"Personalized Fluid Administration Using an AFM System for Goal Directed Fluid Therapy on Postoperative Outcome in High-risk Patients Undergoing High-risk Abdominal Surgery: A Multicenter Stepped-wedge, Cluster-randomized Clinical Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,007
- 试验地点
- 37
- 主要终点
- Composite endpoint ("any event versus none") of major postoperative complications within 30 days after surgery
研究概览
简要总结
Goal directed fluid therapy (GDFT) or "Personalized fluid therapy" may benefit high-risk surgical patients but these strategies are infrequently implemented. It has also been shown that without any goal or protocol for fluid resuscitation, large inter- and intra-provider variability exist that have been correlated with poor patient outcomes.
Recently, an "Assisted Fluid Management" (AFM) system has been developed to help ease some of the work associated with GDFT protocol implementation. The AFM system may help increase GDFT protocol adherence while leaving direction and guidance in the hands of the care providers. This artificial intelligence-based system can suggest administration of fluid boluses, analyse the hemodynamic effects of the bolus, and continually re-assess the patient for further fluid requirements.
To date, there are no large outcome study using this AFM system. The primary objective of this trial is thus to evaluate the impact of this AFM system to guide fluid bolus administration on a composite of major postoperative complications in high-risk patients undergoing high-risk abdominal surgery.
详细描述
Many trials have indicated that goal-directed fluid therapy (GDFT) strategies or more recently "personalized fluid therapy" may benefit high-risk surgical patients but these strategies are infrequently implemented. It has also been shown that without any goal or protocol for fluid resuscitation, large inter- and intra-provider variability exist that have been correlated with poor patient outcomes. Even under ideal study conditions, strict adherence to GDFT protocols is hampered by the workload and concentration required for consistent implementation. Hemodynamic monitors and protocols alone do not enable optimal fluid titration to be provided consistently to all patients - there must also be appropriate and timely interpretation and intervention.
To address this problem of consistency and protocol adherence, a decision support system, "Assisted Fluid Management" (AFM), has been developed to help ease some of the work associated with GDFT protocol implementation. The AFM system (released on the European market in March 2017) may help increase GDFT protocol adherence while leaving direction and guidance in the hands of the care providers. This artificial intelligence-based system can suggest administration of fluid boluses, analyse the hemodynamic effects of the bolus, and continually re-assess the patient for further fluid requirements.
This system was recently implemented in a before-and-after study in a Belgian academic hospital, where the authors reported that the implementation of this AFM software system allowed a better adherence to the GDFT algorithm. However, as this was a pilot study with a small number of patients, the study was not powered to demonstrate a beneficial effect on the incidence of postoperative complications. More recently, a group from the Cleveland Clinic demonstrated that using AFM system resulted in more boluses being effective when compared to the administration of boluses without AFM support.
There are no randomized controlled studies to date comparing this AFM system to standard of care on patient outcome. We therefore aim to conduct a multicenter stepped-wedge, cluster-randomized trial involving patients undergoing high risk abdominal surgery to compare a GDFT strategy guided by the AFM system with usual care.
A stepped wedge, cluster-randomized trial approach was chosen in which clusters will be randomized to commence the intervention at different times following an initial control period in which outcomes will be measured for usual care.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
盲法说明
Outcome assessor will be blinded and a data monitoring willbe done on data
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Any adult patient (aged 18 years or older) admitted to the operating room for an elective high-risk abdominal surgery (both open and laparoscopically assisted).
- •Patients must fulfill at least one of the following high-risk criteria:
- •American Society of Anesthesiologists physical status > 2
- •classification exercise tolerance < 4 metabolic equivalents as defined by the guidelines of the American College of Cardiology/ American Heart Association
- •renal impairment (serum creatinine ≥1.3mg/dL or >115 mmol/l or estimated glomerular filtration rate < 90 mL/min/1.73 m2 within the last 6 months) or renal replacement therapy
- •coronary artery disease (any stage)
- •chronic heart failure (New York Heart Association Functional Classifcation ≥ II)
- •valvular heart disease (moderate or severe);
- •history of stroke
- •peripheral arterial occlusive disease (any stage)
- •chronic obstructive pulmonary disease (any stage) or pulmonary fibrosis (any stage)
- •diabetes mellitus requiring oral hypoglycemic agent or insulin; immunodeficiency due to a disease (e.g., HIV, leukemia, multiple myeloma, solid organ cancer) or therapy (e.g., immunosuppressants, chemotherapy, radiation, steroids)
- •liver cirrhosis (any Child-Pugh class)
- •-- body mass index ≥30 kg/m2
- •current smoking or 15 pack-year history of smoking
- •All participants must receive clear study information and give signed informed consent
排除标准
- •Patients with preoperative cardiac arrhythmias (atrial fibrillation) as the monitoring devices are not accurate under cardiac arrhythmias.
- •No affiliation with the French health care system
- •Patients participating in another randomized controlled trial with the same clinical endpoint, or interventions possibly compromising the primary outcome.
- •Pregnant patients
- •Patient on AME (state medical aid) (unless exemption from affiliation)
- •Patients guardianship/legal protection/curatorship
研究组 & 干预措施
Routine care
During the pre-implementation period, fluid therapy will be done as routine care.
Mean arterial pressure (MAP) will be maintained between 65-70 mmHg per standard of care
干预措施: Routine care (Procedure)
Assisted fluid management system
In the post-implementation period, fluid bolus administration will be guided by the AFM recommandation.
MAP will be maintained between 65-70 mmHg per standard of care
干预措施: AFM (Device)
结局指标
主要结局
Composite endpoint ("any event versus none") of major postoperative complications within 30 days after surgery
时间窗: Postoperative day 30
It includes : acute myocardial injury, including myocardial infarction, acute kidney injury, severe infectious complications (including deep surgical site infection, pneumonia, sepsis, peritonitis), anastomotic leakage, pulmonary embolism or venous thrombosis, pulmonary edema, acute respiratory distress syndrome, de novo arrhythmia, stroke, reoperation for any cause, non-fatal cardiac arrest, and mortality within 30 days after surgery
次要结局
- Comprehensive complication index (CCI)(Postoperative day 30)
- Incidence of each of the individual components of the composite primary outcome within 30 days after surgery(Postoperative day 30)
- Incidence of unplanned hospital re-admission within 30 days after surgery(Postoperative day 30)
- Incidence of the composite primary outcome within 7 days after surgery(Postoperative day 7)
- Incidence of a composite of postoperative infection rate within 30-day of surgery.(Postoperative day 30)
- Clavien-dindo classification score(Postoperative day 30)
- Length of stay in the hospital(Postoperative day 30)
- Mortality rate at 90 days after surgery.(Postoperative day 90)