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国际脊髓损伤核心数据集(第2.0版)——包括报告的标准化。

International Spinal Cord Injury Core Data Set (version 2.0)-including standardization of reporting.

作者信息

Biering-Sørensen F, DeVivo M J, Charlifue S, Chen Y, New P W, Noonan V, Post M W M, Vogel L

机构信息

Clinic for Spinal Cord Injuries, Neuroscience center, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Department of Physical Medicine and Rehabilitation, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Spinal Cord. 2017 Aug;55(8):759-764. doi: 10.1038/sc.2017.59. Epub 2017 May 30.

Abstract

STUDY DESIGN

The study design includes expert opinion, feedback, revisions and final consensus.

OBJECTIVES

The objective of the study was to present the new knowledge obtained since the International Spinal Cord Injury (SCI) Core Data Set (Version 1.0) published in 2006, and describe the adjustments made in Version 2.0, including standardization of data reporting.

SETTING

International.

METHODS

Comments received from the SCI community were discussed in a working group (WG); suggestions from the WG were reviewed and revisions were made. All suggested revisions were considered, and a final version was circulated for final approval.

RESULTS

The International SCI Core Data Set (Version 2.0) consists of 25 variables. Changes made to this version include the deletion of one variable 'Total Days Hospitalized' and addition of two variables 'Date of Rehabilitation Admission' and 'Date of Death.' The variable 'Injury Etiology' was extended with six non-traumatic categories, and corresponding 'Date of Injury' for non-traumatic cases, was defined as the date of first physician visit for symptoms related to spinal cord dysfunction. A category reflecting transgender was added. A response category was added to the variable on utilization of ventilatory assistance to document the use of continuous positive airway pressure for sleep apnea. Other clarifications were made to the text. The reporting of the pediatric SCI population was updated as age groups 0-5, 6-12, 13-14, 15-17 and 18-21.

CONCLUSION

Collection of the core data set should be a basic requirement of all studies of SCI to facilitate accurate descriptions of patient populations and comparison of results across published studies from around the world.

摘要

研究设计

研究设计包括专家意见、反馈、修订和最终共识。

目的

本研究的目的是展示自2006年国际脊髓损伤(SCI)核心数据集(第1.0版)发布以来获得的新知识,并描述第2.0版所做的调整,包括数据报告的标准化。

地点

国际。

方法

在一个工作组(WG)中讨论了从SCI社区收到的意见;审查了工作组的建议并进行了修订。考虑了所有建议的修订,并分发了最终版本以供最终批准。

结果

国际SCI核心数据集(第2.0版)由25个变量组成。此版本的更改包括删除一个变量“住院总天数”,添加两个变量“康复入院日期”和“死亡日期”。变量“损伤病因”扩展了六个非创伤性类别,非创伤性病例的相应“损伤日期”定义为首次因脊髓功能障碍相关症状就诊的日期。增加了一个反映跨性别者的类别。在通气辅助使用变量中增加了一个应答类别,以记录用于睡眠呼吸暂停的持续气道正压通气的使用情况。对文本进行了其他澄清。儿科SCI人群的报告更新为0-5岁、6-12岁、13-14岁、15-17岁和18-21岁年龄组。

结论

核心数据集的收集应是所有SCI研究的基本要求,以便准确描述患者群体并比较世界各地已发表研究的结果。

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