Endocrinology Flashcards

1
Q

What viruses can trigger T1D?

A

Coxsackie B and enterovirus

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2
Q

What is a normal glucose range?

A

4.4-6.1

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3
Q

How does hyperglycaemia present?

A

Polyuria
Polydipsia
Weight loss

(bedwetting and recurrent infections)

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4
Q

What tests should be done for T1DM?

A
FBC, U+E, Lab glucose
HbA1C
Thyroid function
Anti-TTG (Coeliac)
Insulin/islet/Anti-GAD Abs (pancreatic destruction)
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5
Q

Name a type of long acting insulin

A

Lantus

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6
Q

Name a short acting insulin

A

Actrapid

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7
Q

How does hypoglycaemia present?

A

hunger, tremor, sweating, confusion, pale, dizziness

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8
Q

In hospital setting how does you treat hypoglycaemia?

A

IV dextrose and IM glucagon

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9
Q

How do you treat DKA?

A

Fluid resus followed by fixed rate insulin

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10
Q

What do you need to be aware of in DKA treatment?

A

Potassium levels, hypokalaemia

Cerebral oedema

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11
Q

How does cerebral oedema present?

A

Headache, confusion, altered behaviour, bradycardia

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12
Q

What is primary adrenal insufficiency?

A

Addison’s - damaged adrenal gland with decreased cortisol and decreased aldosterone

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13
Q

What is secondary adrenal insufficiency?

A

Damaged pituitary (caused by infection, congenital, radiotherapy, etc)
Not enough ACTH released
Adrenal glands aren’t stimulated enough
Not enough cortisol produced in adrenal glands

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14
Q

What causes tertiary adrenal insufficiency?

A

Inadequate CRH from hypothalamus as a result of long term steroid use suppressing the hypothalamus

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15
Q

What are the symptoms and signs of adrenal insufficiency?

A
Lethargy, vomiting, hypoglycaemia, jaundice, failure to thrive.
Bronze pigmentation (in Addison's only as there's an increase in ACTH which then stimulates melanocytes).
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16
Q

What is a test for Addison’s?

A

Short Synacthen Test (ACTH stimulation test - if cortisol doesn’t rise less than double the baseline then positive test)

17
Q

What investigation results are expected in Addison’s?

A

Low cortisol
Low aldosterone
High ACTH
High Renin

18
Q

What results are expected in 2’ Adrenal Insufficiency tests?

A

Low cortisol
Normal aldosterone
Low ACTH
Normal renin

19
Q

How are adrenal insuff treated?

A

Hydrocortisone - cortisol

Fludrocortisone - aldosterone

20
Q

How does Addisonian Crisis present?

A

Reduced consciousness + hypotension

Hypoglycaemia, hyponatraemia, hyperkalaemia.

21
Q

How do you manage a Addisonian Crisis?

A

IV hydrocortisone
IV fluid resus
Correct hypoglycaemia

22
Q

What is Congenital Adrenal Hyperplasia?

A

Congenital deficiency of 21-hydroxylase enzyme

This causes a decrease in the production of cortisol and aldosterone from progesterone and an overproduction of testosterone from progesterone.

23
Q

What signs + symptoms in CAH?

A

Female: ambiguous genitalia

After birth: Hypoglycaemia, hyponatraemia and hyperkalaemia.

Could see bronzing from increased ACTH due to cortisol decrease.

24
Q

What is the pathophysiology of Growth Hormone Deficiency?

A

Damage to anterior pituitary which stimulates the release of ILGF-1 by the liver.

25
Q

What are congenital causes of GHD?

A

Mutations - GH1 and GHRHR genes

Empty Sella Syndrome (damanged pituitary)

26
Q

How does GHD present?

A

micropenis, hypoglycaemia + severe jaundice

27
Q

How do you test for GHD?

A

Growth hormone stimulation test using glucagon, insulin, arginine and clonidine.

28
Q

How do you treat GHD?

A

Daily injections of somatropin.

29
Q

What investigations should be done in suspected GHD?

A

Thryoid
MRI brain
Genetic testing
DEXA Scan