How to manage Hyperosmolar Non-Ketotic Coma (HONK)?

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Last updated: December 18, 2025View editorial policy

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Management of Hyperosmolar Nonketotic Coma (HONK)

Begin immediate fluid resuscitation with 0.9% sodium chloride at 15-20 mL/kg/hour during the first hour to restore circulatory volume and tissue perfusion, followed by insulin therapy once hemodynamic stability is achieved. 1

Initial Stabilization and Assessment

Immediate priorities:

  • Secure airway, breathing, and circulation; intubate if necessary for airway protection in obtunded patients 1
  • Establish intravenous access and begin aggressive fluid resuscitation before detailed laboratory workup 2
  • Draw initial labs: glucose, electrolytes (especially potassium), BUN, creatinine, serum osmolality, venous pH, and complete blood count 1
  • Monitor vital signs continuously and assess for precipitating causes (infection most common, followed by MI, stroke) 1, 2

Key diagnostic features to confirm:

  • Severe hyperglycemia (typically >600 mg/dL) with marked hyperosmolality 2
  • Absence of significant ketoacidosis (distinguishes from DKA) 3
  • Profound dehydration with typical water deficit of 9 liters 1

Fluid Resuscitation Protocol

First hour:

  • Administer 0.9% normal saline at 15-20 mL/kg/hour to restore intravascular volume 1
  • Continue isotonic saline until hemodynamic stability achieved (stable blood pressure, adequate urine output) 2

After hemodynamic stabilization:

  • Switch to 0.45% (half-normal) saline to address free water deficit 2
  • Continue fluid replacement to correct estimated deficits within 24 hours 1
  • Critical safety parameter: Ensure osmolality decrease does not exceed 3-8 mOsm/kg/hour to prevent cerebral edema 1

Pitfall to avoid: Overly aggressive fluid resuscitation with crystalloids increases risk of cerebral edema and adult respiratory distress syndrome; if hypovolemia persists despite adequate crystalloid administration, consider colloid solutions like albumin 3

Insulin Therapy

Timing and dosing:

  • Delay insulin until after initial fluid resuscitation has begun (unlike DKA, insulin is not first-line) 3, 2
  • Administer IV bolus of regular insulin 0.1 units/kg body weight 1
  • Follow with continuous infusion at 0.1 units/kg/hour 1

Glucose management during treatment:

  • When glucose reaches 250-300 mg/dL, add 5% dextrose to IV fluids 1
  • Reduce insulin infusion rate but continue to prevent rebound hyperglycemia 1
  • Maintain glucose initially around 250 mg/dL (14 mmol/L) as rapid lowering increases cerebral edema risk 3

Transition to subcutaneous insulin:

  • Administer basal insulin 2-4 hours before stopping IV insulin to prevent rebound hyperglycemia 1
  • Many elderly patients with HONK will not require long-term insulin and can be managed with diet or oral agents after recovery 2

Electrolyte Management

Potassium replacement (critical priority):

  • Monitor potassium levels every 2-4 hours as insulin therapy drives potassium intracellularly, causing potentially fatal hypokalemia 1, 4
  • Begin potassium replacement when serum level falls below 5.5 mEq/L, assuming adequate urine output 1
  • Warning: Hypokalemia can cause respiratory paralysis, ventricular arrhythmia, and death if untreated 4

Phosphate and magnesium:

  • Replace when serum concentrations fall below normal range, particularly in critically ill patients 3
  • While clinical benefit not definitively established, replacement is justified given potential for complications 3

Monitoring Protocol

Glucose monitoring:

  • Check blood glucose at least every 2-4 hours 1

Laboratory monitoring:

  • Draw blood every 2-4 hours for: electrolytes, glucose, BUN, creatinine, osmolality, venous pH 1
  • Pay particular attention to potassium given rapid shifts with insulin therapy 1

Clinical monitoring:

  • Assess mental status frequently for improvement or deterioration 2
  • Monitor urine output to ensure adequate renal perfusion 1
  • Watch for signs of cerebral edema (headache, altered consciousness, seizures) especially in younger patients 1

Identify and Treat Precipitating Causes

Most common precipitants:

  • Infection (most frequent cause) - obtain cultures, start empiric antibiotics if suspected 1, 2
  • Myocardial infarction - obtain ECG and cardiac biomarkers 1
  • Stroke - perform neurological examination and imaging as indicated 1
  • Medications: diuretics, corticosteroids, beta-blockers, phenytoin increase risk 2

Critical point: Associated diseases cause most fatalities in HONK, not the metabolic derangement itself; aggressive management of precipitating conditions is essential 5

Special Populations and Complications

Elderly patients:

  • HONK predominantly affects elderly patients with type 2 diabetes 2, 5
  • Higher risk of thromboembolic complications; two-thirds of deaths result from thrombosis and infection 3
  • Monitor for congestive heart failure with aggressive fluid administration 5

Pediatric patients (rare):

  • Greater risk of fatal cerebral edema compared to adults 6
  • Fluid therapy takes priority over insulin in initial management 6
  • Focus on slowly returning serum tonicity to normal 6

Mortality considerations:

  • Overall mortality remains 20-30% despite treatment, primarily due to severe underlying conditions 3
  • Thromboembolic disorders are leading cause of death alongside infections 3

Discharge Planning

Develop structured discharge plan including:

  • Diabetes education to prevent recurrence 1
  • Medication reconciliation (discontinue precipitating drugs if possible) 2
  • Follow-up arrangements to reduce readmission rates 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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