Long-term outcome of vagus nerve stimulation for drug-resistant epilepsy using continuous assessment, with a note on mortality.


Journal

Seizure
ISSN: 1532-2688
Titre abrégé: Seizure
Pays: England
ID NLM: 9306979

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 26 11 2021
revised: 22 01 2022
accepted: 25 01 2022
pubmed: 13 2 2022
medline: 26 3 2022
entrez: 12 2 2022
Statut: ppublish

Résumé

To examine the outcome of vagus nerve stimulation (VNS) for drug-resistant epilepsy using data from a National Health Service VNS clinic. Clinical records of patients implanted with VNS for epilepsy between1995 and 2010 were examined. Patients were selected for study who had at least one year of therapeutic stimulation (minimum 1 mA stimulator current) and follow-up by our service with analysable electronic records, providing continuous assessment of seizure control during available follow-up. Seizure status at each attendance was assessed and graded 1-4 (1=seizure free or <5 seizures/year; 2 =≥50%reduction in seizure frequency; 3=<50% reduction; 4=no improvement compared to baseline). Responders were those whose grades improved consistently (Grades 1,2 and 3). Of 464 patients, 171 fulfilled the inclusion criteria and were divided into three groups: a) Responders (n = 81); b) non-responders (n = 80) and c) others (n = 10), the latter showing a late step-wise change (six improved; four deteriorated). After initial ramping up of current, groups were very stable over subsequent periods varying from one to 12 years (median 3.8 years). Sixteen patients died, 10 of non-epilepsy causes with 6 epilepsy-related deaths. There was a significant relation between epilepsy-related deaths and response (p < 0.00001). Patients with longer time as non-responders had more likelihood of suffering an epilepsy death than responders, though numbers were small. This study shows that meaningful data can be obtained retrospectively from routine clinic records. In this cohort about half of patients treated with VNS responded and the response generally remaining stable over time.

Identifiants

pubmed: 35151152
pii: S1059-1311(22)00025-5
doi: 10.1016/j.seizure.2022.01.017
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

74-78

Informations de copyright

Copyright © 2022 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

Auteurs

Charles E Polkey (CE)

Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), King's College London (KCL), London, UK; Division of Clinical Neurosciences, Kings College Hospital NHS Trust, London, UK.

Lina Nashef (L)

Division of Clinical Neurosciences, Kings College Hospital NHS Trust, London, UK.

Cathy Queally (C)

Division of Clinical Neurosciences, Kings College Hospital NHS Trust, London, UK.

Richard Selway (R)

Division of Clinical Neurosciences, Kings College Hospital NHS Trust, London, UK.

Antonio Valentin (A)

Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), King's College London (KCL), London, UK; Department of Clinical Neurophysiology, King's College Hospital NHS Trust, London, UK. Electronic address: Antonio.Valentin@kcl.ac.uk.

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Classifications MeSH