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Uvulopalatal flap for obstructive sleep apnea on an outpatient basis

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dc.contributor.author Neruntarat C.
dc.date.accessioned 2021-04-05T04:33:09Z
dc.date.available 2021-04-05T04:33:09Z
dc.date.issued 2002
dc.identifier.issn 13412051
dc.identifier.other 2-s2.0-0036236782
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/15241
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-0036236782&partnerID=40&md5=52899023bba51b99dda1e888ea60c004
dc.description.abstract Objective: Obstructive sleep apnea (OSA) is now seen as one end of a spectrum of sleep-related breathing disorders. It is associated with hypertension, cardiovascular diseases, daytime sleepiness and risk for general anesthesia. Since the introduction of uvulopalatopharyngoplasty (UPPP), many other procedures have been introduced to alleviate palatal abnormalities seen in patients with OSA. A reversible uvulopalatal flap (UPF) performed under general anesthesia also achieves the same results as UPPP, but with less postoperative discomfort. The purpose of this study was to assess the safety and efficacy of UPF for the treatment of OSA on an outpatient basis. Methods: UPF was performed in 36 OSA patients on an outpatient basis under local anesthesia. The mucosa on the lingual surface of the uvula and soft palate was removed with cold-knife dissection. The uvular tip was amputated. The uvula was reflected back toward the soft palate and sutured. Data on patients were compared from preoperative to postoperative assessment points. Statistical analysis was performed using Student t test. Results: Patients had a mean age of 30.2 years and a mean body mass index of 28.5 kg/m2. Most of the patients were male. All patients tolerated the procedure well and it was performed in an average of 20 minutes. The mean follow-up was 6 months (range 4-8 months). Responders were defined as OSA patients who had a reduction in RDI of 50% or more and RDI of 10 or less after surgery. By these criteria, 52% of patients were considered to have responded to UPF. Mean RDI improved from 45.2±10.2 to 10.1±4.2 (p<0.001). The Epworth sleepiness scale improved from 12.5 ± 5.4 to 8.2 ± 4.8 (p<0.001). Postoperative complications included transient nasal regurgitation in 11.1% and foreign body sensation in 8.3%. Bleeding, dysphasia, infection, and nasopharyngeal stenosis were not observed. Most patients had mild-to-moderate pain (visual analog scale ≤ 7) for 5 to 7 days after procedure. Conclusion: UPF results in both significant reductions in respiratory disturbance index and clinical improvements in snoring and sleepiness. It appears to be a well-tolerated outpatient surgical procedure for the treatment of OSA.
dc.subject adult
dc.subject ambulatory surgery
dc.subject article
dc.subject bleeding
dc.subject body mass
dc.subject breathing disorder
dc.subject dysphagia
dc.subject female
dc.subject foreign body
dc.subject general anesthesia
dc.subject human
dc.subject infection
dc.subject local anesthesia
dc.subject major clinical study
dc.subject male
dc.subject muscle flap
dc.subject nasopharynx stenosis
dc.subject nose regurgitation
dc.subject pain assessment
dc.subject patient selection
dc.subject polysomnography
dc.subject postoperative complication
dc.subject respiratory distress
dc.subject scoring system
dc.subject sleep apnea syndrome
dc.subject snoring
dc.subject somnolence
dc.subject statistical analysis
dc.subject uvulopalatal flap
dc.subject uvulopalatopharyngoplasty
dc.title Uvulopalatal flap for obstructive sleep apnea on an outpatient basis
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation International Medical Journal. Vol 9, No.1 (2002), p.45-49


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