Endocrinology - hypoglycaemia/growth Flashcards

1
Q

Diagnostic criteria of hypoglycaemia

A

plasma glucose < 2.2-2.6mmol/L

Clinical features:
sweating
pallor
CNS (irritability, headache, seizures, coma)

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2
Q

Long-term complications from hypoglycaemia?

A

If it persists:

Epilepsy
Severe learning difficulties
Microcephaly

This risk is greatest in early childhood

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3
Q

Endocrine causes of hypoglycaemia

A
Hyperinsulinism
Hypopituitarism
Growth hormone insufficiency
Hypothyroidism
Congenital adrenal hyperplasia
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4
Q

Metabolic causes of hypoglycaemia

A
Glycogen storage disease
Galactosaemia
Organic acidaemia
Carnitine deficiency
Acyl-coA dehydrogenase deficiency
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5
Q

Toxic causes of hypoglycaemia

A

Salicylates
Alcohol
Insulin
Valproate

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6
Q

Hepatic causes of hypoglycaemia

A

Hepatitis
Cirrhosis
Reye syndrome

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7
Q

Systemic causes of hypoglycaemia

A

Starvation even after 4 hrs (infants have high energy requirements and poor reserves of glucose)

Malnutrition
Sepsis
Malabsorption

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8
Q

Which children should have their blood glucose measured?

A

Septicaemia
Appears seriously ill
Has prolonged seizure
Develops and altered state of consciousness

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9
Q

What is ketotic hypoglycaemia

A

In young children

Hypoglycaemia after a short period of starvation - child often short. Resolves in later life

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10
Q

Age group of endocrine and metabolic disorders leading to hypoglycaemia

A

Any age

Hepatomegaly may suggest inherited storage disorder

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11
Q

Epidemiology and nature of recurrent hypoglycaemia caused by PHHI

A

Infancy (rare)

Persistent hypoglycaemic hyperinsulinism of infancy

Gene mutation

Treat with high concentration dextrose solutions and diazoxide to maintain safe levels while investigating:

40% there is a localized lesion in the pancreas amenable to partial resection.
Majority require long-term meds or total pancreatectomy

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12
Q

Transient neonatal hypoglycaemia

A

In neonates

Possibly due to exposure of high levels of insulin in utero if mothers are diabetic or glucose intolerant

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13
Q

investigatons for hypoglycaemia

A

laboratory blood glucose to confirm.

U and Es
LFTs
Osmolality
Blood gas

Test for:
Growth hormone
IGF-1
Cortisol
Insulin
C-peptide
Fatty acids
Ketones
Glycerol
Lactate
Pyruvate
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14
Q

Treatment of hypoglycaemia

A

IV infusion of glucose:
2ml/kg of 10% dextrose bolus followed by infusion

CAREFUL to avoid excess - the hypertonic solution can cause CEREBRAL OEDEMA

If delay in establishing infusion OR failure to respond:
IM glucagon (0.5-1mg)

In a neonate, if the 10% dextrose has not worked, cause is likely to be HYPERINSULINAEMIA

If hypopituitarism or hypoadrenalism is suspected, corticosteroids

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15
Q

Epidemiology of insulin dependent diabetes mellitus (IDDM)

A

Steadily increasing in children.
Now 1 in 500 by 16yrs.

Almost all cases are T1DM.
Some severely obese have T2DM

Risk is 1/40 if father is affected. 1/80 if mother

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16
Q

Associated problems with IDDM

A
Few weeks of:
Polyuria
Excessive thirst
Weight loss
Nocturnal enuresis - young children

Enuresis
Skin sepsis
Candida infections

17
Q

Education programme in T1DM covers

A
Basic understanding
Injection techniques
Diet
Adjustment of insulin for sickness or exercise
Blood glucose check
Recognize hypoglycaemia
Where to get help
Support groups and psychological support
18
Q

How can insulin be administered. Correct technique

A

Infusion
Pump
Injection (SC in upper arm, anterior thigh, buttocks, abdomen)

Pinch the skin and insert needle at 45° to avoid complications such as lipohypertrophy.
Rotate sites frequently

19
Q

Insulin administration in infants

A

Insulin pump or 3-4 times/day injection regimen

Short-acting insulin before snacks and a long acting insulin in the evening

20
Q

What are normally the requirements of insulin in children?

