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What is an I gel?: A Comprehensive Guide to this Innovative Airway Device

3 min read

The i-gel supraglottic airway device was introduced in 2007 and quickly gained popularity for its innovative non-inflatable design. This advanced medical tool revolutionized airway management by offering a less traumatic alternative for securing a patient's breathing, especially in emergency situations where rapid airway access is critical.

Quick Summary

An i-gel is a single-use, supraglottic airway management device made from a soft, gel-like thermoplastic elastomer, designed to provide a non-inflating anatomical seal for airway patency.

Key Points

  • Non-inflatable Design: The i-gel uses a unique, gel-like elastomer cuff that conforms to the patient's anatomy, eliminating the need for inflation and reducing trauma.

  • Gastric Channel: A built-in channel allows for decompression of the stomach and suctioning, significantly lowering the risk of aspiration in patients.

  • Intuitive Insertion: Designed for rapid, blind insertion, the i-gel can be used effectively by both experienced and novice healthcare professionals in emergency settings.

  • Single-Use and Safe: The device is single-use, latex and PVC-free, which prevents cross-contamination and minimizes the potential for allergic reactions.

  • Advanced Safety Features: An integral bite block and buccal cavity stabilizer enhance safety by preventing airway occlusion and device rotation.

  • Wide Application: Suitable for use in routine anesthesia, emergency airway management, and resuscitation, the i-gel has a broad range of clinical indications.

In This Article

Understanding the I-gel's Core Technology

Unlike traditional laryngeal masks that use an inflatable cuff, the i-gel uses a soft, gel-like material that conforms to the pharyngeal, laryngeal, and perilaryngeal anatomy, providing a non-inflating seal. This medical-grade thermoplastic elastomer is latex and PVC-free. The non-inflating design minimizes pressure on tissues, potentially reducing trauma.

Key Features and Anatomical Design

The i-gel includes a buccal cavity stabilizer for insertion guidance and position maintenance, and an integral bite block to protect the airway tube. A significant feature is the gastric channel (in most sizes), which allows for stomach decompression via a nasogastric tube and can provide an early indicator of regurgitation, helping to reduce the risk of aspiration.

Indications and Clinical Applications

The i-gel is used to manage airways in various situations, including routine and emergency anesthesia for fasted patients, during ventilation, and for resuscitating unconscious individuals. Its design facilitates rapid, blind insertion, which is advantageous in emergency and pre-hospital settings. Studies indicate a high first-attempt success rate, even for novice users.

I-gel vs. The Laryngeal Mask Airway (LMA)

The LMA has historically been a standard for supraglottic airway management. The i-gel, a second-generation device, differs primarily in its cuff design. The LMA has an inflatable cuff requiring careful pressure management, while the i-gel's non-inflatable cuff naturally conforms to anatomy, removing the need for cuff pressure monitoring and potentially reducing user error.

Feature I-gel Laryngeal Mask Airway (LMA)
Cuff Type Non-inflatable, gel-like elastomer Inflatable cuff, requires inflation pressure monitoring
Material Medical-grade thermoplastic elastomer, latex/PVC-free Often silicone, can be reusable or single-use
Gastric Channel Yes (most sizes) No (classic LMA), some newer generations have it
Insertion Rapid, blind insertion with anatomical guides Requires inflation after insertion, potential for user error with inflation
Trauma Risk Low, due to non-inflating cuff and soft material Higher risk with improper cuff inflation
Ease of Use Considered easier for novices to insert successfully Can be more technically demanding to achieve optimal seal

How to Properly Insert an I-gel

Effective i-gel insertion requires proper technique:

  1. Preparation: Choose the correct size based on weight and prepare equipment, including lubricant. Position the patient with head extended and neck flexed.
  2. Lubrication: Apply water-based lubricant to the i-gel cuff.
  3. Insertion: Insert the device towards the hard palate and glide it downwards and backwards until resistance is met. Avoid excessive force.
  4. Confirmation: Verify placement by checking breath sounds and using capnography (ETCO2).
  5. Securing: Secure the device with a strap or tape to prevent movement.

Potential Complications and Considerations

While generally safe, improper i-gel use can lead to minor trauma like bruising. Rare but serious complications include aspiration, nerve injuries, and laryngospasm. Postoperative sore throat is also possible. Contraindications include an intact gag reflex, known esophageal issues, and certain anatomical abnormalities. Training is crucial to minimize risks.

The Historical Development of the I-gel

The i-gel was developed by Dr. Muhammed A. Nasir with Intersurgical Ltd. and launched in 2007. Its development involved years of research, including anatomical studies on cadavers and testing numerous prototypes, leading to its distinctive anatomical design. For further details on its creation, you can refer to relevant research.

Conclusion

The i-gel is a significant advance in supraglottic airway management, offering an easier-to-insert device with reduced tissue trauma risk and features like a gastric channel, moving beyond traditional inflatable cuffs. Its effectiveness and relative simplicity make it a valuable tool in both routine anesthesia and emergency care.

Frequently Asked Questions

The i-gel is designed for use by appropriately trained and experienced medical professionals, including anesthetists, paramedics, and other healthcare providers skilled in airway management.

In an emergency, the i-gel is used to secure and maintain a patent airway in unconscious or apneic patients, particularly during resuscitation, when quick and effective ventilation is needed.

The i-gel device comes in various sizes, from neonatal to large adult. The correct size is selected based on the patient's body weight, with clear guidance provided on the product packaging.

No, one of the primary contraindications for using the i-gel is a patient with an intact gag reflex. It is only suitable for unresponsive or anesthetized patients.

The non-inflatable cuff minimizes the risk of tissue compression and associated trauma that can occur with over-inflated cuffs. It also removes the need for cuff pressure monitoring, simplifying the procedure.

Many studies and clinical experiences suggest the i-gel is easier and faster to insert than traditional laryngeal masks, even for less experienced users, due to its anatomical design.

While the integrated gastric channel significantly reduces the risk of aspiration by allowing for venting and gastric tube passage, no airway device can provide absolute protection against it. Proper technique and monitoring are still essential.

References

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Medical Disclaimer

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