Why are epilepsy mortality rates rising in the United States? A population-based multiple cause-of-death study

Abstract

Introduction

Epilepsy mortality rates are rising. It is unknown whether rates are rising due to an increase in epilepsy prevalence, changes in epilepsy causes of death, increase in the lethality or epilepsy or failures of treatment. To address these questions, we compare epilepsy mortality rates in the USA with all-cause and all-neurological mortality for the years 1999 to 2017.

Objectives

To determine changes in US epilepsy mortality rates versus all-cause mortality, and to evaluate changes in the leading causes of death in people with epilepsy.

Design

Retrospective population-based multiple cause-of-death study.

Primary outcome

Change in age-adjusted epilepsy mortality rates compared with mortality rates for all-cause and all-neurological mortality.

Secondary outcome

Changes in the leading causes of death in epilepsy.

Results

From 1999 to 2017, epilepsy mortality rates in the USA increased 98.8%, from 5.83 per million in 1999 to 11.59 per million (95% CI 88.2%–110.0%), while all-cause mortality declined 16.4% from 8756.34 per million to 7319.17 per million (95% CI 16.3% to 16.6%). For the same period, all-neurological mortality increased 80.8% from 309.21 to 558.97 per million (95% CI 79.4%–82.1%). The proportion of people with epilepsy who died due to neoplasms, vascular dementia and Alzheimer’s increased by 52.3%, 210.1% and 216.8%, respectively. During the same period, the proportion who died due to epilepsy declined 27.1%, while ischaemic heart disease as a cause of death fell 42.6% (p<0.001).

Conclusions

Epilepsy mortality rates in the USA increased significantly from 1999 to 2017. Likely causes include increases in all-neurological mortality, increased epilepsy prevalence and changes in the underlying causes of death in epilepsy, led by increases in vascular dementia and Alzheimer’s. An important finding is that ischaemic heart disease and epilepsy itself are declining as underlying causes of death in people with epilepsy.

Correspondence to Dr Christopher M DeGiorgio; [email protected]

Strengths and limitations of this study

• Large population-based study of epilepsy mortality, using the Centers for Disease Control multiple cause-of-death database.

• Comparison between epilepsy mortality, all-cause and all-neurological mortality.

• Study reports change in the seven leading causes of death in epilepsy.

• Death certificates may under-report epilepsy-related mortality.

• Physicians completing death certificates may not be able to fully discern the underlying and contributing causes of death

Introduction

People with epilepsy are at higher risk for premature death.¹ Nelligan et al,¹ in a large prospective cohort study of newly diagnosed epilepsy, found that people with epilepsy had a standardised mortality rate of 2.55, significantly higher than expected from the general population. Recent data from the USA and Great Britain (UK) indicate that epilepsy mortality rates are rising significantly.^{2 3} Greenlund et al² reported that epilepsy mortality rates in the USA increased 47% between 2005 and 2014. Similarly, Public Health England reported epilepsy mortality rates in the UK increased 33% between 2003 and 2014.³ Globally, epilepsy deaths have increased 18.9% from 1990 to 2015, while the worldwide prevalence of epilepsy increased 39.2%.⁴ These reports have generated significant concern from stakeholders and advocacy groups that the increase in epilepsy mortality may represent a failure to effectively treat epilepsy and prevent premature death.^{5 6}

The underlying causes for the increase in epilepsy mortality rates in the USA are poorly understood and raise several questions. How is epilepsy mortality changing in comparison to all-cause mortality and all-neurological mortality? Are rising epilepsy mortality rates a result of an increase in epilepsy prevalence? Could changes in the underlying causes of death in people with epilepsy contribute to the increase in epilepsy mortality rates? Is the lethality of epilepsy increasing? Is this increasing mortality due to failure to effectively treat epilepsy or address preventable causes of death?

To address these questions, we analysed vital statistics data obtained from the Centers for Disease Control (CDC) multiple cause-of-death database.⁷ We compare changes in epilepsy mortality rates with all-cause mortality, all-neurological mortality and mortality of major neurological diseases over the years 1999 to 2017. We also report and analyse changes in the underlying causes of death in people with epilepsy.

