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Guideline:

Acute seizures and seizure disorder

National Guideline Clearinghouse (NGC). Guideline summary: Acute seizures and seizure disorder In: National Guideline Clearinghouse (NGC) [Web site]. Rockville (MD): cited 1998 Mar (revised 2003 Apr). Available: http://www.guideline.gov.


Bibliographic Source(s)

  • Texas Tech University Managed Health Care Network Pharmacy & Therapeutics Committee. Acute seizures and seizure disorder. Conroe (TX): University of Texas Medical Branch Correctional Managed Care; 2003 Apr. 4 p. [6 references]

Guideline Status

This is the current release of the guideline.

This guideline updates a previous version: Texas Tech University Managed Health Care Network Pharmacy & Therapeutics Committee. Acute seizures and seizure disorders. Conroe (TX): Texas Department of Criminal Justice University of Texas Medical Branch; 1998 Mar. 4 p.

Guideline Category

Evaluation
Treatment

Intended Users

Health Care Providers
Physicians

Guideline Objective(s)

To provide appropriate recommendations for the evaluation and treatment of acute seizures and seizure disorder

Target Population

Incarcerated offenders within the Texas Department of Criminal Justice with acute seizures or seizure disorder

Interventions and Practices Considered

Evaluation

  1. Observation of seizure activity
  2. Vital signs
  3. Electrocardiograph (EKG) monitoring
  4. Laboratory evaluations: glucose finger stick; venous samples for glucose chemistries hematology parameters toxicology screens and antiepileptic drug levels; determination of oxygenation with oximetry or arterial blood gases

Treatment

  1. Oxygen administration
  2. Administration of:
    • Glucose
    • Thiamine
    • Oral antiepileptic drugs (AED) (formulary agents: carbamazepine phenytoin primidone valproic acid ethosuximide; non-formulary agents: gabapentin lamotrigine phenobarbitol topiramate tiagabine clonazepam)
    • Lorazepam
    • Diazepam
  3. Evaluation of responses to medications and subsequent medication adjustments as appropriate
  4. Neurology consult as indicated

Major Outcomes Considered

Not stated

Methods Used to Collect/Select Evidence

Searches of Electronic Databases

Description of Methods used to Collect/Select the Evidence

Not stated

Number of Source Documents

Not stated

Methods Used to Assess the Quality and Strength of the Evidence

Not stated

Rating Scheme for the Strength of the Evidence

Not applicable

Methods Used to Analyze the Evidence

Review

Description of the Methods Used to Analyze the Evidence

Not stated

Methods Used to Formulate the Recommendations

Not stated

Rating Scheme for the Strength of the Recommendations

Not applicable

Cost Analysis

A formal cost analysis was not performed and published cost analyses were not reviewed.

Method of Guideline Validation

Not stated

Description of Method of Guideline Validation

Not applicable

Major Recommendations

The major recommendations are provided in the form of algorithms for: Acute Seizures and Seizure Disorder.

Seizure Disorder

Most Commonly Used Drugs for Specific Seizure Disorders

Begin treatment with single drug using recommended initial daily dosing. Up to 80% of patients can be managed with monotherapy. Ensure proper medication adherence prior to modifying regimen. Refer to the original guideline document for formulary and non-formulary agents used in the treatment of seizure disorders.

Monitoring Parameters for Formulary Anticonvulsant Medications

Carbamazepine

  • Complete blood count (CBC) with platelets at baseline then twice monthly first two months and annually or as clinically indicated
  • Blood chemistries with emphasis on hepatic and renal function and electrolytes at baseline then at one month and annually or as clinically indicated
  • Electrocardiogram (EKG) at baseline for patients >40 years old and as clinically indicated
  • Carbamazepine level weekly for two weeks then at one month and annually or as clinically indicated

Phenytoin

  • CBC at baseline and as clinically indicated
  • Blood chemistries with emphasis on hepatic and renal functions at baseline annually and as clinically indicated
  • EKG at baseline for patients >40 years old and as clinically indicated
  • Phenytoin level in one week then in one month and annually or as clinically indicated

