Interactive Guide to Hyperglycemic Crises
DKA & HHS: Diagnosis and Management Insights (2024 Consensus Update)
Welcome!
Diabetic Ketoacidosis (DKA) and Hyperglycemic Hyperosmolar State (HHS) are serious, acute complications of diabetes. This guide provides an interactive overview of their diagnosis and management, based on the 2024 Consensus Report by leading diabetes organizations.
Navigate through the sections to learn more. The "Management Algorithm" and "Case Studies" sections are designed to be interactive.
Disclaimer: This tool is for educational purposes only and should not replace clinical judgment or established institutional protocols. Information is derived from "Hyperglycemic Crises in Adults With Diabetes: A Consensus Report" (Diabetes Care 2024;47:1257-1275) and "Hyperglycemic crises in adults: A look at the 2024 consensus report" (Cleveland Clinic Journal of Medicine 2025;92:152-158).
Understanding Hyperglycemic Crises
DKA and HHS differ primarily in the degree of insulin insufficiency and the presence of ketoacidosis.
Pathogenesis of DKA
Key Driver: Absolute Insulin Deficiency & Increased Counterregulatory Hormones
- Reduced glucose utilization.
- Increased glucose production (gluconeogenesis, glycogenolysis).
- Increased lipolysis & free fatty acids (FFAs).
- Increased ketone body production in the liver from FFAs.
- Results in: Hyperglycemia, Ketonemia, Metabolic Acidosis.
- Osmotic diuresis leads to volume depletion.
Pathogenesis of HHS
Key Driver: Relative Insulin Deficiency (enough to prevent ketosis, not hyperglycemia)
- Reduced glucose utilization.
- Increased glucose production.
- Minimal or no significant ketogenesis.
- Profound hyperglycemia leads to severe osmotic diuresis.
- Results in: Severe Hyperglycemia, Hyperosmolality, Dehydration.
- Volume depletion impairs renal function, worsening hyperglycemia.
Inflammation and oxidative stress are also common contributors in both conditions.
Diagnosing DKA & HHS (2024 Criteria)
Diagnostic Criteria (Based on 2024 Consensus Report)
DKA Diagnostic Criteria
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✓
Diabetes/Hyperglycemia (D): Glucose ≥200 mg/dL (11.1 mmol/L) OR prior history of diabetes (irrespective of presenting glucose).
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✓
Ketosis (K): β-Hydroxybutyrate (blood) ≥3.0 mmol/L OR urine ketone strip ≥2+.
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✓
Metabolic Acidosis (A): Venous pH <7.3 AND/OR serum bicarbonate <18 mmol/L.
All three components (D, K, A) must be present. Anion gap is no longer a primary diagnostic criterion but may be useful if ketone measurement is unavailable.
Severity | pH | Bicarbonate (mmol/L) | β-OHB (mmol/L) | Mental Status |
---|---|---|---|---|
Mild | >7.25 to <7.30 | 15-18 | ≤6.0 (typically 3.0-6.0) | Alert |
Moderate | 7.0-7.25 | 10 to <15 | ≤6.0 (typically 3.0-6.0, can be >6.0) | Alert/Drowsy |
Severe | <7.0 | <10 | >6.0 | Stupor/Coma |
Level of care based on severity and clinical judgment.
HHS Diagnostic Criteria
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✓
Hyperglycemia: Plasma glucose ≥600 mg/dL (33.3 mmol/L).
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✓
Hyperosmolarity: Calculated effective serum osmolality >300 mOsm/kg OR total serum osmolality >320 mOsm/kg.
Effective: [2xNa⁺ (mmol/L) + glucose (mmol/L)]
Total: [2xNa⁺ (mmol/L) + glucose (mmol/L) + urea (mmol/L)]
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✓
Absence of significant ketonemia: β-Hydroxybutyrate (blood) <3.0 mmol/L OR urine ketone strip <2+.
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✓
Absence of significant acidosis: Venous pH ≥7.3 AND serum bicarbonate ≥15 mmol/L.
All four components must be present. Mental status is no longer a diagnostic criterion.
Note: Mixed DKA/HHS presentations occur in about 1/3 of hyperglycemic emergencies.
