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Peptide receptor radionuclide therapy for patients with somatostatin receptor expressing tumours German Guideline (S1)

机译:肽受体放射性核素治疗生长抑素受体表达肿瘤的患者德国指南(S1)

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This document describes the guideline for peptide receptor radionuclide therapy (PRRT) published by the German Society of Nuclear Medicine (DGN) and accepted by the Association of the Scientific Medical Societies in Germany (AWMF) to be included in the official AWMF Guideline Registry. These recommendations are a prerequisite for the quality management in the treatment of patients with somatostatin receptor expressing tumours using PRRT. They are aimed at guiding nuclear medicine specialists in selecting likely candidates to receive PRRT and to deliver the treatment in a safe and effective manner. The recommendations are based on an interdisciplinary consensus. The document contains background information and definitions and covers the rationale, indications and contraindications for PRRT. Essential topics are the requirements for institutions performing the therapy, e.g. presence of an expert for medical physics, intense cooperation with all colleagues involved in the treatment of a patient, and a certificate of instruction in radiochemical labelling and quality control are required. Furthermore, it is specified which patient data have to be available prior to performance of therapy and how treatment has to be carried out technically. Here, quality control and documentation of labelling are of great importance. After treatment, clinical quality control is mandatory (work-up of therapy data and follow-up of patients). Essential elements of follow-up are specified in detail. The complete treatment inclusive after-care has to be realised in close cooperation with the involved medical disciplines. Generally, the decision for PRRT should be undertaken within the framework of a multi-disciplinary tumour board.
机译:本文档介绍了由德国核医学学会(DGN)发布,并由德国科学医学会协会(AWMF)接受的肽受体放射性核素治疗(PRRT)指南,该指南将被纳入官方AWMF指南注册表。这些建议是使用PRRT治疗生长抑素受体表达肿瘤患者的质量管理的前提。它们旨在指导核医学专家选择可能的候选者接受PRRT并以安全有效的方式进行治疗。这些建议是基于跨学科共识的。该文件包含背景信息和定义,并涵盖了PRRT的基本原理,适应症和禁忌症。基本主题是执行治疗的机构的要求,例如需要医学物理学专家的存在,与所有参与治疗患者的同事的密切合作以及放射化学标记和质量控制的使用证明。此外,规定了在进行治疗之前哪些患者数据必须是可用的以及如何在技术上进行治疗。在这里,标签的质量控制和文件记录非常重要。治疗后,必须进行临床质量控制(治疗数据的检查和患者的随访)。详细规定了后续行动的基本要素。必须与相关医学学科密切合作,以实现包括治疗在内的完整治疗。通常,PRRT的决定应在多学科肿瘤委员会的框架内进行。

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