Associate Professor of Internal Medicine and Pediatrics Med Peds Conference January 2018 Gout The king of diseases and the disease of kings History Identified in 2640 BC by the Egyptians 5 ID: 775430
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Slide1
Vijay Aswani MD, PhD, FACP, FAAPAssociate Professor of Internal Medicine and PediatricsMed-Peds ConferenceJanuary, 2018
Gout
The king of diseases and the disease of kings
Slide2History
Identified in 2640 BC by the Egyptians5th century BC: Hippocrates identified podagra as “the unwalkable disease”Dominican monk Randolphus of Bocking (1197-1258) wrote gutta quam podagram vel articam vocant – ‘the gout that is called podagra or arthritis’
Nuki
&
Simkin
, 2006. Arthritis Research & Therapy 2996, 8(
Suppl
1):S1
Slide3History
Antoni van Leeuwenhoek described crystals from gouty typhus in 1679: “I observed the solid matter which to our eyes resembles chalk, and saw to my great astonishment that I was mistaken in my opinion, for it consisted of nothing but long, transparent little particles, many pointed at both ends and about 4 ‘axes’ of the globules in length. I can not better describe that by supposing that we with naked eye pieces from the horse-tail cut to a length of one sixth of an inch.”
Nuki
&
Simkin
, 2006. Arthritis Research & Therapy 2996, 8(
Suppl
1):S1
Slide4History
1961: McCarty and Hollander introduced polarizing light microscopy during synovial fluid analysis for acute or chronic arthritis:Different kinds of microcrystals:Monosodium urate (MSU)Calcium pyrophosphate (CPP)Calcium apatite (apatite)Calcium oxalate (CaOx)
Harrison’s Principles of Internal Medicine,
19e. 2015
Slide5The Gout by James
Gilliray
, Lettered with title and publication line: "
Pubd
. May 14th. 1799, by H. Humphrey 27 St James's Street".
Slide6Pathophysiology
4 stages:Hyperuricemia without evidence of MSU depositionCystal deposition without symptomatic goutCrystal deposition with acute gout flaresAdvanced gout characterized by tophi, chronic gouty arthritis and erosions
Dalbeth
et al, 206. Lancet: 388: 2039-54
Slide7Dalbeth
et al, 206. Lancet: 388: 2039-54
Slide8Neogi
, T. Gout. N
Engl
J
Med 364(5
):
443-452. February
3, 2011
Slide9Dalbeth
et al, 206. Lancet: 388: 2039-54
Slide10Epidemiology
Prevalence in western countries: 3-6% in men and 1-2% in womenPrevalence in developing countries: < 1%Men : women 2-6 times greater until age 70s.US prevalence in 2007-08: 3.9%
Dalbeth
et al, 206. Lancet: 388: 2039-54
Slide11Clinical Presentation
Acute
arthritis is the most common early manifestation of gout
Usually one joint initially, polyarticular acute gout in subsequent
MTP join of first toe is often involved
Tarsal joints, ankles and knees also commonly involved
Finger joints in advanced
Inflamed Heberden’s or Bouchard’s nodes may be first manifestation
1
st
episode of acute gouty arthritis begins at night with dramatic joint pain and swelling
Joints become warm, red and tender and may mimic cellulitis
Early attacks may subside spontaneously in 3-10 days
Events that precipitate attack: dietary excess, trauma, surgery , excessive EtOH, hypouricemic therapy, MI and stroke
After any attacks, pts may present with chronic
non-symmetric
synovitis – confused with rheumatoid
arthritis
Slide12Lab Diagnosis
Confirm diagnosis by needle aspiration of joint
MSU crystals – needle shaped intra- and extracellular
Brightly birefringent with negative elongation
Synovial fluid WBC 2k to 60k
Effusions are
cloudy
Serum uric acid levels normal in acute attack
24h urine collection n useful for assessing risk
fo
stones from overproduction or
under-excretion
of uric acid
Excretion
of >800 mg per 24 h on regular diet,: overproduction of
purine
Slide13Dalbeth
et al, 206. Lancet: 388: 2039-54
Slide14Slide15Case Vignette
A 54-year-old man with crystal-proven gout has a history of four attacks during the previous year.Despite receiving 300 mg of allopurinol daily, his serum urate level is 7.2 mg per deciliter (428 μmol per liter).He is moderately obese and has hypertension, for which he receives hydrochlorothiazide, and his serum creatinine level is 1.0 mg per deciliter (88 μmol per liter).How should his case be managed?
Neogi
, T. Gout. N
Engl
J
Med 364(5
):
443-452. February
3, 2011
Slide16Management Strategies in Patients with Hyperuricemia.
Neogi
, T. Gout. N
Engl
J
Med 364(5
):
443-452. February
3, 2011
Slide17Pharmacologic Management Options for Acute Gout Attacks.
Neogi
, T. Gout. N
Engl
J
Med 364(5
):
443-452. February
3, 2011
Slide18Pharmacologic Options for Hyperuricemia Therapy in Gout.
Neogi
, T. Gout. N
Engl
J
Med 364(5
):
443-452. February
3, 2011
Slide19Conclusions and Recommendations
In patients presenting with suspected gout, the diagnosis should be confirmed by examination of synovial fluid or tophus aspirate for monosodium urate crystals.Management should be tailored to the stage of disease and coexisting illnesses.The patient who is described in the vignette has crystal-proven gout, with multiple attacks and a serum urate level of more than 6 mg per deciliter despite receipt of allopurinol at a dose of 300 mg per day.Since his renal function is normal, the allopurinol dose should be increased (e.g., 100-mg increments every 2 to 4 weeks until the target urate level is reached), with monitoring of renal function and serum urate levels and assessment for potential adverse reactions.Colchicine prophylaxis (0.6 mg once or twice daily) is reasonable while the dose of allopurinol is escalated.If target serum urate levels cannot be achieved or if the patient has serious side effects at higher allopurinol doses, the use of either febuxostat or a uricosuric agent is another option, given his normal renal function.
Neogi
, T. Gout. N
Engl
J
Med 364(5
):
443-452. February
3, 2011
Slide20Conclusions and Recommendations
The patient should understand that the intake of alcohol and an excessive amount of meat or seafood and sugar-sweetened drinks may contribute to elevated urate levels and should be minimized.He should be advised to keep well hydrated and to lose weight.Associated cardiovascular risk factors should be identified and treated.Although the use of hydrochlorothiazide may contribute to the increased urate level, I would not necessarily change that medication if it is effectively controlling his blood pressure [controversial], and I would advise him to take the diuretic consistently, since intermittent use may precipitate flares.The addition of losartan for the hypertension might be considered.He should be advised to maintain his urate-lowering regimen during flares, which can be managed with colchicine.Follow-up is necessary to ensure that appropriate serum urate levels are achieved and maintained and to monitor the patient for adverse effects.
Neogi
, T. Gout. N
Engl
J
Med 364(5
):
443-452. February
3, 2011
Slide21Take-home Points
Slide22Questions?
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