Clinical Presentation Comparison
Feature | DKA | HHS |
---|---|---|
Onset | Hours to days | Days to a week |
Mental Status | Usually alert (can be altered in severe DKA) | Change in cognitive state common |
Common Symptoms | Polyuria, polydipsia, weight loss, dehydration, nausea, vomiting, abdominal pain | Polyuria, polydipsia, weight loss, profound dehydration. Often co-presenting with other acute illness. N/V/abd pain less common. |
Respiration | Kussmaul respiration (deep, rapid breathing, fruity odor) | Tachypnea if dehydrated or due to underlying illness |
Management Algorithm (Interactive - 2024 Guidelines)
Click on the main treatment components to see details and decision pathways. This is a simplified representation for learning.
Isotonic saline (0.9% NaCl) or balanced crystalloid solutions (e.g., LR, Plasmalyte).
- Choice of fluid (0.9% NaCl vs. 0.45% NaCl vs. balanced crystalloid) depends on corrected serum sodium and hydration status. 0.45% NaCl only if osmolality not declining in HHS despite adequate fluid/insulin.
- When plasma glucose reaches <250 mg/dL (13.9 mmol/L) in DKA AND HHS:
Add 5% or 10% dextrose to IV fluids (e.g., D5W/0.45% NaCl or D5W/0.9% NaCl). - In euglycemic DKA (glucose <200 mg/dL & positive ketones): Start 5% or 10% dextrose with 0.9% NaCl/crystalloid at the start of insulin treatment.
Balanced crystalloids may lead to faster DKA resolution and less hyperchloremic acidosis vs. 0.9% NaCl.
IMPORTANT: If serum K+ <3.5 mmol/L, HOLD insulin and replete K+ first!
- Initial bolus: 0.1 units/kg s.c.
- Then: 0.1 units/kg s.c. every 1 hour OR 0.2 units/kg s.c. every 2 hours.
- If close monitoring available & non-critical.
- Optional: 0.1 units/kg IV bolus (if delay in starting infusion).
- Start fixed-rate infusion: 0.1 units/kg/h (or nurse-driven protocol).
- When glucose reaches <250 mg/dL, reduce insulin to 0.05 units/kg/h.
- Adjust to maintain glucose 150-200 mg/dL until DKA resolution.
- Start fixed-rate infusion: 0.05 units/kg/h (if no significant ketosis).
- If mixed DKA/HHS (significant ketosis/acidosis): Treat as DKA (0.1 units/kg/h).
- Target glucose 200-250 mg/dL until HHS resolution. Adjust insulin.
- HHS glucose reduction: not >90-120 mg/dL/h. Osmolality fall: not >3-8 mOsm/kg/h.
- Goal glucose decline: 50-75 mg/dL/hour. If not achieved, reassess hydration and consider increasing insulin infusion rate.
- Continue IV insulin until DKA/HHS resolves AND patient can eat.
- Overlap IV insulin with first s.c. basal insulin dose by 1-2 hours.
- If on basal insulin pre-admission, can continue at usual dose (adj. as needed) with IV insulin.
Total body potassium is depleted in DKA/HHS. Hypokalemia is a risk during treatment.
- Routine use NOT recommended.
- Consider ONLY if venous pH <7.0 after initial hydration.
- If given: e.g., 100 mmol sodium bicarbonate in 400 mL sterile water + 20 mEq KCl over 2 hours. Recheck pH.
- Routine replacement NOT recommended.
- Consider if severe hypophosphatemia (<1.0 mg/dL or <0.32 mmol/L) AND cardiac dysfunction, respiratory depression, or muscle weakness.
- If given: e.g., 20-30 mmol/L of potassium phosphate can be added to replacement fluids.
- Plasma/capillary β-hydroxybutyrate <0.6 mmol/L
- AND (Venous pH ≥7.3 OR Bicarbonate ≥18 mmol/L)
- AND Patient is able to eat.
- Glucose ideally <200 mg/dL.
- Serum osmolality <300 mOsm/kg
- AND Urine output >0.5 mL/kg/hour
- AND Cognitive status improved/returned to baseline
- AND Blood glucose <250 mg/dL
- AND Patient is able to eat.
