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先天性胆道闭锁:全球研究架构和科学发展的科学计量分析。

Biliary atresia: a scientometric analysis of the global research architecture and scientific developments.

机构信息

Department of Pediatric Surgery, King's College Hospital, Denmark Hill, London SE5 9RS, UK.

Department of Pediatric Surgery, The Royal London Hospital, London, UK.

出版信息

J Hepatobiliary Pancreat Sci. 2019 Jun;26(6):201-210. doi: 10.1002/jhbp.628. Epub 2019 May 21.

Abstract

Biliary atresia (BA) is a rare cholangiopathy of largely unknown etiology and unpredictable outcome. There has been an increasing number of BA-related publications, which may challenge researchers to determine their actual scientific value. This study aimed to evaluate the global research activity and developments relating to BA using a combination of scientometric methodologies and visualization tools. A comprehensive search strategy for the Web of Science™ database was designed to obtain bibliographic data on scientific BA publications for the timespan 1900-2018. Research output of countries, institutions, individual authors and collaborative networks was analyzed. Semi-qualitative research measures including citation rate and h-index were assessed. Choropleth mapping and network diagrams were used to visualize results. In total, 4,459 publications on BA were identified (88.5% in English), originating from 63 countries. The largest number was published by the USA (n = 991; 22.2%), Japan (n = 667; 15.0%) and the UK (n = 294; 6.6%). The USA combined the highest number of cooperation articles (n = 140). The most productive collaborative network was established between the USA and Canada (n = 17). Scientific papers from the UK received the highest average citation rate (16.7), whereas the USA had the highest country-specific h-index (59). Eighty-eight (2.0%) items were published under the auspices of multicenter consortiums and registries. The most productive institutions and authors were based in the USA, the UK, Japan, France, Canada and Taiwan. BA-related research has constantly been progressing, becoming more multidisciplinary but with main research endeavors concentrated in a few high-income countries. Studies into pathogenesis of BA remain uncommon, but are sorely needed to foster true scientific progress with this rare disease. Hence, international collaborative and translational research should be strengthened to allow further evolution in this field.

摘要

先天性胆道闭锁(BA)是一种罕见的胆管疾病,其病因和预后尚不清楚。关于 BA 的研究数量不断增加,这可能会使研究人员难以确定其实际的科学价值。本研究旨在采用科学计量学方法和可视化工具相结合,评估全球与 BA 相关的研究活动和进展。设计了一种全面的 Web of ScienceTM数据库检索策略,以获取 1900 年至 2018 年期间有关 BA 的科学出版物的书目数据。分析了国家、机构、个人作者和合作网络的研究成果。评估了半定量研究措施,包括引文率和 h 指数。使用面域图和网络图可视化结果。共确定了 4459 篇关于 BA 的出版物(88.5%为英文),来自 63 个国家。发表数量最多的国家是美国(n=991;22.2%)、日本(n=667;15.0%)和英国(n=294;6.6%)。美国合作文章数量最多(n=140)。最具生产力的合作网络是在美国和加拿大之间建立的(n=17)。英国的科学论文平均引文率最高(16.7),而美国的国家特定 h 指数最高(59)。88 项(2.0%)是在多中心联盟和注册机构的支持下发表的。生产力最高的机构和作者位于美国、英国、日本、法国、加拿大和中国台湾。BA 相关研究一直在不断进展,变得更加多学科化,但主要研究工作集中在少数高收入国家。BA 发病机制的研究仍然很少,但对于推动这种罕见疾病的真正科学进步非常必要。因此,应加强国际合作和转化研究,以促进该领域的进一步发展。

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