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

A
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

22
Q
A
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?

A
25
Q

what are the clinical features of hypercalcaemia

A
26
Q

how would you examen hypercalcaemia?

A

Lymph nodes

– Concerns about malignancy (breast, lung etc.)

27
Q

what are the investigations of hypercalcaemia?

A

U&Es

– Ca
– PO4
– Alk phos
– Myeloma screen – Serum ACE
– PTH

28
Q

what are the causes of primary hyperparathyroidism?

A

nephrolithiasis

bone disease

asymptomatic

29
Q

what are the investigations of primary hyperparathyroidism?

A

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
Q

what are the indications for surgery in primary hyperparathyroidism?

A
31
Q

what is the treatment for primary hyperparathyroidism?

A

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
Q

what is familial hypocalciuric hypercalcaemia?

A

low levels of urinary calcium

Autosomal dominant disorder of the calcium sensing receptor

Benign, no therapy indicated

33
Q

what is the management of hypercalcaemia?

A

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
Q

what is the 2nd line management?

A

glucocorticoids

calcitonin

calcimimetics

parathyroidectomy

35
Q
A