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首页> 外文期刊>The Journal of neuroscience nursing: journal of the American Association of Neuroscience Nurses >The Experience of a Neurocritical Care Admission and Discharge for Patients and Their Families: A Qualitative Analysis
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The Experience of a Neurocritical Care Admission and Discharge for Patients and Their Families: A Qualitative Analysis

机译:为患者及其家属提供神经关键护理录取和排放的经验:定性分析

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INTRODUCTION:A qualitative assessment of discharge resource needs is important for developing evidence-based care improvements in neurocritically ill patients.METHODS:We conducted a quality improvement initiative at an academic hospital and included all patients admitted to the neuroscience intensive care unit (ICU) during an 18-month period. Telephone assessments were made at 3 to 6 months after admission. Patients or caregivers were asked whether they had adequate resources upon discharge and whether they had any unanswered questions. The content of responses was reviewed by a neurointensivist and a neurocritical care nurse practitioner. A structured codebook was developed, organized into themes, and applied to the responses.RESULTS:Sixty-one patients or caregivers responded regarding access to resources at discharge with 114 individual codable responses. Responses centered around 5 themes with 23 unique codes: satisfied, needs improvement, dissatisfied, poor post-ICU care, and poor health. The most frequently coded responses were that caregivers believed their loved one had experienced an unclear discharge (n = 11) or premature discharge (n = 12). Two hundred four patients or caregivers responded regarding unanswered questions or additional comments at follow-up, with 516 codable responses. These centered around 6 themes with 26 unique codes: positive experience, negative experience, neutral experience, medical questions, ongoing medical care or concern, or remembrance of time spent in the ICU. The most frequent response was that caregivers or patients stated that they received good care (n = 115). Multiple concerns were brought up, including lack of follow-up after hospitalization (n = 15) and dissatisfaction with post-ICU care (n = 15).CONCLUSIONS:Obtaining qualitative responses after discharge provided insight into the transition from critical care. This could form the basis for an intervention to provide a smoother transition from the ICU to the outpatient setting.
机译:介绍:对储能资源需求的定性评估对于制定神经科病患者的循证护理改善至关重要。一个18个月的时间。录取后3至6个月进行电话评估。患者或护理人员被问到他们是否有足够的资源,以及他们是否有任何未答复的问题。由神经节目和神经关注护士从业者审查了响应的内容。制定了一个结构化的码本,组织成主题,并申请答复。结果:六十一名患者或护理人员在出院时响应了114个单独的可编码反应。响应围绕5个主题,有23个独特的代码:满意,需要改善,不满意,后ICU后差,健康状况不佳。最常见的响应是,护理人员认为他们所爱的人经历了不明确的排出(n = 11)或过早放电(n = 12)。有关未经答造的问题或随访的额外评论,有两百八名患者或护理人员,有516名可编码响应。这些以6个主题为中心,有26个独特的代码:积极经验,负面体验,中性经验,医疗问题,正在进行的医疗或担忧,或在ICU中所花费的时间纪念。最常见的反应是,护理人员或患者表示他们收到了良好的护理(n = 115)。提出了多次担忧,包括住院后缺乏随访(n = 15),并且对后ICU护理(n = 15)的不满意。结论:在卸货后获得定性响应,提供了对从关键护理的过渡的洞察力。这可以构成干预从ICU到门诊设置的更平滑转换的基础。

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