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Alosetron in irritable bowel syndrome: strategies for its use in a common gastrointestinal disorder.

机译:阿罗司琼在肠易激综合症中的应用:在常见胃肠道疾病中的应用策略。

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摘要

Irritable bowel syndrome (IBS) is a common gastrointestinal disorder characterised by recurrent abdominal pain and altered bowel habits in the absence of any discernible structural, biochemical and physiological abnormalities. Although there is no specific biological marker for the diagnosis of this disorder, recently developed symptom-based criteria provide the tools necessary to make a diagnosis. The precise underlying pathophysiology of IBS remains unknown. However, disturbances in the brain-gut axis involving the central nervous system and the enteric nervous system have emerged as an underlying concept for IBS. In this regard, conventional treatment has been recognised as unsatisfactory for many patients with IBS and novel, neuroenteric modulatory compounds have been introduced for use by clinicians. Specifically, compounds interacting with the 5-hydroxytryptamine (5-HT, serotonin) receptors of the 5-HT3 and 5-HT4 subtype have been demonstrated of benefit in some patients for the treatment of IBS.In this leading article, we present the current data on the pharmacology, clinical trials, indications and adverse effects of alosetron, a potent and selective 5-HT3 antagonist. As a result of the recognition of serious adverse effects, the indication for alosetron has been restricted and it is now indicated only for women with severe diarrhoea-predominant IBS who have symptoms for at least 6 months and who have failed to respond to conventional therapy. Prescribing restrictions and the risk-management programme implemented as required by the US FDA is reviewed along with a summary of the studies to be performed after reintroduction of alosetron to monitor safety.
机译:肠易激综合症(IBS)是一种常见的胃肠道疾病,其特征是在没有任何可辨别的结构,生化和生理异常的情况下,反复发作的腹痛和肠道习惯改变。尽管没有用于诊断该疾病的特定生物学标记,但最近开发的基于症状的标准提供了进行诊断所必需的工具。 IBS的确切基础病理生理学仍然未知。但是,涉及中枢神经系统和肠神经系统的脑肠轴紊乱已经成为IBS的基本概念。在这一点上,对于许多患有IBS的患者而言,常规治疗已被认为是不令人满意的,并且已经引入了新颖的神经肠调节化合物供临床医生使用。具体而言,已证明与5-HT3和5-HT4亚型的5-羟色胺(5-HT,5-羟色胺)受体相互作用的化合物在某些患者中对IBS的治疗有益。在这篇领先文章中,我们介绍了当前有效的选择性5-HT3拮抗剂阿洛司琼的药理,临床试验,适应症和不良反应的相关数据。由于认识到严重的不良反应,阿洛司琼的适应症受到了限制,现在仅适用于腹泻为主的IBS严重且症状至少持续六个月且对常规治疗无效的女性。审查了规定限制和根据美国FDA要求实施的风险管理计划,以及重新引入阿洛司琼以监测安全性后将要进行的研究的摘要。

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