Hypoglycamia Flashcards

1
Q

acute management of hypoglycaemia in alert

A

oral carbs, rapid acting - juice, longer acting - sandwich

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2
Q

acute management of hypoglycaemia if drawsy

A

buccal glucose, glucogel, IV access

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3
Q

Acte management of hypo in unconcious

A

IV access, 20% glucose IV,

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4
Q

when would you consider 1mg glucagon

A

deteriorating, refractory, insulin induced, difficult IV access

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5
Q

how does gthe body naturally counter regulate low glucose

A

decreases insulin, increases glucagon (reduce peripheral uptake of glucose, increased glycongenolysis, increase gluconeogenesis, increased lipolysis) increases flucose ND FFA which re oxidised into ketones, low neuronal glucose sensed in hypothalamus and catecholamines, ACTH cortisol and GH are produced

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6
Q

how is glucose measured

A

venous glucose is gold standard, capillary blood glucose is point of case but poor precision

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7
Q

causes of hypos

A

diabetes, paeds, critically unwell, organ failure, hyperinsulinism, insuulinoma, gastric bypass, drugs, extremem weight loss, facticious

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8
Q

which diabetic meds lower glucose

A

sulphonylureas, GLP1, meglitinides, insulin, b blockers, salicyltes , alcohol

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9
Q

what is c peptide

A

cleavage product of insulin, secreted in equimolar amounts to insulin, half life 2 hours, interferes with insulin measurement,s inddicates how much insulin body is making

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10
Q

low insulin low c peptide

A

hypoinsulinaemic hypoglycaemia - due to fasting, starving, strenous exercise, critical illness, endocrine deficiencies, liver failrue

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11
Q

high insulin high c peptide

A

hyperinsulinaemic hypoglycaemia - insulinoma, sulphonylurea excess

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12
Q

high insulin low c peptide

A

exogenous insulin

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13
Q

what does absence of ketones signify in low glucose

A

insulin deficiency, fatty acid oxidation defect, starvation

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14
Q

causes of neonatla hypoglycaemia

A

premature, iugr, indadequate glycogen and fat sttores - should improve with feeding
pathological - inborn metabolic defecgt

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15
Q

inherited metabolic disorders

A

fatty acid oxidation defect, gluconeogentic disorder type 1, medium chain acyl coa dehydrogenase defect, carnitine disorders

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16
Q

what is 3 hydroxybutyrate

A

product of FFA

17
Q

ffa raised 3 hydroxybutyrate raised and no hepatomegaly

A

maple syrup urine, growth hormone deficiency, tyrosinaemia, drug toxicity, sepsis

18
Q

innapropriately raiased insulin causes

A

insulinoma, sulphonylurea, islet cell hyperplasia, beckwith weidmann syndrome, infant of diabetic mum, hyperinsulinism, rare autoimmune

19
Q

how do sulphonylureas work

A

binds to k+ atp channel independently of glucose causng membrane dedpoloratisation and insulin release

20
Q

low glucose low insulin low c peptide low ffa low ketones

A

non islet cell tumour hypoglycaemia - paraneoplastic syndrome secreting big igf2 which acts like insulin