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1.
Acta Otolaryngol ; 143(3): 231-236, 2023 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-36939022

RESUMEN

BACKGROUND: The surgical treatment of otosclerosis consists of the replacement of the stapes using a piston. AIMS/OBJECTIVES: The objective of this study is to assess the audiometric results and quality of life (QOL) of patients who underwent surgery for otosclerosis by stapedectomy with fascia interposition (STIP) or by stapedotomy using CO2 laser (SLaser) without fascia interposition. MATERIAL AND METHODS: Ninety-one patients operated on for otosclerosis by STIP (40 patients) and by SLaser (51 patients) were included. Audiometric results were graphically displayed using the Amsterdam Hearing Evaluation Plot and were compared to the Common Otology Database (COD) comprising 660 patients. The patients' QOL was assessed with an otological validated survey. The significance level was p < .05. RESULTS: There was no significant difference in hearing improvement between SLaser and STIP-operated patients. There was no significant difference between our results and that of COD. QOL was significantly improved (+3.5/10) postoperatively for both STIP and SLaser in both social and professional fields. CONCLUSIONS AND SIGNIFICANCE: By comparing QOL and hearing gain of STIP and SLaser, our results suggest that both surgical techniques are a safe and successful treatment for otosclerotic stapes fixation. Further studies aiming at comparing larger series may confirm and refine these results.


Asunto(s)
Audiometría , Láseres de Gas , Otosclerosis , Cirugía del Estribo , Humanos , Dióxido de Carbono/uso terapéutico , Láseres de Gas/uso terapéutico , Prótesis Osicular , Otosclerosis/complicaciones , Otosclerosis/diagnóstico , Otosclerosis/cirugía , Calidad de Vida , Estudios Retrospectivos , Cirugía del Estribo/métodos , Resultado del Tratamiento , Audiometría/métodos , Pérdida Auditiva/diagnóstico , Pérdida Auditiva/etiología , Pérdida Auditiva/cirugía
2.
Oral Maxillofac Surg ; 21(2): 227-232, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28365803

RESUMEN

PURPOSE: The aim of this study is to determine patients' opinion regarding listening to music before an ambulatory maxillofacial surgery and effects on anxiety and pain reduction. METHODS: This study was conducted on outpatients having a maxillofacial surgery between December 2015 and April 2016 at Poissy/Saint-Germain-en-Laye hospital (France). Patients listened with headphones to an easy-listening music in the operation theater before the first ambulation. A questionnaire including a visual analog scale (VAS) for pain and anxiety was given to participants. The primary endpoint was to determine patients' opinion regarding listening to music before surgery. Secondary endpoints were to determine VAS pain mean, VAS anxiety mean before surgery, VAS anxiety mean after surgery, and if patients wanted to listen to their own playlist. We decided to compare VAS anxiety and pain mean between patients who accepted to listen to music (ALM) and who refused to listen to music (RLM). RESULTS: Nineteen patients ALM and 8 patients RLM to music. 78.9% of patients considered that listening to music before surgery decreased their anxiety. In patients who ALM, the mean (standard deviation, SD) of VAS pain after surgery was 3.42 (1.95), the mean (SD) of VAS anxiety before surgery was 3.1 (2.3), and the mean (SD) of VAS anxiety was 1.21 (0.85). There was a statistically significantly difference of the VAS anxiety mean (SD) before surgery between patients who ALM 3.10 (2.30) and who RLM 6.12 (1.88) (p = 0.005). There was a statistically significantly difference of the VAS anxiety mean (SD) after surgery between patients who ALM 1.21 (0.85) and who RLM 2.62 (1.30) (p = 0.009). Fifty percent of the patients wanted to choose their own music. CONCLUSION: Music seems to reduce anxiety before maxillofacial surgery. An interventional randomized study is needed to demonstrate the positive impact of music on anxiety before maxillofacial surgery.


Asunto(s)
Procedimientos Quirúrgicos Ambulatorios/psicología , Trastornos de Ansiedad/psicología , Trastornos de Ansiedad/terapia , Ansiedad al Tratamiento Odontológico/psicología , Ansiedad al Tratamiento Odontológico/terapia , Musicoterapia , Procedimientos Quirúrgicos Otorrinolaringológicos/psicología , Dolor Postoperatorio/psicología , Dolor Postoperatorio/terapia , Cirugía Bucal/psicología , Adolescente , Adulto , Estudios de Evaluación como Asunto , Humanos , Persona de Mediana Edad , Dimensión del Dolor , Satisfacción del Paciente , Encuestas y Cuestionarios , Adulto Joven
3.
J Appl Physiol (1985) ; 121(1): 343-7, 2016 07 01.
Artículo en Inglés | MEDLINE | ID: mdl-27283916

RESUMEN

Nasal valve collapse is a dynamic abnormality that is currently diagnosed purely on the basis of clinical features and thus subject to certain interpretation. The aim of this study was to develop a new and reliable functional test to objectively characterize nasal valve collapse. This was an observational prospective study including consecutive patients referred to our center for exploration of chronic nasal congestion. The patients were classified into two groups according to their symptoms and clinical abnormalities: the nasal valve collapse (NV+) group when nasal valve collapse was clinically detected during moderate forced inspiration and/or when the feeling of nasal congestion improved during passive nasal lateral cartilage abduction (n = 32); and the no-nasal valve collapse (NV-) group for the others (n = 23). All patients underwent nasal functional tests (posterior rhinomanometry and acoustic rhinometry) before and after topical nasal decongestion. We compared the difference between the pressure flow of the inspiratory and expiratory phases during posterior rhinomanometry [flow rate inspiratory-expiratory difference (FRIED) test] between the two groups. The difference between the absolute value of inspiratory and expiratory flow was significantly higher in the NV+ group than in the NV- group both before and after topical decongestion. The cutoff value for the FRIED test was -0.008 l/s with a good sensitivity (82%) and a specificity of 59%. We suggest that the FRIED test constitutes an objective and easy-to-apply technique to diagnose nasal valve collapse in daily practice.


Asunto(s)
Obstrucción Nasal/fisiopatología , Nariz/fisiología , Adulto , Pruebas Respiratorias/métodos , Espiración/fisiología , Femenino , Humanos , Estudios Longitudinales , Masculino , Presión , Estudios Prospectivos , Rinomanometría/métodos , Sensibilidad y Especificidad
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