Disease understanding

疾病理解
  • 文章类型: Journal Article
    目的:晚期肺癌患者身体症状负担的增加会破坏患者的情绪健康,目前的文献表明,医生良好的沟通技巧可能是一个缓冲。然而,对于哪一组患者,这种缓冲作用最有效,我们知之甚少。基于对晚期肺癌患者的横断面研究,本研究调查了医师沟通技巧对身体症状和情绪困扰之间关联的调节作用是否进一步取决于患者对疾病的认知。
    方法:晚期肺癌患者(n=199)填写了一份问卷,包括与肺癌相关的身体症状的测量,焦虑,和抑郁症状,对医生沟通技巧的看法,并自我报告了解他们的疾病。
    结果:分层回归分析表明,身体症状之间存在显着的三向相互作用,对医生沟通技巧的看法,以及对焦虑和抑郁的感知疾病理解。具体来说,医生良好的沟通技巧仅对疾病理解水平较低的患者产生缓冲作用。
    结论:我们的研究结果表明,对于疾病理解有限的患者,提高医生的沟通技巧可能对减少症状负担的适应不良情绪反应特别有益。当通信的时间和资源受到限制时,增强的意识和集中的培训可能旨在与对其疾病知识有限的患者进行沟通。
    OBJECTIVE: The elevated physical symptom burden in advanced lung cancer can disrupt patients\' emotional well-being, and current literature suggests that physicians\' good communication skills might be a buffer. However, little is known about for which group of patients this buffering effect is most effective. Based on a cross-sectional study in patients with advanced lung cancer, the present study examined whether the moderating effect of physicians\' communication skills on the association between physical symptoms and emotional distress would further depend on patients\' perceived disease understanding.
    METHODS: Patients with advanced lung cancer (n = 199) completed a questionnaire including measures of physical symptoms related to lung cancer, anxiety, and depressive symptoms, perceptions of physicians\' communication skills, and self-reported understanding of their disease.
    RESULTS: Hierarchical regression analyses indicated a significant three-way interaction among physical symptoms, perceptions of physicians\' communication skills, and perceived disease understanding on both anxiety and depression. Specifically, physicians\' good communication skills exerted a buffering effect only for patients with lower levels of disease understanding.
    CONCLUSIONS: Our findings indicate that improving physicians\' communication skills may be especially beneficial for reducing the maladaptive emotional reactions to symptom burden for patients with limited disease understanding. When time and resources for communication are restricted, enhanced awareness and focused training may be directed at communicating with patients who possess limited knowledge about their disease.
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  • 文章类型: Journal Article
    Drug repurposing has become a widely used strategy to accelerate the process of finding treatments. While classical de novo drug development involves high costs, risks, and time-consuming paths, drug repurposing allows to reuse already-existing and approved drugs for new indications. Numerous research has been carried out in this field, both in vitro and in silico. Computational drug repurposing methods make use of modern heterogeneous biomedical data to identify and prioritize new indications for old drugs. In the current paper, we present a new complete methodology to evaluate new potentially repurposable drugs based on disease-gene and disease-phenotype associations, identifying significant differences between repurposing and non-repurposing data. We have collected a set of known successful drug repurposing case studies from the literature and we have analysed their dissimilarities with other biomedical data not necessarily participating in repurposing processes. The information used has been obtained from the DISNET platform. We have performed three analyses (at the genetical, phenotypical, and categorization levels), to conclude that there is a statistically significant difference between actual repurposing-related information and non-repurposing data. The insights obtained could be relevant when suggesting new potential drug repurposing hypotheses.
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  • 文章类型: Journal Article
    BACKGROUND: Within the global endeavour of improving population health, one major challenge is the identification and integration of medical knowledge spread through several information sources. The creation of a comprehensive dataset of diseases and their clinical manifestations based on information from public sources is an interesting approach that allows one not only to complement and merge medical knowledge but also to increase it and thereby to interconnect existing data and analyse and relate diseases to each other. In this paper, we present DISNET (http://disnet.ctb.upm.es/), a web-based system designed to periodically extract the knowledge from signs and symptoms retrieved from medical databases, and to enable the creation of customisable disease networks.
    METHODS: We here present the main features of the DISNET system. We describe how information on diseases and their phenotypic manifestations is extracted from Wikipedia and PubMed websites; specifically, texts from these sources are processed through a combination of text mining and natural language processing techniques.
    RESULTS: We further present the validation of our system on Wikipedia and PubMed texts, obtaining the relevant accuracy. The final output includes the creation of a comprehensive symptoms-disease dataset, shared (free access) through the system\'s API. We finally describe, with some simple use cases, how a user can interact with it and extract information that could be used for subsequent analyses.
    CONCLUSIONS: DISNET allows retrieving knowledge about the signs, symptoms and diagnostic tests associated with a disease. It is not limited to a specific category (all the categories that the selected sources of information offer us) and clinical diagnosis terms. It further allows to track the evolution of those terms through time, being thus an opportunity to analyse and observe the progress of human knowledge on diseases. We further discussed the validation of the system, suggesting that it is good enough to be used to extract diseases and diagnostically-relevant terms. At the same time, the evaluation also revealed that improvements could be introduced to enhance the system\'s reliability.
