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 Vijay  Aswani   MD, PhD, FACP, FAAP  Vijay  Aswani   MD, PhD, FACP, FAAP

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Vijay Aswani MD, PhD, FACP, FAAP - PPT Presentation

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

gout urate arthritis med gout urate arthritis med 2011 february 452 443 364 serum neogi engl acute levels allopurinol

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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

Slide2

History

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

Slide3

History

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

Slide4

History

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

Slide5

The Gout by James

Gilliray

, Lettered with title and publication line: "

Pubd

. May 14th. 1799, by H. Humphrey 27 St James's Street".

Slide6

Pathophysiology

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

Slide7

Dalbeth

et al, 206. Lancet: 388: 2039-54

Slide8

Neogi

, T. Gout. N

Engl

J

Med 364(5

):

443-452. February

3, 2011

Slide9

Dalbeth

et al, 206. Lancet: 388: 2039-54

Slide10

Epidemiology

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

Slide11

Clinical 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

Slide12

Lab 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

Slide13

Dalbeth

et al, 206. Lancet: 388: 2039-54

Slide14

Slide15

Case 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

Slide16

Management Strategies in Patients with Hyperuricemia.

Neogi

, T. Gout. N

Engl

J

Med 364(5

):

443-452. February

3, 2011

Slide17

Pharmacologic Management Options for Acute Gout Attacks.

Neogi

, T. Gout. N

Engl

J

Med 364(5

):

443-452. February

3, 2011

Slide18

Pharmacologic Options for Hyperuricemia Therapy in Gout.

Neogi

, T. Gout. N

Engl

J

Med 364(5

):

443-452. February

3, 2011

Slide19

Conclusions 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

Slide20

Conclusions 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

Slide21

Take-home Points

Slide22

Questions?

You can download take-away notes to this presentation to your phone here, using your smartphone.Either type in the URL:http://www.buffalo.edu/~vaswani/ or scan the QR code below using a free QR scanner

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