Altered Conscious Level Flashcards
What is DKA?
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
When does DKA usually occur?
At diagnosis of DM During a growth spurt/puberty Insulin omission When ill When an insulin pump gets blocked
When do you diagnose DKA?
Acidosis - pH <7.3 (Severe <7.1)
Ketonaemia (Blood beta-hydroxybutyrate >3mmol/L)
Blood glucose >11
What is Kussmaul breathing?
Form of hyperventilation
Deep and labored breathing pattern associated with severe metabolic acidosis, particularly diabetic ketoacidosis (DKA)
Also kidney failure
Treatment for DKA
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
Calculating a fluid requirement for children with DKA
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
Neccesary monitoring in DKA
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
Assess child for cerebral oedema if which conditions are present?
Headache
Agigitation or irritability
Unexpected ↓HR & ↑BP
What is the treatment of cerebral oedema?
Mannitol or
Hypertonic sodium chloride
When to treat for cerebral oedma
Deterioration in level of consciousness
Abnormalities of breathing pattern (for example respiratory pauses)
Oculomotor palsies
Pupillary inequality or dilatation
When to suspend insulin infusion
Hypokalemia (<3mmol/L)
Child may need a central line to deliver IV K+
Symptoms of T1DM
Polyuria
Polydipsia
Weight loss
Excessive tiredness
Diagnosisng diabetes
Fasting glucose >7
2hr palsma glucose >11.1
Monitor children ith T1DM for: (4)
Thyroid disease (at diagnosis, then anually)
Diabetic retinopathy - anually from 12
ACR for albuminuria - anually from 12
Hypertension - anually from 12
Rare complications to be aware of in T1DM
Juvenile cataracts
Necrosis Lipoidica
Addison’s Disease
Initial management of DKA
O2 IV fluids IV insulin Consider NGT if drowsy Consider Abx Discussion with diabetes team
Indications for T2DM in children
Strong family history Signs of insulin resistance - acanthos nigricans Obese at prsentation Black or Asian family origin Have no insuin requirement/ <0/5units/kg
Indications for caauses other than T1 or T2DM
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)
What is the main danger of childhood DKA?
Cerebral oedema
- Occurs in ~1% of DKA cases
- Mortality rate of 25%
(Hypokalemia, aspirational pneumonia)
What may be the cause if ketonuria but glucose normal
Alcohol
What to consider if acidosis but normal glucose?
Poisoning - aspirin
Amylase in DKA
Often raised (up to ten fold) with non-specific abdominal pain even in absence of pancreatitis