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物质使用障碍的治疗:比利时治疗需求指标登记协议。

Treatment for substance use disorders: the Belgian Treatment Demand Indicator registration protocol.

作者信息

Antoine Jérôme, De Ridder Karin, Plettinckx Els, Blanckaert Peter, Gremeaux Lies

机构信息

WIV-ISP: Scientific Institute of Public Health, Brussels, Belgium, Rue Juliette Wytsmanstraat, 14, 1050 Brussels, Belgium.

出版信息

Arch Public Health. 2016 Jul 1;74:27. doi: 10.1186/s13690-016-0139-7. eCollection 2016.

Abstract

BACKGROUND

Registration of patients with substance use disorders is of key importance to get insights and to study trends in patients characteristics and substance use patterns. The Treatment Demand Indicator (TDI) is gathering this information at European level since 2000. In Belgium, this registration started at national level in 2011 and an increasing number of facilities of different types are participating in this data collection since then.

METHODS/DESIGN: This surveillance register collects information on every treatment episode started by patients for their substance use disorder. Information is collected on socio-demographic characteristics of the patient, treatment history and substance use patterns. Patients are identified uniquely using their national identification number in order identify multiple episodes followed by a same person. A large range of treatment facilities have the possibility to participate in this registration to allow a wide coverage of the population.

DISCUSSION

The objective of the paper is to facilitate the use of data by authorities or researchers by correctly describing all aspects of the indicator. The case definition, the variables collected and the way data should be reported are of key importance to use and interpret the data correctly. An overview of the data registered in 2014 gives also an idea of the content of the database. The article also pictures the strengths and limitations of the register and foresees some future improvements.

摘要

背景

对物质使用障碍患者进行登记对于深入了解和研究患者特征及物质使用模式的趋势至关重要。自2000年以来,治疗需求指标(TDI)一直在欧洲层面收集此类信息。在比利时,该登记工作于2011年在国家层面启动,自那时起,越来越多不同类型的机构参与到这一数据收集工作中。

方法/设计:该监测登记册收集患者因物质使用障碍开始的每一次治疗情况的信息。收集的信息包括患者的社会人口学特征、治疗史和物质使用模式。通过患者的国家身份证号码对患者进行唯一识别,以便识别同一人后续的多次治疗情况。众多治疗机构都有可能参与此次登记,从而实现对人群的广泛覆盖。

讨论

本文的目的是通过正确描述该指标的各个方面,方便当局或研究人员使用数据。病例定义、收集的变量以及数据的报告方式对于正确使用和解释数据至关重要。2014年登记数据的概述也能让人了解数据库的内容。本文还阐述了该登记册的优势和局限性,并展望了未来的一些改进方向。

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