The register of epilepsy related deaths has been conceived and developed by bereaved relatives of those who died from epilepsy. The register is run as a collaborative project by Epilepsy Ireland and SUDEP Action with the purpose of reducing the risk of epilepsy deaths in the future. Both charities are fully committed to supporting and developing the register.
The paramount principle behind the register is to collect information from as many bereaved families and other reporters as possible to try and make some sense of what happened, why the death occurred and how to prevent future tragedies.
Protecting the individual
The interests of the individual who died are acknowledged by the non-intrusive way of gathering information. The register will only hold data volunteered to us through contact with the Epilepsy Deaths Register team either on the web, by phone or by post. Nothing will be used for the register unless consent is obtained and this consent can be withdrawn at any time. All data will be anonymised and held securely.
Protecting the family
During this difficult time, support will be available to relatives and friends of the person who has died and again any family information will be anonymised.
The benefits of the register
Until now, there is nowhere to collect and store information about circumstances leading up to death or about the circumstances and investigations after death. The charities are driven by a need to better understand the cause of death and how to reduce the risk of death. That is why the charities have strong links with researchers with a range of research interests relevant to epilepsy deaths.
The risks of having a register
The risks are small as long as the information is anonymous and is held securely. Any research that uses information from the register must get permission from the charities and then get appropriate approval for this research.