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首页> 外文期刊>International endodontic journal >Preferred Reporting Items for Animal Studies in Endodontology: a development protocol
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Preferred Reporting Items for Animal Studies in Endodontology: a development protocol

机译:末痛动物研究的首选报告项目:发展方案

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Abstract The regulated use of animals in endodontic research is often necessary to investigate the biological mechanisms of endodontic diseases and to measure the preclinical efficacy, biocompatibility, toxicology and safety of new treatments, biomaterials, sealers, drugs, disinfectants, irrigants, devices and instruments. Animal testing is most crucial in situations when research on humans is not ethical, practical or has unknown health risks. Currently, there is a wide variability in the quality of manuscripts that report the results of animal studies. Towards the goal of improving the quality of publications, guidelines for preventing disability, pain, and suffering to animals, and enhanced reporting requirements for animal research have been developed. These guidelines are referred to as Animals in Research: Reporting In Vivo Experiments ( ARRIVE ). Henceforth, causing any form of animal suffering for research purposes is not acceptable and cannot be justified under any circumstances. The present report describes a protocol for the development of welfare and reporting guidelines for animal studies conducted in the specialty of Endodontology: the Preferred Reporting Items for Animal Studies in Endodontology ( PRIASE ) guidelines. The PRIASE guidelines will be developed by adapting and modifying the ARRIVE guidelines and the Clinical and Laboratory Images in Publication ( CLIP ) principles. The development of the new PRIASE guidelines will include a five‐step consensus process. An initial draft of the PRIASE guidelines will be developed by a steering committee. Each item in the draft guidelines will then be evaluated by members of a PRIASE Delphi Group ( PDG ) for its clarity using a dichotomous scale (yes or no) and suitability for its inclusion using a 9‐point Likert scale. The online surveys will continue until each item achieves this standard, and a set of items are agreed for further analysis by a PRIASE Face‐to‐face Consensus Meeting Group ( PFCMG ). Following the consensus meeting, the steering committee will finalize and confirm the PRIASE guidelines taking into account the responses and comments of the PFCMG . The PRIASE guidelines will be published and disseminated internationally and updated periodically based on feedback from stakeholders.
机译:摘要探讨了牙髓性疾病的生物机制,并测量新治疗,生物材料,封口剂,药物,消毒剂,灌溉剂,器件和仪器的生物学机制,往往是必要的牙​​髓性研究中的受管制使用。当人类的研究不是道德的,实用或有未知的健康风险时,动物测试是最重要的。目前,报告动物研究结果的手稿质量方面存在广泛的变化。为了提高出版物质量的目标,已经制定了预防残疾,疼痛和患动物的准则,并提高了动物研究的报告要求。这些准则被称为研究中的动物:在体内实验中报告(到达)。此后,造成任何形式的研究目的的动物是不可接受的,并且在任何情况下都无法理解。本报告介绍了开发末端专业中进行的动物研究福利和报告准则的议定书:脊髓症(PRIASE)指导方针的首选报告项目。通过在出版物(CLIP)原则中调整和修改到达和修改到达指南和临床和实验室图像,将开发前方指南。新的前瞻指南的发展将包括五步共识过程。指导委员会将制定前瞻性指南的初步草案。然后,指南草案中的每个项目都将由查看德尔福集团(PDG)的成员来评估使用二分量表(是或否),并使用9点李克特规模纳入其含量的清晰度。在线调查将继续,直到每个物品实现本标准,并一定的物品达成一组项目,以便通过前方面对面共识会议组(PFCMG)进一步分析。在协商一致会议之后,指导委员会将终止并确认提出的指导方针,同时考虑到PFCMG的答复和评论。预指导方针将在国际上发布和传播,并根据利益攸关方的反馈定期更新。

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