Tracheostomy is one of the most frequently performed techniques in intensive care units. For some authors endoscopic guide as part of the percutaneous tracheostomy (PT) might reduces the incidence of serious complications. However, for others, endoscopic guide increases the procedure cost, increases airway pressure and PaCO2 and sometimes requires the presence of another physician. International guidelines conclude that there is insufficient evidence to support the routine use of bronchoscopy during PT in order to decrease the number of complications. In addition the routine use of endoscopic guide is heterogeneous according the results of six published nation surveys. Extensive randomized trials to compare PT with endoscopic guide and without endoscopic guide are needed in order to clarify this controversial issue. This constitutes the justification of this trial. Hypothesis: Percutaneous tracheotomy performed under endoscopic guide decreases the incidence of perioperative complications of the procedure.
Background Tracheostomy is one of the most frequently performed techniques in intensive care units (ICU). A few years after the description of the percutaneous dilatational tracheostomy (PDT), endoscopic guide as part of the technique was performed in four patients. The authors concluded that the endoscopic guide provided advantages to the realization of PDT. Other authors have state that endoscopy, significantly reduces the incidence of serious complications such as posterior tracheal tears, false passage, pneumothorax and subcutaneous emphysema. However, currently endoscopic guide as part of the percutaneous tracheostomy is controversial. Although for some authors its use reduces the number of complications, others found that endoscopic guide increases the procedure cost, increases airway pressure and PaCO2 and sometimes requires the presence of another physician. Thus, some do not consider it necessary when the physicians have enough experience with percutaneous tracheostomy. International guidelines conclude that there is insufficient evidence to support the routine use of bronchoscopy during percutaneous tracheostomy in order to decrease the number of complications. In addition the routine use of endoscopic guide is heterogeneous according the published surveys. Specifically, in Spain its use was the lowest of the six published nation surveys. Extensive randomized trials to compare percutaneous tracheostomy with endoscopic guide and without endoscopic guide are needed in order to clarify this controversial issue. This constitutes the justification of this trial. Hypothesis Percutaneous tracheostomy performed under endoscopic control does not reduce the incidence of perioperative complications of the procedure in critically ill patients when it is performed by experienced physicians in patients without anatomical abnormalities. Main goal 1. \- To assess the incidence of perioperative complications of percutaneous tracheotomy under endoscopic guide versus blind percutaneous tracheotomy. 2. \- To assess the ventilatory parameters during percutaneous tracheostomy with and without endoscopic control. Methodology Prospective, multicenter randomized study. Patients admitted to the ICU who need tracheostomy due to prolonged mechanical ventilation, who do not have neither contraindications to perform the percutaneous technique nor contraindications to perform fibrobronchoscopy will be randomized. The percutaneous tracheostomy will be carried out with the single-step dilation method. For its realization, the usual protocol will be followed. The included patients will be randomized 1:1 (percutaneous tracheostomy with endoscopic guide vs percutaneous tracheostomy without endoscopic guide). The randomization system will be by closed envelope. A sample size of 221 patients in each branch has been calculated. The percutaneous tracheostomy and fiberoptic bronchoscopy will be performed by staff with experience with both procedures.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
442
Percutaneous tracheotomy performed by endoscopic guidance
Hospital Universitario La Paz
Madrid, Spain
Hospital Universitario Infanta Leonor
Madrid, Spain
Hospital Universitario Rey Juan Carlos
Madrid, Spain
Hospital Universitario de Toledo
Toledo, Spain
Number of patients with bleeding
Bleeding with haemodynamic derangement or needing surgical review or transfusion of packed red cells.
Time frame: From date of randomization until 24 hours later
Number of patients with hypoxemia
Hypoxemia: Oxygen arterial saturation (SaO2) \< 85% during more than 90 seconds and/or arrhythmia or cardiac arrest related to hypoxemia.
Time frame: From date of randomization until 24 hours later
Number of patients in whom a loss of airway has ocurred
Loss of airway: Failure to be able to access the airway \> 30 seconds.
Time frame: From randomization until the end of the procedure
Number of patients with atelectasis
Atelectasis: Total or partial lung collapse not present before the technique, evidenced at postoperative control.
Time frame: From date of randomization until 24 hours later
Number of patients with hypotension
Hypotension requiring treatment with vasopressors or \>1000 ml of fluids during the procedure.
Time frame: From randomization until the end of the procedure
Number of patients with barotrauma
Barotrauma: Subcutaneous emphysema, mediastinal emphysema or pneumothorax related to the technique.
Time frame: From date of randomization until 24 hours later
Number of patients with posterior tracheal wall injury
Posterior tracheal wall injury: Injury to membranous trachea by the needle, guide or dilator along with any related consequences (pneumomediastinum, pneumothorax, subcutaneous emphysema, tracheo-esophageal fistula)
Time frame: From date of randomization until 24 hours later
Number of patients in whom false passage has ocurred
False passage: Dilatation or insertion of the cannula out of the trachea lumen.
Time frame: From randomization until the end of the procedure
Number of patients in whom cardiac arrest or death directly related to any complication arising from the technique occurred
Cardiac arrest or death
Time frame: From date of randomization until the ICU discharge
Peak airway pressure
Maximum peak airway pressure (cmH2O)
Time frame: From randomization until the end of the procedure
Plateau pressure
Maximum plateau pressure (cmH2O)
Time frame: From randomization until the end of the procedure
Tidal volume
Minimum tidal volume (mL)
Time frame: From randomization until the end of the procedure
Arterial Blood Gas
Arterial blood gase at the beginning and the end of the procedure
Time frame: From randomization until 15 minutes after the procedure
Oxygen saturation (SaO2)
Minimum arterial oxygen saturation (SaO2)
Time frame: From randomization until the end of the procedure
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