Prepared by :
B.Pharm, Southeast University
M.Pharm, East West University, Bangladesh
Gout is characterized biochemically as a disorder of uric
acid metabolism and clinically by hyperuricaemia and
recurrent attacks of acute arthritis. Gouty arthritis is most
frequently seen as an acute inflammation primarily in the
large toe, instep, ankle, or heel,less often in the knee or
Most hyperuricemic persons are asymptomatic between
acute attacks.Uric acid stones may form in the lumen of the
urinary tract, and progressive renal failure often occurs in the
later stages of untreated Gout.
► Urate: end product of purine metabolism
► Gout: deposition of monosodium urate crystals in tissues
► Hyperuricemia: serum urate > urate solubility (> 6.8
► And in rapid weight loss (dieting)
Breakdown of cellular nucleoprotein is increased
Excess formation of uric acid
Old aged peopleOld aged people
Diuretics, ASA,Diuretics, ASA,
Alcohol intakeAlcohol intake
Highest with beerHighest with beer
Not increased withNot increased with
High BMI (obesity)High BMI (obesity)
Diet high in meat &Diet high in meat &
• Urinary Calculi
• Gouty Nephropathy
It is essential to identify the condition early to
avoid the complications that result from a
prolonged elevated uricaemia.
• The diagnosis of acute gout can
only be made through
examination of synovial fluid
aspirated from the inflamed
• Sudden onset of acute
particularly in the foot or ankle,
should always raise the
suspicion of gout
• In 10% of patients acute gouty arthritis is
• Hyperuricaemia alone is not diagnostic of gout
as many hyper-patients with acute gout have a
normal serum uric acid concentration
• The diagnosis of gout is thus confirmed only by
microscopic examination of synovial fluid
aspirated from the affected joint
• The differential diagnosis
in acute gouty arthritis
must include septic
• Patients with commonly
present with acute
swelling and tenderness
of the joint with a fever
• Patients with joint sepsis are usually more ill
and have other systemic signs of infection
such as a swinging fever and severe malaise
• Large joint are most frequently infected, and
the joint is hot
Synovial fluid analysis (Polarized Light Microscopy)Synovial fluid analysis (Polarized Light Microscopy)
The Gold standard
Crystals intracellular during attacks
Needle & rod shapes
Strong negative birefringence
• Initial treatment of gout and its
associated hyperuricemia must
involve therapy directed
toward terminating painful
inflammatory process that is a
prominent feature of acute
• A variety of nonsteroidal
naproxen, sulindac) can be
administered either alone or in
combination with colchicine, a
relatively specific agent for use
acute gouty attacks.
Clinically used drugs ( for gout and
• NSAIDs (indomethacin, ibuprofen & naproxen )
•Narcotic Pain Relievers
Improves uric acid removal
Block uric acid production
-gastrointestinal diarrhea, nausea, vomiting, hemorrhagic
colitis, occurs in 70-80% of patients on oral therapy, less
frequent with IV therapy but may see with high doses
-bone marrow depression: cumulative toxicity
-renal dysfunction: toxic side effect seen after large doses,
Hematuria , oliguria .
-necrosis of soft tissue after extravasation : do not give IM/SQ
-may include thinning bones, poor wound healing and a
decreased ability to fight infection.
Adverse Effects (continue……)
NSAIDs( Indomethacin, Ibuprofen and
-nausea, vomiting , diarrhea constipation ,
decreased appetite, rash, dizziness ,
headache, and drowsiness.
-NSAIDs may also cause fluid retention, leading
-The most serious side effects are kidney failure,
liver failure, ulcers and prolonged bleeding
after an injury or surgery.
Adverse Effects (continue….)
-hypersensitivity: rashes +/- fever, anaphylaxis
-gastrointestinal: take with food or milk
- stomach pain and kidney stones.
-hypersensitivity reactions (uncommon) rash, may cause
bronchoconstriction in patients with ASA intolerance,
contraindicated in patients allergic to phenylbutazone /
-gastrointestinal irritation: take with food or milk
Adverse Effects (continue……)
-usually occurs within 1st
5 weeks with ampicillin
-severe hypersensitivity more common in pts
with impaired renal function
-gastrointestinal: nausea, vomiting, abdominal
-hepatomegaly/nephritis: may be manifestation
of a hypersensitivity reaction
penicillin, or other beta-lactams,
clarithromycin, erythromycin, cyclosporine,
Lithim, methotrexate and warfarin
sulfonamides and sulfonylureas , methotrexate
rifampin , penicillin antibiotics , salicylates (large doses
(>2 gms) inhibit the uricosuric effect of probenecid )
A 45 years old asymptomatic aircrew reported for periodic
medical examination. Except for being overweight (BMI:
27kg/m2), the general and systemic examination was within
normal limits. The routine laboratory investigations revealed
a serum uric acid of 8.8 mg/dl. The individual denied
consumption of alcohol/ medication and had no symptoms
referable to joints. The various issues involved in the
aeromedical decision making in this aircrew are as follows -
a) Does he require medication for his condition?
b)What are the underlying pathology and the prognosis?
c) What life style and preventive therapy will you suggest
to this aircrew?
a) Does he require medication for
• The serum uric acid level in the body is a function of
balance between the breakdown of purine and the
rate of urate excretion.
