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Anxiety, depression and quality of life in a group of rheumatic patients after joining a web-based self-help community

机译:加入基于网络的自助社区后,一组风湿病患者的焦虑,抑郁和生活质量

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Introduction: Rheumatic diseases are common chronic conditions that can have a profound influence on both physical and mental health of the patients. Internet-based self-help groups are very popular among chronic patients, as a substitute of classic face-to-face self-help groups.Objective: To investigate the possibility that joining an internet-based patient group can positively affect the general and mental health of rheumatic patients.Results: We administered four different questionnaires to 34 rheumatic patients before and after joining an italian web-based self-help community. Joining the community led to a significant improvement in general health measures and in levels of anxiety and depression.Conclusions: Participating in a web-based patient community can positively affect quality of life and mental health of rheumatic patients. Introduction Rheumatic diseases are chronic conditions that can have a profound influence on the psychological status of the patient. Depression is at least two times more common in rheumatic patients than in general population 1 and it’s estimated that major depressive disorder affects between 13% and 17% of patients with rheumatoid arthritis 23. In common with other painful conditions, depression associated with rheumatoid arthritis is often considered to result from the experience of chronic pain 4, and pain have a predictive value in the risk of developing depression 5. On the opposite, depression can affect pain perception 6 and the general clinical course of the disease 7. Other factors leading to depression are degree of physical disability 8, disease activity 9, and duration of disease 10. Also anxiety have been studied in rheumatic patients. Levels of anxiety are elevated in rheumatic patients and often coexist with depression 11, infact those with rheumatoid arthritis have a 4-fold probability to suffer from anxiety disorders than control 12. Patients And Methods PatientsFor the present study 34 rheumatic patients with different diseases (RA, spondyloarthritis, SLE, other connectivitis, vasculitis) were recruited thanks to the collaboration with the italian patient association ReumAmici. This association owns a website that patients can join and therefore participate in the community activities, especially in communicating through a patient web forum. QuestionnairesFour different questionnaires exploring physical and mental health were administered to all patients at time 0 (before joining the website) and after 3 months of active and continuous participation to the community activities: SF-36, HAQ, Zung self-rated anxiety scale and Zung self-rated depression scale. All the questionnaires were submitted by email and self-reported by the patients.SF-36 questionnaire 13 was used to evaluate the Quality of Life (QoL) of the patients. This survey contains 36 questions that evaluate eight health domains in both physical health and mental health. These eight domains are physical functioning (PF, ten items), social functioning (SF, two items), role limitations caused by physical problems (RP, four items), role limitation caused by emotional problems (RE, three items), mental health (MH, five items), energy and vitality (VT, four items), pain (BP, two items), and general perception of health (GH, five items). For each item score are collected and transformed to a scale from 0 (worst possible health state) to 100 (best possible health state). The italian form of SF-36 questionnaire was used 14. HAQ questionnaire 15 was used to assess physical function of the patients. This questionnaire was developed as a comprehensive measure of outcome in patients with a wide variety of rheumatic diseases including RA, osteoarthritis, SLE, ankylosing spondylitis, fibromyalgia and psoriatic arthritis. The HAQ contains 20 items distributed across 8 components. The scores for each item range from 0 (without any difficulty) to 3 (unable to do). The highest score on any item within one component represent the dim
机译:简介:风湿病是常见的慢性病,​​会对患者的身心健康产生深远影响。基于Internet的自助小组在慢性患者中非常流行,可以代替经典的面对面自助小组。目的:研究加入基于Internet的自助小组可以对普通和心理患者产生积极影响的可能性结果:在加入意大利基于网络的自助社区之前和之后,我们对34名风湿病患者进行了四种不同的问卷调查。加入社区导致总体卫生措施以及焦虑和抑郁水平得到显着改善。结论:参加基于网络的患者社区可以积极影响风湿病患者的生活质量和心理健康。简介风湿性疾病是慢性病,会对患者的心理状况产生深远影响。在风湿病患者中,抑郁症的发病率至少是普通人群1的两倍。据估计,主要抑郁症影响的类风湿关节炎患者为13%至17%。与其他痛苦状况一样,与风湿性关节炎相关的抑郁症是通常被认为是由于慢性疼痛4而引起的,并且疼痛对于患抑郁症的风险具有预测价值。5相反,抑郁症可以影响疼痛感6以及疾病的一般临床过程7。抑郁症是身体残疾的程度8,疾病活动9和疾病持续时间10。风湿病患者还研究了焦虑症。风湿病患者的焦虑水平升高,通常与抑郁症共存11。事实上,类风湿关节炎患者患焦虑症的几率是对照组12的四倍。患者和方法患者对于本研究,34名风湿病患者患有不同的疾病(RA由于与意大利患者协会ReumAmici的合作,招募了脊柱关节炎,SLE,其他结缔组织炎,血管炎)。该协会拥有一个网站,患者可以参加,因此可以参与社区活动,尤其是通过患者网络论坛进行交流。问卷调查在0时(加入网站之前)以及在连续3个月积极连续参与社区活动后,向所有患者发放了四份调查问卷,探讨身体和精神健康状况:SF-36,HAQ,Zung自评焦虑量表和Zung自评抑郁量表。所有问卷通过电子邮件提交并由患者自行报告。SF-36问卷13用于评估患者的生活质量(QoL)。这项调查包含36个问题,评估了身体健康和心理健康的八个健康领域。这八个领域是身体机能(PF,十项),社会功能(SF,二项),由身体问题引起的角色限制(RP,四项),由情绪问题引起的角色限制(RE,三项),心理健康(MH,五项),精力和活力(VT,四项),疼痛(血压,两项)和一般健康状况(GH,五项)。收集每个项目的分数并将其转换为从0(最糟糕的健康状态)到100(最佳可能的健康状态)的等级。使用意大利形式的SF-36问卷14。使用HAQ问卷15评估患者的身体功能。编制此调查表是对患有多种风湿性疾病(包括RA,骨关节炎,SLE,强直性脊柱炎,纤维肌痛和牛皮癣关节炎)的患者的结局进行的全面评估。 HAQ包含20个项目,分布在8个组件中。每个项目的分数范围从0(没有任何难度)到3(无法做到)。一个组成部分内任何一项的最高分代表暗淡

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