Increased mortality persists in an adult drug-resistant epilepsy prevalence cohort

• Published in: Journal of neurology, neurosurgery and psychiatry Vol. 85; no. 10; pp. 1084 - 1090
• Main Authors: Callaghan, Brian, Choi, Hyunmi, Schlesinger, Malka, Rodemer, William, Pollard, John, Hesdorffer, Dale C, Hauser, W Allen, French, Jacqueline
• Format: Journal Article
• Language: English
• Published: England 01.10.2014
• Subjects: Adult; Age Factors; Cause of Death; Cohort Studies; Drug Resistance; Epilepsy - etiology; Epilepsy - mortality; Female; Follow-Up Studies; Humans; Kaplan-Meier Estimate; Male; Middle Aged; Prevalence; Anticonvulsants; Epilepsy; Neuroepidemiology
• ISSN: 0022-3050; 1468-330X; 1468-330X
• DOI: 10.1136/jnnp-2013-307074

To investigate the cumulative probability of death and the standardised mortality ratio (SMR) in an adult drug-resistant epilepsy (DRE) population. In two separate centres during 2003-2006, we identified a total of 433 patients with DRE defined as at least one seizure per month and failure of at least two antiepileptic drugs. These patients were subsequently followed for a total follow-up of 6 years. We examined the cumulative probability of death, using Kaplan-Meier methodology, and the SMR based on mortality data from the Social Security Death Index. Clinical predictors of death were evaluated using Cox regression analysis. The cumulative probability of death was 8.7% (95% CI 6.2% to 12.1%) at 6 years. The overall SMR was 2.4 (95% CI 1.7 to 3.3). It was 3.1; 95% CI 2.0 to 4.6 in subjects with remote or progressive aetiology and 1.7; 95% CI 0.8 to 2.8 in subjects with unknown aetiology. The SMR was significantly increased in those with a known remote aetiology (2.5; 95% CI (1.4 to 3.8)). Older age at enrolment and symptomatic generalised epilepsy syndrome were significant predictors of death. Mortality is increased in this drug-resistant population; largely driven by those with a known epilepsy aetiology. The increased mortality remains even after exclusion of those with a progressive aetiology. Previous studies of incident epilepsy cohorts revealed increased mortality that declines to near-normal levels after the first several years, but in our DRE cohort, mortality remains elevated despite a median duration of epilepsy of 25 years at study entry.