Workload burden

  • 文章类型: Journal Article
    COVID-19大流行及其社会限制加速了虚拟临床护理的扩展,据报道这是安全的,低成本和灵活。
    本研究旨在检查糖尿病患者的护理实践和患者对计划外护士主导的虚拟护理的满意度。
    对临床护士专家和患者进行了横断面描述性调查,使用活动日志进行护理实践,并对来电者进行满意度和支持调查。
    患者报告说,在接受虚拟护理后,患者对保持健康的满意度和更大的自信心。大多数来自患者的电话(74.8%)是为了咨询和教育。每个电话平均导致临床护士专家采取2.5次行动。
    该服务具有很高的价值和有效性,但增加了护士的工作量负担。
    UNASSIGNED: The COVID-19 pandemic and its social restrictions accelerated the expansion of virtual clinical care, and this has been reported to be safe, low cost and flexible.
    UNASSIGNED: This study aimed to examine nursing practices and patient satisfaction with unscheduled nurse-led virtual care for people with diabetes.
    UNASSIGNED: A cross-sectional descriptive survey of clinical nurse specialists and patients was carried out, using an activities log for nursing practices and a satisfaction and enablement survey for callers.
    UNASSIGNED: Patients reported high satisfaction levels and greater self-confidence in keeping themselves healthy after receiving virtual care. Most calls (74.8%) from patients were for advice and education. Each call led to an average of 2.5 actions for the clinical nurse specialist.
    UNASSIGNED: The service is highly valued and is effective, but adds to the nurse workload burden.
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  • 文章类型: Journal Article
    BACKGROUND: Although there has been growing research on the burden of treatment, the current state of evidence on measuring this concept is unknown. This scoping review aimed to provide an overview of the current state of knowledge as well as clear recommendations for future research, within the context of chronic disease.
    METHODS: Four health-based databases, Scopus, CINAHL, Medline, and PsychInfo, were comprehensively searched for peer-reviewed articles published between the periods of 2000-2016. Titles and abstracts were independently read by two authors. All discrepancies between the authors were resolved by a third author. Data was extracted using a standardized proforma and a comparison analysis was used in order to explore the key treatment burden measures and categorize them into three groups.
    RESULTS: Database searching identified 1458 potential papers. After removal of duplications, and irrelevant articles by title, 1102 abstracts remained. An additional 22 papers were added via snowball searching. In the end, 101 full papers were included in the review. A large number of the studies involved quantitative measures and conceptualizations of treatment burden (n = 64; 63.4%), and were conducted in North America (n = 49; 48.5%). There was significant variation in how the treatment burden experienced by those with chronic disease was operationalized and measured.
    CONCLUSIONS: Despite significant work, there is still much ground to cover to comprehensively measure treatment burden for chronic disease. Greater qualitative focus, more research with cultural and minority populations, a larger emphasis on longitudinal studies and the consideration of the potential effects of \"identity\" on treatment burden, should be considered.
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