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Evolving Strategies for Hyponatremia Management in the ICU Mazen Kherallah, MD, FCCP Infectious Disease & Critical Care Medicine Assistant Professor, University of North Dakota Critical Care Patients at Increased Risk of Hyponatremia* Increased age1 Up to 30% of patients with subarachnoid hemorrhage2 Up to 30% of ICU patients3 Over 30% of AIDS patients4 Postoperative patients – 25%-35% of pituitary surgery for tumor resection5 ~30% of acute spinal cord injury6 Psychiatric inpatients: 6%-17%7 *Data not exclusive to patients with euvolemic hyponatremia. 1. Hawkins RC. Clin Chim Acta. 2003;337:169-172; 2. Mayer SA. The Neurologist. 1995;1:71-85; 3. DeVita MV et al. Clin Nephrol. 1990;34:163-166; 4. Tang WW et al. Am J Med. 1993;94:169-174; 5. Bhardwaj A. Ann Neurol. 2006;59:229-236; 6. Peruzzi WT et al. Crit Care Med. 1994;22:252-258; 7. Siegler EL et al. Arch Intern Med. 1995;155:953-957. Mortality Related to Hyponatremia Among Hospitalized Patients 25% 20% 15% 10% 5% 0% Anderson1 Terzian2 [Na+] <130 mEq/L 1. Anderson RJ et al. An Intern Med. 1995,102: 164-168 2. Terzian C et al. J Gen Intern Md. 1994,9:89-91 3. Tierney WM et al. J Gen Intern Med. 1986;1: 380-385 Tierney3 Normonatremia Morbidities in Hospitalized Patients with Symptomatic Hyponatremia 60% 50% Altered Sensorium 40% 30% 20% 10% Seizures Nausea & Gait Disturbance Vomiting & Falls 0% • • • • Dysarthria Coma Single center, retrospective over 4 years (1997-2001) 168 patients with serum [Na+] <115 mEq/L Symptoms of hyponatremic encephalopathy in 89 of 168 patient (53%) No documented symptoms in 79 of 168 patients (47%) Nzenue CM et al. J Natl Med Assoc. 2003;95: 335-343 Mechanisms of Hyponatremia ↓ [Na+] 𝑁𝑎 = ↑𝐻2𝑂 ↓ [Na+] ↓𝑁𝑎 = 𝐻2𝑂 Brain CT Scan: Cerebral Edema Normal CT Scan Fatal Hyponatremia Case I 44 year old man with schizophrenia is brought to the ED from his group home after a witnessed tonic-clonic generalized seizure. He was well until earlier in the day at which time he became progressively somnolent. His medications include haloperidol, quetiapine and citalopram. On exam he is afebrile, BP 120/78, HR 92. He is somnolent but arousable and following commands, is euvolemic, and there are no focal findings. His urine output is 120 ml/hour Serum Urine Na 116 mEq/L Na 35 mEq/L K 3.9 mEq/L K 15 mEq/L Creat 0.8 mg/dL Osm 92 mOsm/kg Osm 240 mOsm/kg Question What is the most likely etiology of this man’s hyponatremia? a) b) c) d) e) Syndrome of inappropriate antidiuresis Psychogenic polydipsia Pseudohyponatremia Adrenal insufficiency Cerebral sat wasting The Diagnosis of Hyponatremia: Three Critical Questions Is it real? Is water excretion appropriate? Is ADH excretion “appropriate”? Assessment of Hyponatremia: Three Critical Questions 1. Is it real? Plasma Osmolality Normal or High Pseudohyponatremia Hyperglycemia Azotemia, ETOH Intoxication 92 Low mOsm/kg (< 100 mOsm/kg) Psychogenic polydipsia 240 Low mOsm/kg 2. Is water excretion appropriate? Urine Osmolality High (>100 mOsm/kg) 3. Is ADH secretion appropriate? (Volume Status) Hypovolemia Euvolemia Hypervolemia Appropriate ADH Secretion Inappropriate ADH Maladaptive ADH Secretion Total body water ↓ Total body Na+ ↓↓ Total body water ↑ Total body Na+ ↔ Total body water ↑↑ Total body Na+↑ U[Na+] >20 mEq/L Renal Losses Diuretic excess Mineralocorticoid deficiency Bicarbonaturia with tubal acidosis and metabolic alkalosis Ketonuria Osmotic diuresis U[Na+] <20 mEq/L U[Na+] >20 mEq/L Extrarenal losses Vomiting Diarrhea Third spacing of fluids Burns Pancreatitis Trauma Glucocorticoid deficiency Hypothyroidism Syndrome of inappropriate ADH secretion U[Na+] >20 mEq/L Acute or chronic renal failure U[Na+] 20 <mEq/L Nephrotic syndrome Cirrhosis Cardiac failure Case II 46-year-old woman admitted to Neurocritical Care Unit confused and mildly lethargic secondary to subarachnoid hemorrhage Past medical history: hypertension, tobacco smoker BP 170/78 mm Hg, HR 71 bpm 0.9% saline administered at 100 mL/h CVP 6-8 mm Hg Mildly positive fluid balance Remained confused and disoriented, but lethargy gradually resolved In the Step-Down Unit Day 9 post-SAH Patient transferred to step-down unit Central venous IV catheter discontinued IV fluid: normal saline administered at 100 mL/h through peripheral IV Day 10 post-SAH The patient appeared to be more confused Serum [Na+] = 126 mEq/L Serum Urine Na 126 mEq/L Na 45 mEq/L K 3.6 mEq/L K 17 mEq/L Creat 0.7 mg/dL Osm 292 mOsm/kg Osm 258 mOsm/kg Question What is the most likely etiology of this patient’s hyponatremia? a) b) c) d) e) SIADH