The term gout is derived from the Latin gutta, which means a drop. In the 13th century, it was thought that gout resulted from a drop of evil humor affecting a vulnerable joint.
Causes of hyperuricemia
¤ Nutrition: food rich in purine and fructose, fasting
¤ Myelo- and lymphoproliferative syndromes
¤ Psoriasis, tumor lysis syndrome
¤ Drugs: loop and thiazide diuretics, cyclosporine, ASS
¤ Renal: chronic renal failure was different. Aetiology
¤ Metabolic/endocrine: obesity, dehydration,hypothyroidism, lactic acidosis, ketosis
¤ Alcohol, shock
is a disease in which tissue deposition of monosodium urate (MSU)
crystals occurs as a result of hyperuricemia (MSU supersaturation of
extracellular fluids), resulting in one or more of the following
Tophi (aggregated deposits of MSU occurring in articular, osseous, cartilaginous, or soft tissue areas)
Uric acid nephrolithiasis
Gout is the most common cause of inflammatory arthritis in men over 40 years of age.
Hyperuricemia and gout are strongly associated with obesity and the metabolic syndrome.
Dietary and lifestyle modifications are recommended for the management of gout.
The rheumatologist should always look for gout in all undiagnosed joint conditions even if the serum uric acid level is normal, the involved joint is atypical, and the flare is chronic and polyarticular.
The patient’s comorbid medical conditions should be assessed, including renal and hepatic function, to guide the safest treatment options for acute gout and chronic symptomatic hyperuricemia, with a serum uric acid goal of <6.0 mg/dL.
- Prevalence - depending on country - at 0.9-2.5
- Hyperuricemia, with or without crystal deposits, is associated with an increased risk of developing renal, cardiovascular and metabolic complications and increased cardiovascular and all-cause mortality
Joints involved in gout:
The joints of the lower limbs are typically involved more often than those of the upper limbs. The first metatarsophalangeal (MTP) joint of the great toe is involved in >50% of initial attacks and over time is affected in >90% of patients.
Acute gout of the first MTP is termed podagra. In order of frequency of involvement after the MTP joints are the instep, ankle, heel, knee, wrist, fingers, and elbow.
- Joint effusion (earliest sign)
- Preservation of joint space until late stages of the disease
- Absence of periarticular osteopenia
- Eccentric erosions
- Typical appearance “punched-out” erosions with sclerotic margins in a marginal and juxta-articular distribution, with overhanging edges
- Punched-out lytic bone lesions
- Overhanging sclerotic margins
- Avascular necrosis
- Mineralisation is normal
- Surrounding soft tissues
- Tophi: pathognomonic
- Olecranon and prepatellar bursitis
- Periarticular soft tissue swelling due to crystal deposition in tophi around the joints is common
- Soft tissue swelling may be hyperdense due to the crystals, and the tophi can calcify (uncommon in the absence of renal disease)
Diagnostics: Detection of urate crystals in the joint point or from tophus material: Needle-shaped, negative in the polarization microscope birefringent crystals
Ultrasound: Double contour is very specific. While there can be variation in appearance, tophi tend to be hyperechoic, heterogeneous, have poorly defined contours. They can be multiple grouped and surrounded by anechoic halos.
