Florence Nightingale Faculty of Nursing, Midwifery and Palliative Care, King's College London, London, United Kingdom.
Lane Fox Clinical Respiratory Physiology Research Centre, St Thomas' Hospital, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Crit Care Explor. 2024 Sep 10;6(9):e1146. doi: 10.1097/CCE.0000000000001146. eCollection 2024 Sep.
Increasing numbers of patients experience a prolonged stay in intensive care. Yet existing quality improvement (QI) tools used to improve safety and standardize care are not designed for their specific needs. This may result in missed opportunities for care and contribute to worse outcomes. Following an experience-based codesign process, our objective was to build consensus on the most important actionable processes of care for inclusion in a QI tool for adults with prolonged critical illness.
Items were identified from a previous systematic review and interviews with former patients, their care partners, and clinicians. Two rounds of an online modified Delphi survey were undertaken, and participants were asked to rate each item from 1 to 9 in terms of importance for effective care; where 1-3 was not important, 4-6 was important but not critical, and 7-9 was critically important for inclusion in the QI tool. A final consensus meeting was then moderated by an independent facilitator to further discuss and prioritize items.
Carried out in the United Kingdom.
PATIENTS/SUBJECTS: Former patients who experienced a stay of over 7 days in intensive care, their family members and ICU staff.
None.
We recruited 116 participants: 63 healthcare professionals (54%), 45 patients (39%), and eight relatives (7%), to Delphi round 1, and retained 91 (78%) in round 2. Of the 39 items initially identified, 32 were voted "critically important" for inclusion in the QI tool by more than 70% of Delphi participants. These were prioritized further in a consensus meeting with 15 ICU clinicians, four former patients and one family member, and the final QI tool contains 25 items, including promoting patient and family involvement in decisions, providing continuity of care, and structured ventilator weaning and rehabilitation.
Using experience-based codesign and rigorous consensus-building methods we identified important content for a QI tool for adults with prolonged critical illness. Work is underway to understand tool acceptability and optimum implementation strategies.
越来越多的患者在重症监护病房(ICU)中经历长时间的停留。然而,现有的用于提高安全性和标准化护理的质量改进(QI)工具并非专门针对他们的特定需求而设计。这可能导致错失护理机会,并导致更差的结果。在基于经验的共同设计过程之后,我们的目标是就成人重症疾病延长患者最重要的可操作护理流程达成共识,以便将其纳入成人重症疾病的 QI 工具。
项目从先前的系统评价和对前患者、其护理伙伴和临床医生的访谈中确定。进行了两轮在线修改 Delphi 调查,参与者被要求根据对有效护理的重要性对每项内容进行 1-9 分的评分;其中 1-3 分为不重要,4-6 分为重要但非关键,7-9 分为纳入 QI 工具的关键重要性。然后,由一位独立的主持人主持一次最终的共识会议,进一步讨论和确定优先级。
在英国进行。
患者/研究对象:在 ICU 中停留超过 7 天的前患者、他们的家庭成员和 ICU 工作人员。
无。
我们招募了 116 名参与者:63 名医疗保健专业人员(54%)、45 名患者(39%)和 8 名亲属(7%),参与了第一轮 Delphi 调查,并在第二轮中保留了 91 名(78%)。最初确定的 39 项内容中,有 32 项内容被 Delphi 参与者中的 70%以上投票认为“至关重要”,应纳入 QI 工具。在与 15 名 ICU 临床医生、4 名前患者和 1 名家属的共识会议上对这些内容进行了进一步的优先级排序,最终的 QI 工具包含 25 项内容,包括促进患者和家属参与决策、提供护理连续性以及结构化的呼吸机脱机和康复。
使用基于经验的共同设计和严格的共识建立方法,我们确定了成人重症疾病 QI 工具的重要内容。目前正在努力了解工具的可接受性和最佳实施策略。