Do not use urine ketones for DKA resolution. Clinical judgment is key.
Transition to Maintenance Insulin (2024 Guidelines)
Once DKA/HHS is resolved and the patient can eat, transition from IV to subcutaneous (s.c.) insulin.
Key Principles:
- Overlap: Administer first s.c. basal insulin dose 1-2 hours BEFORE stopping IV insulin infusion.
- Regimen: Basal-bolus regimen is preferred. Ensure 24-hour insulin coverage.
- Calculate Total Daily Dose (TDD):
- Weight-based: 0.3-0.6 units/kg/day (lower end for renal impairment, frailty).
- Preadmission regimen: Consider if appropriate.
- IV insulin requirements: Summation of stable hourly IV rates (e.g., prior 6-8h), use with caution.
- Distribution: Typically 40-60% of TDD as basal, rest as prandial. If NPO, basal + correction.
Non-Insulin Agents:
- SGLT2 inhibitors: Do NOT initiate or continue during hospitalization for DKA/HHS.
- Not recommended in T1D. Other non-insulin agents may be considered for T2D or ketosis-prone T2D.
Discharge Planning:
- Ensure 24-h insulin coverage. Discharge dosing may differ from transition dosing.
- Schedule timely follow-up. Provide comprehensive education.
Guideline Changes: 2024 vs. 2009 Consensus
The 2024 consensus report introduces several key updates to the diagnosis and management of hyperglycemic crises compared to the 2009 guidelines. (Source: CCJM 2025;92:152-158, summarizing the 2024 report)
DKA Diagnostic Criteria Changes
Diagnostic Criterion | 2009 Consensus Statement | 2024 Consensus Report |
---|---|---|
Plasma Glucose (D) | Glucose >250 mg/dL | Glucose ≥200 mg/dL OR History of diabetes (irrespective of presenting glucose) |
Ketosis (K) | Serum ketones: positive Urine ketones: positive |
Beta-hydroxybutyrate ≥3 mmol/L OR Urine ketone strip ≥2+ |
Metabolic Acidosis (A) | pH ≤7.3 Bicarbonate ≤18 mmol/L Anion gap >10 |
pH <7.3 with or without bicarbonate <18 mmol/L (Anion gap removed as a primary diagnostic criterion) |
Key Takeaway for DKA Diagnosis: Lower glucose cutoff, inclusion of diabetes history for euglycemic DKA, emphasis on quantitative β-hydroxybutyrate, and removal of anion gap as a primary criterion.
HHS Diagnostic Criteria Changes
Diagnostic Criterion | 2009 Consensus Statement | 2024 Consensus Report |
---|---|---|
Hyperglycemia | Plasma glucose >600 mg/dL | Plasma glucose ≥600 mg/dL |
Hyperosmolality | Calculated effective serum osmolality >320 mOsm/kg | Calculated effective osmolality >300 mOsm/kg OR Total osmolality >320 mOsm/kg |
Absence of Significant Ketosis | Serum ketones: Small Urine ketones: Small |
Beta-hydroxybutyrate <3 mmol/L OR Urine ketones <2+ |
Absence of Significant Acidosis | pH >7.3 Bicarbonate >18 mmol/L |
pH ≥7.3 AND Bicarbonate ≥15 mmol/L |
Mental Status | Stupor or coma (often implied as part of severity) | Removed as a diagnostic criterion |
Key Takeaway for HHS Diagnosis: Lowered effective osmolality cutoff, addition of total osmolality, quantitative ketone cutoffs, slightly lowered bicarbonate threshold, and removal of mental status as a direct diagnostic criterion.
Main Treatment Recommendation Changes (Fluids & Insulin)
Aspect | 2009 Consensus Statement | 2024 Consensus Report |
---|---|---|
Fluids - Type & Initial Rate | Initial: 0.9% NaCl (15-20 mL/kg/hr or 1-1.5L in 1st hr) | Initial: Isotonic saline or balanced crystalloid solutions (500-1,000 mL/hr for first 2-4 hrs) |
Subsequent: 0.45% NaCl if Na high/normal; 0.9% NaCl if Na low. | Subsequent: Choice depends on hemodynamics, fluid balance, Na. 0.45% NaCl only if osmolality not declining in HHS despite adequate fluid/insulin. | |
Dextrose when glucose reaches 200 mg/dL (DKA) or 300 mg/dL (HHS), usually with 0.45% NaCl. | Add 5% or 10% dextrose when glucose reaches <250 mg/dL for BOTH DKA and HHS. | |
Fluids - Correction Time | Estimated deficit in 24 hours. | Estimated deficit in 24-48 hours (50% in first 8-12 hrs). |
Insulin - Initial (DKA) | IV Bolus 0.1 units/kg, then 0.1 units/kg/hr IV infusion OR 0.14 units/kg/hr IV infusion (no bolus). | Moderate/Severe DKA: 0.1 units/kg/hr IV infusion (optional 0.1 units/kg IV bolus if delay). OR Nurse-driven protocol. |
(SubQ insulin for mild DKA mentioned but less emphasized) | Mild/Uncomplicated Moderate DKA: Subcutaneous rapid-acting analog 0.1 units/kg q1h or 0.2 units/kg q2h recommended. | |
Insulin - Initial (HHS) | Same as DKA (0.1 units/kg bolus then 0.1 units/kg/hr OR 0.14 units/kg/hr). | 0.05 units/kg/hr IV infusion. (If mixed DKA/HHS, treat as DKA: 0.1 units/kg/hr). |
Insulin - Glucose Goal until Resolution | DKA: 150-200 mg/dL HHS: 200-300 mg/dL |
DKA: 150-200 mg/dL HHS: 200-250 mg/dL |
Key Takeaway for Treatment: More emphasis on balanced crystalloids, slightly more conservative initial fluid rates, unified glucose target for adding dextrose, stronger recommendation for SubQ insulin in mild/mod DKA, different initial insulin dose for HHS, and refined glucose targets for HHS.
Case Studies: Apply Your Knowledge
Read each case scenario. Click "Attempt Question" to see the options, then select the best answer. Click "Show Explanation" to review the rationale.
Case 1: Initial Diagnosis
A 22-year-old female with a known history of type 1 diabetes presents to the ED with nausea, vomiting, and abdominal pain. Labs show: Glucose 350 mg/dL, Venous pH 7.20, Serum Bicarbonate 12 mmol/L, Blood β-hydroxybutyrate 5.5 mmol/L. Which of the following best describes her condition according to the 2024 guidelines?
Correct Answer: B) Moderate DKA
Rationale: The patient meets all criteria for DKA: Glucose ≥200 mg/dL (350), β-hydroxybutyrate ≥3.0 mmol/L (5.5), and pH <7.3 (7.20) with bicarbonate <18 mmol/L (12). According to the 2024 DKA severity classification:
- pH 7.0-7.25 falls into Moderate DKA.
- Bicarbonate 10 to <15 mmol/L (12) falls into Moderate DKA.
- β-hydroxybutyrate of 5.5 mmol/L is consistent with moderate DKA (typically 3.0-6.0 mmol/L, though can be higher).
Mild DKA has pH >7.25 to <7.30 and Bicarb 15-18. Severe DKA has pH <7.0 and Bicarb <10. She does not meet criteria for HHS due to significant ketosis and acidosis.
Case 2: HHS Diagnosis
A 68-year-old male with type 2 diabetes is brought in by family due to altered mental status. Labs: Glucose 850 mg/dL, Na+ 150 mmol/L, Urea 80 mg/dL (BUN ~37 mg/dL), Venous pH 7.35, Bicarbonate 20 mmol/L, Blood β-hydroxybutyrate 1.5 mmol/L. What is his calculated effective serum osmolality, and does he meet criteria for HHS?
Correct Answer: A) Eff Osm: 347 mOsm/kg; Yes, meets HHS criteria.
Rationale: Calculated Effective Serum Osmolality = [2 x Na⁺ (mmol/L)] + [Glucose (mg/dL) / 18]. Eff Osm = (2 x 150) + (850 / 18) = 300 + 47.22 = 347.22 mOsm/kg.
