Use of the Microcuff® During General Anesthesia for Patients With Scoliosis
Scoliosis may often be associated with a variety of cardiovascular and respiratory conditions or diseases, and depending on the severity of the spinal deformity, it may also complicate anesthetic management because of the difficulty of neck extension and tracheal deformity. Therefore, patients with scoliosis may require careful perioperative anesthetic considerations. A 14-year-old girl was scheduled to undergo extractions and restorative treatment for dental caries under general anesthesia. Her medical history was significant for intellectual disability and autism as well as previously undiagnosed scoliosis. After fixation of a 6.0 Portex® endotracheal tube (ETT), percutaneous oxygen saturation (SpO2) decreased to 93%, peak airway pressures increased, and unilateral lung ventilation was noted. Inadvertent mainstem bronchial intubation was immediately suspected, prompting removal of the Portex ETT and reintubation with a shorter 6.0 Microcuff® ETT. The dental treatment was completed successfully without further incident. Assessment of the ETTs used intraoperatively led to the determination that the distance from the glottis to the carina was considerably shorter than normal for this patient. It was speculated that the Microcuff ETT may be optimal for anesthetic management of scoliosis patients because of its shorter lengths compared with other style ETTs, which may reduce the risk of bronchial intubation in such cases.

(A) Perioperative chest radiographs. (B) Chest radiographs after tracheal intubation with a pediatric Microcuff® ETT (Halyard® Microcuff® Pediatric Endotracheal Tube, Oral/Nasal Magill, I.D. 6.0 mm, Halyard Healthcare Inc, Atlanta, Ga), with fixation in the right nostril at 21 cm. The red line indicates the level of the carina. Preoperative chest radiographs (A) showed pronounced scoliosis with a Cobb angle of 50°.

Comparison of the distal ends of the tracheal tubes (cuff inflated to 20 cm H2O): (A) Microcuff® ETT (Halyard® Microcuff® Pediatric Endotracheal Tube, Oral/Nasal Magill, I.D. 6.0 mm, Halyard Healthcare Inc, Atlanta, Ga); (B) Portex® ETT (Portex® Oral/Nasal Ivory, I.D. 6.0 mm, Smiths Medical, Keene, NH) I.D. 6.0 mm; (C) Portex® ETT, I.D. 5.5 mm. DM indicates length from the distal edge of the intubation guide/depth mark to distal end of the ETT; DC, length from the distal edge of cuff to the distal end of the ETT; C, length from the distal edge of cuff and proximal edge of cuff; PM, length from the distal edge of intubation guide/depth mark and the proximal edge of cuff; I.D., internal diameter.
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