Valproic Acid

  • CBC with platelets at baseline then twice monthly first two months and annually or as clinically indicated
  • Blood chemistries with emphasis on hepatic function at baseline then at one month and annually or as clinically indicated
  • Protime international normalized ratio (INR) partial prothrombin time (PPT) at baseline and annually
  • Valproic acid level weekly for two weeks then annually or as clinically indicated

Clinical Algorithm(s)

Algorithms are provided for:

Type of Evidence supporting the Recommendations

The guideline was adapted from the following sources:

McAuley JW Biederman TS Smith JC Moore JL. Newer therapies in the treatment of epilepsy. Ann Pharmacother 2002; 36:119-29.

Anderson GD Miller JW. The newer antiepileptic drugs: Their collective role and defining characteristics. Formulary. 2001; 36:114-31.

Baker GA Camfield P et al. Commission on the outcome measurement in epilepsy 1994-1997: final report. Epilepsia. 1998: 39:213-31.

Quality Standards Subcommittee of AAN. Practice parameter: a guideline for discontinuing antiepileptic drugs in seizure-free patients – summary statement. Neurology. 1996: 47:600-2.

Working Group on Status Epilecticus Treatment of Convulsive Status Epilecticus. JAMA. 1993; 270:854-859

Potential Benefits

Appropriate evaluation and treatment of acute seizures and seizure disorder

Potential Harms

Adverse effects of drugs

Qualifying Statements

The pathways do not replace sound clinical judgment nor are they intended to strictly apply to all patients.

Description of Implementation Strategy

An implementation strategy was not provided.

Implementation Tools

Clinical Algorithm

For information about availability see the "Availability of Companion Documents" and "Patient Resources" fields below.

IOM Care Need

Getting Better
Living with Illness

IOM Domain

Effectiveness

Bibliographic Source(s)

  • Texas Tech University Managed Health Care Network Pharmacy & Therapeutics Committee. Acute seizures and seizure disorder. Conroe (TX): University of Texas Medical Branch Correctional Managed Care; 2003 Apr. 4 p. [6 references]

Adaptation

The guideline was adapted from the following sources:

McAuley JW Biederman TS Smith JC Moore JL. Newer therapies in the treatment of epilepsy. Ann Pharmacother 2002; 36:119-29.

Anderson GD Miller JW. The newer antiepileptic drugs: Their collective role and defining characteristics. Formulary. 2001; 36:114-31.

Baker GA Camfield P et al. Commission on the outcome measurement in epilepsy 1994-1997: final report. Epilepsia. 1998: 39:213-31.

Quality Standards Subcommittee of AAN. Practice parameter: a guideline for discontinuing antiepileptic drugs in seizure-free patients – summary statement. Neurology. 1996: 47:600-2.

Working Group on Status Epilecticus Treatment of Convulsive Status Epilecticus. JAMA. 1993; 270:854-859

Source(s) of Funding

University of Texas Medical Branch Correctional Managed Care

Guideline Committee

Texas Tech University Managed HealthCare Network Pharmacy & Therapeutics Committee

Composition of Group that Authored the Guideline

Not stated

Financial Disclosures/Conflicts of Interest

Not stated

Guideline Status

This is the current release of the guideline.

This guideline updates a previous version: Texas Tech University Managed Health Care Network Pharmacy & Therapeutics Committee. Acute seizures and seizure disorders. Conroe (TX): Texas Department of Criminal Justice University of Texas Medical Branch; 1998 Mar. 4 p.

Guideline Availability

Print copies: Available from University of Texas Medical Branch (UTMB) 3009A HWY 30 West Huntsville TX 77340.

Availability of Companion Documents

None available

Patient Resources

None available

NGC STATUS

This summary was updated by ECRI on April 21 2004. This summary was updated by ECRI on November 16 2006 following the FDA advisory on Lamictal (lamotrigine). This summary was updated by ECRI Institute on January 10 2008 following the U.S. Food and Drug Administration advisory on Carbamazepine.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline which is subject to the guideline developer's copyright restrictions.

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