Clozapine-Induced Hypersalivation: A Review of Treatment Strategies

  • Sanjeev Sockalingam
    Resident, Department of Psychiatry, University of Toronto, Toronto, Ontario; Resident, Centre for Addiction and Mental Health, Toronto, Ontario
  • Chekkera Shammi
    Chief, Early Psychosis Unit, Schizophrenia Program, Centre for Addiction and Mental Health, Toronto, Ontario; Assistant Professor, Department of Psychiatry, University of Toronto, Toronto, Ontario
  • Gary Remington
    Director, Medication Assessment Program for Schizophrenia (MAPS) Clinic, Schizophrenia Program, Centre for Addiction and Mental Health; Professor of Psychiatry, Faculty of Medicine, University of Toronto, Toronto, Ontario

書誌事項

公開日
2007-06
権利情報
  • https://journals.sagepub.com/page/policies/text-and-data-mining-license
DOI
  • 10.1177/070674370705200607
公開者
SAGE Publications

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説明

<jats:sec><jats:title>Objective:</jats:title><jats:p> Clozapine-induced hypersalivation (CIH) is a significant side effect affecting about one-third of patients treated with clozapine. CIH can be stigmatizing, can affect quality of life, and can result in discontinuation of clozapine treatment. The purpose of this review is to provide an understanding of CIH, specifically, its pathophysiology, measurement, and the evidence for CIH treatment alternatives. </jats:p></jats:sec><jats:sec><jats:title>Methods:</jats:title><jats:p> We searched MEDLINE from 1980 to June 2006 for all reported pharmacologic treatment studies related to CIH. We identified additional references by a manual search of the bibliographies of retrieved articles. </jats:p></jats:sec><jats:sec><jats:title>Results:</jats:title><jats:p> Several studies reported improvement of CIH with both selective and nonselective anticholinergic medications. However, with the exception of local anticholinergic agents such as ipratropium bromide and atropine eye drops, potential systemic adverse effects limit the effectiveness of this class of medications. Open-label studies of clonidine, an alpha<jats:sub>2</jats:sub> antagonist, suggest that it may be beneficial in managing CIH. Other pharmacologic treatments, such as amisulpride and botulinum toxin, may be useful in refractory CIH cases. </jats:p></jats:sec><jats:sec><jats:title>Conclusion:</jats:title><jats:p> Although few randomized controlled trials were found in the literature, this review highlights potential treatment alternatives for this common and disabling cause of hypersalivation. Prompt and effective treatment of CIH may assist with treatment tolerability, adherence, and outcomes in patients with treatment-refractory schizophrenia. </jats:p></jats:sec>

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