HHS Diagnostic Criteria (2024):
- Hyperglycemia: Glucose ≥600 mg/dL (850 mg/dL - Met)
- Hyperosmolarity: Effective serum osmolality >300 mOsm/kg (347 mOsm/kg - Met) OR Total osmolality >320 mOsm/kg.
- Absence of significant ketonemia: β-hydroxybutyrate <3.0 mmol/L (1.5 mmol/L - Met)
- Absence of significant acidosis: pH ≥7.3 (7.35 - Met) AND Bicarbonate ≥15 mmol/L (20 mmol/L - Met)
The patient meets all four criteria for HHS. Option D is incorrect because a normal pH is part of HHS criteria (absence of acidosis).
Case 3: Initial Fluid Management
A 45-year-old, 70 kg patient presents with DKA and signs of severe hypovolemia (hypotension, tachycardia). According to the 2024 guidelines, what is the most appropriate initial IV fluid administration rate for the first 2-4 hours, assuming no cardiac compromise?
Correct Answer: C) 500-1000 mL/hour of isotonic saline or balanced crystalloid
Rationale: The 2024 guidelines recommend for patients with DKA or HHS without cardiac or renal compromise, initial administration of isotonic saline (0.9% NaCl) or balanced crystalloid solutions at a rate of 500-1000 mL/hour during the first 2-4 hours, especially if severe hypovolemia is present. This can also be thought of as 15-20 mL/kg/hour.
- Option A is too slow for severe hypovolemia.
- Option B suggests hypotonic saline (0.45% NaCl) initially, which is not the first choice; isotonic fluids are preferred for initial resuscitation.
- Option D (D5W) is inappropriate for initial resuscitation as it does not effectively expand intravascular volume and would worsen hyperglycemia without insulin. Dextrose is added later when glucose levels fall.
Case 4: Insulin Initiation - Potassium Concern
A patient is diagnosed with severe DKA. Initial labs include a serum potassium of 3.1 mmol/L. Urine output is adequate. According to the 2024 guidelines, what is the immediate next step regarding insulin and potassium management?
Correct Answer: B) Hold insulin. Administer 10-20 mmol/hour of potassium until K+ is >3.5 mmol/L, then start insulin.
Rationale: The 2024 guidelines state that if initial serum K+ is <3.5 mmol/L (patient's K+ is 3.1 mmol/L), insulin therapy should be HELD. Potassium replacement should be initiated at a rate of 10-20 mmol/hour until the serum K+ rises to >3.5 mmol/L. Once K+ is corrected, insulin therapy can be started. Administering insulin with hypokalemia can drive potassium further into cells, leading to life-threatening arrhythmias.
- Options A and C are incorrect because insulin should be held.
- Option D is incorrect; IV push potassium is dangerous, and insulin should still be held.
Case 5: Adding Dextrose to IV Fluids
A patient with DKA is being treated with IV fluids and an insulin infusion. Their plasma glucose has decreased from 450 mg/dL to 230 mg/dL. Ketones are still elevated, and acidosis persists. What is the next appropriate step regarding IV fluids according to the 2024 guidelines?
Correct Answer: C) Add 5% or 10% dextrose to the IV fluids (e.g., D5W/0.45% NaCl).
Rationale: The 2024 guidelines recommend adding 5% or 10% dextrose to the IV fluids when the plasma glucose reaches <250 mg/dL in both DKA and HHS. The patient's glucose is 230 mg/dL. This allows the insulin infusion to continue (to resolve ketosis and acidosis) without causing hypoglycemia.
- Option A is incorrect because dextrose is needed to prevent hypoglycemia while insulin continues.
- Option B is incorrect as fluid therapy is still essential.
- Option D is incorrect because dextrose is specifically indicated at this glucose level to allow continued insulin therapy.
Case 6: DKA Resolution Criteria
Which set of parameters best defines the resolution of DKA according to the 2024 guidelines, allowing for consideration of transition to subcutaneous insulin?
Correct Answer: B) Blood β-hydroxybutyrate <0.6 mmol/L, AND (Venous pH ≥7.3 OR Bicarbonate ≥18 mmol/L), AND patient able to eat.
