Gout and pseudogout (chondrocalcinosis, pyrophosphate arthropathy) are common disorders causing arthritis in one or few joints.
A synovial fluid sample should be taken whenever gout (sodium urate crystals) or pseudogout (pyrophosphate crystals) is suspected..
Acute arthritis in a patient with arthrosis of large joints may be due to pseudogout requiring topical treatment with a glucocorticoid and anti-inflammatory analgesics.
Brief oral courses of glucocorticoids are increasingly used for the treatment of acute gout, and treatment can be intensified by topical intra-articular injections.
After the very first gout attack, provision of dietary instructions, survey of any cardiovascular disease or risk factors for such disease, as well as their treatment, as necessary, are indicated.
The treatment of intermittent or chronic gout aims to remove monosodium urate deposits from the body to make the patient completely asymptomatic.
Plasma urate levels should be lowered to below 360 µmol/l or, in a severe disease, to below 300 µmol/l to speed up the dissolving of accumulated gouty masses.
The treatment of intermittent and chronic gout is insufficient. Providing patients with comprehensive information on the clinical picture of gout, the importance of lifestyle changes and the aims of medication, as well as regular follow-up, improve the results of treatment.
Causes and prevalence
The prevalence of gout in western countries is 1.5-2.5%. Most patients are male (80-90%).
In men over 65 and women over 85, the prevalence of gout is 7% and 3%, respectively.
Gout is preceded by hyperuricaemia for several years. About 20% of the population have serum urate levels exceeding the reference range.
The main reasons for hyperuricaemia and gout becoming more common are the increasing prevalence of the metabolic syndrome Metabolic Syndrome and renal insufficiency Treatment of Chronic Renal Failure, the increasing average age of the population and increased use of alcohol, diuretics and low-dose aspirin.
Gout rarely occurs in premenopausal women or men below 25.
In pseudogout, calcium (calcium pyrophosphate) accumulates in articular cartilage and menisci as a result of local metabolism, and may be released into the joint, causing acute inflammation.
Pseudogout occurs particularly in people over 65 with arthrosis of large joints.
There may also be hereditary forms of gout and pseudogout.
Symptoms, findings and diagnosis
Acute intermittent gout
The typical symptom is sudden nocturnal onset of redness, heat, pain and swelling of the first metatarsophalangeal joint of the big toe. Other joints that are most commonly affected are other foot joints, the ankle and the knee.
An attack may be triggered by exposure to cold, mechanical stress or injury, surgery, alcohol, starting to take antihyperuricaemic medication, diuretics or aspirin, or a meal high in purines.
The joint may be sensitive to even the lightest touch, and it is difficult or impossible to place weight on the foot.
Joints of the upper limbs are less frequently involved, and their possible involvement causes problems for differential diagnosis.
During an acute attack, the patient may have a slightly elevated body temperature.
Initially, the arthritis will resolve within a few days or in no more than a couple of weeks.
In a typical case, the diagnosis can be based on the clinical picture. A history of paroxysmal joint symptoms or high plasma urate levels support the diagnosis.
The diagnosis of gout is confirmed if a sample taken from an inflamed joint shows sodium urate crystals partly phagocytosed by leucocytes. For the preparation of synovial fluid samples for dispatch, see Investigation of Synovial Fluid.
The leucocyte count in synovial fluid is elevated (even over 50 000 × 106 /l) with a predominance of granulocytes.
During a gout attack, plasma urate levels are often low.
High urate levels and unspecific joint complaints do not confirm the diagnosis of gout.
Arthrosis Osteoarthritis of the Hip and Knee, erysipelas Erysipelas, pseudogout, purulent arthritis, seronegative spondyloarthropathy and palindromic rheumatism should be considered in differential diagnosis.
Chronic gout
Untreated, acute intermittent gout may become chronic.
Gout attacks become more frequent and longer and, finally, joints may be painful and swollen between attacks.
Tophi (subcutaneous accumulation of sodium urate) may occur particularly in fingers, wrists, ear lobes or extensor aspects of the limbs. Skeletal tophi may be associated with neurological symptoms (paresis).
A patient may have bursitis, tendinitis, cellulitis and urolithiasis.
Gout and purulent arthritis should be considered in differential diagnosis of acute pseudogout; in chronic disease, rheumatoid arthritis as well as arthrosis.
