• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/22

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

22 Cards in this Set

  • Front
  • Back

Juvenile Idiopathic Arthritis onset is before 17 yrs, usually before 9.



What are the 5 different subtypes?

1. Systemic Onset


(1 joint)


2. Pauciarticular (oligoarticular)


(< 5 joints)


3. Juvenile Spondylitis


(<5 joints)


4. Psoriatic Arthritis


(<5 joints)


5. Polyarticular


(> 5 joints)

what is the most common subtype?

Pauciarticular (oligoarticular)

Juvenile arthritis is more common in females EXCEPT in ......

juvenile spondylitis (<5 joints)


(^more commonly male)



& systemic JA (1 joint)


(equal male & female child <5)



How can you differentiate JIA from normal growth pains?

growth pains:


-btwn 6-13


-pain localized to thighs, calves, etc (lower extr)


(JIA localized to joints)


-pain more frequent late in day


(JIA worse in morning, better w/ use)


-normal growth & development


-good response to heat, massage, analgesics

6 yr old pt presents w/ high fever & macular (flat) non-itchy rash, both of which come & go throughout the day (rash goes away as fever drops). PE reveals splenomegally & nodes. Blood culture shows leukocytosis.


Dx?


Dx: Systemic Onset JIA


Systemic Onset disease: management

NSAID*


splint to prevent deformity


corticosteroids in severe

T/F


The younger the patient is at onset of systemic onset JIA, the worse the prognosis


TRUE

4 yr old female pt presents with arthritic pain in knee, ankle, elbow, & hand (4 joints). Blood tests show (+) ANA.


Dx?


Pauciarticular JIA (type I)

What may happen if Pauciarticular JIA goes undiagnosed?

chronic uveitis---> blindness


growth abnormalities (uneven limb lengths)


Pauciarticular JIA: management

Intra-artic steroid injections


NSAIDs


Frequent opthalmic assessments (& tx if necessary)

8 yr old male pt presents w/ a dilated achilles tendon (enthesopathy), acute iritis, & sacroiliac pain. PE shows + Schobers test (can't bend lumbar spine). Blood culture shows (+) HLA-B27.


Dx?

Juvenile Spondyloarythropathy


(pauciarticular type II)

Juvenile Spondyloarthropathy may lead to serious problems, such as;

fusion of the spine


(progresses upward)

Juvenile Spondyloarthropathy: Management

Anti-TNF agents (bilogical agents)

8 yr old female pt comes in with swollen digits (dactylitis), asymmetric DIP pain, peripheral joint pain. On PE you find nail pitting & psoriatic rash.


Dx?

Psoriatic JIA

Psoriatic JIA can also progress & cause.....

iritis or spondylitis

Psoriatic JIA: management

Methotrexate (immunosuppressives)


NSAIDs


Biologic agents

Young female pt comes in with joint pain in more than 5 joints, that has been present for 2 months.


Dx?

Polyarticular JIA

There are 2 subtypes of Polyarticular JIA, based on blood culture ______ results.

RF (+) or RF (-)

A pt complaining of reduced neck & TMJ ROM & flexor tenosynovitis, would likely be RF __



RF (-)



(milder form of polyarticular JIA)

A pt complaining of joint pain presents w/ rheumatoid nodules & vasculitis, would likely be RF __



What else would be present in this blood culture?

RF (+)



(more severe form)



likely ANA + also

Polyarticular JIA: Management

both types;



NSAIDs


DMARDs (MTX)


Biologic agents (anti-TNF)


What is the gold standard tx for ALL types of JIA?

NSAIDs