Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34564
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dc.contributor.authorMula, Marco-
dc.contributor.authorBorghs, Simon-
dc.contributor.authorFerro, Bruno-
dc.contributor.authorZaccara, Gaetano-
dc.contributor.authorDainese, Filippo-
dc.contributor.authorFerlazzo, Edoardo-
dc.contributor.authorRomigi, Andrea-
dc.contributor.authorGambardella, Antonio-
dc.contributor.authorPerucca, Emilio-
dc.date2023-
dc.date.accessioned2023-12-18T00:04:41Z-
dc.date.available2023-12-18T00:04:41Z-
dc.date.issued2023-12-11-
dc.identifier.citationEpilepsia 2023-12-11en_US
dc.identifier.issn1528-1167-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34564-
dc.description.abstractTo investigate changes in depressive and suicidality status and their relationship with seizure outcomes after addition or substitution of another antiseizure medication (ASM) in adults with drug-resistant focal epilepsy. 770 consecutively enrolled patients were assessed and followed prospectively for seizure outcome and depressive status over a 6-month period after starting treatment with a newly introduced ASM. The Neurological Disorders Depression Inventory for Epilepsy (NDDIE) was used to screen for depression and suicidality. Correlations of NDDIE results with clinical and treatment-related variables were assessed by using a stepwise logistic regression model. At baseline, 50.0% of patients had a positive screening test result for depression and 13.0% had a positive screening test result for suicidal ideation. A psychiatric comorbidity at baseline was associated with a 2.3 times increased risk of an initially negative NDDIE screening result becoming positive at re-assessment after 6 months. Number of ASMs taken at baseline also correlated with an increased risk of a change in depression screening test results from negative to positive during follow-up, whereas no association was identified with sociodemographic and epilepsy-related variables, including seizure outcomes. Approximately 6% of patients initially negative at screening for suicidal ideation became positive at the 6-month re-assessment. The risk of switch from a negative to a positive screening test result for suicidal ideation was increased more than two-fold in individuals who screened positive for depression at baseline, and was unrelated to type of ASM introduced, sociodemographic variables or seizure outcomes. Almost 1 in 5 adults with drug resistant focal epilepsy who screen negative for depression become positive when re-assessed 6 months after a treatment change. 6.1% who screen initially negative for passive suicidal ideation become positive at re-assessment 6 months later. These changes in screening status are independent of type of ASM introduced or seizure outcomes, but correlate with psychiatric status at baseline.en_US
dc.language.isoeng-
dc.subjectNDDI-Een_US
dc.subjectantiseizure medicationsen_US
dc.subjectdepressionen_US
dc.subjectepilepsyen_US
dc.subjectoutcomeen_US
dc.subjectsuicidalityen_US
dc.subjecttreatmenten_US
dc.titleEffect of drug treatment changes and seizure outcomes on depression and suicidality in adults with drug-resistant focal epilepsy.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleEpilepsiaen_US
dc.identifier.affiliationInstitute of Medical and Biomedical Education, St George's University of London and the Atkinson Morley Regional Neuroscience Centre, St George's University Hospitals NHS Foundation Trust, London, United Kingdom.en_US
dc.identifier.affiliationUCB Pharma, Slough, UK.en_US
dc.identifier.affiliationUCB Pharma, Milan, Italy.en_US
dc.identifier.affiliationRegional Health Agency of Tuscany, Firenze, Italy.en_US
dc.identifier.affiliationDepartment of Neuroscience, Unit of Neurology and Neurophysiology, University Hospital of Padova, Padova, Italy.en_US
dc.identifier.affiliationDepartment of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italy; Regional Epilepsy Centre, Great Metropolitan Hospital BMM, Reggio Calabria, Italy.en_US
dc.identifier.affiliationIRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Pozzilli (IS) Italy; Psychology Faculty, International Telematic University Uninettuno, Rome, Italy.en_US
dc.identifier.affiliationDepartment of Neurology, University of Catanzaro, Catanzaro, Italy.en_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationDepartment of Neuroscience, Monash University, Melbourne, Victoria, Australia.en_US
dc.identifier.doi10.1111/epi.17856en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-9415-3395en_US
dc.identifier.orcid0000-0002-2416-147Xen_US
dc.identifier.orcid0000-0002-4505-2600en_US
dc.identifier.orcid0000-0001-7384-3074en_US
dc.identifier.orcid0000-0001-8703-223Xen_US
dc.identifier.pubmedid38073337-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
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