Comparison of Pressure Support Ventilation and T-Piece as Spontaneous Breathing Trials Before Extubation Among Obese and Overweight Patients
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 100
- 试验地点
- 2
- 主要终点
- Successful extubation within 72 hours
研究概览
简要总结
This study aims to find out which method of spontaneous breathing trial (SBT) better helps overweight and obese ICU patients prepare for extubation, which is the removal of the breathing tube. The two methods being compared are pressure support ventilation (PSV) and the T-piece.
Participants are adults with a body mass index (BMI) of 25 or higher who have been on a breathing machine (invasive mechanical ventilation) for more than 24 hours. Before removing the breathing tube, participants will be randomly assigned to receive either a PSV or a T-piece trial for 1 hour. After that, doctors will decide if they are ready for extubation.
The main question this study wants to answer is: Which method leads to a higher rate of successful extubation-defined as not needing to be reintubated within 72 hours?
研究设计
- 研究类型
- Interventional
- 分配方式
- 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
- 否
入选标准
- •1. Patients had undergone intubation and mechanical ventilation for more than 24 hours prior to the first spontaneous breathing trial.
- •2. Adult patients aged ≥ 18 years.
- •BMI ≥ 25 kg/m².
- •Meeting all the Inter national Consensus Conference on weaning criteria:
- •Stable vital signs: heart rate < 140 beats/min, systolic blood pressure: 90-160 mmHg, and no use of vasopressors or use of minimal doses (<0.2 µg/kg per min).
- •Respiratory rate ≤ 35 breaths/min.
- •Adequate oxygenation, defined as either SpO2 > 90% with FiO2 ≤ 0.4, or PaO2/FiO2 > 150 mmHg with positive end-expiratory pressure (PEEP) ≤ 8 cmH2O.
- •Adequate cough strength (MIP < -20 cmH2O).
- •An awake state, defined as a score of Richmond Agitation-Sedation Scale between +1 and -2, or Glasgow Coma Scale >
- •No continuous sedation.
- •Informed consent provided by the patient or their relatives.
排除标准
- •Patients with tracheostomy.
- •Patients who had been admitted for traumatic brain injury.
- •Patients who had preexisting peripheral neuromuscular disease (underlying myopathy or myasthenia gravis).
- •Patients who had a do-not-reintubate order at the time of the initial spontaneous breathing trial were excluded
- •Patients who have already undergone a first spontaneous breathing trial.
- •Patients who had undergone extubation without an SBT
- •Protected populations: pregnant or breastfeeding women, individuals under guardianship, or those under legal protection.
- •Patients who refused to participate during the study.
结局指标
主要结局
Successful extubation within 72 hours
时间窗: Within 72 hours after extubation
Successful extubation within 72 hours
时间窗: Within 72 hours after extubation
次要结局
未报告次要终点