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艾司氯胺酮与氯胺酮在肾脏和泌尿系统疾病方面的用药安全性比较:药物警戒视角

Comparative safety of prescribed Esketamine and ketamine in relation to renal and urinary disorders: A pharmacovigilance perspective.

作者信息

Chiappini S, Guirguis A, Schifano N, Corkery J M, Semeraro F, Mosca A, D'Andrea G, Duccio Papanti G, Arillotta D, Floresta G, Martinotti G, Schifano F

机构信息

UniCamillus University of Medical Sciences, Via di S. Alessandro 8, Rome, Italy.

Pharmacy, Swansea University Medical School, The Grove, Swansea University, SA2 8PP, Swansea, Wales, UK.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2025 Jan 10;136:111213. doi: 10.1016/j.pnpbp.2024.111213. Epub 2024 Dec 6.

Abstract

Intranasal esketamine, approved with oral antidepressants for adults with treatment-resistant depression (TRD), is the S-enantiomer of ketamine and has higher potency and affinity for N-Methyl-d-Aspartate receptors. Administered intranasally, it offers rapid absorption and onset, essential for severe depressive symptoms or suicidal impulses. Comparative studies on esketamine and ketamine's urological safety profiles show esketamine has lower or comparable risks of renal and urinary disorders. Ketamine, however, has documented cases of nephrotoxicity and severe urological issues in recreational users. The study aims to further evaluate and compare these profiles against other antidepressants and antipsychotics using the Food and Drug Administration (FDA) Adverse Events Reporting System (FAERS) data. ADR cases were reported to the FDA up to May 12, 2024, being drugs listed including esketamine, ketamine, quetiapine, aripiprazole, olanzapine, risperidone, citalopram, escitalopram, paroxetine, fluoxetine, sertraline, duloxetine, venlafaxine, amitriptyline, and clomipramine. Risperidone showed the highest ADRs (107,418) and serious cases (71,515), with significant renal and urinary disorders reported, including acute kidney injury and urinary incontinence. Olanzapine, quetiapine, and aripiprazole also had high serious ADRs. Venlafaxine and fluoxetine were notable among antidepressants for acute kidney injury. Esketamine and ketamine were associated with lower urinary tract symptoms and nephrolithiasis. Disproportionality analysis revealed ketamine had higher odds of renal and urinary disorders compared to other drug classes, while esketamine had lower or comparable odds. The data suggest a relatively favorable tolerability profile for these drugs, especially esketamine. However, the results highlight the necessity for more extensive studies to evaluate long-term safety and optimize treatment protocols.

摘要

鼻内给予艾司氯胺酮,与口服抗抑郁药联合用于治疗难治性抑郁症(TRD)成人患者,它是氯胺酮的S-对映体,对N-甲基-D-天冬氨酸受体具有更高的效力和亲和力。经鼻给药,吸收和起效迅速,这对于严重抑郁症状或自杀冲动至关重要。关于艾司氯胺酮和氯胺酮泌尿系统安全性的比较研究表明,艾司氯胺酮发生肾脏和泌尿系统疾病的风险较低或与之相当。然而,氯胺酮在娱乐性使用者中已有肾毒性和严重泌尿系统问题的记录病例。该研究旨在利用美国食品药品监督管理局(FDA)不良事件报告系统(FAERS)的数据,进一步评估和比较这些药物与其他抗抑郁药和抗精神病药的安全性。截至2024年5月12日向FDA报告的药物不良反应(ADR)病例,涉及的药物包括艾司氯胺酮、氯胺酮、喹硫平、阿立哌唑、奥氮平、利培酮、西酞普兰、艾司西酞普兰、帕罗西汀、氟西汀、舍曲林、度洛西汀、文拉法辛、阿米替林和氯米帕明。利培酮的ADR(107,418例)和严重病例(71,515例)最多,报告了显著的肾脏和泌尿系统疾病,包括急性肾损伤和尿失禁。奥氮平、喹硫平、阿立哌唑的严重ADR也较多。在抗抑郁药中,文拉法辛和氟西汀导致急性肾损伤较为显著。艾司氯胺酮和氯胺酮与下尿路症状和肾结石有关。不成比例分析显示,与其他药物类别相比,氯胺酮发生肾脏和泌尿系统疾病的几率更高,而艾司氯胺酮的几率较低或与之相当。数据表明这些药物,尤其是艾司氯胺酮,具有相对良好的耐受性。然而,结果突出了进行更广泛研究以评估长期安全性和优化治疗方案的必要性。

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