慢性肾脏疾病患者:与经验健康状况和生活满意度相关的背景因素

IF 1.8 Q3 HEALTH CARE SCIENCES & SERVICES
Patient Related Outcome Measures Pub Date : 2024-11-28 eCollection Date: 2024-01-01 DOI:10.2147/PROM.S475723
Mari Pesonen, Aino Vesikansa, Juha Mehtälä, Maria Grönman, Maarit Heinimäki, Sari Högström, Päivi Schenk
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引用次数: 0

摘要

目的:慢性肾脏疾病(CKD)的患病率正在增加,而CKD往往未得到诊断和治疗,直到其晚期发生不可逆转的损害。据报道,CKD患者的生活质量低于一般人群,但芬兰患者报告的CKD患者结局数据有限。患者和方法:这项结构性、多项选择调查研究的主要结果是评估芬兰CKD患者的生活满意度和健康状况。结果以数字(n)和百分比(%)表示。次要结局是使用基于预选反应变量的k均值聚类方法确定患者组,并评估相关背景因素。结果:共有558名CKD患者响应了电子调查。在完成整个调查的395名患者中,39.7%的人报告他们的健康状况为良好、相当好或极好,59.9%的人对他们的生活感到一般或非常满意。根据患者的健康状况和生活满意度,可以确定两类患者:(1)较差的患者和(2)较好的患者。与健康状况较好的患者相比,健康状况较差的患者更有可能患有至少3种合并症(66.8%对44.3%),并且完全缺乏随访(10.5%对1.9%)。与健康状况较好的患者相比,健康状况较差的患者对疾病、病因(35.5%对48.1%)及其护理(30.7%对20.3%)的了解程度较低,并且他们对生活方式干预(如遵循饮食指导)的依从性较弱(30.3%对40.5%)。结论:对CKD进行筛查以实现早期诊断,早期承诺治疗,并通过提供教育来增强患者的能力是改善CKD患者健康和生活满意度的关键。因此,应将资源分配给这些行动措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patients with Chronic Kidney Disease: Background Factors Associated with Experienced Health Status and Life Satisfaction.

Purpose: The prevalence of chronic kidney disease (CKD) is increasing and CKD often goes undiagnosed and untreated until its later stages when irreversible damage has occurred. Patients with CKD have been reported to have lower quality of life than the general population, but the patient-reported outcome data on CKD patients in Finland are limited.

Patients and methods: The primary outcome of this structural, multiple-choice survey study was to assess life satisfaction and experienced health status in Finnish patients with CKD. The results were presented as numbers (n) and percentages (%). The secondary outcome was to identify patient groups using the K-means clustering method based on preselected response variables and to assess the associated background factors.

Results: In total, 558 patients with CKD responded to the electronic survey. Of the 395 patients who completed the whole survey, 39.7% reported their health status as good, pretty good, or excellent, and 59.9% were fairly or very satisfied with their life. Two clusters of patients could be identified based on their health status and life satisfaction: patients with (1) poorer or (2) better well-being. Patients with poorer well-being were more likely to have at least 3 comorbidities (66.8% vs 44.3%) and lack follow-up visits entirely (10.5% vs 1.9%), compared with patients with better well-being. The patients with poorer well-being were less often knowledgeable about the disease, its causes (35.5% vs 48.1%), and its care (30.7% vs 20.3%) than patients with better well-being, and they showed weaker adherence to lifestyle interventions such as following dietary instructions (30.3% vs 40.5%).

Conclusion: Screening for CKD to enable early diagnosis, early commitment to treatment, and empowering the patient by providing education are key for improvement of health and life satisfaction in patients with CKD. Therefore, resources should be allocated to these measures of action.

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Patient Related Outcome Measures
Patient Related Outcome Measures HEALTH CARE SCIENCES & SERVICES-
自引率
4.80%
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27
审稿时长
16 weeks
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