François Hervé, Patrik Aronsson, D Carolina Ochoa, Gommert Van Koeveringe, Giovanni Mosiello, Marcio Augusto Averbeck, George Bou Kheir, Michel Wyndaele, Paul Abrams
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This initiative involved a thorough review of existing literature, expert presentations, and consensus-driven discussions. The methodology ensured a comprehensive exploration of KIU from both clinical and pre-clinical perspectives, leading to actionable research recommendations.</p><p><strong>Results: </strong>Understanding the mechanisms of KIU is crucial for developing effective treatment options targeting specific pathophysiological pathways. Key findings include bladder fibrosis driven by transforming growth factor-β1 (TGF-β1), elevated purinergic responses and upregulated P2X1 purinoceptor expression, decreased barrier function due to increased expression of antiproliferative factor (APF), and functional loss of the bladder through Cav1.2 channel blockade. Research indicates that fibrosis, typically considered irreversible, may be mitigated. However, the exact timing and extent of fibrosis initiation and its impact on long-term outcomes require further research. LUTS typically improve after ketamine cessation but relapse upon resumption, indicating a hypersensitivity mechanism involving elevated serum IgE levels. Advanced stages of KIU do not always correlate with LUTS severity, shedding light on potential systemic effects and the need for evaluating liver enzymes. Furthermore, psychological dependency on ketamine, due to its positive perceptive and mood-altering effects, complicates cessation efforts. Long-term management requires a holistic approach, integrating medical treatments and supportive measures to help patients navigate life with potentially irreversible complications.</p><p><strong>Conclusion: </strong>This comprehensive review spans from fundamental pathology to practical clinical management, addressing both urological and systemic complications, and bridging insights from animal models to human applications. 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引用次数: 0
摘要
简介:氯胺酮是一种用途广泛的麻醉剂,越来越多的人在娱乐中使用氯胺酮,这导致了严重的健康问题,包括氯胺酮诱发的尿病(KIU)。KIU 表现为下尿路症状(LUTS),也可累及上尿路。本研究旨在全面概述 KIU,探讨其病理生理学、诊断策略和治疗方案,并确定/识别未来的研究重点:方法:在 2024 年于布里斯托尔召开的尿失禁研究学会(ICI-RS)国际磋商会议期间,召集了一个专门的提案(P)来探讨 KIU。该倡议包括对现有文献、专家发言和共识驱动型讨论的全面回顾。该方法确保了从临床和临床前角度对 KIU 进行全面探讨,从而提出可操作的研究建议:结果:了解 KIU 的发病机制对于开发针对特定病理生理途径的有效治疗方案至关重要。主要发现包括转化生长因子-β1(TGF-β1)驱动的膀胱纤维化、嘌呤能反应升高和 P2X1 嘌呤受体表达上调、抗增殖因子(APF)表达增加导致的屏障功能下降,以及通过 Cav1.2 通道阻断导致的膀胱功能丧失。研究表明,通常被认为不可逆转的纤维化可能会得到缓解。然而,纤维化开始的确切时间和程度及其对长期疗效的影响还需要进一步研究。氯胺酮停用后,尿路症状通常会有所改善,但复用后又会复发,这表明存在血清 IgE 水平升高的超敏机制。KIU 的晚期并不总是与 LUTS 的严重程度相关,这说明了潜在的全身影响以及评估肝酶的必要性。此外,由于氯胺酮具有积极的感知和情绪改变作用,对氯胺酮的心理依赖也使戒毒工作变得更加复杂。长期管理需要采取综合方法,将医学治疗和支持性措施结合起来,帮助患者在可能出现不可逆并发症的情况下渡过难关:本综述从基础病理学到实际临床管理,涉及泌尿系统和全身并发症,并将动物模型的见解与人体应用相结合。要制定有效的治疗策略,就必须从生理和心理两方面解决氯胺酮依赖问题。
Can We Better Understand, Diagnose, and Treat Ketamine-Induced Uropathy, and Can It Be Reversed? ICI-RS 2024.
Introduction: Ketamine, a versatile anesthetic, has seen increased recreational use, leading to significant health issues, including ketamine-induced uropathy (KIU). KIU manifests with lower urinary tract symptoms (LUTS) and can involve the upper urinary tract. This study aims to provide a comprehensive overview of KIU, addressing its pathophysiology, diagnostic strategies, and treatment options; and to define/identify future research priorities.
Methods: During the 2024 meeting of the International Consultation on Incontinence Research Society (ICI-RS) in Bristol, a dedicated Proposal (P) convened to explore KIU. This initiative involved a thorough review of existing literature, expert presentations, and consensus-driven discussions. The methodology ensured a comprehensive exploration of KIU from both clinical and pre-clinical perspectives, leading to actionable research recommendations.
Results: Understanding the mechanisms of KIU is crucial for developing effective treatment options targeting specific pathophysiological pathways. Key findings include bladder fibrosis driven by transforming growth factor-β1 (TGF-β1), elevated purinergic responses and upregulated P2X1 purinoceptor expression, decreased barrier function due to increased expression of antiproliferative factor (APF), and functional loss of the bladder through Cav1.2 channel blockade. Research indicates that fibrosis, typically considered irreversible, may be mitigated. However, the exact timing and extent of fibrosis initiation and its impact on long-term outcomes require further research. LUTS typically improve after ketamine cessation but relapse upon resumption, indicating a hypersensitivity mechanism involving elevated serum IgE levels. Advanced stages of KIU do not always correlate with LUTS severity, shedding light on potential systemic effects and the need for evaluating liver enzymes. Furthermore, psychological dependency on ketamine, due to its positive perceptive and mood-altering effects, complicates cessation efforts. Long-term management requires a holistic approach, integrating medical treatments and supportive measures to help patients navigate life with potentially irreversible complications.
Conclusion: This comprehensive review spans from fundamental pathology to practical clinical management, addressing both urological and systemic complications, and bridging insights from animal models to human applications. Developing effective treatment strategies necessitates addressing both the physical and psychological aspects of ketamine dependency.
期刊介绍:
Neurourology and Urodynamics welcomes original scientific contributions from all parts of the world on topics related to urinary tract function, urinary and fecal continence and pelvic floor function.