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1.
Int J Pediatr Otorhinolaryngol ; 76(2): 272-7, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22177319

RESUMEN

OBJECTIVE: To compare the audiologic outcome and feasibility of bone-anchored hearing aid (BAHA) and external auditory canal reconstruction (EACR) surgeries in pediatric patients presenting a congenital aural atresia (CAA). METHODS: A retrospective chart review of 40 patients operated in our tertiary pediatric care center between 2002 and 2010 was performed. 20 patients underwent EACR, whereas another 20 patients were implanted with a BAHA device. Air conduction (AC), bone conduction (BC), pure tone average (PTA) and speech discrimination score (SDS) were compared preoperatively, and hearing gain (HG) postoperatively at 6 and at 12 months at frequencies of 500, 1000, 2000 and 4000 Hz. Operative time, complications and associated microtia were documented as well. EACR patients were graded retrospectively upon Jahrsdoerfer's classification. RESULTS: Preoperative AC were significantly different between groups, at 500, 1000 and 2000 Hz but not at 4000 Hz. BAHA group compared postoperatively to EACR group showed significantly a superior HG of 46.9 ± 7.0 dB (p<0.001) and of 39.8(7) ± 7.2(6.9)dB (p<0.001) at 6 months and at 1 year, respectively. Moreover, aided air thresholds from the EACR group revealed an audiologic status similar to those of the BAHA group patients, at 6 months and one year postoperatively. Both groups had a similar evolution of their BC, as well as of the incidence of complications. We report one case of transient facial paralysis in the EACR group. Total operative time is significantly lower (p<0.001) for a BAHA implantation (56 ± 21 min) than for EACR surgery (216 ± 174 min). No preoperative or postoperative correlation (Pearson correlation test; p>0.05) was found between patient's Jahrsdoerfer's score and their audiologic outcome. HG does not seem to be influenced by the presence of microtia. CONCLUSION: EACR, although constituting an attractive option, does not give acceptable results alone. It can however, when combined to conventional air conduction hearing aids, provide excellent audiologic outcomes comparable to BAHA. BAHA implantation is a reliable, safe and efficient therapeutic option that allows a significantly better audiologic outcome when compared to unaided EACR for patients with CAA.


Asunto(s)
Conducto Auditivo Externo/anomalías , Conducto Auditivo Externo/cirugía , Audífonos , Procedimientos de Cirugía Plástica/métodos , Implantación de Prótesis/instrumentación , Anclas para Sutura , Adolescente , Audiometría de Tonos Puros , Percepción Auditiva , Conducción Ósea/fisiología , Niño , Preescolar , Estudios de Cohortes , Anomalías Congénitas/diagnóstico , Anomalías Congénitas/cirugía , Microtia Congénita , Oído/anomalías , Oído/cirugía , Estudios de Factibilidad , Femenino , Estudios de Seguimiento , Pérdida Auditiva Conductiva/congénito , Pérdida Auditiva Conductiva/rehabilitación , Pérdida Auditiva Conductiva/cirugía , Pruebas Auditivas , Humanos , Masculino , Implantación de Prótesis/métodos , Estudios Retrospectivos , Medición de Riesgo , Resultado del Tratamiento
2.
Int J Pediatr Otorhinolaryngol ; 76(2): 194-201, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-22154779

