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急性发作的氯氮平所致高血糖症:一例报告。

Acute onset clozapine-induced hyperglycaemia: A case report.

作者信息

Kumar Pradeep, Mishra Dheerendra Kumar, Mishra Nimisha, Ahuja Sunil, Raghuvanshi Gyanendra, Niranjan Vijay

机构信息

Department of Psychiatry, Shyam Shah Medical College Rewa, Rewa, India.

Department of Psychiatry, Mahatma Gandhi Memorial Medical College, Indore, India.

出版信息

Gen Psychiatr. 2019 Apr 11;32(2):e100045. doi: 10.1136/gpsych-2018-100045. eCollection 2019.

DOI:10.1136/gpsych-2018-100045
PMID:31179433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6551436/
Abstract

Clozapine is an atypical antipsychotic which is described to have higher efficacy among all available antipsychotic medications. Clozapine is reserved especially for resistant schizophrenia due to its side effects. Clozapine-induced metabolic syndrome and hyperglycaemia are common long-term side effects and are responsible for increased mortality in patients with schizophrenia. In this case, a patient with resistant schizophrenia was presented with acute-onset hyperglycaemia and delirium with the use of clozapine within a week. Withdrawal of clozapine in the patient led to the improvement in delirium and hyperglycaemia without the use of any hypoglycaemic agent. This case supports the notion that in certain cases clozapine can induce hyperglycemia through possible direct pathophysiological mechanisms within a shorter time frame.

摘要

氯氮平是一种非典型抗精神病药物,在所有可用的抗精神病药物中疗效较高。由于其副作用,氯氮平特别适用于难治性精神分裂症。氯氮平诱发的代谢综合征和高血糖是常见的长期副作用,也是精神分裂症患者死亡率增加的原因。在本病例中,一名难治性精神分裂症患者在使用氯氮平一周内出现急性高血糖和谵妄。该患者停用氯氮平后,谵妄和高血糖症状得到改善,且未使用任何降糖药物。该病例支持了这样一种观点,即在某些情况下,氯氮平可通过可能的直接病理生理机制在较短时间内诱发高血糖。

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本文引用的文献

1
Rapid-onset clozapine-induced loss of glycaemic control: case report.氯氮平快速诱发血糖控制丧失:病例报告
BJPsych Open. 2017 May 11;3(3):138-140. doi: 10.1192/bjpo.bp.117.004481. eCollection 2017 May.
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Treatment-resistant schizophrenia: current insights on the pharmacogenomics of antipsychotics.难治性精神分裂症:抗精神病药物基因组学的当前见解
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Pharmacol Ther. 2010 Sep;127(3):210-51. doi: 10.1016/j.pharmthera.2010.04.008. Epub 2010 May 20.
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Metabolic side effects of antipsychotic drug treatment--pharmacological mechanisms.抗精神病药物治疗的代谢副作用——药理学机制。
Pharmacol Ther. 2010 Jan;125(1):169-79. doi: 10.1016/j.pharmthera.2009.10.010. Epub 2009 Nov 17.
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Results of phase 3 of the CATIE schizophrenia trial.CATIE精神分裂症试验第三阶段的结果。
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Research on adverse drug events. I. Muscarinic M3 receptor binding affinity could predict the risk of antipsychotics to induce type 2 diabetes.药物不良事件的研究。I. 毒蕈碱M3受体结合亲和力可预测抗精神病药物诱发2型糖尿病的风险。
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