Paediatric aspects of diabetes and endocrinology Flashcards

1
Q

What are common signs of T1DM in children?

A

Drinking ++
Peeing +++
Bedwetting
Wt loss

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2
Q

What are symptoms of DKA in children?

A

Vomiting
Stomach pain
Sighing breathing
Pear drops on breath

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3
Q

What immunological tests should be in suspection of T1DM?

A

GGAD (glutamic acid decarboxylase)
ICA (islet cell antibodies)
IAA (insulin antibodies)
IA2

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4
Q

What is C peptide?

A

Will still be present in early diabetes

Connects the alpha and beta chains of insulin together and is a direct measure of insulin production

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5
Q

What is a common history of diabetes?

A

Young boy vomiting at school
Bed wetting
Risk of dehydration

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6
Q

How is T1DM diagnosed?

A

FBG over 7

RBG over 11.1

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7
Q

Why is fluid carfeully managed in children presenting with DKA?

A

Fluid overload in DKA can lead to cerebral oedema = death

Insulin commences 1 hour after IV fluids stared

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8
Q

What are the targets of the childrens diabetes team?

A
All children to attend specialised childrens diabetic clinic 
MDT team 
Normal growth and development 
Aim for HbA1c below 58 mmol/mol
Microvascular screening from age 12
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9
Q

What are early changes of vascular disease in children with T1DM?

A
Microalbuminuria
CV autonomic neuropathy
Sensory nerve damage
Reinopathy
Cheiroarthropathy
Skin vascular changes
Vascular endothelial pathology
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10
Q

What is the insulin carb ratio?

A

1 unit of insulin = 10g of carbs

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11
Q

What is the insulin sensitivity factor?

A

How much your BG drops with a unit of insulin

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12
Q

What is primary congenital thyroid disease?

A

Gland dysplastic +/- abnormal site (sublingual)

Inborn error of thyroid hormone metabolism

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13
Q

What is secondary/tertiary congenital thyroid disease?

A

Congenital pituitary disease

Usually associated with hypopituitarism (GH, ACTH, gonadotrophin deficiency)

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14
Q

What are the clinical symptoms of congenital thyroid disease?

A

Delayed jaundice
Poor feeding but normal weight gain
Hypotonia (umbilical hernia, constipation)
Skin and hair changes

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15
Q

What screening test is done on newborn babies?

A

Guthrie test on day 5 post birth

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16
Q

What does the guthrie test screen for?

A

Sickle cell disease
CF
Congenital hypothyroidism
6 metabolic conditions

17
Q

Why will a fetus not be harmed by hypothyroidism?

A

Protected by placental thyroid hormones

18
Q

What will occur if hypothyroidism is not treated by 3 months?

A

Permanent developmental delay

19
Q

What is acquired thyroid disease in the young?

A

Delayed congenital
Post infectious
Autoimmune
Iodine deficiency

20
Q

In what other autoimmune conditions would you screen for thyroid disease of the young?

A

T1DM
Down syndrome
Coeliac disease

21
Q

What are the signs of hypothyroidism?

A
Slow progress
Growth failure 
Poor general health
Educational difficulties
Goitre
Thyroid function tests (high TSH, low fT3/4) 
High thyroid cell antibody titres
22
Q

What is the treatment for hypothyroidism in the child?

A

Thyroxine replacement for life

Dose related to size of child

23
Q

What are the general symptoms of hyperthyroidism?

A

Behaviour problems, sleep disturbance, eating difficulties
Goitre, high RH
Precocious puberty
Thyroid function tests (low TSH, high fT3/4)
High thyroid cell antibody titres

24
Q

What is the treatment of hyperthyroidism?

A

Beta blockade
Suppressant therapy: carbimazole +/- thyroxine
Radioiodine
Surgery

25
What does the adrenal cortex produce?
Mineralocorticoids Glucocorticoids Adrenal androgens
26
What does the adrenal medulla produce?
Catecholamines
27
What is primary adrenal disease?
Adrenal hypoplasia (absent/dysplastic/destroyed) Inborn error of metabolism Congenital adrenal hyperplasia
28
What is secondary adrenal disease?
Pituitary disease | Suppression secondary to steroid therapy
29
What can cause an overproduction of steroids?
``` High dose cortisol therapy Cushing disease (primary adrenal or secondary pituitary) ```
30
What can congenital adrenal hyperplasia lead to?
Hyperpigmentation of scrotum | Virilisation of female
31
What lead to congenital adrenal hyperplasia?
Defect in the enzyme 21-hydroxylase in the steroid hormone synthesis pathway in the adrenal gland which leads to a lack of aldosterone, cortisol and an excess of testosterone
32
What is virilisation in males and females?
Female: ambigous genitalia Male: precocious puberty
33
What is an addison crisis?
Absent aldosterone and cortisol: hyponatremia, hyperkalemia and hypotension Need to give salt and cortisol
34
What can cause ambigous genitalia?
CAH or other steroid abnormalities Gene or chormosomal abnormalities Congenital defects