Clinical Calcium Homeostasis Flashcards

1
Q

what are the dietry sources of calcium?

A

milk, cheese and other dairy foods • green leafy vegetables – such as broccoli, cabbage and okra, but not spinach • soya beans • Tofu • nuts • bread and anything made with fortified flour • fish where you eat the bones – such as sardines and pilchards

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2
Q

what are the functions of calcium?

A

bone formation cell division and growth muscle contraction neurotransmitter release

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3
Q

wat proportion of calcium is bound in plasma?

A

45% bound- mainly to albumin 10%non ionised 45% ionised

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4
Q

what is the normal range of plasma calcium?

A

2.20-2.60 mmol/l

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5
Q

how do we calculate free calcium?

A

increased albumin decreases free calcium – Decreased albumin increases free calcium – Adjust Ca2+ by 0.1mmol/l for each 5g/l reduction in albumin from 40g/l

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6
Q

acidosis…. ionised calcium thus predisposing to …..

A

increases hypercalcaemia

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7
Q

what are the soures of vitamin D?

A

vitamin D is also found in a small number of foods. Good food sources are: • oily fish – such as salmon, sardines and mackerel • eggs • fortified fat spreads • fortified breakfast cereals • some powdered milks 

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8
Q

an increase in calcium does what to PTH?

A

decreases

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9
Q

a decrease in calcium does what to PTH?

A

increases

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10
Q

how are alteratioins in ECF Ca levels transmitted into the parathyroid cells?

A

via calcium-sensing receptor (CaSR)

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11
Q

when is PTH secreted in response to calcium

A

a fall in calcium

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12
Q

true or false: PTH mediates the conversion of vitamin D from its inactive to active form

A

true

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13
Q

what is hypocalcaemia?

A

serum calcium <2.20

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14
Q

these are the clinical features of hypocalcaemia

A
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15
Q

what are the causes of hypocalcaemia?

A

Disruption of parathyroid gland due to total thyroidectomy. May be temporary or permanent

Followingselectiveparathyroidectomy(usually transient & mild)

Severe vitamin D deficiency

Mg2+ deficiency (which drug can cause this?)

Cytotoxicdrug-inducedhypocalcaemia

Pancreatitis, rhabdomyolysis and large volume blood tranfusions

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16
Q

what are the investigations of hypocalcaemia?

A

ECG

– Serum calcium – Albumin
– Phosphate
– PTH

– U&Es
– Vitamin D
– Magnesium

17
Q

this is the investigation of hypocalcaemia flow chart

18
Q

what does hypoparathyroidism result from

A

agenesis (e.g. DiGeorge syndrome)

– destruction (neck surgery, autoimmune disease)

– Infiltration (e.g. haemochromatosis or Wilson’s disease)

– reduced secretion of PTH (neonatal hypocalcaemia, hypomagnesaemia)

– Resistance to PTH (discussed on next slide)

19
Q

when does Pseudohypoparathyroidism present?

A

which presents in childhood, refers to a group of heterogeneous disorders defined by target organ (kidney and bone) unresponsiveness to PTH

20
Q

what are the characteristics of Pseudohypoparathyroidism

A

t is characterized by hypocalcemia, hyperphosphatemia and, in contrast to hypoparathyroidism, elevated rather than reduced PTH concentrations

21
Q

what is the treatment of hypocalcaemia?

A

Commence oral calcium tablets
• If post thyroidectomy repeat calcium 24 hours

later

  • If vit D deficient, start vitamin D
  • If low Mg2+, stop any precipitating drug and replace Mg2+

“Severe” hypocalcaemia (Symptomatic or <1.9mmol/L)

This is a medical emergency

Administer IV calcium gluconate

Initial bolus (10-20ml 10% calcium gluconate in 50-100ml of 5% dextrose IV over 10 minutes with ECG monitoring)

Calcium gluconate infusion

Treat the underlying cause

23
Q

what are some vitamin D requirements?

A

Vitamin D requires hydroxylation by the kidney to its active form, therefore the hydroxylated derivatives alfacalcidol or calcitriol should be prescribed if patients with severe renal impairment require vitamin D therapy

24
Q

what are the causes of hypercalcaemia?

25
what are the clinical features of hypercalcaemia
26
how would you examen hypercalcaemia?
Lymph nodes – Concerns about malignancy (breast, lung etc.)
27
what are the investigations of hypercalcaemia?
U&Es – Ca – PO4 – Alk phos – Myeloma screen – Serum ACE – PTH
28
what are the causes of primary hyperparathyroidism?
nephrolithiasis bone disease asymptomatic
29
what are the investigations of primary hyperparathyroidism?
Ca, PTH • U&Es: check renal function • Abdominal imaging: renal calculi • DEXA: osteoporosis • 24 hour urine collection for calcium: Excl. FHH • Vitamin D ultrasound
30
what are the indications for surgery in primary hyperparathyroidism?
31
what is the treatment for primary hyperparathyroidism?
Medical management – Generous fluid intake – Cinacalcet (acts as a calcimetic, i.e. mimics the effect of calcium on the calcium sensing receptor on Chief cells, this leads to a fall in PTH and subsequently calcium levels)
32
what is familial hypocalciuric hypercalcaemia?
low levels of urinary calcium Autosomal dominant disorder of the calcium sensing receptor Benign, no therapy indicated
33
what is the management of hypercalcaemia?
Rehydration – 0.9% Saline 4-6 litres over 24 hours – Monitor for fluid overload – Consider dialysis if severe renal failure Afterrehydration, intravenous bisphosphonates – Zolendronic acid 4mg over 15 mins – Give more slowly and consider dose reduction if renal impairment – Calcium will reach nadir at 2-4 days
34
what is the 2nd line management?
glucocorticoids calcitonin calcimimetics parathyroidectomy
35