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Pathological airway issues frequently masquerade as more severe forms of the physiological respiratory and airway symptoms that many pregnant patients describe. Disorders of the airway are often exacerbated by pregnancy; persistent or worsening dyspnea must be investigated. Gold standard investigations that involve radiation exposure should be used appropriately for diagnosis and surveillance. Goitre is endemic in many countries and often worsens in pregnancy, which places the patient at risk for tracheomalacia. Idiopathic subglottic stenosis is a disease of women in the child-bearing years, and while easily treated, needs to be first diagnosed. Anterior mediastinal masses are unfortunately frequently missed as the presenting symptoms are ascribed to pregnancy changes. Airway changes in pregnancy lead to sleep-disordered breathing and are worsened by preeclampsia. The airway worsens in labor and can transform an awkward airway into a difficult one. Current airway management guidelines should be followed, with specificity for the pregnant patient, ensuring equivalent airway equipment and airway expertise are available for women with known airway issues. Finally, the pregnant patient with a known structural airway issues must be managed in a centre with access to airway experts, surgeons, and cardiopulmonary bypass or ECMO to ensure outcomes are good for both mother and baby.
By studying the odds of developing idiopathic subglottic stenosis in the isolated and genetically unique Hutterite population, this study sought to strengthen the hypothesis that an underlying genetic predisposition may exist for its development.
Methods
A retrospective chart review examined the medical records of all adult patients treated for idiopathic subglottic stenosis in Saskatchewan between 2008 and 2018. Cases were segregated into Hutterite and non-Hutterite.
Results
Four out of 36 cases of idiopathic subglottic stenosis occurred among Hutterites. The odds of a Hutterite developing idiopathic subglottic stenosis are 21.89 times higher than for non-Hutterites. Positive family history was only observed in the Hutterite population.
Conclusion
The study strengthens the hypothesis that genetics may play a role in the aetiology of idiopathic subglottic stenosis by demonstrating that the genetically and socially unique Hutterites are more likely to develop this rare disease. This study is the first to demonstrate that a specific subpopulation is at a higher risk for developing idiopathic subglottic stenosis.
Laryngotracheal reconstruction with costal cartilage graft is a cornerstone procedure in treatment of multiple paediatric airway pathologies. The current study aimed to report on the experience of laryngotracheal reconstruction and document post-operative outcomes and complications.
Method
Records of laryngotracheal reconstruction procedures performed between 2016 and 2020 were retrospectively reviewed. Primary indication, clinical data, decannulation rate, voice assessment, need for revision surgery and possible complications were analysed.
Results
A total of 41 patients were treated with laryngotracheal reconstruction. Subglottic stenosis formed the largest percentage of cases followed by congenital glottic web (20 and 14 patients, respectively). Three patients (7.3 per cent) underwent single stage surgery, and the remaining cases had a double stage procedure. Revision laryngotracheal reconstruction was needed in a single case, and 38 out of 39 tracheostomised patients were successfully decannulated.
Conclusion
Favourable outcomes were reported with costal cartilage laryngotracheal reconstruction as a definitive treatment for a large range of paediatric airway problems.
This chapter, provides an overview of the care and evaluation for patients undergoing laryngotracheal reconstruction. The authors present the evaluation process, grading and considerations surround patients with subglottic stenosis. The anesthetic considerations for these procedures including the postoperative transfer of care to the critical care team are presented.
The development of advanced neonatal care and anesthesia techniques enabled patients to be intubated for prolonged periods leading to a rise in incidence of acquired subglottic stenosis and the survival of patients with ventilator-dependent respiratory failure. The decision for tracheotomy tube placement should entail a detailed thought process and individualized plan for each patient. When evaluating children for tracheotomy tube placement, it is important to communicate openly with anesthesia staff. Correct size and positioning of the tracheotomy tube can be confirmed with a post-operative chest radiograph and/or passage of a small pediatric flexible endoscope. After tracheotomy, the patient should be closely monitored in the intensive care unit for 5-7 days. Careful dissection and ligature techniques are used for anterior jugular veins and the thyroid isthmus to avoid complications. Patients with tracheotomies have been shown to exhibit difficulties with speech and language development, even after decannulation.
In patients with Wegener’s granulomatosis, subglottic stenosis can develop due to active disease; however, some patients develop subglottic stenosis with no clear evidence of airway inflammation. In some cases of idiopathic subglottic stenosis, an association with gastroesophageal reflux disease has been found. Our study assessed the potential role of gastroesophageal reflux as an aetiological factor in the development of subglottic stenosis in patients with Wegener’s granulomatosis.
Design:
We assessed evidence of active reflux disease, using 24-hour pH monitoring and assessment of bile salts in bronchoalveolar lavage fluid.
Subjects:
Ten Wegener’s granulomatosis patients with subglottic stenosis underwent 24-hour pH monitoring and bronchoscopy and lavage of the right middle lobe. A similar number of control patients were included.
Results:
There was no statistically significant difference in the occurrence of bronchoalveolar bile salts in patients with subglottic stenosis (n = 2) versus control patients (zero) (p = 0.457). There was good correlation between the detection of reflux by 24-hour pH monitoring and the detection of bronchoalveolar bile salts (κ = 0.769).
Conclusion:
In this small study of patients with Wegener’s granulomatosis, there was no evidence of an association between the development of subglottic stenosis and gastroesophageal reflux.
In order to improve the outcome and to reduce the post-operative care burden following the anterior cricoid split procedure, we modified the procedure to involve splitting only the cricoid cartilage, not the mucosa deep to the cartilage. In addition, we transposed the cricoid cartilage segment after division of the cricoid ring in the midline.
Case report:
We present the use of our modification in a 19-month-old boy with early-stage subglottic stenosis.
Results:
The technique was performed in one surgical field, and the graft material obtained had the same thickness as the cricoid cartilage. Because there was no intraluminal break, this procedure allowed the patient to avoid the complications of prolonged stenting, and resulted in more rapid extubation.
Conclusion:
The anterior cricoid split procedure with transposition of the cricoid cartilage segment may be a useful treatment option for early-stage subglottic stenosis, with improved outcomes and a reduced post-operative care burden.
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