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临床试验/NCT06733168
NCT06733168招募中不适用

The Impact of PEEP-guided Electrical Impedance Tomography on Oxygenation and Pulmonary Mechanics in Moderate-to-severe ARDS

Vietnam Military Medical University1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2024年8月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
76
试验地点
1
主要终点
Oxygenation

研究概览

简要总结

Acute respiratory distress syndrome (ARDS) in its moderate to severe forms is associated with high mortality. Mechanical ventilation (MV) remains the cornerstone of ARDS management but carries a significant risk of ventilator-induced lung injury (VILI). Positive end-expiratory pressure (PEEP), a fundamental component of MV, is widely utilized in clinical practice; however, optimal PEEP selection for patients with moderate to severe ARDS remains a complex and unresolved challenge. Electrical impedance tomography (EIT), a bedside imaging modality that evaluates regional ventilation distribution, offers a means of individualizing PEEP settings in mechanically ventilated patients. By balancing the competing risks of alveolar overdistension and collapse, EIT facilitates precision in PEEP titration. This study compares the impact of EIT-guided PEEP selection versus the conventional low FiO2-PEEP table on blood oxygenation and pulmonary mechanics.

详细描述

This is a prospective, single-center, randomized controlled trial designed to evaluate the effects of PEEP settings guided by electrical impedance tomography (EIT) on clinical outcomes in patients with moderate to severe ARDS undergoing lung-protective ventilation. Adult intubated patients with moderate to severe ARDS will be enrolled in the study.

Patients in the intervention group will receive PEEP titrated using EIT with a stepwise decremental PEEP trial, while those in the control group will have PEEP set based on the FiO2-PEEP table. Other ventilator parameters will be managed according to the ARDSnet protocol.

The primary outcomes are blood oxygenation and pulmonary mechanics. Secondary outcomes include 28-day mortality, ventilator-free and shock-free days at 28 days, length of ICU and hospital stay, rate of successful weaning, the proportion requiring rescue therapies, complications, respiratory variables, and the Sequential Organ Failure Assessment (SOFA) score.

Before initiating recruitment maneuver, all patients were placed on mechanical ventilation set according to the ARDS network strategy for 10 minutes, ensuring SpO2 of 88-95%, PaO2 of 55-80 mmHg, and a mean arterial pressure (MAP) ≥ 65 mmHg.

  • Patients received sedation and neuromuscular blockade to achieve full synchronization with the ventilator (RASS ≤ -3).
  • The mode was set to Pressure-Controlled Ventilation (PCV): ΔP = 15 cmH2O, which was maintained constant during the recruitment maneuver, while FiO2, PEEP, and respiratory rate were kept as previously set.
  • PEEP was incrementally increased by 5 cmH2O every minute: from 10 to 15, to 20, and finally to 25 cmH2O, with a maximum pressure limit of 40 cmH2O.
  • Following the recruitment maneuver at the final PEEP level, the process of identifying the optimal PEEP was initiated.
  • Then, PEEP will be set to 20 cmH2O and gradually decreased by 2 cmH2O every 30 seconds until it reached 6 cmH2O or SpO2 dropped to ≤ 80%.
  • Selection of optimal PEEP: The optimal PEEP was defined as the intersection point between the alveolar overdistension and collapse curves as measured by the EIT system.

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
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

  • Age ≥ 18 years.
  • Intubated moderate and severe ARDS according to the New Global Definition (PaO2/FiO2 ≤200 mmHg).
  • Used continuous sedation with or without paralysis.

排除标准

  • Presence of pneumothorax that is either undrained or newly occurred.
  • Unstable hemodynamics with a mean arterial pressure < 60 mmHg and unresponsive to resuscitation measures, and/or heart rate < 60 bpm.
  • Contraindications for EIT (pacemakers, automatic external defibrillators, cases of chest trauma or recent chest surgery limiting EIT belt application).
  • Pregnancy.
  • Severe neuromuscular disease.

结局指标

主要结局

Oxygenation

时间窗: at day 1, 2, 3, 4, 5, 6, 7

PaO2/FiO2 will be evaluated via arterial blood gas analysis every day during the first week treatment.

Pulmonary Mechanic

时间窗: at day 1, 2, 3, 4, 5, 6, 7

Static Compliance

次要结局

  • Ventilator free days(up to 28 days)
  • Length of ICU stay(up to 28 days)
  • Length of mechanical ventilated days(up to 28 days)
  • Pneumothorax or barotrauma(up to 28 days)
  • Rescue therapies(up to 7 days)
  • SOFA(at day 1, 3, 7)
  • Mortality(up to 2 months)

研究者

发起方
Vietnam Military Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Nguyen Dang Thu

PhD, MD

Vietnam Military Medical University

研究点 (1)

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