Psychogenic polydipsia Pseudohyponatremia Adrenal insufficiency Cerebral sat wasting Assessment of Hyponatremia: Three Critical Questions 1. Is it real? Plasma Osmolality Normal or High 258 Low mOsm/kg 2. Is water excretion appropriate? Urine Osmolality Low (< 100 mOsm/kg) Pseudohyponatremia Hyperglycemia Azotemia, ETOH Intoxication Psychogenic polydipsia High 292 (>100 mOsm/kg) mOsm/kg 3. Is ADH secretion appropriate? (Volume Status) Hypovolemia Euvolemia Hypervolemia Appropriate ADH Secretion Inappropriate ADH Maladaptive ADH Secretion Total body water ↓ Total body Na+ ↓↓ Total body water ↑ Total body Na+ ↔ Total body water ↑↑ Total body Na+↑ U[Na+] >20 mEq/L Renal Losses Diuretic excess Mineralocorticoid deficiency Bicarbonaturia with tubal acidosis and metabolic alkalosis Ketonuria Osmotic diuresis U[Na+] <20 mEq/L U[Na+] >20 mEq/L Extrarenal losses Vomiting Diarrhea Third spacing of fluids Burns Pancreatitis Trauma Glucocorticoid deficiency Hypothyroidism Syndrome of inappropriate ADH secretion U[Na+] >20 mEq/L Acute or chronic renal failure U[Na+] 20 <mEq/L Nephrotic syndrome Cirrhosis Cardiac failure Question How would you treat this patient? a) b) c) d) e) Fluid restriction (<2 L/d) Salt tablets (NaCl 2 g/d) Normal saline infusion 3% hypertonic saline IV Conivaptan Treatment Considerations • Often unknown • >2 days • Acute reduction in chronic state • More brain adaptation with chronic Acute or Chronic Severity of Hyponatremia • Mild: >129 • Moderate: 121-129 • Severe <120 • Severe Symptoms or Intracranial Pathology: seizures, impaired mental status or coma • Moderate: confusion, lethargy, • Mild: fatigue, nausea, dizziness, gait disturbances, forgetfulness nd muscle cramps • Asymptomatic Severity of Symptoms Treatment Goals • Treat cerebral edema • Relieve symptoms and prevent progression of neurologic dysfunction • Prevent osmotic demyelination syndrome • 4-6 meq/24 hrs (<9 meq/L in any 24 hrs) Treatment Strategies • Treat pain, nausea, vomiting,.. • cessation of therapy with certain drugs • glucocorticoids to patients with adrenal insufficiency Treat Underlying Cause Restoration of Euvolemia • Saline to patients with true volume depletion • Diuretics in edematous states (such as heart failure and cirrhosis) •Fluid restriction in SIADH Balancing the Effect of ADH Correction of Na and Rate of Correction • Hypertonic saline • Normal saline • Salt tablets Sodium deficit= TBW (desired SNa-actual SNa) Increase in SNa= (infusate [Na]-SNa) ÷ (TBW+1) Treatment Options • Rapid increase in Na 46 meq/L (in 6 hours) • 3% saline 100 mL IV bolus • Repeat 1-2 X at 10 minutes intervals if symptoms persist • ≤ 9 meq/L in 24 hours • (NS in hypovolemia) • Hypertonic saline • Increase Na 0.5-1 meq/hour in the first 4 hours • 4-6 meq in 24 hours Severe Symptoms: Seizure or coma Moderate Symptoms: Confusion and/or lethargy Mild or abscent symptoms: Na ≤120 meq/L Mild or abscent symptoms: Na > 120 meq/L • Hypertonic saline • Increase Na 0.5-1 meq/hour in the first 4 hours • 4-6 meq in 24 hours (<9 meqin any 24 hours) • (NS in hypovolemia) • Fluid restriction (<UO or <800 ml/day) • Salt tablets • V2 receptors antagonists Treatment Course for This Patient A 20 mg loading dose of conivaptan followed by a continuous infusion of 20 mg/d 24 hour after the start of the loading dose, the serum [Na+] increased from 126 to 132 A second 24 hour contineous infusion given SAH Day Serum [Na+] (mEq/L) 24 Hour Fluid Balance (L) Conivaptan Treatment Day 10 126 +0.2 1 11 132 -0.8 2 12 138 -1.2 3 Day 2 of Treatment The next day serum [Na+] increased from 132 to138 mEq/L Mental status: less confused Conivaptan discontinued Patient discharged to rehabilitation on SAH Day 13 Receptor-Mediated Effects of VAP Receptor Subtype Site of Action Activation Effects V1a Vascular smooth muscle cells Platelets Lymphocytes and monocytes Adrenal cortex Vasoconstriction Platelet aggregation Coagulation factor release Glyconeogenesis V1b Anterior pituitary ACTH and ß-endorphin release V2 Renal collecting duct principal cells Free water absorption Lee CR et al. AM Heart J. 2003;143:9-18 Hyponatremia in Acute Brain Injury Therapeutic Options Speed Situation Pluses Minuses Free water restriction Slow Hard to regulate NS+furosemide Sow Electrolyte depletion Fludrocortisone Slow Fluid overload AVP Inhibitor Faster Asymptomatic Reliable effect hyponatremia Infusion site reactions Mannitol Fatsest Symptomatic hyponatremia Reduce Edema Can worsen hypovolemia Electrolyte depletion Hypertonic saline Fastest Symptomatic hyponatremia Reduce brain edema Fluid overload Thank you