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  • 文章类型: Journal Article
    Over a decade ago, a new discipline called network medicine emerged as an approach to understand human diseases from a network theory point-of-view. Disease networks proved to be an intuitive and powerful way to reveal hidden connections among apparently unconnected biomedical entities such as diseases, physiological processes, signaling pathways, and genes. One of the fields that has benefited most from this improvement is the identification of new opportunities for the use of old drugs, known as drug repurposing. The importance of drug repurposing lies in the high costs and the prolonged time from target selection to regulatory approval of traditional drug development. In this document we analyze the evolution of disease network concept during the last decade and apply a data science pipeline approach to evaluate their functional units. As a result of this analysis, we obtain a list of the most commonly used functional units and the challenges that remain to be solved. This information can be very valuable for the generation of new prediction models based on disease networks.
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  • 文章类型: Journal Article
    背景:本研究旨在确定自我监控实践,身体残疾的2型糖尿病患者对饮食调整和药物依从性障碍的认识。
    方法:在槟城综合医院糖尿病诊所进行访谈。受邀的与会者代表了马来西亚的三个主要族裔群体(马来人,中国人和印度人)。使用开放式方法来征求参与者的答案。面试问题与参与者对自我监测血糖实践的看法有关,对饮食管理的认识,糖尿病药物的行为和行动线索。
    结果:共有21名年龄在35-67岁之间的身体残疾的糖尿病患者(P1-P21)接受了访谈。队列参与者以男性为主(n=12),并且分布模式显示大多数参与者是马来人(n=10),其次是中国人(n=7)和其余印度人(n=4)。当参与者被问及他们认为记录血糖测试的首选方法时,来自低社会经济地位和离婚或丧偶的一些参与者拒绝适应远程监护,而是倾向于手动记录。关于控制饮食/卡路里的障碍有不同的反应。即使是经济地位很高的患者,35-50岁的中年人和5-10年的糖尿病病史受到替代治疗的影响.
    结论:研究得出结论,身体残疾患者需要广泛的护理和有效的策略来控制糖代谢。
    结论:本研究探讨了患者对肢体残疾治疗管理的看法。
    BACKGROUND: This study aimed to determine self-monitoring practices, awareness to dietary modifications and barriers to medication adherence among physically disabled type 2 diabetes mellitus patients.
    METHODS: Interview sessions were conducted at diabetes clinic-Penang general hospital. The invited participants represented three major ethnic groups of Malaysia (Malay, Chinese and Indians). An open-ended approach was used to elicit answers from participants. Interview questions were related to participant\'s perception towards self-monitoring blood glucose practices, Awareness towards diet management, behaviour to diabetes medication and cues of action.
    RESULTS: A total of twenty-one diabetes patients between the ages 35-67 years with physical disability (P1-P21) were interviewed. The cohort of participants was dominated by males (n = 12) and also distribution pattern showed majority of participants were Malay (n = 10), followed by Chinese (n = 7) and rest Indians (n = 4). When the participants were asked in their opinion what was the preferred method of recording blood glucose tests, several participants from low socioeconomic status and either divorced or widowed denied to adapt telemonitoring instead preferred to record manually. There were mixed responses about the barriers to control diet/calories. Even patients with high economic status, middle age 35-50 and diabetes history of 5-10 years were influenced towards alternative treatments.
    CONCLUSIONS: Study concluded that patients with physical disability required extensive care and effective strategies to control glucose metabolism.
    CONCLUSIONS: This study explores the patients\' perspectives regarding treatment management with physical disability.
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  • 文章类型: Journal Article
    BACKGROUND: Disability is a key indicator implicating both overall morbidity and success of public health efforts to compress the period of morbidity among geriatrics for the overall population. Disabilities are more prevalent among diabetics than among those without diabetes.
    OBJECTIVE: This study aimed to determine self-monitoring practices, awareness to dietary modifications and barriers to medication adherence among physically disabled type 2 diabetes mellitus patients.
    METHODS: Interview sessions were conducted at diabetes clinic - Penang general hospital. The invited participants represented three major ethnic groups of Malaysia (Malay, Chinese & Indians). An openended approach was used to elicit answers from participants. Interview questions were related to participant\'s perception towards self-monitoring blood glucose practices, Awareness towards diet management, behaviour to diabetes medication and cues of action.
    RESULTS: A total of twenty-one diabetes patients between the ages 35 - 67 years with physical disability (P1-P21) were interviewed. The cohort of participants was dominated by Males (n=12) and also distribution pattern showed that majority of participants were Malay (n=10), followed by Chinese (n=7) and rest Indians (n=4). When the participants were asked in their opinion what was the preferred method of recording blood glucose tests, several participants from low socioeconomic status and either divorced or widowed denied to adapt telemontoring instead preferred to record manually. There were mixed responses about the barriers to control diet/calories. Even patients with high economic status, middle age 35-50 and diabetes history of 5-10 years were influenced towards alternative treatments.
    CONCLUSIONS: Study concluded that patients with physical disability required extensive care and effective strategies to control glucose metabolism.
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