disorders of calcium homeostasis part 2 W2 Flashcards

1
Q

what causes the symptoms of hypocalcaemia

A

increase in neuromuscular excitability due to increased inward Na+ movement.
resting potential of membrane is increased in hypocalcaemia
action potentials may be spontaneously generated

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2
Q

neuromuscular clinical manifestations of hypocalcaemia?

A

numbness and paraesthesia (tingling) in fingertips, toes, around mouth
anxiety and fatigue
muscle cramps, carpo-pedal spasm, bronchial or laryngeal spasm
seizures

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3
Q

clinical manifestations of hypocalcaemia - mental state?

A

personality change
confusion, psychoneurosis
impaired intellectual ability

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4
Q

clinical manifestations of hypocalcaemia other than neuromuscular and mental state

A

ECG changes (prolongation of QT interval) - can lead to cardiac arrest
eye problems - cloudiness

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5
Q

Chvostek’s sign?

A

contraction of muscles of eyes/mouth/nose elicited by tapping along the course of the facial nerve (in front of ear)

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6
Q

neurological signs of hypocalcaemia?

A

Chvostek’s sign
Trousseau’s sign

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7
Q

Trousseau’s sign

A

bp cuff used, brachial artery occluded for 3 minutes.
causes involuntary spasm of muscles resulting in adducted thumb, grouped fingers, flexed wrist

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8
Q

factitious hypocalcaemia causes?

A

consequence of low plasma albumen
-acute phase response
-malnutrition/malabsorption
-liver disease
-nephrotic syndrome

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9
Q

common cause of hypocalcaemia

A

vitamin D deficiency!! caused by

lack of sunlight exposure
inadequate dietary source
malabsorption
chronic renal disease (common)
chronic liver disease (rare)
rare genetic causes

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10
Q

vitamin D deficiency risk factors?

A

those confined indoors (esp elderly)
dark skin
high latitudes
lack of sunlight exposure (via dress, suncream, etc)

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11
Q

biochemical features of vitamin D deficiency

A

low 25-D3 and 1,25-D3 (
low Ca2+
high PTH
phosphate tends to be low
often raised ALP

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12
Q

clinical features of vitamin D deficiency

A

symptoms related to low Ca2+
osteomalacia (bone pain, fractures disordered growth in children as a consequence of defective mineralisation)

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13
Q

what is osteomalacia called in children?

A

Rickets

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14
Q

osteomalacia pathophysiology?

A

pathological bone problem classically associated with vitamin D deficiency
osteoid laid down by osteoblasts is not adequately calcified
osteoid content in bone increases as expense of normal calcified osteoid (bone matrix)
bones are softened, weak and susceptible to fracture

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15
Q

inherited causes of osteomalacia/rickets?

A

deficient 1-hydroxylase (vitamin D-resistant rickets type 1)

defective receptor for calcitriol (vitamin D-resistant rickets type 2)

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16
Q

hypoparathyroidism causes

A

acquired
-surgical damage/removal
-suppressed secretion

inherited
-developmental parathyroid problems
-genetic/familial disorders

17
Q

hypoparathyroidism biochemistry?

A

low Ca2+
inappropriately low PTH
phosphate may be increased

18
Q

what is magnesium required for

A

required for PTH action

19
Q

what can cause suppressed secretion in acquired hypoparathyroidism

A

low magnesium
maternal hypercalcaemia

20
Q

treatment of hypocalcaemia

A

acute - IV calcium
normally oral calcium and vitamin D are given (sometimes Mg)
vitamin D given in various forms
-by injection if malabsorption
-as 10H form if renal function
impaired
close monitoring of plasma calcium concentration necessary

21
Q

osteoporosis features

A

reduced bone mineral density, disruption of microarchitecture
routine biochemistry unaffected

22
Q

osteoporosis vs osteomalacia in terms of biochemistry

A

osteoporosis - normal biochem
osteomalacia - abnormal biochem