Shapiro Jason S
Columbia University, Department of Biomedical Informatics, 622 West 168th Street, VC5, New York, NY 10032, USA.
J Biomed Inform. 2007 Dec;40(6 Suppl):S46-9. doi: 10.1016/j.jbi.2007.08.003. Epub 2007 Aug 31.
Health information exchange (HIE) initiatives are in various stages of development across the United States. They aim to bring previously unavailable clinical data from patients' disparate health records, which may be spread over multiple provider and payer networks, to the point of care where clinicians and their patients need it most. The implications of these initiatives on public health are numerous. This article provides general evaluation methods for measuring the impact of HIE on public health in six use cases: (1) mandated reporting of laboratory diagnoses, (2) mandated reporting of physician-based diagnoses, (3) public health investigation, (4) disease-based non-reportable laboratory data, (5) antibiotic-resistant organism surveillance, and (6) population-level quality monitoring.
健康信息交换(HIE)计划在美国正处于不同的发展阶段。它们旨在将患者分散的健康记录中以前无法获取的临床数据汇集起来,这些记录可能分布在多个医疗服务提供者和支付方网络中,并将其提供给临床医生及其患者最需要的医疗点。这些计划对公共卫生的影响是多方面的。本文提供了在六个用例中衡量HIE对公共卫生影响的一般评估方法:(1)实验室诊断的强制报告,(2)基于医生诊断的强制报告,(3)公共卫生调查,(4)基于疾病的不可报告实验室数据,(5)抗药生物体监测,以及(6)人群层面的质量监测。