Rheumatology Flashcards

(23 cards)

1
Q

Septic arthritis presentation in a child

A
Acute fever
Joint pain and swelling
Ill appearance
Irritable
Tachycardia
Joint effusion
Periarticular warmth and tenderness
Pain on movement
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2
Q

Investigations for septic arthritis

A

CRP and ESR - raised
White cells and platelets - raised
US joint
Blood cultures

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3
Q

Management of septic arthritis

A

Referral to orthopaedics
IV antibiotics
Joint aspiration

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4
Q

Describe slipped upper femoral epiphysis (SUFE)

A

Displacement of capital femoral epiphysis from femoral neck

Most common hip disorder of adolescence

Associated with obesity

Pain and altered gait

Worse with activity

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5
Q

Management of SUFE

A

Xray; ice cream slipping off cone

Refer to ortho

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6
Q

Describe transient synovitis

A

Pain and limited movement hip

Relatively common

3-8yrs

Symptoms <1week

Fever absent or low grade

not unwell looking

US bilateral effusion

Resolves gradually with conservative therapy

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7
Q

Describe perthes

A

idiopathic avascular necrosis of hip

Insidious hip pain and limp

Pain not relieved by rest or medication

3-12 years, peak 5-7

males>females

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8
Q

Management of perthes

A

minimal weight bearing

paediatric ortho

Contain head within acetabulum with use of splints

Occasional surgery (osteotomy)

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9
Q

What are symptoms of juvenile idiopathic arthritis?

A

Arthritis at least 6 weeks

Morning stiffness of gelling

Irritability or refusal to walk in toddlers

School absence or limited ability to take part in physical activity

rash/fever

Fatigue

Poor appetite/weight loss

Delayed puberty

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10
Q

What are differential diagnoses for swollen/painful joint?

A
Septic arthritis
Osteomyelitis
Transient synovitis
Malignancies
Recurrent haemarthrosis
Vasular abnorms
Trauma
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11
Q

What are signs of JIA?

A

Swelling; periarticular, soft tissue oedema, intraarticular effusion, hypertrophy of synovial membrane

Tenosynovitis
Pain
Joint help in position of max comfort
Range of movement limited at extremes

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12
Q

What are types of JIA?

A

Oligoarthritis (<5joints)

Polyarthritis (more than 5 joints) (RF -ve vs RF +ve)

Enthesitis Related Arthritis

Psoriatic arthritis

Systemic onset JIA

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13
Q

Describe enthesitis related arthritis

A

tendons involved more than joints

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14
Q

DEscribe oligoarthritis vs polyarthritis

A

Oligo - <5joints

Poly - > 5 joints

Poly is split into RF +ve and -ve (+ve poorer prognosis)

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15
Q

Describe systemic JIA

A

5-15% of JIA

Unwell
Arthritis
Intermittent fever >2weeks
Salmon pink erythematous rash
Generalised lymphadenopathy
Serositis
Hepatomegaly/splenomegaly
High inflammatory markers
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16
Q

Investigations for JIA

A

Labs (ESR raised, CRP not)
Plain xray
US
MRI with contrast

17
Q

Treatment for JIA

A

NSAIDs (short term not long term)

DMARDs
biologic agents
intraarticular and oral steroids

Physio, OT, school discussions

18
Q

Describe IA steroids in JIA

A

Efficacious

Greater success in oligoarticular

No long term side effects

19
Q

What is DMARD of choice in JIA?

A

Methotrexate

Injectable (most common) or oral

If poor response to IAS in olgio JIA

Blood monitoring

20
Q

What are biological agents in JIA?

A

Used if failure to respond DMARD

Anti TNF agents common

21
Q

Describe uveitis

A

Associated with JIA

If untreated can become chronic

All children with JIA undergo screening

More common in ANA positive oligoJIA, <5yrs

Rarely symptomatic

Red eyes, headache, reduced vision

Cataracts, glaucoma and blindness if untreated

22
Q

Treatment of uveitis

A

Slit lamp examination

All JIA patients seen within 6 weeks diagnosis

Initially topical steroids to reduce inflammation, more severe need systemic steroids

If poor steroid response, DMARD and biologics introduced

23
Q

What are complications of JIA?

A
poor growth
Osteopenia
Localised growth disturbances
Micrognathia (TMJ involvement)
Contractures
Ocular complications