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      Awake supraglottic airway guided flexible bronchoscopic intubation

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      Korean Journal of Anesthesiology
      Korean Society of Anesthesiologists

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          Abstract

          I read with great interest the narrative review on awake supraglottic airway guided flexible bronchoscopic intubation in patients with anticipated difficult airways by Lim and Wong [1]. Undoubtedly, awake intubation is indicated in a patient when difficulty in maintaining or securing the airway after induction of general anesthesia is expected. The natural airway is better maintained in the awake patient. The normal muscle tone helps to maintain the anatomy and easier identification of upper airway structures relative to each other. There is less likelihood of aspiration with preservation of the lower esophageal sphincter tone and maintenance of spontaneous breathing; besides, the patient can follow instructions while awake. However, awake intubation requires careful patient preparation, adequate topical anesthesia of the airway, and judicious use of sedative agents; besides, an appropriate level of operator expertise. The insertion of a supraglottic airway device (SAD) seated in the pharynx above the laryngeal inlet attenuates the pressor and laryngeal responses [2]. It is reasonable to assume that in the awake patient, an SAD may be better tolerated than an endotracheal tube. The SAD serves as a conduit for fiberoptic bronchoscope-guided endotracheal intubation and, if positioned correctly, leads to easier and more rapid endotracheal intubation. The Difficult Airway Society guidelines for the management of the unanticipated difficult airway [3] and the American Society of Anesthesiologists Difficult Airway algorithm [4] suggest intubation through an SAD in case of failed tracheal intubation. Insertion of an SAD in the awake patient under topical anesthesia followed by tracheal intubation after induction of general anesthesia has been reported previously [3]. In their narrative review, Lim and Wong describe inserting an Ambu AuragainTM SAD after topical anesthesia of the airway and remifentanil infusion. Fiberoptic bronchoscope-guided tracheal intubation was achieved through the SAD. However, it is not clear why the authors did not inflate the SAD cuff. The position of an SAD is usually confirmed after cuff inflation. Cuff inflation permits the formation of a seal between the device and the pharyngeal mucosa; besides, the use of a second-generation SAD also allows isolation of the respiratory and alimentary tracts. Cuff inflation also prevents device displacement. There seems to be no recommendation in literature to leave the SAD cuff uninflated. Furthermore, insufflation of oxygen at 10–15 L/min through an oxygen tubing attached to the proximal end of the ventilation port of the SAD may lead to gastric insufflation, regurgitation, and pulmonary aspiration. The authors report supraglottic airway guided flexible bronchoscopic intubation in several cases. However, when coughing or patient movement during intubation is undesirable, as in patients with intracranial lesions or an unstable cervical spine, it may be prudent to administer general anesthesia with or without the use of muscle relaxants after confirmation of SAD position by fiberoptic bronchoscopy. This may be followed by assisted ventilation before attempting tracheal intubation through the SAD.

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          Awake supraglottic airway guided flexible bronchoscopic intubation in patients with anticipated difficult airways: a case series and narrative review

          Awake intubation is indicated in difficult airways if attempts at securing the airway after induction of general anesthesia may lead to harm due to potential difficulties or failure in those attempts. Conventional awake flexible bronchoscopic intubation is performed via the nasal, or less commonly, oral route. Awake oral flexible bronchoscopic intubation (FBI) via a supraglottic airway device (SAD) is a less common technique; we refer to this as ‘supraglottic airway guided’ FBI (SAGFBI). We describe ten cases with anticipated difficult airways in which awake SAGFBI was performed. After sedation and adequate airway topicalization, an Ambu AuragainTM SAD was inserted. A flexible bronchoscope, preloaded with a tracheal tube, was then inserted through the SAD. Finally, the tracheal tube was railroaded over the bronchoscope, through the SAD and into the trachea. The bronchoscope and the SAD were carefully removed, whilst keeping the tracheal tube in-situ. The technique was successful and well tolerated by all patients, and associated complications were rare. It also offered the advantages of performing an ‘awake test insertion’ of the SAD, an ‘awake look’ at the periglottic region, and an ‘awake test ventilation.’ In certain patients, awake SAGFBI offers advantages over conventional awake FBI or awake videolaryngoscopy. More research is required to evaluate its success and failure rates, and identify associated complications. Its place in difficult airway algorithms may then be further established.
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            Assessment of awake i-gel™ insertion for fiberoptic-guided intubation in patients with predicted difficult airway: A prospective, observational study

