Description |
1 online resource |
Series |
Stahl's handbooks |
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Stahl's handbooks
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Contents |
Sampling times for oral and long acting injectable agents -- The therapeutic threshold and the point of futility -- Level interpretation including laboratory reporting issues, responding to high plasma issues, responding to high plasma levels, special situations (hepatic dysfunction, renal dysfunction and hemodialysis, bariatric surgery) -- Tracking oral antipsychotic adherence -- What is an adequate antipsychotic trial-using plasma levels to optimize psychiatric response and tolerability -- Important concepts about first generation antipsychotics -- Haloperidol and haloperidol decanoate -- Fluphenazine and fluphenazine decanoate -- Perphenazine and perphenazine decanoate -- Zuclopenthixol and zuclopenthixol decanoate; flupenthixol and flupenthixol decanoate -- Chlorpromazine, loxapine, thiothixene, trifluoperazine -- Important concepts about second generation antipsychotics -- Clozapine -- Risperidone oral and long acting injectable, paliperidone oral and long acting injectable -- Olanzapine and olanzapine pamoate -- Aripiprazole, aripiprazole monohydrate and aripiprazole lauroxil -- Amisulpride, asenapine, lurasidone, brexpiprazole, cariprazine |
Summary |
"The use of antipsychotics to treat schizophrenia is fraught with many layers of complexity, as prescribers try to tailor the pharmacodynamic properties of an agent to a specific patient based primarily on subjective response. Variations in drug metabolism related to genetic polymorphisms, or to medication or environmental exposures (e.g. smoking), and variable adherence with oral medications lead to scenarios that confound even seasoned clinicians. Excluding the realization that up to one-third of schizophrenia patients may not respond adequately to non-clozapine antipsychotics, 60 years of antipsychotic research has demonstrated that dose is a poor correlate of response likelihood, whereas plasma drug levels represent the best clinically available tool that quantifies the relationship between drug exposure and central nervous system (CNS) activity.[1] The classic equation by psychopharmacologist Sheldon Preskorn illustrates the variables involved in clinical drug response (Figure 1.1)"-- Provided by publisher |
Bibliography |
Includes bibliographical references and index |
Notes |
Description based on print version record and CIP data provided by publisher; resource not viewed |
Subject |
Antipsychotic drugs.
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Psychoses -- Chemotherapy.
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Drugs -- Dose-response relationship.
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Antipsychotic Agents -- blood
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Dose-Response Relationship, Drug
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Antipsychotic Agents -- therapeutic use
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Psychotic Disorders -- drug therapy
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Schizophrenia -- drug therapy
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Antipsychotic Agents
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MEDICAL / Mental Health.
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Drugs -- Dose-response relationship
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Antipsychotic drugs
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Psychoses -- Chemotherapy
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Form |
Electronic book
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Author |
Stahl, Stephen M., 1951- author
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LC no. |
2021012649 |
ISBN |
9781009002103 |
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1009002104 |
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