Rationale: The 2024 guidelines define DKA resolution as:
- Plasma/capillary β-hydroxybutyrate <0.6 mmol/L
- AND (Venous pH ≥7.3 OR Bicarbonate ≥18 mmol/L)
- AND Patient is able to eat.
- Glucose ideally should also be <200 mg/dL.
Option A is incorrect because anion gap is no longer a primary resolution criterion, and "feeling better" is subjective. Option C is incorrect as urine ketones are not recommended for monitoring resolution, and the other criteria are incomplete. Option D lists some criteria for HHS resolution, not DKA.
Case 7: Subcutaneous Insulin for Mild DKA
A 30-year-old patient with type 1 diabetes presents with mild DKA (pH 7.28, bicarb 16 mmol/L, blood ketones 4.0 mmol/L, glucose 280 mg/dL, alert and oriented). The ED is busy, but nursing can provide close monitoring on a step-down unit. According to 2024 guidelines, which insulin regimen is an acceptable alternative to IV insulin infusion?
Correct Answer: B) Subcutaneous rapid-acting insulin analog (e.g., lispro) 0.1 units/kg every 1 hour or 0.2 units/kg every 2 hours.
Rationale: The 2024 guidelines explicitly recommend that most individuals with uncomplicated mild or moderate DKA can be treated with subcutaneous rapid-acting insulin analogs every 1 to 2 hours, with close nursing supervision, as an alternative to IV insulin infusion. This can often be done outside an ICU setting.
- Option A (NPH) is a long-acting insulin and not suitable for acute DKA management requiring frequent adjustments.
- Option C (SubQ regular insulin) has a slower onset and longer duration than rapid-acting analogs, making it less ideal for the frequent dosing and rapid adjustments needed in DKA protocols that use SubQ insulin. While historically used, rapid-acting analogs are preferred for these protocols.
- Option D is incorrect as the 2024 guidelines support SubQ insulin for select DKA cases.
Case 8: Management of HHS - Insulin Rate
An 80-year-old patient is diagnosed with HHS (glucose 950 mg/dL, effective osmolality 345 mOsm/kg, no significant ketosis or acidosis). After initial fluid resuscitation, an IV insulin infusion is to be started. What is the recommended initial fixed-rate IV insulin infusion for this patient according to the 2024 guidelines?
Correct Answer: A) 0.05 units/kg/hour
Rationale: For HHS without significant ketosis or acidosis, the 2024 guidelines recommend starting a fixed-rate IV insulin infusion at 0.05 units/kg/hour. A higher rate (0.1 units/kg/hr) is used if there are mixed DKA/HHS features (significant ketosis/acidosis). An insulin bolus is generally not recommended for HHS and is optional in DKA only if there's a delay in starting the infusion. Insulin is a key component of HHS management, not just fluids. The goal for glucose reduction in HHS is also more gradual (not >90-120 mg/dL/hr) to prevent rapid shifts in osmolality.
Case 9: Euglycemic DKA
A 35-year-old patient with type 1 diabetes on an SGLT2 inhibitor (off-label) presents with nausea and malaise. Labs: Glucose 180 mg/dL, Venous pH 7.15, Bicarbonate 10 mmol/L, Blood β-hydroxybutyrate 6.5 mmol/L. According to 2024 DKA diagnostic criteria, does this patient have DKA?
Correct Answer: B) Yes, all criteria for DKA are met.
Rationale: The 2024 DKA diagnostic criteria are:
- Diabetes/Hyperglycemia (D): Glucose ≥200 mg/dL OR prior history of diabetes. This patient has a history of type 1 diabetes, so this criterion is met even with glucose at 180 mg/dL (this is euglycemic DKA).
- Ketosis (K): β-hydroxybutyrate ≥3.0 mmol/L. The patient's value is 6.5 mmol/L (Met).
- Metabolic Acidosis (A): pH <7.3 AND/OR bicarbonate <18 mmol/L. The patient's pH is 7.15 and bicarbonate is 10 mmol/L (Met).
