PMID- 25458101 OWN - NLM STAT- MEDLINE DCOM- 20150831 LR - 20191210 IS - 1532-2688 (Electronic) IS - 1059-1311 (Linking) VI - 24 DP - 2015 Jan TI - Adult nonconvulsive status epilepticus in a clinical setting: Semiology, aetiology, treatment and outcome. PG - 102-6 LID - S1059-1311(14)00258-1 [pii] LID - 10.1016/j.seizure.2014.09.007 [doi] AB - PURPOSE: Our objective was to study the semiology, aetiology, treatment and outcome of nonconvulsive status epilepticus (NCSE) in adults. METHODS: All NCSE episodes in an unselected hospital cohort in the period 2004-2009 were identified, and the files reviewed. STESS (Status Epilepticus Severity Scale) was conducted retrospectively and correlated to outcome. Follow-up was undertaken after >2 years. RESULTS: 48 NCSEs in 39 patients, 22 men and 17 women, were found. Mean age was 63 years. 23/39 (59%) patients had established epilepsy. The underlying cause of NCSE was cerebrovascular disease in 17/39 (44%). 37/48 (77%) NCSEs were complex focal status epilepticus. 3/48 NCSEs (6.3%) lead to death, whereas 8.5% lead to severe sequelae. Cognitive sequelae were found after 14.9% of NCSEs. The outcome was worst in the group with no prior epilepsy (p=0.013). STESS had a negative predictive value of 96% (cut-off value of 3) for severe sequelae and death combined (p<0.002). CONCLUSIONS: NCSE has a potential for severe sequelae and represents an emergency in need of intensive treatment. The major determinant of outcome is the underlying cause. The outcome was worse in patients without epilepsy than in patients with epilepsy. STESS is of value in predicting outcome. Cognitive sequelae following NCSE can occur, but need further investigation with prospective, systematic studies. CI - Copyright (c) 2014 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved. FAU - Power, Kjersti Nesheim AU - Power KN AD - Department of Neurology, Haukeland University Hospital, Bergen, Norway; Department of Clinical Medicine, Section for Neurology, University of Bergen, Norway. Electronic address: kjersti.nesheim.power@helse-bergen.no. FAU - Gramstad, Arne AU - Gramstad A AD - Department of Neurology, Haukeland University Hospital, Bergen, Norway; Department of Biological and Medical Psychology, University of Bergen, Norway. FAU - Gilhus, Nils Erik AU - Gilhus NE AD - Department of Neurology, Haukeland University Hospital, Bergen, Norway; Department of Clinical Medicine, Section for Neurology, University of Bergen, Norway. FAU - Engelsen, Bernt A AU - Engelsen BA AD - Department of Neurology, Haukeland University Hospital, Bergen, Norway; Department of Clinical Medicine, Section for Neurology, University of Bergen, Norway. LA - eng PT - Journal Article DEP - 20141002 PL - England TA - Seizure JT - Seizure JID - 9306979 RN - 0 (Anticonvulsants) SB - IM EIN - Seizure. 2015 Dec;33:103 CIN - Seizure. 2015 Dec;33:99. PMID: 26341145 CIN - Seizure. 2015 Dec;33:100. PMID: 26385398 MH - Adolescent MH - Adult MH - Aged MH - Aged, 80 and over MH - Anticonvulsants/therapeutic use MH - Cohort Studies MH - Electroencephalography MH - Epilepsy, Generalized/complications/*etiology/*therapy MH - Female MH - Humans MH - Male MH - Middle Aged MH - Outcome Assessment, Health Care MH - Severity of Illness Index MH - Status Epilepticus/complications/*etiology/*therapy MH - *Treatment Outcome MH - Young Adult OTO - NOTNLM OT - Aetiology OT - Epilepsy OT - Nonconvulsive status epilepticus OT - Outcome OT - Status epilepticus EDAT- 2014/12/03 06:00 MHDA- 2015/09/01 06:00 CRDT- 2014/12/03 06:00 PHST- 2014/06/19 00:00 [received] PHST- 2014/09/08 00:00 [revised] PHST- 2014/09/24 00:00 [accepted] PHST- 2014/12/03 06:00 [entrez] PHST- 2014/12/03 06:00 [pubmed] PHST- 2015/09/01 06:00 [medline] AID - S1059-1311(14)00258-1 [pii] AID - 10.1016/j.seizure.2014.09.007 [doi] PST - ppublish SO - Seizure. 2015 Jan;24:102-6. doi: 10.1016/j.seizure.2014.09.007. Epub 2014 Oct 2.