...
首页> 外文期刊>Patient Related Outcome Measures >The health and life path of rare disease patients: results of the 2015 French barometer
【24h】

The health and life path of rare disease patients: results of the 2015 French barometer

机译:罕见病患者的健康和生活道路:2015年法国晴雨表的结果

获取原文
           

摘要

Purpose: A barometer has been set up to provide better knowledge about the daily situation of French rare disease (RD) patients, their families and relatives, in order to contribute to the elaboration of improvement measures. This report focuses on the care and life path of RD patients. Patients and methods: A preliminary survey was carried out with three patients, five parents and three RD experts to identify the main hurdles and disruptions in the life path of RD patients. It was used to design a larger survey comprising 60 questions as well as open fields allowing free expression. Respondents (448) comprised patients, parents of RD children and close relatives of patients. The Percentage of Maximum Deviation, Yates’ correction for continuity and Fisher’s test were employed to compare the responses between groups. Results: Large disparities in the delays to obtain a diagnosis were identified (20 years), and longer delays were associated with negative perception of care conditions. While good interactions with education teams were reported (59% of respondents), the professional situation of both patients and parents was strongly and negatively impacted by the disease (51% did not work or stopped working). Three hundred respondents expressed various needs and psychological and personal issues were reported by 62% and 75% of respondents, respectively. Interestingly, the medical care path and daily life of RD patients were positively impacted by the follow-up in a specialized consultation, as reflected by changes in scores measured by our barometer (Fisher’s test, p <0.05). Conclusion: Some of the main hurdles and sources of disruption in the life path of RD patients were identified, as well as some positive outcomes. These data could serve not only as a background for further studies, but also to better adapt the support to real needs and to improve the synergies between the many people involved in the life path of RD patients.
机译:目的:已经建立了一个晴雨表,以提供有关法国罕见病(RD)患者,其家人和亲属的日常状况的更多信息,从而有助于制定改善措施。本报告重点介绍RD患者的护理和生活路径。患者和方法:对三名患者,五名父母和三名RD专家进行了初步调查,以确定RD患者生活路径中的主要障碍和障碍。它被用来设计一个更大的调查,包括60个问题以及允许自由表达的开放领域。受访者(448名)包括患者,RD儿童的父母以及患者的近亲。使用最大偏差百分比,Yates的连续性校正和Fisher检验来比较各组之间的响应。结果:确定延迟诊断的巨大差异(20年),并且延迟较长与对护理条件的负面看法有关。虽然与教育团队的互动良好(59%的受访者),但患者和父母的职业状况均受到该疾病的强烈和负面影响(51%没工作或停止工作)。 300名受访者表达了各种需求,分别有62%和75%的受访者报告了心理和个人问题。有趣的是,RD病人的医疗路径和日常生活受到专门咨询中随访的积极影响,这反映在我们的晴雨表测量的得分变化上(Fisher检验,p <0.05)。结论:确定了RD患者生活路径中的一些主要障碍和来源,以及一些积极的成果。这些数据不仅可以作为进一步研究的背景,而且可以更好地使支持适应实际需求,并改善参与RD患者生活路径的许多人之间的协同作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号