Juvenile Iodiopathic Arthritis Flashcards

1
Q

what is juvenile idiopathic arthritis?

A

systemic inflammatory disorders affecting children less than 16 years old

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2
Q

what is the pathogenesis of juvenile idiopathic arthritis?

A

> autoimmune disease

> string subset of specific genetic markers affect the immune response

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3
Q

what is the criteria for diagnosis of JIA?

A
> less than 16 years age of onset
> duration of disease more than 6 weeks
> presence of arthritis
 - joint swelling
 - 2 of: painful limited joint motion, warmth or tenderness
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4
Q

describe the epidemiology of type 1 pauci-articular JIA

A

before 5 years and affecting girls more 9:1

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5
Q

how does pauci-articular JIA present?

A
> limp
> mainly lower limb joints
> irregular iris
> asymptomatic
> chronic uveitis
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6
Q

what percentage of type 1 Pauci-articular JIA is ANA positive?

A

40-75%

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7
Q

what is the epidemiology of type 2 pauci-articular JIA?

A

after 8/9years and a ration of girls 1: boys 7

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8
Q

hoe does type 2 pauci-articular JIA present?

A

> limp
lower limb joints
hip can be affected early and may evolve into spodyloarthritis

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9
Q

what is the epidemiology of type 3 pauci-articular JIA?

A

> can occur any age during childhood girls4:boys1

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10
Q

how does type 3 pauci-articular JIA present?

A

> dactylitis
asymmetric arthritis
family history of psoriasis (nail pitting)
chronic iridocyclitis

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11
Q

what percentage of pauci-articular cases go onto extended oligoarthritis?

A

30%

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12
Q

what is the epidemiology of RF negative poly-articular JIA?

A

> girls 9:1 boys

> any age

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13
Q

what is the presentation of RF -ve poly-articular JIA?

A
> hepatosplenomegaly
> low grade fever
> symmetric joints (large and small)
> growth abnormalities
> mild anaemia
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14
Q

what is the epidemiology of RF +ve poly-articular JIA?/

A

> late childhood

> girls 7: 1 boys

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15
Q

what is the presentation of RF positive poly-articular JIA?

A
> anaemia
> fever
> nodules
> malaise
> weight loss
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16
Q

what are some complications of RF positive polyarticular JIA?

A

> sjogrens
vasculitis
pulmonary fibrosis

17
Q

true or false

in RF positive poly-articular JIA erosions occur early in xrays?

A

true

18
Q

what is systemic polyarticular JIA?

A

extraarticular features define the disease. it starts early and disappears after 2-5 years

19
Q

what is the epidemiology of systemic poly-articular JIA?

A

can occur throughout childhood and girls 1.5 to 1 boys

20
Q

how does systemic polyarticular JIA present?

A
> fever
 - late evenings and afternoon
 - 39.5 degrees daily at least 2 weeks
> rash
 - thighs
 - trunk
 - salmon red eruption
 - brought on by scratching
> lymph nodes (generalised)
> abdo. pain
> hepatosplenomegaly
> transaminases
> serositis
> pericarditis
> pulmonary
 - fibrosis
 - effusion
> arthritis within 3-12 months of fever onset
21
Q

what is first line therapy in JIA?

A

> NSAIDs

22
Q

what is second line therapy in juvenile idiopathic arthritis?

A

> methotrexate
Anti-TNF
IL-1 R antagonist [anakinra]
IL-6 antagonist [tocilizumab]

23
Q

when are systemic steroids indicated?

A

> systemic JIA
serious disease complications
undergoing surgery
as a bridge between DMARDs

24
Q

what are the risks with systemic steroids?

A

> growth abnormalities
infections
osteoporosis

25
Q

what are local intraarticular steroids used for?

A

> oligoarticular JIA

> eye disease

26
Q

what surgeries can be used in JIA?

A

> synovectomy
reconstruction
replacement