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镰状细胞病:英国成年人研究中的疼痛、应对方式与生活质量

Sickle cell disease: Pain, coping and quality of life in a study of adults in the UK.

作者信息

Anie Kofi A., Steptoe Andrew, Bevan David H.

机构信息

Imperial College School of Medicine, Brent Sickle Cell and Thalassaemia Centre/Department of Haematology, Central Middlesex Hospital, London, UK.

出版信息

Br J Health Psychol. 2002 Sep;7(Part 3):331-344. doi: 10.1348/135910702760213715.

Abstract

OBJECTIVE

To examine the relationship between pain, coping, and quality of life in adult patients with sickle cell disease (SCD) in the UK, and to assess the influence of these factors on the utilization of health services. DESIGN: This cross-sectional study involved 96 adult patients with SCD attending hospitals in London. METHOD: Interview and questionnaire study involving standard measures of pain, health service utilization, coping responses (measured with the Coping Strategies Questionnaire - revised for SCD), and quality of life (measured by the SF36). Data concerning clinical history, complications and haemoglobin levels were also collected. RESULTS: The number and duration of painful sickle cell episodes in the past 12 months varied widely between patients. We found that 49.5% of accident and emergency visits and 45% of hospitalizations were of 10.4% (10) patients. Pain experience accounted for 12.3% of hospital and general practice service use, independently of age, sex, number of SCD complications and haemoglobin levels. Three higher order factors emerged from analysis of the coping strategies questionnaire, reflecting active behavioural and cognitive coping, affecting coping, and passive adherence (e.g. resting, taking fluids). Active coping was positively associated with the number of pain episodes, while passive adherence coping was related to pain intensity. Psychological coping was unrelated to health service utilization. Marked impairment on many dimensions of quality of life was apparent in the analyses of the SF36. Affective coping was associated with impaired quality of life independently of demographic and clinical variables. CONCLUSIONS: It is evident that sickle cell disease involves not only severe recurrent pain, but also other impairments in health-related quality of life. Psychological coping patterns are relevant both to the experience of pain, and to broader adjustment. Patients may benefit from interventions that enhance the use of appropriate pain coping techniques and other strategies to improve quality of life.

摘要

目的

研究英国成年镰状细胞病(SCD)患者疼痛、应对方式与生活质量之间的关系,并评估这些因素对医疗服务利用的影响。设计:这项横断面研究纳入了96名在伦敦医院就诊的成年SCD患者。方法:采用访谈和问卷调查,涉及疼痛、医疗服务利用、应对反应(使用针对SCD修订的应对策略问卷进行测量)和生活质量(通过SF36进行测量)的标准指标。还收集了有关临床病史、并发症和血红蛋白水平的数据。结果:过去12个月中,患者镰状细胞疼痛发作的次数和持续时间差异很大。我们发现,49.5%的急诊就诊和45%的住院是由10.4%(10名)患者导致的。疼痛经历占医院和全科医疗服务使用的12.3%,与年龄、性别、SCD并发症数量和血红蛋白水平无关。应对策略问卷分析得出三个高阶因素,反映了积极的行为和认知应对、情感应对以及被动依从(如休息、补充液体)。积极应对与疼痛发作次数呈正相关,而被动依从应对与疼痛强度相关。心理应对与医疗服务利用无关。SF36分析显示,生活质量的许多维度存在明显损害。情感应对与生活质量受损相关,与人口统计学和临床变量无关。结论:显然,镰状细胞病不仅涉及严重的复发性疼痛,还涉及与健康相关生活质量的其他损害。心理应对模式与疼痛体验以及更广泛的适应都相关。患者可能会从增强使用适当疼痛应对技巧和其他改善生活质量策略的干预措施中受益。

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