| Literature DB >> 27810515 |
Monica S Cooper1, Anne Mcintosh2, Douglas E Crompton3, Jacinta M McMahon4, Amy Schneider4, Kevin Farrell5, Vijeya Ganesan6, Deepak Gill7, Sara Kivity8, Tally Lerman-Sagie9, Ailsa McLellan10, James Pelekanos11, Venkateswaran Ramesh12, Lynette Sadleir13, Elaine Wirrell14, Ingrid E Scheffer15.
Abstract
We measured the mortality rate and the rate of Sudden Unexpected Death in Epilepsy (SUDEP) in Dravet Syndrome (DS). We studied a cohort of 100 consecutively recruited, unrelated patients with DS; 87 had SCN1A mutations. Living cases had a median follow-up of 17 years. Seventeen patients died, at a median age of seven years (inter-quartile range 3-11 years) with causes of death: 10 SUDEP, four status epilepticus, two drowning and one asphyxia. The SUDEP classification included three Definite, one Definite Plus and six Probable. The Dravet-specific mortality rate/1000-person-years was 15.84 (98% CI 9.01-27.85). The Dravet-specific SUDEP rate was 9.32/1000-person-years (98% CI 4.46-19.45). The Dravet-specific SUDEP rate is the only documented syndrome-specific SUDEP rate. SUDEP in DS occurs mainly in childhood. It is also the highest SUDEP rate, considerably higher than the recent 5.1 SUDEP rate/1000-person-years for adults with refractory epilepsy. Copyright ÂEntities:
Keywords: Dravet syndrome; Epilepsy; Mortality; Sudden unexpected death in epilepsy
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Year: 2016 PMID: 27810515 DOI: 10.1016/j.eplepsyres.2016.10.006
Source DB: PubMed Journal: Epilepsy Res ISSN: 0920-1211 Impact factor: 3.045