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1000 Titel
  • Urothelial toxicity of esketamine in the treatment of depression
1000 Autor/in
  1. Findeis, Hannelore |
  2. Sauer, Cathrin |
  3. Cleare, Anthony |
  4. Bauer, Michael |
  5. Ritter, Philipp |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-07-26
1000 Erschienen in
1000 Quellenangabe
  • 237(11):3295-3302
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00213-020-05611-y |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561544/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Rationale!#!Ketamine is the first widely used substance with rapid-onset antidepressant action. However, there are uncertainties regarding its potential urothelial toxicity, particularly after repeated application. In the context of rising recreational ketamine use, severe side effects affecting the human urinary tract have been reported. It is assumed that ketamine interacts with bladder urothelial cells and induces apoptosis.!##!Objectives!#!This study aimed to assess whether single or repeated doses of esketamine used in an antidepressant indication are associated with urinary toxicity.!##!Methods!#!We included male and female inpatients with a current episode of depression and a diagnosis of recurrent depressive disorder, bipolar disorder or schizoaffective disorder according to ICD-10 criteria (n = 25). The esketamine treatment schedule involved a maximum of 3× weekly dosing at 0.25-0.5 mg/kg i.v. or s.c. The primary outcome was the change in urine toxicity markers (leukocytes, erythrocytes, protein and free haemoglobin). Description of demographic, clinical and laboratory data was conducted using means, standard deviations, frequencies and percentages. Changes in urinary toxicity markers over time were evaluated using linear mixed models with gender as a covariate.!##!Results!#!The participants received an average of 11.4 (SD 8) esketamine treatments, and an average number of 11.2 (SD 8) urine samples were analysed over the course of treatment. Neither urinary leukocyte concentration (F(20; 3.0) = 3.1; p = 0.2) nor erythrocyte concentration (F(20;2.2) = 4.1; p = 0.2) showed a significant trend towards increase during the course of esketamine treatment. Similarly, free haemoglobin and protein concentrations, which were analysed descriptively, did not display a rise during treatment. There was a significant improvement in depression ratings after esketamine treatment (p < 0.001).!##!Conclusions!#!This study is, to the best of our knowledge, the first to focus on urothelial toxicity of esketamine used in antidepressant indication and dose. The results indicate that the use of single or repeated doses of esketamine is unlikely to cause urothelial toxicity. The results are in need of confirmation as sample size was small.
1000 Sacherschließung
lokal Antidepressive Agents/adverse effects [MeSH]
lokal Depressive Disorder/drug therapy [MeSH]
lokal Urothelium/metabolism [MeSH]
lokal Original Investigation
lokal Depression
lokal Ketamine/administration
lokal Male [MeSH]
lokal Depressive Disorder/urine [MeSH]
lokal Esketamine
lokal Ketamine/urine [MeSH]
lokal Dose-Response Relationship, Drug [MeSH]
lokal Urothelium/drug effects [MeSH]
lokal Antidepressive Agents/administration
lokal Female [MeSH]
lokal Depressive Disorder/diagnosis [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Antidepressive Agents/urine [MeSH]
lokal Middle Aged [MeSH]
lokal Affective disorder
lokal Injections, Subcutaneous [MeSH]
lokal Urothelial toxicity
lokal Injections, Intravenous [MeSH]
lokal Ketamine/adverse effects [MeSH]
lokal Side effects
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/RmluZGVpcywgSGFubmVsb3Jl|https://frl.publisso.de/adhoc/uri/U2F1ZXIsIENhdGhyaW4=|https://frl.publisso.de/adhoc/uri/Q2xlYXJlLCBBbnRob255|https://frl.publisso.de/adhoc/uri/QmF1ZXIsIE1pY2hhZWw=|https://frl.publisso.de/adhoc/uri/Uml0dGVyLCBQaGlsaXBw
1000 Hinweis
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1000 Dateien
  1. Urothelial toxicity of esketamine in the treatment of depression
1000 Objektart article
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1000 Erstellt am 2023-11-17T04:28:27.615+0100
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1000 Zuletzt bearbeitet 2023-12-01T05:01:51.728+0100
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