheumatoid arthritis cannot be overemphasized — early intervention with DMARDs as well as biologics has been shown to improve long-term outcomes, and once joint damage has occurred erosion and joint instability are irreversible.

If rheumatoid arthritis is mild and in its early stages many rheumatologists favour using hydroxychloroquine (Plaquenil) because it is safe and convenient. If control is suboptimal after 2 months, other DMARDs are often prescribed.

A recent study reported some efficacy with minocycline for patients with early rheumatoid arthritis. However, long-term efficacy data for patients treated with minocycline are not available, and x-rays show that damage progresses at the same rate as in placebo-treated patients.

If a patient has moderate or severe rheumatoid arthritis, especially if the rheumatoid factor is positive, methotrexate is the drug of choice. Methotrexate is relatively convenient and well tolerated. Sulfasalazine is safe as a second-line agent and can be used in combination with methotrexate and other DMARDs.

There is frequently a delay between the presentation of polyarthritis and the confirmed diagnosis, and there is always a delay before a prescribed DMARD has the expected benefit. When optimal DMARD therapy or a combination of DMARDs does not control synovitis, low-dose prednisone can provide symptom relief, acceptable low toxicity and joint protection.

Biologics should be started within three months of diagnosis if disease is either not in remission or is not at an acceptable low disease level.

The aim of therapy is to minimize pain, stiffness and joint swelling; retard joint damage; and reduce future disability.

Psoriatic arthritis is almost as common as rheumatoid arthritis. This condition should be suspected when the patient or the patient's family has a history of psoriasis, when distal interphalangeal joints are affected or when there is a history of unexplained chronic or recurring back pain with prolonged inactivity. Another common feature of psoriatic arthritis and the spondyloarthropathies is bursitis or enthesitis (i.e., inflammation of the muscular or tendinous attachment to bone).

Typical examples of bursitis, tendinitis and enthesitis include trochanteric bursitis, Achilles tendinitis and lateral epicondylitis. Heel pain or plantar fasciitis are commonly associated with psoriatic arthritis, and nails may show pitting and onycholysis. Careful examination may reveal psoriatic plaques on the scalp or ears that the patient has not noticed. Interestingly, the severity of psoriasis has little correlation with the presence or severity of psoriatic arthritis.

Psoriatic arthritis may be indistinguishable from rheumatoid arthritis in onset and progression, and there are no diagnostic laboratory tests for psoriatic arthritis. However, it more typically is asymmetric or monoarticular. Most cases of psoriatic arthritis are controlled with NSAIDs; for those whose arthritis is not satisfactorily controlled with NSAIDs and for those who are experiencing joint damage the DMARDs and biologics used for the treatment of rheumatoid arthritis are effective.

Seronegative spondyloarthopathies such as reactive arthritis and Reiter's syndrome most commonly present as asymmetric oligoarthritis affecting the lower extremity joints. Reactive arthritis is an inflammatory arthritis that occurs as a consequence of infection at a remote site.

It should be suspected when there is a recent history of diarrhea, chlamydial infection, unexplained genitourinary symptoms, prostatitis, cystitis or conjunctivitis. Reiter's syndrome is a reactive arthritis that occurs within 3 weeks of a chlamydia infection of the genitourinary tract or after an intestinal infection, typically caused by Salmonella spp., Shigella spp., Campylobacter spp. or Yersinia spp. Extra-articular symptoms associated with the full-blown syndrome include conjunctivitis, circinate balanitis and hyperkeratotic skin lesions on the soles called keratoderma blennorrhagica.

The triggering infection should be treated as appropriate; screening of contacts at risk must be included in the management of patients with genitourinary reactive arthritis and selected patients with intestinal Reiter's syndrome. Management of the arthritis must be individualized and may include NSAIDs, oral or intra-articular steroids and, in resistant cases, DMARDs.

Patients with SLE (female:male ratio is about 10:1) frequently present with polyarthritis — typically a peripheral polyarthritis with symmetric involvement of both small and large joints. Symptoms reflect multisystem involvement, particularly photosensitivity, unexplained rashes, malar rash, pleuritic chest pain, history of seizures, oral ulcers, hair loss, Raynaud's phenomenon, fevers and sweats. Deformities including subluxation at the MCP joints, ulnar deviation, "swan neck" and boutonniere deformities (Jaccoud's arthropathy) may develop in about approximately 15% of patients with SLE.

