Altered Conscious Level Flashcards

1
Q

What is DKA?

A

Severe lack of insulin means the body cannot use intracellular glucose
Body breaks down other body tissue as an alternative energy source
Ketones are the by-product of this process which build up and cause the body to become acidic

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2
Q

When does DKA usually occur?

A
At diagnosis of DM
During a growth spurt/puberty
Insulin omission
When ill
When an insulin pump gets blocked
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3
Q

When do you diagnose DKA?

A

Acidosis - pH <7.3 (Severe <7.1)
Ketonaemia (Blood beta-hydroxybutyrate >3mmol/L)
Blood glucose >11

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4
Q

What is Kussmaul breathing?

A

Form of hyperventilation
Deep and labored breathing pattern associated with severe metabolic acidosis, particularly diabetic ketoacidosis (DKA)
Also kidney failure

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5
Q

Treatment for DKA

A

Treat DKA with oral fluids and subcutaneous insulin only if the child or young person is:
Alert
Not nauseated or vomiting, Not clinically dehydrated

IV fluids and IV insulin if the child or young person is:
Not alert
Nauseated or vomiting
Clinically dehydrated

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6
Q

Calculating a fluid requirement for children with DKA

A

Assume a:
5% fluid deficit in mild to moderate DKA
10% fluid deficit in severe DKA

Lower than usual - Large fluid volumes associated with increased risk of cerebral oedema

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7
Q

Neccesary monitoring in DKA

A
1 hourly monitoring of:
BM
Ketones
Vital Signs
Fluid balance
GCS
@ 2 hours and then evey 4
monitor:
Glucose
Blood pH
pCO2
Na, K, urea

Monitor children receiving IV therapy with ECG

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8
Q

Assess child for cerebral oedema if which conditions are present?

A

Headache
Agigitation or irritability
Unexpected ↓HR & ↑BP

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9
Q

What is the treatment of cerebral oedema?

A

Mannitol or

Hypertonic sodium chloride

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10
Q

When to treat for cerebral oedma

A

Deterioration in level of consciousness
Abnormalities of breathing pattern (for example respiratory pauses)
Oculomotor palsies
Pupillary inequality or dilatation

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11
Q

When to suspend insulin infusion

A

Hypokalemia (<3mmol/L)

Child may need a central line to deliver IV K+

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12
Q

Symptoms of T1DM

A

Polyuria
Polydipsia
Weight loss
Excessive tiredness

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13
Q

Diagnosisng diabetes

A

Fasting glucose >7

2hr palsma glucose >11.1

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14
Q

Monitor children ith T1DM for: (4)

A

Thyroid disease (at diagnosis, then anually)
Diabetic retinopathy - anually from 12
ACR for albuminuria - anually from 12
Hypertension - anually from 12

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15
Q

Rare complications to be aware of in T1DM

A

Juvenile cataracts
Necrosis Lipoidica
Addison’s Disease

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16
Q

Initial management of DKA

A
O2
IV fluids
IV insulin
Consider NGT if drowsy
Consider Abx
Discussion with diabetes team
17
Q

Indications for T2DM in children

A
Strong family history
Signs of insulin resistance - acanthos nigricans
Obese at prsentation
Black or Asian family origin
Have no insuin requirement/ <0/5units/kg
18
Q

Indications for caauses other than T1 or T2DM

A

Diabetes in the first year of life
Rarely or never develop ketone bodies in the blood (ketonaemia) during episodes of hyperglycaemia
Associated features: optic atrophy, retinitis pigmentosa, deafness, or another systemic illness or syndrome
Strong family history of diabetes(however type 1 diabetes also has a genetic component)

19
Q

What is the main danger of childhood DKA?

A

Cerebral oedema

  • Occurs in ~1% of DKA cases
  • Mortality rate of 25%

(Hypokalemia, aspirational pneumonia)

20
Q

What may be the cause if ketonuria but glucose normal

A

Alcohol

21
Q

What to consider if acidosis but normal glucose?

A

Poisoning - aspirin

22
Q

Amylase in DKA

A

Often raised (up to ten fold) with non-specific abdominal pain even in absence of pancreatitis