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Improving the Patient Experience by Implementing an ICU Diary for Those at Risk of Post-intensive Care Syndrome

机译:通过为重症监护综合症风险患者实施ICU日记来改善患者体验

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摘要

The critical care literature in the US has recently brought attention to the impact an ICU experience can have long after the patient survives critical illness, particularly if delirium was present. Current recommendations to mitigate post-intensive care syndrome (PICS) are embedded in patient and family-centered care and aim to promote family presence in the ICU, provide support for decision-making, and enhance communication with the health-care team. Evidence-based interventions are few in number but include use of an ICU diary to minimize the psychological and emotional sequelae affecting patients and family members in the months following the ICU stay. In this paper we describe our efforts to implement an ICU diary and solicit feedback on its role in fostering teamwork and communication between patients, family members, and ICU staff. Next steps will involve a PICS follow-up clinic where trained staff will coordinate specialty referrals and perform long-term monitoring of mental health and other quality of life outcomes.
机译:最近,美国的重症监护文献引起了人们对重症患者幸存的ICU经历的影响的关注,特别是如果存在del妄。当前减轻重症监护综合症(PICS)的建议已嵌入以患者和家庭为中心的护理中,旨在促进家庭在ICU中的存在,为决策提供支持,并加强与医疗团队的沟通。以证据为基础的干预措施很少,但包括使用ICU日记以最大程度地减少在ICU住院后的几个月内影响患者和家庭成员的心理和情感后遗症。在本文中,我们描述了实施ICU日记的努力,并征求了其在促进患者,家庭成员和ICU员工之间的团队合作和沟通方面的作用的反馈。下一步将涉及PICS跟踪诊所,训练有素的工作人员将协调专科医生的转诊,并对精神健康和其他生活质量进行长期监测。

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