II. Epidemiology
- Age distribution of DKA Cases
- Age over 70 years: 14%
- Age 51 to 70 years: 23%
- Age 30-50 years: 27%
- Age under 30 years: 36%
- Henricksen (2007) Diabetes Res Clin Pract 76(1): 51-6 [PubMed]
-
Incidence of DKA in children
- Up to 30% of children present with DKA at the time of diagnosis
- Incidence of DKA after initial diagnosis 6 to 8% per year
- References
III. Pathophysiology
-
Insulin deficiency
- Diabetes Mellitus
- Type I Diabetes Mellitus
- Type II Diabetes Mellitus with Ketosis-prone diabetes (accounts for 20-50% of DKA cases)
- Black or latino
- Male
- Overweight
- Middle-aged
- Diabetes MellitusFamily History
- Uncontrolled Blood Sugars (see precipitating factors below)
- See Medication Causes of Hyperglycemia
- New onset Diabetes Mellitus
- Insulin non-compliance
- Acute Infection (e.g. Pneumonia, Urinary Tract Infection)
- Insulin Pump failure
- Diabulimia (Eating Disorder variant of skipping Insulin to lose weight)
- Physiologic stressors (Myocardial Infarction, Cerebrovascular Accident)
- Diabetes Mellitus
- Compensatory response to lack of usable fuel sources (in the absence of Insulin)
- Paradoxical exacerbation of Hyperglycemia
- Release of Glucagon, Catecholamines, Cortisol, and Growth Hormone
- Catabolism to Glucose of Proteins and glycogen by liver
- Lipase secretion results in increased Ketones
- Free Fatty Acid Metabolism (lipolysis)
- Results in increased Ketone production (acetone, acetoacetone, Beta hydroxybutyrate)
- Results in Metabolic Acidosis
- Increased Renal Clearance of Ketones and Glucose
- Results in osmotic diuresis, Dehydration and hyperosmolar state
- Paradoxical exacerbation of Hyperglycemia
IV. Risk Factors: Precipitating Factors
- Uncontrolled Diabetes Mellitus
- New onset Diabetes Mellitus
- Insulin Pump failure
- Insulin non-compliance
- Infection
- Medical condition
- Other Endocrine Disorder
- Medications
V. Symptoms
- Timing
- Rapid onset of symptoms
- Follows febrile illness (40%)
-
Hyperglycemia symptoms
- Polyuria and polydipsia (98%)
- Polyphagia (23%)
- Gastrointestinal symptoms
- Nausea and Vomiting (50-80% of cases)
- Abdominal Pain (30% of patients)
- May present as a vague Abdominal Pain with minimal tenderness on exam
- Consider Pancreatitis or Pyelonephritis (both are common in DKA)
- Miscellaneous symptoms
VI. Signs
- Mental clouding (lethargy to coma)
-
Metabolic Acidosis findings
- Tachypnea with Kussmaul Breathing
- Acetone on breath (sweet or fruity breath smell)
-
Dehydration (often >10% dehydrated)
- Dry Skin with loss of Skin Turgor
- Eyes sunken
- Tachycardia and possibly Hypotension
- Temperature below normal
VII. Differential Diagnosis
VIII. Labs
- Bedside Glucose
- Glucose >250 mg/dl
-
Urinalysis
- Glucosuria
- Urinary Tract Infection
- Ketonuria
- See Urine Ketones
- High Test Sensitivity (98%) for Diabetic Ketoacidosis
- High Negative Predictive Value
- Negative Urine Ketone excludes DKA diagnosis
- Schwab (1999) Ann Emerg Med 34:342-6 [PubMed]
- Poor Test Specificity (35%)
- Confirm with Serum Beta Hydroxybutyrate
- Beta hydroxybutyrate is converted to Acetoacetate which is then detected on the Urine Dipstick as Ketones
- Normal serum bicarbonate and Anion Gap suggests resolving DKA or False Positive ketonuria
- Confirm with Serum Beta Hydroxybutyrate
- Chemistry Panel (Chem8)
- Serum Glucose increased (Hyperglycemia)
- Serum Sodium decreased (Hyponatremia)
- See Corrected Serum Sodium for Hyperglycemia
- Requires correction for Glucose (Pseudohyponatremia secondary to Hyperglycemia)
- Serum Sodium correction calculation: sNa + 0.016 * (Glu - 100)
- Serum Potassium
- Metabolic Acidosis results in initial underestimation of Serum Potassium
- Hypokalemia is present in only 5-10% of Diabetic Ketoacidosis presentations
- As acidosis corrects, Potassium enters cells in exchange for Hydrogen Ion and Serum Potassium falls
- Hypokalemia develops in in up to 80% of Diabetic Ketoacidosis cases with management
- Low Serum Potassium on presentation suggests severe Hypokalemia
- Must be corrected before Insulin initiation
- Metabolic Acidosis results in initial underestimation of Serum Potassium
- Serum Chloride depressed (Hypochloremia)
- Serum Bicarbonate depressed (<15 to 18 mEq/L)
- Anion Gap elevated
- Typically >10-12 and often >16 in DKA
- Anion Gap calculation: Na - (Cl + HCO3)
- Serum Osmolality (calculate and measure if available)
- Should be >320 mOsm/kg if DKA present
- Serum Osmolality calculation: 2*(Na + K) + (glu/18) + (BUN/2.8)
