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首页> 外文期刊>Cureus. >Olanzapine-Associated Rhabdomyolysis: A Case Report
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Olanzapine-Associated Rhabdomyolysis: A Case Report

机译:奥拉齐滨相关的横纹肌溶解:案例报告

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摘要

This paper presents the case of a 20-year-old patient with a suspected diagnosis of paranoid schizophrenia. He was prescribed oral olanzapine at a dose of 10 mg per day, and the treatment was associated with rhabdomyolysis (serum creatine kinase = 9,725 U/L on day four of the therapy). On suspicion of its contribution to rhabdomyolysis, olanzapine was immediately withdrawn. Pharmacogenetic testing demonstrated that the patient’s CYP2D6 genotype was *4/*4 (1846GA, rs3892097). Based on these results, the patient was switched to trifluoperazine, a medication that is not metabolized by the CYP2D6 isoenzyme. Subsequently, the patient recovered well and was discharged without any nephrological sequelae. The presented case demonstrates that pharmacogenetic‐guided personalization of treatment may allow selecting the best medication and determining the right dosage, resulting in the reduced risk of adverse drug reactions and pharmacoresistance.
机译:本文呈现了一个20岁患者的患者,涉嫌诊断偏执精神分裂症。 他每天服用10毫克的剂量的口服奥腊扎丁,治疗与横纹肌分解(血清肌酸激酶= 9,725 u / l治疗)。 涉嫌对横纹肌溶解的贡献,立即撤回奥氮滨。 药物发生测试表明,患者的CYP2D6基因型为* 4 / * 4(1846g& A,RS3892097)。 基于这些结果,患者切换到三氟吡嗪,一种未被CYP2D6同工酶代谢的药物。 随后,患者恢复良好并在没有任何肾病后遗症的情况下排出。 所提出的病例证明了治疗的药物发生引导的个性化可以允许选择最佳的药物和确定右剂量,导致不良药物反应和药物阻能度的风险降低。

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