Atypical Antipsychotics Part I: Pharmacology, Pharmacokinetics, and Efficacy
Abstract
OBJECTIVE: To compare the pharmacology, pharmacokinetics, and efficacy of the newer atypical antipsychotics with those of conventional agents and existing atypical agents. DATA SOURCES: Information was retrieved from a MEDLINE English-literature search from July 1986 to June 1998 and by review of references. Indexing terms included neuroleptics, atypical antipsychotics, clozapine, risperidone, olanzapine, sertindole, quetiapine, and ziprasidone. STUDY SELECTION: Comparative studies were selected when possible; placebo-controlled studies were included when data were limited on newer atypical antipsychotics. DATA EXTRACTION: Emphasis was placed on properly designed clinical trials that assessed dosage, expanded efficacy, enhanced adverse effect profile, and cost. DATA SYNTHESIS: Like other atypical antipsychotics, the newer agents have an enhanced 5-hydroxytryptophan/dopaminergic receptors (5-HT 2 /D 2 ) affinity ratio and undergo extensive biotransformation. Risperidone and olanzapine demonstrate more favorable efficacy/adverse effect ratios than clozapine, sertindole, and conventional antipsychotics in nonrefractory and refractory schizophrenics. Future studies will more clearly define the role of quetiapine and ziprasidone in antipsychotic therapy. CONCLUSIONS: Data from controlled trials on efficacy and extrapyramidal side effects support risperidone or olanzapine as first-line agents for the treatment of schizophrenia. Pharmacologic and pharmacokinetic factors do not distinguish between agents sufficiently for drug selection.
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Prolonged exposure to ketamine may predispose to neurotoxicity.
“In addition, a prolonged exposure to ketamine may predispose to neurotoxicity [142].”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [142]
The use of ketamine in psychiatry is at risk of replicating the 2016 opioid US epidemic abuse with the risk to induce neurotoxicity, which might be associated with persistent post-withdrawal disorders.
“In view of the inevitable decay of the response to ketamine due to pharmacological tolerance [148] and its possible benefit as maintenance therapy in treatment-resistant depression [142], and considering that some clinicians use ketamine formulations for chronic use despite the alarm regarding 'the rapid proliferation of off-label ketamine administration in the absence of evidence of”
From Acute and Persistent Withdrawal Syndromes Following Discontinuation of Psychotropic Medications (2020) · cites this paper as [142]
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- Authors
- Markowitz, J. S., Brown, C. S., & Moore, T. R.
- Affiliations
- Medical University of South Carolina (US)
- University of Tennessee Health Science Center (US)
- Florida Agricultural and Mechanical University (US)
- Venue
- Annals of Pharmacotherapy
- Publisher
- SAGE Publications
- Published
- 1999-01
- Volume
- 33
- Issue
- 1
- Pages
- 73-85
- ISSN
- 0012-6578 (ISSN-L)
- 1060-0280
- 1542-6270
- OpenAlex
- W2153226419
- Cited by
- 208
- References
- 76
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 2 · 2023: 6 · 2022: 2 · 2020: 7 · 2019: 3 · 2018: 6 · 2017: 4 · 2016: 5 · 2015: 4 · 2014: 4 · 2013: 7 · 2012: 5
- FWCI
- 2.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of Pharmacotherapy (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- atypical antipsychotics, schizophrenia, pharmacology, pharmacokinetics, efficacy, adverse effects, clozapine, risperidone, olanzapine, sertindole, quetiapine, ziprasidone, typical antipsychotics, extrapyramidal symptoms, drug selection
- MeSH terms
- Clinical Trials as Topic, Humans, Receptors, Serotonin, Schizophrenia, Antipsychotic Agents, MEDLINE, Receptors, Dopamine D2
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