Clozapine augmentation with long‐acting antipsychotic injections: A case series and systematic review

氯氮平 医学 利培酮 帕潘立酮棕榈酸酯 观察研究 奥氮平 抗精神病药 精神分裂症(面向对象编程) 帕利哌酮 临床试验 儿科 精神科 内科学
作者
Ebenezer Oloyede,Aikaterini Dima,David Taylor,Henry Cheung,Olubanké Dzahini,Sukhwinder S. Shergill,Eromona Whiskey
出处
期刊:Acta Psychiatrica Scandinavica [Wiley]
卷期号:148 (6): 538-552 被引量:4
标识
DOI:10.1111/acps.13621
摘要

Abstract Background Up to 30% of patients with a diagnosis of treatment‐resistant psychosis remain symptomatic despite an optimal trial with the gold standard treatment, clozapine. Emerging evidence suggests the clinical utility of long‐acting injections (LAI) in such clinical scenarios. In this study, we aimed to describe clozapine augmentation with LAIs in an inner London hospital and explore the literature on the clinical effectiveness of this treatment modality. Methods Patients prescribed clozapine, who were commenced on a LAI between 2007 and 2023 by the United Kingdom's largest mental health trust, were identified from electronic patient records. First, routine clinical data were used to describe the use, effectiveness, and safety of this augmentation strategy. Second, we conducted a literature search up to 1st June 2023 to identify published studies describing clinical outcomes after clozapine augmentation with a LAI. Clinical outcomes were collated and presented in a table, including hospitalisation rates and quantitative clinical assessments using validated scales. Results Of the 1248 patients prescribed clozapine in SLaM, three patients (0.2%) received augmentation with the following LAIs: olanzapine embonate, paliperidone palmitate and pipotiazine palmitate. This treatment strategy was clinically effective and generally well tolerated in all three cases. Twelve published studies between 2010 and 2022 were included in the review. Eight distinct LAIs were reported (4 first and 4 second generation antipsychotics), with risperidone and paliperidone most widely studied. All the identified studies were observational including mirror‐image studies, case series and case reports. Duration of follow up varied from 3 months to 3 years. There was evidence that the use of LAIs with clozapine can significantly reduce clinical symptoms, hospitalisation rates and bed days. No serious adverse effects were reported. Conclusion This preliminary evidence suggests clinical utility of LAIs in alleviating residual symptoms and subsequently reducing hospitalisation rates in patients optimised on clozapine treatment. The current study warrants further investigations including a randomised controlled study to establish the clinical efficacy, tolerability, and place in therapy of this treatment modality.
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