Highlights
- •We analyzed mortality data of 11,968 patients who died of COVID-19 in order to find the prevalence of epilepsy.
- •The risk factors for COVID-19 mortality in young adults may be different than in the general population.
- •Epilepsy is overrepresented among young patients who died from COVID-19.
Abstract
Background
Methods
Results
Conclusion
Keywords
1. Introduction
- Nørgaard S.K.
- Vestergaard L.S.
- Nielsen J.
- Richter L.
- Schmid D.
- Bustos N.
- et al.
- Booth A.
- Reed A.B.
- Ponzo S.
- Yassaee A.
- Aral M.
- Plans D.
- et al.
- Balestrini S.
- Koepp M.J.
- Gandhi S.
- Rickmann H.M.
- Shin G.Y.
- Houlihan C.F.
- et al.
- Asadi-Pooya A.A.
- Emami A.
- Akbari A.
- Javanmardi F.
- Turk M.A.
- Landes S.D.
- Formica M.K.
- Goss K.D.
- Malle L.
- Gao C.
- Bouvier N.
- Percha B.
- Malle L.
- Gao C.
- Bouvier N.
- Percha B.
2. Methods and materials
2.1 COVID-19 epidemic in Hungary
NY times: Coronavirus world map: tracking the global outbreak, Updated Updated March 23, 2021, 2:29 PM. E.T., Accessed March 23, 2021https://www.nytimes.com/interactive/2020/world/coronavirus-maps.html.
2.2 Analysis of the Hungarian COVID-related death data
2.3 Statistical methods
2.4 Data availability and ethical consideration
3. Results
All patients N = 11,686 | Epilepsy patients N = 255 | Patients without epilepsy N = 11,431 | p value | |
---|---|---|---|---|
Age (y, mean±SD) | 75.73±11 | 68.24±15 | 75.89±12 | <0.001 |
N (% of all patients) | N (% of epilepsy patients) | N (% of patients without epilepsy) | ||
Male sex | 5912 (50.6%) | 150 (58.8%) | 5762 (50.4%) | <0.01 |
Died during the first wave | 674 (5.8%) | 12 (4.7%) | 662 (5.8%) | 0.45 |
Intellectual disability | 84 (0.7%) | 28 (11.0%) | 56 (0.5%) | <0.001 |
Down syndrome | 15 (0.13%) | 5 (2.0%) | 10 (0.09%) | <0.001 |
Brain tumor | 55 (0.5%) | 8 (3.1%) | 47 (0.4%) | <0.001 |
History of stroke | 1072 (9.2%) | 56 (22.0%) | 1016 (8.9%) | <0.001 |
- Turk M.A.
- Landes S.D.
- Formica M.K.
- Goss K.D.
- Malle L.
- Gao C.
- Bouvier N.
- Percha B.
Age groups | Number of all patients | Epilepsy (N,% of all patients in the age group) | Intellectual disability | Down syndrome | Brain tumor | history of stroke |
---|---|---|---|---|---|---|
all age groups | 11,686 | 255 (2.2%) | 84 (0.7%) | 15 (0.13%) | 55 (0.5%) | 1072 (9.2%) |
age 49 or younger | 334 | 31 (9.3%) | 33 (9.9%) | 9 (2.7%) | 5 (1.5%) | 13 (3.9%) |
50–59 years | 696 | 33 (4.7%) | 21 (3%) | 5 (0.72%) | 6 (0.9%) | 36 (5.2%) |
60–69 years | 2189 | 66 (3%) | 13 (0.6%) | 1 (0.047%) | 13 (0.6%) | 159 (7.3%) |
70–79 years | 3517 | 61 (1.7%) | 12 (0.2%) | 0 (0%) | 20 (0.6%) | 336 (9.6%) |
≥80 years | 4950 | 64 (1.3%) | 5 (0.1%) | 0 (0%) | 11 (0.2%) | 528 (10.7%) |

4. Discussion
Age groups | Estimated prevalence of epilepsy in Croatia | Patients with epilepsy among those who died of COVID-19 in Hungary (% of all patients in the particular age group) |
---|---|---|
19–45 years | 0.5% (CI:0.47–0.53) | 10.5% (N = 21/200) |
46–65 years | 0.47% (CI:0.44–0.5) | 4.1% (N = 77/1877) |
>65 years | 0.44% (CI:0.41–0.48) | 1.6% (N = 157/9608) |
Age groups | Estimated prevalence of epilepsy in Croatia | Patients with epilepsy among those who died of COVID-19 in Hungary (% of all patients in the particular age group) |
---|---|---|
19–45 years | 0.5% (CI:0.47–0.53) | 10.5% (N = 21/200) |
46–65 years | 0.47% (CI:0.44–0.5) | 4.1% (N = 77/1877) |
>65 years | 0.44% (CI:0.41–0.48) | 1.6% (N = 157/9608) |
