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Sorry You Cant Have That Information: Data Holder Confusion Regarding Privacy Requirements for Personal Health Information and the Potential Chilling Effect on Health Research

机译:抱歉您无法获得该信息:关于个人健康信息的隐私要求以及对健康研究的潜在影响数据持有人感到困惑

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摘要

This study, conducted in Newfoundland and Labrador, assessed the level of awareness, perceptions and concerns of healthcare providers, health researchers, data managers and the general public about the collection, use and disclosure of personal health information (PHI) for research purposes. Data collection involved surveys and follow-up focus groups with participants. Results indicate a poor understanding generally with regard to privacy rights and responsibilities. Many professionals are unfamiliar with the legislative environment for PHI, particularly as it pertains to the access and use of PHI for research purposes. Lack of familiarity with basic requirements for patient-based research, coupled with heightened sensitivity to privacy issues owing to various federal and provincial regulatory initiatives, could have a chilling effect on health research. Importantly, our results indicate that the public is much less concerned about the use of their PHI for health research purposes than are professionals who collect, store and share it.
机译:这项在纽芬兰和拉布拉多进行的研究评估了医疗保健提供者,健康研究人员,数据管理人员和公众对于出于研究目的而收集,使用和披露个人健康信息(PHI)的认识,看法和关注水平。数据收集涉及调查和参与者的后续焦点小组。结果表明总体上对隐私权和责任的理解不佳。许多专业人士不了解PHI的立法环境,尤其是与出于研究目的而使用和使用PHI有关。缺乏对以患者为基础的研究的基本要求的认识,再加上由于联邦和省的各种监管措施,对隐私问题的敏感度提高,可能对健康研究产生令人不寒而栗的影响。重要的是,我们的结果表明,与收集,存储和共享PHI的专业人员相比,公众对于PHI的卫生使用的关注要少得多。

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