Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications

F. Cosci*, G. Chouinard

*Corresponding author for this work

Research output: Contribution to journal(Systematic) Review article peer-review

Abstract

Studies on psychotropic medications decrease, discontinuation, or switch have uncovered withdrawal syndromes. The present overview aimed at analyzing the literature to illustrate withdrawal after decrease, discontinuation, or switch of psychotropic medications based on the drug class (i.e., benzodiazepines, nonbenzodiazepine benzodiazepine receptor agonists, antidepressants, ketamine, antipsychotics, lithium, mood stabilizers) according to the diagnostic criteria of Chouinard and Chouinard [Psychother Psychosom. 2015;84(2):63-71], which encompass new withdrawal symptoms, rebound symptoms, and persistent post-withdrawal disorders. All these drugs may induce withdrawal syndromes and rebound upon discontinuation, even with slow tapering. However, only selective serotonin reuptake inhibitors, serotonin noradrenaline reuptake inhibitors, and antipsychotics were consistently also associated with persistent post-withdrawal disorders and potential high severity of symptoms, including alterations of clinical course, whereas the distress associated with benzodiazepines discontinuation appears to be short-lived. As a result, the common belief that benzodiazepines should be substituted by medications that cause less dependence such as antidepressants and antipsychotics runs counter the available literature. Ketamine, and probably its derivatives, may be classified as at high risk for dependence and addiction. Because of the lag phase that has taken place between the introduction of a drug into the market and the description of withdrawal symptoms, caution is needed with the use of newer antidepressants and antipsychotics. Within medication classes, alprazolam, lorazepam, triazolam, paroxetine, venlafaxine, fluphenazine, perphenazine, clozapine, and quetiapine are more likely to induce withdrawal. The likelihood of withdrawal manifestations that may be severe and persistent should thus be taken into account in clinical practice and also in children and adolescents.
Original languageEnglish
Pages (from-to)283-306
Number of pages24
JournalPsychotherapy and Psychosomatics
Volume89
Issue number5
DOIs
Publication statusPublished - 1 Aug 2020

Keywords

  • antidepressant
  • antipsychotic
  • atypical antipsychotics
  • benzodiazepine
  • cognitive-behavioral therapy
  • discontinuation
  • dopamine supersensitivity psychosis
  • dose benzodiazepine use
  • double-blind
  • generalized anxiety disorder
  • lithium
  • long-term treatment
  • mood stabilizers
  • rebound insomnia
  • selective serotonin reuptake inhibitor
  • serotonin noradrenaline reuptake inhibitor
  • serotonin reuptake inhibitor
  • tolerance
  • treatment-resistant schizophrenia
  • withdrawal
  • Antidepressant
  • REBOUND INSOMNIA
  • Lithium
  • Selective serotonin reuptake inhibitor
  • COGNITIVE-BEHAVIORAL THERAPY
  • Antipsychotic
  • GENERALIZED ANXIETY DISORDER
  • Discontinuation
  • DOSE BENZODIAZEPINE USE
  • Withdrawal
  • Benzodiazepine
  • Mood stabilizers
  • Tolerance
  • Serotonin noradrenaline reuptake inhibitor
  • DOPAMINE SUPERSENSITIVITY PSYCHOSIS
  • ATYPICAL ANTIPSYCHOTICS
  • TREATMENT-RESISTANT SCHIZOPHRENIA
  • SEROTONIN REUPTAKE INHIBITOR
  • DOUBLE-BLIND
  • LONG-TERM TREATMENT

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