Rheum Flashcards

1
Q

List DDX for arthritis

A

MONOARTICULAR

  • Septic arthritis
  • GOUT
  • psedogout
  • OA
  • Trauma

POLYARTICULAR SYMMETRICLA

  • rheumatoid flare
  • psoratic arthrtiis
  • polymylagia rheumatica
  • ank spont

POLYARTICULAR ASSYMETRICAL

  • gonoccal arthritis
  • ARF
  • Reactive arthritis
  • viral arthritides
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2
Q

Discuss indications and contraindications for joint aspiration

A

INDICATIONS

  • Obtain joint fluid for anaylsis
  • drain tense haemarthroses in patients with trauma and haemophilia
  • to evaluate whether a laceration communicates with the joint space.

Contraindications - relative

  • cellulitis overlying the injection site
  • coaguloapthy
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3
Q

Describe technique for knee tap

A
  • Aseptic
  • Local anaethetics
  • Flex knee to 15-20 degrees
  • palpate the anteromedial patellar edge at the patellar midpoint or superior portion
  • Insert 18g needle 1cm medial to this point direted toward the posterior surface of the patella
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4
Q

Discuss different synovial fluid finding by arthritis type

A

NON INFLAMMATORY

  • colour : yellow
  • Viscosity ; thick and stringy
  • Synovial WBC: 200-2000
  • PMN- variable
  • Gram stain -ve

INFLAMMATORY

  • Colour : yellow/white
  • Viscosity: variable
  • WBC 2000-50000/mm3
  • PMN- variable
  • Gram stain -ve

SEPTIC

  • Colour : Cloudy/opaque
  • Viscosity: thin/watery
  • WBC >25000/mm3 +LR 2.9, >50000 +LA 7.7, >100000 LA28
  • PMN- >90%
  • Gram stain +ve in 30-65% of cases
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5
Q

Describe septic arthritis

A

Bacterial infection of diarthrotic joint space

Can occur simultaneously with other forms of inflammatory arthritis - fever is common with inflammatory flares and infection can cause precipitation of crystals

Risk factors

  • Age over 80
  • Low socioeconoic status
  • IVDU
  • alcoholism
  • diabetes
  • skin infection
  • advanced HIV or other immunocompromised sate
  • chronic arthritis (particularly RA, crystalline and degenerative)
  • recent injection
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6
Q

List Microbiology of septic joint by age groups and demographic groups

A

NEONATES

  • Staph aureas
  • GBS
  • GNR bacteria

CHILDREN

  • HIB
  • Staph aurea

Adolescents and Young adults

  • N. Gonorrhoea
  • chlaymydia
  • stah

Older adult

  • S aureas
  • strep
  • GNR bacteria

SICKLE CELL
-Salmonella

IVDA

  • Pseudomonas,
  • S. aureas
  • GNR bacteria
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7
Q

Discuss management of septic arthritis

A

ORTHO review
Fluclox 2g Q6 hourly
if MRSA suspected use Vancomycin 30mg/kg

If IVDU consider psuedomonas coverage with cipro or ceftazadime

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8
Q

Discuss gonococcal arthritis

A

Represents a clinical and pathologic course distinctly different from that of other bacterial infections.

Systemic gonococcal infection complicates 0.5%-3% of mucosal infection and is manifested with two somewhat overlapping MSK syndromes

1) localised septic arthritis - more commonly oligo than mono predominatnly in the knees and wrist.
2) true disseminated gonococcal is manigested with bacteremia, and a triad of tenosynovitis, dermatitis and migratory polyarthralgia +- puruelent arthritis
- skin lesions are usually painfless visculopustular

Risk factors for DGI

  • Recent mensturation –
  • pregnancy or the immediate postpartum state
  • congenitial or acquired complement deficienes
  • SLE

WBC in synovial fluid tend to be lower than than in nongonococcal arthritis.

Treat with IV ceftriaxone 24 hourly + 1gram of oral azithromycin

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9
Q

Describe GOUT and its risk factors

A

Acute intermittent gout typically is manifested in middle aged men or postmenopausal women often in the setting of excess alcohol, or dietary indiscretion, acute physioloigcal stress or new medications.

Risk factors

  • Chronic obesity
  • htn
  • diabetes
  • thiazide diuretics
  • cyclosporine
  • purine rich diets ( meat, seafood (ancovies and shellfish), beer and legumes)

Acute precipitation of uric acid crystals from supersaturated extracellular fluid. Uric acid is a normal metabolic endpoint of purine metabolism

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10
Q

Discuss clinical features of gout

A

Most common joint is the great toe MTP, the knee the ankle and the trasal joints.

Pain is often exquisite at onset. Systemic features include fever can be present. Without treatment the attack is self limited peaking during the 24-48 hour mark and lasting about a week

Subsequent attacks tend to be closer together involve more joints and last longer.

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11
Q

Discuss management of GOUT

A

ACUTE

1) Nsaids - indomethasin is typically given 50mg TDS, Ibuprofen 800mg DS - if initiated promptly relief occurs in the first 24 hours
2) -Colchicine -inhibits microtuble formation and impedes the inflammatory response to the presence of cyrstals
- 1mg followed by 500mic one hour later
- contraindicated in haematological, renal or hepatic insufficiency
3) Steroids
- prednisone 15-30mg dialy until symptoms abate

Chronic
-Allopurinol 50mg daily for 4 weeks than increase by 50mg every 2-4 weeks max dose of 900mg dialy

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12
Q

Describe pseudogout (calcium pyrophosphate, dihydrate deposition)

A

Results when calcium complex cyrstals form across articular surfaces. CPPD is manifest on radiographs as chondrocalcinosis

When precipitating crystals trigger an inflammatory synovitis termed pseudogout.

