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Diabetic Ketoacidosis (DKA) & Hyperglycemic Hyperosmolar State (HHS). Ulrich K. Schubart, MD JMC/AECOM. DKA/HHS Presenting Symptoms. Nausea and Vomiting Polyuria and Polydipsia Weakness and/or Anorexia Abdominal Pain Visual Disturbances Somnolence. DKA/HHS Presenting Signs. Tachycardia
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Diabetic Ketoacidosis (DKA) &Hyperglycemic Hyperosmolar State (HHS) Ulrich K. Schubart, MD JMC/AECOM
DKA/HHSPresenting Symptoms • Nausea and Vomiting • Polyuria and Polydipsia • Weakness and/or Anorexia • Abdominal Pain • Visual Disturbances • Somnolence
DKA/HHSPresenting Signs • Tachycardia • Hypotension • Dehydration • Hypothermia • Warm dry Skin • Kussmaul Respiration • Lethargy or Coma • Fruity Odor
Compensatory Hyperventilation in DKA From UpToDate Kety et al. JCI 1948
DKA/HHSPrecipitating Factors Any major Stress/Acute Illness • Infection • Pneumonia • Gastroenteritis • UTI • Sepsis • Meningitis • Influenza • Mucormycosis • Emotional Problems • Trauma • Acute Pancreatitis • Myocardial Infarction • Stroke • Endocrine • Acromegaly • Thyrotoxicosis • Cushing’s S. • Omission of Antidiabetic Mx’s • Drugs
DKA/HHSDrugs that can Precipitate • Psychotropic Drugs • Chlorpromazine • Clozapine • Risperidone • Loxapine • Steroids • Immunosuppressants • Beta Blockers • Calcium Channel Blockers • Diuretics • Anticonvulsants • Diazoxide
DKA/HHSPathogenesis Precipitating Factors Absolute Insulin Deficiency Relative Insulin Deficiency Glucagon Catecholamines Cortisol Growth Hormone Lipolysis Proteolysis Minimal Lipolysis Gluconeogenic Substrates FFAs Ketogenesis Gluconeogenesis Glycogenolysis Ketoacidosis Hyperglycemia Hyperosmolality Glucosuria (Osmotic Diuresis) Triglycerides Decreased GFR Hyperlipidemia Loss of Water & Electrolytes Dehydration
- + + PKA PFK-1 F1,6BP DKA/HHSEnhanced Glucose Production Glucagon cAMP Glycogen Glucose G-6-P PFK-2 F-6-P F-2,6P2 F-1,6-P2 Glycerol Alanine PYR CO2 Fat
Insulin DKA/HHSKetone Body Formation in Liver Glucagon Fatty Acids Glucose Fatty Acyl-CoA Triglycerides Fatty Acyl-CoA Acetyl-CoA Acetoacetyl-CoA b-Hydroxy-b-methylglutaryl CoA Acetoacetate b -Hydroxybutyrate NADH NAD Acetone
Fatty Acid Oxidation DKA/HHSGlucagon-inducedCatabolic Cascade in Liver Glucose Glucose Glycogenolysis Gluconeogenesis Glycogen Formation Glycolysis Fatty Acids Fatty acyl CoA CPT1 Malonyl-CoA ACC Acetyl-CoA Ketones
NAD NADH + H+ DKA/HHSKetone Body Utilization in Muscle EXTACELLULAR MITOCHONDRION b -Hydroxybutyrate b -Hydroxybutyrate Acetoacetate Acetoacetate Succinyl-CoA Succinate Acetoacetyl-CoA CoA Acetyl-CoA Fatty Acids Citric Acid Cycle
DKA/HHSGlucotoxicty & Lipotoxicity • Relatively Short Term: Reversible Inhibition of: a) Glucose Uptake and Utilization in Insulin-Responsive Target Tissues b) Insulin Secretion • Long-term: a) & b) +Apoptosis of Beta-Cells
DKA/HHSEssential to R/o Infection • Look for meningeal signs - Head CT/MR followed by LP may be indicated • Look for necrotic lesions in nasal turbinates to r/o mucormycosis • For abdominal pain consider appendicitis cholecystitis pancreatitis diverticulitis PID • Obtain CXR • Check urine sediment
