About this trial
The goal of this clinical trial is to learn whether a brief suction of the airway going to the surgical lung (bronchus) can help the lung collapse faster and more completely during uniportal video-assisted thoracoscopic surgery (UVATS). This type of surgery is performed through a small incision in the chest, and good lung collapse helps the surgeon see and work safely. The main questions it aims to answer are
1. Does brief bronchial suction improve the quality of lung collapse 1 minute after chest cavity is opened? 2. Does brief bronchial suction help reach satisfactory lung collapse faster?
Researchers will compare patients who receive brief bronchial suction and those who do not. This is to see if suction improves and fastens lung collapse, reduce the need for additional steps if lung is not adequately collapsed, affect inflammation, oxygenation, postoperative pulmonary complications, operative time, and the duration of one-lung ventilation. Participants will
1. Undergo UVATS under general anesthesia 2. Have a double-lumen breathing tube placed as part of the standard anesthetic care 3. Be randomly assigned to either receive bronchial suction for one minute or receive no bronchial suction 4. Have the surgical team assess the quality of lung collapse at different time points 5. Have blood samples taken for interleukin-6, a marker related to inflammation, once during and once after surgery. These samples are collected through a small tube in a vein that is placed as a standard anesthetic care while the participant is under general anesthesia. No extra puncture is required for blood collection. 6. Have information collected from the routine anesthesia and surgical records such as oxygen levels during surgery, length of surgery and lung-related complications within 7 days after surgery
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age ≥ 18 years old
BMI ≤ 35 kg/m2
American Society of Anesthesiologists (ASA) physical status I to III
Scheduled for elective single-port video-assisted thoracoscopic surgery (VATS) at Siriraj Hospital
Disqualifiers
Previous thoracic surgery
Known or suspected severe pleural adhesions based on preoperative imaging or clinical history
Tracheobronchial anatomical abnormalities
Pulmonary bullae identified on chest radiography or computed tomography, or a history of recurrent pneumothorax
Trial design
Parallel
Treatments tested in this trial
bronchial suction
Other interventionBronchial suction will be performed through the operative lumen of the double-lumen endobronchial tube on two occasions: before pleural opening, and immediately after pleural opening. The suction pressure is at -30 cmH2O and each suction period will last for 60 seconds.
Treatment groups
Trial outcomes
Primary outcomes
Quality of lung collapse at 1 minute after pleural opening
Surgical team to assess quality of lung collapse at 1 minute after pleural opening by using lung collapse score (LCS). The higher the LCS, the better the lung collapse.
Secondary outcomes
Quality of lung collapse at pleural opening, 5 minutes and 10 minutes after pleural opening
Quality of lung collapse assessed by the surgical team using the Lung Collapse Score (LCS) immediately after pleural opening, and at 5 minutes and 10 minutes after pleural opening.
Time to satisfactory lung collapse
Time from pleural opening to the first Lung Collapse Score (LCS) of 8 or greater
Requirement for rescue maneuvers for inadequate lung collapse
Need for additional intraoperative maneuvers to improve lung collapse due to inadequate surgical exposure
Change in interleukin-6 level from baseline to after one-lung ventilation
Plasma interleukin-6 level measured at baseline after induction of anesthesia and 30-60 minutes after completion of one-lung ventilation in the post-anesthesia care unit.
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