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临床试验/NCT03753022
NCT03753022Unknown不适用

Effects of PEEP on Parameters of Tissue Perfusion and Clinical Outcomes After Coronary Artery Bypass Graft Surgery - a Randomized Clinical Trial

Federal University of São Paulo0 个研究点目标入组 125 人开始时间: 2012年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
125
主要终点
Pulmonary events

研究概览

简要总结

Pulmonary dysfunction is a condition inherent in cardiac surgery because of various interventions, such as general anesthesia, a median sternotomy, cardiopulmonary bypass and establishment of internal thoracic artery dissection.

In situations when there is a deterioration in oxygenation, increased positive pressure on the airways end pressure (PEEP) can be used as therapeutic mode by reversing severe hypoxemia resulting pulmonary shunt. But the use of PEEP has been associated to reduced cardiac output, due mainly to decrease systemic venous return consequent to increased intrathoracic pressure, and thus might reduce tissue oxygenation. Moreover, the increased transpulmonary gradient may also impair right ventricular ejection exacerbating the hemodynamic consequences in some patients, which in clinical practice this diagnosis may be difficult to perform.

In hypovolemic patients or those with cardiac changes may become even more pronounced, resulting in accentuation of low flow and systemic hypotension entailing changes in markers of tissue perfusion commonly measured by venous saturation central difference venoarterial carbon dioxide and lactate. The hypothesis of the investigators is that PEEP of 10 cmH2O and 15 cmH2O can be applied to reverse lung damage in patients in the immediate postoperative myocardial revascularization without repercussion tissue importantly in markers of tissue perfusion.

The objective is to evaluate the effects of different optimization levels of PEEP on gas exchange and influences the tissue perfusion after coronary artery bypass graft surgery.

详细描述

This is a prospective, randomized study and will be performed on patients who accept coronary artery bypass grafting with cardiopulmonary bypass, the conscious openness to participate in the study. Age, sex, body mass index (BMI), smoking habits, diagnosis, additional diseases, drugs used, surgery, intervention, peroperative supportive treatments, left ventricular ejection fraction, post operative blood and cardiopulmonary bypass (CPB) time (min), cross clamp time (min), duration of operation, postoperative extubation period, intensive care day of hospitalization, day of hospitalization will be recorded.The study was planned in 3 groups. Group G5 (control group: no changes will be made to the value of PEEP). Group G10 [after 30 minutes of admission (time 0) the PEEP will be raised to 10 cmH2O (time1) for 30 minutes and then returned to 5 cmH2O (time 2)]. Group G15 [after 30 minutes of admission (time 0) the PEEP will be raised to 15 cmH2O (time 1) for 30 minutes and then returned to 5 cm H2O (time 2)]. At each time of protocol (0, 1 and 2) will be collected: arterial blood gas measurements (partial pressure of arterial oxygen [PaO2] and partial pressure of carbon dioxide ([PaCO2]), the ratio between the partial oxygen pressure, inspired oxygen fraction (PaO2/FiO2) and pH. Also, will be performed parameters of tissue perfusion: central venous oxygen saturation ([SVO2]), arterial blood lactate, venoarterial CO2 difference ([Dif VA CO2]) and vital signs. In all other respects, treatment will follow the standard of care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • elective and isolated CABG, ejection fraction greater than 40%

排除标准

  • patients with a diagnosis of pulmonary disease, emergency surgery and mechanical ventilation prior to surgery.
  • Postoperative patients who had radiological abnormalities suggestive of pneumothorax, atrial or ventricular arrhythmias, electrical ischemic changes on ECG, pulse pressure variation of more than 13, hemodynamic instability characterized by mean arterial pressure less than 60 mmHg, nor epinephrine greater than 0.5 mcg/Kg/ min and the presence of increased bleeding through the drains (greater than 2 ml \ kg \ h) the protocol was discontinued and the patient excluded from the study.

研究组 & 干预措施

Group G10

Experimental

Patients submitted to CABG and peep 10

干预措施: Group G10 (Other)

Group G15

Experimental

Patients submitted to CABG and peep 15

干预措施: Group G15 (Other)

Group G5

Sham Comparator

Patients submitted to CABG and peep 5

干预措施: Group G5 (Other)

结局指标

主要结局

Pulmonary events

时间窗: Through study completion, an average of 24 hours after surgery

Pleural effusion was considered relevant when exceeding the phrenicocostal angle and fluid drainage was monitored hourly. Atelectasis was acknowledged when a clear atelectasis radiologic shadow exceeded 15 mm in width, with linear atelectasis

Arterial oxygenation

时间窗: Immediately after arrival at the intensive care unit until the end of protocol (around 5 hours)

arterial blood gas measurements (partial pressure of arterial oxygen \[PaO2\]

Tissue oxygenation

时间窗: Immediately after arrival at the intensive care unit until the end of protocol (around 5 hours)

(central venous oxygen saturation , arterial blood lactate and venoarterial CO2 difference

次要结局

  • Length of Hospital Stay(From the day of surgery up to Hospital discharge, maximum censoring at day 28 after surgery ])
  • Length of intensive care unit (ICU) stay(From the day of surgery up to ICU discharge, maximum censoring at day 28 after surgery ])
  • Duration of mechanical ventilation(Through study completion, an average of 24 hours after surgery)

研究者

发起方
Federal University of São Paulo
申办方类型
Other
责任方
Principal Investigator
主要研究者

Solange Guizilini

Principal Investigator

Federal University of São Paulo

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