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[2009年的《智利医学杂志》]

[Revista Médica de Chile in the year 2009].

作者信息

Reyes B Humberto, Andresen H Max, Palma H Joaquín

出版信息

Rev Med Chil. 2009 Aug;137(8):1089-94. Epub 2009 Nov 4.

PMID:19915775
Abstract

During the first semester of 2009 Revista Médica de Chile has received an increasing number of manuscripts. Close to 30% were rejected while most other are in the process of being improved by the authors after receiving criticisms by external peer reviewers and the editors. The time lag between acceptance and publication of manuscripts is on an average six months. During 2008, 10% of articles published were submitted by authors from countries other than Chile and most of them were printed in English. Impact factor and other indexes provided by the ISI Web of Knowledge showed a promising improvement in 2008. The International Advisory Committee and the National Editorial Committee were renewed, a new Section on Laboratory Medicine was incorporated and several minor changes were done in design and format, in the title page and the issues' content. The main problems to be faced relate to the increasing cost of editing and printing, with a reduction in commercial advertising historically contributed by the pharmaceutical industry. Another major concern is to stimulate governmental agencies, scientific societies and universities to establish a national independent registry of clinical trials, that should become a mandatory requisite for every manuscript submitted to Chilean medical journals, reporting clinical trials performed in the country; foreign manuscripts should document the satisfaction of an identical requisite in their original source.

摘要

2009年第一学期,《智利医学杂志》收到的稿件数量不断增加。近30%的稿件被拒,而其他大多数稿件在收到外部同行评审员和编辑的批评后,作者正在对其进行修改完善。稿件接受发表之间的平均时间间隔为六个月。2008年,发表的文章中有10%是由智利以外国家的作者提交的,其中大部分文章用英文发表。科学信息研究所(ISI)的《科学引文索引》(Web of Knowledge)提供的影响因子和其他指标显示,2008年有了令人鼓舞的提升。国际咨询委员会和国家编辑委员会进行了换届,新设了检验医学板块,并在设计和格式、标题页及各期内容方面做了一些小改动。面临的主要问题涉及编辑和印刷成本不断增加,以及制药行业以往提供的商业广告减少。另一个主要问题是激励政府机构、科学学会和大学建立一个全国性的独立临床试验注册机构,这应成为提交给智利医学期刊的每篇稿件的一项强制性要求,用以报告在该国进行的临床试验;外国稿件应证明其原始出处满足相同要求。

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