fundamental nursing care

基础护理
  • 文章类型: Randomized Controlled Trial
    目的:评估常规护理加基本护理指南与仅对COVID-19住院患者的常规护理相比对患者体验的影响,护理质量,功能能力,治疗结果,护士道德困扰,患者健康相关的生活质量和成本效益。
    方法:平行双臂,整群随机对照试验。
    方法:在2021年1月18日至12月20日之间,我们招募了(i)18岁及以上患有COVID-19的成年人,不包括侵入性通风者,在英国医院信托基金住院至少三天或三个晚上;(ii)照顾他们的护士。我们随机分配医院使用基本护理指南和常规护理或仅常规护理。我们的患者报告的共同主要结果是护理问卷的关系方面和来自患者观点问卷的质量的四个量表。我们进行了意向治疗分析。
    结果:我们随机分为15组,招募了581名患者和418名护士参与者。主要结果数据可用于14个集群中的570-572名(98.1%-98.5%)患者参与者。我们没有发现任何患者的组间差异的证据,护士或经济结果。随着时间的推移,我们发现了组间的差异,赞成干预,对于我们五个共同主要结果中的三个,和一个主要患者的种族结局的显着相互作用(英国白人与其他)并分配组支持对“其他”种族亚组的干预。
    结论:与常规护理相比,我们没有发现基本护理指南的患者体验总体差异。我们有迹象表明,随着时间的推移,该指南可能有助于维持良好的实践,并对非白人英国患者的护理体验产生了更积极的影响。
    我们不建议在常规护理实践中全面实施我们的指南。进一步的干预发展,可行性,需要进行试点和评估研究。
    结论:基础护理驱动患者体验,但在大流行中受到严重影响。我们的指导方针并不优于常规护理,尽管它可以维持良好的实践,并对非白人英国患者的护理体验产生积极影响。
    CONSORTandCONSERVE.
    有COVID-19住院经历的患者参与了指南的制定和编写,试验管理和结果解释。
    OBJECTIVE: To evaluate the impact of usual care plus a fundamental nursing care guideline compared to usual care only for patients in hospital with COVID-19 on patient experience, care quality, functional ability, treatment outcomes, nurses\' moral distress, patient health-related quality of life and cost-effectiveness.
    METHODS: Parallel two-arm, cluster-level randomized controlled trial.
    METHODS: Between 18th January and 20th December 2021, we recruited (i) adults aged 18 years and over with COVID-19, excluding those invasively ventilated, admitted for at least three days or nights in UK Hospital Trusts; (ii) nurses caring for them. We randomly assigned hospitals to use a fundamental nursing care guideline and usual care or usual care only. Our patient-reported co-primary outcomes were the Relational Aspects of Care Questionnaire and four scales from the Quality from the Patient Perspective Questionnaire. We undertook intention-to-treat analyses.
    RESULTS: We randomized 15 clusters and recruited 581 patient and 418 nurse participants. Primary outcome data were available for 570-572 (98.1%-98.5%) patient participants in 14 clusters. We found no evidence of between-group differences on any patient, nurse or economic outcomes. We found between-group differences over time, in favour of the intervention, for three of our five co-primary outcomes, and a significant interaction on one primary patient outcome for ethnicity (white British vs. other) and allocated group in favour of the intervention for the \'other\' ethnicity subgroup.
    CONCLUSIONS: We did not detect an overall difference in patient experience for a fundamental nursing care guideline compared to usual care. We have indications the guideline may have aided sustaining good practice over time and had a more positive impact on non-white British patients\' experience of care.
    UNASSIGNED: We cannot recommend the wholescale implementation of our guideline into routine nursing practice. Further intervention development, feasibility, pilot and evaluation studies are required.
    CONCLUSIONS: Fundamental nursing care drives patient experience but is severely impacted in pandemics. Our guideline was not superior to usual care, albeit it may sustain good practice and have a positive impact on non-white British patients\' experience of care.
    UNASSIGNED: CONSORT and CONSERVE.
    UNASSIGNED: Patients with experience of hospitalization with COVID-19 were involved in guideline development and writing, trial management and interpretation of findings.
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  • 文章类型: Journal Article
    目的:由于肿瘤手术后的恢复时间可能很长,家庭照顾者通常在患者出院后的护理中发挥重要作用。为了让护理人员做好这个角色的准备,我们制定了家庭参与计划(FIP),以加强他们在住院期间积极参与肿瘤术后护理.这项定性研究的目的是探索家庭护理人员参与FIP的经验。
    方法:我们对参与家庭参与计划的12名家庭照顾者进行了半结构化访谈。该计划包括两个主要组成部分:(1)对医生和护士的培训和指导;(2)家庭护理人员积极参与基本护理活动。这种积极参与包括六项活动。使用解释现象学分析对数据进行分析。
    结果:家庭照顾者积极评价该计划。积极参加手术后护理是可以接受的负担。该计划使参与者能够简单地出现(“在那里”),这被认为是必不可少的,并提高了他们对护理的理解,虽然家庭照顾者有时会经历情绪激动的时刻。积极的参与加强了家庭照顾者与患者之间的关系。参与者认为临床监督。护士很重要。
    结论:亲密关系似乎是家庭参与计划的重要组成部分。它帮助护理人员感到他们为亲人的福祉做出了有意义的贡献。要求家庭参与肿瘤术后护理的基本护理活动是可以接受的,也不要对护理人员要求过高。
    OBJECTIVE: As recovery time after oncological surgery can be long, family caregivers often play an important role in the delivery of care after patients\' discharge. To prepare carers for this role, we developed a family involvement program (FIP) to enhance their active involvement in post-surgical oncology care during hospitalization. The purpose of this qualitative study was to explore family caregivers experience of participating in a FIP.
    METHODS: We conducted semi-structured interviews with 12 family caregivers who participated in the family involvement program. The program is comprised of two main components (1) training and coaching of physicians and nurses; (2) active involvement of family caregivers in fundamental care activities. This active involvement included six activities. Data were analyzed using interpretative phenomenological analysis.
    RESULTS: Family caregivers positively valued the program. Active participation in post-surgical care was experienced as an acceptable burden. The program gave participants the ability to simply be present (\'being there\') which was considered as essential and improved their understanding of care, although family caregivers sometimes experienced emotional moments. Active involvement strengthened existent relationship between the family caregiver and the patient. Participants thought clinical supervision. by nurses is important.
    CONCLUSIONS: Physical proximity appeared as an essential part of the family involvement program. It helped carers to feel they made a meaningful contribution to their loved ones\' wellbeing. Asking families to participate in fundamental care activities in post-surgical oncology care was acceptable, and not over-demanding for caregivers.
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