Juvenile idiopathic arthritis Flashcards

1
Q

What is JIA?

A

Group of systemic inflammatory disorders affecting children below 16

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2
Q

What is the pathogenesis of JIA?

A

Autoimmune

Genetic markers

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3
Q

What is the criteria for diagnosis of JIA?

A

Onset <16
Duration of disease >6 weeks
Presence of arthritis- joint swelling or 2 of: painful or limited joint movement, tenderness, warmth

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4
Q

What are the types of JIA?

A

Periarticular
Polyarticular
Systemic

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5
Q

What is periarticular JIA?

A

Affects 4 joints or less

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6
Q

What are the types of periarticular JIA?

A

Type 1, 2 and 3

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7
Q

What is type 1 periarticular JIA?

A

Majority girls, presents before age 5, normally age 1-3

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8
Q

What is the presentation of type 1 periarticular JIA?

A
Limp due to arthritis normally in knee or ankle
Asymptomatic in 50%
Chronic uveitis in 20%
Irregular iritis
\+ ANA in 40-75%
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9
Q

What is type 2 periarticular JIA?

A

Mainly boys

Onst after 8 years

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10
Q

What is the presentation of type 2 periarticular JIA?

A

Limp due to mainly knee and ankle, but occasionally hip

Acute iridocyclitis in 10-20%

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11
Q

What is type 3 periarticular JIA?

A

Mainly girls

Onset at any age in childhood

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12
Q

What is the presentation of type 3 periarticular JIA?

A
Asymmetric upper and lower limb arthritis
Dactylitis
Nail pitting
Psoriasis- FH in 40%
Chronic iridocyclitis in 10-20%
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13
Q

What is polyarticular JIA?

A

5 or more joints affected

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14
Q

What are the types of polyarticualr JIA?

A

Rheumatic factor -

Rheumatic factor +

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15
Q

When does rheumatic - JIA present?

A

Any age but often earlier

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16
Q

Who is rheumatic - JIA seen in?

A

Mainly girls

17
Q

What is the presentation of rheumatic - JIA?

A
Behaves like rheumatoid arthritis in adults
Symmetric
Large and small joints affected
Systemic- fever, malaise
Hepatosplenomegaly
Mild anaemia
Growth abnormalities
18
Q

What is the presentation of rheumatic + JIA?

A

Systemic- fever, malaise, weight loss
Anaemia
Nodules
Early erosions on xray

19
Q

Who is rheumatic + JIA seen in?

A

Mainly girls

Later onset, 12-16 years

20
Q

What is systemic onset JIA?

A

Least common but most dangerous form

21
Q

Who is systemic onset IA seen in?

A

4-6 year olds

Slightly more girls- 3:2

22
Q

What is the presentation of systemic JIA?

A

Any joint, starting 3-12 months after onset of fever
Fever- high and persistent and worse in evening
Generalised non tender lymphadenopathy in 50-75%
Salmon pink rash on trunk and thighs in 90%
Polyserositis
Pericarditis
Hepatosplenomegaly and abode pain in 50-75%

23
Q

What are the rare presentations of systemic JIA?

A

Pleural effusion
Pulmonary fibrosis
Tamponade
Myocarditis

24
Q

How is systemic JIA diagnosed?

25
What is the 1st line treatment of JIA?
NSAIDs Local steroids Physio OT
26
When and how are steroids used in JIA?
Joint steroid injections, mainly in oligoarticular disease | Eye disease
27
What are the 2nd line pharm treatments of JIA?
``` Methotrexate Anti TNF IL-1 R antagonist IL-6 antagonist Systemic steroids ```
28
When are IL-1 R antagonists and IL-6 antagonists used?
Refractory systemicc disease
29
What are the indications for steroid use in JIA?
Systemic disease Serious disease complications Undergoing surgery
30
What are the risks of using steroids in JIA?
Osteoporosis Infections Growth abnormalities
31
What are the surgical options in JIA?
Synovectomy | Reconstructive/joint replacement