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首页> 外文期刊>BMC Health Services Research >Telephone health services in the field of rare diseases: a qualitative interview study examining the needs of patients, relatives, and health care professionals in Germany
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Telephone health services in the field of rare diseases: a qualitative interview study examining the needs of patients, relatives, and health care professionals in Germany

机译:罕见病领域的电话医疗服务:定性访谈研究,考察了德国患者,亲戚和医疗保健专业人员的需求

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Rare diseases are, by definition, very serious and chronic diseases with a high negative impact on quality of life. Approximately 350 million people worldwide live with rare diseases. The resulting high disease burden triggers health information search, but helpful, high-quality, and up-to-date information is often hard to find. Therefore, the improvement of health information provision has been integrated in many national plans for rare diseases, discussing the telephone as one access option. In this context, this study examines the need for a telephone service offering information for people affected by rare diseases, their relatives, and physicians. In total, 107 individuals participated in a qualitative interview study conducted in Germany. Sixty-eight individuals suffering from a rare disease or related to somebody with rare diseases and 39 health care professionals took part. Individual interviews were conducted using a standardized semi-structured questionnaire. Interviews were analysed using the qualitative content analysis, triangulating patients, relatives, and health care professionals. The fulfilment of qualitative data processing standards has been controlled for. Out of 68 patients and relatives and 39 physicians, 52 and 18, respectively, advocated for the establishment of a rare diseases telephone service. Interviewees expected a helpline to include expert staffing, personal contact, good availability, low technical barriers, medical and psychosocial topics of counselling, guidance in reducing information chaos, and referrals. Health care professionals highlighted the importance of medical topics of counselling—in particular, differential diagnostics—and referrals. Therefore, the need for a national rare diseases helpline was confirmed in this study. Due to limited financial resources, existing offers should be adapted in a stepwise procedure in accordance with the identified attributes.
机译:顾名思义,罕见疾病是非常严重的慢性疾病,对生活质量造成很大的负面影响。全球约有3.5亿人患有罕见病。由此产生的高疾病负担触发了健康信息搜索,但是有用的,高质量的和最新的信息通常很难找到。因此,改善健康信息的提供已被纳入许多国家罕见病计划,并将电话作为一种上网选择。在这种情况下,本研究探讨了对电话服务的需求,该电话为受罕见疾病影响的人们,其亲属和医生提供信息。总共有107个人参加了在德国进行的定性访谈研究。六十八名患有罕见疾病或与某种罕见疾病有关的人和39名卫生保健专业人员参加了会议。使用标准化的半结构化问卷进行个人访谈。访谈采用定性内容分析法,对患者,亲属和医疗保健专业人员进行三角剖分。定性数据处理标准的实现已得到控制。在68位患者和亲属中,以及39位医生中,分别有52位和18位主张建立罕见病电话服务。受访者希望热线电话包括专家人员配备,个人联系,可用性高,技术障碍低,咨询的医学和社会心理主题,减少信息混乱的指导以及转介。卫生保健专业人员强调了咨询医学主题的重要性,尤其是鉴别诊断和转诊。因此,这项研究证实了需要全国罕见病热线的帮助。由于财务资源有限,应根据确定的属性以逐步的方式调整现有报价。

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