• The normal serum uric acid as measured by
automated enzymatic (uricase) method is less than
7.0 mg/dl for adult male and any value more than 7.0
mg/dl is considered to represent hyperuricemia.
• As the air crew has a creatinine level more than the
normal level (8.8 mg/dl), Yess, he needs some
b) What are the underlying pathology
and the prognosis?
• The laboratory investigations can be divided in to the
1. Test directed towards establishing the diagnosis
(a) Serum uric acid
(b) Joint aspiration and demonstration of strongly
birefringent needle shaped intra and extracellular crystals in
cases of gout.
2. Test directed towards the pathophysiology
- 24 hours urinary uric acid estimation: Excretion of >800
mg of uric acid per 24hr on a regular diet suggests
overproduction of purine as the etiology. It is also useful in
assessing the risk of stone formation. and in deciding whether
to start uricosuric therapy or not.
b) What are the underlying pathology and
3. Tests directed towards establishing the etiology
(a) Complete blood counts: for hemolytic anemia or hematological
(b) Liver function test: base line liver function is required before initiation
of allopurinol therapy. It also aids in the detection of metabolic disorders.
(c) Blood sugars: for underlying diabetes mellitus and glycogen storage
(d) Renal function test and serum electrolytes: for underlying renal
disease and acidosis
(e) Serum calcium and phosphate: for hyperparathyroidism, sarcoidosis
(f) Thyroid stimulating hormone: to rule out hypothyroidism.
4. Radiological evaluation
Radiological feature of advanced chronic gouty arthritis includes soft tissue
masses, cystic changes and well-defined erosions with sclerotic margins
and overhanging bony edges.
c) What life style and preventive therapy will
you suggest to this aircrew?
Life StyleLife Style
c) What life style and preventive therapy will
you suggest to this aircrew? (Cont.)
a) High protein diet is associated with increase
urinary uric acid excretion and may reduce the
serum uric acid level. The amount of red meat
and seafood however has to be reduced. Diet
should include, consumption of more of low
fat dairy product and complex carbohydrate
which helps in reducing the serum uric acid
Preventive therapyPreventive therapy
b) Purine rich vegetables (peas, lentils, spinach, mushroom,
cauliflower) may not affect serum uric acid to desirable
extent and hence purine restricted diet is rarely necessary.
Vitamin C in dosages of 500mg/ day has mild urate lowering
(c) High-fructose corn syrup containing foods and drinks increase
blood urate levels and are hence not recommended to be
consumed. Coffee may decrease the risk of gout attacks .
(d) Alcohol increases the urate levels by increasing the
production of uric acid as well as by impairing its excretion.
Beer with its high purine content causes more elevation of
serum urate levels than wine.
Preventive therapy (Cont.)Preventive therapy (Cont.)
Case Study- 2
• A 52-year-old male presented with severe pain in his wrists
and right big toe, which was accompanied by inflammation
and erythema of the joints. The patient had previously been
diagnosed with acute gouty arthritis approximately 7 years
ago, but had not experienced another acute attack since his
original diagnosis. He had been taking simvastatin 40 mg
nightly for hyperlipidemia for 7 years, 20 mg lisinopril daily for
hypertension for 10 years, and hydrochlorothiazide 25 mg,
also for hypertension, which was recently added two months
ago. The patient had been steadily gaining weight over the
last few years and was now about 50 lbs overweight. He
stated that he drinks about a six pack of beer every day.
• Gout is influenced by numerous factors, including overeating,
obesity, alcohol abuse, hyperlipidemia, and insulin resistance
• A low purine and protein diet along with alcohol restriction,
weight loss through caloric restriction, and management of
associated disease, may be extremely beneficial.
• Also, since patients with gout are at an increased risk for
developing nephrolithiasis, health care providers should
emphasize the importance of increasing fluid intake and
decreasing salt consumption.
• In addition, joint rest and local application of ice may be
• Nonsteroidal anti-inflammatory drugs (NSAIDs) remain the
primary therapy for acute gouty arthritis for patients without
complications or contraindications.
• Although ketoprofen and ibuprofen are often used, the FDA
currently has approved only three NSAIDs for treatment of
acute gouty arthritis: indomethacin, naproxen, and sulindac.
• The most important determinant of therapeutic success is
probably not which NSAID is selected, but rather how soon
NSAID therapy is initiated.
• In patients with contraindications to NSAIDs, Colchicine is a
highly effective alternative treatment. Colchicine, which has
been used for gout for a rather long time, interferes with the
migration of neutrophils to the inflammation site, inhibiting
the underlying inflammatory cascade.
• Corticosteroids can also be used for acute gouty arthritis but
generally are reserved as the last treatment option because
of their associated short- and long-term side effects.
• Corticosteroids can either be injected into the involved
intraarticular joints or administered systemically. Because
rapid removal of corticosteroids can precipitate a rebound
attack, steroid withdrawal should be done gradually.