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An exploration of patient-reported symptoms in systemic lupus erythematosus and the relationship to health-related quality of life

机译:探索患者报告的系统性红斑狼疮症状及其与健康相关的生活质量的关系

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Objective: The aim of this study was to explore the most distressing symptoms of systemic lupus erythematosus (SLE) and determine how these relate to health-related quality of life (HRQoL), anxiety/depression, patient demographics, and disease characteristics (duration, activity, organ damage). Methods: In a cross-sectional study, patients with SLE (n = 324, age 18-84 years) gave written responses regarding which SLE-related symptoms they experienced as most difficult. Their responses were categorized.Within each category, patients reporting a specific symptom were compared with non-reporters and analysed for patient demographics, disease duration, and results from the following questionnaires: the Medical Outcomes Study 36-item Short Form Health Survey (SF-36), the Hospital Anxiety and Depression Scale (HADS), the Systemic Lupus Activity Measure (SLAM), the SLE Disease Activity Index (SLEDAI), and the Systemic Lupus International Collaboration Clinics/American College of Rheumatology (SLICC/ACR) damage index. Results: Twenty-three symptom categories were identified. Fatigue (51%), pain (50%), and musculoskeletal distress (46%) were most frequently reported. Compared with non-reporters, only patients reporting fatigue showed a statistically significant impact on both mental and physical components of HRQoL. Patients with no present symptoms (10%) had higher HRQoL (p < 0.001) and lower levels of depression (p < 0.001), anxiety (p < 0.01), and disease activity (SLAM) (p < 0.001). Conclusion: Fatigue, pain, or musculoskeletal distress dominated the reported symptoms in approximately half of the patients. Only patients reporting fatigue scored lower on both mental and physical aspects of HRQoL. Our results emphasize the need for further support and interventions to ease the symptom load and improve HRQoL in patients with SLE. Our findings further indicate that this need is particularly urgent for patients with symptoms of pain or fatigue.
机译:目的:本研究旨在探讨系统性红斑狼疮(SLE)最令人困扰的症状,并确定这些症状与健康相关的生活质量(HRQoL),焦虑/抑郁,患者人口统计学特征以及疾病特征(持续时间,活动,器官损伤)。方法:在一项横断面研究中,SLE患者(n = 324,年龄18-84岁)给出了书面回答,说明他们经历了最困难的与SLE相关的症状。在每个类别中,将报告特定症状的患者与未报告患者进行比较,并分析患者的人口统计学特征,疾病持续时间以及以下调查表的结果:医学成果研究36项简短健康调查(SF- 36),医院焦虑和抑郁量表(HADS),系统性狼疮活动量度(SLAM),SLE疾病活动指数(SLEDAI)和系统性狼疮国际合作诊所/美国风湿病学院(SLICC / ACR)损伤指数。结果:鉴定了二十三个症状类别。疲劳(51%),疼痛(50%)和肌肉骨骼困扰(46%)的报道最多。与未报告者相比,只有报告疲劳的患者对HRQoL的精神和身体成分均显示出统计学显着的影响。没有症状(10%)的患者HRQoL较高(p <0.001),抑郁水平(p <0.001),焦虑(p <0.01)和疾病活动(SLAM)较低(p <0.001)。结论:在大约一半的患者中,疲劳,疼痛或肌肉骨骼困扰占主导。只有报告疲劳的患者在HRQoL的精神和身体方面得分较低。我们的结果强调需要进一步的支持和干预以减轻SLE患者的症状负荷并改善HRQoL。我们的发现进一步表明,对于有疼痛或疲劳症状的患者,这一需求尤为迫切。

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