Endocrine Flashcards

1
Q

What are some risk factors for Type 1 diabetes?

A

identical twin has 30-40% chance of developing disease

increased risk if parent has insulin-dependant diabetes

increased risk of HLA-DR3 or HLA-DR4

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2
Q

When does Type 1 Diabetes normally present?

A

preschool or teen years

spring and autumn

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3
Q

How does Type 1 diabetes normally present?

A

polyuria

polydipsia

weight loss

less common : enuresis, skin sepsis and candida

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4
Q

How is Type 1 diabetes diagnosed?

A

usually confirmed in symptomatic child - >11.1 mmol/L random blood glucose

> 7mmol/L fasting blood glucose

increased HbA1c

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5
Q

When should Type 2 be suspected?

A

Fam Hx

Indian Subcontinent

Severely Obese

Signs of insulin resistance (acanthosis nigricans)

PCOS

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6
Q

What are some signs of diabetic ketoacidosis?

A

acetone on breath

vomiting

dehydration

abdo pain

hyperventilation (Kussmaul)

hypovolaemic shock

drowsiness

coma and death

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7
Q

How would you manage Diabetic Ketoacidosis?

A

hosp admission

subcut insulin

IV fluids

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8
Q

What are some general non-medical ways of Type 1 diabetic management?

A

Injection of Insulin - technique and sites

Diet - less refined carbs, less than 30% fat intake, ‘carb counting’ for insulin calculation

‘sick-day-rule’ during illness to prevent DKA

blood glucose monitoring

recognition and treatment of hypoglycaemia

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9
Q

Why is it impt to keep rotating insulin injection sites?

A

avoid lipohypertrophy

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10
Q

What is the typical insulin regime for a child with Type 1 diabetes?

A

insulin pump OR

short-acting (Lispro, Glulisine) before each meal and snack

long-acting (Glurgine or Detemir) in late evening/and or before breakfast

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11
Q

What should the blood glucose range be in children? HbA1c?

A

4-10 in children

4-8 in adolescents

HbA1c - 58 mmol/mol (7.5%)

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12
Q

What is hypoglycaemia in children and neonates?

A

Diabetic children <4 mmol/L (very rare in non-diabetic children)

Neonates <2.6 mmol/L

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13
Q

How would hypoglycaemia present?

A

hunger

tummy ache

sweatiness

faint

irritability

seizures

coma

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14
Q

In children, what is an easy cure for hypoglycaemia?

A

Lucozade tablets

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15
Q

What are some problems with glucose control w children?

A

sweets and snacks

illness (increased insulin)

exercise (decreased insulin)

puberty (GH, oestrogen and testosterone all antagonise insulin) > increase from 0.5-1U/Kg/day > 2U/kg/day

can learn that glycosuria can be used to aid losing weight

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16
Q

What are some consequences of prolonged hypoglycaemia in neonates?

A

epilepsy

severe learning difficulties

microcephaly

17
Q

Why are infants at higher risk of hypoglycaemia?

A

high energy requirements

relatively poor reserves of glucose from gluconeogenesis and glycogenesis

18
Q

How would you treat hypoglycaemia in infants?

A

IV infusion glucose

corticosteroid

19
Q

After birth what are the levels of TSH like?

A

surge in TSH&raquo_space; increase T3 and T4, then TSH drops to adult levels

preterm infants may have very low levels of T4, and normal TSH

20
Q

What is the biggest complication associated with hypothyroidism?

A

learning difficulties

21
Q

What are some causes of hypothyroidism?

A

maldescent of thyroid and athyrosis

dyshormogensis (inbred)

iodine deficiency

tsh deficiency

22
Q

What is normally seen on the Guthrie test if hypothyroidism?

A

increased TSH

23
Q

What is most common cause of hyperthyroid?

A

Graves

24
Q

What is a cause of hypoparathyroidism?

A

DiGeorge syndrome

Addison’s

25
Q

What syndrome is hyperparathyroidism associated with?

A

William syndrome

26
Q

What is Cushing’s? What are some causes?

A

Glucocorticoid excess

normally side effect of long-term gluco-corticoid treatment - nephrotic syndrome, asthma

27
Q

How does Cushing’s present?

A

growth failure

short

face and trunk obesity

red cheeks

hirsutism

striae

HTN

bruising

carb intolerance

osteopenia

*normally obese and short children

28
Q

Diagnosis and Treatment of Cushing’s?

A

diurnal variation of cortisol - 24 hr urine free cortisol

Dex

29
Q

What is congenital adrenal hyperplasia?

A

group of autosomal recessive disorders

affect adrenal steroid biosynthesis

in response to resultant low cortisol levels the anterior pituitary secretes high levels of ACTH

ACTH stimulates the production of adrenal androgens that may virilize a female infant

30
Q

How does CAH present?

A

virilisation of the external genitalie in female infants (clitorial hypertrophy and variable fusion of labia)

enlarged penis and scrotum pigmented

salt-losing adrenal crisis - vomiting, weight loss, floppiness and circulatory collapse

tall stature in male non salt losers

muscular build, adult body odour, pubic hair and acne

precocious puberty

31
Q

How would you diagnoses CAH?

A

increased 17 alpha -hydroxyprogesterone

low sodium

high potassium

metabolic acidosis

hypoglycaemia

32
Q

How would you manage CAH?

A

females - corrective surgery to ext genitalia (as they have uterus and ovaries)

males in salt-losing crisis - saline, dextrose and hydrocortisone IV

long term - glucocorticoids

fludrocortisone

monitor growth, skeletal maturity and plasma androgens and 17 alpha-hydroxyprogesterone