Methods

This is a retrospective population-based multiple cause-of-death study using the CDC wide-ranging online database (CDC Wonder). CDC Wonder compiles cause-of-death data based on information reported on death certificates.⁷ This information is then coded and aggregated at the county level. The CDC Wonder Database was accessed for the years 1999 to 2017.^{7 8} These years were selected to provide the longest contiguous period for which the same International Classification of Diseases codes (ICD-10) were utilised. The CDC migrated to the ICD-10 classification in 1999. County health departments and CDC coded all data from 1999 to 2017 with the same ICD-10 system. The multiple cause-of-death database was utilised for this study.^{7 8} The multiple cause-of-death database reports the underlying cause of death plus up to 20 contributing conditions listed on the death certificate. In the case of epilepsy, epilepsy or another cause (myocardial infarction, stroke, accidental death, etc) may be identified as the underlying or associated cause of death. Multiple cause-of-death mortality rates better reflect the complex constellation of conditions that contributed to death rather than a single cause-of-death analysis.⁹

The primary outcomes of this study are the following: change in age-adjusted epilepsy mortality rates compared with mortality rates for all-causes, all-neurological disorders, stroke and degenerative dementia (Alzheimer’s). Secondary outcomes include changes in the seven leading underlying causes of death in epilepsy. The number of deaths per year, crude death rates, age-adjusted death rates and standard errors were obtained. Mortality rates were calculated as the number of deaths per 1 000 000. For measures of variability, standard errors were utilised. Data were exported to a text file and transferred to an Excel spreadsheet (2013 version) for statistical analysis.

Statistical analysis

Age-adjusted rate ratios were computed by dividing the age-adjusted rate for year 2017 by the corresponding rate for year 1999. To calculate the statistical significance for the standardised rate ratios, we used approximate formulas by Smith.¹⁰ In addition, the weighted linear regression model was used to compute the per cent changes per year (slope) in age-adjusted mortality rates for a given cause, and the corresponding slopes were compared under the weighted linear regression model.¹¹ We used the weighted linear regression model with piecewise linear splines to assess whether the per cent change in epilepsy mortality per year differed before and after year 2010. The per cent changes per year in epilepsy mortality for underlying cause-of-death versus epilepsy mortality using the multiple cause-of-death was compared under the regression model. The above models were weighted by the inverse of the variance estimates for the age-adjusted mortality rates. The underlying causes of death among people who died from epilepsy were compared between years 1999, 2008 and 2017 using the Cochran-Armitage test for trend, taking into account the overall trend over time and ensuring that the results would not be influenced by outliers. Level of significance was defined as p<0.05.

Patient and public involvement

Patients and/or the public were not involved in the design, or conduct, or reporting or dissemination plans of this research.

Results

Table 1 summarises changes in age-adjusted mortality rates from 1999 to 2017 for all causes, all neurological disorders, stroke, central nervous system (CNS) degenerative disorders (Alzheimer’s) and epilepsy. Note that during the study period, mortality rates for all causes and stroke declined, while the mortality rates for epilepsy, all neurological disorders and degenerative dementia increased significantly, p<0.001 (table 1).

Table 1

Changes in age-adjusted mortality rates 1999 to 2017 for major causes of death in the USA

	ICD-10 code	1999 Age-adjusted mortality rate per million	2017 Age-adjusted mortality rate per million	Per cent change, 95% CI	P value	Per cent change per year
All-cause mortality		8756.34	7319.17	−16.4%, 16.3% to 16.6%	<0.001	<0.001
Stroke	I60–I69	616.03	375.90	−39.0%, 38.5% to 39.4%	<0.001	<0.001
All neurological disorders	G00–G98	309.21	558.97	+80.8%, 79.4% to 82.1%	<0.001	<0.001
Degenerative disorders of the CNS	G30–G31	168.90	367.58	+117.6%, 115.5% to 119.7%	<0.001	<0.046
Epilepsy: multiple cause of death	G40.0–G40.9	5.83	11.59	+98.8%, 88.2% to 110.0%	<0.001	<0.001

Rates are expressed as number per million. Mortality per cent changes per year were evaluated using the weighted linear regression model; approximate formulas by Smith et al.¹⁰

CNS, central nervous system; ICD, International Classification of Diseases.

