Calcium and Bone Disorders Flashcards

1
Q

what is osteoporosis

A

progressive skeletal disease characterised by low bone mass and deterioration of bone tissue

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2
Q

what causes osteoporosis to occur

A

increased bone turnover with increased osteoclast activity/increased bone resorption

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3
Q

list the risk factors for developing osteoporosis

A
age
family history 
low BMI
rheumatoid arthritis 
liver or renal failure 
early menopause
steroid use
coeliac disease
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4
Q

does osteoporosis present with symptoms

A

typically asymptomatic unless have pathological fracture

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5
Q

where are the common site of fractures seen in osteoporosis

A

colles
hip
vertebral wedge

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6
Q

what is the best investigation for diagnosing osteoporosis

A

dexa bone scan

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7
Q

how is a dexa bone scan interpreted

A

T score shows the number of standard deviations away from a young persons bone density

  • 1 to -2.5 is osteopenia
  • 2.5 or more is osteoporosis
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8
Q

outline the lifestyle management for osteoporosis

A

smoking cessation
alcohol reduction
resistance training
calcium supplements

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9
Q

what classes of drugs are used to treat osteoporosis

A

bisphosphonates
strontium ranelate
teriparatide - s/c injection only indicated if patient doesnt respond to other therapies

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10
Q

list examples of bisphosphonates

A

alendronate

risedronate

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11
Q

how do bisphosphonates work

A

kill off osteoclasts which reduces bone reasorption

one tablet taken once a week

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12
Q

what are the side effects of bisphosphonates

A

photosensitivity
GI upset
osteonecrosis of the jaw

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13
Q

what is Pagets disease of the bone

A

metabolic disease causing increased bone turnover, osteoblast and osteoclast activity increased and bone is deposited in a disorganised manner

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14
Q

how does Pagets disease present

A

deep bone pain that is worse at night and weight bearing

pathological fracture - commonly tibia, femur, skull and pelvis

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15
Q

state the complications of Pagets disease

A

pathological fractures
hypercalcaemia
nerve compression

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16
Q

describe alkaline phos, calcium and phosphate levels in Pagets disease

A

raised alk phos

normal calcium and phosphate

17
Q

other than bloods tests, what investigations are done for Pagets disease

A

x-ray
early disease shows lytic lesions
late disese shows cortical thickening and deformity

18
Q

how is Pagets disease managed

A

analgesia

bisphosphonates

19
Q

describe the pathophysiology of osteomalacia and rickets

A

normal amount of bone but the mineral content of the bone is low

20
Q

what is the difference between rickets and osteomalacia

A

rickets occurs during active periods of bone growth before growth plates have fused
osteomalacia occurs once the epiphyseal growth plates have fused

21
Q

what causes osteomalacia and rickets

A

vitamin D deficiency
renal bone disease in context of CKD
cirrhosis - vitamin D cannot be activated
anti-convulsants

22
Q

how does Rickets present

A

growth retardation
bow legged/knock knees
hypotonia
apathy

23
Q

how does osteomalacia present

A

bone pain
fractures - neck of femur
proximal myopathy
waddling gait

24
Q

outline the investigations done for osteomalacia and rickets

A

bloods showing hypocalcaemia

x-ray showing reduced cortical bone and scleritic lines

25
Q

how is osteomalacia and rickets managed

A

calcium and vitamin D supplements

if renal disease - restrict fluids, phosphate binders

26
Q

what causes primary hyperparathyroidism and how does it present

A

usually parathyroid adenoma or hyperplasia of all 4 glands

presents with hypertension, increased bone resorption and hypercalcaemia

27
Q

what are the main symptoms of hypercalcaemia

A
fatigue 
thirst 
renal stones 
abdo pain 
depression
28
Q

state the blood test findings for primary hyperparathyroidism

A

PTH and calcium high

phosphate low

29
Q

what is the best investigation to diagnose hyperparathyroidism

A

sesatimbi scan to visualise the glands

30
Q

how is primary hyperparathyroidism managed

A

watchful waiting

removal or adenoma or glands

31
Q

what is the difference between secondary and tertiary hyperparathyroidism

A

secondary - physiological response in response to hypocalcaemia
tertiary - hyperplastic change due to prolonged hypercalcaemia, not a normal response

32
Q

outline the biochemical profile of secondary and tertiary hyperparathyroidism

A

secondary - low calcium, raised phosphate and PTH

tertiary - raised calcium and PTH, low phosphate

33
Q

how is secondary/tertiary hyperparathyroidism managed

A

treat underling cause with Vit D supplements

diet restriction if renal disease

34
Q

what is hypoparathyroidism

A

low PTH hormone due to gland failure

35
Q

what causes hypoparathyroidism

A

decreased Mg
Di George syndrome
haemochromatosis/Wilsons disease
thyroid surgery

36
Q

how does hypoparathyroidism present (symptoms of hypocalcaemia)

A
numbness
muscle cramps 
spasms 
wheeze 
anxiety
37
Q

what is the biochemical profile of hypoparathyroidism

A

low calcium
low PTH
high phosphate