DUAL-CT: Imaging of the crystals
MRI (not necessary):Signal characteristics of gouty tophi are usually: T1: isointense T2: variable, majority of lesions are characteristically heterogeneously hypointense T1 C+ (Gd): tophus often enhances
Management of acute attacks of gout
- non-steroidal anti-inflammatory drugs (NSAIDs)
- peroral steroids at a dosage of 20-40 mg prednsion equivalent for 3-6 days or prednisone per os: 0.5mg/kg bw/d for 3-5 days, followed by a period of 7-10 days > Option for severe renal failure
- Colchicine (Colchicine: (not authorised in Switzerland). Dosage: 1mg immediately, 0.5mg after 1 hour, then from the 2nd day: 2x0.5mg per day. Dose adjustment for renal failure (GFR 30-60), hepatic failure Child A/B, weak CYP3A4 inhibitors: 1mg first day, 1x0.5mg from day 2. For therapy with strong CYP3A4 inhibitors: avoid colchicine)
- Infiltration of corticoids
- Interleukin-1 inhibitors (Anakinra or Canakinumab) for Patients with frequent attacks and contraindication for NSAIDs, colchicines, steroids: IL-1 Blocker: Anakinra (not approved in CH) 100mg s.c. 1x/d (approx. Fr. 60/injection). Canakinumab (approved for CAPS, syst. Juvenile idipath. Arthritis) 150mg s.c. every 3 months (approx. Fr. 14'000/injection)
Management of hyperuricemia
- Limit the consumption of purine-rich foods such as meat or seafood
- give preference to low-fat milk products as sources of protein
- avoid alcohol (especially beer and spirits) and sweet drinks containing fructose and fruit juices as far as possible
- drink enough water
- Regular consumption of coffee and cherry juice is protective
- For obesity reduction diet
- Does the patient have medication that causes hyperuricemia?aspirin, diuretics (thiazide diuretics, loop diuretics), cyclosporine and other cytotoxic/cytostatic drugs, ethambutol/pyrazinamide, levodopa, nicotinic acid. Consider switching to drugs with uric acid-lowering effects: Losartan, calcium antagonists.
Drug therapy of hyperuricemia
- Consider the use of urate lowering therapy (ULT) for every patient with a definitive diagnosis of gout. Objective: Prevention of the formation of urate crystals, dissolution of crystals, tophi. Correctly performed prophylaxis can prevent further gout attacks.
- ULT is indicated in patients with two or more attacks of gout per year and in the presence of tophi, urate arthropathy and/or kidney stones
- Target value <360μmol/l (= 6 mg/dl)
- lower target value (<300 μmol/l) for severe gout (tophi, chronic arthropathy, frequent attacks)
- ULT especially in younger patients (<40 years), in case of very high uric acid levels (>480 μmol/l) and/or comorbidities (impaired renal function, hypertension, coronary heart disease, heart failure)
- Start ULT after the acute gout flare has subsided (e.g. after one week) and adjust the low dose until the target value is reached.
- Do not pause if gout occurs below ULT, do not pause ULT
- In principle, continue therapy in the long term
- advise patients that initiating ULT may cause acute attacks (often in the first three to six months of therapy)
- In the first three to six months of ULT use prophylaxis with NSAID, colchicine (0.5-1 mg daily) or low-dose corticosteroids p.o.
- ad Colchicine: dose adjustment is necessary in renal and liver failure
- ad Colchicine: interaction with cytochrome 3A4 inhibitors such as protease inhibitors, calcium antagonists and antimycotics type triazoles
- By gradually increasing the ULT dose, seizure rates can be reduced and, in the case of allopurinol, the occurrence of allergic side effects can be minimized
Xanthine oxidase inhibitors (allopurinol, febuxostat)
- prefer allopurinol in patients without impaired renal function
- Start dose of Allopurinol at 100mg/day, increase by 100 mg/day (up to 900mg) every two to five weeks until the uric acid target value is reached. Only 28% reach therapy goal with 300mg but 78% with 600mg!
- Adjust allopurinol dose to creatinine clearance in case of impaired kidney function
- If kidney function improves under Allopurinol, increase dosage
- If serum uric acid target value is not reached with allopurinol, switch to febuxostat (febuxostat reaches uric acid target value more frequently): Non-purine-based XO inhibitor. No dose adjustment for renal failure (KreaCl≥30). Dosage: 40mg 1x/d, after 2-4 Wo increase to 80mg/d if uric acid >360umol/l
- Febuxostat can be used without dose adjustment in patients with mild or moderate kidney function impairment.
- (Probenecid, Lesinurad) recommended as second-line therapy alone or in combination with allopurinol
- Not for kidney stones
- Probenecid (Santuril®): also possible as monotherapy. Dose initial 2x250mg, after 1 Wo 2x500mg/d. Contraindicated for renal insufficiency/nephrolithiasis
- Lesinurad in combination with allopurinol is indicated if serum uric acid targets are not achieved with allopurinol alone, dose of Lesinurad is 200 mg 1 × daily (morning), only in combination with allopurinol. Lesinurad (Zurampic®): URAT1 inhibitor, approved in combination with allopurinol Dose 200mg/d, no therapy start for creatinine clearance <45