DKA/HHSHyperosmolality Measure and Calculate Serum Osmolality = 2 x measured Na+ (mEq/l) + glucose (mg/dl) /18 + BUN (mg/dl)/2.8 Osmolar Gap = Measured – Calculated Serum Osmolality Effective Serum Osmolality OsmEff (>320 =HHS) =2 x measured Na+ (mEq/l) + glucose (mg/dl) /18
DKA/HHSSodium Correction Corrected Sodium = Measured Sodium + 1.6 x plasma glucose (mg/dl) – 100 100
DKA/HHSMetabolic Acidosis Plasma Anion Gap = Na+ - [Cl-+ HCO3-] (mEq/l)
DKA/HHSPoor Prognostic Indicators • Advanced Age • Low pH • Hypotension • Marked Hyperosmolality • High BUN • Associated Diseases
DKA/HHSTreatment Considerations • Precipitating Cause evident in 80% • ECG indicated in all adult patients • Isotonic NaCl preferred for initial rehydration • IV Insulin preferred mode of administration • Potassium depletion in all patients • Prevention is long-term goal of management • Bicarbonate administration rarely indicated
DKA/HHSOther Considerations in Tx • Type & Cross-match as indicated • Blood (and other) Cultures as indicated • Aspirate Gastric Contents if Comatose • Catherize if needed for Output Measurement • Give Oxygen if indicated • Keep patient NPO
DKA/HHSEssential Components in Tx • IV Fluids • Insulin • Potassium
DKA/HHSEssential Components in Tx IV Fluids • 2-3 L 0.9% saline during first 3 h • Subsequently, 0.45% saline at 150-300 ml/h • Add 5% dextrose when plasma glucose reaches 250 mg/dl
DKA/HHSEssential Components in Tx Insulin • 10 U/h iv infusion of short-acting insulin • Increase rate 2-10 fold if no response by 4 h • Decrease to 1-2 U/h when acidosis is corrected • Administer sc insulin before stopping iv infusion
DKA/HHSEssential Components in Tx Potassium • 10-20 mEq/h when plasma K<6.0, ECG normal, urine flow documented • 40-80 mEq/h when plasma K <3.5 or if bicarb is given
+ + F1,6BP PFK-1 DKA/HHSStimulation of Glucose Utilization and Glycogen Formation by Insulin Glycogen G-6-P Glucose PFK-2 F-6-P F-2,6P2 F-1,6-P2 PYR CO2 Fat
Fatty Acid Oxidation - DKA/HHS-inducedAnabolic Cascade in Liver Insulin Glucose Glucose Glycogenolysis Gluconeogenesis Glycolysis Glycogen Formation Fatty Acids Fatty acyl CoA Malonyl-CoA CPT1 ACC TG Acetyl-CoA Ketones
DKA/HHSAdverse Effects of Severe Acidosis • Impaired Cardiac Contractility • Decreased Response to Vasoconstrictors • Inhibition of Respiration
DKA/HHSPotential Adverse Effect of Bicarbonate Administration • Significantly Increased Risk of Hypokalemia • Decreased Tissue Oxygen Delivery
DKA/HHSIndications for ConsideringBicarbonate Administration • pH < 7.0 or HCO3- < 5.0 • K+> 6.5 • Hypotension refractory to fluid replacement • Severely impaired LV function • Respiratory depression • Marked late hyperchloremic acidosis • Significant lactic acidosis
Compensatory Hyperventilation in DKA From UpToDate Kety et al. JCI 1948
DKA/HHSComplications of Therapy • Hypoglycemia • Hypokalemia or Hyperkalemia • Fluid Overload • Hyperchloremic Acidosis • Cerebral Edema • ARDS • Thromboembolic Episodes
DKA/HHSPrevention • Education of Patient and Health Care Providers