Cardiovascular Risk Reduction in Epilepsy

NCT ID: NCT05704439

Last Updated: 2024-07-25

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-01-31
• Study Completion Date: 2027-01-31

Brief Summary

Epilepsy is a disabling and lethal neurological disease which affect 3.47 million Americans. Significant health care disparities exist in people with epilepsy (PWE). Hypertension and hyperlipidemia are highly prevalent and often go undertreated, and cardiovascular (CV) mortality is higher in people with epilepsy (PWE) than the general population. Preliminary data from our group shows that PWE have higher ACC-ASCVD risk scores than an age matched NHANES cohort without epilepsy. Preliminary data also demonstrate mortality rates in PWE due to hypertension, stroke, and diabetes are rising in the US, counter to the US general population.

This proposal seeks to test the feasibility, acceptability, and preliminary efficacy of a new care model for the underserved PWE in a public health setting. In this new model, neurologists guided by standardized treatment algorithms (ACC-ASCVD estimator+) propose and initiate pharmacological interventions for hypertension and hyperlipidemia.

Detailed Description

Epilepsy is a disabling and lethal neurological disease which affect 3.47 million Americans. Significant health care disparities exist in people with epilepsy (PWE). PWE are more likely to be Hispanic, Black, developmentally disabled and unemployed. Hypertension and hyperlipidemia are highly prevalent and often go undertreated, and cardiovascular (CV) mortality is higher in people with epilepsy (PWE) than the general population. Preliminary data from our group shows that PWE have higher ACC-ASCVD risk scores than an age matched NHANES cohort without epilepsy. Preliminary data also demonstrate mortality rates in PWE due to hypertension, stroke, and diabetes are rising in the US, counter to the US general population.

PWE on Medicaid, Medi-Cal and without insurance are more likely to experience delays to treatment and follow aberrant care pathways. Unexpected seizures and status epilepticus often result in transport to community and public health hospitals, where they are referred to neurology clinics, a process which may bypass primary care. As a result, PWE may have as their primary point of contact neurologists who traditionally do no monitor or treat hypertension or hyperlipidemia. This leads to gaps in care and missed opportunities to reduce CV risk.

This proposal seeks to test the feasibility, acceptability, and preliminary efficacy of a new care model for the underserved PWE in a public health setting. In this new model, neurologists guided by standardized treatment algorithms (ACC-ASCVD estimator+) propose and initiate pharmacological interventions for hypertension and hyperlipidemia.

We propose enrolling 150 subjects ages 40-79 with untreated or incompletely treated hypertension and/or hyperlipidemia. Subjects will be randomized 2:1 to Neurologist-initiated treatment (Model 1) versus usual care (Model 2). Subjects will be evaluated for blood pressure, blood chemistries, lipids, and HgA1C at baseline, one and three months. At 3-months, subjects randomized to usual care (Model 2) will be offered treatment if not yet initiated by primary care. If successful, results of this pilot study will provide needed feasibility and preliminary efficacy data for a large multicenter randomized trial of Neurologist initiated treatment of cardiovascular risk in the underserved with epilepsy

Conditions

Epilepsy; Hypertension; Hyperlipidemia (E.G., Hypercholesterolemia)

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: HEALTH_SERVICES_RESEARCH
• Blinding Strategy: NONE

Study Groups

Model 1-Neurologist Initiation of Treatment for Hypertension or Hyperlipidemia

Neurologist Initiation of antihypertensive or treatment for hyperlipidemia

Group Type: ACTIVE_COMPARATOR

Neurologist Initiated Treatment

Intervention Type: DRUG

Neurologist Initiated Treatment for Hypertension or Hyperlipidemia

Model 2-Usual Care

Usual care

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Usual care

Interventions

Neurologist Initiated Treatment

Neurologist Initiated Treatment for Hypertension or Hyperlipidemia

Intervention Type: DRUG

Placebo

Usual care

Intervention Type: OTHER

Other Intervention Names

antihypertensive agent or Hyperlipidemia agent; Usual Care

Eligibility Criteria

Inclusion Criteria

• Epilepsy defined as G40.0-G40.9 in the electronic medical record, or seizure disorder prescribed at least one antiseizure medication
• Age 40-79 (age range defined by ACC-ASCVD risk estimator+)
• Untreated HTN defined as at least two sitting BPs > 130/80 in the last year prior to enrollment or on enrollment
• Hyperlipidemia defined as LDL > 70 mg/dl with 10-year ACC-ASCVD score > 7.5% or total LDL > 190, or ASCVD recommendation to initiate lipid lowering agent
• Intellectual Disability, developmental disorder or autism recorded in the electronic medical record (ICD-10 codes F70-F79, F84)

Exclusion Criteria

• Stroke or cerebral hemorrhage < 1 year
• Documented poor compliance with treatment
• If intellectually disabled, if there is no caregiver to support or initiate therapy
• Pregnancy or person actively trying to become pregnant
• Blood Pressure > 180/110
• Known secondary cause of hypertension that causes concern regarding safety of the protocol.
• Arm circumference too large or small to allow accurate blood pressure measurement with available devices
• Diabetes mellitus,
• Glomerulonephritis treated with or likely to be treated with immunosuppressive therapy
• eGFR < 20 ml/min /1.73m2 or end-stage renal disease (ESRD)
• Cardiovascular event, procedure or hospitalization for unstable angina within last 3 months
• Symptomatic heart failure within the past 6 months
• A medical condition likely to limit survival to less than 3 years or a malignancy other than non-melanoma skin cancer within the last 2 years
• Any factors judged by the clinic team to be likely to limit adherence to interventions.
• Failure to obtain informed consent from participant
• Any organ transplant

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 79 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Olive View-UCLA Education & Research Institute

OTHER

Sponsor Role: collaborator

University of California, Los Angeles

OTHER

Sponsor Role: lead

Responsible Party

Christopher Degiorgio, MD FAAN

Professor of Neurology in Residence

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Christopher M DeGiorgio, MD

Role: PRINCIPAL_INVESTIGATOR

University of California, Los Angeles

Other Identifiers

CMD01

Identifier Type: -

Identifier Source: org_study_id