SUDEP and mortality in epilepsy: The role of routinely collected healthcare data, registries, and health inequalities.

SUDEP and mortality in epilepsy: The role of routinely collected healthcare data, registries, and health inequalities.
Epilepsy Behav. 2019 Aug 17;:106453
Authors: Pickrell WO, Kerr MP
Abstract
Routinely collected data are a powerful research resource and offer the opportunity to further our understanding of epilepsy mortality and Sudden Unexpected Death in Epilepsy (SUDEP). The advantages of using routinely collected data include that it often covers whole populations, is already collected, and can be easily linked to other data sources. A significant disadvantage is the difficulty in obtaining accurate causes of death and correctly identifying cases of SUDEP. Using and linking data from epilepsy death registries can improve the quality of mortality data for research. Epilepsy prevalence, incidence, and mortality rates are associated with socioeconomic deprivation. Further research into understanding the link between deprivation and epilepsy mortality could lead to ways to reduce epilepsy mortality. This paper is for the Special Issue :Prevent 21: SUDEP Summit - Time to Listen.
PMID: 31427266 [PubMed - as supplied by publisher]

Source: Epilepsy and Behaviour - August 16, 2019 Category: Neurology Authors: Pickrell WO, Kerr MP Tags: Epilepsy Behav Source Type: research