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dc.contributor.authorAnzolin, Ana Paulapt_BR
dc.contributor.authorGoularte, Jeferson Ferrazpt_BR
dc.contributor.authorPinto, Jairo Vinícius Merege de Mello Cruzpt_BR
dc.contributor.authorBelmonte-de-Abreu, Paulo Silvapt_BR
dc.contributor.authorCruz, Luciane Nascimentopt_BR
dc.contributor.authorCordova, Victor Hugo Schalypt_BR
dc.contributor.authorMagalhães, Lucas Suetipt_BR
dc.contributor.authorRosa, Adriane Ribeiropt_BR
dc.contributor.authorCeresér, Keila Maria Mendespt_BR
dc.contributor.authorKauer-Sant'Anna, Márciapt_BR
dc.date.accessioned2024-11-27T06:52:28Zpt_BR
dc.date.issued2023pt_BR
dc.identifier.issn1664-0640pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/281575pt_BR
dc.description.abstractBackground: Psychiatric disorders are associated with more than 90% of reported suicide attempts worldwide, but few treatments have demonstrated a direct effect in reducing suicide risk. Ketamine, originally an anesthetic, has been shown anti-suicide effects in clinical trials designed to treat depression. However, changes at the biochemical level were assessed only in protocols of ketamine with very limited sample sizes, particularly when the subcutaneous route was considered. In addition, the inflammatory changes associated with ketamine effects and their correlation with response to treatment, dose-effect, and suicide risk warrant further investigation. Therefore, we aimed to assess whether ketamine results in better control of suicidal ideation and/or behavior in patients with depressive episodes and whether ketamine affects psychopathology and inflammatory biomarkers. Materials and methods: We report here the design of a naturalistic prospective multicenter study protocol of ketamine in depressive episodes carried out at Hospital de Clínicas de Porto Alegre (HCPA) and Hospital Moinhos de Vento (HMV). The study was planned to recruit adult patients with Major depressive disorder (MDD) or Bipolar disorder (BD) types 1 or 2, who are currently in a depressive episode and show symptoms of suicidal ideation and/or behavior according to the Columbia-Suicide Severity Rating Scale (C-SSRS) and have been prescribed ketamine by their assistant psychiatrist. Patients receive ketamine subcutaneously (SC) twice a week for 1 month, but the frequency can be changed or the dose decreased according to the assistant physician’s decision. After the last ketamine session, patients are followed-up via telephone once a month for up to 6 months. The data will be analyzed using repeated measures statistics to evaluate the reduction in suicide risk as a primary outcome, as per C-SSRS. Discussion: We discuss the need for studies with longer follow-ups designed to measure a direct impact on suicide risk and that additional information about the safety and tolerability of ketamine in particular subset of patients such as those with depression and ideation suicide. In line, the mechanism behind the immunomodulatory effects of ketamine is still poorly understood.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofFrontiers in psychiatry. Lausanne. Vol. 14 (2023), 1147298, 14 p.pt_BR
dc.rightsOpen Accessen
dc.subjectDepressãopt_BR
dc.subjectSuicideen
dc.subjectTranstorno bipolarpt_BR
dc.subjectBipolar depressionen
dc.subjectSuicídiopt_BR
dc.subjectUnipolar depressionen
dc.subjectDepressionen
dc.subjectKetaminapt_BR
dc.subjectKetamineen
dc.titleKetamine study : protocol for naturalistic prospective multicenter study on subcutaneous ketamine infusion in depressed patients with active suicidal ideationpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001211136pt_BR
dc.type.originEstrangeiropt_BR


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