Tag: Airway management

According to a systematic review published by the National Institutes of Health, hypoxia was the most common adverse event during procedural sedation, occurring in 40.2 out of every 1,000 sedations. This is primarily caused by drug-induced respiratory depression, considered the most common serious complication of sedation.

Procedural sedation carries a low risk of complications for properly screened patients, but a thorough pre-procedure evaluation is essential to identify high-risk cases. Understanding what are the absolute contraindications for procedural sedation is crucial for ensuring patient safety and determining if the procedure can proceed safely outside of an operating room setting.

While under general anesthesia, potent medications temporarily suppress a patient's natural respiratory drive and paralyze the muscles responsible for breathing. To ensure patient safety, a dedicated anesthesia provider is always present to manage and support breathing throughout the entire procedure.

First described as a vital airway management skill, the C and E technique for anesthesia is a fundamental method used to provide manual bag-mask ventilation. This critical skill involves a specific hand position to secure a tight mask seal and maintain an open airway, ensuring adequate oxygenation for a patient during the induction of anesthesia or a medical emergency.

First launched in 2007, the IGEL has since become a standard tool in anesthesia and resuscitation worldwide, reflecting a major advancement in airway management technology. When asking "what is an IGEL considered?" the definitive answer is a second-generation supraglottic airway (SGA) device, known for its unique non-inflatable cuff and ease of insertion.

The i-gel® supraglottic airway device (SAD) has gained popularity not only as a primary ventilation device but also as a conduit for endotracheal intubation [1.2.1]. This article explores the central question: can you intubate down an iGel, and what determines a successful outcome?

Developed over years of extensive research, the i-gel is a unique single-use, non-inflatable supraglottic airway management device that has transformed modern airway control. This innovative tool, designed to work in perfect unison with the patient's anatomy, has a distinct set of applications. So, for what purpose is I gel used, and how does it compare to other airway adjuncts?

First introduced in 2007, the I-gel supraglottic airway device is used globally for anesthesia and resuscitation, and its unique non-inflatable design offers specific benefits that improve patient outcomes and procedural efficiency. Made from a soft, medical-grade thermoplastic elastomer, the I-gel creates a precise anatomical seal without the need for cuff inflation.

While not all surgical procedures require a breathing tube, **do patients get intubated during surgery?** Yes, it is a routine and critical part of airway management for many major or lengthy operations performed under general anesthesia.

Over one-third of all general anesthesia cases do not require a breathing tube, dispelling the common myth that everyone gets intubated when having surgery. The method of airway management is a critical decision made by the anesthesia care team based on several factors, including the type of procedure and the patient's health.