Juvenile Idiopathic Arthritis Flashcards

1
Q

What is juvenile Idiopathic arthritis?

A

Group of systemic inflammatory disorders affecting children below the age of 16

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2
Q

Criteria for diagnosis of juvenile idiopathic arthritis?

A

Age of onset - <16 years
Duration of disease- >6 weeks
Presence of arthritis

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3
Q

What criteria would indicate the presence of arthritis?

A

Joint swelling or 2 of the following:
Painful or limited joint motion,
Tenderness,
Warmth

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4
Q

After 6 months what are the 3 subtypes of JIA identified?

A

Pauciarticular,
Polyarticular,
Systemic onset

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5
Q

What is pauciarticular JIA?

A

JIA of 4 or less joints

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6
Q

Age of onset of pauciarticular JIA type 1

A

Peak 1-3 years,

More common in females

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7
Q

Presentation of pauciarticular JIA type 1?

A
Limp, 
Mainly lower limb joints,
Chronic uveitis (can lead to blindness),
Irregular iris 
ANA +ve
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8
Q

Age of onset of pauciarticular JIA type 2?

A

After 8-9,

More common in boys

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9
Q

Presentation of pauciarticular JIA type 2

A
Limp,
Mainly lower limbs, 
Acute iridocyclitis 
Hip can be affected,
? Enthesitis,
? AS or spondyloarthritis,
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10
Q

Age onset and gender of pauciarticular JIA type 3?

A

Any childhood age,

Girls more common than boys

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11
Q

Presentation of pauciarticular JIA type 3?

A
Asymmetrical UL and LL arthritis, 
Dactylitis,
FH of psoriasis,
? Nail pitting,
Chronic iridocyclitis
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12
Q

What gender is more liokely to get polyarticular JIA RF -ve?

A

Female

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13
Q

Presentation of polyarticular JIA RF -ve

A
Constitutional manifestations, 
Hepato-splenomegaly, 
Mild anaemia, 
Growth abnormalities,
Arthritis of symmetric large and small joints
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14
Q

What is polyarticular JIA?

A

Arthritis of 5 or more joints

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15
Q

Age onset and gender of polyarticular JIA RF +Ve?

A

Late childhood,

Girls more common

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16
Q

Presentation of polyarticular JIA RF +ve?

A

Constitutional manifestations,
Anaemia,
Nodules,
Erosions in Xray

17
Q

Extra-articular symptoms that define systemic onset JIA?

A
Fever, 
Rash,
Lymphadenopathy,
Heptosplenomegaly, 
Abdominal pain,
Serositis,
Arthritis,
18
Q

Fever presentation of systemic onset JIA

A

Rises to 39.5C daily for at least 2 week,
Late afternoon/ evening worse,
Normal/subnormal in morning,
Fever +/- chills

19
Q

Rash presentation of systemic onset JIA

A

Evanescent salmon red eruption,
Trunk and thighs,
Fever,
+ve Koebner’s phenomenon (brought on my scratching)

20
Q

Lymph node presentation of systemic onset JIA

A

Generalised lymphadenopathy,

Non-tender

21
Q

Abdominal presentation of systemic onset JIA

A

Hepatosplenomegaly,
Abdominal pain,
+/- transaminases

22
Q

Serositis presentation of systemic onset JIA

A

Polyserositis,
Pericarditis,
Tamponade,
Myocarditis

23
Q

Pulmonary presentation of systemic onset JIA

A

Pleural effusion,

Pulmonary fibrosis

24
Q

Arthritis presentation of systemic onset JIA

A

Within 3-12 months of onset of fever,

Wrists, knees, ankles, cervical spine, hips and TMJ

25
Q

Complications of uveitis

A

Posterior synechiae,
Cataract,
Band keratopathy

26
Q

Treatment of uveitis?

A
Steroids,
Mydriatic and cycloplegic agents, 
Methotrexate, 
Cyclosporin, 
Anti-TNF
27
Q

1st line therapy of JIA?

A

NSAIDs,

28
Q

2nd line therapy for JIA?

A

Methotrexate,
Anti-TNF Rex,
IL-1 R-antagonist (anakinra)
IL-6 antagonist (toclilzumab)

29
Q

When are systemic steroids used in JIA?

A

Systemic JIA,
Serious disease complications,
Bridge between DMARDs,
Undergoing surgery

30
Q

Risk of using systemic steroids?

A

Osteoporosis,
Infections,
Growth abnormalities

31
Q

Surgical treatment of JIA?

A

Synovectomy,

Reconstructive/ joint replacement surgery

32
Q

Growth failures that can occur in JIA?

A
Leg length discrepancies, 
Micrognathia,
Shortening of fingers, hands, forearms, toes, feet, 
Short stature, 
Delayed puberty