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Perform a stat sodium and glucose level in patients with refractory seizures

Perform a stat sodium and glucose level in patients with refractory seizures: Excerpt from Avoiding Common Pediatric Errors

Author: Caroline Rassbach, MD

What to Do - Interpret the Data

Seizures are one of the most common neurologic conditions affecting children. The majority are short, self-limited seizures that occur secondary to disorders originating outside the brain. Examples include high fever, infection, head trauma, hypoxia, and toxins. Less than one third of seizures in children occur as a result of epilepsy. When a child presents with a first-time seizure, or when a child with a known seizure disorder presents with prolonged seizure, metabolic causes should be considered. Obtaining stat serum glucose and sodium levels are essential in these children.

Initialassessmentofanychildwithaseizureshouldincludeevaluationof the airway, breathing, and circulation (ABCs). The provider should perform vital signs and place the patient on a cardiac monitor and on supplemental oxygen. The provider should then obtain a detailed history and perform a quick physical examination, including a neurologic examination, searching for clues to the etiology of the seizure. Life-threatening conditions, such as meningitis, sepsis, head trauma, and toxin ingestion, should be considered in the differential diagnosis.

When a seizure lasts >5 minutes, intravenous access should be attained and stat serum glucose and sodium levels drawn. Serum calcium, phosphorus, magnesium, blood urea nitrogen, and a complete blood count may also be indicated. Urine for toxicology and serum anticonvulsant levels may be helpful. A benzodiazepine such as lorazepam or a barbiturate should be administered as a first-line drug to stop the seizure. Lorazepam administration can be repeated every 10 to 15 minutes if needed.

If the seizure continues for >10 minutes, a second anticonvulsant, such as phenobarbital or phenytoin, should be administered. Metabolic derangements, such as hypoglycemia and hyponatremia, should be treated as soon as they are diagnosed.

When the seizure activity persists >30 minutes, it is referred to as status epilepticus. Administration of a second long-acting anticonvulsant is indicated for status epilepticus. In addition, the practitioner should prepare for intubation and general anesthesia as the seizure approaches 45 minutes.

Complications of status epilepticus include hypoxia, lactic acidosis, hyperkalemia, hypoglycemia, shock, hyperpyrexia, renal and respiratory failure, and death.

Hypoglycemia and hyponatremia are the most frequent metabolic derangements that cause seizure. Hypoglycemia occurs most commonly in neonates in the setting of hypoxia, toxemia, gestational diabetes, or a normal delivery. In older children, it occurs because of prolonged fasting, malabsorption and malnutrition, systemic disease, and hyperinsulinemia. Hypoglycemia in infants presents as cyanosis, apnea, hypothermia, hypotonia, poor feeding, lethargy, or seizures. In older children, signs of hypoglycemia includeanxiety,tachycardia,sweating,tremulousness,weakness,hunger,and seizures. At any age, hypoglycemia should be considered as a cause of a seizure.Seizuressecondarytohypoglycemiashouldbetreatedwith2mL/kg of 50% glucose intravenously.

Hyponatremia, another metabolic cause for seizure, is one of the most common electrolyte disturbances occurring in hospitals. It usually results from excess free water intake in the presence of impaired free water excretion. Examples include syndrome of inappropriate secretion of antidiuretic hormone (SIADH), postoperative hyponatremia, water intoxication, overdilution of infant formula, and diuretic use. When hyponatremia occurs, water shifts into the intracellular space, resulting in cellular swelling. This may present clinically as cerebral edema and encephalopathy with headache, nausea, vomiting, emesis, and weakness. It may progress to altered mental status, seizures, respiratory arrest, and cerebral herniation.

Symptomatic hyponatremia is a medical emergency and should be treated with hypertonic 3% saline intravenously. For seizing patients or for those with increased intracranial pressure, the hypertonic saline should be infused rapidly enough to raise the serum sodium level by 4 to 8 mEq/L during the first hour or until seizure activity ceases. For less severe symptoms, hypertonic saline should be infused with a goal of raising the serum sodium by 1 mEq/L/hr. In general, 1 mL/kg of hypertonic saline will raise the serum sodium level by 1 mEq/L. Practitioners should be aware that overly fast correction of hyponatremia can result in devastating cerebral demyelination.

Practitioners should remember to consider metabolic derangements in patients with seizures. Stat serum glucose and sodium levels should be checked for all patients with prolonged or refractory seizures.

Suggested Readings

Johnston MV. Seizures in childhood. In: Behrman RE, Kliegman RM, Jenson HB, eds. Nelson Textbookof Pediatrics. 17thed.Philadelphia: Saunders;2004: chapter586,pages1993–2009.
Moritz ML, Ayus JC. Disorders of water metabolism in children: hyponatremia and hypernatremia. Pediatr Rev. 2002;23(11):371–380.
Sabo-Graham T, Seay AR. Management of status epilepticus in children. Pediatr Rev. 1998;19(9)306–310.
SperlingMA.Hypoglycemia.In:BehrmanRE,KliegmanRM,JensonHB,eds.NelsonTextbook of Pediatrics. 17th ed. Philadelphia: Saunders; 2004: - .

Book Source Details

  • Book Title: Avoiding Common Pediatric Errors
  • Author(s): Anthony D Slonim MD, DrPH; Lisa Marcucci MD
  • Year of Publication: 2008
  • Copyright Details: Avoiding Common Pediatric Errors, Copyright © 2008 Lippincott Williams & Wilkins.

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Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.




More About This Book:
Title: Avoiding Common Pediatric Errors
Authors: Anthony D Slonim MD, DrPH; Lisa Marcucci MD
Publisher: Lippincott Williams & Wilkins
Copyright: 2008
ISBN: 0-7817-7489-6

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