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首页> 外文期刊>International endodontic journal >A protocol for developing reporting guidelines for laboratory studies in Endodontology
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A protocol for developing reporting guidelines for laboratory studies in Endodontology

机译:制定脊髓症实验室研究报告指南的议定书

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Abstract Laboratory‐based research studies are the most common form of research endeavour and make up the majority of manuscripts that are submitted for publication in the field of Endodontology. The scientific information derived from laboratory studies can be used to design a wide range of subsequent studies and clinical trials and may have translational potential to benefit clinical practice. Unfortunately, the majority of laboratory‐based articles submitted for publication fail the peer‐review step, because unacceptable flaws or substantial limitations are identified. Even when apparently well‐conducted laboratory‐based articles are peer‐reviewed, they can often require substantial corrections prior to the publication. It is apparent that some authors and reviewers may lack the training and experience to have developed a systematic approach to evaluate the quality of laboratory studies. Occasionally, even accepted manuscripts contain limitations that may compromise interpretation of data. To help authors avoid manuscript rejection and correction pitfalls, and to aid editors/reviewers to evaluate manuscripts systematically, the purpose of this project is to establish and publish quality guidelines for authors to report laboratory studies in the field of Endodontology so that the highest standards are achieved. The new guidelines will be named–‘Preferred Reporting Items for Laboratory studies in Endodontology’ ( PRILE ). A steering committee was assembled by the project leads to develop the guidelines through a five‐phase consensus process. The committee will identify new items as well as review and adapt items from existing guidelines. The items forming the draft guidelines will be reviewed and refined by a PRILE Delphi Group ( PDG ). The items will be evaluated by the PDG on a nine‐point Likert scale for relevance and inclusion. The agreed items will then be discussed by a PRILE face‐to‐face consensus meeting group ( PFCMG ) formed by 20 individuals to further refine the guidelines. This will be subject to final approval by the steering committee. The approved PRILE guidelines will be disseminated through publication in relevant journals, presented at congresses/meetings, and be freely available on a dedicated website. Feedback and comments will be solicited from researchers, editors and peer reviewers, who are invited to contact the steering committee with comments to help them update the guidelines periodically.
机译:摘要基于实验室的研究研究是最常见的研究形式努力,并弥补了在脊髓源性领域出版的大部分手稿。源自实验室研究的科学信息可用于设计各种后续研究和临床试验,并且可能具有促进临床实践的平移潜力。不幸的是,大多数基于实验室的文章为出版物出版而失败了同行评审步骤,因为确定了不可接受的缺陷或实质性限制。即使在对同行评审的基于实验室的物品的明显进行了良好的实验室的物品时,它们通常可以在出版物之前需要大量校正。很明显,一些作者和审查人员可能缺乏制定了系统化的培训和经验来评估实验室研究的质量。偶尔,甚至被接受的稿件包含可能损害数据解释的限制。为了帮助作者避免稿件拒绝和纠正陷阱,并援助编辑/审核人员系统地评估手稿,本项目的目的是建立和公布作者的质量准则,以报告肢体胚源学领域的实验室研究,以便最高标准实现。新的准则将被命名为 - 末端的实验室研究报告项目'(普利)。转向委员会被项目组建,导致通过五阶段共识进程制定指导方针。委员会将确定新项目,以及从现有指南中审查和适应项目。形成准则草案草案的物品将由普利式德尔福集团(PDG)进行审查和修整。这些项目将由PDG评估九点李克特规模以进行相关性和包含。然后,由20个人组成的普利面对面共识会议组(PFCMG)讨论约定的物品,以进一步完善指南。这将受到指导委员会的最终批准。通过在大会/会议上提出的相关期刊上的出版物将通过出版,并在专门的网站上自由提供批准的普利指南。反馈和评论将由研究人员,编辑和同行评审员征求,该审核人员被邀请联系指导委员会的意见,以帮助他们定期更新指导方针。

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