首页> 美国卫生研究院文献>International Journal of Environmental Research and Public Health >How Do Patients and Doctors Perceive Medical Services for Rare Diseases Differently in China? Insights from Two National Surveys
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How Do Patients and Doctors Perceive Medical Services for Rare Diseases Differently in China? Insights from Two National Surveys

机译:患者和医生如何在中国不同地感知医疗服务罕见疾病?两个国家调查的见解

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摘要

: Increasing attention is being paid to improve the quality of life of patients with rare diseases in China. However, we are currently unaware of the problems encountered in the medical services of rare diseases from the viewpoints of doctors and patients. This study addressed the differences in the perceived barriers of diagnosis and treatments for rare diseases between doctors and patients in China. : Two independent cross-sectional surveys on the perception of Chinese doctors’ and patients’ experiences with rare diseases were launched online between January and February 2018. A non-probability, convenience sampling method was employed to recruit participants. In all, 45 rare diseases were reported by 139 doctors and 1853 patients. Patients with rare diseases faced significantly more difficulties in receiving accurate diagnosis (72.0%) and accessing information related to diagnosis and treatment (77.3%) as compared with doctors (34.5% and 40.3%, < 0.0001, respectively). Specially, patients felt more difficulties than doctors in obtaining sustainable treatment for rare diseases (84.3% vs. 49.6%, < 0.001). A higher percentage of patients (58.7%) than that of doctors (39.1%) had concerns in terms of the affordability of drugs. Further, 66.3% patients claimed that the drugs used to treat their conditions were not covered by their current medical insurances, whereas only 21.6% for doctors ( < 0.0001). Moreover, 35.3% of doctors responded that they recommended patients to visit the specialist they knew or were acquainted with, whereas 30.0% of patients said that their doctors chose to treat them based on their past experiences ( < 0.001). : The perceived experience of patients with regard to diagnosis and treatment was significantly different from that of doctors. An integrated medical service platform should be established to facilitate better communication and mutual understanding of rare diseases between patients and doctors.
机译::正在增加注意力,以提高中国罕见疾病患者的生活质量。然而,我们目前没有意识到从医生和患者的角度来看,我们的稀有疾病遇到的问题。本研究解决了中国医生与患者稀有疾病的诊断和治疗的感知障碍的差异。 :在2018年1月至2月在线在线推出了对中国医生和患者对罕见疾病的看法的两个独立横断面调查。雇用了招聘参与者的非概率,方便抽样方法。总共有139名医生和1853名患者报告了45例罕见疾病。含有罕见疾病的患者在接受准确的诊断(72.0%)并获得与诊断和治疗相关的信息(分别为34.5%和40.3%,<0.0001),获得诊断和治疗相关信息(77.3%)。特别是,患者比医生获得更困难,以获得稀有疾病的可持续治疗(84.3%,vs.49.6%<0.001)。比医生(39.1%)的患者(58.7%)较高的百分比对药物的负担能力有所担忧。此外,66.3%的患者声称,用于治疗其条件的药物未被其目前的医疗保险涵盖,而医生只有21.6%(<0.0001)。此外,35.3%的医生回答说,他们推荐患者访问他们所知道或熟悉的专家,而30.0%的患者表示他们的医生选择根据他们过去的经历来对待他们(<0.001)。 :诊断和治疗的患者的感知经验与医生的诊断和治疗有显着差异。应建立综合医疗服务平台,以促进对患者与医生之间的罕见疾病的更好的沟通和相互理解。

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