Hypoglycaemia Flashcards

(34 cards)

1
Q
  1. Outline the first step in the management of hypoglycaemic patients in the following states:
    a. Alert and orientated
    b. Drowsy/confused but swallow intact
    c. Unconscious or concerned about swallow
A

a. Alert and orientated
Oral carbohydrates (e.g. juice/sweets or long-acting forms such as a sandwich)
b. Drowsy/confused but swallow intact
Buccal glucose (e.g. glucogel)
c. Unconscious or concerned about swallow
IV 50 mL 50% glucose
NOTE: or 100 mL 20% glucose

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2
Q
  1. What should be considered if a hypoglycaemic patient is deteriorating or does not appear to be responding to the first step in their management?
A

IM/SC 1 mg glucagon

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3
Q
  1. What is the benefit of giving glucose sublingually?
A

Bypasses hepatic first-pass metabolism

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4
Q
  1. How long is it likely to take for IM glucagon to cause an increase in blood glucose?
A

15-20 mins

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5
Q
  1. Which group of patients may not respond to IM glucagon?
A

Starving
Anorexic
Hepatic failure
These patients will have poor liver glycogen stores that can be accessed by glucagon

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6
Q
  1. Describe the triad of features that is used to define hypoglycaemia.
A

Low glucose
Symptoms
Relief of symptoms by administration of glucose

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7
Q
  1. List some symptoms of hypoglycaemia.
A

Adrenergic: tremors, palpitations, sweating
Neuroglycopaenic: confusion, coma

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8
Q
  1. What is a consequence of recurrent episodes of hypoglycaemia?
A

Hypoglycaemia awareness (loss of adrenergic symptoms with hypoglycaemia)

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9
Q
  1. Describe the order in which physiological compensatory changes in response to hypoglycaemia take place.
A

Suppression of insulin
Release of glucagon
Release of adrenaline
Release of cortisol

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10
Q
  1. What effect do these measures have on blood glucose and FFA production?
A

Increases blood glucose
Increases FFAs
Not all FFAs can be used to generate ATP by beta-oxidation so some of them will become ketone bodies

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11
Q
  1. What investigation may need to be performed to demonstrate hypoglycaemia in an otherwise healthy person?
A

Prolonged fast

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12
Q
  1. List some causes of hypoglycaemia in people without diabetes.
A
Fasting 
Paediatric
Critically unwell
Organ failure 
Hyperinsulinism
Post-gastric bypass 
Drugs 
Extreme weight loss 
Factitious (artefact)
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13
Q
  1. List some causes of hypoglycaemia in diabetics.
A
Medications (inappropriate insulin)
Inadequate carbohydrate intake (missed meal)
Impaired awareness
Excessive alcohol 
Strenuous exercise 
Co-existing autoimmune conditions
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14
Q
  1. List some diabetic medications that can cause hypoglycaemia.
A

Oral hypoglycaemics: sulphonylureas, meglitinides, GLP1 analogues
Insulin

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15
Q
  1. List some non-diabetic medications that can cause hypoglycaemia.
A

Beta-blockers
Salicylates
Alcohol

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16
Q
  1. How could co-morbidities in a diabetic patient lead to increased risk of hypoglycaemia?
A

Renal/liver failure could lead to impaired drug clearance

Concurrent Addison’s disease could result in hypoglycaemia (polyglandular autoimmune syndrome)

17
Q
  1. What is continuous glucose monitoring?
A

The device is applied to the abdominal wall with a small cannula that sits in the interstitial space in the subcutaneous fat

The sensor does not accurately read blood glucose when < 2.2 mmol/L

18
Q
  1. List some biochemical tests that may help differentiate between causes of hypoglycaemia.
A

Insulin levels (NOTE: exogenous insulin can interfere with assays)
C-peptide (marker of endogenous insulin production)
Drug screen
Autoantibodies
Cortisol/GH
Free fatty acids/ketone bodies
Lactate

