The impact of fluphenazine withdrawal: a mirror-image study.

IF 1.8 Q3 PSYCHIATRY
S Meehan, S Moran, A Rainford, C McDonald, B Hallahan
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Abstract

Background: Fluphenazine decanoate licenced as a long-acting injectable (LAI) first-generation antipsychotic (FGA) was withdrawn from sale in 2018. This study evaluates if its withdrawal resulted in increased relapse rates of psychosis in an Irish patient cohort and examines which prescribed alternative antipsychotic medications were associated with more optimal outcomes.

Methods: Fifteen participants diagnosed with a psychotic disorder were included. A mirror-image study over 24-months' pre-and post-withdrawal of fluphenazine was conducted. Kaplan-Meier survival and proportional hazards analyses were conducted. The impact of alternate antipsychotic agents (LAI flupenthixol compared to other antipsychotic medications) was evaluated. Semi-structured interviews with participants examined subjective opinions regarding the change in their treatment.

Results: Seven participants (46.7%) relapsed in the 24-month period subsequent to fluphenazine discontinuation compared to one individual (6.7%) in the previous identical time-period (p = 0.035). Flupenthixol treatment was associated with reduced relapse rates compared to other antipsychotics (χ2 = 5.402, p = 0.02). Thematic analysis revealed that participants believed that the discontinuation of fluphenazine deleteriously impacted the stability of their mental disorder.

Conclusion: The withdrawal of fluphenazine was associated with increased relapse rate in individuals previously demonstrating stability of their psychotic disorder. While acknowledging the limitation of small sample size, preliminary evidence from this study suggests that treatment with the first-generation antipsychotic (FGA) flupenthixol was associated with a lower risk of relapse compared to SGAs. Reasons for this lower risk of relapse are not fully clear but could be related to dopamine hypersensitivity with this treatment change.

氟奋乃静戒断的影响:镜像研究。
背景:作为长效注射剂(LAI)第一代抗精神病药物(FGA)获得许可的癸酸氟奋乃静于2018年停售。本研究评估了停售是否会导致爱尔兰患者队列中的精神病复发率上升,并研究了哪些处方替代抗精神病药物与更理想的治疗效果相关:方法:纳入15名被诊断患有精神病性障碍的参与者。方法:纳入了 15 名被诊断为精神病性障碍的患者,对他们停用氟奋乃静前后 24 个月的情况进行了镜像研究。进行了卡普兰-梅耶生存分析和比例危险度分析。评估了替代抗精神病药物(LAI氟奋乃静与其他抗精神病药物相比)的影响。对参与者进行的半结构式访谈考察了他们对治疗改变的主观看法:结果:在氟奋乃静停药后的 24 个月内,有 7 名参与者(46.7%)复发,而在之前的相同时间段内,只有一人(6.7%)复发(p = 0.035)。与其他抗精神病药物相比,氟苯尼考治疗可降低复发率(χ2 = 5.402,p = 0.02)。主题分析显示,参与者认为停用氟奋乃静会对其精神障碍的稳定性产生有害影响:结论:停用氟奋乃静会增加之前精神障碍表现稳定的患者的复发率。虽然承认样本量较小的局限性,但本研究的初步证据表明,与SGAs相比,使用第一代抗精神病药物(FGA)氟奋乃静治疗的复发风险较低。复发风险降低的原因尚不完全清楚,但可能与改变治疗方法后多巴胺过敏有关。
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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来源期刊
CiteScore
9.10
自引率
3.90%
发文量
51
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