Receptor-binding profiles of antipsychotics: Clinical strategies when switching between agents

Peter F. Buckley

Research output: Contribution to journalReview article

33 Scopus citations

Abstract

In spite of apparent improvements in the pharmacotherapy of schizophrenia, many patients still demonstrate an incomplete therapeutic response to antipsychotic medication and/or intolerable adverse effects, necessitating a change in their medication regimen. The switch from one antipsychotic to another, however, is not without challenges and can be complicated by withdrawal-emergent adverse effects that prompt the patient or the clinician to abort the switch. The extent to which these adverse events can be predicted by comparing the effects of the old and new antipsychotic medications on various receptor systems, including dopaminergic, muscarinic, and histaminergic receptors, is of considerable clinical and research interest. For example, patients receiving a sedating antipsychotic with high affinity for histamine H, receptors could experience rebound insomnia if switched to a less sedating agent with a low affinity for H1 receptors. An understanding of the differential receptor-binding profiles of the various antipsychotics can help clinicians anticipate and manage potential clinical issues that may be encountered when switching antipsychotic therapy.

Original languageEnglish (US)
Pages (from-to)5-9
Number of pages5
JournalJournal of Clinical Psychiatry
Volume68
Issue numberSUPPL. 6
StatePublished - Jul 10 2007

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Clinical Psychology

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