[抗精神病和抗胆碱能治疗对精神分裂症患者认知功能的影响]。

Q3 Medicine
M A Tumova, A A Stepanova, Y S Zazulina, Z T Guseinova, M M Zaitseva, I V Dyment, A P Kotsyubinsky, M V Ivanov
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引用次数: 0

摘要

目的:探讨抗精神病药物和抗胆碱能药物与精神分裂症患者认知功能的关系。材料和方法:观察性前瞻性研究在别赫捷列夫国家精神病学和神经病学医学中心进行。本研究纳入41例偏执型精神分裂症患者(男22例,女19例),符合ICD 10标准,年龄30.12±8.24岁,采用稳定的抗精神病单药治疗或联合抗胆碱能药物(三己苯肼)治疗。认知功能采用《精神分裂症患者认知功能简要评估》(BACS)量表进行评估,精神状态和锥体外系障碍的严重程度采用《阳性和阴性综合征量表》(PANSS)和《辛普森-安格斯锥体外系副作用评估量表》(SAS)进行测量。所有检查程序在治疗第2周和第8周进行两次。根据抗精神病药物治疗类型将患者分为两组。12例患者接受第一代抗精神病药(FGAs)治疗(1组),29例患者接受第二代抗精神病药(SGAs)治疗(2组)。结果:与第2周的数据相比,接受SGAs治疗的患者在治疗第8周的SAS总分显著下降,认知功能有所改善,与接受FGAs治疗的患者不同。仅在2组患者的BACS测试中,数字排序(V=51.5, p=0.007)、标记运动任务(V=75.5, p=0.007)和伦敦塔(V=52, p=0.027)也有变化。结论:服用SGAs的患者在第8周时对药物的耐受性和认知功能均有所改善。我们的研究证实了在精神分裂症治疗中坚持最低有效剂量的抗精神病药物对预防认知障碍的重要性,并在治疗选择中优先考虑SGAs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[An effect of antipsychotic and anticholinergic treatment on cognitive function in patients with schizophrenia].

Objective: To reveal the relationships between antipsychotic and anticholinergic drugs and cognitive functions in patients with schizophrenia.

Material and methods: The observational prospective study was conducted at the Bekhterev National Medical Center of Psychiatry and Neurology. The study involved 41 patients (22 men and 19 women) with paranoid schizophrenia, according to ICD 10 criteria, aged 30.12±8.24 years on stable antipsychotic monotherapy or in combination with anticholinergic drug (trihexiphenidyl). Cognitive functions were assessed using the «Brief Assessment of Cognitive Function in Patients with Schizophrenia» (BACS) scale, severity of mental state and extrapyramidal disturbances were measured using the «Positive and Negative Syndrome Scale (PANSS) and the Simpson-Angus Scale for Assessment of Extrapyramidal Side Effects (SAS). All examination procedures were performed twice at weeks 2 and 8 of therapy. Patients were divided into 2 groups according to the type of antipsychotic therapy. Twelve patients received first generation antipsychotics (FGAs) (group 1), 29 patients received second generation antipsychotics (SGAs) (group 2).

Results: Patients receiving SGAs had a significant decrease in the overall SAS score at week 8 of therapy compared with data at week 2, and there was an improvement in cognitive function, unlike patients receiving FGAs. There were also changes on BACS tests the digit sequencing (V=51.5, p=0.007), token motor task (V=75.5, p=0.007) and Tower of London (V=52, p=0.027) only in patients of group 2.

Conclusion: The improved tolerance to the drug, as well as cognitive measures, was shown in patients taking SGAs by week 8. Our study confirms the importance of adhering to the minimum effective dose of antipsychotic drugs for the treatment of schizophrenia to prevent cognitive impairment, and to give preference to SGAs in the choice of treatment.

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Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova Medicine-Psychiatry and Mental Health
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