Risk factors

  • aging
  • joint surgery
  • haemochromatosis
  • hypothyroidism
  • hyperparathyroidsm
  • amyloidosis
  • hypomagnesemia
  • Wilsons diseaes

Clinical feature and mangement are similar to gout

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13
Q

Discuss Rheumatoid arthritis

A

Women 2-3x more commonly then men with a peak incidence in the 4th and 5th decade of life.

Common presentation is that of a prodromal period of fatigue, weakness and MSK pain with or wihtout fever and weight loss that may have been present for weeks to months.

Acute presentation may have only warm, tender and swollen joints that may be difficult to distinguish from a viral arthropathy

Long standing changes of RA include MCP and PIP joint swellling, ulnar deviation, swan neck and boutoneire deformities of the hand and limitation of dorsiflexion of the wrist.

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14
Q

Discuss extra-articular features of RA

A

Occur in up to half of patient with RA and include

  • subcut nodules
  • vasculitis of the skin
  • pulmonary fibrosis
  • mononeuritis multiplex
  • pericarditis
  • Sjogrens and Felty’s syndrome.
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15
Q

Discuss IX of RA

A

Focused on ruling out other cause of arthritis in the ED. But diffinitive diagnosis can be challenging and involves confirmatory serology.

Synovial fluid analysis is helpful to rule out infectious or cyrstalline processes. Arthrocentesis reveals inflammaotry fluid with WBC between 4000-50000 with more PMN than would be expected for crystaline inflammation up to 75%

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16
Q

Discuss treatment of RA

A

Steroids for acute flares
NSAIDS
DMARDS including sulfasalazine, hydroxychloroquine, methotrexate

17
Q

Describe seronegative spondyloarhtropathies

A

All share the characteristics of

1) sacroiliac involvement,
2) peripheral inflammatory arthropathy,
3) absence of rheumatoid factor,
4) pathalogical changes around the enthesis (ligamentous and tendinous insertion into bone)
5) geneitc component related to HLA-B27

The most importnat being ankylosing spondylitis, reactive arthritis the arthroapthy of IBD and psoritic arthritis

18
Q

Briefly describe Ankylosing spondylitis

A

Generally are male patients younger than 40 years old with chronic insidious back discomfort for more than 3 months with radiological evidence of sacroilitiis.

Uveitis is the most common extra-articular manifestation but life threatening aortic root disease can rarely occur.
Peripheral joints are involved in 30% of cases with enthesopathic involvement such as plantar fasciits and achilles tendinitis.

Can develop atraumatic cauda and spinal compression

Goals of therapy are to control pain, to decrease inflammation and to being physiotherapy and strengthening exercises. NSIADS with DMARDS including slafasalazine, methotrexate and MABS

19
Q

Describe reactive arthritis (previously reiter’s syndrome)

A

Occurs in genetically susceptible hosts after infection with chlamydia trachomatis in the gen urinary tract or Salmonella, shigella, yersinia or campylobacter organisms of the GIT.

Reactive arthritis is generally a disease of patients from 20-40 years old in whom arthritis develops 2-6 weeks after an episode of urethritis, cervicitis or dysentry.

The syndrome is predominatly polyarticular, asymmetrical and often additve.

Conjunctivitis is seen early in the disease and can progress to uveitis.

Synovial fluid sjows inflammatory range white cells with chlamydia, salmonella and yersinia antigens found in the synovial membrane

MANAGEMNT

  • respond well ot NSAIDS particularly indomethacin up to 200mg/day
  • Antibiotics improve recovery time for patients with chlamydia-triggered reactive arthritis. nil benifit for gi causes
20
Q

Describe enteropathic arthritis

A

Up to 46% of patients with IBP experience MSK manifestations

Typically an acute migratory asymmetrical inflammatory polyarthritis of the peripheral joints especially the knees
The arthritis generally correlates with flare-ups of the bowel dissease but the spinal manifestations do not.

21
Q

Describe polymyalgisa rheumatica

A

Manifested with symmetric MSK aching and morning stiffness of several weeks duration especially of the shoulder and pelvic girdle almost always in patients over the age of 50 years old.

Physical signs are modest
THe disease usual shows an elevated ESR >40 with many above 100

Usually self limited and systemic review suggest most patients will respond to low dose prednisone.

22
Q

Describe systemic sclerosis (scleroderma)

A

Hallmark of the disease is thickening or hardening of the skin
Scleroderma can cause serious damge to internal organs including the lugns heart, kidney and GIT

Manifestations include

  • skin thickening of the fingers of both hands extending above the elbow in diffuse disease
  • sclerodactyly
  • telangiectasia
  • raynaud phenomenon
  • digital tip ulcers
  • pulmonary arterial htn
  • interstitial lung disease
  • scleroderma renal crsis
23
Q

Describe scleroderma renal crisis

A

Severe life threatening renal disease develops in 10-15% of pateitns is charachterised by

1) acute onset renal failure
2) abrupt onset of moderate to marked hypertension
3) urinary sediment that is normal or has mild proteinuria.