Diabetic Ketoacidosis
Precipitants
- insulin deficiency (unknown or due to mistaken with-holding of insulin)
- excessive glucagon
- excessive glucocorticoids
- infection or other illness
- vomiting
- MI
- trauma, burns, surgery
- stress
Pathogenesis
Lack of insulin means that glucose in the blood cannot be taken up into cells. Therefore the body perceives itself to be in a state of starvation and so begins lipolysis -> ketones and glycerol and gluconeogenesis using glycerol + alanine.
Ketones such as acetoacetate and 3-hydroxybutyrate have 3 effects - acidosis
- central action -> nausea and vomiting
- ketone excretion in urine (ketonuria) -> osmotic diuresis (losing Na+, K+, and Cl-)
Proteolysis occurs to produce the alanine required for gluconeogenesis.
High blood glucose with exacerbation by glucose production -> glycosuria and osmotic diuresis. Biochemical consequences
- Hyperglycaemia and plasma hyperosmolality -> cellular dehydration
- Metabolic acidosis with low HCO3-
- Glycosuria -> hyponatraemia and ketonuria
- May also have
- hyperkalaemia secondary to the metabolic acidosis; however there is an overall lack of body potassium as it is being lost via the osmotic diuresis - therefore give potassium during treatment to prevent severe hypokalaemia
- mild uraemia due to decreased GFR
- hyperlipidaemia (NB this may produce a pseudohyponatraemia)
Clinical consequences
- Dehydration ->
- Hypovolaemia ->
- Renal Hypoperfusion ->
- Acidosis ->
- Cardiac arrest, by affecting enzyme function once buffering capacity is exceeded
Clinical features at presentation
- 2-3 day history of gradual deterioration
- Hyperventilation (Kussmaul respiration) - deep and sighing
- Acetone / ketone odour on breath
- Nausea and vomiting
- Hypothermia due to peripheral vasodilatation - may mask pyrexia due to precipitating infection
- Drowsiness and coma - late signs
Investigations
To assess severity of DKA
- venous blood for glucose and U's and E's
- arterial blood for pH and blood gases
- urine for ketones
To assess cause of DKA
- venous blood for FBC, cardiac enzymes, blood cultures
- CXR
- ECG
- urine culture
Management
- 1) Correct dehydration with
- initially isotonic saline until blood glucose < 12 mmol/l
- then 10% dextrose
- 2) Decrease blood glucose with insulin, and monitor blood glucose hourly
- 3) Prevent hypokalaemia with i.v. K+ if necessary, monitor K+ hourly
- 4) Some doctors correct severe acidosis pH < 7.1 with HCO3- ie if cardiac arrest has occurred or is imminent as correction may induce cerebral oedema
- 5) Treat underlying condition - start broad spectrum antibiotics in case of infection
- 6) Be ready for
- shock
- cerebral oedema (treat with mannitol)
- DVT
- DIC
Emergency protocol - as for vivas
- 1) i.v. line for fluid
- usually 90% saline
- >1·5 litres/hr for 2 hrs
- 500ml/hr for 4 hrs
- 500ml/2hr
- 2) Investigations
- blood samples
- glucose
- should be monitored every hour
- once blood glucose < 12mmol/litre change infusion to dextrose saline
- U &Es
- hyponatraemia is common, but if Na+ <120mmol/litre consider another cause eg hypertriglyceridaemia
- if there is hypernatraemia (Na+ >150mmol/l) give first litre of saline as 0.45% instead of 0·9%
- beware the fact that some assays for creatinine cross-react with ketones, so creatinine may not reflect true renal function
- osmolality
- bicarbonate & blood gases
- if acidosis is severe pH < 7·1 some physicians give bicarbonate (100mmol over 1hr); other physicians don't because it affects the oxygenHb dissociation curve
- if there is acidosis without gross elevation of glucose consider overdose (aspirin) or lactic acidosis (esp. if elderly diabetic patients)
- FBC
- patient may have an elevated WCC (even leukaemoid) even in the absence of infection; however even with infection patient may be apyrexial
- blood cultures
- urine tests
- glucose
- ketones
- ketonuria does not equate with ketoacidosis
- normal individuals have ketonuria after a night's fast
- if glucose is normal consider alcohol
- can do test on blood to look for plasma ketonaemia
- MSU (for MC&S)
- 3) Nasogastric tube to prevent gastric dilatation and aspiration
- 4) Detailed Hx (relatives) + examination
- 5) CXR & ECG
- 6) Insulin
- preferably i.v. soluble insulin by pump
- 50u in 50ml 0·9% saline at 6ml/hr (ie 6 units insulin per hr)
- if infection use 10u/hr
- when blood glucose < 14mmol/litre halve infusion rate
- if no pump give 6units/hr i.m.
- 7) Potassium
- monitor serum K+ every hour
- hypokalaemia is likely (since when glucose enters cells it takes K+ with it)
- target range for K+ should be 4-5mmol/litre
- protocol
- if K+ < 3mmol/l give 40mmol K+ over 1 hr by i.v. and then recheck K+
- if K+ 3-4 mmol/l give 30mmol K+ over 1hr
- if K+ 4-5mmol/l give 20mmol K+ over 1 hr
- remember to monitor urine output
- withold K+ if oliguric (rare) or if initial plasma K+ is raised
- 8) If unconsciousness is prolonged give heparin 5000 units/6hr s.c.
- since dehydrated and stationary - to prevent DVT & PE
- 9) Monitor vital signs and glucose every hour, also K+
- 10) Treat any manifest infection - broad-spectrum antibiotics at first, change to more appropriate treatment when organism and sensitivity known
- 11) Be prepared for
- shock
- cerebral oedema (Rx- mannitol 20% 1g/kg = 5ml/kg i.v. over 15 mins)
- DVT
- DIC (Rx - 2 units fresh frozen plasma i.v. immediately, may need platelets and blood so consult expert; maintain accurate fluid balance and monitor urine output with catheter)
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