第二代抗精神病药物激活未抗精神病和未抗精神病的精神分裂症患者的血小板:一项回顾性研究

Hyun-Ah Kim, J. W. Lee, S. Kim, H. Oh, W. Im, Ji-Woong Kim
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引用次数: 0

摘要

目的在第二代抗精神病药物引起的脑血管/心血管疾病或血栓栓塞事件的危险因素中,临床医生主要关注代谢副作用,而对血小板活性的影响兴趣较少。由于血小板活性过高会增加脑血管/心血管疾病的风险,本研究的目的是探讨第二代抗精神病药物对精神分裂症患者血小板活性的影响。方法回顾性分析二代抗精神病药物治疗精神分裂症患者的临床资料。通过测定血小板平均成分来评估血小板活化程度。结果Wilcoxon符号秩检验显示,服用第二代抗精神病药物后,平均血小板成分水平显著降低(V = 20;P < 0.05),提示第二代抗精神病药物可能增加血小板活化。结论血小板活化是脑血管/心血管疾病发生的另一个危险因素,本研究结果提示临床医生在服用第二代抗精神病药物后应仔细监测血小板活化程度。
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Second-generation antipsychotics activate platelets in antipsychotic-naive and antipsychotic-free patients with schizophrenia: A retrospective study
Objective Among the risk factors for cerebrovascular/cardiovascular disease or thromboembolic events caused by the administration of second-generation antipsychotics, clinicians have mainly focused on metabolic side effects, with little interest in the effects on platelet activity. Because excessive platelet activity can increase the risk for cerebrovascular/cardiovascular disease, the aim of this study was to investigate the effect of second-generation antipsychotics on platelet activity in patients with schizophrenia. Methods The medical records of patients with schizophrenia who were treated with second-generation antipsychotics were retrospectively reviewed. The degree of platelet activation was assessed by measuring the mean platelet component. Results Wilcoxon signed-rank test revealed that mean platelet component levels were significantly decreased by the administration of second-generation antipsychotics (V = 20; p < 0.05), suggesting that the administration of second-generation antipsychotics may increase platelet activation. Conclusion Because platelet activation is an additional risk factor for the occurrence of cerebrovascular/cardiovascular disease, results of this study suggest that clinicians should carefully monitor the degree of platelet activation after the administration of second-generation antipsychotics.
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