Tanya K Meyer1, Jeffrey Wolf. 1. Department of Otolaryngology Head & Neck Surgery, University of Washington, Seattle, Washington 98195-6515, USA. meyertk@uw.edu
Abstract
BACKGROUND: The Type I Posterior Glottic Stenosis (PGS-I) is a well-described but uncommon clinical entity. Despite this, there is little known about the outcome of surgical treatment. METHODS: Retrospective case series. RESULTS: Thirteen cases met inclusion criteria. All but one patient had a tracheostomy at the time of initial evaluation. At the postoperative visit, seven patients (54%) had completely normal vocal fold motion. Of the verbal patients, 6 (50%) had normal vocal function as reported by both the patient/caregiver and the physician, and 10 (83%) patients were successfully decannulated. CONCLUSIONS: Patients with an isolated interarytenoid synechia have an excellent prognosis with regard to decannulation. Although many patients regain normal vocal fold motion and a return to their preintubation vocal function, a significant proportion can have persistent deficits in vocal fold mobility and some level of dysphonia. This report represents the largest known series of PGS-I cases.
BACKGROUND: The Type I Posterior Glottic Stenosis (PGS-I) is a well-described but uncommon clinical entity. Despite this, there is little known about the outcome of surgical treatment. METHODS: Retrospective case series. RESULTS: Thirteen cases met inclusion criteria. All but one patient had a tracheostomy at the time of initial evaluation. At the postoperative visit, seven patients (54%) had completely normal vocal fold motion. Of the verbal patients, 6 (50%) had normal vocal function as reported by both the patient/caregiver and the physician, and 10 (83%) patients were successfully decannulated. CONCLUSIONS:Patients with an isolated interarytenoid synechia have an excellent prognosis with regard to decannulation. Although many patients regain normal vocal fold motion and a return to their preintubation vocal function, a significant proportion can have persistent deficits in vocal fold mobility and some level of dysphonia. This report represents the largest known series of PGS-I cases.