Endocrinology Flashcards

1
Q

Insulin infusion rate in children in DKA?

A

0.05 - 0.1 units/ kg /hr

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2
Q

Single best test to assess thyroid function

A

TSH

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3
Q

HbA1c threshold to diagnose diabetes

A

48

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4
Q

Desmopressin test, results in

Craniogenic DI

Nephrogenic DI

A
  1. Responds, increase urine osmolality
  2. opposite
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5
Q

Glucose % and ml/hr once BGL <14 in DKA

A

10 % 125ml/hr

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6
Q

Fluid resus in adults with DKA

A

500ml NaCl initially over 10-15 mins
+ another 500ml if BP <90

Then 1L NaCl over 90 mins

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7
Q

Initial immediate treatment for a thyroid storm

A

beta blockers

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8
Q

Osmolality formula

A

2Na + glucose + urea

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9
Q

DKA CRITERIA

A

Glucose >11 or known diabetes
Ketones - >3 serum or 2+ on urine dip
Bicarb <15 and or pH <7.3

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10
Q

Complications of HSS

A

Re-hydrating too quickly
Cerebral oedema
Pulmonary oedema

cental pontine myelionsis

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11
Q

Congenital adrenal hypoplasia, deficiency in what?

A

deficiency of the enzyme 21-hydroxylase.

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12
Q

Test for congenital adrenal hypoplasia

A

ACTH stimulation test

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13
Q

HHS and advice regarding VTE

A

The risk of thromboembolism is very high in patients with HHS, and low molecular weight heparin should be routinely given. In patients such as this with a serum osmolality greater than 350 mmol/l full heparinisation should be considered.

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14
Q

Diabetic amyotrophy

(Proximal diabetic neuropathy)

A

second most common type of diabetic neuropathy

initially presents with pain in the buttocks, hips or thighs and is frequently unilateral initially.

Weakness and wasting of the proximal muscles of the lower limbs follow, and it can result in the patient being unable to go from sitting to standing without assistance.

Reflexes can also be affected in the corresponding areas involved. Diabetic amyotrophy is reversible with good glycaemic control, physiotherapy and lifestyle measures.

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15
Q

Nelson’s syndrome

A

Nelson’s syndrome is a rare condition that occurs many years after a bilateral adrenalectomy for Cushing’s syndrome. It is thought that it develops due to the loss of the negative feedback control that usually suppresses high cortisol levels. This, in turn, results in the re-establishment of CRH production by the hypothalamus, which subsequently stimulates the growth of an adrenocorticotrophic hormone (ACTH) producing pituitary adenoma.

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16
Q

Biochemical features of Addison’s disease

A

The classical biochemical features of Addison’s disease are as follows:
Increased ACTH levels
Elevated serum renin level
Hyponatraemia
Hyperkalaemia
Hypercalcaemia
Hypoglycaemia
Metabolic acidosis

17
Q

Type A vs B lactic acidosis

A

Type-B lactic acidosis is defined as not having to do with tissue hypoxia or hypoperfusion.

18
Q

Cushing’s disease vs Cushing’s syndrome

A

Cushing’s disease - an adenoma of the pituitary gland that secretes large amounts of ACTH and in turn elevates cortisol levels.

19
Q

Metabolic acidosis
(with raised anion gap) causes:

(4)

A

Lactic acidosis (e.g. hypoxaemia, shock, sepsis, infarction)
Ketoacidosis (e.g. diabetes, starvation, alcohol excess)
Renal failure
Poisoning (e.g. late stages of aspirin overdose, methanol, ethylene glycol)

20
Q

Metabolic acidosis
(with normal anion gap) causes:

(4)

A

Renal tubular acidosis
Diarrhoea
Ammonium chloride ingestion
Adrenal insufficiency

21
Q

Metabolic alkalosis causes:

(4)

A

Vomiting
Potassium depletion (e.g. diuretic usage)
Cushing’s syndrome
Conn’s syndrome

22
Q

Respiratory acidosis causes:

(5)

A

COPD
Life-threatening asthma
Pulmonary oedema
Sedative drug overdose (e.g. opiates, benzodiazepines)
Neuromuscular disease
Obesity

23
Q

Respiratory alkalosis cause:

(6)

A

Hyperventilation (e.g. anxiety)
Pulmonary embolism
CNS disorders (e.g. CVA, SAH, encephalitis)
Altitude
Pregnancy
Early stages of aspirin overdose

24
Q

How often is hydrocortisone given in adrenal crisis?

A

100mg IV 6hrly until the patient is haemodynamically stable and clinical improvement (alternative 200mg/24hrs by continuous IV infusion).

25
Q

Glucose concentration criteria in diabetes

A

Random > 11
Fasting > or equal to 7
OGTT > 11

(if asymptomatic, must be on two separate occasions)

26
Q

HBA1C criteria in diabetes

A

> or equal to 48 (confirmed with a second sample)

27
Q

Parameters for diagnosis of HHS

A

Glucose >30

Osmolality > 320

Hypovolaemia

Absence of significant ketonaemia (<3) and acidosis (pH 7.3 / Bicarb <15)

28
Q

Hyponatraemia with neurological sx

At what rate should Na be increased by

A

1-2 mmol/L/hr until symptoms resolve

29
Q

Markers for 5% dehydration for children in DKA

A

ph < 7.3 / Bicarb <15

30
Q

Markers for 7% dehydration for children in DKA

A

pH <7.2 or serum bicarbonate <10mmol/L

31
Q

Markers for 10% dehydration for children in DKA

A

pH <7.1 or serum bicarbonate <5mmol/L

32
Q

Fluid bolus in children in DKA who are shocked

A

20ml/kg of 0.9% (normal) saline over 15 minutes

If required, further 10ml/kg boluses up to a maximum of 40ml/kg at which point inotropes should be considered

33
Q

Fluid bolus in children in DKA who are NOT shocked

A

10ml/kg bolus of 0.9% (normal) saline over 60 minutes

Boluses for non-shocked patients should be subtracted from the fluid deficit

34
Q

Calculate fluid deficit in children with DKA

Given over what time period

A

Deficit (ml) = % dehydration X weight (kg) X 10

48hrs

35
Q

Calculate insulin rate in DKA in children

A

0.05 units/kg/hour

36
Q

Diabetic amyotrophy

A

proximal diabetic neuropathy, is the second most common type of diabetic neuropathy.

37
Q

Treatment for myxoedema

A

Thyroid hormones
Glucocorticoids
Treat infection if present

38
Q

When should insulin be stopped in DKA?

A

Ketones <0.6
pH >7.3 / Bicarb >18