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心力衰竭患者的疾病感知、自我护理行为和生活质量:一项纵向问卷调查。

Illness perception, self-care behaviour and quality of life of heart failure patients: a longitudinal questionnaire survey.

机构信息

Royal Brompton & Harefield NHS Foundation Trust, London, UK.

出版信息

Int J Nurs Stud. 2013 Jul;50(7):945-53. doi: 10.1016/j.ijnurstu.2012.11.007. Epub 2012 Dec 1.

Abstract

OBJECTIVES

To examine the associations between illness perception, self-care behaviour, and quality of life in patients admitted to hospital with a primary diagnosis of heart failure (HF), and the changes in these at 2 and 6 months after discharge.

DESIGN

Longitudinal questionnaire-based study.

SETTING

Three London hospitals with specialist heart failure services.

PARTICIPANTS

A convenience sample of 88 patients (70% male, mean age 70) admitted to hospital with a primary diagnosis of heart failure were recruited prior to discharge. Participants were over the age of 18, able to understand English, and with the cognitive ability to complete the questionnaires. Thirty-eight patients did not provide follow-up data: 21 (24%) died during the 6-month follow-up period, and 17 (19%) did not return their post-discharge questionnaires.

METHODS

The Revised Illness Perception Questionnaire, the Self-Care Heart Failure Index, Hospital Anxiety and Depression scale, and the Minnesota Living with Heart Failure (MLHF) Questionnaires were completed prior to discharge from hospital, and 2 and 6 months after discharge.

RESULTS

HF symptoms improved over time (MLHF score co-efficient [95%CI] -0.915 [-1.581, -0.250], P<0.001). Patients appeared to believe that many of the causes of their illness were outside their control. Although self-care maintenance (e.g. weighing daily) improved over time, this did not translate into increased involvement in self-care management (e.g. adjusting diuretic dose) or the ability to act on changes in symptoms. Self-care confidence was lower in those who reported a more negative emotional impact of their illness, but was higher in those who had high scores on illness coherence.

CONCLUSIONS

Six months following hospital discharge, patients' symptom control had improved. Many continued to believe that their illness was outside their control, and although self-care maintenance improved this was not associated with greater self-care management, particularly if the patient's emotional state was negative, and their understanding of their condition was poor. Our data suggest that a more participative person-centred approach, tailoring the disease management programme to address the patient's illness beliefs and emotional state, assisting the individual to identify barriers and solutions, may help increase self-care confidence and management.

摘要

目的

探讨首发心力衰竭住院患者的疾病感知、自我护理行为与生活质量之间的相关性,以及出院后 2 个月和 6 个月时这些因素的变化。

设计

基于问卷调查的纵向研究。

地点

伦敦 3 家具有专科心力衰竭服务的医院。

参与者

在出院前招募了 88 例(70%为男性,平均年龄 70 岁)首发心力衰竭住院患者进行方便抽样。参与者年龄在 18 岁以上,能够理解英语,且具有完成问卷的认知能力。38 例患者未提供随访数据:21 例(24%)在 6 个月随访期间死亡,17 例(19%)未返回出院后调查问卷。

方法

在出院前、出院后 2 个月和 6 个月时,使用修订后的疾病感知问卷、自我护理心力衰竭指数、医院焦虑抑郁量表和明尼苏达州心力衰竭生活质量问卷进行评估。

结果

心力衰竭症状随时间改善(MLHF 评分系数[95%CI] -0.915 [-1.581, -0.250],P<0.001)。患者似乎认为许多疾病的病因都超出了他们的控制范围。尽管自我护理维持(如每天称重)随时间改善,但这并未转化为自我护理管理的增加(如调整利尿剂剂量)或对症状变化的应对能力。自我护理信心较低的患者报告疾病对情绪的负面影响更大,但疾病一致性得分较高的患者自我护理信心较高。

结论

出院后 6 个月,患者的症状控制有所改善。许多患者仍然认为自己的疾病无法控制,尽管自我护理维持有所改善,但这与自我护理管理的增加无关,尤其是当患者的情绪状态为负性时,且对病情的理解较差。我们的数据表明,采用更具参与性的以患者为中心的方法,根据患者的疾病信念和情绪状态调整疾病管理方案,帮助患者识别障碍和解决方案,可能有助于提高自我护理信心和管理水平。

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