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The impact and financial burden of pulmonary arterial hypertension on patients and caregivers: results from a national survey

机译:肺动脉高压对患者和护理人员的影响和财务负担:国家调查的结果

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Pulmonary arterial hypertension (PAH) is a chronic progressive devastating disease. Symptom burden might impair health-related quality of life of patients. Furthermore, treatment on this disease brings significant financial burden to patients’ families. Both physiological and psychological symptoms have been reported, but limited evidence regarding the impact of PAH on patients and caregivers exists, especially the emotional issues and their association with patients’ health quality. The main purpose of this study was to describe the impact of PAH on patients and their caregivers in a Chinese population. This large-scale national survey enrolled 174 participants to complete questionnaires using face-to-face semistructured interviews. PAH influenced all aspects of patients’ lives including daily activities, work, emotions, and personal relationships. Both patients and caregivers reported a major impact on family finances and on their work. The majority of patients had feelings of isolation. A lack of public understanding about PAH contributes to social isolation. Most patients and caregivers would like to get information regarding PAH doctors and patient organization contacts to obtain support. This survey-based report provides information regarding the way and extent to which PAH impacts both patients and their caregivers and provides some means for comparison with non-Chinese populations. It is important for physicians and the community to offer more support and information for PAH patients and their families.
机译:肺动脉高压(PAH)是一种慢性进行性破坏性疾病。症状负担可能会损害患者健康相关的生活质量。此外,对这种疾病的治疗给患者家庭带来了巨大的经济负担。生理和心理症状都有报道,但是关于PAH对患者和护理人员影响的证据有限,尤其是情绪问题及其与患者健康状况的关系。这项研究的主要目的是描述PAH对中国人群患者及其护理人员的影响。这项大规模的全国性调查招募了174名参与者,使用面对面的半结构化访谈来完成问卷。 PAH影响了患者生活的方方面面,包括日常活动,工作,情绪和人际关系。患者和护理人员都报告了对家庭经济和工作的重大影响。大多数患者有孤立感。公众对PAH缺乏了解导致社会孤立。大多数患者和护理人员希望获得有关PAH医生和患者组织联系人的信息,以获得支持。这份基于调查的报告提供了有关PAH影响患者及其护理人员的方式和程度的信息,并提供了一些与非华裔人群进行比较的方法。对于医生和社区来说,为PAH患者及其家人提供更多支持和信息非常重要。

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