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临床试验/NCT03968120
NCT03968120已完成不适用

Effect of Lung Protective One-lung Ventilation With Fix and Variable Positive End-expiratory Pressure (PEEP) on Oxygenation and Outcome: Randomized, Controlled Trial

University of Debrecen2 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2018年2月1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
140
试验地点
2
主要终点
Intraoperative oxygenation

研究概览

简要总结

During One-lung ventilation, the use of lower tidal volumes (VT) is helpful to avoid over-distension, provide sufficient oxygenation, but can result in increased atelectasis.

Nevertheless, it is not known if, during one-lung ventilation with constant low VT, moderate levels of PEEP combined with lung recruitment maneuvers are superior to variable PEEP for intraoperative oxygenation and protection against PPCs.

Aim of the study is to compare a strategy using constant tidal volume with recruitment maneuvers versus variable PEEP with recruitment maneuvers during thoracic surgery in adults.

The investigators hypothesize that in adult, non-obese patients undergoing thoracic surgery under standardized OLV with variable PEEP and recruitment maneuvers as compared to constant PEEP without recruitment maneuvers prevent PPCs.

Patients will be randomly assigned to one of two groups:

FIX PEEP VOLUME GROUP (Groupfix): mechanical ventilation with constant (6 ml/kgIBW) tidal volume and PEEP of 5 cmH2O with recruitment maneuvers

VARIABLE PEEP GROUP (Groupvar): mechanical ventilation with constant (6 ml/kgIBW) tidal volume with variable PEEP with recruitment maneuvers.

详细描述

Lung separation will be performed by DLT technique. Mechanical ventilation will be applied in volume-controlled mode. During two-lung ventilation, VT will be set at 8 mL/kg predicted body weight. During one-lung ventilation, in GroupFix VT will be decreased to 6 mL/kg PBW with 5 cmH2O PEEP.

In GroupVar VT mechanical ventilation with constant (6 ml/kgIBW) tidal volume with variable PEEP with recruitment maneuvers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

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

  • Patient scheduled for open thoracic or video-assisted thoracoscopic surgery under general anesthesia requiring OLV (no emergency surgery)
  • BMI < 35 kg/m2
  • Age ≥ 18 years
  • Expected duration of surgery > 60 min
  • Expected duration of anesthesia > 90 min

排除标准

  • COPD GOLD 3+4, lung fibrosis, documented bullae, severe emphysema, pneumothorax
  • uncontrolled asthma
  • NYHA 3+4, CCS 3+4
  • previous thoracic surgery
  • ARDS (Berlin definition)
  • documented pulmonary arterial hypertension > 40 mmHg syst
  • documented or suspected neuromuscular disease (thymoma, myasthenia)
  • planned mechanical ventilation after surgery
  • bilateral procedures
  • lung separation with other method than DLT (eg diff. airway, trachestomy)
  • surgery in prone position
  • persistent hemodynamic instability, intractable shock
  • intracranial injury or tumor
  • enrollment in other interventional study or refusal of informed consent
  • pregnancy (excluded by anamnesis and/or laboratory analysis)

结局指标

主要结局

Intraoperative oxygenation

时间窗: 1 day

PaO2 \< 60 mmHg

次要结局

  • Postoperative pulmonary complications(90 days)
  • 30 day survival/mortality(30 days)
  • Postoperative oxygenation(90 days)
  • 90 day survival/mortality(90 days)
  • Postoperative extra-pulmonary complications(90 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tamas Vegh, MD

Head, Division General, Vascular and Thoracic Anaesthesia

University of Debrecen

研究点 (2)

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