All three criteria are met. SGLT2 inhibitors are a known risk factor for euglycemic DKA. Anion gap is no longer a primary diagnostic criterion. When treating euglycemic DKA, dextrose-containing fluids should be started with insulin from the beginning.
Case 10: Transition to Subcutaneous Insulin
A patient's DKA has resolved. They are now eating. The plan is to transition from IV insulin to a subcutaneous basal-bolus regimen. The patient's weight is 80 kg, and they were insulin-naive prior to this admission. Which is a reasonable starting Total Daily Dose (TDD) of insulin for this patient according to the 2024 guidelines?
Correct Answer: B) 0.3 - 0.6 units/kg/day (24-48 units)
Rationale: The 2024 guidelines suggest that for estimating TDD when transitioning to subcutaneous insulin, a weight-based calculation can be used, especially for insulin-naive patients. The typical range is 0.3-0.6 units/kg/day. For an 80 kg patient, this would be 24-48 units.
- Option A is too low.
- Option C is too high for an initial estimate in an insulin-naive patient.
- Option D (using only the last few hours of IV insulin) can be one method, but it should be used with caution as glucotoxicity can overestimate needs, and a weight-based approach is also a primary consideration, especially for naive patients. The guidelines suggest considering weight-based, pre-admission regimen, or IV requirements. For a naive patient, weight-based is a good starting point.
The chosen TDD would then be split, typically 40-60% as basal insulin and the remainder as prandial insulin, divided among meals. Remember to overlap subcutaneous basal insulin with the IV infusion by 1-2 hours.
Complications During Treatment
Hypoglycemia
Risk: Common. Severe hypoglycemia associated with increased mortality.
Mitigation: Frequent glucose monitoring (q1-2h). Add dextrose to IV fluids when glucose <250 mg/dL. Reduce insulin infusion rate as glucose falls.
Hypokalemia
Risk: Common due to intracellular K+ shift with insulin. Severe hypokalemia associated with increased mortality.
Mitigation: Careful K+ monitoring (baseline, 2h post-insulin, then q4h). Start K+ replacement once K+ ≤5.0 mmol/L and renal function adequate. Hold insulin if K+ <3.5 mmol/L until corrected.
Hyperchloremic Normal Anion Gap Metabolic Acidosis
Risk: Can occur during recovery, especially with large volumes of 0.9% NaCl.
Mitigation: Usually self-limiting. Use of balanced crystalloid solutions may reduce risk. Do not delay transition if this is the only remaining "acidosis."
Cerebral Edema
Risk: Rare in adults, but serious. Associated with rapid shifts in osmolality.
Mitigation: Gradual correction of hyperglycemia and hyperosmolality, especially in HHS (avoid glucose drop >90-120 mg/dL/h, osmolality drop >3-8 mOsm/kg/h). Monitor mental status. If suspected, brain imaging, mannitol, consider hyperventilation.
Thrombosis
Risk: DKA/HHS are prothrombotic states, especially HHS.
Mitigation: Consider prophylactic anticoagulation (e.g., LMWH) based on individual risk assessment, especially in HHS or prolonged immobility.
Acute Kidney Injury (AKI)
Risk: Common due to dehydration.
Mitigation: Adequate fluid resuscitation. Usually resolves with rehydration. Monitor renal function.
Preventing Recurrence
- Education: Crucial for patients and families. Focus on:
- Sick day management (continue insulin, monitor glucose/ketones, hydration, when to seek help).
- Insulin administration techniques and adherence.
- Glucose and ketone (blood or urine) monitoring.
- Recognizing early symptoms of DKA/HHS.
- Access to Care & Supplies: Ensure adequate supply of insulin, monitoring equipment. Address socioeconomic barriers.
- Follow-up: Prompt follow-up post-discharge (2-4 weeks) to review regimen and address issues.
- Mental Health: Screen for and address mental health conditions (depression, eating disorders, diabetes distress) and psychosocial factors, which are strong predictors of recurrence.
- Technology: Consider CGM for eligible patients to improve glycemic control and potentially reduce DKA.
- Address Precipitating Factors: Identify and manage common triggers like infection, insulin omission, and intercurrent illnesses.