Health Information Systems and Migrant Health in Europe

L. Biddle, K. Bozorgmehr, R. Jahn
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引用次数: 2

Abstract

Ensuring the health of migrants and access to appropriate health services presents a challenge to health systems in the age of global migration. Reliable and timely information is key to decision-making in all sectors of the health system to ensure that health system goals are met. Such information is even more important among a mobile, sometimes rapidly changing, dynamic and heterogeneous migrant population. While health information systems (HIS) are crucial for effective functioning of other health system blocks as well as for evidence-informed decision-making, they are often sidelined in health system policy and development. Looking across the World Health Organization (WHO) European Region, HIS for migrants are deficient both in their overall availability and their integration into regular monitoring structures. Less than half of the 53 member states routinely report health data for refugees and migrants. Most of the routinely collected data on migrant and refugee health can be identified in countries with strong population-based records, with some good practice examples of well-integrated and high-quality health monitoring surveys, disease-specific registries, and “parallel” HIS in migrant-specific settings. Overall, however, HIS in the WHO European Region are not able to provide data of sufficient quality and comparability to be well integrated into regular health monitoring structures. The reasons for this can be highlighted by five key barriers to improved information systems for migrant health: barriers in recording data, standardizing data collection, harmonizing migrant indicators, producing high-quality data, and sharing information. Better integration can be achieved through increased multilateral collaboration for the harmonization of indicators, strengthening of governance frameworks for data-sharing and protection measures, and the increased use of currently underutilized data collection mechanisms, including health monitoring surveys and medical records from refugee reception facilities. These steps will remain essential for the adequate planning and provision of needs-based care for refugees and migrants.
欧洲的卫生信息系统和移民健康
在全球移徙时代,确保移徙者的健康和获得适当的卫生服务对卫生系统提出了挑战。可靠和及时的信息是卫生系统所有部门做出决策以确保实现卫生系统目标的关键。这种信息在流动的、有时变化迅速的、动态的和异质的移民人口中更为重要。虽然卫生信息系统对于卫生系统其他部门的有效运作以及基于证据的决策至关重要,但它们在卫生系统政策和发展中往往处于次要地位。纵观世界卫生组织(世卫组织)欧洲区域,移徙者卫生信息系统在总体可得性和纳入定期监测结构方面都存在不足。在53个成员国中,不到一半的国家定期报告难民和移民的健康数据。大多数例行收集的移徙者和难民健康数据都可以在具有良好人口记录的国家中确定,并有一些良好做法的例子,包括综合良好和高质量的健康监测调查、特定疾病登记以及移徙者特定环境中的“平行”卫生保健。然而,总的来说,卫生组织欧洲区域的卫生信息系统无法提供足够高质量和可比性的数据,无法很好地纳入定期卫生监测结构。改善移徙者健康信息系统的五个主要障碍可以突出说明这一原因:记录数据、标准化数据收集、协调移徙者指标、产生高质量数据和共享信息方面的障碍。通过加强多边协作以统一各项指标,加强数据共享和保护措施的治理框架,以及更多地利用目前未充分利用的数据收集机制,包括健康监测调查和难民接待设施的医疗记录,可以更好地实现一体化。这些步骤对于为难民和移徙者充分规划和提供基于需要的照顾仍然是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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