Cited by 18Pharmacovigilance and Adverse Drug ReactionsEpilepsy research and treatmentElectroconvulsive Therapy Studies

Seizures during antidepressant treatment in psychiatric inpatients—results from the transnational pharmacovigilance project “Arzneimittelsicherheit in der Psychiatrie” (AMSP) 1993–2008

Köster, M., Grohmann, R., Engel, R. R., Nitsche, M. A., Rüther, E., Degner, D.·2013·Psychopharmacology

Abstract

Rationale There is little clinical data available about seizure rates in psychiatric inpatients, and there are no studies with reference data to the frequencies of antidepressant (AD) use for this important clinical population.Objective This study investigates seizure rates during AD treatment in psychiatric inpatient settings, drawn from the transnational pharmacovigilance programme Arzneimittelsicherheit in der Psychiatrie (AMSP) in relation to the known frequencies of ADs used in the participating clinics. Comparisons are made to former publications and their limitations.Results Seventy-seven cases were identified with grand mal seizures (GMS) during AD treatment between 1993 and 2008, with a total number of 142,090 inpatients under surveillance treated with ADs in the participating hospitals. The calculated overall rate of reported seizures of patients during AD treatment in this collective is 0.05 % for ADs imputed alone or in combination with other psychotropic drug groups and 0.02 % when only ADs were given and held responsible for GMS. The patients receiving tri- or tetracyclic ADs (TCAs) had a 2-fold risk to develop a seizure as compared to the overall average rate in this sample. In 11 cases, there was only one AD imputed--the majority of these cases (9/11) were TCA. Monotherapy with selective serotonin reuptake inhibitors (SSRI) or dual serotonin and noradrenaline reuptake inhibitors (SNRI) were never imputed alone in this sample.Conclusions The results of the study favour the assumption that SSRIs, noradrenergic and specific serotonergic antidepressants (NaSSA) and dual SNRI might be more appropriate than TCAs for the treatment of psychiatric patients with an enhanced seizure risk.

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Crossref · 10.1007/s00213-013-3281-8

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References 71 · Cited by 18

Authors
Köster, M., Grohmann, R., Engel, R. R., Nitsche, M. A., Rüther, E., & Degner, D.
Affiliations
  • Klinik und Poliklinik für Psychiatrie und Psychotherapie (DE)
  • Universitätsmedizin Göttingen (DE)
  • University of Göttingen (DE)
Corresponding author
Köster, M.
Venue
Psychopharmacology
Published
2013-09-26
Volume
230
Issue
2
Pages
191-201
ISSN
  • 0033-3158 (ISSN-L)
  • 1432-2072
OpenAlex
W2118710609
Cited by
18
References
71
Citations by year
2025: 2 · 2024: 1 · 2021: 2 · 2020: 2 · 2018: 4 · 2017: 1 · 2016: 1 · 2015: 2 · 2014: 2 · 2013: 1
FWCI
1.48
Type
journal article
Language
en
Open access
closed
Locations
  • Psychopharmacology (publishedVersion)
  • PubMed (publishedVersion)
  • GRO (submittedVersion)
Funders
  • Bristol-Myers Squibb
  • Sanofi
  • Ludwig-Maximilians-Universität München
  • H. Lundbeck A/S
  • Cilag
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Pharmacovigilance and Adverse Drug Reactions
  • Health Sciences › Medicine › Psychiatry and Mental health › Epilepsy research and treatment
  • Health Sciences › Medicine › Psychiatry and Mental health › Electroconvulsive Therapy Studies
Keywords
generalized tonic-clonic seizures, tricyclic antidepressants, selective serotonin reuptake inhibitors, serotonin-norepinephrine reuptake inhibitors, noradrenergic and specific serotonergic antidepressants, seizure risk, psychiatric inpatients, pharmacovigilance, drug safety
MeSH terms
Adolescent, Adult, Aged, Antidepressive Agents, Epilepsy, Tonic-Clonic, Female, Germany, Humans, Inpatients, Male, Middle Aged, Risk, Young Adult, Pharmacovigilance

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