Epilepsy mortality: multiple cause-of-death database

In 2017 there were 4131 deaths with epilepsy as either the underlying cause of death or 1 of 20 contributing causes, for an age-adjusted mortality of 11.59 per million (SE 0.18). Compared with 1999, the multiple cause-of-death mortality rate in 2017 increased by 98.8% (95% CI 88.2% to 110.0%, p<0.001). For the period 1999 to 2010, epilepsy multiple cause-of-death mortality increased by only 0.4% per year (95% CI −0.3% to 1.1%%, p=0.26). From 2010 to 2017, epilepsy multiple cause-of-death mortality increased 9.7% per year (95% CI 8.4% to 11.0%, p<0.001). When compared with all-cause mortality for 2017, the epilepsy multiple cause-of-death mortality rate was equal to 0.06% of all-cause mortality. Figure 1 displays the changes in age-adjusted mortality for the years 1999 to 2017. The slopes for two periods 1999–2010 and 2010–2017 were significantly different (p=0.001).

Figure 1. Epilepsy age-adjusted mortality rates, 1999 to 2017: multiple cause-of-death mortality rates. Rates are expressed as number per million. The change in slope from 2010 to 2017 was significantly increased compared with 1999 to 2009 (weighted linear regression model with piecewise linear splines, p=0.001).

Leading causes of death in people with epilepsy

Table 2 summarises the leading causes of death in people with epilepsy for the years 1999 and 2017 using the multiple cause-of-death database. Of the 4131 deaths in people with epilepsy in 2017, only 1578 (38.2%) were directly due to epilepsy itself, while 2553 (61.8%) deaths were due to the other leading causes. When compared with 1999, the proportion of deaths as a direct result of epilepsy declined from 52.4% to 38.2%, for a net reduction of 27.1% (p<0.001). Malignant neoplasms, degenerative dementia (Alzheimer’s) and organic mental disorders (vascular dementia and delirium) increased by 52.3%, 216.8% and 210.1%, respectively. Ischaemic heart disease as a cause of death in people with epilepsy declined 42.6% (table 2).

Table 2

Underlying Causes of death in people With epilepsy 1999–2017

All deaths in people with epilepsy			1999	2008	2017	Per cent change	P value
			1613	1786	4131
Rank	Underlying cause of death	ICD-10 codes	Number and proportion of deaths due to the underlying cause
1	Epilepsy	G40–G47	845 (52.39%)	881 (49.33%)	1578 (38.19%)	−27.1%	<0.001
2	Malignant neoplasms	C00–C97	91 (5.64%)	83 (4.64%)	355 (8.59%)	+52.3%	<0.001
3	Cerebrovascular disease	I60–I69	105 (6.51%)	120 (6.72%)	284 (6.87%)	+5.5%	0.62
4	Ischaemic heart disease	I20–I25	174 (10.79%)	123 (6.89%)	256 (6.19%)	−42.6%	<0.001
5	Degenerative diseases of the CNS (ie, Alzheimer’s)	G30–G31	24 (1.49%)	55 (3.08%)	195 (4.72%)	+216.8%	<0.001
6	Cerebral palsy	G80–G83	28 (1.74%)	52 (2.91%)	149 (3.61%)	+107.5%	<0.001
7	Organic mental disorders (vascular dementia and delirium)	F01–F09	16 (0.99%)	35 (1.95%)	127 (3.07%)	+210.1%	<0.001

Data are expressed as the number and proportion of deaths due to the underlying cause, Cochran-Armitage test for trend.

CNS, central nervous system; ICD, International Classification of Diseases.

Discussion

Epilepsy age-adjusted mortality rates in the USA increased 98.8%, from 5.83 per million in 1999 to 11.59 per million in 2017, p=0.001. (figure 1). However, epilepsy was a rare cause of death, representing only 0.13% of all-cause mortality in 2017.

Three key factors may be contributing to the increase in epilepsy mortality rates from 1999 to 2017. First, the crude number of deaths due to all neurological disorders, of which epilepsy is a subset, increased from 84 077 in 1999 to 216 352 in 2017. The age-adjusted mortality rate for all-neurological causes increased 80.8% (95% CI 79.4% to 82.1%, p<0.001). Neurological disorders are the leading cause of disability in the world, and the global burden of neurological disease is rising due to population growth and ageing.⁴ Epilepsy contributes to up to 25% of the global burden of neurological disease and many neurological diseases are associated with seizures and epilepsy.⁴ Given the association between epilepsy and neurological disorders, the increased burden and mortality of all-neurological disorders are likely major contributors to the increase in epilepsy mortality rates reported here.