            Background and Aims: Orotracheal intubation (OTI) with fiberoptic bronchoscope (FOB) in spontaneous ventilation is one of the main techniques for patients with predicted difficult airway. Latest generation supraglottic airway devices have been designed to allow OTI through them. We assessed the safety and effectiveness of FOB-guided OTI through i-gel™ device which was inserted in spontaneously breathing patients with predicted difficult airway. Material and Methods: Eighty-five patients with difficult airway predictors were included. The i-gel was inserted under oropharyngeal local anaesthesia and sedation. After checking the adequate ventilation through the i-gel with capnography curve, general anaesthesia was induced in order to introduce the endotracheal tube guided by FOB. We recorded the i-gel insertion time (t gel), intubation time (t int), O2 saturation in pulse oximetry (SpO2) at different times: basal (t 0), after 3 min of preoxygenation with a face mask at 100% FiO2 (t 1), after i-gel mask insertion (t 2) and after intubation (t 3). Adverse events during the procedure were also recorded. Results: All patients were successfully intubated. SpO2 values were: 96.9 ± 1.2 (t 0), 99.0 ± 0.9 (t 1), 96.2 ± 2.4 (t 2), 96.0 ± 2.5 (t 3). t gel and t int were 38.0 ± 7.8 s and 36.5 ± 5.6 s, respectively. No serious adverse events were recorded and no patient suffered airway trauma. Conclusion: I-gel insertion in spontaneous ventilation secures the airway before achieving fiberoptic intubation without the occurrence of adverse events. More studies might be necessary in order to confirm the results presented, but we consider that the technique described is a safe and effective alternative to classic OTI with FOB in spontaneously breathing patients with predicted difficult airway.
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              Hemodynamic and catecholamine stress responses to insertion of the Combitube, laryngeal mask airway or tracheal intubation.

              In a prospective, randomized, and controlled trial, we compared the stress responses after insertion of the Combitube (CT; Kendall-Sheridan Catheter Corp., Argyle, NY), the laryngeal mask airway (LMA), or endotracheal intubation (ET). Seventy-five patients scheduled for routine urological or gynecological surgery were randomly allocated to one of three groups and were ventilated via either an ET, a LMA, or a CT. All three devices could be inserted easily and rapidly, providing adequate ventilation and oxygenation. Insertion of the CT was associated with a significant increase in mean maximal systolic arterial pressure (160+/-32 mm Hg) and diastolic arterial pressure (91+/-17 mm Hg) compared with ET (140+/-24, 78+/-11 mm Hg; P < 0.05, P < 0.01, respectively) or insertion of the LMA (115+/-33,63+/-22 mm Hg, both P < 0.001). The mean maximal epinephrine and norepinephrine plasma concentrations after insertion of the CT (37.3+/-31.1 and 279+/-139 pg/mL, respectively) were significantly higher than those after ET (35.8+/-89.8 and 195+/-58 pg/mL, respectively) or insertion of a LMA (17.3+/-13.3 and 158+/-67 pg/mL, respectively). This might be attributed to the pressure of the pharyngeal cuff of the CT on the anterior pharyngeal wall. We conclude that insertion of the CT causes a pronounced stress response and that precautions should be taken when used in patients at risk of hypertensive bleeding.
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                Author and article information

                Journal
                Korean J Anesthesiol
                Korean J Anesthesiol
                KJA
                Korean Journal of Anesthesiology
                Korean Society of Anesthesiologists
                2005-6419
                2005-7563
                April 2020
                31 January 2020
                : 73
                : 2
                : 173-174
                Affiliations
                Department of Anesthesiology, Maulana Azad Medical College and Associated Lok Nayak Hospital, New Delhi, India
                Author notes
                Corresponding author: Anju Romina Bhalotra, M.D. Department of Anesthesiology, Maulana Azad Medical College and Associated Lok Nayak Hospital, A-1/59 Safdarjang Enclave, New Delhi 110029, India Tel: +91-01126183684 Email: drakgk@ 123456yahoo.co.in
                Author information
                http://orcid.org/0000-0003-0700-2941
                Article
                kja-20013
                10.4097/kja.20013
                7113161
                32008276
                01d324db-8a34-4aea-8378-64b95fd23d00
                Copyright © The Korean Society of Anesthesiologists, 2020

                This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 January 2020
                : 28 January 2020
                Categories
                Letter to the Editor

                Anesthesiology & Pain management
                Anesthesiology & Pain management

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