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
Q

marfan syndrome clinical features

A

tall thin, armspan that exceeds ehight

26
Q

osteogenesis imperfecta

A

brittle bone disease (genetic)

27
Q

diagnosising hypermobility

A

beighton scale
2 main criteria

-4 or more beighton score
-joint stiffness longer than 3 months in 4 or more joints

28
Q
A