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Senin, 12 Desember 2011

Diabetic Ketoacidosis


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 ->
  • 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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