19
Q
  1. What would you expect the insulin and C-peptide levels to be in a hypoglycaemic patient who has anorexia nervosa but not diabetes?
A

Low insulin and low C-peptide
The patient is hypoglycaemic because of poor liver glycogen stores (not an issue with insulin) so their insulin response will be normal

20
Q
  1. List some causes of Hypoinsulinaemic hypoglycaemia.
A

Fasting/starvation
Strenuous exercise
Critical illness
Endocrine deficiencies (adrenal failure, hypopituitarism)
Liver failure
Anorexia nervosa
NOTE: this is a normal response to hypoglycaemia

21
Q
  1. Name 3 ketone bodies.
A

3-hydroxybutyrate
Acetone
Acetoacetate

22
Q
  1. What does hypoglycaemia with high FFAs and low ketones suggest?
A

Fatty acid oxidation defect

23
Q
  1. List some physiologically explicable causes of neonatal hypoglycaemia.
A

Prematurity
IUGR
Inadequate glycogen/fat stores
NOTE: this should improve with feeding

24
Q
  1. List some tests that may be useful in the investigation of neonatal hypoglycaemia.
A
Insulin/C-peptide
FFA 
Ketone bodies 
Lactate 
Hepatomegaly
25
31. List some causes of neonatal hypoglycaemia with high FFAs and low ketones.
``` Fatty acid oxidation defects MCAD deficiency Carnitine disorders HMG-CoA lyase deficiency GSD type 1 ```
26
32. List some causes of neonatal hypoglycaemia with low FFAs and low ketones.
Hyperinsulinism | Hypopituitarism
27
33. List some causes of neonatal hypoglycaemia with high FFAs and high ketones.
``` Galactosaemia Glycogen storage disease Neonatal haemochromatosis GH deficiency Glucocorticoid deficiency Septicaemia ```
28
34. List some causes of inappropriately high insulin levels in neonates.
Islet cell tumours (e.g. insulinoma) Drugs (e.g. insulin, sulphonylureas) Islet cell hyperplasia • Infant with diabetic mother • Beckwith-Wiedemann syndrome (overgrowth disorder) • Nesidioblastosis (excessive function of beta cells with abnormal microscopic appearance)
29
35. State two causes of Hyperinsulinaemic hypoglycaemia with a high C-peptide.
Insulinoma Sulphonylurea abuse DOURINE OR SERUM SULPHONYLUREAS
30
37. Describe the mechanism by which beta cells release insulin in response to blood glucose.
Glucose crosses the membrane of beta cells and enters glycolysis via glucokinase Glycolysis produces ATP The rise in ATP leads to the closure of ATP-sensitive K+ channels This leads to membrane depolarisation, calcium influx and insulin exocytosis
31
38. Describe the mechanism of action of sulphonylureas.
They bind to the ATP-sensitive K+ channel making it close independently of ATP
32
41. What can cause the following: low glucose, low insulin, low C-peptide, low FFAs and low ketones?
This suggests that something is pretending to be insulin This is non-islet cell hypoglycaemia caused by secretion of big IGF-2 Big IGF-2 binds to IGF-1 receptors and insulin receptors It behaves like insulin, so it causes hypoglycaemia and suppresses insulin and FFA/ketone production It is a paraneoplastic syndrome usually caused by mesenchymal tumours (e.g. mesothelioma, fibroblastoma) and epithelial tumours (carcinoma)
33
42. Describe two autoimmune causes of hypoglycaemia.
Autoimmune conditions – antibodies against insulin receptors can cause insulin resistance and hypoglycaemia (rarely) Autoimmune insulin syndrome – antibodies are directed towards insulin so sudden dissociation of the antibodies can precipitate hypoglycaemia (could be caused by drugs e.g. hydralazine, procainamide)
34
43. List some genetic causes of hypoglycaemia.
``` Glucokinase activating mutation Congenital hyperinsulinism (GLUD-1, HNF4A, HADH, KNJJ11) ```