T1DM Flashcards

1
Q

define T1DM

A

loss of beta cells due to progressive AI destruction

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2
Q

presentation

A

usually acute onset of severe symptoms e.g. weight loss, polyuria, thirst, etc.
DKA
pre-school and peri-puberty (but can be any age group)
non-obese (not necessarily)
insulin dependent
FH uncommon

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3
Q

diagnosis

A
  • antibodies GAD, IA-2 and ZnT8
  • C-peptide is usually still present at diagnosis. for this to be positive it must be low, even undetectable. it becomes low by 3 years in children and 5 years in adults (CONFIRMATORY test)
  • genetic risk score (high if 50th centile, 5th T2DM)
  • ketones e.g. ketonuria/ketonemia
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4
Q

how can C-peptide by investigated?

A

random or post meal C-peptide
fasted C-peptide
urine or plasma C-peptide 120 minutes after largest meal

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5
Q

aims of management

A

avoid hyperglycaemia
avoid hypoglycaemia
reduce complications

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6
Q

management

A

insulin
annual review of weight, BP, bloods (HbA1c, renal function and lipids), retina and feet
pancreas transplant either kidney-pancreas auto-transplant or islet auto-transplant
admit to hospital if persistent vomiting, diarrhoea, ketones, etc.

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7
Q

describe the use of insulin

A

never omit
alcohol predisposes to hypo, so reduce insulin dose before drinking and don’t take insulin for alcohol
less insulin with meal if exercising
advanced carb counting with MDI (risk of lipohypertrophy) and SCII (insulin pump)
blood glucose monitoring every 4 hours
sick day rules

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8
Q

different types of insulin used

A
prandial insulin (analogue or soluble)
basal insulin (isophane or analogue)
most T1DM are on an analogue basal insulin
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9
Q

blood glucose target pre-meal

A

3.9-7.2mmol/L

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10
Q

blood glucose target 1-2 hours post-meal

A

<10mml/L

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11
Q

how many grams of carbohydrate is one unit of insulin?

A

10g of carb

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12
Q

limitations to exogenous insulin

A

secreted into subcutaneous tissue so peak too slow to prevent post-meal hyperglycaemic spike
slow clearance

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13
Q

hypoglycaemia management

A

dextrose

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