A review on side effect management of second-generation antipsychotics to treat schizophrenia: a drug safety perspective
Publication date
2024-06
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Document Type
Article
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taverne
Abstract
INTRODUCTION: Effective side effects management present a challenge in antipsychotic treatment with second-generation antipsychotics (SGAs). In recent years, most of the commonly used SGAs, except for clozapine, have been shown to differ only slightly in their effectiveness, but considerably regarding perceived side effects, safety profiles, and compatibility to preexisting medical conditions. AREAS COVERED: The current state of available evidence on side-effect management in SGA treatment of patients with schizophrenia spectrum disorders (SSD) is reviewed. In addition, current guideline recommendations are summarized, highlighting evidence gaps. EXPERT OPINION: SGA safety and side effects needs to be considered in treatment planning. Shared decision-making assistants (SDMA) can support patients, practitioners and relatives to orient their decisions toward avoiding side effects relevant to patients' adherence. Alongside general measures like psychosocial and psychotherapeutic care, switching to better tolerated SGAs can be considered a relatively safe strategy. By contrast, novel meta-analytical evidence emphasizes that dose reduction of SGAs can statistically increase the risk of relapse and other unfavorable outcomes. Further, depending on the type and severity of SGA-related side effects, specific treatments can be used to alleviate induced side effects (e.g. add-on metformin to reduce weight-gain). Finally, discontinuation should be reserved for acute emergencies.
Keywords
Safety aspects, schizophrenia, second-generation antipsychotics (SGA), shared decision making assistants (SDMA), side effect management, Taverne, Pharmacology (medical), Journal Article, Review
Citation
Strube, W, Wagner, E, Luykx, J J & Hasan, A 2024, 'A review on side effect management of second-generation antipsychotics to treat schizophrenia : a drug safety perspective', Expert Opinion on Drug Safety, vol. 23, no. 6, pp. 715-729. https://doi.org/10.1080/14740338.2024.2348561