Potential impact on mental health in patients with treatment-resistant schizophrenia - clozapine augmentation with long-acting parenteral antipsychotics: a case series.

Q3 Pharmacology, Toxicology and Pharmaceutics
Ceska a Slovenska Farmacie Pub Date : 2023-01-01
M Nováková, T Hammer, E Nováková, M Mayerová, L Ustohal, Hana Kotolová
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引用次数: 0

Abstract

Introduction: The rate of pharmacoresistance among in patients diagnosed with schizophrenia is around 30%. Clozapineis the drug of choice for these patients; however, an adequate response to treatment doesn't always occur. One of the possible augmentation approaches, specifically for non-adherent patients, is the administration of long-acting parenteral antipsychotics. Our goal was to evaluate previous experiences of administering a combination of the atypical antipsychotic clozapine and long-acting injectable antipsychotics to pharmacoresistant patients at the Department of Psychiatry the Czech Republic and to assess the safety and effectiveness of such administration.

Methods: A retrospective evaluation of patient case studies was conducted for those who were hospitalized in the Ward for the therapy of Psychotic disorders between 2016 and 2020 and had a medication history of combining clozapine and depot antipsychotics.

Results: Over half of the patients had no illness relapses during the observed period. The clinical manifestation of adverse effects from combination therapy appears low in our patient sample, primarily involving mild and pharmacologically manageable side effects (tachycardia). Only one of the cases recorded neutropenia, which led to discontinuation of clozapine; the patient was maintained on long-acting injectable antipsychotics medication.

Conclusion: From our findings, it can be inferred that augmenting clozapine with depot antipsychotics is a potential therapeutic intervention that pharmacoresistant patients could benefit from. However, it is essential to emphasize that this therapeutic approach should only be administered after carefully considering the patient's existing treatment. It should be strictly individualized based on the treating physician's or clinical pharmacist's sufficient professional experience.

用长效肠外抗精神病药增服氯氮平对耐药精神分裂症患者心理健康的潜在影响:病例系列。
简介被诊断为精神分裂症的患者中,耐药率约为 30%。氯氮平是这些患者的首选药物,但并不总是能对治疗产生足够的反应。特别是对于非依从性患者,一种可能的增效方法是使用长效肠外抗精神病药物。我们的目标是评估捷克共和国精神病学系以往对药理耐药性患者联合使用非典型抗精神病药物氯氮平和长效注射用抗精神病药物的经验,并评估这种用药的安全性和有效性:方法:对2016年至2020年期间在精神障碍治疗病房住院、有氯氮平和去势抗精神病药物联合用药史的患者病例研究进行了回顾性评估:超过一半的患者在观察期内没有复发。在我们的患者样本中,联合治疗的不良反应临床表现似乎较少,主要涉及轻微且药物可控的副作用(心动过速)。只有一个病例出现了中性粒细胞减少症,因此停用了氯氮平;该患者继续服用长效注射抗精神病药物:从我们的研究结果中可以推断,用去势抗精神病药物辅助氯氮平治疗是一种潜在的治疗干预措施,耐药患者可以从中获益。然而,有必要强调的是,只有在仔细考虑了患者的现有治疗方案后,才可采用这种治疗方法。应严格根据主治医生或临床药剂师的充分专业经验进行个体化治疗。
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
Ceska a Slovenska Farmacie
Ceska a Slovenska Farmacie Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.90
自引率
0.00%
发文量
22
期刊介绍: Přehledový článek je zaměřen zejména na metody přípravy, charakterizaci mikročástic a dále na charakteristiku a příklady jejich možného využití ve farmakoterapii. Mikročástice jako...
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