Age groups | Estimated prevalence of epilepsy in Estonia | Patients with epilepsy among those who died of COVID-19 in Hungary (% of all patients in the particular age group) |
---|---|---|
20–29 | 0.43% (CI:0.33–0.53) | 4% (N = 1/25) |
30–39 | 0.57% (CI:0.45–0.69) | 12.9% (N = 9/70) |
40–49 | 0.6% (CI:0.46–0.74) | 8.8% (N = 21/239) |
50–59 years | 0.61% (CI:0.47–0.75) | 4.7% (N = 33/696) |
60–69 years | 0.63% (CI:0.48–0.78) | 3.0% (N = 66/2189) |
70–79 years | 0.22% (CI:0.1–0.34) | 1.7% (N = 61/3517) |
≥80 years | 0.48% (CI:0.23–0.73) | 1.3% (N = 64/4950) |
- Booth A.
- Reed A.B.
- Ponzo S.
- Yassaee A.
- Aral M.
- Plans D.
- et al.
- Balestrini S.
- Koepp M.J.
- Gandhi S.
- Rickmann H.M.
- Shin G.Y.
- Houlihan C.F.
- et al.
- Asadi-Pooya A.A.
- Emami A.
- Akbari A.
- Javanmardi F.
- Turk M.A.
- Landes S.D.
- Formica M.K.
- Goss K.D.
- Malle L.
- Gao C.
- Bouvier N.
- Percha B.
- Booth A.
- Reed A.B.
- Ponzo S.
- Yassaee A.
- Aral M.
- Plans D.
- et al.
5. Limitations
- (1)There are no available reliable epidemiological data on epilepsy in Hungary. Hungary is located in Eastern-Central Europe (“post-communist region”). The prevalence of epilepsy in the immediate neighbor Croatia and in Estonia (both are located in the same region of Europe as Hungary) is similar, and does not differ significantly from general European prevalence of epilepsy [[18],[19],[20]]. Thus, we can assume that the epilepsy prevalence data in Hungary may also be similar.
- (2)The diagnosis on chronic disorders in people who died of COVID-19 was provided to the National Public Health Center by GPs or physicians working at the COVID centers, so the diagnosis of epilepsy may not be completely reliable, although in Hungary the diagnosis of epilepsy in general is made by neurologists, often with the involvement of epilepsy centers [[37]].
- (3)We examined the absolute number of COVID-related deaths, thus, our study does not provide any direct information on whether epilepsy is a risk factor for COVID-related death. The absolute number of COVID-related deaths in epilepsy depends on the incidence rate of the infection in the population, individual susceptibility to a serious infections and the probability of fatal outcome of a serious illness. At the same time, however, the absolute number of deaths may demonstrate the magnitude of the effect of COVID-19 pandemic on epilepsy community in a country in many ways better than separate data on susceptibility, predisposition to a serious illness and the risk of a death during serious illness. The absolute number of deaths were those that highlighted that young PWE may be much more affected by COVID-19 than previously thought, as nearly 10% of young deaths had epilepsy, 10–20 times more than what we could have expected from epidemiological studies. The exact mechanism of the causal relationship between death of young adult epileptic patients and COVID-19 infection cannot be established with certainty based on our results.
- (4)The database does not contain information on the type or etiology of epilepsy, thus we have no results on mortality data for different subgroups of epileptic patients [[38]].
- Pack A.M.
Epilepsy overview and revised classification of seizures and epilepsies.Continuum (Minneap Minn). 2019; 25 (PMID: 30921011): 306-321https://doi.org/10.1212/CON.0000000000000707
6. Conclusions
Financial disclosure
Conflicts of Interest
Acknowledgments
Appendix. Supplementary materials
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