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临床试验/NCT04487054
NCT04487054已完成不适用

Outcomes of Early Palliative Care Intervention for High-Risk Patients in the Intensive Care Unit- A Pilot Study

West Virginia University2 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2019年5月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
104
试验地点
2
主要终点
Length Of Stay (LOS) in the medical ICU

研究概览

简要总结

The investigators propose to conduct a feasibility study of identifying high-risk ICU patients using previously validated integrated prediction model and employing early palliative care intervention. The study will consist of two four-month time periods: usual care in time period one and usual care plus targeted pro-active palliative care intervention within 48 hours of ICU admission in time period two.

详细描述

The emerging challenge in critical care medicine focuses on improving patient- and family-centered outcomes. (1) The gold standard for patient-centered care is that which aligns with patients' values, preferences, and goals. (2) Palliative care consultants are known for utilizing shared decision making conversations in the intensive care unit (ICU) in which they elicit patients' values and goals. Accurate prognostic information based on the patient's overall condition sets the context for shared decision-making. With the gravity of the decisions made every day in the ICU, prognostic information is invaluable to patients, families, and clinicians. Historically, prognostic models in the ICU have focused on short-term mortality, such as death prior to hospital discharge, but studies have shown that information about post-ICU quality of life outcomes is important to patients and families as is information about survival for six months or more. Researchers have identified that future work in ICU prognostication must focus on accurately predicting the scope of patient-centered outcomes without losing sight of the higher mortality risk faced by ICU patients and survivors. The investigators propose to perform a proof of concept study based on our previously validated integrated prognostic model to identify medical ICU patients with high risk of mortality in six months and determine the utility of this model in terms of improving quality of life and quality of care. The study will consist of two 4-month time periods: usual care and usual care + targeted pro-active palliative care intervention within 48 hours of ICU admission, respectively. For both phases, the investigators will use the previously validated and published integrated prognostic model consisting of the 'surprise question' of "Would you be surprised if this patient died in the next six months?" with a response of "No", the APACHE IV score, and the Charlson Comorbidity Index (CCI) score to identify ICU patients within 24 hours of their ICU admission with a probability estimate of six-month mortality greater than 40 percent.

Six weeks after ICU discharge, we will contact the legal decision maker for the patient (family member or friend who is the medical power of attorney or healthcare surrogate) regarding their satisfaction with critical care services the patient received during the ICU stay. After obtaining verbal consent, questions will be asked from the modified Family Survey-ICU (FS-ICU) and the global performance measure #18 from the Bereaved Family Survey (BFS). The investigators hypothesize that the systematic identification of ICU patients at highest risk of six-month mortality as a prompt for a targeted pro-active palliative care approach will decrease length of ICU and hospital stay, reduce ICU readmissions, lead to earlier treatment limitation orders according to patients' wishes, and increase family satisfaction with the quality of care.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients greater than 18 years of age admitted to the medical ICU at West Virginia University Hospital.
  • Patients with a predicted six-month mortality greater than 40% on the integrated prognostic model.
  • Patients who live longer than 48 hours after medical ICU admission.

排除标准

  • Patient who did not meet inclusion criteria will be excluded.
  • Pregnant female/incarcerated patients will be excluded.
  • Since this is a study in an adult patient population, children will be excluded.

结局指标

主要结局

Length Of Stay (LOS) in the medical ICU

时间窗: From enrollment to Discharge from the ICU, an average of 24 weeks

Number of days subject was admitted to the medical ICU

Length Of Stay in hospital

时间窗: From enrollment to Discharge from the hospital, an average of 24 weeks

Number of total days subject was hospitalized

Medical ICU re-admission during the hospital stay

时间窗: From enrollment to discharge from the hospital, up to 16 weeks

Number of times a patient was re-admitted to the medical ICU

Treatment limitation orders within 48 hours of admission

时间窗: From enrollment to discharge from the hospital, an average of 24 weeks

Count of subjects that had or completed any treatment limitation orders (do-not-resuscitate, do-not-intubate, no vasopressors, etc) within 48 hours of admission

Family satisfaction with care in ICU

时间窗: From enrollment to six weeks post ICU discharge

Six-weeks post discharge, a telephone survey will be conducted with health care surrogate or medical power attorney to determine their satisfaction with the care received in ICU. 5 point scale with 1= very dissatisfied and 5= Completely Satisfied

Advance directive completion

时间窗: From enrollment to hospital discharge, an average of 24 weeks

Difference in completion rate of advance directives \[a written statement of a person's wishes regarding medical treatment\] between the baseline period (Standard of Care Patients) and following the intervention (Early Palliative Care Patients)

Physician Orders for Scope of Treatment (POST) form completion

时间窗: From enrollment to hospital discharge, an average of 24 weeks

Difference in completion rate of the Physician Orders for scope of Treatment (POST) form between the baseline period (Standard of Care Patients) and following the intervention (Early Palliative Care Patients)

Discharge Outcome Location-Home

时间窗: From enrollment to six weeks post ICU discharge

Difference in discharge outcome location from the baseline period (Standard of Care Patients) and following the intervention (Early Palliative Care Patients)

Discharge Outcome Location-Skilled Nursing Facility

时间窗: From enrollment to six weeks post ICU discharge

Difference in discharge outcome location from the baseline period (Standard of Care Patients) and following the intervention (Early Palliative Care Patients)

Discharge Outcome Location-LTACH

时间窗: From enrollment to six weeks post ICU discharge

Difference in discharge outcome location from the baseline period (Standard of Care Patients) and following the intervention (Early Palliative Care Patients)

Discharge outcomes-Death

时间窗: From enrollment to six weeks post ICU discharge

Difference in discharge outcome location from the baseline period (Standard of Care Patients) and following the intervention (Early Palliative Care Patients)

Site of death-ICU

时间窗: From enrollment to six weeks post ICU discharge

Count of subjects that passed in specific locations.

Site of death-Hospital

时间窗: From enrollment to six weeks post ICU discharge

Count of subjects that passed in specific locations.

Site of death-Home

时间窗: From enrollment to six weeks post ICU discharge

Count of subjects that passed in specific locations.

Site of death-Hospice

时间窗: From enrollment to six weeks post ICU discharge

Count of subjects that passed in specific locations.

Site of death-Skilled Nursing Facility

时间窗: From enrollment to six weeks post ICU discharge

Count of subjects that passed in specific locations.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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