A second cause for the increase in epilepsy mortality rates is an increase in the prevalence of epilepsy in the USA. For the period 2010–2015, the CDC reported that the number of adults with epilepsy increased from 2.3 million to 3.0 million, and the number of children with epilepsy increased to 470 000, for an overall epilepsy prevalence of 1.2%.¹² This represents a 30.4% increase in epilepsy prevalence in 2010 to 2015.¹² For the same 5-year period, epilepsy underlying cause-of-death mortality rates increased 49.2% (figure 1), similar in magnitude to the 30.4% increase in prevalence reported by the CDC.¹² Given the increase in both mortality rates and prevalence, we hypothesise that an increase in epilepsy prevalence is contributing to the increase in epilepsy mortality rates. The CDC states ‘The increase [in epilepsy prevalence] is likely because of population growth over the past decade, or other unknown factors (eg, an increased willingness to disclose one has epilepsy)’.¹² Immigration from regions where epilepsy prevalence is high, such as Latin America may also contribute to the increase in prevalence of epilepsy in the USA. In Latin America, reported epilepsy prevalence ranges from 1.58% to 1.78%, which is higher than the USA prevalence of 1.2%.^{13 14}

A third factor contributing to the increase in epilepsy mortality in the USA is a significant change in the underlying causes of death in epilepsy. An unexpected finding is that epilepsy as the underlying cause of death declined significantly from 52.4% of all epilepsy-related deaths in 1999 to 38.2% in 2017 (p<0.0001). This finding provides strong evidence against an increase in the lethality of epilepsy as a driver of increased epilepsy mortality. This is consistent with the observation by Neligan et al¹ who found that the leading causes of death in people with epilepsy in the UK were not epilepsy related. Rather, cancer, cerebrovascular disease, pneumonia and ischaemic heart disease were the leading causes of death in people with epilepsy. Deaths directly due to epilepsy were rare. Comorbidities like Alzheimer’s and organic mental disorders (vascular dementia and delirium) are increasing significantly in people with epilepsy in the USA (table 2 and figure 2). The proportion of deaths in people with epilepsy due to vascular dementia and Alzheimer’s increased to 210.1% and 216.8%, respectively. This is higher than the increase in dementia mortality in the general population reported in table 1 (117.6%). Epilepsy affects 7% of the elderly, and 4%–5% of persons with Alzheimer’s disease. These rates are substantially higher than the 1.2% in the general population.^{15 16} At the same time, the prevalence of Alzheimer’s in people with epilepsy is six times higher than those without epilepsy.¹⁷ As the population ages and the global burden of neurologic disease increases, dementia will likely continue to grow as a comorbidity and cause of death in people with epilepsy, contributing to an increase in epilepsy mortality rates in the future.⁵

Figure 2. Relative change in key leading causes of death, 1999 to 2017. Note the significant reduction in heart disease as a leading cause of death in epilepsy, and increase in Alzheimer’s, Vascular Dementia, and Neoplasms, Cochran Armitage Test for Trend, p < 0.001.

For neoplasms, there is strong evidence that systemic cancer is associated with a high lifetime risk of epilepsy, especially in those with brain metastasis and primary neoplasms.^{18 19} As survival in systemic cancers increase and mortality rates decrease, it is reasonable to conclude that more survivors will develop epilepsy as a consequence of CNS involvement with cancer (table 2 and figure 2).^{18 19}

An important and unexpected finding of this study is the significant decline in heart disease as a leading cause of death in epilepsy (table 2 and figure 2). Ischaemic heart disease as a cause of death in people with epilepsy declined 43% from 1999 to 2017. The reduction in heart disease mortality in epilepsy is even better than that reported in the general population, which was 22% from 1990 to 2013.²⁰ The results suggest that people with epilepsy are benefitting from the improvements in primary prevention strategies seen in the general population.²⁰ This is an unexpected finding given the higher risk of cardiovascular disease and stroke reported in multiple large population studies.^{21 22} There is evidence that older antiepileptic drugs may increase people with vascular risk factors and with epilepsy, possibly increasing the risk for stroke and heart disease.^23–25 The newer antiepileptic drugs are associated with significant improvements in biomarkers like C-reactive protein, low-density lipoproteins and homocysteine when compared with older agents such as carbamazepine.^23–25 Many of these new agents (eg, Levetiracetam, Lacosamide) were introduced since 1999, the timeframe of this study. Further investigation of this important finding or a reduction in cardiovascular disease as a cause of death in epilepsy is needed.^{21 22}

