Stewart Rachelle S
Department of Biomedical and Health Information Sciences, College of Applied Health Sciences, University of Illinois at Chicago, USA.
Perspect Health Inf Manag. 2007 Jun 1;4:5.
This study measured attitudes about patient privacy. Participants ranked a collection of 25 patient- specific health information protection measures that have been established as a part of the Health Insurance Portability and Accountability Act (HIPAA), effective in April 2003. Individual points of view were surveyed to determine which information protection measures patients felt to be least effective and most effective with regard to protection of patient privacy. The researcher, being interested in subjects with the human immuno deficiency virus (HIV), conducted an exploratory Q-Methodology study to capture individual participants' points of view. A by-person factor analysis was performed on the intercorrelated Q-sort matrix. The subjects clustered into three groups; however, the concern for privacy was similar for subjects with and without HIV. Recommendations for policy changes are discussed for four areas: usage of the "Notice of Privacy Practices," patient sign-in procedures, the role of the privacy officer, and staff education.
本研究测量了对患者隐私的态度。参与者对作为2003年4月生效的《健康保险流通与责任法案》(HIPAA)一部分而制定的25项特定患者健康信息保护措施进行了排序。调查了个人观点,以确定患者认为哪些信息保护措施在保护患者隐私方面最无效和最有效。研究人员对感染人类免疫缺陷病毒(HIV)的受试者感兴趣,开展了一项探索性Q方法研究,以获取个体参与者的观点。对相互关联的Q分类矩阵进行了个人因素分析。受试者分为三组;然而,有HIV和无HIV的受试者对隐私的关注相似。针对四个领域讨论了政策变更建议:《隐私实践通知》的使用、患者签到程序、隐私官员的角色以及员工教育。