Jean-Maxime Côté, William Beaubien-Souligny, Lauriane Hamel, Josée Bouchard
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We asked about their awareness and perceptions on how AKI should be disclosed and followed, the barriers encountered regarding the process of care following hospital discharge, and their level of comfort and expertise in offering dedicated post-AKI care. The survey integrated direct and scenario-based questions and was conducted from December 2022 to April 2023.</p><p><strong>Participants: </strong>We distributed the survey to practicing family physicians and nurse practitioners through the mailing list of the <i>Fédération des Médecins Omnipraticiens du Québec</i>, and the <i>Association des infirmières praticiennes spécialisées du Québec</i>, respectively. No incentives were provided.</p><p><strong>Methods: </strong>We conducted descriptive analyses and used chi-squared analysis to compare responses between family physicians and nurse practitioners and between hospital-based and cabinet-based practice.</p><p><strong>Results: </strong>The survey was opened by 779 potential participants. Of these, the response rate was 9% (70/779). Most participants were family physicians (79%) and dedicated 70% (±32) of their time in community outpatient clinics. Participants reported that 59% (±20) of all patients seen daily had at least 1 risk factor for AKI, whereas they estimated that 21% (±12) of recently discharged patients suffered from an AKI episode. The lack of awareness by the patient and lack of details on the discharge summary were the barriers most frequently reported impacting the overall process of care at follow-up. Most nurse practitioners (60%) and 33% of family physicians reported at least some levels of discomfort and lack of expertise when offering post-AKI.</p><p><strong>Limitations: </strong>The generalizability of our study is limited by its response rate. However, this is comparable with typical response rates seen in electronic surveys. The distribution was limited to a single province of Canada.</p><p><strong>Conclusions: </strong>We reported significant barriers regarding the hospital-to-community transition of care in patients who experienced AKI and the suboptimal comfort and expertise of primary care providers when offering dedicated post-AKI care. 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引用次数: 0
摘要
背景:急性肾损伤(AKI)患者出院后可能会受益于专门的护理。这些患者中的大多数将由初级保健提供者随访。目前还缺乏有关这些医疗服务提供者在提供 AKI 后护理时的做法和舒适度的数据:我们对执业护士和家庭医生进行了调查,以评估他们对 AKI 后护理的认识、看法、实践模式和舒适度:我们向魁北克省的临床医生发放了一份基于网络的自填式调查问卷。我们询问了他们对如何披露和跟踪 AKI 的认识和看法、出院后护理过程中遇到的障碍,以及他们在提供 AKI 后专门护理方面的舒适度和专业知识水平。调查综合了直接问题和情景问题,调查时间为 2022 年 12 月至 2023 年 4 月:我们分别通过魁北克全科医师联合会和魁北克专科护士协会的邮件列表向执业家庭医生和执业护士发放了调查问卷。没有提供任何奖励:我们进行了描述性分析,并使用卡方分析比较了家庭医生和执业护士之间以及医院执业和内阁执业之间的回复情况:779 名潜在参与者打开了调查问卷。其中,回复率为 9%(70/779)。大多数参与者是家庭医生(79%),70%(±32)的时间在社区门诊工作。参与者报告说,在每天接诊的所有患者中,59%(±20)的患者至少有一个导致 AKI 的危险因素,而他们估计最近出院的患者中有 21%(±12)的患者曾发生过 AKI。患者缺乏意识和出院摘要缺乏细节是影响随访护理整体流程的最常见障碍。大多数执业护士(60%)和 33% 的家庭医生表示,在提供 AKI 后护理时至少会有一定程度的不适和缺乏专业知识:我们研究的推广性受到了回复率的限制。然而,这与电子调查中的典型回复率相当。调查范围仅限于加拿大的一个省:我们报告了经历过 AKI 的患者在从医院到社区的护理过渡中遇到的重大障碍,以及初级医疗服务提供者在提供专门的 AKI 后护理时的舒适度和专业知识不够理想。这反映出需要加强与初级医疗服务提供者的沟通、合作和 AKI 培训。
Primary Care Providers Barriers, Comfort and Awareness in Follow-up Care of Acute Kidney Injury Patients: A Comprehensive Survey on Current Practices.
Background: Patients who experienced acute kidney injury (AKI) may benefit from dedicated care following hospital discharge. Most of these patients will be followed by primary care providers. There is a lack of data on current practices and comfort for these care providers when offering post-AKI care.
Objective: We surveyed nurse practitioners and family physicians to assess their awareness, perceptions, practice patterns and comfort regarding post-AKI care.
Design/setting: We distributed a web-based self-administered survey among clinicians from the Province of Quebec. We asked about their awareness and perceptions on how AKI should be disclosed and followed, the barriers encountered regarding the process of care following hospital discharge, and their level of comfort and expertise in offering dedicated post-AKI care. The survey integrated direct and scenario-based questions and was conducted from December 2022 to April 2023.
Participants: We distributed the survey to practicing family physicians and nurse practitioners through the mailing list of the Fédération des Médecins Omnipraticiens du Québec, and the Association des infirmières praticiennes spécialisées du Québec, respectively. No incentives were provided.
Methods: We conducted descriptive analyses and used chi-squared analysis to compare responses between family physicians and nurse practitioners and between hospital-based and cabinet-based practice.
Results: The survey was opened by 779 potential participants. Of these, the response rate was 9% (70/779). Most participants were family physicians (79%) and dedicated 70% (±32) of their time in community outpatient clinics. Participants reported that 59% (±20) of all patients seen daily had at least 1 risk factor for AKI, whereas they estimated that 21% (±12) of recently discharged patients suffered from an AKI episode. The lack of awareness by the patient and lack of details on the discharge summary were the barriers most frequently reported impacting the overall process of care at follow-up. Most nurse practitioners (60%) and 33% of family physicians reported at least some levels of discomfort and lack of expertise when offering post-AKI.
Limitations: The generalizability of our study is limited by its response rate. However, this is comparable with typical response rates seen in electronic surveys. The distribution was limited to a single province of Canada.
Conclusions: We reported significant barriers regarding the hospital-to-community transition of care in patients who experienced AKI and the suboptimal comfort and expertise of primary care providers when offering dedicated post-AKI care. This reflects the need to improve communication, collaboration, and AKI training with primary care providers.
期刊介绍:
Canadian Journal of Kidney Health and Disease, the official journal of the Canadian Society of Nephrology, is an open access, peer-reviewed online journal that encourages high quality submissions focused on clinical, translational and health services delivery research in the field of chronic kidney disease, dialysis, kidney transplantation and organ donation. Our mandate is to promote and advocate for kidney health as it impacts national and international communities. Basic science, translational studies and clinical studies will be peer reviewed and processed by an Editorial Board comprised of geographically diverse Canadian and international nephrologists, internists and allied health professionals; this Editorial Board is mandated to ensure highest quality publications.