Clozapine use in the first two years after first-episode psychosis in a real-world clinical sample.

0 PSYCHIATRY
Emilio Pechuán, Alba Toll, Daniel Bergé, Teresa Legido, Laura Martínez-Sadurní, Amira Trabsa, Gonzalo De Iturbe, Sara García Fernández, Beltran Jiménez-Fernández, Aurea Fernández, Víctor Pérez-Solà, Anna Mané
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引用次数: 0

Abstract

Background: Approximately 20-30% of patients with schizophrenia fail to respond to antipsychotic treatment and are considered treatment resistant (TR). Although clozapine is the treatment of choice in these patients, in real-world clinical settings, clinicians often delay clozapine initiation, especially in first-episode psychosis (FEP).

Aim: The main aim of this study was to describe prescription patterns for clozapine in a sample of patients diagnosed with FEP and receiving specialized treatment at a university hospital. More specifically, we aimed to determine the following: (1) the proportion of patients who received clozapine within two years of disease onset, (2) baseline predictors of clozapine use, (3) time from starting the first antipsychotic to clozapine initiation, (4) concomitant medications, and (5) clozapine-related adverse effects.

Methods: All patients admitted to a specialized FEP treatment unit at our hospital between April 2013 and July 2020 were included and followed for two years. The following variables were assessed: baseline sociodemographic characteristics; medications prescribed during follow-up; clozapine-related adverse effects; and baseline predictors of clozapine use. We classified the sample into three groups: clozapine users, clozapine-eligible, and non-treatment resistant (TR).

Results: A total of 255 patients were consecutively included. Of these, 20 (7.8%) received clozapine, 57 (22.4%) were clozapine-eligible, and 178 (69.8%) were non-TR. The only significant variable associated with clozapine use at baseline was the Global Assessment of Functioning (GAF) score (R2=0.09, B=-0.07; OR=0.94; 95% CI: 0.88-0.99; p=0.019). The median time to clozapine initiation was 55.0 (93.3) days. The most common side effect was sedation.

Conclusions: A significant proportion (30.2%) of patients in this cohort were treatment resistant and eligible for clozapine. However, only 7.8% of the sample received clozapine, indicating that this medication was underprescribed. A lower baseline GAF score was associated with clozapine use within two years, suggesting that it could be used to facilitate the early identification of patients who will need treatment with clozapine, which could in turn improve treatment outcomes.

在真实世界的临床样本中,首次发作精神病后两年内氯氮平的使用情况。
背景:约有20%-30%的精神分裂症患者对抗精神病药物治疗无效,被视为治疗耐药(TR)。尽管氯氮平是这些患者的首选治疗药物,但在现实的临床环境中,临床医生往往会推迟氯氮平的用药时间,尤其是在首发精神病(FEP)患者中。目的:本研究的主要目的是描述被诊断为FEP并在一家大学医院接受专门治疗的样本患者的氯氮平处方模式。更具体地说,我们旨在确定以下几点:1)发病两年内接受氯氮平治疗的患者比例;2)使用氯氮平的基线预测因素;3)从开始使用第一种抗精神病药物到开始使用氯氮平的时间;4)伴随药物;5)与氯氮平相关的不良反应:纳入2013年4月至2020年7月期间入住我院FEP专科治疗病房的所有患者,并进行为期两年的随访。我们对以下变量进行了评估:基线社会人口学特征;随访期间的处方药物;氯氮平相关不良反应;使用氯氮平的基线预测因素。我们将样本分为三组:氯氮平使用者、氯氮平合格者和非治疗耐药者(TR):结果:共连续纳入 255 名患者。其中,20 人(7.8%)接受了氯氮平治疗,57 人(22.4%)符合氯氮平治疗条件,178 人(69.8%)为非耐药患者。与基线使用氯氮平相关的唯一重要变量是功能全面评估(GAF)得分(R2 =0.09,B = - 0.07;OR = 0.94;95% CI:0.88 至 0.99;P=0.019)。开始使用氯氮平的中位时间为 55.0 (93.3) 天。最常见的副作用是镇静:该队列中有相当一部分(30.2%)患者对治疗产生耐药性,符合使用氯氮平的条件。然而,只有7.8%的样本接受了氯氮平治疗,这表明该药物的处方量不足。较低的基线GAF评分与两年内氯氮平的使用有关,这表明GAF可用于帮助早期识别需要氯氮平治疗的患者,从而改善治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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