Osteomalacia (MSK) Flashcards

1
Q

Define osteomalacia.

A

Softening of the bones secondary to low vitamin D levels which in turn leads to decreased bone mineral content

(Metabolic bone disease characterised by incomplete mineralisation of the underlying mature organic bone matrix (osteoid) following growth plate closure in ADULTS)

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2
Q

What is rickets?

A

Disorder of impaired mineralisation of cartilaginous growth plates in CHILDREN

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3
Q

What are the causes of osteomalacia? (3)

A
  • vitamin D deficiency:
    • reduced exposure to sunlight
    • low dietary intake
    • reduced intestinal absorption - Coeliac disease, chronic pancreatitis
  • defective vitamin D metabolism - liver cirrhosis, CKD
  • drugs (anticonvulsants)
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4
Q

What does vitamin D deficiency lead to in adults vs children?

A
  • adults - osteomalacia
  • children - rickets
  • rickets and osteomalacia are different manifestations of the same underlying pathological process
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5
Q

What are the clinical features of osteomalacia? (6)

A
  • bone pain and tenderness
  • pathological fractures - especially at femoral neck
  • proximal myopathy - may lead to waddling gait
  • fatigue and weakness
  • malaise
  • hypocalcaemia symptoms - CATs go numb
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6
Q

What are the symptoms of hypocalcaemia (osteomalacia)?

A

CATs go numb:

  • Convulsions
  • Arrhythmias
  • Tetany
  • Paraesthesia
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7
Q

What signs of hypocalcaemia might you see in osteomalacia? (2)

A
  • Chvostek’s sign - tapping over facial nerve causes twitching of ipsilateral facial muscles
  • Trousseau’s sign - inflation of BP cuff to above SBP for >3mins causes tetanic spasm of wrist and fingers
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8
Q

What are the clinical features of rickets? (4)

A
  • hypotonia
  • growth retardation
  • skeletal deformities
  • bow-legged (early childhood), knock knees (later childhood)
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9
Q

What are some risk factors for osteomalacia? (6)

A
  • dietary calcium and vitamin D deficiency
  • CKD
  • limited sunlight exposure
  • inherited disorders of vitamin D and bone metabolism
  • hypophosphatasia
  • anticonvulsant therapy
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10
Q

What are the first-line investigations for osteomalacia? (6)

A
  • serum 25-hydroxyvitamin D (low)
  • serum calcium (low)
  • serum phosphate (low)
  • serum ALP (raised)
  • intact PTH (raised - secondary hyperparathyroidism)
  • serum urea and creatinine (ratio elevated in renal failure)
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11
Q

What might you find on an XR in osteomalacia?

A
  • Looser’s zones (pseudofractures)
  • may see characteristic findings of long-standing secondary hyperparathyroidism, reversible with treatment
  • may show osteopenia
  • may appear normal
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12
Q

What are some differential diagnoses for osteomalacia? (2)

A
  • osteoporosis - painless and insidious until a fracture develops, advancing age and high-dose glucocorticoids, normal Ca/PO4/ALP/vitamin D/PTH, bone biopsy
  • Paget’s disease - ASx, markedly raised ALP, XR
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13
Q

What is the main management for osteomalacia?

A

Vitamin D + calcium replacement:

Ergocalciferol + calcium carbonate

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14
Q

How do we manage osteomalacia if renal disease or vitamin D resistance?

A

Alfacalcidol (1a-hydroxyvitamin D3) or calcitriol (1,25-hydroxyvitamin D3)

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15
Q

How do we manage inherited/acquired disorders of phosphate wasting or oncogenic osteomalacia?

A

Calcitriol + calcium carbonate + sodium phosphate

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16
Q

What are some complications of osteomalacia? (4)

A
  • pseudofractures
  • hypercalcaemia
  • secondary hyperparathyroidism
  • hypocalcaemia symptoms - CATs go NUMB
17
Q

What is prognosis of osteomalacia dependent on? (2)

A
  • underlying cause
  • compliance with therapies