An antinuclear antibody test is a useful screening test because a negative test result will virtually exclude SLE. If the test is positive and there is clinical suspicion of multisystem disease, the physician should consider further lab tests.

For SLE patients without serious internal organ involvement hydroxychloroquine is the drug of choice because it has been shown to improve disease control, prevent flares and improve long-term outcomes. Arthritis and pleurisy respond to NSAIDs. Steroid medications may also be required in low and moderate doses either intermittently or continuously. Immunosuppressant drugs are required for those with serious internal organ involvement (e.g., cerebritis or glomerulonephritis).

Diseases such as primary Sjögren's syndrome, polymyositis, dermatomyositis, limited and diffuse scleroderma and mixed connective tissue disease may also manifest as polyarthritis.

Primary Sjögren's syndrome may be extremely difficult to differentiate from rheumatoid arthritis when the main feature is polyarthritis. Prominent muscle weakness is a clue to myositis, and patients with scleroderma almost always have sclerodactyly (fusiform swelling of the fingers) and Raynaud's phenomenon. Mixed connective tissue disease may present with features of rheumatoid arthritis in conjunction with those of other autoimmune diseases.

Elderly-onset polyarthritis is distinguished from rheumatoid arthritis on the basis of a negative rheumatoid factor, a markedly elevated erythrocyte sedimentation rate, usual age of onset over 60 years and marked improvement in response to low doses of steroids. Although it is uncommon it is not rare. Onset is often sudden, and there is typically swelling of the wrists and pain, stiffness and restriction of the shoulder joints. The clinical course of this syndrome closely resembles polymyalgia rheumatica in its sudden onset and response to prednisone.

Polymyalgia rheumatica typically presents with shoulder and pelvic girdle involvement and an absence of clinically detectable synovitis; elderly onset polyarthritis syndrome presents with peripheral synovitis that may be indistinguishable from seronegative rheumatoid arthritis except in its response to prednisone and its course over time. The synovitis disappears with 10–15 mg/day of prednisone, and the condition is nonprogressive and nonerosive. Once the disease is under control the dose of prednisone can be lowered every 1–3 months, aiming for the lowest dose that will control symptoms. Strategies to prevent steroid-induced osteoporosis, specifically anti-osteoporosis drugs, are required. If the prednisone dose cannot be lowered or if pain and swelling persist in spite of low-dose prednisone, the physician should reassess the patient and consider alternative diagnoses, such as rheumatoid arthritis, psoriatic arthritis, temporal arteritis and other vasculitides.

Gout or pseudogout can result in inflammatory polyarthritis. The typical patient with polyarticular gout has had acute attacks of monoarthritis and typical attacks of gout for many years. Any joint may be affected and, in severe cases, the patient may have fever and have an elevated white blood cell count; tophi are commonly found on careful examination. Patients are usually over 50 years of age or have identifiable risk factors for gout such as diuretic use, renal disease or alcohol abuse. Although serum uric acid level is often high this is not always the case. Synovial fluid aspiration will demonstrate the typical urate crystals.

Calcium pyrophosphate dihydrate deposition disease (i.e., pseudogout) may also cause polyarthritis. Patients are usually over 60 years of age, and this condition commonly coexists with osteoarthritis. The presentation may resemble rheumatoid arthritis — typical distribution of joint inflammation includes the wrists, knees, shoulders, hips and finger joints. X-rays commonly show chondrocalcinosis, but the diagnosis is confirmed when calcium pyrophosphate dihydrate crystals are found in the synovial fluid of inflamed joints.

Osteoarthritis affecting DIP, PIP and CMC joints may be associated with symptoms and signs of inflammation. Onset is common in perimenopausal women, and there is often a family history of Heberden's osteoarthritis. Patients complain of joint tenderness and episodes of swelling usually in 1 or several finger joints at a time. Examination discloses Heberden's and Bouchard's nodes in finger and sometimes toe joints; MCP and MTP joints are not affected. Radiographs of affected joints show narrowing, osteophytes, sclerosis and, in the advanced stages, PIP or DIP joint erosions. Because of the prominent involvement of DIP joints, it may be difficult to distinguish inflammatory osteoarthritis from psoriatic arthritis, which may also develop in older patients. It is important to remember that rheumatoid arthritis can occur in patients who also have osteoarthritis.



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