Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2002;16(7):473-84.
doi: 10.2165/00023210-200216070-00004.

Relapse and rehospitalisation rates in patients with schizophrenia: effects of second generation antipsychotics

Affiliations
Review

Relapse and rehospitalisation rates in patients with schizophrenia: effects of second generation antipsychotics

John G Csernansky et al. CNS Drugs. 2002.

Abstract

Recent studies suggest that the risk of relapse in patients with schizophrenia is approximately 3.5% per month. Predictors of more frequent relapses include poor compliance with antipsychotic drug treatment, severe residual psychopathology, poor insight into the illness and the need for treatment, comorbid substance abuse, and poor relationships between patients, families and care providers. Although conventional antipsychotic drugs, such as haloperidol and fluphenazine, are effective in preventing relapse, second generation antipsychotic drugs, such as clozapine, risperidone and olanzapine, appear to be superior in preventing relapse and improving the patient's quality of life. The development of adverse events can undermine treatment response and relapse prevention. Minimising adverse effects thus helps to improve treatment compliance and prevent relapse. Second generation antipsychotic drugs tend to have fewer adverse effects than conventional agents, especially pseudoparkinsonism and akathisia. The societal costs of treating patients with schizophrenia can be lessened by employing strategies that decrease relapse and the need for rehospitalisation, the most costly treatment alternative.

PubMed Disclaimer

References

    1. Eur Arch Psychiatry Clin Neurosci. 1994;244(5):241-6 - PubMed
    1. J Clin Psychiatry. 2001;62 Suppl 23:5-12 - PubMed
    1. Br J Psychiatry. 1999 Jan;174:23-30 - PubMed
    1. Acta Psychiatr Scand. 1992 Apr;85(4):295-305 - PubMed
    1. Drug Saf. 2000 Mar;22(3):195-214 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources