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What is iGel anesthesia?

4 min read

Introduced into clinical practice in 2007, the i-gel supraglottic airway device has become a widely used and trusted tool in airway management for general anesthesia. iGel anesthesia involves using this single-use, gel-like device to secure a patient's airway, providing a fast and effective alternative to traditional intubation for many procedures.

Quick Summary

The iGel is a second-generation supraglottic airway device with a soft, non-inflatable cuff that anatomically seals around the laryngeal inlet. It is utilized in general anesthesia and resuscitation due to its ease of insertion, high success rate, and reduced patient trauma compared to an endotracheal tube.

Key Points

  • Non-inflatable design: The i-gel features a soft, gel-like cuff that creates an anatomical seal without requiring inflation, significantly reducing trauma to throat tissues.

  • Fast and easy insertion: Its anatomical design allows for quick and reliable placement, making it suitable for routine anesthesia and emergency airway management.

  • Reduced postoperative morbidity: Patients experience lower rates of complications like sore throat and hoarseness compared to those with endotracheal tubes.

  • Integrated gastric channel: Most sizes include a separate lumen for gastric drainage, which enhances patient safety by reducing the risk of aspiration.

  • Versatile application: It can be used for both spontaneous and controlled positive pressure ventilation in a wide range of patient sizes, from neonates to large adults.

  • Used as a rescue device: The i-gel is a reliable option for difficult airways and as a rescue device in failed intubation scenarios.

  • Safe for laparoscopy: Studies show i-gel can be a safe alternative to an ETT during laparoscopic surgeries, with comparable ventilation efficacy at moderate pressures.

In This Article

Understanding the i-gel Supraglottic Airway Device

For many medical procedures requiring general anesthesia, maintaining a clear and open airway is paramount. The i-gel supraglottic airway device (SAD) offers a modern and often less invasive alternative to traditional methods like endotracheal tubes (ETT). It is a single-use, second-generation SAD that provides a reliable seal in the pharynx without the need for an inflatable cuff.

The i-gel is made from a soft, medical-grade thermoplastic elastomer that has a unique gel-like texture. This material is designed to work in harmony with a patient's anatomy, creating a perfect, impression-fit seal over the laryngeal inlet. The lack of an inflatable cuff means there is no risk of over-inflation causing damage or compression trauma to the surrounding tissues. The device was developed by inventor Dr. Muhammed A. Nasir and launched by Intersurgical Ltd in 2007, after years of research and testing.

How the i-gel Device Works During Anesthesia

When inserted, the soft, non-inflatable cuff of the i-gel conforms to the perilaryngeal anatomy, using the patient's body temperature to further soften and create an anatomical impression fit. This provides a high-pressure seal that is effective for both spontaneous and controlled (positive pressure) ventilation, essential during general anesthesia.

The device's specific design includes several key features that contribute to its efficacy and safety:

  • Non-inflatable cuff: The innovative design of the gel-like cuff eliminates the need for inflation, simplifying insertion and reducing the risk of tissue compression and associated trauma.
  • Gastric channel: Most adult and pediatric i-gel sizes incorporate a separate gastric channel. This allows for the insertion of a nasogastric tube to decompress the stomach and manage potential gastric regurgitation, significantly enhancing patient safety.
  • Epiglottic rest: A built-in feature helps prevent the epiglottis from folding down and causing an airway obstruction.
  • Integral bite block: This feature reduces the possibility of the patient occluding the airway channel by biting down on the device.
  • Anatomical mirror: The overall shape of the device is designed to accurately mirror the curves of the pharyngeal and laryngeal anatomy, which aids in quick and reliable placement.

Comparing i-gel to Endotracheal Tubes

While an endotracheal tube (ETT) is considered the gold standard for full airway protection, especially in procedures with a high risk of aspiration, the i-gel offers a suitable and often preferable alternative for many short-duration surgeries.

