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Tumour necrosis factor inhibitors in the treatment of psoriatic arthritis: a view on effectiveness, clinical practice and toxicity

机译:肿瘤坏死因子抑制剂治疗银屑病关节炎:有效性,临床实践和毒性的看法

摘要

Introduction: Psoriatic arthritis is a common and often severe chronic joint disorder associated with the skin disease psoriasis (PsO). Treatment options for psoriatic arthritis patients have changed considerably over the last decade with the widespread use of biological therapies, in particular tumour necrosis factor inhibitors. Current clinical experience based on large registries and careful observations now allows us to understand the true value of these interventions in daily clinical practice. Areas covered: Literature searches were performed targeting effectiveness, drug survival, toxicity and safety of biological therapies as well as treatment strategies specifically focused on patients with psoriatic arthritis. Expert opinion: Tumour necrosis factor inhibition is a powerful and effective option for the treatment of severe psoriatic arthritis. The different available drugs have good survival rates and show an excellent balance between effectiveness and toxicity. Switching of inhibitor is feasible, but treatment changes should be carefully considered. Novel biological therapies are introduced into the market and will further provide better perspectives for the patient. New questions are also emerging: How to handle long-term remission, can biological therapies be successfully stopped and are co-morbidities sufficiently managed? These questions should be addressed for optimal long-term management of a severe chronic disease.
机译:简介:银屑病关节炎是一种常见的且经常是严重的慢性关节疾病,与皮肤病牛皮癣(PsO)相关。在过去的十年中,随着生物疗法,尤其是肿瘤坏死因子抑制剂的广泛使用,牛皮癣关节炎患者的治疗选择发生了巨大变化。基于大量注册资料和仔细观察的当前临床经验现在使我们能够了解这些干预措施在日常临床实践中的真正价值。涵盖领域:针对生物疗法的有效性,药物存活率,毒性和安全性以及针对银屑病关节炎患者的治疗策略进行了文献检索。专家意见:抑制肿瘤坏死因子是治疗严重牛皮癣关节炎的有效方法。不同的可用药物具有良好的存活率,并且在有效性和毒性之间显示出极好的平衡。更换抑制剂是可行的,但应仔细考虑治疗的改变。新型生物疗法被引入市场,并将进一步为患者提供更好的前景。还出现了新的问题:如何处理长期缓解,能否成功停止生物疗法并充分控制合并症?这些问题应予以解决,以对严重的慢性疾病进行最佳的长期治疗。

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    Lories Rik; De Vlam Kurt;

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  • 年度 2014
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  • 正文语种 en
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