RESUMEN

OBJECTIVES: Rigid bronchoscopy (RB) is the principal method used for the extraction of a tracheo-bronchial foreign body (FB), but its use as a diagnostic tool implies a certain rate of negative exams, exposing the child to the risk of procedure and anesthesia-related complications. Technological progress has improved the accuracy and availability of non-invasive modalities, such as CT scan and fluoroscopy. Our aim is to review our experience in the routine use of bronchoscopy for a suspected FB aspiration, and evaluate the adequacy of our current attitude in light of these alternatives. METHODS: We performed a retrospective review of cases where bronchoscopy was used in the management of a suspected airway FB, and analysis of the correlation between the clinical and radiological data and the bronchoscopy's results. In addition we reviewed the literature concerning the use of RB and alternative means of diagnosis such as CT scan, fluoroscopy and flexible bronchoscopy. RESULTS: Thirty-two patients underwent bronchoscopy to rule out a FB aspiration under general anesthesia. No FB was found in 8 cases (25%). Cough and a history of choking were the most sensitive parameters (sensitivity 100% and 80% respectively), but had a low specificity. Stridor was the most specific sign (88% specificity), but was not sensitive. Chest radiography had 25% sensitivity, and 62.5% specificity. Flexible bronchoscopy changed the management in 22% of cases, sparing RB. CONCLUSIONS: Basing the decision to perform RB solely on the clinical findings and chest radiography entails a 25% rate or more of negative exams. CT scan appears to be the most accurate non-invasive tool for ruling out the presence of a FB but its use cannot be systematic due to its complexity and the risks of exposure to radiation. Digital substraction fluoroscopy is a safe and simple mean to confirm the presence of air trapping generated by a bronchial obstruction, but it is not sensitive enough to definitively rule out a FB. We propose a stepwise approach using fluoroscopy or possibly flexible bronchoscopy under sedation, in order to reduce the number of negative RBs while restricting the use of the CT scan.


Asunto(s)
Bronquios , Broncoscopios , Broncoscopía/estadística & datos numéricos , Cuerpos Extraños/diagnóstico , Aspiración Respiratoria/diagnóstico , Adolescente , Niño , Preescolar , Estudios de Cohortes , Diseño de Equipo , Femenino , Cuerpos Extraños/diagnóstico por imagen , Humanos , Lactante , Masculino , Radiografía Torácica , Aspiración Respiratoria/diagnóstico por imagen , Estudios Retrospectivos , Administración de la Seguridad , Tomografía Computarizada por Rayos X/métodos
3.
Arch Otolaryngol Head Neck Surg ; 137(12): 1210-6, 2011 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22183899

RESUMEN

OBJECTIVES: To compare the efficiency of the subannular T-tube (SAT) vs that of the repetitive transtympanic Duravent tube (TTT) in children with recurrent or chronic otitis media (OM) with effusion or tympanic membrane retraction and to establish which population would be more likely to benefit from TTTs vs SATs. DESIGN: Medical record review. SETTING: Tertiary care pediatric center. PATIENTS: Children receiving an SAT (234 in 160 patients) or at least 2 TTTs (216 in 111 patients) between January 1, 2002, and December 31, 2006, to allow at least 4 years of follow-up from that period until 2010. MAIN OUTCOME MEASURES: Average tube duration and complication rates. RESULTS: The tubes remained in place for a median of 35 months with SAT and 7 months with TTT (P < .001). Overall complication rates were lower with SAT (otorrhea, 21.4%; perforation, 7.7%; plugged tube, 13.7%; new acute OM, 13.7%; new serous OM, 5.1%; and cholesteatoma, 1.7%) than with TTT (otorrhea, 26.9%; perforation, 5.1%; blocked tube, 20.8%; new acute OM, 23.1%; new serous OM, 37.5%; and cholesteatoma, 0.46%). Differences were statistically significant for otorrhea, blocked tube, and new acute and serous OM (P < .001). With similar rates, TTTs and SATs were used more frequently in acute (P = .26) and serous (P = .32) OM, whereas SATs were placed more often in adhesive OM and retracted tympanic membrane (P < .001). CONCLUSIONS: Insertion of an SAT is a safe and effective method for long-term middle ear ventilation in recurrent or refractory OM, adhesive OM, and retracted tympanic membrane. Associated with fewer complications, SATs offer an alternative to repeated use of the short-term TTTs without damaging the tympanic membrane.