Finally, while epilepsy mortality in the USA is increasing, the evidence for status epilepticus is more nuanced.^26–28 The incidence of status epilepticus has increased fourfold over the last 30 years.²⁶ However, the mortality rate of status epilepticus has remained unchanged.^26–28 The stability of status epilepticus mortality in the face of rising incidence is likely due to earlier recognition and treatment, better diagnosis and coding and more effective treatment algorithms.^26–28

Limitations and strengths of this study

Limitations: this study relies on mortality rates calculated from death certificates. Death certificates likely under-report epilepsy-related mortality, since there may be uncertainty about the underlying mechanism of death in people with epilepsy (status epilepticus, sudden unexplained death in epilepsy, hypoxia, etc). Data from Bell et al²⁹ indicate that death certificates can significantly underestimate the number of deaths in epilepsy. For this reason, we utilised the multiple cause-of-death database, rather than the single underlying cause-of-death database.^{7–9 29} When using the single underlying cause-of-death database, epilepsy mortality rate in 2017 was only 4.6 per million compared with 11.56 per million when using the multiple cause-of-death database.⁸ In a recent position paper, the National Association of Medical Examiners state:

The investigation and certification of deaths in patients with seizures and epilepsy vary within and between medical examiners’ and coroners’ offices. This variation, together with varied terms and criteria to diagnose and classify seizures and epilepsies…challenges the determination of cause of death (COD) in seizure and epilepsy-related death, and likely underestimates the frequency of these deaths.³⁰

Strengths: strength of this study is the use of the largest vital record population database in the USA, incorporating data from all 50 states, the District of Columbia and Puerto Rico. It is likely that the multiple cause-of-death mortality rates reported in this study better reflect the varied and complex mechanisms of death in people with epilepsy, because it includes the 113 leading causes of death as defined by the CDC.^{7–9 31} Indeed, when evaluating the impact of multiple causes of death in chronic diseases, Fedeli et al³¹ write that multiple cause-of-death analyses allows ‘…more complete assessment of the burden of mortality related to chronic diseases but are also useful to monitor patterns and inconsistencies in cause of death certification’.

Conclusions

Epilepsy mortality rates in the USA increased significantly from 1999 to 2017. The results from this large US population-based multiple cause-of-death study indicate the increases in epilepsy mortality rates are likely caused by at least three factors: (1) increased all-neurological mortality, which is related to the increase in the burden of neurological disorders overall; (2) increased epilepsy prevalence in the USA; (3) significant increases in degenerative dementia, vascular dementia and malignant neoplasms as causes of death in people with epilepsy. Importantly, ischaemic heart disease as a cause of death declined 42.6% while epilepsy-related causes declined 27.1% (p=0.001).

The authors thank Kenneth D Kochanek, Statistician, National Center for Health Statistic for his advice and assistance.

Footnote

Contributors AsCu created and edited the excel spreadsheet and contributed to the literature review and manuscript. DH, ArCa and AK reviewed and edited the manuscript for intellectual content. DM performed the statistical analysis and reviewed and edited the manuscript. CMdG has overall responsibility for the concept, research questions, data analysis, drafting and preparing the manuscript for publication.

Funding Supported by an unrestricted grant to the David Geffen School of Medicine, UCLA Department of Neurology by James and Beverly Peters and Family. The grantees had no role in the study design, data collection, interpretation of the data, writing of the report or decision to submit the paper for publication.

Competing interests None declared.

Patient consent for publication Not required.

Provenance and peer review Not commissioned; externally peer reviewed.

Data availability statement Data are available in a public, open access repository. Source data were obtained from the Centers for Disease Control, Wonder Database. The database is open access, and interested parties may check the link https://wonder.cdc.gov/. Data access is subject to certain conditions, see https://wonder.cdc.gov/ucd-icd10.html.

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