Department of Endocrinology, Diabetes and Rheumatology, University Hospital Duesseldorf, Heinrich-Heine-University Düsseldorf, Germany.
Clin Exp Rheumatol. 2010 Mar-Apr;28(2):261-4. Epub 2010 May 13.
The Internet supports interactive patient assessments, online documentation and access to online electronic health records (EHRs), but little is known about the acceptance of these features and trends in rheumatology patients. Therefore, we studied patients' attitudes and willingness to participate in online patient (self-)documentation.
We interviewed 153 consecutive outpatients with rheumatoid arthritis, systemic lupus erythematosus or spondyloarthritis using a paperbased self-administered questionnaire. To detect recent trends in patients' perception we compared our 2006 data to the results of our survey conducted in 2001. P-values provided in the abstract reflect the comparisons from 2001 and 2006.
Patients were predominantly female (69.3%; n.s.), mean age was 45.7+/-14.4 years (n.s.), and 68.6% (+18.6% compared to 2001; p<0.001) reported regular Internet use. Confidence in the Internet and reliability of online information were rated unchanged to 2001. Internet users appreciated to access their EHR online in 68.6% (+13.8% compared to 2001; p<0.01), (self-)monitor the course of their disease online in 80.0%, and answer outcome questionnaires online in 67.6%. Internet users considered computers as valuable instruments in the patient-doctor relationship (88.4%), 58.8% were not convinced that computer use influences the relationship positively.
Attitudes of patients with rheumatic disorders (Internet users and non-users) towards online EHRs have improved since 2001, online applications for patient assessments and disease (self-)management in rheumatology seem feasible now. Nevertheless, unchanged low confidence rates in the Internet and in the reliability of medical information derived from the Internet should sound a note of caution regarding the implementation of such services.
互联网支持交互式患者评估、在线文档记录以及在线电子健康记录(EHR)的访问,但对于风湿病患者对这些功能和趋势的接受程度知之甚少。因此,我们研究了患者对在线患者(自我)文档记录的态度和参与意愿。
我们使用纸质自我管理问卷对 153 名连续就诊的类风湿关节炎、系统性红斑狼疮或脊柱关节炎门诊患者进行了访谈。为了检测患者感知的最新趋势,我们将 2006 年的数据与我们在 2001 年进行的调查结果进行了比较。摘要中提供的 P 值反映了 2001 年和 2006 年的比较。
患者主要为女性(69.3%;n.s.),平均年龄为 45.7+/-14.4 岁(n.s.),68.6%(比 2001 年增加 18.6%;p<0.001)报告经常使用互联网。对互联网的信心和在线信息的可靠性与 2001 年相比保持不变。互联网用户在以下方面表示赞赏:在线访问他们的 EHR(68.6%,比 2001 年增加 13.8%;p<0.01),在线(自我)监测疾病的进程(80.0%),以及在线回答结果问卷(67.6%)。互联网用户认为计算机是医患关系中的有价值工具(88.4%),58.8%的患者不相信计算机的使用会对关系产生积极影响。
自 2001 年以来,风湿性疾病患者(互联网用户和非用户)对在线 EHR 的态度有所改善,在线患者评估和风湿病疾病(自我)管理的应用现在似乎可行。然而,互联网和源自互联网的医疗信息可靠性的信心率保持不变,这应该引起对实施此类服务的谨慎态度。