DIABETES IN CHILDHOOD

 

DR SIMON ATTARD MONTALTO

 

 

Aetiology:

genetic susceptibility (DR3, DR4; chr.6),

environmental trigger (?CMV, reovirus),

autoimmune injury to beta cells (islet cell antibodies in 80%, )insulin autoantibodies in 18-20%

 

Presentation:

often in 'clusters',

weight loss, thirst, polydipsia, polyuria,

occasionally 'crisis' (ketoacidosis).

 

Diagnosis:

blood glucose - fasting >8mmol/l, postprandial >12mmol/l.

urinalysis - glycosuria.

 

MANAGEMENT

 

A. Initial Presentation

 

1 Admission:

stabilise,

initiate/establish treatment,

familiarise with 'diabetic team',

familiarise with insulin, injections, skin pricks,

dietary advice.

? induce hypo attack.

 

Insulin: medium acting preparation, initially 0.5U/kg/day; 60% before b'fast, 40% before evening meal.

 

 If weight loss, metabolic derangement severe -

 insulin requirement upto 1.0U/kg/day.

 Add short acting insulin (0.25-0.5U/kg/day).

 

2. Transition:

close supervision by diabetic health visitor.

5% experience 'honeymoon period'.

 

3. Follow-up:

close supervision,

educate and involve family.

 

B. Outpatient Clinic

 

1.      Routine:

B.D. regimen (occasionally t.d.s.).

Mixed short and medium acting insulin,

dose approximately. 0.5-0.8U/kg/day.

Check skin, liver size, urine for protein, C&S.

 

2.      Puberty:

Often difficult, especially girls.

Increased insulin requirements (1.5U/kg/day) due to surge in growth hormone.

 

3.      Difficult pts:

Convert to Pen injections.

Continuous s.c. insulin infusion as last resort.

Semi residential special school.

 

4.      Brittle diabetics:

Frequent ketoacidoses, usually due to:

§         Problem with diabetic management.

§         Concurrent illness.

§         Disrupted child/family dynamics.

 

Monitor:

Weight, growth.

Frequency of hypo attacks.

Sugars: 3-4/day twice a week or once daily,

  - (more frequently if instable),

  - use finger prick (BM stix) or autolets.

Urine glucose if needle phobic.

% HbA1 : normal=8%; 11-11.5% is acceptable

Serum fructosamine - measures % albumin  glycation. quick, cheap but ? too sensitive  to brief hyperglycaemic spells.

Ophthalmic review (if IDDM >10 years)

BP

 

COMPLICATIONS

 

A. Hypoglycaemia

 

1. Daytime: 10-15% will have at least one attack/year.

 Frequency increases with tighter control.

 Very rarely result in brain damage (even +fits).

 

2. Nocturnal: Potentially serious problem: - check BM late p.m, especially after busy day to obtain warning.

Partly due to surge in growth hormone at night.

May present with rebound hyperglycaemia first thing a.m. ('dawn phenomenon'/Somogyi effect).

 

Treatment:

 

Glucose drink, sweet etc.

Provide glucose buccal gel (Hypostop).

Provide (and instruct) glucagon injection.

Educate family, school etc.

 

B. Hyperglycaemia

 

1.       History:

Short illness; insulin omitted

Vomiting, abdominal pain

Drowsiness, confusion, coma

 

2. Examination:

Dehydrated,

ketotic

decreased consciousness,

tachycardia

Kussmaul respiration

diffuse abdo tenderness

? signs of infection

 

3. Investigations:

Urinalysis: 3+ glucose; 3+ ketones,

BM stix 'high',

Blood glucose >15mmol/l (often much higher),

Na+ normal; K+ normal (initially); urea, creatinine raised,

osmolality raised: (2x(Na+ + K+) + urea + glucose).

FBC: Hb, white cell count raised.

Blood gas: pH, HCO3- low; pO2 normal/high; pCO2 low.

CXR

Blood cultures

 

Management of Diabetic Ketoacidosis [DKA]

 

 1. CORRECT FLUID IMBALANCE

 2. CORRECT ACIDOSIS

 3. CORRECT ELECTROLYTE IMBALANCE

 4. CORRECT HYPERGLYCAEMIA

 5. TREAT PRECIPITATING CAUSE

 

1.      Fluids:

 

If shock is present resuscitate with boluses of 10 ml/kg of 0.9% saline (or 5% albumin) IV over 30 minutes, and repeat whilst signs of shock remain.

 

Calculate the fluid requirement = maintenance + deficit

 

(a) Maintenance:

first 10 kg: 100 ml/kg/24h

next 10 kg: 50 ml/kg/24h

over first 20 kg: 20 ml/kg/24h

 

(b) Deficit = %dehydration × body weight (kg).

 

The total fluid requirement should be given evenly over 24 hours.

 

Fluid used as replacement:

 

 - 0.9% (normal) saline until BM/glucose <15mmol/l,

 - 0.18% saline/4% dextrose thereafter.

 

2. Acidosis:

 

 - generally rehydration suffices.

 - if pH <7.1 give 8.4% NaHCO3, 1ml/kg/dose.

 

3. Electrolytes:

 

 - connect ECG monitor.

 - as hydration proceeds, K+ moves into the cells to  replace the net intracellular deficit resulting in  hypokalaemia.

 - add K+ to replacement fluids (depending on U & E).

 

4. Hyperglycaemia

 

 - start insulin infusion.

 - use rapid acting insulin.

 - initially 0.1U/kg/hour.

 - adjust according to sliding scale.

 - repeated s.c. doses may replace infusion.

 

5. Monitoring in ketoacidosis

 

- Continuous ECG monitoring.

- Vital signs (pulse, BP, resp. rate, abdo tenderness) - hourly.

- BM stix, 2-4 hourly.

- Blood glucose, U & E (especially K+), 4 hourly.

- Blood gas - repeated if initial pH <7.1.

- Urinalysis - assess every sample for glucose, ketones.