A

0.5-1U/kg usually

Can increase to >2U/kg/day in puberty

21
Q

Dietary advice in IDDM

A

Match to insulin regimen
Aim to maintain control while getting good growth

High complex carbohydrates are recommended
Low fat content (<30% of calories)

High in fibres
Avoid foods that cause rapid sugar highs

22
Q

Different types of insulin

A

Rapid acting - short duration
Short acting - onset 30-60 minutes and peak at 2-4hrs (duration 8hrs). Give 15 min before meal.

Intermediate acting - onset after 1-2 hrs and peak at 4-12 hrs

A lot of preparations have predetermined preparations of short and intermediate acting insulin

23
Q

Blood glucose monitoring in IDDM

A

Aim is to keep blood glucose at 4-6mmol/L.
In practice more like 4-10 in children
-to avoid hypoglycaemia!

HbA1c for long-term control over 6-12 weeks - at least x3 per year. Keep below 7.5% (<58mmol/L)

24
Q

What to do if start getting symptoms of hypoglycaemia?

A

Try a sugary drink/snack. Then give a complex carbohydrate to maintain control

Otherwise IM glucagon

25
Why does the level of insulin needed rise in adolescence?
Antagonism by GH, oestrogen and testosterone
26
Appreciate that IDDM needs MDT
Same as any long-term condition (GP, paediatric consultant, dietician etc) Specialist Diabetic nurse
27
What are the difficulties in diabetic control in children
Eating too many sweets at parties Infrequent or unreliable blood glucose monitoring Illness - influences appetite and insulin (dose needs titrating) Exercise - prolonged exercies requires decrease in insulin Eating disorders Family disturbances (eg. divorce) Poor motivation and support
28
Long-term complications of IDDM (and prevention)
Growth and pubertal development - there may be delay/obesity Check yearly for HTN Renal disease (screen yearly for microalbuminuria) Eyes - retinopathy rare in children but should be checked 5 years after diagnosis Feet - encourage good care and avoid tight shoes or infections by treating early
29
Which diseases are commonly associated with T1DM and should not be missed
Coeliac disease Thyroid disease Other autoimmune disorders Low threshhold for investigating
30
Clinical features of DKA
``` Smell of acetone on breath Vomiting Dehydration Abdo pain Hyperventilation due to acidosis Hypovolaemic shock Drowsiness Coma and death ```
31
6 stages of DKA treatment
1. Fluids 2. Insulin 3. Potassium 4. Acidosis 5. Re-establish oral fluids, subcutanoeus insulin and diet 6. Identification and treatment of underlying cause
32
Managing fluids in DKA (1.)
If shock - resuscitate with normal saline. Rehydrate over 48-72h to avoid cerebral oedema. Monitor: Fluid input and output Electrolytes, creatinine and acid-base status regularly. Neurological state. Insert central venous line and urinary catheter if shocked. NG tube is passed for acute gastric dilatation if there is vomiting
33
The role of insulin in DKA management (2.)
Insulin infusion (0.5-1 U/kg per h). Titrate dose according to blood glucose. No bolus. Aim for gradual reduction of blood glucose by 2mmol/h. (faster is dangerous). Change to 4% dextrose/0.18% saline after 24h (should be <14mmol/L) to prevent hypoglycaemia.
34
The role of Potassium in DKA management (3.)
High initially. Will fall after treatment is initiated. Replacement must be instituted as soon as urine is passed. Continuous cardiac monitoring and regular plasma potassium measurement until stable
35
The role of acidosis in DKA management (4)
Metablic acidosis is present, but do not use bicarbonate unless there is shock or no response to therapy. Acidosis will self-correct with fluid and insulin. Monitor capillary ketones.
36
When can iv insulin be stopped in DKA?
1 hour after successful SC insulin has been given
37
What can precipitate ketoacidosis?
intercurrent infection Antibiotics may be indicated