| Literature DB >> 31263293 |
Andrea S Huang1,2, John Hajduk1, Catherine Rim1, Sarah Coffield1, Narasimhan Jagannathan1,2.
Abstract
Management of the difficult paediatric airway management may be associated with a high rate of complications. It is important that clinicians understand the patient profiles associated with difficult airway management, and the equipment and techniques available to effectively manage these children. The goal of this focused review is to highlight key airway management concepts when managing the paediatric difficult airway. This includes understanding the advantages and limitations of various airway equipment designed for children and reviewing the difficult airway algorithm with its unique considerations for the paediatric patient. Early recognition of known risk factors and thorough preparation may be helpful in reducing the risk of complications during difficult airway management in children.Entities:
Keywords: Airway devices; airway; complications; difficult; pediatric
Year: 2019 PMID: 31263293 PMCID: PMC6573050 DOI: 10.4103/ija.IJA_250_19
Source DB: PubMed Journal: Indian J Anaesth ISSN: 0019-5049
Syndromes in children associated with difficult airways with key airway features observed
| Syndrome | Airway Features |
|---|---|
| Pierre Robin sequence | Micrognathia; glossoptosis (backward displacement of tongue); airway obstruction at rest; and improves with age |
| Treacher Collins | Micrognathia; limited mouth opening; airway obstruction at rest; and worsens with age (in spite having mandibular distraction) |
| Goldenhar syndrome | Micrognathia; hemifacial macrosomia; occipitalization of atlas; and limited mouth opening |
| Mucopolysaccaridoses (Hunter’s and Hurler’s syndromes) | Accumulation of mucopolysaccharides in various tissues, including airway; short, immobile neck; cervical instability, airway obstruction at rest; difficult mask ventilation and tracheal intubation; and worsens with age |
| Apert syndrome | Midface hypoplasia; possible choanal stenosis; progressive calcification of cervical spine; and airway obstruction |
| Down syndrome | Macroglossia; atlantoaxial instability; and pharyngeal hypotonia |
| Crouzon syndrome | Midface hypoplasia; maxillary hypoplasia; short neck; and restricted neck movement |
| Pfeiffer syndrome | Midface hypoplasia and airway obstruction |
| Klippel-Feil syndrome | Fusion of variable number of cervical vertebrae and limited neck movement |
| Beckwith-Wiedemann syndrome | Macroglossia |
| Freeman-Sheldon syndrome | Circumoral fibrosis and microstomia |
Figure 1Paediatric difficult airway management algorithm
Pros and Cons of various airway techniques/equipment
| Device | Pros | Cons |
|---|---|---|
| Direct laryngoscopy | Widely available | Requires alignment of axis to obtain laryngeal view; requires degree of mouth opening; multiple attempts are associated with increased complications; greater workforce needed to displace tissue vs. other techniques |
| Video laryngoscopy | Easy to acquire skill; portability; less force; panoramic and/or wide magnified view; and proven efficacy in the difficult airway | Requires moderate degree of mouth opening; the view can be easily obstructed with blood, secretions; time to intubate typically longer than DL |
| Supraglottic airway | Rescue device; conduit for tracheal intubation; can be used as a primary airway; and strong evidence base in difficult airways | Requires some degree of mouth opening; risk of pulmonary aspiration when used in patients with a “full stomach” |
| Flexible fiberoptic bronchoscope | Can be used in limited mouth opening; nasal or oral route; and can be used in conjunction with SAD | Steep learning curve to be proficient with its use; expensive; and suboptimal view in airway with blood, secretions |
| Optical stylet | Shorter learning curve than the FFB | Cannot use for nasal intubations and suboptimal view in airway with blood, secretions |