Ortho/Rheum Flashcards

1
Q

What is Henoch-Schonlein purpura?

A

IgA vasculitis
presents with purpuric rash affecting lower limbs and buttocks in children
Inflammation occurs in the affected organs due to IgA deposits in the blood vessles

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2
Q

Where does HSP affect?

A
  • skin
  • kidneys
  • GI tract
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3
Q

What triggers HSP?

A
  • upper airway infection
  • gastroenteritis
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4
Q

Most common age group to be affected by HSP?

A

Under 10

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5
Q

4 Classic features of HSP?

A
  • purpura
  • joint pain
  • abdo pain
  • renal involvement
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6
Q

How does HSP present?

A
  • Purpura- usually starts on legs and spread to the buttocks and can also affect trunk and arms- skin ulceration and necrosis may develop
  • Arthralgia or arthritis- knees and ankles, joints may become swollen and painful
  • Abdo pain- can lead to GI haemorrhage, intussuception and bowel infarction
  • IgA nephritis- haematuria (micro or macro) and proteinuria–> 2+ or more protein on dipstick–> nephrotic syndrome
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7
Q

Investigations for HSP?

A
  • A-E- EXCLUDE: meningoccocal septicaemia, leukaemia
  • Bedside:
    urine dipstick- for proteinuria, BP- for hypertension
  • Bloods:
    FBC and blood film- thrombocytopenia, sepsis and leukaemia
    Renal profile: kidney involvement
    Serum albumin: nephrotic syndrome
    CRP: sepsis
    Blood cultures: sepsis
    Urine protein: creatinine ration: quantity of proteinuria
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8
Q

What is the criteria to diagnose HSP?

A
  • EULAR/PRINTO/PRES criteria
  • Requires: palpable purapura + at least one of:
  • Diffuse abdo pain
  • Arthritis
  • IgA depostis on histology
  • proteinuia or haematuria
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9
Q

Management of HSP?

A
  • Supportive with simple analgesia, rest and hydration
  • steroid may be considered if severe GI or renal involvement
  • Monitor closely:
    Urine dipstick: renal involvement
    BP: hypertension
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10
Q

Prognosis of HSP?

A
  • Abdo pains settles within a few days
  • Pts w/o kidney involvement expect to recover within 4-6 weeks
  • 1/3 pts have recurrence of diease within 6 months
  • v small proportion will develop ESRD
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11
Q

What is transient synovitis?

triggers, aetiology

A
  • Irritable hip
  • generally presents as acute hip pain following a recent viral infection
  • commonest cause of hip pain in children.
  • typical age group is 3-8 years.
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12
Q

Features of transient synovitis?

A
  • limp/refusal to weight bear
  • groin or hip pain
  • a low-grade fever is present in a minority of patients
  • high fever should raise the suspicion of other causes such as septic arthritis
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13
Q

What is imp to exlucude if child presents with ?transient synovitis?

A
  • SEPTIC ARTHIRITIS
  • if child has fever- red flag- needs specialist assessment
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14
Q

Managment of transient synovitis?

A
  • Self-limiting
  • requiring rest and analgesia
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15
Q

Ddx for purpuric rash?

A
  • meningococcal septicaemia
  • Leukaemia
  • HSP
  • idiopathic thrombocytopenic purpura
  • Haemolytic uraemic syndrome
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16
Q

Epidemiology of septic arthritis in children?

A

4-5 in 100,000
More common in M:F= 2:1

17
Q

Where is most commonly affected in septic arthritis?

A
  • hip
  • knee
  • ankle
18
Q

Symptoms of septic arthritis?

A
  • joint pain
  • limp
  • fever
  • systemically unwell; lethargy
19
Q

Signs of septic arthritis?

A
  • swollen red joint
  • typically, only minimal movement of affected joint is possible
20
Q

Investigations in septic arthritis?

A
  • joint aspiration for culture- will show increase WBC
  • raised inflammatory markers
  • blood cultures
21
Q

What is the Kocher criteria for the diagnosis of septic arthritis?

A
  • fever > 38.5 degrees
  • non-weight bearing
  • raised ESR
  • raised WCC
22
Q

What is reactive arthritis?

A
  • HLA-B27 associated seronegative spondyloarthropathies
  • Defined as: arthritis that develops following an infection where the organism cannot be recovered from the joint
23
Q

What is the ‘classic’ triad of reactive arthritis?

A

Urethritis, conjunctivitis and arthritis
* this used to be called Reiter’s syndrome- now reactive arthritis encompasses this

can’t pee, can’t see, can’t climb a tree

24
Q

What is the ‘classic’ triad of reactive arthritis?

A

Urethritis, conjunctivitis and arthritis
* this used to be called Reiter’s syndrome- now reactive arthritis encompasses this

can’t pee, can’t see, can’t climb a tree

25
Q

What organisms are associated with reactive arthritis?

A
  • Shigella felxneri
  • Salmonella typhimurium
  • Salmonella enteritidis
  • Yersinia enterocolitica
  • Camplylobacter

Chamydia can also cause it- not AS relevant in children

26
Q

What is the time course of reactive arthritis?

A
  • Typically develops 4 weeks of initial infection
  • Symptoms last around 4-6 months
  • 25% of patients have recurrent episodes
  • 10% of patients develop chronic disease
27
Q

Features of reactive arthritis?

A
  • Arthritis: asymmetrical oligoarthritis of lower limbs
  • Dactylitis
  • Symptoms of urethritis
  • Conjunctivitis
  • Anterior uveitis
  • circinate balanitis (painless vesicles on the coronal margin of the prepuce)
  • keratoderma blenorrhagica (waxy yellow/brown papules on palms and soles)
28
Q

Management of reactive arthritis?

A
  • Symptomatic: Analgesia, NSAIDs, intra-articular steroids
  • Sulfasalzine and methotrexate are sometimes used for persistent disease
  • Symptoms rarely last more than 12 months