为重症患者开发并试行以患者为导向的出院摘要。

Anmol Shahid, Bonnie Sept, Shelly Kupsch, Rebecca Brundin-Mather, Danijela Piskulic, Andrea Soo, Christopher Grant, Jeanna Parsons Leigh, Kirsten M Fiest, Henry T Stelfox
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引用次数: 0

摘要

背景:离开重症监护病房(ICU)的患者往往会因出院沟通不足而在护理方面出现缺失,使他们容易受到更多压力、不良事件、再次入住重症监护病房以及死亡的影响。为了促进出院沟通,我们采用了书面总结的方式,为患者及其家属提供有关药物、活动和饮食限制、复诊预约、预期症状以及如有疑问应致电谁等方面的信息。虽然为患者及其家属提供的书面出院摘要在外科、康复科和儿科环境中经常使用,但在重症监护病房环境中却很少使用。目的:开发重症监护病房专用的以患者为导向的出院摘要工具(PODS-ICU),并对该工具进行试点测试,以确定其可接受性和可行性:方法:患者伙伴(即有 ICU 患者生活经历的个人或 ICU 患者家属)、ICU 临床医生(即医生、护士)和研究人员会聚一堂,讨论 ICU 患者的特定信息需求,并通过多次讨论和反复修改设计出 PODS-ICU。研究小组的护士在加拿大卡尔加里的两家重症监护病房与患者和家属一起试用了 PODS-ICU。对患者、家属参与者和 ICU 护士进行了关于 PODS-ICU 及其对出院影响的后续调查:结果:大多数参与者认为他们从重症监护室出院的情况良好或更好(n = 13;87.0%),一些参与者(n = 9;60.0%)表示很好地理解了病人住重症监护室的原因。大多数参与者(n = 12;80.0%)表示,他们了解重症监护室事件及其对患者健康的影响。虽然许多患者和家属表示 PODS-ICU 信息丰富且有用,但 ICU 护士表示,由于 "时间限制",PODS-ICU 在他们的日常临床工作流程中 "并不合理":PODS-ICU 工具为从重症监护室出院的患者及其家属提供了重要信息。该工具有可能让患者及其家属参与进来,并增强他们的能力,以确保 ICU 出院后护理的连续性。不过,PODS-ICU 需要与早期出院实践配对,并与电子临床信息系统整合,以更好地适应 ICU 护士的临床工作流程。需要在不同的重症监护环境中进一步完善和测试 PODS-ICU 工具,以更好地评估其可行性及其对患者健康结果的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development and pilot implementation of a patient-oriented discharge summary for critically Ill patients.

Development and pilot implementation of a patient-oriented discharge summary for critically Ill patients.

Development and pilot implementation of a patient-oriented discharge summary for critically Ill patients.

Development and pilot implementation of a patient-oriented discharge summary for critically Ill patients.

Background: Patients leaving the intensive care unit (ICU) often experience gaps in care due to deficiencies in discharge communication, leaving them vulnerable to increased stress, adverse events, readmission to ICU, and death. To facilitate discharge communication, written summaries have been implemented to provide patients and their families with information on medications, activity and diet restrictions, follow-up appointments, symptoms to expect, and who to call if there are questions. While written discharge summaries for patients and their families are utilized frequently in surgical, rehabilitation, and pediatric settings, few have been utilized in ICU settings.

Aim: To develop an ICU specific patient-oriented discharge summary tool (PODS-ICU), and pilot test the tool to determine acceptability and feasibility.

Methods: Patient-partners (i.e., individuals with lived experience as an ICU patient or family member of an ICU patient), ICU clinicians (i.e., physicians, nurses), and researchers met to discuss ICU patients' specific informational needs and design the PODS-ICU through several cycles of discussion and iterative revisions. Research team nurses piloted the PODS-ICU with patient and family participants in two ICUs in Calgary, Canada. Follow-up surveys on the PODS-ICU and its impact on discharge were administered to patients, family participants, and ICU nurses.

Results: Most participants felt that their discharge from the ICU was good or better (n = 13; 87.0%), and some (n = 9; 60.0%) participants reported a good understanding of why the patient was in ICU. Most participants (n = 12; 80.0%) reported that they understood ICU events and impacts on the patient's health. While many patients and family participants indicated the PODS-ICU was informative and useful, ICU nurses reported that the PODS-ICU was "not reasonable" in their daily clinical workflow due to "time constraint".

Conclusion: The PODS-ICU tool provides patients and their families with essential information as they discharge from the ICU. This tool has the potential to engage and empower patients and their families in ensuring continuity of care beyond ICU discharge. However, the PODS-ICU requires pairing with earlier discharge practices and integration with electronic clinical information systems to fit better into the clinical workflow for ICU nurses. Further refinement and testing of the PODS-ICU tool in diverse critical care settings is needed to better assess its feasibility and its effects on patient health outcomes.

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