- Serum Creatinine (and eGFR)
- Acute Kidney Injury is common (prerenal related to severe Dehydration and Metabolic Acidosis)
- Other Electrolytes (Phosphorus and Magnesium)
- Serum Phosphorus decreased (Hypophosphatemia)
- Serum Magnesium decreased (Hypomagnesemia)
-
Arterial Blood Gas (ABG) or Venous Blood Gas (VBG)
- Metabolic Acidosis (serum pH <7.30)
- Venous Blood Gas is equivalent to monitoring Arterial Blood Gas for pH and bicarbonate
- Beta hydroxybutyrate (or Serum Ketones if not available)
- Beta hydroxybutyrate is the most important Ketone in Diabetic Ketoacidosis
- Test Sensitivity: High
- Test Specificity: 85%
- Levels do not correlate with disease severity
- Arora (2011) Diabetes Research and Clinical Practice 94(3): e86-8
- Precipitating factor evaluation
- Complete Blood Count with differential
- Leukocytosis is often present in DKA regardless of underling infection
- Bandemia (Neutrophil band forms or Left Shifts) is highly predictive of infection
- Blood Culture
- Urine Culture
- Chest XRay
- Electrocardiogram (EKG)
- Detects Hypokalemia related changes
- Also indicated for ischemia evaluation over age 40 or over 10 years of Diabetes Mellitus
- Complete Blood Count with differential
- Evaluation of Diabetes and Endocrine Status
- Hemoglobin A1C
- Anti-GAD65 Antibody (identifies Type I diabetics)
- Thyroid Stimulating Hormone (TSH)
- Complications (obtain as needed)
- Serum Lipase
- Frequently increased regardless of Pancreatitis
- Pancreatitis is present in 10-15% of DKA patients
- Hepatic Transaminases (AST and ALT)
- Typically increased in non-Alcoholic Fatty Liver disease (NASH)
- Troponin I
- Troponin I is increased in absence of myocardial injury in more than 25% of DKA patients
- Serum Lipase
IX. Diagnosis: Criteria - Hyperglycemia, Ketosis, Acidosis
- Blood Glucose >250 mg/dl (>200 mg/dl in children)
-
Metabolic Acidosis
- Serum pH < 7.30 or
- Serum Bicarbonate < 15 to 18 meq/L
-
Serum Ketones or Beta hydroxybutyrate
- Increased Serum Ketones (>3-4 mmol/L or >1:2 dilution)
- Anion Gap (using uncorrected Serum Sodium)
X. Evaluation: Severity
- Arterial pH (or venous pH) in Adults
- Mild DKA: 7.25 to 7.30
- Moderate DKA: 7.00 to 7.24
- Severe DKA: < 7.00
- Arterial pH (or venous pH) in Infants and Children
- Mild DKA: 7.25 to 7.30 (some guidelines list pH 7.2 to 7.3)
- Moderate DKA: 7.2 to 7.25 (some guidelines list pH 7.1 to 7.2)
- Severe DKA: < 7.2 (some guidelines list pH<7.1)
- Serum bicarbonate
- Mild: 15-18
- Moderate: 10 to 14
- Severe: < 10
- Mental status
- Mild: Alert
- Moderate: Drowsy
- Severe: Stupor
XI. Management
- See Diabetic Ketoacidosis Management in Adults
- See Diabetic Ketoacidosis Management in Children
- Evaluate and manage underlying causes
- Underlying infection (e.g. urosepsis, Pneumonia, Cellulitis)
- Consider noncompliance due to financial concerns
- Facilitate lower cost options for medications
- See Diabetes Cost Reduction
XII. Complications
- See Diabetic Ketoacidosis Related Cerebral Edema
- Metabolic Complications
- Non-metabolic Complications
- Septic Shock
- Hypovolemic Shock
- Vascular Thrombosis
- Pulmonary Edema (aggressive rehydration)
- Acute Renal Failure
- Rhabdomyolysis
- Prolonged QT Interval
- Cerebral Edema (See Diabetic Ketoacidosis Related Cerebral Edema)
XIII. Prevention
- See Diabetes Sick Day Management
- Diabetic action plan based on Blood Glucose Monitoring
- Home monitoring of beta hydroxybutyrate or Ketones when Serum Glucose >240 mg/dl
- Plan for adjusting short acting Insulin
- Sick day Insulin coverage (reduced dose but not eliminated)
- Liquid diets when sick
- Back-up plan for Insulin Pump failure
- Early contact with medical provider when Glucose control acutely changes
- Case management
- Diabetic educator
- Frequent phone contact
- Consider Insulin Pump
XIV. Prognosis
- Case fatality rate: 1-5%
- Mortality typically due to cerebral edema
- Leading cause of death in diabetes under age 24 years
- Wang (2006) Diabetes Care 29(9): 2018-22 [PubMed]
XV. References
- Fahlsing and Ponce (2024) Crit Dec Emerg Med 38(3): 18-9
- Kirschke (2020) Crit Dec Emerg Med 34(8): 3-7
- Orland in Stine (1994) Emergency Med, p. 204-5
- Orman and Willis in Herbert (2017) EM:Rap 17(9): 19-20
- Chiasson (2003) CMAJ 168:859-66 [PubMed]
- Kitabchi (2001) Diabetes Care 24:131-53 [PubMed]
- Trachtenbarg (2005) Am Fam Physician 71(9): 1705-22 [PubMed]
- Trence (2001) Endocrinol Metab Clin North Am 30:817-31 [PubMed]
- Westerberg (2013) Am Fam Physician 87(5): 337-46 [PubMed]