JIA Flashcards

(45 cards)

1
Q

Diagnosis by ARA

A

Onset before 16
Sx must persist min 6 weeks
Arthritis in 1 or more joints (defined as swelling within a joint or limitation in the ROM with joint pain or tenderness)
Exclusion of other diseases

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2
Q

Etiology

A

Autoimmune, multifactorial inheritance (genetics + environmental trigger), involvement of T-cells & HLA genes

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3
Q

Is there a lab test to diagnose JIA?

A

No.

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4
Q

When does a child get assigned to a subtype?

A

After 6 mo of active disease

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5
Q

What are the 7 subtypes?

A
Oligoarticular persistent and extended
Seronegative Polyarticular
Seropositive Polyarticular
Systemic
Psoriatric
Enthesitis
Undifferentiated
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6
Q

How many joints are affected in Oligoarticular JIA

A

4 or fewer (50% have only 1)

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7
Q

What joints are often affected with Oligoarticular JIA?

A

KNEE, ankle, wrist (often asymmetric joint involvement)

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8
Q

What is the most common kind of JIA?

A

Oligoarticular JIA

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9
Q

What other condition is common with Oligoarticular JIA?

A

Iridocyclitis (anterior uveitis) - may be asymptomatic

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10
Q

What is Persistent Oligoarticular JIA?

A

Affects no more than 4 joints throughout the course of the disease

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11
Q

What is Extended Oligoarticular JIA?

A

Affects more than 4 joints after the first 6 mo of the disease

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12
Q

How many joints need to be affected to be considered Polyarticular JIA?

A

5 or more joints

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13
Q

What joints are affected in Polyarticular JIA?

A

Knees, ankles, elbows, wrists, cervical spine and TMJ

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14
Q

What are the subtypes of Polyarticular JIA?

A

Seronegative (RF-) & Seropositive (RF+)

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15
Q

Peak ages and type of joint involvement in Seronegative Polyarticular JIA

A

2-4 & 6-12 y.o.

ASYMMETRIC

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16
Q

Peak ages and type of joint involvement in Seropositive Polyarticular JIA

A

Girls in late childhood/early adolescence.
SYMMETRIC - similar to adult RA
(wrists/small joints in hands/feet)

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17
Q

Severe constitutional symptoms of Systemic JIA

A
High Spiking fever
Salmon colored rash (tunk/proximal extremities)
Hepatosplenomegaly
Pleuritis
Pericarditis
Lymphadenopathy
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18
Q

What is the life threatening syndrome associated with Systemic JIA?

A

MAS (macrophage activation system) - activation of T cells and macrophages leads to overwhelming inflammatory response

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19
Q

When does joint pain develop with Systemic JIA?

A

Later in the process. 25-50% develop significant joint destruction

20
Q

Common clinical manifestations

A
Morning "gelling"/after immobility
IL-1 & tumor necrosis factor alpha (mediates joint damage)
Pannus formation 
Ligamentous Laxity
Decreased ROM
Dec Physical Activity/Weakness
Osteopenia
Growth disturbance
Micrognathia
21
Q

Medical Treatment

A
NSAID
DMARDS (methotrexate)
Anti-malarial (Plaquenil)
Gold Salts
Corticosteroids
Biologic Agents
22
Q

Methotrexate

A

Gold standard, Treats all types except systemic

23
Q

What is inactive disease?

A
No joints with active arthritis
No fever, rash, serositis
No active uveitis/eye inflammation
Normal CRP and ESR
No disease activity on physician global assessment of disease activity
24
Q

What is clinical remission on medication?

A

criteria for inactive disease are met for a minimum of 6 continuous months while on meds

25
What is clinical remission off medication?
criteria for inactive disease are met for a minimum of 12 continuous months off meds
26
Whats one of the first things a parent might notice with JIA?
Decreased activity, not wanting to play etc (d/t pain)
27
Pediatric pain scales
``` NIPS - babies FLACC- birth+, developmentally delayed (excluding paralyzed or those with spasticity) Oucher - ages 3 to 12 Faces Pain Rating Scale VAS COMFORT - unconscious/ventilator ```
28
What should you assess with a child with JIA?
``` The joint (look, feel, move, test) ROM Muscle strength (Observation of functional skills, MMT, handheld dynamometer) Posture/gait Functional abilities Physical Fitness ```
29
What is the PEDI-CAT?
Computer Adaptive Test. 3 functional domains & responsibility domain (daily activities, mobility, social-cognitive)
30
What is age range for the Wee-FIM?
6 mo - 7 years may be used with children above 7 as long as their functional abilities (as measured by wee fim) are below those expected of children aged 7 who do not have disabilities
31
How many items and what domains are on the wee-fim
18 items, Self care, mobility, cognition.
32
What are the FIM levels?
No Helper 7 Complete Independence (timely, safe) 6 Modified ind (device) Helper - Modified Dependence 5 Supervision (subject = 100%) 4 Minimal assistance (subject = 75% or more) 3 Moderate assistance (subject = 50% or more) Helper - Complete Dependence 2 Maximal assistance (subject = 25% or more) 1 Total assistance (subject = less than 25%)
33
Juvenile Arthritis Assessment Scale age range
7-16 y.o.
34
What does Juvenile Arthritis Assessment Scale observe?
the child’s actual performance of typical activities under standardized conditions. 10 items - ADLs (dressing, picking up an object off the floor)
35
What is teh Juvenile Arthritis Assessment Scale scale?
``` 0= task performed in less than or equal to criterion time 1= task performed in more time than the criterion time 2= unable to do the task ```
36
Activities Scale for Kids (ASK) age range
5-15 years old
37
What does ASK measure?
Measures physical disability and monitors functional change in children with limitations due to musculoskeletal disorders
38
How many items are on ASK
30 items - scored 0-4
39
What is the ASK scale?
0-4. 0 is with no problem and 4 is the child could not (personal care, dressing, locomotion, play, standing, transfers, other skills)
40
Physical Fitness in pts with JIA
Peak oxygen uptake reduced in comparison to healthy peers Lower peak work rate, peak exercise HR and exercise time Impaired aerobic capacity appears to be related to hypoactivity more so than the severity of the disease
41
Recommendations for physical fitness in pts with JIA
2X/week | Moderate to vigorous intensity (60-85%max HR) for 45-60 minutes for at least 6-12 weeks
42
Tx of acute active joint swelling: AROM
go to point of discomfort and hold 10 reps 2-3x day Proper hand placement to isolate the joint without stressing other joints
43
Tx of acute active joint swelling: isometric exercises
Submax contraction for 6 seconds for 5-6 reps
44
Tx of acute active joint swelling: other
Pain management, splinting/casting, activity modification
45
Tx: resolving joint inflammation
Progress home program Antigravity activities May add light resistance 8-10 reps against gravity without pain (TB, etc) Aquatic therapy Strengthening (observe joint protection principles) Return to activity (consider appropriateness of activities) Continue ROM exercises