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Emergence of general anesthesia is a critical period, in the same way as the induction of anesthesia, during which several adverse events may occur. Extubation may even be more difficult than the intubation, with a higher respiratory complications rate. Among these, cough is common and expected. It can be associated with significant complications including hypertension, tachycardia, increased intracranial pressure, bleeding at the surgical site or even wound dehiscence.
The incidence of coughing during emergence of general anesthesia varies depending on the type of airway instrumentation, the population under study, agents used for the maintenance of the anesthesia and techniques used to prevent coughing. In the literature, the incidence of coughing during emergence of general anesthesia under endotracheal intubation varies from 38 to 96%. In our center, the incidence of coughing during emergence of general anesthesia under desflurane and endotracheal intubation is 30 % according to a local preliminary study.
Propofol is well-known to inhibit airway reflexes. Total intravenous anesthesia (TIVA) is associated with a lower incidence of coughing compared to inhalated anesthesia. The efficacy of propofol at a subhypnotic dose to reduce coughing during emergence has recently been demonstrated in patients undergoing nasal surgery under sevoflurane. However, the most effective antitussive dose remains unknown and its efficacy during anesthesia under desflurane has not yet been demonstrated.
Propofol is rapidly available, simple to administer and has an interesting pharmacological profile, among others due to its short half-life.
The aim of this study is to evaluate if an intravenous bolus of 0.5 mg/kg of propofol is more effective than placebo administration to decrease the incidence of coughing during emergence of general anesthesia under desflurane (PROPOREV). Propofol could also reduce the incidence of postoperative nausea and vomiting (PONV).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Propofol | Active Comparator | Active drug given to patients as an intravenous dose of 0.5 mg/kg of propofol |
|
| Saline solution | Placebo Comparator | Placebo drug given to patients as an intravenous dose of 0.05 mL/kg of saline solution (NaCl 0.9%) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Intravenous dose of 0.5 mg/kg of propofol | Drug |
| ||
| Intravenous dose of 0.05 mL/kg of saline solution |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of coughing (between discontinuation of desflurane and minimum alveolar concentration (MAC) of 0.15 of desflurane) | Incidence of coughing during emergence of general anesthesia (between discontinuation of desflurane and MAC of 0.15 of desflurane) and its severity based on a 4-grade scale | one day, perioperative period |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of coughing (between discontinuation of desflurane, MAC of 0.1 and 0.2 of desflurane, at extubation, as well as 5 and 10 min after extubation) | Incidence of coughing during emergence of general anesthesia (between MAC of 0.15 of desflurane and until 10 min after extubation) and its severity based on a 4-grade scale | one day, perioperative period |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Pierre Beaulieu, MD, PhD | CHUM | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHUM | Montreal | Quebec | H2W 1T8 | Canada |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 36829104 | Derived | Ouellet MF, Moore A, Williams S, Girard F, Desroches J, Ruel M, Beaulieu P. Efficacy of a propofol bolus against placebo to prevent cough at emergence from general anesthesia with desflurane: a randomized controlled trial. Can J Anaesth. 2023 May;70(5):842-850. doi: 10.1007/s12630-023-02401-w. Epub 2023 Feb 24. |
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| Drug |
|
| Extubation time | Interval between discontinuation of desflurane and extubation | one day, perioperative period |
| Sedation of the patient | Sedation of the patient two, five and ten minutes following extubation, then at 15 minutes interval in the recovery room, based on the Observer's Assessment of Alertness/Sedation Scale (OAA/A), until 30 minutes after the admission in the recovery room | one day, perioperative period |
| Incidence of hypoventilation | incidence of hypoventilation (breathing rate < 8/min) | one day, perioperative period |
| Incidence of hypoxic episode | incidence of hypoxic episode (oxygen saturation < 90%) | one day, perioperative period |
| Blood pressure | Measurement of blood pressure before the induction and during emergence (every 5 min) in order to calculate incidence of fluctuation of non invasive blood pressure and heart rate of more than 20% between the values before induction of anesthesia until 10 min after extubation | one day, perioperative period |
| Heart rate | Measurement of heart rate before the induction and during emergence (every 5 min) in order to calculate incidence of fluctuation of non invasive blood pressure and heart rate of more than 20% between the values before induction of anesthesia until 10 min after extubation | one day, perioperative period |
| Agitation of the patient during emergence | Note the possible agitation of the patient during emergence | one day, perioperative period |
| Complications | Describe potential complications secondary to the bolus of the substance under study at the emergence | one day, perioperative period |
| Cumulative incidence of nausea/vomiting | Calculate cumulative incidence of nausea/vomiting between extubation and 30 minutes after the admission in the recovery room | one day, perioperative period |
| Swallowing pain scores | Evaluate swallowing pain scores evaluated using a verbal simple numeric scale (0 = no pain et 10 = worst pain imaginable) 30 min after extubation | one day, perioperative period |
| ID | Term |
|---|---|
| D003371 | Cough |
| ID | Term |
|---|---|
| D012120 | Respiration Disorders |
| D012140 | Respiratory Tract Diseases |
| D012818 | Signs and Symptoms, Respiratory |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| D015742 | Propofol |
| D000077330 | Saline Solution |
| ID | Term |
|---|---|
| D010636 | Phenols |
| D001555 | Benzene Derivatives |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D000077324 | Crystalloid Solutions |
| D007552 | Isotonic Solutions |
| D012996 | Solutions |
| D004364 | Pharmaceutical Preparations |
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