Asunto(s)
Ventilación del Oído Medio/métodos , Otitis Media con Derrame/cirugía , Otitis Media Supurativa/cirugía , Niño , Preescolar , Femenino , Estudios de Seguimiento , Humanos , Masculino , Complicaciones Posoperatorias/etiología , Complicaciones Posoperatorias/cirugía , Recurrencia , Reoperación , Estudios Retrospectivos
4.
Int J Pediatr Otorhinolaryngol ; 75(4): 527-31, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21257210

RESUMEN

OBJECTIVE: To assess different clinical scales of TM perforation size; to evaluate the effect of the size and the site of a perforation on the hearing level and frequencies. METHODS: Prospective study. Observers had subjectively estimated the size in millimeter and in percentage of a particular perforation; objectively computerized measures of TM perforations area were analyzed. Agreement between different measures was studied. Cases with postoperative intact TM and an air-bone gap (ABG) of 10 dB or less were studied. RESULTS: Global mean preoperative ABG was 21.8 ± 17 dB. Preoperative ABG was different between small-large and small-total perforations (p=0.001). Difference of the preoperative ABG was statistically significant between perforations filling up the four quadrants and perforation limited to one quadrant in the postero-inferior, antero-superior and antero-inferior site. No statistically difference between perforation sites was identified for each affected frequency. Difference is statistically significant (p=0.001) between the 250 Hz and the other frequencies for the medium, large and total perforations. After myringoplasty bone conduction improvement was statistically significant for the frequencies 500 (p=0.04), 1000 (p=0.04) and 2000 Hz (p=0.011). Agreement was large enough when TM perforation size was expressed in percentage and absent when expressed in millimeter. CONCLUSION: TM perforation can be clinically estimated quite precisely as a percentage of the TM area. Conductive hearing loss is frequency dependent; with the greatest loss occurring at the lowest sound frequencies. Hearing loss does not depend on the perforation's location.


Asunto(s)
Audiometría de Tonos Puros/métodos , Conducción Ósea/fisiología , Diagnóstico por Computador/métodos , Miringoplastia/métodos , Perforación de la Membrana Timpánica/diagnóstico , Umbral Auditivo/fisiología , Distribución de Chi-Cuadrado , Estudios de Cohortes , Femenino , Estudios de Seguimiento , Pérdida Auditiva Conductiva/diagnóstico , Pruebas Auditivas/métodos , Humanos , Masculino , Variaciones Dependientes del Observador , Cuidados Posoperatorios/métodos , Estudios Prospectivos , Índice de Severidad de la Enfermedad , Programas Informáticos , Resultado del Tratamiento , Perforación de la Membrana Timpánica/cirugía
6.
J Otolaryngol Head Neck Surg ; 37(5): 616-22, 2008 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-19128665

RESUMEN

OBJECTIVES: To determine whether there is an increase in the incidence of nontuberculous mycobacteria (NTM) adenitis at our tertiary care pediatric hospital and to determine whether there is an association between geographic location and prevalence of cases. Also, to investigate the role of nongeographic risk factors such as bacille Calmette-Guérin (BCG) vaccination in the incidence of NTM adenitis. METHOD: We conducted a retrospective chart review of 153 pediatric patients with NTM adenitis diagnosed between 1994 and 2004 and a prospective telephone survey of geographic and nongeographic risk factors for 82 patients. RESULTS: The annual incidence, calculated with the number of hospitalizations for that year as the denominator, was 25.1 in 100,000 during the 1994-1998 period and 107.4 in 100,000 for 1999-2004. A statistically significant increase in the incidence of NTM adenitis was observed after 1999, with an incidence ratio of 4.28 (95% confidence interval 2.84-6.65; p < .0000). We found a nonsignificant increase in incidence for cases in the suburbs compared with the city. The survey did not reveal any significant risk factors for NTM adenitis in our population. However, none of the affected children had had the BCG vaccination. CONCLUSION: There has been a significant increase in the incidence of NTM adenitis at our tertiary care centre, particularly since 1999. No clear risk factors could be identified to account for this increase, even though geographic location and discontinuation of BCG vaccination could be implicated. More studies are needed to confirm those hypotheses.


