健康期刊为作者提供了哪些简明扼要的写作指导?范围审查。

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Karen M Gainey, Jenna Smith, Kirsten J McCaffery, Sharon Clifford, Danielle M Muscat
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引用次数: 5

摘要

背景:简单的语言摘要(pls)是为非专业观众设计的,目的是使公众能够访问和理解卫生研究。这一点很重要,因为大多数研究都是用行话写成的,阅读水平也很高。然而,在编写公共服务清单的说明中存在着高度的可变性,这可能会妨碍它们作为向公众传播卫生研究的工具的作用。目的:本范围综述的目的是对主要生物医学和卫生期刊提供的pls作者说明进行详细分析。方法:我们筛选了534种卫生期刊,涵盖11个类别,从InCites期刊引文报告中选择了与十大非传染性疾病相关的期刊。我们纳入了推荐纳入PLS(由国家卫生研究所定义)的英文期刊,并向作者提供了如何撰写PLS的文本指导。两个独立的审稿人提取与作者说明中确定的公共元素相关的数据,例如字数/PLS长度、内容、结构、目的、支持简单语言的措辞,以及术语、首字母缩略词和缩写的使用。记录了PLS的其他方面,如使用的标签(例如,简单的语言摘要,外行摘要和患者摘要),期刊出版商,消费者参与以及PLS是可选的还是强制性的。我们记录了每个元素的频率和具体指令的定性细节。结果:尽管我们回顾了10个非传染性疾病领域和11个期刊类别的534种期刊,但我们发现只有27种(5.1%)期刊包含基于文本的PLS说明,在这27种期刊中,大多数(70%)不需要PLS说明,大约70%的期刊有PLS说明,包括关于术语、缩写和首字母缩略词的使用建议。只有一份期刊建议使用可读性工具,但五份期刊指出应考虑读者的阅读水平或PLS的可读性。不同期刊的作者说明差异很大。在字数/PLS长度(例如,在100到850个单词之间)、结构(例如,段落或要点)以及说明书中其他元素的不同细节级别方面存在不一致。虽然只有一家期刊建议消费者参与pls的开发,但许多被推荐的作者在提交之前会咨询那些不是该领域专家的人来审查他们的摘要。结论:制定统一的作者说明书可提高pls的有效性和应用。应与消费者一起制定此类说明,以确保它们满足非专业受众的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

What Author Instructions Do Health Journals Provide for Writing Plain Language Summaries? A Scoping Review.

What Author Instructions Do Health Journals Provide for Writing Plain Language Summaries? A Scoping Review.

Background: Plain language summaries (PLSs) are intended for a non-expert audience in order to make health research accessible and understandable to the public. This is important because most research is written with jargon and at a high reading level. However, there is a high degree of variability in the instructions for writing PLSs, which may impede their usefulness as a tool for communicating health research to the public.

Objective: The aim of this scoping review was to conduct a detailed analysis of the author instructions for PLSs provided by leading biomedical and health journals.

Method: We screened 534 health journals covering 11 categories selected from the InCites Journal Citation Reports linked to the top 10 non-communicable diseases. We included journals published in English that recommended the inclusion of a PLS (as defined by the National Institute for Health Research) and provided authors with text-based instructions on how it should be written. Two independent reviewers extracted data pertaining to common elements identified in author instructions, such as word count/PLS length, content, structure, purpose, wording to support plain language, and the use of jargon, acronyms and abbreviations. Other aspects of PLSs were recorded, such as the label used (e.g., plain language summary, lay summary, and patient summary), journal publisher, consumer involvement and whether the PLS is optional or mandatory. We recorded the frequency of each element and qualitative details of specific instructions. A consumer representative provided ongoing and iterative feedback on the methods, results, and reporting of this study RESULTS: Despite reviewing 534 journals across 10 non-communicable disease areas and 11 journal categories, we found only 27 (5.1%) contained text-based instructions for PLS. Of the 27 journals included in this review, most (70%) did not require a PLS. Approximately 70% of journals with PLS instructions included advice about the use of jargon, abbreviations, and acronyms. Only one journal recommended the use of a readability tool, however five noted that the reading level of the audience or readability of the PLS should be considered. Author instructions were highly heterogeneous between journals. There was inconsistency regarding the word count/PLS length (e.g., between 100 and 850 words), structure (e.g., paragraphs or bullet points), and varying levels of detail for other elements in the instructions. Although only one journal recommended consumer involvement in the development of PLSs, many recommended authors consult those who are not an expert in their field to review their summary prior to submission.

Conclusion: The development of consistent author instructions could enhance the effectiveness and use of PLSs. Such instructions should be developed with consumers to ensure they met the needs of a lay non-expert audience.

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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
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