DKA Management Protocol
Initial Assessment and Diagnosis
Confirm DKA by meeting all three criteria: blood glucose >250 mg/dL, venous pH <7.3, and serum bicarbonate <15 mEq/L with moderate ketonuria or ketonemia. 1, 2
Immediate Laboratory Workup
- Draw venous blood gases (arterial not required after initial diagnosis), complete metabolic panel, serum β-hydroxybutyrate (preferred over nitroprusside-based ketone tests), BUN, creatinine, calculated anion gap, urinalysis, CBC with differential, and ECG 3, 1, 2
- Calculate anion gap using [Na+] - ([Cl-] + [HCO3-]); should be >10-12 mEq/L in DKA 1, 2
- Correct serum sodium by adding 1.6 mEq/L for every 100 mg/dL glucose above 100 mg/dL 1, 2
- Obtain bacterial cultures (blood, urine, throat) if infection suspected, as infection is the most common precipitating factor 3, 1, 4
Identify Precipitating Causes
Look specifically for: infection (most common), myocardial infarction, cerebrovascular accident, insulin omission/inadequacy, pancreatitis, SGLT2 inhibitor use, glucocorticoid therapy, or pregnancy 3, 1, 4
Fluid Resuscitation Protocol
Begin with isotonic saline (0.9% NaCl) at 15-20 mL/kg/hour (approximately 1-1.5 L in the first hour) to restore intravascular volume and renal perfusion. 3, 1, 2, 4
After the First Hour
- Calculate corrected serum sodium (add 1.6 mEq/L per 100 mg/dL glucose above 100) 1, 2
- If corrected sodium is normal or elevated: switch to 0.45% NaCl at 4-14 mL/kg/hour 3, 1, 2
- If corrected sodium is low: continue 0.9% NaCl at 4-14 mL/kg/hour 3, 1, 2
- Aim to correct total fluid deficit (typically 6-9 L) within 24 hours while limiting osmolality change to ≤3 mOsm/kg/hour to prevent cerebral edema 3, 1
When Glucose Reaches 250 mg/dL
Switch to 5% dextrose with 0.45-0.75% NaCl while continuing insulin infusion to prevent hypoglycemia and ensure complete ketoacidosis resolution, as ketonemia clears more slowly than hyperglycemia 3, 1, 2, 4
Potassium Management
Total body potassium depletion is universal in DKA (3-5 mEq/kg) even when serum levels appear normal or elevated. 3, 1
Critical Potassium Thresholds
- If K+ <3.3 mEq/L: HOLD insulin and replace potassium aggressively at 20-40 mEq/hour until K+ ≥3.3 mEq/L to prevent fatal arrhythmias, cardiac arrest, and respiratory muscle weakness 3, 1, 2
- If K+ 3.3-5.5 mEq/L: Add 20-30 mEq/L potassium to IV fluids (2/3 KCl + 1/3 KPO4) once adequate urine output confirmed 3, 1, 2, 4
- If K+ >5.5 mEq/L: Withhold potassium initially but monitor every 2-4 hours, as levels will drop rapidly with insulin therapy 3, 1
- Target serum potassium: 4-5 mEq/L throughout treatment 3, 1, 4
Insulin Therapy
Confirm serum potassium ≥3.3 mEq/L before starting insulin to avoid life-threatening hypokalemia. 1, 2, 4
Standard IV Insulin Protocol (Moderate-Severe DKA or Critically Ill Patients)
- Give IV bolus of 0.1-0.15 units/kg regular insulin (optional but not required) 3, 1
- Start continuous IV regular insulin infusion at 0.1 units/kg/hour 3, 1, 2
- Target glucose decline: 50-75 mg/dL per hour 3, 1, 4
- If glucose does not fall ≥50 mg/dL in first hour despite adequate hydration: double the insulin infusion rate each hour until steady decline achieved 3, 1
Alternative Protocol for Mild-Moderate Uncomplicated DKA
For hemodynamically stable, alert patients: subcutaneous rapid-acting insulin analogs at 0.15 units/kg every 2-3 hours combined with aggressive fluid management are equally effective, safer, and more cost-effective than IV insulin 1
Critical Insulin Management Rules
- Never stop insulin based on glucose levels alone—continue until ALL resolution criteria met 1, 2
- When glucose reaches 250 mg/dL, add dextrose to IV fluids while maintaining insulin infusion 3, 1, 2
- Stopping insulin prematurely is a common cause of recurrent ketoacidosis 3, 1
Monitoring During Treatment
Draw blood every 2-4 hours for serum electrolytes, glucose, BUN, creatinine, calculated osmolality, venous pH, and β-hydroxybutyrate. 3, 1, 2, 4
- Use venous pH (typically 0.03 units lower than arterial) rather than repeated arterial blood gases after initial diagnosis 3, 1, 4
- Calculate anion gap with each draw to track acidosis resolution 1, 2
- β-hydroxybutyrate measurement in blood is the preferred method for monitoring ketosis resolution; nitroprusside-based tests miss the predominant ketone body and may delay appropriate therapy 3, 1
Bicarbonate Administration
Bicarbonate is NOT recommended for DKA patients with pH >6.9-7.0, as multiple studies show no difference in resolution time or outcomes, and it may worsen ketosis, cause hypokalemia, and increase cerebral edema risk 3, 1
- Only consider bicarbonate if pH <6.9: give 100 mmol sodium bicarbonate diluted in 400 mL sterile water, infused at 200 mL/hour 1
Resolution Criteria
DKA is resolved when ALL of the following are met:
Transition to Subcutaneous Insulin
Administer basal subcutaneous insulin (NPH, detemir, glargine, or degludec) 2-4 hours BEFORE stopping IV insulin infusion to prevent recurrence of ketoacidosis and rebound hyperglycemia 3, 1, 2, 4
- Calculate total daily dose based on pre-admission regimen or estimate 0.5-1.0 units/kg/day for newly diagnosed patients 1, 2
- Once patient can eat, start multiple-dose schedule using combination of short/rapid-acting and intermediate/long-acting insulin 3, 1
- Recent evidence shows adding low-dose basal insulin analog during IV insulin infusion may prevent rebound hyperglycemia without increasing hypoglycemia risk 1
Special Considerations
Euglycemic DKA
- SGLT2 inhibitors are the leading cause of euglycemic DKA (glucose <200-250 mg/dL with ketoacidosis) 1
- Discontinue SGLT2 inhibitors immediately and do not restart until 3-4 days after metabolic stability achieved 1
- Check ketones during illness even if glucose is normal in patients on SGLT2 inhibitors 1
Common Pitfalls to Avoid
- Starting insulin before correcting hypokalemia (K+ <3.3 mEq/L) causes life-threatening arrhythmias 1
- Stopping insulin when glucose falls to 250 mg/dL instead of adding dextrose leads to recurrent ketoacidosis 3, 1
- Inadequate potassium monitoring and replacement is a leading cause of mortality in DKA 3, 1
- Overly rapid correction of osmolality (>3 mOsm/kg/hour) increases cerebral edema risk 3, 1
- Using nitroprusside-based ketone tests misses β-hydroxybutyrate and delays appropriate therapy 3, 1
Discharge Planning
- Ensure structured discharge plan including DKA recognition, prevention, and sick-day management education 1, 2
- Verify adequate outpatient insulin supply and scheduled follow-up appointments 1, 2
- Identify outpatient diabetes care providers before discharge 3, 1
- Educate on glucose monitoring, insulin administration, and recognition/treatment of hyperglycemia/hypoglycemia 1