Asunto(s)
Linfadenitis/epidemiología , Linfadenitis/microbiología , Infecciones por Mycobacterium no Tuberculosas/epidemiología , Mycobacterium/aislamiento & purificación , Distribución por Edad , Antibacterianos/uso terapéutico , Biopsia con Aguja , Niño , Preescolar , Cara , Femenino , Hospitales Pediátricos , Humanos , Incidencia , Escisión del Ganglio Linfático/métodos , Linfadenitis/terapia , Imagen por Resonancia Magnética , Masculino , Infecciones por Mycobacterium no Tuberculosas/diagnóstico , Infecciones por Mycobacterium no Tuberculosas/terapia , Cuello , Pronóstico , Quebec/epidemiología , Estudios Retrospectivos , Medición de Riesgo , Índice de Severidad de la Enfermedad , Distribución por Sexo , Encuestas y Cuestionarios , Tomografía Computarizada por Rayos X
7.
J Otolaryngol ; 35(4): 216-21, 2006 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17176795

RESUMEN

OBJECTIVE: To determine the impact of a provincial choking prevention program (CPP) on the incidence of aerodigestive foreign body cases among children. METHODS: The CPP, including posters, pamphlets, an informative video, and annual participation in the Parents & Kids Fair, was launched throughout Quebec in October 1999. The incidence rates of aerodigestive foreign body cases prior to implementation (during 1997-1998) and subsequently (2000-2002) within the province and our tertiary care centre (Sainte-Justine Hospital) were compared by estimating incidence rate ratios (IRRs) and associated 95% confidence intervals (95% CIs). RESULTS: No significant changes in the incidence of aerodigestive foreign body cases after program implementation were observed in our hospital (age-adjusted IRR 0.92, 95% CI 0.79-1.07). The provincial rates were higher after program implementation (age-adjusted IRR 1.15, 95% CI 1.05-1.25). CONCLUSIONS: To influence choking prevention habits, modifications to the campaign are required. Strategies are discussed.


Asunto(s)
Obstrucción de las Vías Aéreas/prevención & control , Cuerpos Extraños , Promoción de la Salud/métodos , Obstrucción de las Vías Aéreas/epidemiología , Niño , Protección a la Infancia , Preescolar , Humanos , Incidencia , Lactante , Desarrollo de Programa , Evaluación de Programas y Proyectos de Salud , Quebec/epidemiología
9.
J Otolaryngol ; 34(5): 312-6, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16181592

RESUMEN

OBJECTIVE: To evaluate the efficiency of a subannular tube insertion technique in a group of pediatric patients with adhesive otitis or severe atelectasis of the tympanic membrane. DESIGN: Retrospective nonrandomized case series. SETTING: Tertiary referral centre. MAIN OUTCOME MEASURES: The main outcomes of this study are tube duration according to the type of tube used, the complication rate, and the audiometric gain associated with this procedure. RESULTS: The study group consisted of 190 patients (316 tubes) aged between 3 and 19 years (average 9 years old) and operated on between 1993 and 1999 by four pediatric otolaryngologists. The average follow-up was 53 months. The tubes remained in place for an average of 21.8 months, with fluoroplastic tubes lasting 17.8 months and Goode T tubes lasting 23.8 months. When used in children between 5 and 9 years of age and in cases of adhesive otitis, Goode T tubes showed statistically significantly better results than fluoroplastic tubes. The complications of this technique were otorrhea (17.7%), perforation (7.9%), a plugged tube (7.0%), and cholesteatoma (1.6%). The 5- to 9-year-old group and the reintervention group of patients showed statistically higher complication rates compared with all other groups. Sixty-four patients (128 tubes) were eligible for audiogram analysis, which showed a gain of 13.4 dB (speech reception threshold). CONCLUSIONS: The technique of subannular tube insertion is a safe and effective method for long-term middle ear ventilation in cases of adhesive otitis or severely atelectatic tympanic membrane or for patients with pathology related to dysfunction of the eustachian tube. It offers an alternative to repeated short-term tube insertions for otitis media with effusion or recurrent acute otitis media.


Asunto(s)
Ventilación del Oído Medio/métodos , Otitis Media/cirugía , Membrana Timpánica/cirugía , Adolescente , Adulto , Niño , Preescolar , Colesteatoma del Oído Medio , Enfermedades del Oído/cirugía , Femenino , Humanos , Masculino , Ventilación del Oído Medio/instrumentación , Otoscopía , Complicaciones Posoperatorias , Estudios Retrospectivos , Factores de Tiempo , Resultado del Tratamiento , Perforación de la Membrana Timpánica , Timpanoplastia
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