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首页> 外文期刊>Preventive Medicine Reports >Electronic health record access by patients as an indicator of information seeking and sharing for cardiovascular health promotion in social networks: Secondary analysis of a randomized clinical trial
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Electronic health record access by patients as an indicator of information seeking and sharing for cardiovascular health promotion in social networks: Secondary analysis of a randomized clinical trial

机译:病人对电子健康记录的访问,作为社交网络中促进心血管健康的信息寻求和共享的指标:一项随机临床试验的二级分析

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We investigated electronic health record (EHR) access as an indicator of cardiovascular health promotion by patients in their social networks, by identifying individuals who viewed their coronary heart disease (CHD) risk information in the EHR and shared this information in their social networks among various spheres of influence. In a secondary analysis of the Myocardial Infarction Genes trial, Olmsted County MN residents (2013–2015; n?=?203; whites, ages 45–65?years) at intermediate CHD risk were randomized to receive their conventional risk score (CRS; based on traditional risk factors) alone or also their genetic risk score (GRS; based on 28 genomic variants). We assessed self-reported and objectively quantified EHR access via a patient portal at three and six months after risk disclosure, and determined whether this differed by GRS disclosure. Data were analyzed using logistic regression and adjusted for sociodemographic characteristics, family history, and baseline CRS/GRS. Self-reported EHR access to view CHD risk information was associated with a high frequency of objectively quantified EHR access (71(10) versus 37(5) logins;P?=?0.0025) and a high likelihood of encouraging others to be screened for their CHD risk (OR 2.936, CI 1.443–5.973,P?=?0.0030), compared to the absence of self-reported EHR access to view CHD risk information. We thereby used EHR access trends to identify individuals who may function as disseminators of CHD risk information in social networks, compared to individuals on the periphery of their social networks who did not exhibit this behavior. Partnering with such individuals could amplify CHD health promotion.Clinical Trial Registration: Myocardial Infarction Genes (MI-GENES) Study,NCT01936675,https://clinicaltrials.gov/ct2/show/NCT01936675.
机译:我们通过识别在电子病历中查看过冠心病(CHD)风险信息并在各种社交网络中共享此信息的个人,调查了电子健康记录(EHR)的访问情况,以此作为患者在社交网络中促进心血管健康的指标。影响范围。在对心肌梗塞基因试验的次要分析中,患有中度冠心病风险的奥尔姆斯特德县明尼苏达州居民(2013-2015; n == 203; 45-65岁的白人)随机获得常规风险评分(CRS; (仅基于传统风险因素)或其遗传风险评分(GRS;基于28个基因组变体)。我们在风险披露后的三,六个月评估了通过患者门户进行的自我报告和客观量化的EHR访问,并确定GRS披露是否有所不同。使用逻辑回归分析数据,并针对社会人口统计学特征,家族史和基线CRS / GRS进行调整。自我报告的电子病历访问权限可查看冠心病风险信息与客观量化的电子病历访问频率较高(71(10)对37(5)登录; P = 0.0025)和鼓励其他人进行筛查的可能性较高相关与没有自我报告的EHR来查看CHD风险信息的情况相比,他们的CHD风险(OR 2.936,CI 1.443–5.973,P?=?0.0030)。因此,我们使用EHR访问趋势来确定在社交网络中可以充当CHD风险信息传播者的个人,而不是在社交网络外围没有这种行为的个人。与此类人员合作可以扩大冠心病的健康促进。临床试验注册:心肌梗塞基因(MI-GENES)研究,NCT01936675,https://clinicaltrials.gov/ct2/show/NCT01936675。

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