Feature i-gel Supraglottic Airway Endotracheal Tube (ETT)
Insertion Faster and easier insertion; often successful on the first attempt with minimal manipulation. Requires laryngoscopy, which can be more complex and time-consuming, especially for novices.
Airway Seal Achieves a reliable seal for spontaneous and controlled ventilation but may have higher leak pressure at very high ventilation pressures. Provides a superior, tight seal for high-pressure ventilation, protecting the lungs from contents of the stomach.
Hemodynamic Response Minimal hemodynamic changes (pulse rate, blood pressure) during insertion. Can cause a significant and abrupt increase in heart rate and blood pressure upon insertion.
Postoperative Morbidity Significantly lower incidence of complications such as sore throat, hoarseness, and dental or pharyngeal trauma. Can lead to higher rates of postoperative sore throat and potential for dental or pharyngeal injury.
Aspiration Protection Provides protection via the gastric channel but is not a definitive barrier for a high risk of aspiration. Considered the gold standard for preventing aspiration, as the cuff creates a sealed passage directly into the trachea.

Benefits of Choosing i-gel Anesthesia

For many elective surgical procedures, especially those that are shorter in duration, the i-gel is an excellent choice for airway management. The device's primary benefits include:

  • Rapid Insertion: The non-inflatable design and anatomical shape allow for quick and easy placement, even by less experienced practitioners, which is crucial in both routine and emergency scenarios.
  • Reduced Patient Trauma: By eliminating the need for an inflatable cuff, the i-gel minimizes trauma and compression injury to the delicate tissues of the throat and larynx, leading to a lower incidence of postoperative sore throat and other complaints.
  • Increased Patient Safety: The integrated gastric channel provides an extra layer of protection against regurgitation and aspiration by allowing for active or passive venting of stomach contents.
  • Versatility: The i-gel is used in a wide range of settings, from routine anesthesia for healthy patients to emergency resuscitation and even as a conduit for fiberoptic-guided intubation in difficult airway situations.

Limitations and Considerations

While the i-gel is highly effective, it is not suitable for all clinical scenarios. Contraindications typically include patients with a full stomach, conditions with an increased risk of aspiration, and specific airway abnormalities that prevent proper seating of the device. For procedures requiring prolonged mechanical ventilation or high airway pressures (typically over 20-25 cm H2O), an endotracheal tube may provide a more reliable and secure airway seal. Clinical judgment and proper patient selection remain essential for optimal outcomes. Training for novices has shown a predictable learning curve, with proficiency improving with experience to match results from experienced clinicians.

Conclusion

The i-gel supraglottic airway device has cemented its place as a valuable tool in modern anesthesia and airway management. By offering rapid, atraumatic insertion and effective ventilation, it provides a safe and reliable alternative to endotracheal intubation for a broad spectrum of surgical procedures and emergency situations. The device's unique non-inflatable design and integrated gastric channel address some of the major drawbacks of older supraglottic devices, improving both ease of use and patient safety. However, proper patient selection and understanding of its limitations are key to leveraging its full potential.

For more clinical context and comparisons of different supraglottic airway devices, readers may find this comparative review helpful: Comparison of the i-gel and other supraglottic airways in adult patients: a systematic review and meta-analysis.

Frequently Asked Questions

The i-gel differs from traditional laryngeal mask airways primarily because it uses a non-inflatable, gel-like cuff to create an anatomical seal, whereas older masks require an inflated cuff. This eliminates the need for inflation, reduces insertion time, and minimizes compression trauma.

Yes, the i-gel is widely used in emergency situations and for cardiopulmonary resuscitation (CPR). Its fast and reliable insertion makes it a valuable tool for securing an airway quickly when traditional intubation is difficult or not possible.

The i-gel is a safe and effective option for many routine and short-duration surgical procedures, including laparoscopic surgeries where ventilation pressures are moderate. However, for surgeries with a high risk of aspiration or those requiring very high ventilation pressures, an endotracheal tube may be more appropriate.

The gastric channel on the i-gel allows for the passage of a nasogastric tube. This enables the drainage of stomach contents and venting of gas, providing additional protection against regurgitation and pulmonary aspiration.

Compared to endotracheal tubes and other airway devices, the i-gel is associated with a significantly lower incidence of postoperative sore throat and other pharyngolaryngeal complications. Its non-inflatable cuff design is gentler on the tissues of the throat.

The manufacturer provides guidelines for selecting the correct i-gel size based on the patient's body weight. Sizes are available for neonates, pediatric patients, and adults to ensure an optimal fit.

Yes, certain larger sizes of the i-gel (typically 3, 4, and 5) can be used as a conduit for fiberoptic-guided tracheal intubation in cases of difficult intubation.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.