Endocrinology/Growth - Hypoglycaemia/Growth&Puberty Flashcards

1
Q

Why is hypoglycaemia a problem in the neonatal period?

A
  • first 24 hours of life in babies with intrauterine growth restriction or preterm - poor glycogen stores
  • born to mothers with diabetes mellitus - sufficient glycogen but hyperplasia of islet cells in pancreas leading to high insulin
  • large for dates
  • hypothermic
  • polycythaemic
  • Ill
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the symptoms of hypoglycaemia in neonates?

A
jitteriness 
irritability
apnoea 
lethargy 
drowsiness 
seizures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the treatment for hypoglycaemia in neonates?

A

early and frequent milk feeding
if high risk then monitor blood glucose
if symptomatic or 2 low values give IV glucose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the causes of hypoglycaemia in children?

A
  • fasting
  • insulin excess e.g. diabetes mellitus, insulinoma
  • drug induced (sulphonylurea)
  • autoimmune - insulin receptor antibodies
  • liver disease
  • hormone deficiency (low GH, low ACTH) etc
  • galactosaemia
  • maternal DM
  • aspiration/alcohol poisoning
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the symptoms of hypoglycaemia in children?

A

sweating
pallor
CNS symptoms - irritability, headache, seizures, coma
If persists - epilepsy, severe learning disabilities and microcephaly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What investigations should be carried out when hypoglycaemic?

A

lab blood glucose
Bloods - GH, IGF-1, cortisol, insulin, C-peptide, fatty acids, ketones, glycerol, amino acids, acylcarnitine, lactate, pyruvate
Urine - organic acids, toxicology

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is the treatment for hypoglycaemia?

A
Glucose in the form of tablets
Non-diet sugary drink 
Oral glucose gel 
IV glucose 
Glucagon injection - IM if severe 
Corticosteroids is possibility of hypopituitarism or hypoadrenalism
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the epidemiology of insulin dependent diabetes in childhood?

A

2/1000 children by 16 years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How does insulin dependent diabetes present in childhood?

A

two peaks of presentation - preschool and teenagers
few weeks of polyuria, polydipsia and weight loss
young children may develop secondary nocturnal enuresis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the non medical treatment options for childhood diabetes- IDDM?

A

education for parents and children
diet changes - reduced carbs, <30% fat, high fibre
finger prick monitoring - in case of adjustments to changes of lifestyle, food and exercise
blood ketone monitored when ill

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the medical treatment options for IDDM?

A
  • Insulin – continuous infusion by pump or injections by syringe + needle/pen-like devices/jet injectors
  • Inject into upper arm/ant or lat thigh/buttocks/abdo (rotate to prevent liphypertrophy)
  • Usually basal-bolus
  • Need for supportive school environment
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the short term complications of IDDM?

A
  • Hypoglycaemia – hunger, tummy ache, sweatiness, feeling faint/dizzy or ‘wobbly feeling’ in legs
  • Can progress to seizures/coma
  • Treatment = Administer glucose tablets or non-diet sugary drink (or gel if unwilling to eat)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are the long term complications of IDDM?

A
  • Diabetic retinopathy + nephropathy – good diabetic control can delay or prevent complications
  • Growth + pubertal development – some delay of onset of puberty, obesity common if insulin dose not reduced towards end of puberty
  • Hypertension – BP checked once a year
  • Nephropathy – microalbuminaemia early sign
  • Monitor for retinopathy + cataracts
  • Feet – encourage good care + avoid tight shoes, treat infections early
  • Coeliac + thyroid disease common
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the presenting features of DKA?

DKA - blood glucose >11 mmol/L

A
  • Smell of acetone in breath
  • Vomiting
  • Dehydration
  • Abdo pain
  • Hyperventilation due to acidosis
  • Hypovolaemic shock
  • Drowsiness
  • Coma + death
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How should DKA be managed?

A

initial resuscitation if in shock with normal saline, insert central venous line and urinary catheter
correct dehydration - monitor fluids, U&E, creatinine, acid-base status, neuro state
start potassium replacement as soon as urine passed
metabolic acidosis present
re-establish oral fluids
treat underlying cause

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is classified as short stature?

A

height below second centile

17
Q

What are the pathological causes of short stature?

A
  • familial
  • IUGR and extreme prematurity
  • constitutional delay in growth and puberty
  • endocrine (usually child overweight) e.g. hypothyroidism, GH deficiency
  • nutritional/chronic illness e.g. crohns/coeliac
  • psychosocial deprivation
  • chromosomal disorder e.g. downs/turners
  • extreme short stature e.g. primordial dwarfism, resistance to GH
18
Q

What are the important investigations when looking at growth delays?

A

Growth chart + compare measures of height with predicted height based on parental measures
Bone age may be useful

19
Q

What are the important features of Russel-Silver syndrome?

not essential

A

born very small but normal head size

20
Q

How do you calculate the mid parental height?

A
Girl = (½ dads height –12cm) + mum’s height 
Boy = ½ dad’s height + (mum’s height + 12cm)
21
Q

When does puberty occur in girls?

A
8-13 years 
first sign = breast development
pubic hair growth + rapid growth spurt 
menarche average about 2.5 years after start of puberty  
early adrenache RF for PCOS
22
Q

When does puberty occur in boys?

A

9-14 years
first sign = testicular enlargement
pubic hair growth follows
later puberty could be hypogonadotrophic hypogonadism

23
Q

Which syndromes affect growth?

A

Down’s
Turner’s– F with one functioning X choromosome. Short stature, premature ovarian failure. GH resistance
Laron’s Syndrome - GH insensitivity
Prader-Willi – constant hunger and slow metabolic rate. C’some 15
Soto’s/ Weaver’s -overgrowth syndrome but usually become normal-size adults
Russell-Silver Syndrome - born very small but normal-sized heads

24
Q

What is precocious puberty?

A

Development of secondary sexual characteristics before 8 (females) and 9 (males)

25
Q

What are the investigations for precocious puberty?

A

Females - US exam of ovaries and uterus

Males - examination of the testes (look for bilateral/unilateral enlargement and small testes)

26
Q

What is premature thelarche?

A

premature breast development between 6 months and 2 years
non progressive and self limiting
no investigating required

27
Q

What is premature pubarche?

A

premature pubic hair development
no other sexual development signs
self limiting
risk of PCOS in later life

28
Q

What is defined as delayed puberty?

A

Delayed puberty – absence of pubertal development by 14 in females + 15 in males
More common in males
Long legs compared to body (eunuchoid body habitus)

29
Q

What investigations should be carried out in males and females with delayed puberty?

A

Investigations in males:
•Pubertal staging, esp testicular volume
•Identification of chronic systemic disorders

Investigations in females:
•Karyotype to identify Tuner syndrome
•Thyroid + sex steroid hormone measurements