Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15197
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dc.contributor.authorNeruntarat C.
dc.date.accessioned2021-04-05T04:32:57Z-
dc.date.available2021-04-05T04:32:57Z-
dc.date.issued2003
dc.identifier.issn1945998
dc.identifier.other2-s2.0-0141923713
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15197-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0141923713&doi=10.1016%2fS0194-5998%2803%2900636-3&partnerID=40&md5=f727ce90bc255ec391977a5a282a8585
dc.description.abstractOBJECTIVE: Snoring is now seen as one end of a spectrum of sleep-related breathing disorders, and in its extreme form, snoring can cause obstructive sleep apnea syndrome. Since the introduction of uvulopalatopharyngoplasty, many other procedures have been introduced to alleviate palatal abnormalities seen in patients with obstructive sleep apnea syndrome. A reversible uvulopalatal flap (UPF) achieves the same results as the uvulopalatopharyngoplasty but with less postoperative discomfort. The purpose of this study was to assess the safety and efficacy of UPF for the treatment of simple snoring on an outpatient basis. METHODS: UFP was performed 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. Most of the patients were male with simple snoring by history and confirmed by polysomnographic study. Data on patients were compared from preoperative to postoperative assessment points. Statistic analysis was performed. RESULTS: Fifty-six patients tolerated the procedure well, and it was performed in an average of 20 minutes. Patients had a mean age of 48 years and a mean body mass index of 26.5 kg/m2. The mean follow-up was 14 months (range, 12 to 20 months). Significant improvement was observed in snoring scale (8.2 ± 3.4 versus 2.6 ± 1.4, P < 0.05). Mean snoring index decreased from 245.8 ± 40.8 to 42. 5 ± 20.7 events/hr (P < 0.001). The correlations between the changes in the subjective and objective snoring assessments were statistically significant. Postoperative complications included transient nasal regurgitation (4%) and foreign body sensation (2%). Bleeding, dysphagia, infection, and nasopharyngeal stenosis were not observed. Most patients had mild to moderate pain (visual analog scale, ≤7) for 5 to 7 days after the procedures. The overall success rate was 88%. CONCLUSION: Snoring, as reported by subjective and objective results, decreased after UPF. It appears to be a safe and effective procedure, which can be easily performed under local anesthesia on an outpatient basis, in carefully selected patients.
dc.subjectanesthesia induction
dc.subjectarticle
dc.subjectbody mass
dc.subjectcorrelation analysis
dc.subjectdysphagia
dc.subjectfollow up
dc.subjectforeign body sensation
dc.subjecthospital patient
dc.subjectintermethod comparison
dc.subjectlocal anesthesia
dc.subjectnasal regurgitation
dc.subjectnasopharynx stenosis
dc.subjectoperation duration
dc.subjectoral surgery
dc.subjectpain assessment
dc.subjectpatient selection
dc.subjectpolysomnography
dc.subjectpostoperative complication
dc.subjectpostoperative hemorrhage
dc.subjectpostoperative infection
dc.subjectpreoperative evaluation
dc.subjectsafety
dc.subjectsleep apnea syndrome
dc.subjectsnoring
dc.subjectstatistical analysis
dc.subjectsurgical technique
dc.subjectsurvival rate
dc.subjecttreatment indication
dc.subjecttreatment outcome
dc.subjectuvulopalatal flap
dc.subjectuvulopalatopharyngoplasty
dc.subjectvisual analog scale
dc.titleUvulopalatal flap for snoring on an outpatient basis
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationOtolaryngology - Head and Neck Surgery. Vol 129, No.4 (2003), p.353-359
dc.identifier.doi10.1016/S0194-5998(03)00636-3
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