A diabetic patient with hyperglycemia, dehydration, and a history of vomiting and omitted insulin, which treatment approach is correct?

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Low Molecular Weight Heparin Should Be Administered

The correct answer is C: Low molecular weight heparin should be administered. This patient presents with diabetic ketoacidosis (DKA), and thromboprophylaxis is a critical component of management that is often overlooked.

Why Option C is Correct

  • Patients with DKA are at significantly elevated risk for thromboembolic complications due to dehydration, hyperosmolality, and hypercoagulability 1
  • The American Diabetes Association guidelines emphasize that hospitalized patients with diabetes, particularly those with acute hyperglycemic crises, require venous thromboembolism prophylaxis 2
  • Low molecular weight heparin should be administered unless contraindicated to prevent potentially fatal pulmonary embolism and deep vein thrombosis 1

Why the Other Options Are Incorrect

Option A: Total Body Potassium Will Be Elevated - FALSE

  • Total body potassium is severely depleted in DKA, despite initially normal or elevated serum levels 1
  • The acidosis drives an extracellular shift of potassium, creating falsely reassuring serum levels while total body stores are critically low 1
  • Once insulin therapy begins, potassium shifts back intracellularly, and serum levels can drop precipitously, causing life-threatening arrhythmias 3, 1
  • Potassium replacement must begin once renal function is assured and serum potassium is known, typically adding 20-40 mEq/L to IV fluids 2

Option B: Rehydration and Insulin Should Always Commence Immediately Concurrently - FALSE

  • This is dangerously incorrect and represents a common pitfall that can cause death 3, 1
  • If initial serum potassium is <3.3 mEq/L, insulin therapy MUST be delayed until potassium is restored to prevent life-threatening cardiac arrhythmias, cardiac arrest, and respiratory muscle weakness 3, 1
  • The correct sequence is: begin isotonic saline at 15-20 mL/kg/hour while holding insulin, confirm renal function, aggressively replace potassium until K+ ≥3.3 mEq/L, then start insulin 3
  • Only after potassium is safe should insulin be initiated with an IV bolus of 0.1 units/kg followed by continuous infusion at 0.1 units/kg/hour 2, 3

Option D: Intravenous Sodium Bicarbonate Should Be Considered - FALSE

  • Several studies have shown that bicarbonate use in DKA made no difference in resolution of acidosis or time to discharge 2
  • Bicarbonate is generally not recommended and may be considered only in severe acidosis with pH <6.9 2
  • The acidosis resolves with insulin therapy and fluid resuscitation; bicarbonate adds unnecessary risk without benefit 2

Option E: Arterial Blood Gases Would Reveal a Reduced Anion Gap - FALSE

  • DKA is characterized by an ELEVATED anion gap metabolic acidosis, not reduced 2
  • The accumulation of ketoacids (β-hydroxybutyrate and acetoacetate) causes the anion gap to increase 2
  • Resolution of DKA requires anion gap ≤12 mEq/L, along with glucose <200 mg/dL, bicarbonate ≥18 mEq/L, and venous pH >7.3 3

Complete Management Algorithm for This Patient

Immediate Actions (First Hour)

  1. Begin isotonic saline (0.9% NaCl) at 15-20 mL/kg/hour to restore circulatory volume 2, 3
  2. Obtain STAT laboratory evaluation: plasma glucose, electrolytes (especially potassium), venous blood gas, BUN/creatinine, serum ketones (β-hydroxybutyrate preferred), osmolality, urinalysis, CBC, ECG 2, 3
  3. Administer low molecular weight heparin for thromboprophylaxis 1
  4. DO NOT start insulin yet - wait for potassium results 3, 1

Potassium Management (Critical)

  • If K+ <3.3 mEq/L: Continue aggressive fluid resuscitation, add 20-40 mEq/L potassium to IV fluids (2/3 KCl and 1/3 KPO4), obtain ECG, and delay insulin until K+ ≥3.3 mEq/L 3, 1
  • If K+ ≥3.3 mEq/L: Proceed with insulin therapy and add potassium to fluids 3

Insulin Therapy (After Potassium is Safe)

  • IV bolus of regular insulin 0.1 units/kg followed by continuous infusion at 0.1 units/kg/hour 2, 3
  • Target glucose decline of 50-75 mg/dL per hour 3
  • If glucose doesn't fall by 50 mg/dL in first hour, verify hydration status and double insulin infusion rate hourly until achieving steady decline 2

Ongoing Monitoring

  • Check blood glucose every 2-4 hours 3
  • Monitor electrolytes, venous pH, and anion gap every 2-4 hours 2, 3
  • When glucose reaches 250 mg/dL, change fluids to 5% dextrose with 0.45-0.75% NaCl plus potassium 2

Resolution Criteria

DKA is resolved when ALL of the following are met 3:

  • Glucose <200 mg/dL
  • Serum bicarbonate ≥18 mEq/L
  • Venous pH >7.3
  • Anion gap ≤12 mEq/L

Transition to Subcutaneous Insulin

  • Administer basal insulin (glargine or detemir) subcutaneously 2-4 hours BEFORE stopping IV insulin to prevent DKA recurrence 2, 3
  • Continue IV insulin for 1-2 hours after subcutaneous insulin is given 3
  • Never discontinue IV insulin without prior basal insulin administration - this is the most common error leading to DKA recurrence 3, 1

Common Pitfalls to Avoid

  1. Starting insulin before checking potassium - can cause fatal arrhythmias 3, 1
  2. Stopping IV insulin without prior subcutaneous basal insulin - causes DKA recurrence 3, 1
  3. Forgetting thromboprophylaxis - increases risk of potentially fatal pulmonary embolism 1
  4. Using bicarbonate routinely - no proven benefit and may cause harm 2
  5. Correcting osmolality too rapidly (>3 mOsm/kg/hour) - increases risk of cerebral edema 1

References

Guideline

Complications of Diabetic Ketoacidosis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Diabetic Ketoacidosis Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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