Ch 3 - Rheumatology: Juvenile RA Flashcards

1
Q

What is the MC form of childhood arthritis?

A

Juvenile RA

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2
Q

What are the 3 clinical subtypes of Juvenile RA?

A

Systemic
Polyarticular
Pauciarticular

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3
Q

What is the ACR diagnostic criteria for JRA?

A
  • Onset < 16 yo
  • Persistent arthritis in 1 or > joints at least 6 wks
  • Exclusion of other types of childhood arthritis
  • Type of onset of disease during the 1st 6 mo classified as polyarthritis, oligoarthritis, or systemic arthritis with intermittent fever
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4
Q

What are causes of childhood arthritis besides JRA?

A

Rheumatic fever
Infection
SLE
Vasculitis

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5
Q

What is Still’s disease?

A

Systemic JRA

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6
Q

What is the onset of Still’s disease?

A

1 to 6 years old

Male = female

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7
Q

Describe fever in Still’s disease.

A

Persistent intermittent fever daily > 101°F spikes daily or twice daily

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8
Q

Describe the rash seen in Still’s disease.

A

Transient, nonpruritic seen on the trunk

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9
Q

Describe multisystemic involvement in Still’s disease.

A
– Growth delay 
– Osteoporosis, osteopenia 
– Diffuse lymphadenopathy 
– Hepatosplenomegaly 
– Pericarditis 
– Pleuritis 
– Anemia 
– Leukocytosis 
– Acute phase reactants
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10
Q

What is Polyarticular JRA?

A

5 or more joints involved during the first 6 mo

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11
Q

What is the onset of Polyarticular JRA?

A

Females&raquo_space; males

> 8 years old

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12
Q

Describe clinical features of Polyarticular JRA.

A
  • Gradual onset of swelling, stiffness involving the cervical spine and hips
  • Growth retardation—early closure of the epiphyseal plates
  • No extra-articular manifestations of systemic onset disease
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13
Q

Describe clinical features of Polyarticular JRA patients with (+) RF.

A
  • 5-10%
  • Females > 10 years old
  • Erosive and chronic
  • Unremitting disease (worst prognosis)
  • No Uveitis
  • Subcutaneous nodules
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14
Q

Describe clinical features of Polyarticular JRA patients with (-) RF.

A

90-95% of Polyarticular JRA

25% males < 6 years old

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15
Q

What is Pauciarticular JRA?

A

Oligoarticular JRA: 4 or fewer joints affected during the 1st 6 mo

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16
Q

What are the types of Pauciarticular JRA?

A

– Early onset: females,&raquo_space; 5 years old

– Late onset: males

17
Q

What labs are positive in Pauciarticular JRA?

A
  • (+) HLA-B27
  • (+) ANA
  • RF (–) (Only + in < 2%)
18
Q

What are Pauciarticular JRA patients with + ANA at risk for?

A

Greater risk of eye involvement

19
Q

What does chronic iridocyclitis in Pauciarticular JRA lead to?

A

Cataracts, glaucoma, or blindness (often asymptomatic)

20
Q

What is mandatory in Pauciarticular JRA?

A
  • Ophthalmology referral

* Slit lamp exam is required 4x/ year, for 4 to 5 years

21
Q

What are poor prognostic indicators of JRA?

A

– RF (+)
– Nodules
– Bony erosions on x-ray
– Polyarticular group with unremitting disease

22
Q

What medication should be avoided in treatment of JRA?

A

Salicylates should be avoided because of risk of Reyes’ syndrome

23
Q

Which JRA types is methotrexate MC used?

A

Systemic and polyarticular types

24
Q

Which JRA patients are most likely to get chronic iridocyclitis?

A

< 6 yo in 20-40%

MC in females with ANA (+)