[关于间质性膀胱炎(IC/BPS)诊断和治疗的S2K指南:用一个案例研究讨论当前指南]。

Der Urologe. Ausg. A Pub Date : 2022-03-01 Epub Date: 2022-01-17 DOI:10.1007/s00120-021-01753-9
J Tolle, B T Kaftan, Th Bschleipfer
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引用次数: 2

摘要

IC/BPS是一种慢性进行性疾病,通常对患者和治疗治疗师来说是困难和不满意的。因此,治疗应该是全面的、跨学科的、多模式的,并考虑到生物心理社会模型。该指南通过多种诊断和治疗方案形成了一条线索,并提供了关于这种罕见疾病的定义、流行病学和病原发生的广泛背景信息。然而,实践和理论/指南是不同的。因此,适应个别情况是必要的,也是明确需要的。因此,该指南应作为同事编制适合其实践的自己的标准的思想来源。一方面,在日常临床实践中经过尝试和测试的治疗方法被传递。另一方面,经常缺乏证据也应该被批判性地看待。进一步的研究,如果可能的话,多中心,专门为IC/BPS的不同方面设计,将是可取的。私人诊所和特殊中心的治疗师之间的密切联系对于IC/BPS患者的最佳治疗至关重要。该指南旨在表明在实践和门诊诊所可以做的事情的局限性,并为患者何时应转介到“间质性膀胱炎和盆腔疼痛中心”提供指导。总的来说,该指南改善了同事中这种罕见疾病的存在。因此,需要对当前的研究状况进行全面的补充、更新和进一步的证实。
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[S2K guideline on the diagnosis and treatment of interstitial cystitis (IC/BPS) : Discussion of the current guideline using a case study].

IC/BPS is a chronic progressive disorder that is often difficult and unsatisfactory for the person affected and the treating therapist. Treatment should therefore be comprehensive, interdisciplinary, multimodal and take into account the biopsychosocial model. The guideline forms a thread through the diverse diagnostic and therapeutic options and provides extensive background information on the definition, epidemiology and aetiopathogenesis of this rare disease. However, practice and theory/guideline are different. Adaptation to the individual case is therefore necessary and explicitly desired. The guideline should therefore serve as a source of ideas for colleagues to compile their own standards suitable for their practice. On the one hand, therapy approaches that have been tried and tested in everyday clinical practice are passed on. On the other hand, the frequent lack of evidence should also be viewed critically. Further studies, if possible multi-centre, specifically designed for different aspects of IC/BPS would be desirable. Close networking between therapists in private practice and special centres is essential for the best possible treatment of people with IC/BPS. The guideline is intended to show the limits of what can be done in practices and outpatient clinics and to provide guidance on when patients should be referred to a "Centre for Interstitial Cystitis and Pelvic Pain". Overall, the guideline has improved the presence of this rare disease among colleagues. A comprehensive supplement, update and further substantiation with the state of current research is thus desirable.

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