Clinical and Economic Burden of Uncontrolled Epilepsy: Analyses From a Medicaid Database and a Private Health Plan Database

NCT ID: NCT01390909

Last Updated: 2012-10-08

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

12386 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-05-31

Study Completion Date

2011-01-31

Brief Summary

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Antiepileptic drugs (AEDs) are the main therapeutic option for patients with epilepsy; however, complete seizure control remains elusive for many patients. Uncontrolled or refractory epilepsy is associated with a higher risk of mortality, physical injuries, and depression or anxiety compared with patients with controlled epilepsy. Higher resource utilization for patients with poor control is likely to be associated with higher economic costs. While diagnostic criteria for uncontrolled epilepsy are debated by neurologists, recent studies suggest that a diagnosis of uncontrolled epilepsy requires 1.) at least one seizure per month and 2.) a history of drug failures.

The objective of this study is to identify patients with uncontrolled epilepsy in both a Medicaid database and a private health plan database, to describe patient characteristics and AED treatment patterns between cohorts of patients with uncontrolled versus well-controlled epilepsy, and to evaluate the economic burden of uncontrolled versus well-controlled epilepsy.

For this evaluation, the data sources are medical and pharmacy claims in Medicaid databases from Florida (Third quarter 1997 to second quarter 2008), Iowa (First quarter 1998 to second quarter 2006), Kansas (First quarter 2001 to second quarter 2009), Missouri (First quarter 1997 to second quarter 2008) and New Jersey (First quarter 1997 to fourth quarter 2008) and medical and pharmacy claims in an private health plan database.

The study design is a retrospective, longitudinal, matched-cohort study. Eligible patient records will be assigned to one of three mutually-exclusive cohorts: uncontrolled epilepsy (at least 2 consecutive changes in AED therapy in at least 30 days, and at least 1 epilepsy-related inpatient or emergency department (ED) visit within 365 days), well-controlled epilepsy (no AED changes and no epilepsy-related inpatient or ED visits), and intermediate epilepsy (not classified as uncontrolled or well-controlled).

Detailed Description

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Conditions

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Epilepsy

Keywords

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epilepsy anti-epileptic drug polytherapy adherence Medicaid

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Medicaid patients with uncontrolled epilepsy

Database records for patients with 2 or more consecutive changes in anti-epileptic drug (AED) therapy occurring at least 30 days apart and followed by 1 or more epilepsy-related inpatient or emergency department (ED) visits within the 365 days

Anti-epileptic drug (AED)

Intervention Type DRUG

Prescription claim for at least one AED including lamotrigine, tiagabine, pregabalin, ethosuximide, lacosamide, phenytoin, carbamazepine, valproic acid, felbamate, levetiracetam, zonisamide, primidone, oxcarbazepine, vigabatrin, phenobarbital, gabapentin, topiramate.

Medicaid patients with well-controlled epilepsy

Database records for patients with an epilepsy diagnosis but no AED change and no epilepsy-related inpatient or ED visits

Anti-epileptic drug (AED)

Intervention Type DRUG

Prescription claim for at least one AED including lamotrigine, tiagabine, pregabalin, ethosuximide, lacosamide, phenytoin, carbamazepine, valproic acid, felbamate, levetiracetam, zonisamide, primidone, oxcarbazepine, vigabatrin, phenobarbital, gabapentin, topiramate.

Medicaid patients with intermediate epilepsy

Database records for patients who are not classified as uncontrolled or well-controlled

Anti-epileptic drug (AED)

Intervention Type DRUG

Prescription claim for at least one AED including lamotrigine, tiagabine, pregabalin, ethosuximide, lacosamide, phenytoin, carbamazepine, valproic acid, felbamate, levetiracetam, zonisamide, primidone, oxcarbazepine, vigabatrin, phenobarbital, gabapentin, topiramate.

Patients in a private health plan with uncontrolled epilepsy

Database records for patients with 2 or more consecutive changes in AED therapy occuring at least 30 days apart and followed by 1 or more epilepsy-related inpatient or ED visits within 365 days

Anti-epileptic drug (AED)

Intervention Type DRUG

Prescription claim for at least one AED including lamotrigine, tiagabine, pregabalin, ethosuximide, lacosamide, phenytoin, carbamazepine, valproic acid, felbamate, levetiracetam, zonisamide, primidone, oxcarbazepine, vigabatrin, phenobarbital, gabapentin, topiramate.

Patients in a private health plan with well-controlled epileps

Database records for patients with an epilepsy diagnosis but no AED change and no epilepsy-related inpatient or ED visits

Anti-epileptic drug (AED)

Intervention Type DRUG

Prescription claim for at least one AED including lamotrigine, tiagabine, pregabalin, ethosuximide, lacosamide, phenytoin, carbamazepine, valproic acid, felbamate, levetiracetam, zonisamide, primidone, oxcarbazepine, vigabatrin, phenobarbital, gabapentin, topiramate.

Patients in a private health plan with intermediate epilepsy

Database records for patients who are not classified as uncontrolled or well-controlled

Anti-epileptic drug (AED)

Intervention Type DRUG

Prescription claim for at least one AED including lamotrigine, tiagabine, pregabalin, ethosuximide, lacosamide, phenytoin, carbamazepine, valproic acid, felbamate, levetiracetam, zonisamide, primidone, oxcarbazepine, vigabatrin, phenobarbital, gabapentin, topiramate.

Interventions

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Anti-epileptic drug (AED)

Prescription claim for at least one AED including lamotrigine, tiagabine, pregabalin, ethosuximide, lacosamide, phenytoin, carbamazepine, valproic acid, felbamate, levetiracetam, zonisamide, primidone, oxcarbazepine, vigabatrin, phenobarbital, gabapentin, topiramate.

Intervention Type DRUG

Other Intervention Names

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Mysoline® is a registered trademark of Valeant Pharmaceuticals Neurotin® is registered trademark of Pfizer Inc Vimpat® is a registered trademark of UCB Pharma Tegretol® is a registered trademark of Novartis Pharmaceuticals Trileptal® is a registered trademark of Novartis Pharmaceuticals Sabril® is a registered trademark of Lundbeck Inc Felbatol® is a registered trademark of MedPointe Topamax® is a registered trademark of Ortho-McNeill-Janssen Pharmaceuticals Depakote® is a registered trademark of Abbott Laboratories Zonegran® is a registered trademark of Dainippon Pharmaceutical C. Ltd. Gabatril® is a registered trademark of Cephalon Keppra® is registered trademark of UCB Pharma Zarontin® is a registered trademark of Pfizer Lamictal® is a registered trademark of GlaxoSmithKline Luminal® is a registered trademark of Abbott Laboratories Dilantin® is a registered trademark of Pfizer Lyrica is registered trademark of Pfizer

Eligibility Criteria

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Inclusion Criteria

* At least 18 years of age at the initiation of anti-epileptic drug (AED) treatment as noted in the database
* A record of at least one medical visit with a diagnosis of epilepsy (ICD-9-CM 345.xx) or at least two diagnoses of non-febrile convulsions (ICD-9-CM 780.30 or 780.39) occuring more than 30 days apart
* At least one pharmacy claim for an anti-epileptic drug (AED)
* Continuous enrollment throughout the observation period (minimum of 365 days). Patients with gaps in Medicaid enrollment will be observed only during their period of continuous enrollment, provided that all the above criteria are met

Exclusion Criteria

* Age less than 18 years
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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GlaxoSmithKline

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Other Identifiers

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113917

Identifier Type: -

Identifier Source: org_study_id