wk 9 - RA Flashcards

1
Q

ankylosing spondylitis

A

A systemic, progressive disease of inflammatory of the spine, leading to
fusion

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2
Q

AS clinical features

A
  • nocturnal back pain/ stiffness with or without systemic symptoms
  • achillies/patellar tendonitis
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3
Q

AS management

A
  1. exercise - reduce stifness/loss of function
  2. NSAIDs
  3. bDMARDs , CS dont work
    -increased risk of low level infections
  4. surgery
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4
Q

complication of AS

A

enethesitis in foot

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5
Q

psoriatic arthritis

A

chronic inflammatory arthritis that occurs in people with psoriasis of the skin or nails
(may precede or follow skin involvement)

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6
Q

PsA clinical features

A
  • sausage toes
    -have psoriasis first usually
  • nail changes
  • arthritis mutilans
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7
Q

how long after does PsA develop

A

10 years after psoriasis

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8
Q

what is arthritis mutilans

A

Resorption of bone (osteolysis) small joints of digits

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9
Q

PsA management

A
  1. NSAIDS
  2. corticosteroids
  3. csDMARDs- not hydrocycholorquine makes psoriasis worse
  4. bDMARDS
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10
Q

reactive arthritis

A

caused by infection

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11
Q

clinical features of reactive arthritis

A
  1. conjunctivitis
  2. urethritis
  3. arthritis
  4. mucocutaneous symptoms
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12
Q

Reactive arthritis management

A
  1. NSAIDS
  2. corticosteroids
  3. antibiotics
  4. csDMARDs/ bDMARDs
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13
Q

spondyloarthropathies have what?

A

absence of rhematoid factor in serum

genetic association with HLA B27

present with enthesitis, dactylitis, tendonitis

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14
Q

scleroderma

A

rare chronic disorder with diffuse fibrosis of the skin and internal organs

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15
Q

triggers to sclerderma

A
  1. injury
  2. drugs
  3. chemicals
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16
Q

clinical features of scleroderma

A

joint/muscle pain and stiffness
increased sensitvity to cold
digestive problems
skin changes- hard tight skin

17
Q

raynauds phenomonon

A

hyperactivation of the sympathetic nervous system causing extreme
vasoconstriction of the peripheral blood vessels, leading to tissue hypoxia

18
Q

complications of sclerderma

A
  • raynauds
  • increased collagen causing hard tight skin
  • puffy hands and feet
  • ulceration
  • lesser toe deformities/ decreased rom
    -tightening and thickening of tendons
    -calcinosis
19
Q

systemic lupus erythamatous

A

autoimmune inflammatory connective tissue disorder predominantly effecting
young females of non white descent

20
Q

SLE clinicalfeatures

A
  • redness hands/face
    -butterfly rash
    -alopecia
    -photosensitive
    -swelling around nail bed
21
Q

complications of SLE

A

-DVT risk factor

22
Q

what type of joint hypermobility is considered a disordr

A

disrupts normal function
causing pain

23
Q

how to diagnose hypermobility

A

beighton scoring sytem
1. thumb
2. wrist
3. elbow
4. knee
5. hips

24
Q

marfan syndrome

A

gene mutation of the proteins that make healthy connective tissue

25
marfan syndrome clinical features
tall thin, armspan that exceeds ehight
26
osteogenesis imperfecta
brittle bone disease (genetic)
27
diagnosising hypermobility
beighton scale 2 main criteria -4 or more beighton score -joint stiffness longer than 3 months in 4 or more joints
28