endo Flashcards

1
Q

normal range for plasma glucose

A

fasting 3.5-5.6

post prandial <7.8

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2
Q

diabetes diagnosis

A

oral glucose tolerance test
Fasting = ≥7.0mmol/L
Post OGTT = ≥11.1mmol/l
HbA1c = 48mmol (> 6.5%)

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3
Q

type 1 diabetes cause

A

t cell mediated destruction of pancreatic B cells

causes insulin deficiency and hyperglycaemia

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4
Q

type 1 diabetes presentation

A

polyuria
lethargy
polydipsia
weight loss

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5
Q

type 1 diabetes management and OD symptoms (and cure)

A
insulin
weakness
vomiting
abdo pain
give glucogel
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6
Q

diabetic ketoacidosis cause

A

prolonged insulin deficiency

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7
Q

diabetic ketoacidosis signs

A
confusion
vomiting
polyuria
polydipsia
weight loss
abdo pain
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8
Q

diabetic ketoacidosis diagnosis

A

hyperglycaemia
acidosis
ketones in urine and blood >3

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9
Q

diabetic ketoacidosis management

A

correct dehydration - IV fluids
insulin - 1hr after fluids as can cause hypokalaemia
monitor electrolytes - K+

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10
Q
diabetic ketoacidosis fluids 
boluses
weights
maintenance 
insulin
A
correct over 48 hours
boluses - 10ml/kg 0.9% NaCl
<10kg 2ml/kg/hr
10-40kg 1ml/kg/hr
>40kg 40ml/hr

When calculating the fluid requirement for children and young people with DKA, assume:
a 5% fluid deficit in mild to moderate DKA (indicated by a blood pH of 7.1 or above)
a 10% fluid deficit in severe DKA (indicated by a blood pH below 7.1).

maintenance + correction - %dehydration x 10 x kg

insulin - 0.1units/kg/hour (1hour after fluids)

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11
Q

diabetic ketoacidosis complications

A

cerebral oedema - decreased HR, increased BP and ICP, restless, irritable, falling consciousness

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12
Q

hypo signs

A

autonomic - irritable, hungry, nauseous

neuroglycopenic - dizzy, headache confusion, LOC

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13
Q

hypo managment

mild/moderate, severe

A

3-5 glucose tablets, if no improvement after 10mins repeat
Glucagon - s/c or i/m injection
if < 5 years = 0.5mg
if > 5 years = 1mg
Wait 10 minutes, when conscious give sugar

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14
Q

diabetic complications

A

retinopathy
nephropathy
neuropathy

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15
Q

hypothyroidism signs

A
prolonged neonatal jaundice
poor feeding
hypotonia
dry skin/hair
bradycardia
constipation
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16
Q

hypothyroidism investigations

A

low T4

high TSH

17
Q

hypothyroidism what is thyroid hormone important for

A

growth and neurological development

18
Q

hypothyroidism management (+SE and managment)

A

levothyroxine - careful of thyroid storm (IV hydrocortisone, propanolol, fluids)

19
Q

congenital adrenal hyperplasia cause

A

21-hydroxylase (for cortisol biosynthesis) deficiency

excess male steroids and low cortisol and aldosterone

20
Q

congenital adrenal hyperplasia findings

A

cortisol deficient
increased ACTH
adrenal hyperplasia
increased progesterone leading to increased testosterone
21-hydroxylase needed for aldosterone production, as deficient get salt loss (low na, high k, metabolic acidosis)

21
Q

congenital adrenal hyperplasia signs

A

vomiting
dehydration
ambiguous genitalia
precocius puberty

22
Q

congenital adrenal hyperplasia managment

A

hydrocortisone for life (supress ACTH)

23
Q

adrenocortical crisis signs

A

nausea/vomiting
abdo pain
lethargy
hypotension

24
Q

adrenocortical crisis management

A

IV hydrocortisone - glucocorticoid

fludrocortisone - mineralocorticoid

25
Q

androgen insuficiency syndrome presentation

A

x linked recessive
genetically male child with female phenotype
resistant to testosterone

undescended testes
breast development

26
Q

androgen insuficiency syndrome management

A

counselling

bilateral orchidectomy - reduce risk of testicualr cancer

27
Q

precocious puberty definition

A

development of 2nd sexual characteristics before 8 in females and before 9 in males

28
Q

precocious puberty managment

A

synthetic GnRH analogues - supress pituitary gonadotrophins
no affect on androgen secretion so pubic hair still grows
treatment continued up to 11