DKA Flashcards
The management of diabetic ketoacidosis involves
The management of diabetic ketoacidosis involves the replacement of fluid and electrolytes and the administration of insulin.
What are the guidelines
To restore circulating volume if systolic blood pressure is below 90 mmHg (adjusted for age, sex, and medication as appropriate), give 500 mL sodium chloride 0.9% by intravenous infusion over 10–15 minutes; repeat if blood pressure remains below 90 mmHg and seek senior medical advice.
When blood pressure is over 90 mmHg, sodium chloride 0.9% should be given by intravenous infusion at a rate that replaces deficit and provides maintenance.
Include potassium chloride in the fluids unless anuria is suspected; adjust according to plasma-potassium concentration (measure at 60 minutes, 2 hours, and 2 hourly thereafter; measure hourly if outside the normal range).
Start an intravenous insulin infusion: soluble insulin should be diluted (and mixed thoroughly) with sodium chloride 0.9% intravenous infusion to a concentration of 1 unit/mL; infuse at a fixed rate of 0.1 units/kg/hour.
Established subcutaneous therapy with long-acting insulin analogues (insulin detemir or insulin glargine) should be continued during treatment of diabetic ketoacidosis.
Monitor blood-ketone and blood-glucose concentrations hourly and adjust the insulin infusion rate accordingly.
Blood-ketone concentration should fall by at least 0.5 mmol/litre/hour and blood-glucose concentration should fall by at least 3 mmol/litre/hour.
Once blood-glucose concentration falls below 14 mmol/litre, glucose 10% should be given by intravenous infusion (into a large vein through a large-gauge needle) at a rate of 125 mL/hour, in addition to the sodium chloride 0.9% infusion.
Continue insulin infusion until blood-ketone concentration is below 0.3 mmol/litre, blood pH is above 7.3 and the patient is able to eat and drink; ideally give subcutaneous fast-acting insulin and a meal, and stop the insulin infusion 1 hour later.
DKA is commonly seen in
This is most commonly seen in type 1 diabetes however in some cases it can be a complication of type 2 diabetes
Clinical features
High blood glucose (usually, although not always present)
Ketones in blood or urine
Symptoms
Increased frequency of urination Increased thirst Tiredness/ lethargy Blurred vision Abdominal pain Nausea and vomiting Smell of ketones on the breath Collapse/ unconsciousness
Risk factors
Can be seen at point of diagnosis During concurrent illness Missing insulin doses During a growth spurt or puberty Pregnancy Binge drinking Using illegal drugs
Treatment
Rehydrate with intravenous fluids
Replace electrolytes with intravenous electrolytes
Administer intravenous insulin- via a fixed rate insulin infusion.
Intravenous fluids
If patients have a systolic BP less than 90 mmHg a fluid bolus of 500mL sodium chloride 0.9% should be given over 10-15 minutes, this can be repeated if BP remains low.
When the BP is over 90 mmHg sodium chloride 0.9% is given at a rate that replaces deficit and provides maintenance.
Intravenous electrolytes
Potassium chloride should be given in the fluids unless the patient is suspected of being anuric. This
should be adjusted according to plasma-potassium concentration.
Intravenous insulin
- Soluble insulin (Actrapid®, Humulin S) should be given by intravenous injection.
- It is diluted with sodium chloride 0.9% to give a final concentration of 1 unit/mL.
- Initially infuse at a fixed rate of 0.1 units/kg/hour.
- If patient is on a long acting insulin (insulin Lantus® or Levemir®) this should be continues alongside the intravenous insulin infusion.
Monitoring
The patient should have their plasma potassium monitored initially after 60 minutes of commencing
treatment, then at 2 hours after treatment started and then every 2 hours thereafter.
If level is outside of the normal range recheck every hour until back in normal range.
Blood-ketone and blood glucose concentrations need to be checked hourly, the rate of the intravenous insulin infusion can be adjusted accordingly- the ketones should fall by at least 0.5mmol/litre/hour and glucose by at least 3 mmol/litre/hour.
Next steps
- When blood glucose concentration is less than 14 mmol/litre the patient should be started on a glucose 10% infusion at a rate of 125 mL/hour. This needs to be given in addition to sodium chloride 0.9% infusion.
- The insulin infusion can be stopped when the blood ketone concentration is less than 0.3 mmol/litre and blood pH is greater than 7.3 as long as the patient can eat and drink normally.
- When stopping the insulin infusion the patient should be given a subcutaneous fast acting insulin and a meal and the infusion stopped one hour later.
Pathophysiology
Diabetic ketoacidosis (DKA) is a complex disordered metabolic state characterised by hyperglycaemia, acidosis, and ketonaemia. DKA usually occurs as a consequence of absolute or relative insulin deficiency that is accompanied by an increase in counterregulatory hormones (ie, glucagon, cortisol, growth hormone, epinephrine). This type of hormonal imbalance enhances hepatic gluconeogenesis and glycogenolysis resulting in severe hyperglycaemia. Enhanced lipolysis increases serum free fatty acids that are then metabolised as an alternative energy source in the process of ketogenesis. This results in accumulation of large quantities of ketone bodies and subsequent metabolic acidosis. Ketones include acetone, 3-beta-hydroxybutyrate, and acetoacetate. The predominant ketone in DKA is 3-betahydroxybutyrate
There are several mechanisms responsible for fluid
depletion in DKA. These include osmotic diuresis due to hyperglycaemia, vomiting commonly associated with DKA, and eventually, inability to take in fluid due to a diminished level of consciousness. Electrolyte shifts and depletion are in part related to the osmotic diuresis. Hyper and hypokalaemia need particular
attention.
Potassium should be maintained between
4.0 and 5.0 mmol/L
The following groups of patients need specialist input
as soon as possible and special attention needs to be
paid to fluid balance
- Elderly
- Pregnant
- Young people 18 to 25 years of age (see cerebral oedema)
- Heart or kidney failure
- Other serious co-morbidities