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Perception of Disease and Doctor-Patient Relationship Experienced by Patients with Psoriasis: A Questionnaire-Based Study

机译:牛皮癣患者的疾病知觉和医患关系:基于问卷的研究

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Background: Many studies have addressed the impact of psoriasis on quality of life, but few studies have investigated patient perception of the disease or the patient-physician relationship. As with most chronic diseases, improvement in the patient-physician relationship may be important in the proper management of patients with psoriasis. Objectives: To assess how psoriasis and its treatments are subjectively experienced by patients as well as patient expectations with regard to the patient-physician relationship. Methods: A discussion agenda for 'focus group meetings' was organized by a group of sociologists, psychologists, educators, researchers, and clinicians active in the field of psychodermatology. Four meetings were held in Northern and Central Italy and participants included one moderator and either eight dermatologists or eight patients. Discussions were based on a predefined agenda and included: (i) the psychological representation of psoriasis; (ii) the hetero- and self-perception of the patient; (iii) the patient-physician relationship; and (iv) the development of an educational intervention for dermatologists in order to improve the patient-physician relationship. A questionnaire, based on the information gathered at the focus groups, was administered to 323 patients with moderate to severe chronic plaque psoriasis from 17 dermatology clinics throughout Italy. Results: Three hundred patients completed the questionnaire. Psoriasis elicited anger, annoyance at the inconvenience of the disease, and irritation in approximately 50% of the patients, whilst 38% of patients were unable to describe their emotional state. Aspects of life that were limited by psoriasis included clothing (57%), social interactions (43%), and personal hygiene (31%). The disease was often seen by patients as incomprehensible, incurable, and uncontrollable. More than half of the patients stressed their need to be listened to by the treating physician, and their wish that the physician should use simple language and should improve their psychological skills and interpersonal communication techniques. Conclusions: Dermatologists need to convey to patients with psoriasis the feeling of 'understanding the disease,' of hope about its curability, and the 'perception of control.' These elements should be taken into account when treating patients and whenever educational interventions are planned.
机译:背景:许多研究都研究了牛皮癣对生活质量的影响,但是很少有研究调查患者对疾病的认识或患者与医师之间的关系。与大多数慢性疾病一样,改善患者与医师之间的关系对于正确治疗牛皮癣患者可能很重要。目的:评估患者对银屑病及其治疗的主观感受以及患者对医患关系的期望。方法:由活跃在皮肤病学领域的社会学家,心理学家,教育者,研究人员和临床医生组成的小组组织了“焦点小组会议”的讨论议程。在意大利北部和中部举行了四次会议,与会者包括一名主持人和八名皮肤科医生或八名患者。讨论基于预先确定的议程,包括:(i)牛皮癣的心理表征; (ii)患者的异样和自我感知; (iii)医患关系; (iv)开发针对皮肤科医生的教育干预措施,以改善患者与医师之间的关系。根据在焦点小组收集的信息,对意大利的17个皮肤科诊所的323名中度至重度慢性斑块状牛皮癣患者进行了问卷调查。结果:300名患者完成了问卷。牛皮癣在大约50%的患者中引起了愤怒,对疾病的不便烦恼和发炎,而38%的患者无法描述其情绪状态。银屑病限制的生活方面包括衣服(57%),社交(43%)和个人卫生(31%)。患者经常将这种疾病视为难以理解,无法治愈和无法控制。超过一半的患者强调他们需要主治医师的倾听,并希望医师应使用简单的语言,并应改善其心理技能和人际交往技巧。结论:皮肤科医生需要向牛皮癣患者传达“了解疾病”的感觉,对其可治愈性的希望以及“控制感”。在治疗患者时以及计划进行教育干预时,应考虑这些因素。

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