Laboratory test
ESR, CRP
Reflect the severity of the inflammatory reaction.
Oral glucocorticoids are used increasingly often, particularly in cases with relative contraindications for anti-inflammatory analgesics (abdominal discomfort, renal or cardiac failure, hypertension).
The initial dose of prednisone (or prednisolone) is 30-40 mg/day for about 3-5 days. The medication should then be reduced and withdrawn within 1-2 weeks.
The response to treatment can be intensified by giving topical intra-articular methylprednisolone.
All the above treatments can be combined.
If NSAIDs and glucocorticoids are contraindicated, interleukin-1 inhibitors (anakinra, canakinumab, rilonacept) have also been used to alleviate severe gout attacks. These medicines are very expensive and they are not officially indicated in the treatment of gout.
Colchicine is a medicine available for compassionate use, only, and not too often used in Finland. Larger doses easily cause diarrhoea.
Medication can be recommended after the first gout attack already, if the patient is less than 40 years of age or if the urate concentration is clearly increased (> 480 µmol/l) or if the patient has associated diseases.
Antihyperuricaemic medication may lower blood pressure, improve the prognosis of cardiovascular diseases and slow down the worsening of renal failure.
Medication of an asymptomatic patient may be individually considered, if the urate concentration is considerably high (particularly in renal failure).
The most common adverse effects are abdominal discomfort, rashes, elevated liver enzyme values and hypersensitivity reactions. The prevalence of a severe hypersensitivity syndrome is 0.1-0.4%. Agranulocytosis is rare.
In patients with renal insufficiency, the aim of the treatment is the same. At GFR levels > 20 ml/min normal doses, at 10-20 ml/min 100-200 mg/day and in terminal uraemia 100 mg once daily or 300 mg after dialysis.
In practice, allopurinol is started in all haematological patients on cytotoxic medication when beginning treatment.
The initial dose is 80 mg/day. A response can be seen as soon as after 2-4 weeks, and the dose should be increased, depending on the therapeutic target, up to 120 mg/day.
Used if allopurinol is not suitable or sufficiently effective.
The most common adverse effects are abdominal discomfort, rashes and hypersensitivity reactions.
The dose need not be reduced if GFR > 30 ml/min. In severe renal insufficiency, lower doses should be used, depending on the therapeutic target.
Xanthine oxidase inhibitors can also be started during an effectively treated acute gout attack, and existing medication with xanthine oxidase inhibitors should not be interrupted during an attack.
Can be used (also in combination) if xanthine oxidase inhibitors are not suitable or sufficiently effective.
Initial dose 250 mg twice daily, after two weeks 500 mg twice daily. In the beginning of treatment urine should be alkalized (pH > 6) with 1 g sodium bicarbonate 3-4 times daily for at least one month.
In acute intermittent gout, antihyperuricaemic medication can be interrupted after one year after due consideration. In some patients, serum urate levels can be kept on target by lifestyle changes and dietary treatment.
In chronic gout, very long-term or permanent medication will be needed.
A short course of oral glucocorticoids can be used for severe attacks, particularly if affecting several joints (see treatment of acute gout).
The treatment of chronic pseudogout is symptomatic (paracetamol and anti-inflammatory analgesics, as necessary). Arthrosis should be treated conservatively.
The treatment and regular follow-up of gout should be done mainly in primary health care.
Assessment in specialized care is warranted in patients with unclear diagnosis or refractory gout.
After starting antihyperuricaemic medication, follow-up in 2-3 months, checking at least basic blood count with platelet count, ALT, creatinine (GFR), urate
Further follow-up examinations every 6-12 months
References
Neogi T, Jansen TL, Dalbeth N et al. 2015 Gout classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Ann Rheum Dis 2015;74(10):1789-98. [PubMed]
Richette P, Doherty M, Pascual E et al. 2016 updated EULAR evidence-based recommendations for the management of gout. Ann Rheum Dis 2017;76(1):29-42. [PubMed]
Singh JA, Yu S. Are allopurinol dose and duration of use nephroprotective in the elderly? A Medicare claims study of allopurinol use and incident renal failure. Ann Rheum Dis 2017;76(1):133-139. [PubMed]
Drug and Therapeutics Bulletin. Latest guidance on the management of gout. BMJ 2018;362:k2893. [PubMed]