Abstract

ObjectiveTo evaluate outcomes of injection laryngoplasty (IL) and endoscopic surgical repair for the treatment of type 1 laryngeal clefts (LC1) and to determine the most common presentations of LC1. MethodsPrimary studies were searched for in PubMed, Scopus, OVID, and Cochrane Library using search terms laryngeal cleft and laryngotracheoesophageal cleft for articles published from database inception through August 2019. The search identified all articles pertaining to the symptomatology and management of LC1. Meta-analysis was performed on presenting symptoms and improvement of clinical symptoms and swallow function. ResultsTwenty-four studies, comprising 713 patients with a mean age of 33.7 months (range 0–168 months), were included. The most common presenting symptoms were aspiration (80%, CI [55%–96%]), dysphagia (61%, CI [47%–74%]), and choking (57%, CI [37%–76%]). Gastroesophageal reflux disease (GERD) was the most common comorbidity (68%, CI [51%–83%]) and premature birth comprised 27% [21%–32%] of the patients. Overall, 38% of patients received IL as a primary therapy. Prior to injection, 91% [87%–94%] of patients aspirated on swallow evaluations, and 62% [55%–68%] aspirated post-injection. At an average follow-up time of 6.8 months, 90% [70%–100%] of parents reported symptom improvement. An additional 54% of patients underwent endoscopic surgical repair as primary treatment. The rate of aspiration decreased from 73% [43%–94%] to 28% [13%–46%] after repair. At a mean follow-up of 14.2 months, 80% [67%–91%] reported symptom improvement. ConclusionA high level of clinical suspicion is necessary to detect LC1 since its most common presenting symptoms overlap with other diseases commonly found in this patient population. Both IL and formal surgical repair were effective in managing LC1.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.